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US20080299205A1 - Particulate Constructs For Release of Active Agents - Google Patents

Particulate Constructs For Release of Active Agents Download PDF

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Publication number
US20080299205A1
US20080299205A1 US11/632,884 US63288405A US2008299205A1 US 20080299205 A1 US20080299205 A1 US 20080299205A1 US 63288405 A US63288405 A US 63288405A US 2008299205 A1 US2008299205 A1 US 2008299205A1
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US
United States
Prior art keywords
poly
composition
agents
active
hydrophobic
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US11/632,884
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English (en)
Inventor
Lawrence D. Mayer
Robert K. Prud'homme
Christine J. Allen
Walid S. Saad
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Princeton University
Jazz Pharmaceuticals Therapeutics Inc
Original Assignee
Individual
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Priority to US11/632,884 priority Critical patent/US20080299205A1/en
Assigned to THE TRUSTEES OF PRINCETON UNIVERSITY reassignment THE TRUSTEES OF PRINCETON UNIVERSITY ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: SAAD, WALID S., PRUD'HOMME, ROBERT K.
Assigned to CELATOR PHARMACEUTICALS, INC. reassignment CELATOR PHARMACEUTICALS, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: ALLEN, CHRISTINE J., MAYER, LAWRENCE D.
Publication of US20080299205A1 publication Critical patent/US20080299205A1/en
Assigned to DOMAIN PARTNERS VI, L.P., TMP NOMINEE II, LLC, QUAKER BIOVENTURES, L.P., GARDEN STATE LIFE SCIENCES VENTURE FUND, L.P., TMP ASSOCIATES II, L.P., WORKING OPPORTUNITY FUND (EVCC) LTD., THOMAS, MCNERNEY & PARTNERS II, L.P., VENTURES WEST 7 U.S. LIMITED PARTNERSHIP, VENTURES WEST 7 LIMITED PARTNERSHIP, BDC CAPITAL INC. reassignment DOMAIN PARTNERS VI, L.P. SECURITY AGREEMENT Assignors: CELATOR PHARMACEUTICALS, INC.
Assigned to CELATOR PHARMACEUTICALS, INC. reassignment CELATOR PHARMACEUTICALS, INC. RELEASE BY SECURED PARTY (SEE DOCUMENT FOR DETAILS). Assignors: BDC CAPITAL INC., DOMAIN PARTNERS VI, L.P., GARDEN STATE LIFE SCIENCES VENTURE FUND, L.P., QUAKER BIOVENTURES, L.P., THOMAS, MCNERNEY & PARTNERS II, L.P., TMP ASSOCIATES II, L.P., TMP NOMINEE II, LLC, VENTURES WEST 7 LIMITED PARTNERSHIP, VENTURES WEST 7 U.S. LIMITED PARTNERSHIP, WORKING OPPORTUNITY FUND (EVCC) LTD.
Assigned to U.S. BANK NATIONAL ASSOCIATION reassignment U.S. BANK NATIONAL ASSOCIATION SECURITY AGREEMENT Assignors: CAVION, INC., CELATOR PHARMACEUTICALS, INC., JAZZ PHARMACEUTICALS IRELAND LIMITED, Jazz Pharmaceuticals, Inc.
Abandoned legal-status Critical Current

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    • A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
    • A61K9/51—Nanocapsules; Nanoparticles
    • A61K9/5107—Excipients; Inactive ingredients
    • A61K9/513—Organic macromolecular compounds; Dendrimers
    • A61K9/5146—Organic macromolecular compounds; Dendrimers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, polyamines, polyanhydrides
    • A61K9/5153—Polyesters, e.g. poly(lactide-co-glycolide)
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
    • A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B82—NANOTECHNOLOGY
    • B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y5/00—Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/57—Compounds covalently linked to a(n inert) carrier molecule, e.g. conjugates, pro-fragrances

Definitions

  • compositions and methods for improved delivery and performance of active agents relate to compositions and methods for improved delivery and performance of active agents. More particularly, the invention concerns particulate constructs stabilized by an amphiphilic compound and comprising at least one active agent coupled through a linker to a hydrophobic moiety, which agent can be released from the construct by cleavage of the linker.
  • Sustained release is desirable in many applications to provide optimal use and effectiveness of active agents, including pharmaceuticals, cosmetics, food, and fragrances. Attempts have been made to solubilize, target, stabilize, and control the release of substances, including use of microparticles, nanoparticles, and polymer conjugation.
  • Nanoparticulate dimensions may be required in a number of applications, such as drug delivery, in particular to tumors where particulates in the size range ⁇ 200 nm accumulate in tumors whereas larger particles do not. While the art provides many descriptions for preparation of nanoparticles containing active agents, none is completely satisfactory. See, e.g., Mu, L., et al., Journal of Controlled Release (2003) 86:33-48; Fonseca, C., et al., Journal of Controlled Release (2002) 83:273-286.
  • U.S. Pat. Nos. 6,429,200 and 6,673,612 describe reverse micelles for carrying nucleic acids or other actives into cells.
  • U.S. Pat. No. 6,676,963 describes nanoparticulate formulations for targeted drug delivery to tissues and organs.
  • PCT publication WO 02/098465 describes lipid-based vehicles for delivery of pharmaceuticals comprising an internalizing peptide.
  • PCT publication WO 03/028696 describes particulate delivery vehicles for coordinating the release of combinations of drugs. A multiplicity of liposomal formulations have been used for many years to deliver drugs.
  • Chelators for release of platinum-containing antitumor agents are described, for example, by Nishiyama, N., et al., J. Controlled Release (2001) 74:83-94 and by Nishiyama, N., et al, J. Cancer Res. (2003) 63:8977-8983.
  • Drug preparations have been formulated using mixed micellar and emulsion type formulations, including the use of PEG-modified phospholipids to stabilize oil in water emulsions.
  • PEG-modified phospholipids to stabilize oil in water emulsions.
  • U.S. Pat. No. 4,610,868 describes a matrix material having a particle size in the range of 500 nm-100 ⁇ m which is composed of a hydrophobic compound and an amphipathic compound.
  • the resulting “lipid matrix carriers” encapsulate biologically active agents and effect release from the matrix.
  • U.S. Pat. No. 5,869,103 describes particulate compositions in the size range of 10 nm-200 ⁇ m where the particles are formed by combining emulsions of an active agent with mixtures of a biodegradable polymer and a water-soluble polymer.
  • U.S. Pat. No. 5,145,684 describes particulate preparations wherein a crystalline drug substance is itself coated with a surface modifier.
  • U.S. Pat. No. 5,470,583 describes nanoparticles having nonionic surfactants as a surface modifier associated with a charged phospholipid.
  • the biologically active substance itself having a particle size of ⁇ 400 nm, is used as the core of the particles.
  • U.S. Pat. No. 5,891,475 describes drug delivery vehicles which contain hydrophilic cores such as those prepared from polysaccharides.
  • the particles are treated to contain an external layer of fatty acids grafted onto the core by covalent bonds.
  • U.S. Pat. No. 5,188,837 describes microparticles which are generally in the size range of 1-38 ⁇ m which contain a solid hydrophobic polymer as a core and a phospholipid, such as phosphatidyl choline or lecithin as an exterior coating. According to this disclosure, other phospholipids such as phosphatidyl inositol and phosphatidyl glycerol are unworkable in this system.
  • U.S. Pat. No. 5,543,158 discloses 1 nm-1 ⁇ m particles with polymeric cores and a surface layer of PEG, which may be linked covalently to a biologically active agent contained therein.
  • lipocores which are formed from a core of a poorly water-soluble drug surrounded by a PEG-conjugated lipid.
  • Gref, R., et al, Coll and Surf B: Biointerfaces (2000) 18:301-313 describe the nature of protein absorption onto PEG-coated nanoparticles formed from various polymers and copolymers, including polycaprolactone. Although it is recognized that such particles might be useful in pharmaceutical applications, only the particles themselves were studied. Lemoine, D., et al., Biomaterials (1996) 17:2191-2197 reports studies of various nanoparticles composed of, among other polymers, polycaprolactone. While recognizing these as useful in delivery systems, only the particles themselves were studied.
  • Lamprecht, A., et al., Int. J. Pharmaceut . (2000) 196:177-182 reports the study of the effect of the use of microfluidizers on the particle size of nanoparticles obtained using various hydrophobic polymers and copolymers.
  • Particulate constructs for sustained or controlled delivery of active agents is not confined to pharmaceuticals.
  • U.S. Pat. No. 5,928,832 describes latex emulsions containing toner for use in photocopying processes.
  • U.S. Pat. No. 5,766,818 describes latex emulsions containing toner with hydrolyzable surfactants.
  • U.S. patent publication 2004/0221989 describes surfactant compositions designed to decompose so as to reduce viscosity of their surroundings.
  • U.S. 2004/0152913 describes cleavable surfactants for use in MALDI-MS analysis of hydrophobic proteins.
  • U.S. Pat. No. 6,559,243 describes glyoxylic compounds coupled to active ingredients which are released on contact with an aqueous medium.
  • controlled release delivery systems relate to the administration of drug combinations where it is desirable to coordinate the release of such drugs.
  • compositions wherein agents are encapsulated or otherwise associated with particulate delivery vehicles so that the vehicles control the pharmacokinetics and assure coordinated delivery are described in PCT application PCT/CA02/01500 as well as in PCT applications PCT/CA2004/000507 and PCT/CA2004/000508.
  • the formulations of the present invention offer an alternative controlled release mechanism for these drug combinations.
  • the present invention provides particulate constructs that can be adapted to the release of active agents of various types useful in both pharmaceutical and non-pharmaceutical applications. These delivery systems provide high loading capacity for active compounds as well as provide a means for controlled release of the active, reduction in toxicity where relevant, and, if desired, selective delivery to a target site.
  • the active agents may include various therapeutic agents such as platinum agents, taxanes and antibiotics, actives important in other applications such as pigments, dyes, fragrances and flavors, and may be applied in in vivo therapeutic and diagnostic contexts, in agricultural applications and in industrial uses.
  • the invention is directed to a particulate construct comprising an amphiphilic stabilizer
  • n is an integer of 1-100
  • active refers to a compound that has a desired activity
  • linker is a covalent bond, a divalent residue of an organic molecule or a chelator
  • hydrophobic moiety refers to the residue of an organic molecule that is insoluble in aqueous solution.
  • the active may be a fragrance, a pharmaceutical, a diagnostic agent, a toner, or any compound with a desirable activity.
  • a multiplicity of active compounds may be coupled to the same hydrophobic moiety, which may be a hydrophobic polymer with multiple linking sites, or a smaller molecule, such as a vitamin or steroid. More than one type of active agent may also be included, making the constructs particularly useful for combination therapy. In any event, by providing the delivery vehicle in this form, controlled release of the active, either over time or at a desired site, is facilitated.
  • the invention provides a method to deliver active compounds in a controlled manner over time or at a selected target.
  • FIG. 1 provides a depiction of poly (ethylene glycol) based paclitaxel prodrug prepared by the method of Greenwald, et al, J. Med. Chem . (1996) 39:424-431.
  • FIG. 2 provides a depiction of poly (ethylene glycol) based cisplatin complex prepared by the method of Ohya, et al, Polymers for Adv. Tech . (2000) 11:635-641.
  • FIG. 3 provides a depiction of an exemplary delivery vehicle of the present disclosure including a combination of active agents/drugs. Three steps are depicted, including (1) preparation of the polymers, (2) mixture of the polymers and (3) administration of the delivery vehicle.
  • the present invention provides particularly advantageous particulate constructs which are adaptable to the controlled release of a wide variety of active agents.
  • a single active agent may be released from a single particulate construct, or a multiplicity of such agents may be released. This may result from a multiplicity of such actives linked in a single conjugate to a hydrophobic moiety which can support covalent or chelator based linkage to a multiplicity of agents, and/or a multiplicity of such conjugates may be accommodated within a single particulate construct.
  • active agent refers to chemical moieties used in a variety of applications including therapy or diagnosis. Examples are therapeutic agents, imaging agents, diagnostic agents, radionuclides, metal ions, inks, fragrances, viscoelastic agents, flavors, and, indeed, any chemical substance that has a desired behavior or activity.
  • solubility range of the actives ranges from “insoluble” in water or buffer, to those that are “sparingly soluble” or “soluble.”
  • insoluble in aqueous medium means that the substance can be dissolved in an aqueous solution at physiological ionic strength only to the extent of 0.05 mg/ml or less. It is recognized that almost no substances are completely insoluble in aqueous medium, and that the salt concentration or osmolality of the medium may also influence solubility. “Insoluble in aqueous medium,” according to the present definition, assumes the osmolality, ionic strength, and pH of physiologically compatible solutions. Alternatively, “insolubility in pure water” may be used as the standard if so specified. “Insolubility in water” is defined as ⁇ 0.05 mg/ml of pure water.
  • aqueous medium as defined above or in “pure water.”
  • Substances that are “soluble” in aqueous medium dissolve at least to the extent of being equal to or greater than 1.0 mg/ml of the physiological solution; substances that are “sparingly soluble” in aqueous medium dissolve only to the extent of less than 1.0 mg/ml but more than 0.05 mg/ml of the physiological solution.
  • Hydrophobic moiety is defined as a moiety which is insoluble in aqueous solution as defined above.
  • the hydrophobic moiety may be a hydrophobic polymer such as polycaprolactone or may be a hydrophobic small molecule such as a vitamin or a steroid. It may be monovalent—i.e., have a suitable functional group for coupling only to a single active through a linker—or may be multivalent—i.e., able to couple to multiple actives through a linker. Not all of the actives need be the same.
  • an “amphiphilic stabilizer” is a compound having a molecular weight greater than about 500 that has a hydrophilic region and a hydrophobic region. Preferably the molecular weight is greater than about 1,000, or greater than about 1,500, or greater than about 2,000. Higher molecular weight moieties, e.g., 25,000 g/mole or 50,000 g/mole, may be used. “Hydrophobic” is defined as above. “Hydrophilic” in the context of the present invention refers to moieties that have a solubility in aqueous solution (i.e., a physiological solution as defined above) of at least 1.0 mg/ml.
  • aqueous solution i.e., a physiological solution as defined above
  • Typical amphiphilic stabilizers are copolymers of hydrophilic regions and hydrophobic regions.
  • the hydrophobic region if taken alone, would exhibit a solubility in aqueous medium of less than 0.05 mg/ml and the hydrophilic region, if taken alone, would exhibit a solubility in aqueous medium of more than 1 mg/ml.
  • Examples include copolymers of polyethylene glycol and polycaprolactone.
  • a “linker” refers to any covalent bond, to a divalent residue of a molecule, or to a chelator (in the case where the active is a metal ion or organic metallic compound, e.g., cisplatin) that allows the hydrophobic moiety to be attached to the active agent.
  • the linker may be selectively cleavable upon exposure to a predefined stimulus, thus releasing the active agent from the hydrophobic moiety.
  • the site of cleavage in the case of the divalent residue of a molecule may be at a site within the residue, or may occur at either of the bonds that couple the divalent residue to the agent or to the hydrophobic moiety.
  • the predefined stimuli include, for example, pH changes, enzymatic degradation, chemical modification or light exposure.
  • Convenient conjugates are often based on hydrolyzable or enzymatically cleavable bonds such as esters, carbonates, carbamates, disulfides and hydrazones.
  • the conditions under which the active performs its function are not such that the linker is cleaved, but the active is able to perform this function while still attached to the particle.
  • the linker is described as “non-cleavable,” although virtually any linker could be cleaved under some conditions; therefore, “non-cleavable” refers to those linkers that do not necessarily need to release the active from the particle as the active performs its function.
  • the members of the particulate constructs of the invention include: (1) an active agent; (2) a linker; (3) a hydrophobic moiety; and (4) an amphiphilic stabilizer. Examples of each of these follow:
  • the constructs are used to deliver non-pharmaceutical or non-diagnostic agents including but not limited to pigments, inks, pesticides, herbicides, probes (including fluorescent probes), ingredients for sunscreens, fragrances and flavor compounds.
  • the constructs are used to deliver pharmaceuticals or diagnostics in vivo.
  • the active is a therapeutic agent or a diagnostic agent.
  • a wide variety of therapeutic agents can be included. These may be anti-neoplastic agents, anthelmintics agents, antibiotics, anticoagulants, antidepressants, antidiabetic agents, antiepileptics, antihistamines, antihypertensive agents, antimuscarinic agents, antimycobacterial agents, immunosuppressants, antithyroid agents, antiviral agents, anxiolytic sedatives, astringents, beta-adrenoceptor blocking agents, cardiac inotropic agents, contrast media, corticosteroids, cough suppressants, diagnostic agents, diagnostic imaging agents, diuretics, dopaminergics, haemostatics, immunological agents, lipid regulating agents, muscle relaxants, parasympathomimetics, parathyroid calcitonin, biphosphonates, protease inhibitors, prostaglandins, radio-pharmaceuticals, sex hormones, steroids, anti-allergic agents, stimulants, sympathomimetics, thyroid agents, vasodil
  • Anti-neoplastic agent refers to moieties having an effect on the growth, proliferation, invasiveness or survival of neoplastic cells or tumors.
  • Anti-neoplastic therapeutic agents often include disulfide compounds, alkylating agents, antimetabolites, cytotoxic antibiotics, drug resistance modulators and various plant alkaloids and their derivatives. Other anti-neoplastic agents are contemplated.
  • Anti-neoplastic agents include paclitaxel, an etoposide-compound, a camptothecin-compound, idarubicin, carboplatin, oxaliplatin, adriamycin, mitomycin, ansamitocin, bleomycin, cytosine arabinoside, arabinosyl adenine, mercaptopolylysine, vincristine, busulfan, chlorambucil, melphalan, mercaptopurine, mitotane, procarbazine hydrochloride, dactinomycin, mitomycin, plicamycin, aminoglutethimide, estramustine phosphate sodium, flutamide, leuprolide acetate, megestrol acetate, tamoxifen citrate, testolactone, trilostane, amsacrine, asparaginase, interferon, teniposide, vinblastine sulfate, vin
  • Diagnostic agents may also be included as actives. These may comprise, for example, chelated metal ions for MRI imaging, radionuclides, such as 99 Tc or 111 In or other biocompatible radionuclides. These may also be therapeutic agents.
  • the linker component as described above, may be or may include a cleavable bond.
  • the linker may be, for example, cleaved by hydrolysis, reduction reactions, oxidative reactions, pH shifts, photolysis, or combinations thereof; or by an enzyme reaction.
  • Some linkers can be cleaved by an intracellular or extracellular enzyme, or an enzyme resulting from a microbial infection, a skin surface enzyme, or an enzyme secreted by a cell, by an enzyme secreted by a cancer cell, by an enzyme located on the surface of a cancer cell, by an enzyme secreted by a cell associated with a chronic inflammatory disease, by an enzyme secreted by a cell associated with rheumatoid arthritis, by an enzyme secreted by a cell associated with osteoarthritis, or by a membrane-bound enzyme.
  • the linker can be cleaved by an enzyme that is available in a target region.
  • These types of linkers are often useful in that the particular enzyme or class of enzymes may be present in increased concentrations at a target region.
  • the target tissue generally varies based on the type of disease or disorder present in the subject.
  • the linker may also comprise a bond that is cleavable under oxidative or reducing conditions, or may be sensitive to acids.
  • Acid cleavable linkers can be found in U.S. Pat. Nos. 4,569,789 and 4,631,190; and Blattner, et al., Biochemistry (1984) 24:1517-1524. Such linkers are cleaved by natural acidic conditions, or alternatively, acid conditions can be induced at a target site as explained in U.S. Pat. No. 4,171,563.
  • a non-limiting set of molecules that can form acid cleavable bonds include cis-polycarboxylic alkenes (see U.S. Pat. No. 4,631,190), and amino-sulfhydryl cross-linking reagents which are cleavable under mildly acidic conditions (see U.S. Pat. No. 4,569,789).
  • the linker may comprise a time-release bond, such as a biodegradable and/or hydrolyzable bond, such as esters, amides or urethane bonds.
  • linking reagents which contain cleavable disulfide bonds (reducible bonds) include 1,4-di-[3′-(2′-pyridyldithio)propionamido]butane; N-succinimidyl(4-azidophenyl) 1,3′-dithiopropionate; sulfosuccinimidyl (4-azidophenyldithio)propionate; dithiobis(succinimidylpropionate); 3,3′-dithiobis(sulfosuccinimidylpropionate); dimethyl 3,3′-dithiobispropionimidate-2HCl (available from Pierce Chemicals, Rockford, Ill.).
  • oxidation sensitive linking reagents include, without limitation, disuccinimidyl tartarate; and disuccinimidyl tartarate (available from Pierce Chemicals).
  • the linker may also comprise a small molecule such as a peptide linker.
  • the peptide linker is cleavable by base, under reducing conditions, or by a specific enzyme.
  • the linker may be cleaved by an indigenous enzyme, or by an non-indigenous enzyme administered after or in addition to the presently contemplated compositions.
  • a small peptide linker is pH sensitive, for example, the linker may comprise linkers selected from the group consisting of poly L-glycine; poly L-glutamine; and poly L-lysine linkers.
  • the linker may comprise a hydrophobic polymer and a dipeptide, L-alanyl-L-valine (Ala-Val), cleavable by the enzyme thermolysin.
  • This linker is advantageous because thermolysin-like enzyme has been reported to be expressed at the site of many tumors.
  • a linker may also be used that contains a recognition site for the protease furin. Goyal, et al., Biochem. J . (2000) 2:247-254.
  • the chemical and peptide linkers can be bonded between the ligand and the agent by techniques known in the art for conjugate synthesis, i.e., using genetic engineering or chemically.
  • Photocleavable linkers include, for example, 1-2-(nitrophenyl)-ethyl.
  • a photocleavable linker often permits the activation and action of the active agent in a very specific area, for example at a particular part of the target tissue.
  • Activation (light) energy can be localized through a variety of means including catheterization, via natural or surgical openings or via blood vessels.
  • the linkers and techniques for providing coupling of the active to the hydrophobic moiety are similar to those that have been used previously to prepare conjugates to make actives more soluble, in contrast to their application in the present invention.
  • the active is often, but not always, made less soluble in aqueous solution by virtue of forming the conjugate.
  • Greenwald, et al. for attaching PEG to small organic molecules can be adapted to the present invention. Some of these techniques are described in Greenwald, R. B., Journal of Controlled Release (2001) 74:159-171; Greenwald, R. B., et al., Journal of Medicinal Chemistry (1996) 39:424-431; and Greenwald, R.
  • paclitaxel esters have been prepared via conjugation of PEG acids to the ⁇ -position on the paclitaxel molecule. These esters were demonstrated to be an especially effective linking group, as hydrolysis of the ester carbonyl bond and the subsequent release of the attached drug were shown to occur in a predictable fashion in vitro. (Greenwald, R. B., et al., Critical Reviews in Therapeutic Drug Carrier Systems (2000) 17:101-161.)
  • the linker chemistry as applied in the present invention does not enhance solubility, but adapts the active for inclusion in the particulate vehicles of the invention.
  • activated PEGs are based on reactive aryl chlorides, acylating agents and alkylating groups as described by Zalipsky, S., Advanced Drug Delivery Reviews (1995) 16:157-182; and Zalipsky, S., Bioconjugate Chem . (1995) 6:150-165. Tailoring the number of ethylene groups in the linker can additionally be used to adjust the hydrolysis rates of drug-linked ester bonds, to values appropriate for once-a-week administration.
  • Schoenmakers, et al. demonstrated the conjugation of a model paclitaxel molecule to PEG using a hydrolysable linker based on reaction between a thiol and an acrylamide. By changing the length of the linker, the time of drug release was varied between 4 and 14 days.
  • Frerot, et al. prepared a series of carbamoyl esters of maleate and succinate and studied the rate constants for neighboring group assisted alkaline ester hydrolysis. The rates of hydrolysis were found to depend on the structure of the neighboring nucleophile that attacks the ester function.
  • hydrolysis rates may be varied over several orders of magnitude and precursors yielding the desired release profile may be designed.
  • enzymatically cleavable bonds can be used to conjugate active agents to the hydrophobic moiety.
  • An enzymatically cleavable linker generally will comprise amino acids, sugars, nucleic acids, or other compounds which have one or more chemical bonds that can be broken via enzymatic degradation.
  • amino acid spacers were employed for the conjugation of PEG to camptothecin, an anti-tumor drug. Rates of amino acid linker hydrolysis were determined to vary according to the type of amino acid spacer utilized. (Conover, C. D., et al., Anti - Cancer Drug Design (1999) 14:499-506.)
  • Photocleavable linkers have also been extensively employed for the synthesis of conjugates for release of actives.
  • keto-esters have been used as delivery systems for the controlled release of perfumery aldehydes and ketones.
  • Alkyl or aryl ⁇ -keto esters of primary or secondary alcohols decompose upon radiation at 350-370 nm, releasing the active aldehyde.
  • This mechanism has been shown to successfully sustain release of the active agent.
  • light energy can be localized through a variety of means including catheterization, via natural and surgical openings or via blood vessels.
  • the cleavage “of the linker” may be either within the residue itself, or it may be at one of the bonds that couples the linker to the remainder of the conjugate—i.e., either to the active or the hydrophobic moiety.
  • the linker it is unnecessary for the linker to be cleavable.
  • the active is functional while still coupled to the linker, there is no need to release the active from the particulate moiety.
  • the active is printer's ink, which can remain in particulate form when employed.
  • linker need not be cleavable
  • alternative organic moieties may be used to create the divalent residue, or a covalent bond directly coupling the active to the hydrophobic moiety may not be subject to cleavage under conditions contemplated in use.
  • non-cleavable linkers comprise, but are not limited to, (sulfosuccinimidyl 6-[alpha-methyl-alpha-(2-pyridylthio)toluamido]hexanoate; Azidobenzoyl hydrazide; N-Hydroxysuccinimidyl-4-azidosalicyclic acid; Sulfosuccinimidyl 2-(p-azidosalicylamido)ethyl-1,3-dithiopropionate; N- ⁇ 4-(p-azidosalicylamido) buthy ⁇ -3′(2′-pyidyldithio)propionamide; Bis-[beta-(4-azidosalicylamido)ethyl]disulfide; N-hydroxys
  • a third component of the constructs of the invention is a hydrophobic moiety.
  • the hydrophobic moiety may include polymers or natural products.
  • suitable hydrophobic polymeric moieties include but are not limited to polymers of the following: acrylates including methyl acrylate, ethyl acrylate, propyl acrylate, n-butyl acrylate (BA), isobutyl acrylate, 2-ethyl acrylate, and t-butyl acrylate; methacrylates including ethyl methacrylate, n-butyl methacrylate, and isobutyl methacrylate; acrylonitriles; methacrylonitrile; vinyls including vinyl acetate, vinylversatate, vinylpropionate, vinylformamide, vinylacetamide, vinylpyridines, and vinylimidazole; aminoalkyls including aminoalkylacrylates, aminoalkylmethacrylates, and aminoalkyl(meth)acrylamides; sty
  • hydrophobic peptide-based polymers and copolymers based on poly(L-amino acids) Lavasanifar, A., et al., Advanced Drug Delivery Reviews (2002) 54:169-190
  • EVA poly(ethylene-vinyl acetate)
  • silicone rubber polyethylene, polypropylene, polydienes (polybutadiene, polyisoprene and hydrogenated forms of these polymers
  • maleic anhydride copolymers of vinyl-methylether and other vinyl ethers polyamides (nylon 6,6), polyurethane, poly(ester urethanes), poly(ether urethanes), poly(ester-urea).
  • Particularly preferred polymeric hydrophobes include poly(ethylenevinyl acetate), poly (D,L-lactic acid) oligomers and polymers, poly (L-lactic acid) oligomers and polymers, poly (glycolic acid), copolymers of lactic acid and glycolic acid, poly (caprolactone), poly (valerolactone), polyanhydrides, copolymers of poly (caprolactone) or poly (lactic acid)
  • particularly preferred polymeric carriers include polystyrene, polyacrylates, and butadienes. The polymers must contain one or more functionizable groups which may be incorporated into the polymer by derivitization or may be inherent in the polymer chemistry.
  • Polymers as hydrophobic moieties should have molecular weights between 800 and 200,000.
  • the preferred range is 1,000 to 10,000 for polymers with mono or divalent functional sites.
  • the preferred molecular weight of the polymer per conjugated active is 1,000 to 10,000.
  • Natural products with functional groups or groups that can be converted to functional groups for conjugation include: hydrophobic vitamins (for example vitamin E, vitamins K and A), carotenoids and retinols(for example beta carotene, astaxanthin, trans and cis retinal, retinoic acid, folic acid, dihydrofolate, retinyl acetate, retinyl palmitate), cholecalciferol, calcitriol, hydroxycholecalciferol, ergocalciferol, ⁇ -tocopherol, ⁇ -tocopherol acetate, ⁇ -tocopherol nicotinate, and estradiol.
  • the preferred natural product is vitamin E which can be readily obtained as a vitamin E succinate, which facilitates functionalization to amines and hydroxyls on the active species.
  • Hydrophobic, non polymeric and moieties include hydrocarbon molecules with solubilities less than 0.1 mg/ml that contain a functional group for can be derivatized to incorporate a functional group for conjugation.
  • Molecules in this class include hydrophobic dyes and plasticizers. Examples include, but are not limited to, coumarin, diaminonaphthalene and other naphthalene derivatives, anthracene and its derivatives, nile red. Further examples can be found in Handbook of Dyes and pH Indicators .
  • hydrophobic plasticizes include dioctylphthalate, dibutylphthalate, and its derivatives.
  • hydrophobic moiety may be able to accommodate more than one, including substantially more than one active through a multiplicity of linking sites.
  • Polymeric moieties may have as many as 100 sites whereby actives could be linked.
  • Simpler hydrophobic moieties, such as Vitamin E, may provide only one such site.
  • the number of actives coupled to a single hydrophobic moiety may be only 1, or may be 2, 5, 10, 25, 100 and more, and all integers in between.
  • the polymers set forth above can readily be provided with a multiplicity of functional groups for coupling to the active.
  • Difunctional hydrophobic moieties would include the hydrophobic polymer chains listed above that have two terminal OH, COOH, or NH 2 groups.
  • Multifunctional hydrophobic moieties include all of those listed above that have multiple OH, COOH, or NH 2 groups on some or all of the monomer units on the polymer backbone. These functional groups are merely illustrative; other moieties which could form functional groups for linking include phenyl substituents, halo groups, and the like. Typically, when the hydrophobic moiety is a hydrophobic polymer, it may have multiple sites for linkage. When the hydrophobic moiety is a relatively small molecule, it will accommodate only the number of linkers for which it has available functional groups.
  • the fourth component is an amphiphilic stabilizer.
  • the stabilizer is a copolymer of a hydrophilic block coupled with a hydrophobic block.
  • Nanoparticles formed by the process of this invention can be formed with graft, block or random amphiphilic copolymers. These copolymers can have a molecular weight between 1,000 g/mole and 50,000 g/mole or more, or between about 3,000 g/mole to about 25,000 g/mole, or at least 2,000 g/mole.
  • the amphiphilic copolymers used in this invention exhibit a water surface tension of at least 50 dynes/cm 2 at a concentration of 0.1 wt %.
  • suitable hydrophobic blocks in an amphiphilic copolymer include but are not limited to the following: acrylates including methyl acrylate, ethyl acrylate, propyl acrylate, n-butyl acrylate (BA), isobutyl acrylate, 2-ethyl acrylate, and t-butyl acrylate; methacrylates including ethyl methacrylate, n-butyl methacrylate, and isobutyl methacrylate; acrylonitriles; methacrylonitrile; vinyls including vinyl acetate, vinylversatate, vinylpropionate, vinylformamide, vinylacetamide, vinylpyridines, and vinylimidazole; aminoalkyls including aminoalkylacrylates, aminoalkylmethacrylates, and aminoalkyl(meth)acrylamides; styrenes; cellulose acetate phthalate, cellulose acetate succinate, hydroxypropylmethylcellulose phthalate, poly(
  • hydrophobic peptide-based polymers and copolymers based on poly(L-amino acids) Lavasanifar, A., et al., Advanced Drug Delivery Reviews (2002) 54:169-190
  • EVA poly(ethylene-vinyl acetate)
  • silicone rubber polyethylene, polypropylene, polydienes (polybutadiene, polyisoprene and hydrogenated forms of these polymers
  • maleic anhydride copolymers of vinyl methylether and other vinyl ethers polyamides (nylon 6,6), polyurethane, poly(ester urethanes), poly(ether urethanes), poly(ester-urea).
  • Particularly preferred polymeric blocks include poly(ethylenevinyl acetate), poly (D,L-lactic acid) oligomers and polymers, poly (L-lactic acid) oligomers and polymers, poly (glycolic acid), copolymers of lactic acid and glycolic acid, poly (caprolactone), poly (valerolactone), polyanhydrides, copolymers of poly (caprolactone) or poly (lactic acid)
  • particularly preferred polymeric blocks include polystyrene, polyacrylates, and butadienes.
  • suitable hydrophilic blocks in an amphiphilic copolymer include but are not limited to the following: carboxylic acids including acrylic acid, methacrylic acid, itaconic acid, and maleic acid; polyoxyethylenes or poly ethylene oxide; polyacrylamides and copolymers thereof with dimethylaminoethylmethacrylate, diallyldimethylammonium chloride, vinylbenzylthrimethylammonium chloride, acrylic acid, methacrylic acid, 2-acrylamido-2-methylpropane sulfonic acid and styrene sulfonate, polyvinyl pyrrolidone, starches and starch derivatives, dextran and dextran derivatives; polypeptides, such as polylysines, polyarginines, polyglutamic acids; poly hyaluronic acids, alginic acids, polylactides, polyethyleneimines, polyionenes, polyacrylic acids, and polyiminocarboxylates, gelatin, and uns
  • block copolymers for this invention include blocks of polystyrene, polyethylene, polybutyl acrylate, polybutyl methacrylate, polylactic acid, polycaprolactone, polyacrylic acid, polyoxyethylene and polyacrylamide
  • block copolymers for this invention include blocks of polystyrene, polyethylene, polybutyl acrylate, polybutyl methacrylate, polylactic acid, polycaprolactone, polyacrylic acid, polyoxyethylene and polyacrylamide
  • the length of a grafted moiety can vary.
  • the grafted segments are alkyl chains of 12 to 32 carbons or equivalent to 6 to 16 ethylene units in length.
  • the grafting of the polymer backbone can be useful to enhance solvation or nanoparticle stabilization properties.
  • a grafted butyl group on the hydrophobic backbone of a diblock copolymer of a polyethylene and polyethylene glycol should increases the solubility of the polyethylene block.
  • Suitable chemical moieties grafted to the block unit of the copolymer comprise alkyl chains containing species such as amides, imides, phenyl, carboxy, aldehyde or alcohol groups.
  • a commercially available stabilizer is the Hypermer family marketed by Uniqema Co.
  • the amphiphilic stabilizer could also be of the gelatin family such as the gelatins derived from animal or fish collagen.
  • Nano Precipitation a process termed “Nano Precipitation” as described by Johnson, B. K., et al., AIChE Journal (2003) 49:2264-2282 and U.S. 2004/0091546 incorporated herein by reference. This process is capable of producing controlled size, polymer-stabilized and protected nanoparticles of hydrophobic organics at high loadings and yields.
  • the Nano Precipitation technique is based on amphiphilic diblock copolymer arrested nucleation and growth of hydrophobic organics. Amphiphilic diblock copolymers dissolved in a good solvent can form micelles when the solvent quality for one block is decreased.
  • a tangential flow mixing cell (vortex mixer) is used.
  • the vortex mixer consists of a confined volume chamber where one jet stream containing the diblock copolymer and active agent dissolved in a water-miscible solvent is mixed at high velocity with another jet stream containing water, an anti-solvent for the active agent and the hydrophobic block of the copolymer.
  • the fast mixing and high energy dissipation involved in this process provide timescales that are shorter than the timescale for nucleation and growth of particles, which leads to the formation of nanoparticles with active agent loading contents and size distributions not provided by other technologies.
  • Nano Precipitation When forming the nanoparticles via Nano Precipitation, mixing occurs fast enough to allow high supersaturation levels of all components to be reached prior to the onset of aggregation. Therefore, the active agent(s) and polymers precipitate simultaneously, and overcome the limitations of low active agent incorporations and aggregation found with the widely used techniques based on slow solvent exchange (e.g., dialysis).
  • the Nano Precipitation process is insensitive to the chemical specificity of the components, making it a universal nanoparticle formation technique.
  • the active agent conjugated polymer and stabilizing diblock copolymer of methoxy poly(ethylene glycol)-b-poly( ⁇ -caprolactone) (mPEG-PCL, 5,000-2,900 g/mole, respectively)
  • THF time to make a 0.3 wt % solution for each component.
  • the resulting solution is loaded into a 100 ml gas tight syringe, which is fixed on a digitally controlled syringe pump.
  • a 300 mM sucrose solution is prepared, loaded into a 100 ml gas tight syringe, and fixed on a second syringe pump.
  • the syringes are connected to the vortex mixer inlet, and pumped through at flow rates of 12 and 120 ml/min for the active agent and the sucrose solution, respectively.
  • the mixer outlet two samples are collected.
  • the first sample is collected in a scintillation vial and analyzed for particle size by dynamic light scattering (DLS), and the second sample is collected in low temperature freezer vials, and freeze-dried.
  • the freeze-drying cycle is the following: ⁇ 40° C. overnight, ⁇ 10° C. for a day, 4° C. for a day, and then room temperature for one day.
  • DLS measurements are repeated at 1, 2, 8, 16 hours, and daily intervals for each sample to check for stability.
  • the samples are checked visually for crystals/aggregates formation.
  • the freeze-dried material are checked for the presence of any residual solvent (THF).
  • a freeze-dried sample is dissolved in methanol to dissociate the nanoparticles, and the solution is tested for the presence of THF
  • Milling involves precipitating the conjugated active species into a particulate form with a macroscopically large particle size. The precipitate is then pulverized by mechanical means in the presence of a grinding media and a stabilizing polymer or surface active agent. The process is described in U.S. Pat. Nos. 4,726,955; 5,518,738 and 5,145,684).
  • One conventional emulsification method of microencapsulating an agent to form a microencapsulated product is disclosed in U.S. Pat. No. 5,407,609. This method involves dissolving or otherwise dispersing agents, liquids or solids, in a solvent containing dissolved wall-forming materials, dispersing the agent/polymer-solvent mixture into a processing medium to form an emulsion and transferring all of the emulsion immediately to a large volume of processing medium or other suitable extraction medium, to immediately extract the solvent from the microdroplets in the emulsion to form a microencapsulated product, such as microcapsules or microspheres.
  • the most common method used for preparing polymer delivery vehicle formulations is the solvent emulsification-evaporation method.
  • This method involves dissolving the polymer and drug in an organic solvent that is completely immiscible with water (for example, dichloromethane).
  • the organic mixture is added to water containing a stabilizer, most often poly(vinyl alcohol) (PVA) and then typically sonicated.
  • PVA poly(vinyl alcohol)
  • the particulate construct that results may contain one or more than one of the conjugates described.
  • a nanoparticulate size construct will comprise 10 3 -10 4 conjugates; larger microparticles might comprise 10 5 -10 7 conjugates.
  • the resulting particles may have a variety of sizes depending on the nature of the components and on the method used to form them. Typically, the particles range in size from 50 nm to as much as 5 ⁇ m. For in vivo applications, nanometer size particles, typically of the order of 200 nm or less are preferred. For other applications, larger particles may be desirable. Thus, the dimensions of the particles may range from as little as 50 nm to 100 nm, 200 nm, 500 nm, 1 ⁇ m or 5 ⁇ m and the integers between.
  • a composition of these constructs may contain a variety of sizes and can be described in terms of an average or median diameter.
  • particulate constructs After the particulate constructs are formed, they may be assessed for active agent loading content, size, and in vitro active agent release. Methods are available to assess the degree of polymer-active interaction or compatibility, including DSC, powder X-ray diffraction, and FTIR.
  • paclitaxel encapsulated in nanoparticles is assessed as follows. A sample of the freeze-dried material is weighed and dissolved in THF to solubilize the particles, then the sample is placed in a semi-micro spectrophotometer cell, and the paclitaxel concentration is determined using a UV spectrophotometer at 261 nm. In addition, the absorbance is measured at 350 nm, and polymer only solutions is run at 261 nm as controls.
  • UV analysis results obtained by UV analysis are confirmed using high performance liquid chromatography (HPLC) with a C18 column, methanol and water as mobile phases ranging from 10 to 100% methanol by volume, at a flow rate of 1 ml/min and 261 nm detection wavelength.
  • HPLC high performance liquid chromatography
  • the amount of cisplatin encapsulated in the nanoparticles is determined using atomic absorption spectrometry.
  • Particle size may be determined by DLS. For example, in one illustration, measurements are performed using an Nd-YAG laser with a 532 nm wavelength at a scattering angle of 90°. The sample collected in a scintillation vial from the mixer effluent is inserted into the DLS sample cell containing decalin scintillation fluid (maintained at 25° C. using a temperature bath), and left to equilibrate to the cell temperature. The run duration is 60 seconds, replicated three times. The particle size expressed as the hydrodynamic diameter is obtained using an ALV 5000 correlator and a second order cumulant fit.
  • In vitro release can also be measured.
  • 10 mM phosphate, 150 mM NaCl buffer solution is prepared, and active agent nanoparticles are suspended in 2 ml of the buffer solution to form a 1 mg/ml to a 5 mg/ml solution.
  • the solution is introduced into a 12-14K dialysis membrane bag, and placed in 1 liter of the buffer solution at room temperature. 0.05 ml aliquots are collected from the dialysis bag and 1 ml of THF is added to dissociate the nanoparticles.
  • the resulting solution is placed in semi-micro spectrophotometer cells, and the paclitaxel concentration is determined using a UV spectrophotometer at 261 nm.
  • the absorbance is measured at 350 nm, and polymer only solutions is run at 261 nm as controls.
  • the cisplatin amounts are determined using atomic absorption spectrometry. The measurements are repeated at intervals of 1, 2, 4, 8, 16, 24, 48, and 72 hours.
  • the physical state of the active agent can also be studied by DSC. DSC thermograms of pure active agent, empty polymer nanoparticles or films and active agent-loaded polymer nanoparticles or films are recorded. The concentration of active agent ranges from 10-75% (w/w). The values for the heat of melting ( ⁇ H m , J/g of active agent) of the active agent at each active agent concentration are recorded and a plot of ⁇ H m versus concentration is prepared.
  • the solid-state solubility (saturation solubility) of the active agents in the nanoparticles or films is determined by the y-intercept of the plot (Puttipipatkhachorn, et al., J. Controlled Release (2001) 10:75(1-2):143-153). Below the solid-state solubility the active agent is in a dissolved state while above that it exists in both a dissolved state and a crystalline state.
  • the solid-state solubility of the active agent is dependent on the molecular weight of the polymer. The higher the molecular weight of the polymer, the greater the microviscosity of the medium and the more difficult it is for the active agent to crystallize. Therefore, an increase in polymer molecular weight should act to increase the saturation solubility of an active agent.
  • the active agent may act as a plasticizer causing a decrease in the T g of the polymer or as a reinforcing filler resulting in an increase in the T g of the polymer.
  • the criterion for polymer-active agent miscibility often comprises the presence of a single concentration dependent T g lying between the T g 's of the individual components.
  • the miscibility of the polymer blends is frequently assessed using DSC.
  • the DSC thermograms of each polymer and the polymer blend are recorded.
  • the glass transition temperatures (T g ) of each component alone is compared to the T g value(s) in the polymer blends.
  • the criterion for polymer-polymer miscibility is the same as that set out above for polymer-active agent miscibility.
  • the state of the active agent in polymer films or nanoparticles may be determined from diffractograms obtained from Powder X-ray diffraction (PXRD) patterns of the pure active agent, physical mixtures and the active agent-polymer blends.
  • PXRD Powder X-ray diffraction
  • Polymer-active agent interactions may be measured using FTIR spectroscopy.
  • FTIR spectroscopy The transmission infrared spectra of pure active agent, physical mixtures of pure active agent and polymer as well as films of the active agent-polymer blends are obtained. Interactions in the blend will result in band shifts and broadening in the FTIR spectrum when compared to the spectra for the pure polymer and active agent.
  • the particulate constructs are formulated into suitable veterinary or pharmaceutical compositions and administered to subjects as appropriate.
  • the subjects include warm-blooded animals, including humans, domestic avian species, fish and the like.
  • a qualified physician will determine how the compositions of the present invention should be utilized with respect to dose, schedule and route of administration using established protocols.
  • Such applications also frequently utilize dose escalation should agents encapsulated in delivery vehicle compositions of the present invention exhibit reduced toxicity to healthy tissues of the subject.
  • compositions of the present invention may be administered parenterally, i.e., intraarterially, intravenously, intraperitoneally, subcutaneously, or intramuscularly, the pharmaceutical compositions are administered, e.g., by a bolus or infusional injection.
  • parenterally i.e., intraarterially, intravenously, intraperitoneally, subcutaneously, or intramuscularly
  • the pharmaceutical compositions are administered, e.g., by a bolus or infusional injection.
  • a bolus or infusional injection e.g., by a bolus or infusional injection.
  • the formulations of the invention can be contacted with target tissue by direct application of the preparation to the tissue.
  • the application may be made by “topical”, “open” or “closed” procedures.
  • topical it is meant the direct application of the multi-active agent preparation to a tissue exposed to the environment, such as the skin, oropharynx, external auditory canal, and the like.
  • Open procedures are those procedures that include incising the skin of a patient and directly visualizing the underlying tissue to which the pharmaceutical preparations are applied. This is generally accomplished by a surgical procedure, such as a thoracotomy to access the lungs, abdominal laparotomy to access abdominal viscera, or other direct surgical approach to the target tissue.
  • “Closed” procedures are invasive procedures in which the internal target tissues are not directly visualized, but accessed via inserting instruments through small wounds in the skin.
  • the preparations may be administered to the peritoneum by needle lavage.
  • the preparations may be administered through endoscopic devices, pumping devices, stents, wafers, reservoirs, pastes or films.
  • compositions comprising delivery vehicles of the invention are prepared according to standard techniques and may comprise water, buffered water, 0.9% saline, 0.3% glycine, 5% dextrose, iso-osmotic sucrose solutions and the like, including glycoproteins for enhanced stability, such as albumin, lipoprotein, globulin, and the like. These compositions may be sterilized by conventional, well-known sterilization techniques. The resulting aqueous solutions may be packaged for use or filtered under aseptic conditions and lyophilized, the lyophilized preparation being combined with a sterile aqueous solution prior to administration.
  • compositions may contain pharmaceutically acceptable auxiliary substances as required to approximate physiological conditions, such as pH adjusting and buffering agents, tonicity adjusting agents and the like, for example, sodium acetate, sodium lactate, sodium chloride, potassium chloride, calcium chloride, and the like.
  • auxiliary substances such as pH adjusting and buffering agents, tonicity adjusting agents and the like, for example, sodium acetate, sodium lactate, sodium chloride, potassium chloride, calcium chloride, and the like.
  • the formulation similar to those above may also be applied for cosmetic purposes and the excipients modified accordingly.
  • a particularly significant application of the present techniques is its use to deliver combinations of therapeutic agents, including multidrug resistance modulators, and imaging agents.
  • biologically active combinations are used, the pharmacokinetics of the delivery are controlled by the particulate constructs used to deliver them and the nature of the cleavable linkers employed. Coordination of delivery of such agents to target tissues or organs is assured by suitable control of these parameters. It is particularly advantageous to deliver such agents in a ratio that is non-antagonistic, and especially that is non-antagonistic over a wide range of concentrations.
  • algorithms are available such that based on the results of in vitro tests, such non-antagonistic ratios may be determined.
  • coordinated delivery of the specified ratio may be effected by including more than a single active in a particulate construct, or separate particulate constructs may be used. In the present case, if separate constructs are employed, the pharmacokinetics and release mechanisms of each construct are engineered to provide the desired ratio maintenance.
  • D is the dose of the active agent used
  • f a is the fraction of cells affected by that dose
  • D m is the dose for median effect signifying the potency
  • m is a coefficient representing the shape of the dose-effect curve (m is 1 for first order reactions).
  • This equation can be further manipulated to calculate a combination index (CI) on the basis of the multiple active agent effect equation as described by Chou and Talalay, Adv. Enzyme Reg . (1984) 22:27-55; and by Chou, et al., in: Synergism and Antagonism in Chemotherapy (1991)223-244, Chou and Rideout, eds., Academic Press: New York.
  • CI combination index
  • a two-active agent combination may be further used as a single pharmaceutical unit to determine synergistic or additive interactions with a third agent.
  • a three-agent combination may be used as a unit to determine non-antagonistic interactions with a fourth agent, and so on.
  • the underlying experimental data are generally determined in vitro using cells in culture or cell-free systems.
  • the combination index (CI) is plotted as a function of the fraction of cells affected (f a ) as shown in FIG. 1A which, as explained above, is a surrogate parameter for concentration range.
  • Preferred combinations of agents are those that display synergy or additivity over a substantial range of f a values.
  • Combinations of agents are selected that display synergy over at least 5% of the concentration range wherein greater than 1% of the cells are affected, i.e., an f a range greater than 0.01.
  • a larger portion of overall concentration exhibits a favorable CI; for example, 5% of an f a range of 0.2-1.0.
  • f a range More preferably 10% of this range exhibits a favorable CI. Even more preferably, 20% of the f a range, preferably over 50% and most preferably over at least 70% of the f a range of 0.2 to 1.0 are utilized in the compositions. Combinations that display synergy over a substantial range of f a values may be re-evaluated at a variety of agent ratios to define the optimal ratio to enhance the strength of the non-antagonistic interaction and increase the f a range over which synergy is observed.
  • the optimal combination ratio may be further used as a single pharmaceutical unit to determine synergistic or additive interactions with a third agent.
  • a three-agent combination may be used as a unit to determine non-antagonistic interactions with a fourth agent, and so on.
  • the combination of agents is utilized in anti-neoplastic therapy.
  • the combination of agents is intended for leukemia or lymphoma therapy.
  • Appropriate choices will then be made of the cells to be tested and the nature of the test.
  • tumor cell lines are suitable subjects and measurement of cell death or cell stasis is an appropriate end point.
  • other target cells and criteria other than cytotoxicity or cell stasis could be employed.
  • cell lines may be obtained from standard cell line repositories (NCI or ATCC for example), from academic institutions or other organizations including commercial sources. Preferred cell lines would include one or more selected from cell lines identified by the Developmental Therapeutics Program of the NCI/NIH.
  • the tumor cell line screen used by this program currently identifies 60 different tumor cell lines representing leukemia, melanoma, and cancers of the lung, colon, brain, ovary, breast, prostate and kidney.
  • the required non-antagonistic effect over a desired concentration range need be shown only on a single cell type; however, it is preferred that at least two cell lines exhibit this effect, more preferably three cell lines, more preferably five cell lines, and more preferably 10 cell lines.
  • the cell lines may be established tumor cell lines or primary cultures obtained from patient samples.
  • the cell lines may be from any species but the preferred source will be mammalian and in particular human.
  • the cell lines may be genetically altered by selection under various laboratory conditions, and/or by the addition or deletion of exogenous genetic material.
  • Cell lines may be transfected by any gene-transfer technique, including but not limited to, viral or plasmid-based transfection methods. The modifications may include the transfer of cDNA encoding the expression of a specific protein or peptide, a regulatory element such as a promoter or enhancer sequence or antisense DNA or RNA.
  • tissue culture cell lines may include lines with and without tumor suppressor genes, that is, genes such as p53, pTEN and p16; and lines created through the use of dominant negative methods, gene insertion methods and other selection methods.
  • Preferred tissue culture cell lines that may be used to quantify cell viability, e.g., to test antitumor agents include, but are not limited to, P388, L1210, HL-60, MOLT-4, KBM-3, WeHi-3, H460, MCF-7, SF-268, HT29, HCT-116, LS180, B16-F10, A549, Capan-1, CAOV-3, IGROV1, PC-3, MX-1 and MDA-MB-231.
  • the given effect (f a ) refers to cell death or cell stasis after application of a cytotoxic agent to a cell culture.
  • Cell death or viability may be measured using known techniques.
  • a non-limiting set of examples comprise the following: “Signal transduction inhibitors” which interfere with or prevents signals that cause cancer cells to grow or divide; “Cytotoxic agents”; “Cell cycle inhibitors” or “cell cycle control inhibitors” which interfere with the progress of a cell through its normal cell cycle, the life span of a cell, from the mitosis that gives it origin to the events following mitosis that divides it into daughter cells; “Checkpoint inhibitors” which interfere with the normal function of cell cycle checkpoints, e.g., the S/G2 checkpoint, G2/M checkpoint and G1/S checkpoint; “Topoisomerase inhibitors”, such as camptothecins, which interfere with topoisomerase I or II activity, enzymes necessary for DNA replication and transcription; “Receptor tyrosine kinase inhibitors” which interfere with the activity of growth factor receptors that
  • Especially preferred combinations for treatment of tumors are the clinically approved combinations set forth hereinabove. As these combinations have already been approved for use in humans, reformulation to assure appropriate delivery is especially important.
  • Preferred agents that may be used in combination include DNA damaging agents such as carboplatin, cisplatin, cyclophosphamide, doxorubicin, daunorubicin, epirubicin, mitomycin C, mitoxantrone; DNA repair inhibitors including 5-fluorouracil (5-FU) or FUDR, gemcitabine and methotrexate; topoisomerase I inhibitors such as camptothecin, irinotecan and topotecan; S/G2 or G2/M checkpoint inhibitors such as bleomycin, docetaxel, doxorubicin, etoposide, paclitaxel, vinblastine, vincristine, vindesine and vinorelbine; G1/early-S checkpoint inhibitors; G2/M checkpoint inhibitors; receptor tyrosine kinase inhibitors such as genistein, trastuzumab, ZD1839; cytotoxic agents; apoptosis-inducing agents and
  • the mechanism of action of one or more of the agents may not be known or may be incorrectly identified. All synergistic or additive combinations of agents are within the scope of the present invention.
  • combinations that inhibit more than one mechanism that leads to uncontrolled cell proliferation are chosen for use in accordance with this invention.
  • the present invention includes selecting combinations that effect specific points within the cell cycle thereby resulting in non-antagonistic effects.
  • active agents that cause DNA damage can be paired with those that inhibit DNA repair, such as anti-metabolites.
  • the present invention also includes selecting combinations that block multiple pathways that would otherwise result in cell proliferation.
  • DNA damaging agents in combination with DNA repair inhibitors DNA damaging agents in combination with topoisomerase I or topoisomerase II inhibitors, topoisomerase I inhibitors in combination with S/G2 or G2/M checkpoint inhibitors, G1/S checkpoint inhibitors or CDK inhibitors in combination with G2/M checkpoint inhibitors, receptor tyrosine kinase inhibitors in combination with cytotoxic agents, apoptosis-inducing agents in combination with cytotoxic agents, apoptosis-inducing agents in combination with cell-cycle control inhibitors, G1/S or G2/M checkpoint inhibitors in combination with cytotoxic agents, topoisomerase I or II inhibitors in combination with DNA repair inhibitors, topoisomerase I or II inhibitors or telomerase inhibitors in combination with cell cycle control inhibitors, topoisomerase I inhibitors in combination with topoisomerase II inhibitors, and two cytotoxic agents in combination.
  • agents that may be used in combination include cisplatin (or carboplatin) and 5-FU (or FUDR), cisplatin (or carboplatin) and irinotecan, irinotecan and 5-FU (or FUDR), vinorelbine and cisplatin (or carboplatin), methotrexate and 5-FU (or FUDR), idarubicin and araC, cisplatin (or carboplatin) and taxol, cisplatin (or carboplatin) and etoposide, cisplatin (or carboplatin) and topotecan, cisplatin (or carboplatin) and daunorubicin, cisplatin (or carboplatin) and doxorubicin, cisplatin (or carboplatin) and gemcitabine, oxaliplatin and 5-FU (or FUDR), gemcitabine and 5-FU (or FUDR), adriamycin and vin
  • Preferred combinations in general include those set forth hereinabove as already shown to be efficacious in the clinic as recognized by the FDA and those further suggested based on literature reports. While the candidate agents for use in the method of the invention are not limited to these specific combinations, those set forth hereinabove have been disclosed as suitable combination therapies, and are thus preferred for use in the methods and compositions of the present invention.
  • kits which include, in separate containers, a first composition comprising delivery vehicles stably associated with at least a first therapeutic agent and, in a second container, a second composition comprising delivery vehicles stably associated with at least one second therapeutic agent. The containers can then be packaged into the kit.
  • the kit will also include instructions as to the mode of administration of the compositions to a subject, at least including a description of the ratio of amounts of each composition to be administered.
  • the kit is constructed so that the amounts of compositions in each container is pre-measured so that the contents of one container in combination with the contents of the other represent the correct ratio.
  • the containers may be marked with a measuring scale permitting dispensation of appropriate amounts according to the scales visible.
  • the containers may themselves be useable in administration; for example, the kit might contain the appropriate amounts of each composition in separate syringes. Formulations which comprise the pre-formulated correct ratio of therapeutic agents may also be packaged in this way so that the formulation is administered directly from a syringe prepackaged in the kit.
  • Therapeutic activity of delivery vehicle compositions comprising two or more active agents may be measured after administration into an animal model.
  • the animal model comprises a tumor although delivery vehicle compositions may be administered to animal models of other diseases.
  • Rodent species such as mice and rats of either inbred, outbred, or hybrid origin including immunocompetent and immunocompromised, as well as knockout, or transgenic models may be used.
  • ink jet printing inks are based on soluble dyes. These present two problems. First the soluble dyes are prone to “bleeding” and are not as water-fast as is desired, and second, the dye wicks into the paper prior to drying with a corresponding loss in color intensity. To overcome these problems one strategy is to use insoluble pigment particles. However, the range of colors obtained from soluble dyes is not matched by the pigments in particulate form.
  • the current invention would allow the conjugation of dyes to hydrophobic linkers that would allow incorporation into nanoparticle form.
  • the especially preferable embodiment of this technology would couple Flash Nano Precipitation to form narrow size distribution particles in the range of 200 nm with the conjugation scheme to incorporate otherwise soluble dyes.
  • the Flash Nano-Precipitation process allows the incorporation of multiple colors into a single particle to effect color blending.
  • fluorescently labeled particles in the size range 50 nm to 2,000 nm. These are most commonly made from polymeric emulsion polymerized lattices into which dyes are imbibed. Alternatively, fluorescent species are reacted onto the surface of the particles. See Polysciences, Inc., Particle Catalog for a listing of representative particles (website: polysciences.com).
  • the imbibing route has limitations as to the dyes that are hydrophobic enough to be retained in the spheres, and the chemical reacting route has limitations as to the number of fluorescent molecules that can be attached to a single sphere.
  • the production of these tracer particles requires independent steps of particle formation, and then post processing to introduce the fluorescent species.
  • fragrances that are released over time.
  • laundry fabric conditioners spray deodorizers, and perfumes.
  • the fragrance can be released over time by the hydrolytic cleavage of the linking bond, or by light cleavage of a photocleavable bond.
  • UV absorbers can be conjugated with hydrophobic moieties to enable incorporation into nanoparticles in long-lasting formulation.
  • hydrophilic blocks on the particle surface that include cationic and hydrogen bonding monomers, it would be possible to have the nanoparticle formulation adhere to the skin for prolonged periods of time.
  • Nanoparticles with Methoxy Polyethylene Glycol-Polycaprolactone (mPEG-PCL) and Paclitaxel-VitE are Methoxy Polyethylene Glycol-Polycaprolactone (mPEG-PCL) and Paclitaxel-VitE
  • mPEG5-PCL6 was dissolved in THF to make a 0.5 wt % solution (w:w). Then, paclitaxel-PCL prepared as described in Example 2 was added to the solution to make a 0.5 wt % (w:w) of the conjugate. The resulting solution was mixed using the vortex mixer at a flow rate of 12 ml/min against water at 120 ml/min, yielding nanoparticles with an average diameter of 75 nm. The nanoparticles size after 60 hours was 93 nm.
  • Vitamin E succinate (1210 IU/g) (2273.0 mg, 4.28 mMol) was dissolved in 20 ml of anhydrous methylene chloride. To this solution at 0° C. were added DIPC (654.9 ⁇ l, 4.28 mMol), rifampicin (1762.1 mg, 2.14 mMol) dissolved in 20 ml of anhydrous methylene chloride, and DMAP (806.1 mg, 6.55 mMol). The resulting solution was warmed to room temperature and left for 16 hours. The reaction mixture was washed with 0.1 N HCl, dried, and evaporated in vacuo to yield the product as a red powder. 13 C and 1 H NMR and HPLC confirmed the function or Rifampicin-VitES.
  • the particle growth from 170 nm after 2 hours to 532 nm after four hours shows that the drug cannot form stable nanoparticles in the unconjugated form.
  • Conjugated rifampicin from Example 5 was mixed with block copolymer poly (ethylene glycol)-b-poly (caprolactone) (PEG-b-PCL) (5k-5k) as described in Example 6. Stable particles were formed when the initial concentration of conjugated rifampicin in DMF is 4 wt %. And the particles were stable as shown by DLS. The results are shown in the table below,
  • Dicarboxyl PCL (5 kDa) (10700 mg, 2.14 mMol) was dissolved in 20 ml of anhydrous methylene chloride. To this solution at 0° C. were added DIPC (654.9 ⁇ l, 4.28 mMol), rifampicin (1762.1 mg, 2.14 mMol) dissolved in 20 ml of anhydrous methylene chloride, and DMAP (806.1 mg, 6.55 mMol). The resulting solution was taken out of the ice bath to warm to room temperature and left for 16 hours. The reaction mixture was washed with 0.1 N HCl, dried, and evaporated in vacuo to yield the product as a red powder. 13 C and 1 H NMR and HPLC confirmed the structure as rifampicin-PCL.
  • Nanoparticles from Poly (ethylene glycol)-b-poly (caprolactone) and Rifampicin-PCL are Nanoparticles from Poly (ethylene glycol)-b-poly (caprolactone) and Rifampicin-PCL
  • Conjugated rifampicin from Example 8 above was mixed with block copolymer poly (ethylene glycol)-b-poly (caprolactone) (PEG-b-PCL) (5k-5k) as described in Example 6.
  • Stable nanoparticles were formed when the initial concentration of rifampicin-PCL in DMF is 4 wt %. And the particles were stable as shown by DLS.
  • ⁇ -Tocopherol succinate (530.8 g/mol) is dissolved in anhydrous dichloromethane at 0° C. 1,3-diisopropylcarbodiimide (DIPC, 152.9 g/mol), estradiol (272.39 g/mol) and 4-(dimethylamino)-pyridine (DMAP, 123.1 g/mol) are added to the solution at a molar ratio of 1.5:0.25:1.5 with respect to ⁇ -tocopherol succinate. The reaction mixture is warmed to room temperature and aged for a period of 70 hours to achieve near complete conversion to the conjugate. A 0.1 N HCl wash is employed following reaction completion for the removal of residual DMAP. The solution is evaporated to dryness and the solid product, estradiol-VitES, isolated. The product estradiol-VitES was characterized by High Performance Liquid Chromatography (HPLC) and Nuclear Magnetic Resonance (NMR) analysis.
  • HPLC High Performance Liquid Chromatography
  • Estradiol and methoxy-poly(ethylene glycol)-b-poly( ⁇ -caprolactone) are dissolved in THF at a weight ratio of 1:1 to make a 0.3 wt % solution for each component.
  • the resulting solution is loaded into a gas tight syringe, and impingement mixed with an anti-solvent (water) using the Confined Impinging Jet (CIJ) mixer at injection rates of 12 ml/min and 120 ml/min for THF and water, respectively.
  • Estradiol loaded nanoparticles were unstable soon after particle formation ( ⁇ 30 minutes), as indicated by visual observation of aggregates. DLS analysis could not be performed due to the presence of these aggregates.
  • estradiol-VitES loaded nanoparticles with the Confined Impinging Jet (CIJ) mixer.
  • the estradiol-VitES along with the block copolymer were dissolved in THF at the aforementioned weight ratios and impingement mixed with DI water.
  • the resulting nanoparticles demonstrated a less than 10% increase in radius over the course of 48 hours, as indicated by Dynamic Light Scattering (DLS) analysis. Additional stability was observed in particles where the reaction mixture comprises a 3:1 molar ratio of VitES to conjugated to estradiol-VitES with stability noted in excess of 30 days.
  • DLS Dynamic Light Scattering
  • Nanoparticles Containing Estradiol-VitES and Paclitaxel-VitES are Nanoparticles Containing Estradiol-VitES and Paclitaxel-VitES
  • An estradiol-VitES conjugate is prepared as in Example 10.
  • a conjugate of paclitaxel-VitES is prepared as according to Example 1.
  • Nanoparticles comprising both estradiol-VitES and paclitaxel-VitES were made by first dissolving 30 mg of methoxy polyethylene glycol-polycaprolactone (methoxy polyethylene glycol molecular weight of 5 kg/mole, PCL molecular weight of 7 kg/mole) (mPEG5-PCL7) in 3 ml of THF to make a 1 wt % solution (w:w) of mPEG5-PCL7.
  • methoxy polyethylene glycol-polycaprolactone methoxy polyethylene glycol molecular weight of 5 kg/mole, PCL molecular weight of 7 kg/mole
  • paclitaxel-VitES 8.5 mg
  • 6.5 mg of estradiol-VitES prepared as described in the previous examples were added to the mPEG5-PCL7 solution in THF with 15 mg VitES.
  • the weight ratio of paclitaxel-VitES to estradiol-VitES is 1.27.
  • the resulting solution was mixed using the vortex mixer at a flow rate of 12 ml/min against water at 120 ml/min, yielding nanoparticles with an average diameter of 107 nm as determined by DLS (see plot below). No visible crystals or aggregates were observed in the sample.
  • a hydrophobic polymer-paclitaxel conjugate is prepared in accordance with the methods set out in Greenwald, et al., supra (1996), which addressed the formation of water soluble Taxol- poly (ethylene glycol) prodrugs. Instead of using poly (ethylene glycol), we will use poly (caprolactone) with a carboxylic acid end group to form the active agent conjugate. The reaction scheme used by Greenwald is shown in FIG. 1 .
  • cisplatin-polymer complexes The same rationale is used to form cisplatin-polymer complexes.
  • cisplatin is reacted with a mono acid or a diacid end group of a hydrophobic homopolymer to form a cisplatin-polymer complex, then the stabilizing diblock copolymer is added, and finally PEG-protected nanoparticles are formed using the vortex mixer.
  • the cisplatin complex is prepared based on the work of Ohya, et al. supra (2000), where poly (ethylene glycol)- cisplatin complexes were prepared based on a 6-membered chelate-type dicarboxylate coordination bond, as shown in FIG. 2 .
  • active agent combinations include combinations comprising paclitaxel with cisplatin, etoposide with cisplatin, taxotere with doxorubicin, and paclitaxel with doxorubicin. These are formulated at particular ratios shown to be non-antagonistic.
  • hydrophobic active agent-polymer conjugate using hydrophobic biodegradable polymers will provide an active agent release rate determined by the rate of chemical hydrolysis rather than diffusion.
  • covalent attachment of the active agent to the hydrophobic block of the polymer will prevent Ostwald ripening of the nanoparticles and improve the stability of the formulation.
  • linkers are set forth below, a variety of other chemical linkers between the active agent and the polymer are contemplated as set forth herein. Coupling an active agent to a polymer using any of a variety of these linkers is accomplished in accordance with the presently described methods and others known and available in the art.
  • Novel Paclitaxel-polymer conjugates are prepared using hydrophobic polymers.
  • the approach set out herein is based on the conjugation of paclitaxel to a homopolymer backbone before encapsulation using the diblock copolymer; First, paclitaxel is reacted with a hydrophobic homopolymer to form a paclitaxel-polymer conjugate, then the stabilizing diblock copolymer is added, and finally PEG-protected nanoparticles is formed using the vortex mixer.
  • PCL and poly (lactide) with a terminal carboxylic acid group are specifically investigated, but other polymers that are suitable are poly(lactide-co-glycolide)-COOH; poly(lactide)-COOH; poly( ⁇ -caprolactone)-COOH and poly( ⁇ -benzyl-aspartate)-COOH.
  • Paclitaxel-PLA conjugate is prepared following Greenwald's procedure for making mPEG-paclitaxel prodrug.
  • PLA-COOH (16,000 g/mole) is dissolved in dichloromethane to make a 3 wt % solution.
  • the resulting solution is brought to 0° C., and diisopropylcarbodiimide (DIPC) is added at a molar ratio of 1.36:1 DIPC:PLA-COOH.
  • DIPC diisopropylcarbodiimide
  • Paclitaxel is then added at a molar ratio of 1:1 paclitaxel:DIPC.
  • the reaction mixture is. then warmed to room temperature, and left to react for 16 hours.
  • a 0.1 N HCl is used for washing, and the solution is dried and evaporated in vacuo.
  • Nanoparticles of the active agent conjugate are then formed following the method outlined in the Formulation and Characterization section, using the active agent conjugate instead of the pure active agent. The experiment is repeated for paclitaxel-polymer: block copolymer weight ratios of 1:1, 1:3, and 1:10. The resulting nanoparticles are analyzed for size, active agent content, and in vitro release rates as outlined in the Formulation and Characterization section.
  • Kataoka has demonstrated the formation of cisplatin complexes in water with homopolymers of poly ( ⁇ , ⁇ -aspartic acid) and poly(ethylene glycol)-poly(glutamic acid) block copolymers, resulting in nanoparticles with cisplatin release times of approximately 14 hours. See Nishiyama, N., et al., J. of Controlled Release (2001) 74:83-94; see also Nishiyama, N., et al., Cancer Research (2003) 63:8977-8983.
  • cisplatin-polymer conjugates are formulated using hydrophobic polymers.
  • cisplatin is conjugated to a homopolymer end group prior to encapsulation using the diblock copolymer.
  • PCL and poly (lactide) homopolymers having terminal diacid groups are described below. The present method is based on Ohya, Y., et al., (2000) (cited supra), to form poly (ethylene glycol)-cisplatin complexes.
  • Diacid diethyl ester terminated poly (lactide) (PLA-Da(Et) 2 ): 0.5 mMole of poly (lactide) is dissolved in 10 ml of anhydrous THF, and mixed with sodium and naphthalene (1.5 mMole). After refluxing under Ar atmosphere for 4 hours, diethylchloropropylmalonate (3 nMole) in 10 ml of THF is added to the reaction mixture, and refluxed for 4 hours under Ar. The final product is obtained by concentration and re-precipitation using diethyl ether. 1 H-NMR is used to confirm the structure.
  • Cisplatin attachment to PLA-Da(Et 2 ) PLA-Da(Et 2 ) obtained from the above procedure is dissolved in 10 ml of ethanol (aq., 95%) and 243 mg of NaOH, and refluxed for 90 min. The resulting solution is subjected to an anion exchange resin column (QAE-Sephadex A-25, water then 2M-NaCl at 1 ml/min effluent) after refluxing for 90 minutes and re-precipitation using diethyl ether. The solution is then freeze-dried as described in the Formulation and Characterization section (above) to yield PLA-Da (Na salt). 1 H-NMR is used to confirm the reaction.
  • Cisplatin 50 mg is dissolved in water and stirred for 3 h at 60° C., after which 0.22 ml of a 0.1 M silver nitrate solution is added and mixed at 60° C. for 6 h. The solution is filtered to remove precipitated silver chloride, and the filtrate dried in vacuo. The product is dissolved in THF and PLA-Da (Na salt) is added and left to react at 60° C. for 24 h. Gel-filtration chromatography is used to purify the sample, and the higher molecular weight fraction is freeze-dried as described in the Formulation and Characterization section. Atomic absorption spectrometry is used to determine the amounts of platinum in the complex.
  • both agents are encapsulated in one carrier.
  • the nanoparticles encapsulating both paclitaxel (or corresponding polymer conjugate) and the cisplatin complex are formed by the following procedure. Each component (in active agent or complex form) is dissolved in THF to make a 0.3 wt % solution for each active agent. mPEG-PCL is added at a weight ratio of 1:1 mPEG-PCL:active agents. The nanoparticles then form, as outlined in the Formulation and Characterization section, using the cisplatin-polymer complex and the paclitaxel (or paclitaxel-polymer conjugate) instead of one active agent.
  • the experiment is repeated for cisplatin:paclitaxel molar ratios of 1:5 and 5:1, and for active agents:block copolymer weight ratios of 1:1, 1:5 and 1:10.
  • the resulting nanoparticles are analyzed for size, active agent content, and in vitro release rates as outlined in the Formulation and Characterization section.
  • This example demonstrates the stability and controlled release of paclitaxel from polymer-based nanoparticles formed via the presently described methods.
  • a paclitaxel formulation is prepared, lyophilized and redispersed in water to the primary particle size (determined before freeze-drying) using sucrose at a weight ratio of 60:1 sucrose:nanoparticles.
  • the stability of the paclitaxel nanoparticles in freeze-dried form is evaluated over a period of one month to demonstrate long term storage of the lyophilized material.
  • Lyophilized material obtained through the nanoparticle formation process as described in the Formulation and Characterization section is stored at 4° C.
  • a sample is collected every week for the first month, then monthly and analyzed for size, active agent content, and in vitro release rate as outlined in the Formulation and Characterization section. The same procedure is repeated for a sample stored at room temperature.
  • the in vitro paclitaxel release rate from the nanoparticles is controlled to provide release half lives of >4h.
  • Lyophilized nanoparticles containing paclitaxel are dissolved at a target active agent concentration of 1-5 mg/ml in water.
  • the solution is diluted 2-10 fold in serum and incubated at 37° C. Aliquots are collected at 1, 2, 4, 8, 16, and 24 hours intervals, and assayed for paclitaxel.
  • a Biogel A-0.5M gel filtration column is used to separate proteins and free active agent from the polymer-associated active agent.
  • the paclitaxel concentration is determined as described in the Formulation and Characterization section.
  • In vivo paclitaxel release rate are evaluated through the injection of the active agent nanoparticles into mice IV at a paclitaxel dosage of 10 mg/kg.
  • the target paclitaxel half life is 4 hours or longer.
  • the plasma active agent elimination properties of polymer formulations are determined as a function of active agent/polymer ratio as well as hydrophobic/block co-polymer ratio.
  • Lyophilized nanoparticles containing paclitaxel are dissolved at a target active agent concentration of 1-5 mg/ml in water.
  • the solution is diluted as necessary in saline to provide paclitaxel doses of 10 mg/kg in a volume of 0.2 ml.
  • plasma samples are collected at 1, 2, 4, 8, 16, and 24 hours intervals, and assayed for paclitaxel.
  • the paclitaxel concentration is determined by HPLC analysis of a solvent-extracted sample.
  • Nanoparticles containing both cisplatin and paclitaxel are investigated for in vivo release rates.
  • the active agent ratios in the nanoparticles are dictated by the in vitro release rate results.
  • Lyophilized nanoparticles containing paclitaxel and cisplatin are dissolved at a target paclitaxel concentration of 1-5 mg/ml in water.
  • the solution is diluted as necessary in saline to provide paclitaxel doses of 10 mg/kg in a volume of 0.2 ml.
  • plasma samples are collected at 1, 2, 4, 8, 16, and 24 hours and assayed for paclitaxel.
  • the paclitaxel and cisplatin concentrations are determined by HPLC and atomic absorption, respectively.
  • the experiment is repeated at various paclitaxel:cisplatin ratios and for various polymer compositions until the synergistic ratio is maintained after i.v. injection.
  • a CombiPlexTM formulation containing polymer conjugated paclitaxel and cisplatin at a molar ratio shown to be non-antagonistic in vitro and also exhibiting matched release rates for the two active agents is administered IV to mice bearing 100-200 mg solid tumors.
  • the tumor selected is based on in vitro screening data where significant non-antagonism and preferably ratio dependency is observed.
  • Dose range finding studies (3 mice per group) are first performed to establish MTD's in non-tumor bearing mice). For efficacy studies, mice (6 per group) are administered by IV a minimum of two different dose levels of CombiPlexTM and free active agent cocktail at approximate MTD's and at a matched dose of active agents in the CombiPlexTM formulation. Two treatment schedules are evaluated (weekly ⁇ 3 and Q4D ⁇ 3). Tumor weights are determined by measuring tumors using calipers. Animals are also monitored for signs of toxicity (weight loss and physical signs of stress).
  • Additional CombiPlexTM formulations are prepared utilizing a variety of combinations of anti-neoplastic agents.
  • Agent combinations such as paclitaxel with etoposide, paclitaxel with taxotere, paclitaxel with doxorubicin, cisplatin with etoposide, cisplatin with taxotere, cisplatin with doxorubicin, etoposide with taxotere, etoposide with doxorubicin, doxorubicin with taxotere are prepared and evaluated. The chemical linkages are altered and adjusted to provide for desired release rates.
  • active agents can be substituted for those set forth in the above Examples.
  • other platinum analogs such as Carboplatin, Oxaliplatin, Tetraplatin, Platinum-DACH, Ormaplatin, among others, can be substituted for Cisplatin.
  • an active agent is substituted with another active agent within the same class, as discussed above.
  • any of a variety of the active agents set forth herein are combined in a nanoparticle formulation in accordance with the present materials and methods. Frequently, these nanoparticle formulations contain a combination of one or two or three or more active agents.

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Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100203150A1 (en) * 2009-02-06 2010-08-12 National Tsing Hua University Novel amphiphilic copolymers and fabrication method thereof
US20100247668A1 (en) * 2009-03-30 2010-09-30 Scott Eliasof Polymer-agent conjugates, particles, compositions, and related methods of use
US20100285144A1 (en) * 2009-03-30 2010-11-11 Scott Eliasof Polymer-epothilone conjugates, particles, compositions, and related methods of use
WO2010077045A3 (fr) * 2008-12-29 2010-11-18 Samyang Corporation Composition pharmaceutique d'une formule lyophilisée et sa méthode d'élaboration
US20100331290A1 (en) * 2007-11-28 2010-12-30 Celator Pharmaceuticals, Inc Taxane delivery system
US20110064812A1 (en) * 2009-09-16 2011-03-17 Deepak Bahl Oral Solid Dosage Form Containing Nanoparticles and Process of Formulating the Same Using Fish Gelatin
WO2011127255A1 (fr) * 2010-04-08 2011-10-13 Merck Sharp & Dohme Corp. Préparation de nanoparticules de lipide
WO2011112999A3 (fr) * 2010-03-12 2011-12-08 The Regents Of The University Of California Conjugués lipide-peptide-polymère et leurs nanoparticules
US20130017265A1 (en) * 2009-12-16 2013-01-17 Massachusetts Institute Of Technology Particles for multiple agent delivery
WO2013063279A1 (fr) * 2011-10-25 2013-05-02 The Trustees Of Princeton University Formulation à base de nanoparticules à chargement élevé pour des stéroïdes insolubles dans l'eau
US20150265716A1 (en) * 2012-10-09 2015-09-24 The Brigham And Women's Hospital, Inc. Nanoparticles For Targeted Delivery of Multiple Therapeutic Agents and Methods of Use
US9949927B2 (en) 2012-04-10 2018-04-24 The Regents Of The University Of California Bis-polymer lipid-peptide conjugates and nanoparticles thereof
US10347848B2 (en) * 2013-09-03 2019-07-09 Basf Se Amorphous material and the use thereof
US20200360287A1 (en) * 2019-05-16 2020-11-19 Megapro Biomedical Co., Ltd. Pharmaceutical compositions containing mixed polymeric micelles
WO2021113397A1 (fr) * 2019-12-03 2021-06-10 Onselex Inc. Plates-formes et méthodes d'administration de médicament peg polymère
US11160870B2 (en) 2017-05-10 2021-11-02 Graybug Vision, Inc. Extended release microparticles and suspensions thereof for medical therapy
US20230241219A1 (en) * 2008-06-05 2023-08-03 President And Fellows Of Harvard College Polymersomes, colloidosomes, liposomes, and other species associated with fluidic droplets

Families Citing this family (49)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8173167B2 (en) 2005-04-12 2012-05-08 Wisconsin Alumni Research Foundation Micelle composition of polymer and passenger drug
US9943490B2 (en) 2007-11-05 2018-04-17 The Trustees Of Princeton University Composite flash-precipitated nanoparticles
ES2358493B1 (es) * 2008-04-05 2012-06-13 Instituto Cientifico Y Tecnologico De Navarra, S.A Nanopartículas pegiladas que comprenden una molécula biológicamente activa y sus aplicaciones.
CA2737452C (fr) 2008-09-25 2018-05-22 Vive Nano Inc. Procedes de production de nanoparticules de polymere et formulations d'ingredients actifs
WO2010114770A1 (fr) * 2009-03-30 2010-10-07 Cerulean Pharma Inc. Conjugués polymère-agent, particules, compositions et procédés d'utilisation apparentés
US20110262490A1 (en) * 2009-03-30 2011-10-27 Jerry Zhang Polymer-agent conjugates, particles, compositions, and related methods of use
KR101721281B1 (ko) 2009-09-25 2017-04-10 위스콘신 얼럼나이 리서어치 화운데이션 치료제의 미셀 캡슐화
US20110237686A1 (en) 2010-03-26 2011-09-29 Cerulean Pharma Inc Formulations and methods of use
MX2013002051A (es) * 2010-08-20 2013-06-28 Cerulean Pharma Inc Particulas, composiciones y conjugados de peptido terapeutico-polimero y metodos relacionados.
CN103561726A (zh) 2010-11-18 2014-02-05 通用医疗公司 用于癌症治疗的抗高血压剂的新型组合物和用途
WO2012076853A1 (fr) 2010-12-08 2012-06-14 Innovative Carbon Limited Matériaux particulaires, composites les comprenant, préparation et utilisations de ceux-ci
AU2012311247B2 (en) 2011-08-23 2016-10-13 Vive Crop Protection Inc. Pyrethroid formulations
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EP2841486B1 (fr) * 2012-04-23 2020-01-15 NanoProteagen Ltd. Nanoparticules polymères et leur procédé de préparation
BE1022066B1 (nl) * 2013-06-28 2016-02-15 Chemstream Bvba Oppervlakteactief middel en bereiding daarvan
US20170037234A1 (en) 2014-02-26 2017-02-09 The Trustees Of Princeton University Polymer nanoparticles
WO2015153345A1 (fr) 2014-04-03 2015-10-08 Invictus Oncology Pvt. Ltd. Agents thérapeutiques combinatoires supramoléculaires
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US11602512B1 (en) 2016-07-22 2023-03-14 Flamel Ireland Limited Modified release gamma-hydroxybutyrate formulations having improved pharmacokinetics
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US20210085598A1 (en) 2018-04-03 2021-03-25 Vaxess Technologies, Inc. Microneedle comprising silk fibroin applied to a dissolvable base
US12186436B2 (en) 2018-07-19 2025-01-07 The Trustees Of Princeton University Triblock copolymer stabilizers for the formation of nanoparticles encapsulating soluble biologics, therapeutics, and imaging agents
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US20200147032A1 (en) 2018-11-14 2020-05-14 Robert K. Prud'homme Dihydromyricetin hot melt extrusion formulations and methods for forming them
BR112021013766A2 (pt) 2019-03-01 2021-09-21 Flamel Ireland Limited Composições de gama-hidroxibutirato com farmacocinética melhorada no estado alimentado
AU2020303907A1 (en) * 2019-06-28 2022-02-24 Dynamic Biologics Inc. Levodopa polymeric conjugates, formulations thereof, and their uses for the treatment of Parkinson's disease
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US11779557B1 (en) 2022-02-07 2023-10-10 Flamel Ireland Limited Modified release gamma-hydroxybutyrate formulations having improved pharmacokinetics
US11583510B1 (en) 2022-02-07 2023-02-21 Flamel Ireland Limited Methods of administering gamma hydroxybutyrate formulations after a high-fat meal
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WO2024263835A1 (fr) 2023-06-23 2024-12-26 Vaxess Technologies, Inc. Applicateur de timbre médicamenteux

Citations (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4610868A (en) * 1984-03-20 1986-09-09 The Liposome Company, Inc. Lipid matrix carriers for use in drug delivery systems
US4780535A (en) * 1986-11-21 1988-10-25 Spyros Theodoropulos Maleic and phthalic diamides
US5145684A (en) * 1991-01-25 1992-09-08 Sterling Drug Inc. Surface modified drug nanoparticles
US5166319A (en) * 1989-10-10 1992-11-24 Brunswick Corporation Interfacial condensation of bioactive compounds and the site-specific compounds and conjugates thereof
US5188837A (en) * 1989-11-13 1993-02-23 Nova Pharmaceutical Corporation Lipsopheres for controlled delivery of substances
US5330768A (en) * 1991-07-05 1994-07-19 Massachusetts Institute Of Technology Controlled drug delivery using polymer/pluronic blends
US5336506A (en) * 1986-07-03 1994-08-09 Advanced Magnetics Inc. Targeting of therapeutic agents using polysaccharides
US5470583A (en) * 1992-12-11 1995-11-28 Eastman Kodak Company Method of preparing nanoparticle compositions containing charged phospholipids to reduce aggregation
US5543158A (en) * 1993-07-23 1996-08-06 Massachusetts Institute Of Technology Biodegradable injectable nanoparticles
US5766818A (en) * 1997-10-29 1998-06-16 Xerox Corporation Toner processes with hydrolyzable surfactant
US5869103A (en) * 1994-06-18 1999-02-09 Danbiosyst Uk Limited Polymer microparticles for drug delivery
US5891475A (en) * 1993-04-21 1999-04-06 Institut Pasteur Particulate vector and pharmaceutical composition containing it
US5928832A (en) * 1998-12-23 1999-07-27 Xerox Corporation Toner adsorption processes
US6429200B1 (en) * 1998-07-17 2002-08-06 Mirus Corporation Reverse micelles for delivery of nucleic acids
US6482413B1 (en) * 2001-02-26 2002-11-19 Council Of Scientific And Industrial Research Vitamin B12 —biodegradable micro particulate conjugate carrier systems for peroral delivery of drugs, therapeutic peptides/proteins and vaccines
US6500461B2 (en) * 1998-05-20 2002-12-31 The Liposome Company Particulate formulations
US6559243B1 (en) * 1997-10-01 2003-05-06 The Procter & Gamble Company Glyoxylic compound comprising one or more active ingredient
US6589548B1 (en) * 1998-05-16 2003-07-08 Mogam Biotechnology Research Institute Controlled drug delivery system using the conjugation of drug to biodegradable polyester
US6673612B2 (en) * 1999-07-16 2004-01-06 Mirus Corporation Micellar systems
US6676963B1 (en) * 2000-10-27 2004-01-13 Barnes-Jewish Hospital Ligand-targeted emulsions carrying bioactive agents
US20040152913A1 (en) * 2001-05-29 2004-08-05 Caprioli Richard M Cleavable surfactants and methods of use thereof
US20040221989A1 (en) * 2001-02-13 2004-11-11 Jian Zhou Aqueous viscoelastic fluid

Family Cites Families (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3993754A (en) 1974-10-09 1976-11-23 The United States Of America As Represented By The United States Energy Research And Development Administration Liposome-encapsulated actinomycin for cancer chemotherapy
US4086257A (en) 1976-10-12 1978-04-25 Sears Barry D Phosphatidyl quaternary ammonium compounds
CH624011A5 (fr) 1977-08-05 1981-07-15 Battelle Memorial Institute
US4235871A (en) 1978-02-24 1980-11-25 Papahadjopoulos Demetrios P Method of encapsulating biologically active materials in lipid vesicles
US4522803A (en) 1983-02-04 1985-06-11 The Liposome Company, Inc. Stable plurilamellar vesicles, their preparation and use
US4588578A (en) 1983-08-08 1986-05-13 The Liposome Company, Inc. Lipid vesicles prepared in a monophase
DE3611229A1 (de) 1986-04-04 1987-10-08 Basf Ag Verfahren zur herstellung von feinverteilten, pulverfoermigen carotinoidpraeparaten
JPH0781138B2 (ja) * 1986-12-02 1995-08-30 株式会社資生堂 抗酸化剤
US5565215A (en) * 1993-07-23 1996-10-15 Massachusettes Institute Of Technology Biodegradable injectable particles for imaging
GB9409778D0 (en) * 1994-05-16 1994-07-06 Dumex Ltd As Compositions
US5518738A (en) 1995-02-09 1996-05-21 Nanosystem L.L.C. Nanoparticulate nsaid compositions
DE60111352T2 (de) * 2000-01-20 2006-05-04 Supratek Pharma, Inc., Montreal Podophyllotoxin-zusammensetzungen
CA2455170A1 (fr) * 2000-07-31 2002-02-07 Ottawa Heart Institute Research Corporation Compositions lipidiques chargees et procedes d'utilisation desdites compositions
JP3539388B2 (ja) * 2001-01-26 2004-07-07 日本電気株式会社 光ディスク記録方法及び光ディスク記録装置
WO2002076970A2 (fr) * 2001-03-23 2002-10-03 Sonus Pharmaceuticals, Inc. Derives succinate tocopherol et compositions
US8137699B2 (en) 2002-03-29 2012-03-20 Trustees Of Princeton University Process and apparatuses for preparing nanoparticle compositions with amphiphilic copolymers and their use
US6638994B2 (en) * 2001-03-30 2003-10-28 Regan Crooks Aqueous suspension of nanoparticles comprising an agrochemical active ingredient
KR100394770B1 (ko) * 2001-06-05 2003-08-14 주식회사 태평양 토코페롤 유도체를 이용하여 나노유화입자를 안정화시키는방법 및 나노유화입자를 함유하는 피부 외용제 조성물
EP1399191A2 (fr) 2001-06-07 2004-03-24 Celator Technologies Inc. Agent therapeutique de penetration cellulaire
ATE345775T1 (de) 2001-10-03 2006-12-15 Celator Pharmaceuticals Inc Zusammensetzungen zur verabreichung von arzneimittelkombinationen
WO2004087105A1 (fr) 2003-04-02 2004-10-14 Celator Pharmaceuticals, Inc. Formulations associant du platine et des fluoropyrimidines
WO2004087115A2 (fr) 2003-04-02 2004-10-14 Celator Pharmaceuticals, Inc. Compositions combinees de camptothecines et de fluoropyrimidines
US7727969B2 (en) * 2003-06-06 2010-06-01 Massachusetts Institute Of Technology Controlled release nanoparticle having bound oligonucleotide for targeted delivery

Patent Citations (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4610868A (en) * 1984-03-20 1986-09-09 The Liposome Company, Inc. Lipid matrix carriers for use in drug delivery systems
US5336506A (en) * 1986-07-03 1994-08-09 Advanced Magnetics Inc. Targeting of therapeutic agents using polysaccharides
US4780535A (en) * 1986-11-21 1988-10-25 Spyros Theodoropulos Maleic and phthalic diamides
US5166319A (en) * 1989-10-10 1992-11-24 Brunswick Corporation Interfacial condensation of bioactive compounds and the site-specific compounds and conjugates thereof
US5188837A (en) * 1989-11-13 1993-02-23 Nova Pharmaceutical Corporation Lipsopheres for controlled delivery of substances
US5145684A (en) * 1991-01-25 1992-09-08 Sterling Drug Inc. Surface modified drug nanoparticles
US5330768A (en) * 1991-07-05 1994-07-19 Massachusetts Institute Of Technology Controlled drug delivery using polymer/pluronic blends
US5470583A (en) * 1992-12-11 1995-11-28 Eastman Kodak Company Method of preparing nanoparticle compositions containing charged phospholipids to reduce aggregation
US5891475A (en) * 1993-04-21 1999-04-06 Institut Pasteur Particulate vector and pharmaceutical composition containing it
US5543158A (en) * 1993-07-23 1996-08-06 Massachusetts Institute Of Technology Biodegradable injectable nanoparticles
US5869103A (en) * 1994-06-18 1999-02-09 Danbiosyst Uk Limited Polymer microparticles for drug delivery
US6559243B1 (en) * 1997-10-01 2003-05-06 The Procter & Gamble Company Glyoxylic compound comprising one or more active ingredient
US5766818A (en) * 1997-10-29 1998-06-16 Xerox Corporation Toner processes with hydrolyzable surfactant
US6589548B1 (en) * 1998-05-16 2003-07-08 Mogam Biotechnology Research Institute Controlled drug delivery system using the conjugation of drug to biodegradable polyester
US6500461B2 (en) * 1998-05-20 2002-12-31 The Liposome Company Particulate formulations
US6429200B1 (en) * 1998-07-17 2002-08-06 Mirus Corporation Reverse micelles for delivery of nucleic acids
US5928832A (en) * 1998-12-23 1999-07-27 Xerox Corporation Toner adsorption processes
US6673612B2 (en) * 1999-07-16 2004-01-06 Mirus Corporation Micellar systems
US6676963B1 (en) * 2000-10-27 2004-01-13 Barnes-Jewish Hospital Ligand-targeted emulsions carrying bioactive agents
US20040221989A1 (en) * 2001-02-13 2004-11-11 Jian Zhou Aqueous viscoelastic fluid
US6482413B1 (en) * 2001-02-26 2002-11-19 Council Of Scientific And Industrial Research Vitamin B12 —biodegradable micro particulate conjugate carrier systems for peroral delivery of drugs, therapeutic peptides/proteins and vaccines
US20040152913A1 (en) * 2001-05-29 2004-08-05 Caprioli Richard M Cleavable surfactants and methods of use thereof

Non-Patent Citations (6)

* Cited by examiner, † Cited by third party
Title
Cleek et al. J Control Rel. 48, p 259-268, 1997 *
Definition of "coordinate" from Merriam-Webster online, accessed May 12, 2014 *
Muggia et al. J Clin Oncol 18(1), p 106-115, 2000 *
Ohya et al. Polym Adv Technol, 11, p 635- 641, 2000 *
Soppimath et al. Journal of Controlled Release 70, p 1-20, 2001 *
Tracy et al. Biomaterials, 20, p 1057-1062, 1999 *

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100331290A1 (en) * 2007-11-28 2010-12-30 Celator Pharmaceuticals, Inc Taxane delivery system
US8486924B2 (en) * 2007-11-28 2013-07-16 Celator Pharmaceuticals, Inc. Taxane delivery system
US20230241219A1 (en) * 2008-06-05 2023-08-03 President And Fellows Of Harvard College Polymersomes, colloidosomes, liposomes, and other species associated with fluidic droplets
CN102271662B (zh) * 2008-12-29 2013-11-06 株式会社三养生物制药 冻干制剂的药物组合物及其制备方法
WO2010077045A3 (fr) * 2008-12-29 2010-11-18 Samyang Corporation Composition pharmaceutique d'une formule lyophilisée et sa méthode d'élaboration
US20100203150A1 (en) * 2009-02-06 2010-08-12 National Tsing Hua University Novel amphiphilic copolymers and fabrication method thereof
US20110189092A1 (en) * 2009-03-30 2011-08-04 Scott Eliasof Polymer-agent conjugates, particles, compositions, and related methods of use
US20100285144A1 (en) * 2009-03-30 2010-11-11 Scott Eliasof Polymer-epothilone conjugates, particles, compositions, and related methods of use
US20100247668A1 (en) * 2009-03-30 2010-09-30 Scott Eliasof Polymer-agent conjugates, particles, compositions, and related methods of use
US20110064812A1 (en) * 2009-09-16 2011-03-17 Deepak Bahl Oral Solid Dosage Form Containing Nanoparticles and Process of Formulating the Same Using Fish Gelatin
US9775819B2 (en) 2009-09-16 2017-10-03 R.P. Scherer Technologies, Llc Oral solid dosage form containing nanoparticles and process of formulating the same using fish gelatin
US20130017265A1 (en) * 2009-12-16 2013-01-17 Massachusetts Institute Of Technology Particles for multiple agent delivery
WO2011112999A3 (fr) * 2010-03-12 2011-12-08 The Regents Of The University Of California Conjugués lipide-peptide-polymère et leurs nanoparticules
US9044514B2 (en) 2010-03-12 2015-06-02 Regents Of The University Of California Lipid-peptide-polymer conjugates and nanoparticles thereof
WO2011127255A1 (fr) * 2010-04-08 2011-10-13 Merck Sharp & Dohme Corp. Préparation de nanoparticules de lipide
WO2013063279A1 (fr) * 2011-10-25 2013-05-02 The Trustees Of Princeton University Formulation à base de nanoparticules à chargement élevé pour des stéroïdes insolubles dans l'eau
US9949927B2 (en) 2012-04-10 2018-04-24 The Regents Of The University Of California Bis-polymer lipid-peptide conjugates and nanoparticles thereof
US10806702B2 (en) 2012-04-10 2020-10-20 The Regents Of The University Of California Bis-polymer lipid-peptide conjugates and nanoparticles thereof
US9931410B2 (en) * 2012-10-09 2018-04-03 The Brigham And Women's Hospital, Inc. Nanoparticles for targeted delivery of multiple therapeutic agents and methods of use
US20150265716A1 (en) * 2012-10-09 2015-09-24 The Brigham And Women's Hospital, Inc. Nanoparticles For Targeted Delivery of Multiple Therapeutic Agents and Methods of Use
US10347848B2 (en) * 2013-09-03 2019-07-09 Basf Se Amorphous material and the use thereof
US11160870B2 (en) 2017-05-10 2021-11-02 Graybug Vision, Inc. Extended release microparticles and suspensions thereof for medical therapy
US20200360287A1 (en) * 2019-05-16 2020-11-19 Megapro Biomedical Co., Ltd. Pharmaceutical compositions containing mixed polymeric micelles
CN114025743A (zh) * 2019-05-16 2022-02-08 巨生生医股份有限公司 含有混合聚合物胶束的药物组合物
US11541007B2 (en) * 2019-05-16 2023-01-03 Megapro Biomedical Co., Ltd. Pharmaceutical compositions containing mixed polymeric micelles
US11931456B2 (en) 2019-05-16 2024-03-19 Megapro Biomedical Co. Ltd. Pharmaceutical compositions containing mixed polymeric micelles
WO2021113397A1 (fr) * 2019-12-03 2021-06-10 Onselex Inc. Plates-formes et méthodes d'administration de médicament peg polymère

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