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WO2000040220A1 - Method of preparing pharmaceutical active ingredient comprising water-insoluble drug and pharmaceutical composition for oral administration comprising the same - Google Patents

Method of preparing pharmaceutical active ingredient comprising water-insoluble drug and pharmaceutical composition for oral administration comprising the same Download PDF

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Publication number
WO2000040220A1
WO2000040220A1 PCT/KR1999/000025 KR9900025W WO0040220A1 WO 2000040220 A1 WO2000040220 A1 WO 2000040220A1 KR 9900025 W KR9900025 W KR 9900025W WO 0040220 A1 WO0040220 A1 WO 0040220A1
Authority
WO
WIPO (PCT)
Prior art keywords
water
oil
drug
insoluble drug
active ingredient
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.)
Ceased
Application number
PCT/KR1999/000025
Other languages
French (fr)
Inventor
Soon-Hong Yuk
Sun-Hang Cho
Hai-Bang Lee
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Korea Research Institute of Chemical Technology KRICT
Original Assignee
Korea Research Institute of Chemical Technology KRICT
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Korea Research Institute of Chemical Technology KRICT filed Critical Korea Research Institute of Chemical Technology KRICT
Priority to PCT/KR1999/000025 priority Critical patent/WO2000040220A1/en
Priority to EP99901236A priority patent/EP1058539A1/en
Priority to JP2000591977A priority patent/JP2002534371A/en
Publication of WO2000040220A1 publication Critical patent/WO2000040220A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/4841—Filling excipients; Inactive ingredients
    • A61K9/4858—Organic compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605—Excipients; Inactive ingredients
    • A61K9/1629—Organic macromolecular compounds
    • A61K9/1652—Polysaccharides, e.g. alginate, cellulose derivatives; Cyclodextrin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605—Excipients; Inactive ingredients
    • A61K9/1629—Organic macromolecular compounds
    • A61K9/1635—Organic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605—Excipients; Inactive ingredients
    • A61K9/1629—Organic macromolecular compounds
    • A61K9/1641—Organic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, poloxamers

Definitions

  • the mixed solution and air are injected into a spray-dryer body, while raising the ambient temperature by the heated air and mixed solution is changed from solution form to microparticle form by heated air.
  • the drug microparticles combined with polymer may be mixed with oil in the weight of 1 : 1 to 10. It is preferred that the drug microparticles mixed with oil because bioavailability increases.
  • oil amount is lower than 1 , it is difficult to mix the drug micropartices with oil. On the contrary, oil amount exceeds 10, it is difficult to charge the mixture to a capsule.
  • oil corn oil, peanut oil, coconut oil, caster oil, sesame oil, perilla oil, sunflower oil, walnut oil and cacao butter may be used.

Landscapes

  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • Engineering & Computer Science (AREA)
  • Medicinal Preparation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

A method of preparing a pharmaceutical active ingredient comprising a water-insoluble drug is provided. In the method, a water-insoluble drug in an organic solvent is mixed with a water-soluble polymer in an aqueous solvent and spray-dried. Thereafter, the drug microparticles is mixed with oil. The method can easily prepare a pharmaceutical active ingredient including water-insoluble drug, exhibiting good bioavailability. Accordingly, it is not required for specific technology in the preparation.

Description

METHOD OF PREPARING PHARMACEUTICAL ACTIVE INGREDIENT
COMPRISING WATER-INSOLUBLE DRUG AND PHARMACEUTICAL
COMPOSITION FOR ORAL ADMINISTRATION COMPRISING THE SAME
BACKGROUND OF THE INVENTION
(a) Field of the Invention
The present invention relates to method of preparing a pharmaceutical active ingredient comprising water-insoluble drug and a pharmaceutical composition for oral administration comprising the same and, more particularly, to a method of preparing a pharmaceutical active ingredient comprising the water-insoluble improved bioavailability with simple process.
(b) Description of the Related Art
When a water-insoluble drug is orally administrated into a patient, bioavailability is low. Due to the low bioavailability, it is impossible to orally administrate the water-insoluble drug or for increasing the effective concentration of the drug in the blood, the patient frequently takes the water- insoluble drug for a long time. For example, the patient takes the water- insoluble drug three times a day for a week. For improving bioavailability, studies to use oil and a surfactant has been attracted. Korean Patent Laid-open No. 96-21056 discloses that a drug is micro-emulsified by using oil and a surfactant. Furthermore, a drug is dissolved in an organic solvent and the mixture is micro-emulsified by using oil and a surfactant (Sandoz company, Swiss). In addition, Korean Patent Laid-open No. 96-5136 discloses that drug in alcohol such as ethanol or isopopanol or acetone is mixed with excess water under the condition of forming hydrosol and dried by rotary drying or freeze- drying to make preparation.
However, in the methods of Korean Patent Laid-open No. 96-21056 and Sandoz company, the surfactant used hurts gastrointestinal tract. Furthermore, the method of Korean Patent Publication No. 96-5136 has disadvantages in that manufacturing process is complicate and it is required specific manufacturing technology.
SUMMARY OF THE INVENTION
It is an object of the present invention to provide a method of preparing a pharmaceutical active ingredient comprising a water-insoluble drug with simple and economical process.
It is another object of the present invention to provide a pharmaceutical composition for oral administration comprising the water-insoluble drug.
These and other objects may be achieved by a method of preparing a pharmaceutical active ingredient comprising a water-insoluble drug. The method includes the steps of mixing a water-insoluble drug in an organic solvent with a water-soluble polymer in an aqueous solvent and spray-drying the mixture.
Furthermore, the present invention provides the pharmaceutical composition for oral administration including a pharmaceutical active ingredient including water-insoluble drug microparticles combined with a water-soluble polymer. BRIEF DESCRIPTION OF THE DRAWINGS
A more complete appreciation of the invention, and many of the attendant advantages thereof, will be readily apparent as the same becomes better understood by reference to the following detailed description when considered in conjunction with the accompanying drawing, wherein:
FIG. 1 is a graph showing water-insoluble drug excretion rate after pharmaceutical compositions including pharmaceutical active ingredients of examples 1 to 2 and comparative example 1 is oral administrated; and
FIG. 2 is a schematic diagram showing sprayer for producing water- insoluble drug microparticles combined with a water-soluble polymer used in the present invention.
DETAILED DESCRIPTION OF THE INVENTION
The present invention provides a pharmaceutical active ingredient including water-insoluble drug. The pharmaceutical active ingredient exhibits good bioavailability. For that purpose, in the present invention, microparticles is formed by using a water-insoluble drug and water-soluble polymer without a surfactant which causes gastrointestinal tract damage.
The method of preparing pharmaceutical product for oral administrating water-insoluble drug will be described in more detail.
A water-insoluble drug is dissolved in an organic solvent such as acetone to prepare a drug solution. As the water-insoluble drug, ipriflavone, biphenyl dimethyl dicarboxylate and cyclosporin may be used.
A water-soluble polymer is dissolved in an organic solvent such as ethanol aqueous solution to prepare a polymer solution. As the water-soluble polymer, cellulose type compound may be used. The exemplary of cellulose type compound is ethylcellulose, polyethyleneglycol, carboxymethylcellulose, polyethyleneglycol, polyvinylpyrollidone, dextran, poloxamer and a mixture thereof.
The drug is mixed with the polymer in the weight ratio of 1 : 0.1 to 10, preferably 1 : 0.1 to 2. The mixed solution is spray-dried, thereby obtaining water-insoluble drug powder, microparticles combined with water-soluble polymer. For obtaining microparticles, since rotary-evaporation or freeze-dry step has been used in the conventional process, the preparation is complicate, thereby requiring the specific technology. On the contrary, in the present invention, according to the performance of the spray-drying step, the preparation is simple and therefor, it is not required the specific technology. The exemplary of a spray dryer used in the spray-drying step in the present invention is shown in Fig. 2. As shown in Fig.2, the mixed solution and air are injected into a spray-dryer body, while raising the ambient temperature by the heated air and mixed solution is changed from solution form to microparticle form by heated air. For increasing bioavailability, the drug microparticles combined with polymer may be mixed with oil in the weight of 1 : 1 to 10. It is preferred that the drug microparticles mixed with oil because bioavailability increases. When oil amount is lower than 1 , it is difficult to mix the drug micropartices with oil. On the contrary, oil amount exceeds 10, it is difficult to charge the mixture to a capsule. As the oil, corn oil, peanut oil, coconut oil, caster oil, sesame oil, perilla oil, sunflower oil, walnut oil and cacao butter may be used.
The water-insoluble drug microparticles combined with water-soluble polymer may be used as an active ingredient for a pharmaceutical composition for oral administration.
The pharmaceutical composition further includes vehicle or a disintegrant, a lubricant. In addition, the pharmaceutical compositon may inlcude other pharmaceutical excipients such as stabilizer, a preservatives, an electrolyte, etc used in the pharmaceutics The present invention is further explained in more details with reference to the following examples. The examples are not intended to limit the present invention.
Example 1 1 part by weight of ipriflavone was dissolved in 8 parts by weight of acetone to prepare a water-insoluble drug solution. 2 parts by weight of hydroxypropylmethylcellurose was dissolved in an aqueous ethanol solution including 1 part by weight of water and 1 part by weight of ethanol to prepare a water-soluble polymer solution. 4 parts by weight of the polymer solution was added to 9 parts by weight of the drug solution and mixed well by using a
homogenizer. The mixed solution was spray-dried at 50 °C for 20 minutes by
using a spray-dryer shown in Fig.2 to obtain the water-insoluble drug microparticles combined with water-soluble polymer. 3 parts by weight of the drug microparticles was mixed with 10 parts by weight of corn oil to obtain a pharmaceutical active ingredient. Example 2 A pharmaceutical active ingredient was prepared by the same procedure in Example 1 except that corn oil was not used.
Comparative example 1 The commercial product of Ipriflavone was used for oral administrating water-insoluble drug.
Pharmaceutical compositions of the present invention were prepared by the conventional pharmaceutical process with these pharmaceutical active ingredients of examples 1 to 2. Furthermore, pharmaceutical compositions of comparative example 1 was prepared by disintegrating 0.27 parts by weight of Ipriflavone of comparative example 1 in water. These pharmaceutical compositions was used as powder or tablets. These tablets or powder were oral administered into white rats in the amount of 50 mg of drug per kg of rat's weight with conventional method. The amounts of ipriflavone in the tablets or powder which did not absorbed in the rat's body and excreted to the out of the body were determined. The result shows in Fig. 1.
The result of comparative example 1 show that the most of ingredient ipriflavone did not absorbed in the rat's body and excreted to the out of the body were shown in Fig. 1. As shown in Fig. 1 , when the pharmaceutical active ingredient including the drug microparticles and water of the Example 2 was oral administered, absorption in the body increased two times more than the Comparative example 1. Furthermore, when the pharmaceutical active ingredient including oil of example 1 , absorbing in the body is seven times more than the comparative example 1. As described above, when the drug microparticles obtained by the present invention is oral administered with oil, the increased bioavailability is exhibited. Accordingly, the drug of the present invention can be oral administered. Furthermore, it is not required for the drug to administered into a patient three or four times a day rather than the conventional water-insoluble drug.
While the present invention has been described in detail with reference to the preferred embodiments, those skilled in the art will appreciate that various modifications and substitutions can be made thereto without departing from the spirit and scope of the present invention as set forth in the appended claims.

Claims

WHAT IS CLAIMED IS:
1. A method of preparing a pharmaceutical active ingredient composition including water-insoluble drug for oral administration comprising the steps of: mixing water-insoluble drug in an organic solvent with water-soluble polymer in an aqueous solvent; spray-drying the mixture.
2. The method of claim 1 wherein the polymer is selected from the group consisting of ethylcellulose, polyvinylpyrrolidone, polyethyleneglycol, carboxymethylcellulose, hydroxypropylmethylcellurose, dextran and poloxamer.
3. The method of claim 1 wherein the drug is selected from the group consisting of ipriflavone, biphenyldimethyldicarboxylate and cyclosporin.
4. The method of claim 1 wherein the weight ratio of the drug and polymer is 1 : 0.1 to 10.
5. The method of claim 1 further comprising the step of mixing the microparticles with oil.
6. The method of claim 1 wherein the oil is selected from the group consisting of corn oil, peanut oil, coconut oil, castor oil, sesame oil, perilla oil, sunflower oil, walnut oil and cacao butter.
7. The method of claim 5 wherein the weight ratio of the microparticles and oil is 1 : 1 to 10.
8. A pharmaceutical composition for oral administration, comprising a pharmaceutical active ingredient water-insoluble drug microparticles combined with water-soluble polymer.
9. The pharmaceutical composition of claim 8 wherein the drug is selected from the group consisting of ipriflavone, biphenyldimethyldicarboxylate and cyclosporin.
10. The pharmaceutical composition of claim 8 wherein the polymer is selected from the group consisiting of ethylcellulose, polyvinylpyrrolidone, polyethyleneglycol, carboxymethylcellulose, hydroxypropylmethylcellurose, dextran and poloxomer.
PCT/KR1999/000025 1999-01-06 1999-01-06 Method of preparing pharmaceutical active ingredient comprising water-insoluble drug and pharmaceutical composition for oral administration comprising the same Ceased WO2000040220A1 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
PCT/KR1999/000025 WO2000040220A1 (en) 1999-01-06 1999-01-06 Method of preparing pharmaceutical active ingredient comprising water-insoluble drug and pharmaceutical composition for oral administration comprising the same
EP99901236A EP1058539A1 (en) 1999-01-06 1999-01-06 Method of preparing pharmaceutical active ingredient comprising water-insoluble drug and pharmaceutical composition for oral administration comprising the same
JP2000591977A JP2002534371A (en) 1999-01-06 1999-01-06 Method for producing pharmaceutically active ingredient containing water-insoluble drug and pharmaceutical composition for oral administration containing the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/KR1999/000025 WO2000040220A1 (en) 1999-01-06 1999-01-06 Method of preparing pharmaceutical active ingredient comprising water-insoluble drug and pharmaceutical composition for oral administration comprising the same

Publications (1)

Publication Number Publication Date
WO2000040220A1 true WO2000040220A1 (en) 2000-07-13

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JP (1) JP2002534371A (en)
WO (1) WO2000040220A1 (en)

Cited By (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001047492A1 (en) * 1999-12-23 2001-07-05 F H Faulding & Co Limited Improved pharmaceutical compositions for poorly soluble drugs
WO2004050061A1 (en) * 2002-11-29 2004-06-17 Hanmi Pharm. Co., Ltd. Microemulsion composition for oral administration of biphenyldimethyldicarboxylate
US6835396B2 (en) 2001-09-26 2004-12-28 Baxter International Inc. Preparation of submicron sized nanoparticles via dispersion lyophilization
US6869617B2 (en) 2000-12-22 2005-03-22 Baxter International Inc. Microprecipitation method for preparing submicron suspensions
US6884436B2 (en) 2000-12-22 2005-04-26 Baxter International Inc. Method for preparing submicron particle suspensions
US6951656B2 (en) 2000-12-22 2005-10-04 Baxter International Inc. Microprecipitation method for preparing submicron suspensions
US6977085B2 (en) 2000-12-22 2005-12-20 Baxter International Inc. Method for preparing submicron suspensions with polymorph control
US7112340B2 (en) 2001-10-19 2006-09-26 Baxter International Inc. Compositions of and method for preparing stable particles in a frozen aqueous matrix
US7193084B2 (en) 2000-12-22 2007-03-20 Baxter International Inc. Polymorphic form of itraconazole
WO2008006712A3 (en) * 2006-07-13 2009-02-26 Unilever Plc Preparation of nanodispersions
EP2123255A4 (en) * 2007-02-16 2010-06-02 Aska Pharm Co Ltd PHARMACEUTICAL COMPOSITION CONTAINING OIL BASED SUSPENSION OF FINE PARTICLES
WO2010020518A3 (en) * 2008-08-18 2010-10-14 Unilever Plc Improvements relating to nanodisperse compositions
US8067032B2 (en) 2000-12-22 2011-11-29 Baxter International Inc. Method for preparing submicron particles of antineoplastic agents
US20120076838A1 (en) * 2009-05-27 2012-03-29 Samyang Biopharmaceuticals Corporation Poorly soluble drug containing microsphere with improved bioavailabilty and method of preparing the same
WO2012045994A1 (en) * 2010-10-05 2012-04-12 Iota Nanosolutions Limited Processes for preparing improved compositions
US8268349B2 (en) 2003-08-28 2012-09-18 Abbott Laboratories Solid pharmaceutical dosage form
US8377952B2 (en) 2003-08-28 2013-02-19 Abbott Laboratories Solid pharmaceutical dosage formulation
US8470347B2 (en) 2000-05-30 2013-06-25 AbbVie Deutschland GmbH and Co KG Self-emulsifying active substance formulation and use of this formulation
US8613946B2 (en) 2006-12-21 2013-12-24 Isp Investment Inc. Carotenoids of enhanced bioavailability
US8722091B2 (en) 2001-09-26 2014-05-13 Baxter International Inc. Preparation of submicron sized nanoparticles via dispersion lyophilization
US8921374B2 (en) 2012-06-21 2014-12-30 Mayne Pharma International Pty Ltd Itraconazole compositions and dosage forms, and methods of using the same
WO2015071841A1 (en) 2013-11-12 2015-05-21 Druggability Technologies Holdings Limited Complexes of dabigatran and its derivatives, process for the preparation thereof and pharmaceutical compositions containing them
US9700866B2 (en) 2000-12-22 2017-07-11 Baxter International Inc. Surfactant systems for delivery of organic compounds
US10189957B2 (en) 2007-01-26 2019-01-29 Isp Investments Llc Formulation process method to produce spray dried products
US10532028B2 (en) 2005-07-28 2020-01-14 Isp Investments Llc Method to improve characteristics of spray dried powders and granulated materials, and the products thereby produced

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5672880B2 (en) * 2010-09-14 2015-02-18 大正製薬株式会社 Ipriflavone solubilized composition

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EP0012496A1 (en) * 1978-12-08 1980-06-25 Beecham Group Plc A process for the preparation of a solid sodium amoxycillin and aqueous solutions thereof
EP0670166A2 (en) * 1994-03-01 1995-09-06 Eli Lilly And Company Formulations for orally administered pharmaceutical agents
WO1995032726A1 (en) * 1994-06-01 1995-12-07 Yuhan Corporation Cyclosporin containing composition and process for the preparation thereof
US5817343A (en) * 1996-05-14 1998-10-06 Alkermes, Inc. Method for fabricating polymer-based controlled-release devices

Patent Citations (4)

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Publication number Priority date Publication date Assignee Title
EP0012496A1 (en) * 1978-12-08 1980-06-25 Beecham Group Plc A process for the preparation of a solid sodium amoxycillin and aqueous solutions thereof
EP0670166A2 (en) * 1994-03-01 1995-09-06 Eli Lilly And Company Formulations for orally administered pharmaceutical agents
WO1995032726A1 (en) * 1994-06-01 1995-12-07 Yuhan Corporation Cyclosporin containing composition and process for the preparation thereof
US5817343A (en) * 1996-05-14 1998-10-06 Alkermes, Inc. Method for fabricating polymer-based controlled-release devices

Cited By (41)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6881745B2 (en) 1999-12-23 2005-04-19 F H Faulding & Co Limited Pharmaceutical compositions for poorly soluble drugs
US8771739B2 (en) 1999-12-23 2014-07-08 Mayne Pharma International Pty Ltd Pharmaceutical compositions for poorly soluble drugs
WO2001047492A1 (en) * 1999-12-23 2001-07-05 F H Faulding & Co Limited Improved pharmaceutical compositions for poorly soluble drugs
US8470347B2 (en) 2000-05-30 2013-06-25 AbbVie Deutschland GmbH and Co KG Self-emulsifying active substance formulation and use of this formulation
US6869617B2 (en) 2000-12-22 2005-03-22 Baxter International Inc. Microprecipitation method for preparing submicron suspensions
US6884436B2 (en) 2000-12-22 2005-04-26 Baxter International Inc. Method for preparing submicron particle suspensions
US6951656B2 (en) 2000-12-22 2005-10-04 Baxter International Inc. Microprecipitation method for preparing submicron suspensions
US6977085B2 (en) 2000-12-22 2005-12-20 Baxter International Inc. Method for preparing submicron suspensions with polymorph control
US7037528B2 (en) 2000-12-22 2006-05-02 Baxter International Inc. Microprecipitation method for preparing submicron suspensions
US7193084B2 (en) 2000-12-22 2007-03-20 Baxter International Inc. Polymorphic form of itraconazole
US9700866B2 (en) 2000-12-22 2017-07-11 Baxter International Inc. Surfactant systems for delivery of organic compounds
US8067032B2 (en) 2000-12-22 2011-11-29 Baxter International Inc. Method for preparing submicron particles of antineoplastic agents
US8722091B2 (en) 2001-09-26 2014-05-13 Baxter International Inc. Preparation of submicron sized nanoparticles via dispersion lyophilization
US6835396B2 (en) 2001-09-26 2004-12-28 Baxter International Inc. Preparation of submicron sized nanoparticles via dispersion lyophilization
US7112340B2 (en) 2001-10-19 2006-09-26 Baxter International Inc. Compositions of and method for preparing stable particles in a frozen aqueous matrix
WO2004050061A1 (en) * 2002-11-29 2004-06-17 Hanmi Pharm. Co., Ltd. Microemulsion composition for oral administration of biphenyldimethyldicarboxylate
US8268349B2 (en) 2003-08-28 2012-09-18 Abbott Laboratories Solid pharmaceutical dosage form
US8691878B2 (en) 2003-08-28 2014-04-08 Abbvie Inc. Solid pharmaceutical dosage form
US8309613B2 (en) 2003-08-28 2012-11-13 Abbvie Inc. Solid pharmaceutical dosage form
US8333990B2 (en) 2003-08-28 2012-12-18 Abbott Laboratories Solid pharmaceutical dosage form
US8377952B2 (en) 2003-08-28 2013-02-19 Abbott Laboratories Solid pharmaceutical dosage formulation
US8399015B2 (en) 2003-08-28 2013-03-19 Abbvie Inc. Solid pharmaceutical dosage form
US10532028B2 (en) 2005-07-28 2020-01-14 Isp Investments Llc Method to improve characteristics of spray dried powders and granulated materials, and the products thereby produced
AU2007271827B2 (en) * 2006-07-13 2010-10-14 Unilever Plc Improvements relating to nanodispersions
WO2008006712A3 (en) * 2006-07-13 2009-02-26 Unilever Plc Preparation of nanodispersions
US8613946B2 (en) 2006-12-21 2013-12-24 Isp Investment Inc. Carotenoids of enhanced bioavailability
US10189957B2 (en) 2007-01-26 2019-01-29 Isp Investments Llc Formulation process method to produce spray dried products
US8309138B2 (en) 2007-02-16 2012-11-13 Aska Pharmaceutical Co., Ltd. Pharmaceutical composition comprising microparticle oily suspension
EP2123255A4 (en) * 2007-02-16 2010-06-02 Aska Pharm Co Ltd PHARMACEUTICAL COMPOSITION CONTAINING OIL BASED SUSPENSION OF FINE PARTICLES
WO2010020518A3 (en) * 2008-08-18 2010-10-14 Unilever Plc Improvements relating to nanodisperse compositions
US20120076838A1 (en) * 2009-05-27 2012-03-29 Samyang Biopharmaceuticals Corporation Poorly soluble drug containing microsphere with improved bioavailabilty and method of preparing the same
AU2010253578B2 (en) * 2009-05-27 2014-01-30 Samyang Biopharmaceuticals Corporation A poorly soluble drug containing microsphere with improved bioavailability and method of preparing the same
US9511026B2 (en) 2009-05-27 2016-12-06 Samyang Biopharmaceuticals Corporation Poorly soluble drug containing microspheres with improved bioavailability and method of preparing the same
WO2012045994A1 (en) * 2010-10-05 2012-04-12 Iota Nanosolutions Limited Processes for preparing improved compositions
US10463740B2 (en) 2012-06-21 2019-11-05 Mayne Pharma International Pty. Ltd. Itraconazole compositions and dosage forms, and methods of using the same
US9713642B2 (en) 2012-06-21 2017-07-25 Mayne Pharma International Pty. Ltd. Itraconazole compositions and dosage forms, and methods of using the same
US9272046B2 (en) 2012-06-21 2016-03-01 Mayne Pharma International Pty. Ltd. Itraconazole compositions and dosage forms, and methods of using the same
US8921374B2 (en) 2012-06-21 2014-12-30 Mayne Pharma International Pty Ltd Itraconazole compositions and dosage forms, and methods of using the same
US10806792B2 (en) 2012-06-21 2020-10-20 Mayne Pharma International Pty Ltd. Itraconazole compositions and dosage forms, and methods of using the same
US11638758B2 (en) 2012-06-21 2023-05-02 Mayne Pharma International Pty. Ltd Itraconazole compositions and dosage forms, and methods of using the same
WO2015071841A1 (en) 2013-11-12 2015-05-21 Druggability Technologies Holdings Limited Complexes of dabigatran and its derivatives, process for the preparation thereof and pharmaceutical compositions containing them

Also Published As

Publication number Publication date
JP2002534371A (en) 2002-10-15
EP1058539A1 (en) 2000-12-13

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