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US20090281177A1 - Butylphthalide Intravenous Emulsion and Application Thereof - Google Patents

Butylphthalide Intravenous Emulsion and Application Thereof Download PDF

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Publication number
US20090281177A1
US20090281177A1 US12/086,665 US8666506A US2009281177A1 US 20090281177 A1 US20090281177 A1 US 20090281177A1 US 8666506 A US8666506 A US 8666506A US 2009281177 A1 US2009281177 A1 US 2009281177A1
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Prior art keywords
oil
butylphthalide
mixture
emulsion according
amount
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
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US12/086,665
Inventor
Chunshun Zhao
Zhanqi Niu
Zhen Chen
Haibo Guo
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SHIJIAZHUAN PHARMA GROUP NBP PHARMACEUTICAL Co Ltd
Shijiazhuang Pharma Group NBP Pharmaceutical Co Ltd
Original Assignee
SHIJIAZHUAN PHARMA GROUP NBP PHARMACEUTICAL Co Ltd
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Assigned to SHIJIAZHUANG PHARMA GROUP NBP PHARMACEUTICAL CO., LTD. reassignment SHIJIAZHUANG PHARMA GROUP NBP PHARMACEUTICAL CO., LTD. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: ZHAO, CHUNSHUN, CHEN, ZHEN, GUO, HAIBO, NIU, ZHANQI
Publication of US20090281177A1 publication Critical patent/US20090281177A1/en
Abandoned legal-status Critical Current

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    • 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
    • A61K9/10—Dispersions; Emulsions
    • A61K9/107—Emulsions ; Emulsion preconcentrates; Micelles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
    • A61K31/343—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/365—Lactones
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • 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
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis

Definitions

  • the present invention relates to a butylphthalide preparation, and specifically to a butylphthalide intravenous emulsion and application thereof.
  • NBP dl-3-n-Butylphthalide
  • 1-3-n-Butylphthalid is extracted from celery seeds.
  • NBP acts on multiple steps of cerebral ischemia procedure, such as reducing infarct area after focal cerebral ischemia, increasing cerebral blood flow in ischemic area and improving microcirculation in cerebral ischemic area, protecting mitochondrial function, alleviating damage to nerve function, and improving cerebral energy metabolism after total cerebral ischemia.
  • butylphthalide preparations available in market are only soft capsules. Since butylphthalide is of an oily liquid form, it can be dissolved in an oil phase or directly processed to form an emulsion, then can be packaged in hard capsules or soft capsules, or can be orally administered directly. However, butylphthalide has a relatively apparent first pass effect which leads to a relatively low bioavailability.
  • cerebral ischemia patients usually are integrated with dysphagia or coma, so that capsules cannot meet the clinical requirements for these patients. For cerebral ischemia patients, time is life. Therefore, it is vital to develop a new delivery system suitable for clinical application.
  • butylphthalide is an oily liquid and hardly dissoluble in water
  • a specific manufacture technology is employed in the present invention to process butylphthalide into an emulsion for intravenous administration.
  • the butylphthalide intravenous emulsion of the present invention has the following advantages: the drug directly enters into systemic circulation, thus resulting in quick action; the solubility of butylphthalide is improved, resulting in a reduced dosage; and/or the targeting of butylphthalide to brain tissue is improved, thus reducing its toxic side-effects.
  • the emulsion of the present invention has a particle size of between 10 and 2000 nm, and may be administered via intravenous injection or infusion in order to achieve quick action and brain targeting effect.
  • the butylphthalide intravenous emulsion of the present invention comprises butylphthalide or derivatives thereof as an active ingredient in an amount of 0.01 ⁇ 50 wt %, preferably 0.01 ⁇ 20 wt %, more preferably 0.01 ⁇ 10 wt %, and an excipient in an amount of 50 ⁇ 99.99 wt %, preferably 80 ⁇ 99.9 wt %, more preferably 90 ⁇ 99.5 %, based on the total weight of the emulsion.
  • the excipient comprises an oil phase, an aqueous phase, an emulsifier, a stabilizer and/or an osmoregulation agent.
  • Butylphthalide or derivatives thereof may be either a raceme of butylphthalide or derivatives thereof, or l-butylphthalide or derivatives thereof.
  • the excipient may comprise an oil phase in an amount of 0 ⁇ 50 wt %, preferably 0.1 ⁇ 40 wt %, an aqueous phase in an amount of 50 ⁇ 98 wt %, preferably 60 ⁇ 97 wt %, an emulsifier in an amount of 0.01 ⁇ 50 wt %, preferably 0.5 ⁇ 10 wt %, a stabilizer in an amount of 0 ⁇ 50 wt %, preferably 0 ⁇ 15 wt %, and an osmoregulation agent in an amount of 0 ⁇ 10 wt %, all based on the total weight of the excipient.
  • the process for manufacture of the butylphthalide intravenous emulsion of the present invention comprises the steps of, such as preparing a primary emulsion, homogenizing, sterilizing and quality controlling.
  • the step of preparing the primary emulsion is carried out by utilizing ultrasonic method or high-speed shearing method (FA25 Model High Shear Emulsifying Machine, FLUKO Equipment Shanghai Co., Ltd.).
  • the step of homogenizing is carried out by utilizing a two-stage high pressure emulsifying and homogenizing method (Niro-Soavi NS1001L Model High Pressure Homogenizer and Avestin EmulsiFlex-C5 High Pressure Homogenizer) or microfluidizing technology.
  • the step of sterilizing is carried out by using high pressure sterilizing under rotation.
  • the quality controlling is mainly carried out by measuring particle size.
  • the oil phase generally has an amount in mass of 0 ⁇ 50% (w/v). It is required in the present invention that a therapeutically effective amount of drug should be dissolved in a relatively small amount of oil phase, no drug precipitate occurs or no layer separation occurs under cryogenic storage condition, and in the meantime a stable emulsion is able to be formed with an aqueous phase in the presence of an emulsifier.
  • the oil phase as used in the present invention may be a natural vegetable oil with long chain fatty acid ester groups or a vegetable oil or fatty acid ester being subjected to structure modification and hydrolysis.
  • the examples of those may be one of or a mixture of soybean oil (especially in injection grade), castor oil, tea-seed oil, peanut oil, cottonseed oil, sesame oil, rape oil, safflower oil, olive oil, coconut oil, palm oil and cacao oil; or may be a glyceride with a chain length of C 6 ⁇ C 12 fatty acid, such as but not limited to Arlacel 80, Arlacel 86, Capmul MCM, Captex 200 (oil), Captex 355 (oil), Miglyol 812 (oil), Myvacet (oil), Myverol 18-92, glyceride oleate, glyceride linoleate, macrogol glyceryl laurate, ethyl oleate, ethyl linoleate, caprylocaproyl triglyceride, and a mixture thereof; or may be a mixture of the above long chain fatty acid esters and medium-chain fatty acid est
  • oils may also be used in the present invention:
  • the emulsifier as used in the present invention may be one of or a mixture of nonionic surfactants and anionic surfactants.
  • the preferred emulsifier may be but not limited to one of or a mixture of soybean lecithin or modified soybean lecthin (natural or synthesized), ovolecithin or modified ovolecithin (natural or synthesized), Ophase 31, Poloxamer 108, Poloxamer 188, Poloxamer 407, polyoxyethylene (hydrogenated) castor oil, water soluble VE (TPGS), Solutol HS-15, PEG-400 monostearate, PEG-1750 monostearate, Tween-80, Tween-20, and Span-20.
  • the preferred emulsifier has relatively little haemolysis effect and is refined.
  • the following may also be used in the butylphthalide emulsion of the present invention:
  • Suitable stabilizer as used in the present invention may be but not limited to one of or a mixture of oleic acid, sodium oleate, sodium caprylate, cholesterol, cholic acid, deoxycholic acid and sodium salt thereof, vitamin A, vitamin C, and vitamin E.
  • Suitable osmoregulation agent as used in the present invention may be but not limited to one of or a mixture of sodium chloride, glucose, sorbitol, xylitol, mannitol, and glycerol.
  • the ratio of butylphthalide:oil phase:emulsifier:aqueous phase:stabilizer:osmoregulation agent is any ratio (by weight) within the range of 0.01 ⁇ 50 wt %:0 ⁇ 50 wt %:0.01 ⁇ 50 wt %:50 ⁇ 98 wt %:0 ⁇ 50 wt %:0 ⁇ 10 wt %.
  • the butylphthalide intravenous emulsion of the present invention has the following composition:
  • composition (g) Butylphthalide 10 Soybean lecithin 12 Soybean oil 100 Vitamin E 1 Sorbitol 25 Water for injection Added to 1000 ml
  • the preparation process comprises the steps of: butylphthalide, vitamin E and soybean oil were weighed and mixed to form an oil phase, and the oil phase was pre-heated in a 60° C. water bath. Soybean lecithin and sorbitol were weighed and dispersed in water to form an aqueous phase, and the aqueous phase was pre-heated in a 60° C. water bath. The oil phase was slowly poured into the aqueous phase, and the mixture was dispersed by using a high shear emulsifying machine under 10,000 rpm for 5 min. Then the mixture was circulated in a high pressure homogenizer for 5 times, in which the first stage pressure is 100 MPa and the second stage pressure is 10 MPa. Then the emulsion was regulated to have a pH of 8, filtered, subpackaged and sterilized at 121° C. for 15 min. Nitrogen gas is fed for protection during the whole process.
  • composition (g) Butylphthalide 15 Castor oil 100 Soybean lecithin 12 Poloxamer 188 6 Glycerol 25 Oleic acid 10 Water for injection Added to 1000 ml
  • the preparation process comprises the steps of: butylphthalide, soybean lecithin, oleic acid and castor oil were weighed and mixed to form an oil phase, and the oil phase was pre-heated in a 60° C. water bath. Poloxamer 188 and glycerol were weighed and dispersed in water to form an aqueous phase, and the aqueous phase was pre-heated in a 60° C. water bath. The oil phase was slowly poured into the aqueous phase, and the mixture was dispersed by using a high shear emulsifying machine under 10,000 rpm for 5 min.
  • the mixture was circulated in a high pressure homogenizer for 5 times, in which the first stage pressure is 100 MPa and the second stage pressure is 10 MPa. Then the emulsion was regulated to have a pH of 8, filtered, subpackaged and sterilized at 121° C. for 15 min. Nitrogen gas is fed for protection during the whole process.
  • composition (g) Butylphthalide 20 Soybean lecithin 12 Olive oil 100 Cholic acid 1 Mannitol 20 Water for injection Added to 1000 ml
  • the preparation process comprises the steps of: butylphthalide, cholic acid and olive oil were weighed and mixed to form an oil phase, and the oil phase was pre-heated in a 60° C. water bath. Soybean lecithin and mannitol were weighed and dispersed in water to form an aqueous phase, and the aqueous phase was pre-heated in a 60° C. water bath. The oil phase was slowly poured into the aqueous phase, and the mixture was treated with ultrasonic waves for 10 times (10 seconds for each time, power: 400W). Then the mixture was circulated in a high pressure homogenizer for 5 times, in which the first stage pressure is 100 MPa and the second stage pressure is 10 MPa. Then the emulsion was regulated to have a pH of 8, filtered, subpackaged and sterilized at 121° C. for 15 min. Nitrogen gas is fed for protection during the whole process.
  • composition (g) Butylphthalide 25 Cottonseed oil 100 Ovolecithin 12 Poloxamer 188 20 Glycerol 25 Sodium oleate 10 Water for injection Added to 1000 ml
  • the preparation process comprises the steps of: butylphthalide, ovolecithin, sodium oleate and cottonseed oil were weighed and mixed to form an oil phase, and the oil phase was pre-heated in a 60° C. water bath. Poloxamer 188 and glycerol were weighed and dispersed in water to form an aqueous phase, and the aqueous phase was pre-heated in a 60° C. water bath. The oil phase was slowly poured into the aqueous phase, and the mixture was dispersed by using a high shear emulsifying machine under 10,000 rpm for 5 min.
  • the mixture was circulated in a high pressure homogenizer for 5 times, in which the first stage pressure is 100 MPa and the second stage pressure is 10 MPa. Then the emulsion was regulated to have a pH of 8, filtered, subpackaged and sterilized at 121° C. for 15 min. Nitrogen gas is fed for protection during the whole process.
  • composition (g) Butylphthalide 30 Soybean lecithin 12 Soybean oil 200 Tween 80 6 Vitamin E 8 Xylitol 100 Water for injection Added to 1000 ml
  • the preparation process comprises the steps of: butylphthalide, Tween 80, vitamin E and soybean oil were weighed and mixed to form an oil phase, and the oil phase was pre-heated in a 60° C. water bath. Soybean lecithin and xylitol were weighed and dispersed in water to form an aqueous phase, and the aqueous phase was pre-heated in a 60° C. water bath. The oil phase was slowly poured into the aqueous phase, and the mixture was dispersed by using a high shear emulsifying machine under 10,000 rpm for 5 min. Then the mixture was circulated in a high pressure homogenizer for 5 times, in which the first stage pressure is 100 MPa and the second stage pressure is 10 MPa. Then the emulsion was regulated to have a pH of 8, filtered, subpackaged and sterilized at 121° C. for 15 min. Nitrogen gas is fed for protection during the whole process.
  • composition (g) Butylphthalide 40 Caprylocaproyl triglyceride 200 Soybean lecithin 12 Poloxamer 188 20 Glycerol 25 Oleic acid 10 Water for injection Added to 1000 ml
  • the preparation process comprises the steps of: butylphthalide, soybean lecithin, oleic acid and caprylocaproyl triglyceride were weighed and mixed to form an oil phase, and the oil phase was pre-heated in a 60° C. water bath. Poloxamer 188 and glycerol were weighed and dispersed in water to form an aqueous phase, and the aqueous phase was pre-heated in a 60° C. water bath. The oil phase was slowly poured into the aqueous phase, and the mixture was dispersed by using a high shear emulsifying machine under 10,000 rpm for 5 min.
  • the mixture was circulated in a high pressure homogenizer for 5 times, in which the first stage pressure is 100 MPa and the second stage pressure is 10 MPa. Then the emulsion was regulated to have a pH of 8, filtered, subpackaged and sterilized at 121° C. for 15 min. Nitrogen gas is fed for protection during the whole process.
  • composition (g) Butylphthalide 50 Soybean lecithin 15 Sesame oil 100 Vitamin E 8 Glycerol 22.5 Water for injection Added to 1000 ml
  • the preparation process comprises the steps of butylphthalide, vitamin E and sesame oil were weighed and mixed to form an oil phase, and the oil phase was pre-heated in a 60° C. water bath. Soybean lecithin and glycerol were weighed and dispersed in water to form an aqueous phase, and the aqueous phase was pre-heated in a 60° C. water bath. The oil phase was slowly poured into the aqueous phase, and the mixture was dispersed by using a high shear emulsifying machine under 10,000 rpm for 5 min. Then the mixture was circulated in a high pressure homogenizer for 5 times, in which the first stage pressure is 100 MPa and the second stage pressure is 10 MPa. Then the emulsion was regulated to have a pH of 8, filtered, subpackaged and sterilized at 121° C. for 15 min. Nitrogen gas is fed for protection during the whole process.
  • composition (g) Butylphthalide 20 Soybean oil 100 Ovolecithin 12 Poloxamer 188 20 Glycerol 25 Sodium oleate 10 Water for injection Added to 1000 ml
  • the preparation process comprises the steps of butylphthalide, ovolecithin, sodium oleate and soybean oil were weighed and mixed to form an oil phase, and the oil phase was pre-heated in a 60° C. water bath. Poloxamer 188 and glycerol were weighed and dispersed in water to form an aqueous phase, and the aqueous phase was pre-heated in a 60° C. water bath. The oil phase was slowly poured into the aqueous phase, and the mixture was dispersed by using a high shear emulsifying machine under 10,000 rpm for 5 min.
  • the mixture was circulated in a high pressure homogenizer for 5 times, in which the first stage pressure is 100 MPa and the second stage pressure is 10 MPa. Then the emulsion was regulated to have a pH of 8, filtered, subpackaged and sterilized at 121° C. for 15 min. Nitrogen gas is fed for protection during the whole process.
  • composition (g) Butylphthalide 100 Ovolecithin 20 Poloxamer 188 20 Glycerol 25 Sodium oleate 30 Water for injection Added to 1000 ml
  • the preparation process comprises the steps of: butylphthalide, ovolecithin and sodium oleate were weighed and mixed to form an oil phase, and the oil phase was pre-heated in a 60° C. water bath. Poloxamer 188 and glycerol were weighed and dispersed in water to form an aqueous phase, and the aqueous phase was pre-heated in a 60° C. water bath. The oil phase was slowly poured into the aqueous phase, and the mixture was dispersed by using a high shear emulsifying machine under 10,000 rpm for 5 min. Then the mixture was circulated in a high pressure homogenizer for 5 times, in which the first stage pressure is 100 MPa and the second stage pressure is 10 MPa. Then the emulsion was regulated to have a pH of 8, filtered, subpackaged and sterilized at 121° C. for 15 min. Nitrogen gas is fed for protection during the whole process.
  • composition (g) Butylphthalide 0.1 Soybean oil 100 Ovolecithin 19 Poloxamer 188 25 Glycerol 25 Water for injection Added to 1000 ml
  • the preparation process comprises the steps of butylphthalide, ovolecithin and soybean oil were weighed and mixed to form an oil phase, and the oil phase was pre-heated in a 60° C. water bath. Poloxamer 188 and glycerol were weighed and dispersed in water to form an aqueous phase, and the aqueous phase was pre-heated in a 60° C. water bath. The oil phase was slowly poured into the aqueous phase, and the mixture was dispersed by using a high shear emulsifying machine under 10,000 rpm for 5 min. Then the mixture was circulated in a high pressure homogenizer for 5 times, in which the first stage pressure is 100 MPa and the second stage pressure is 10 MPa. Then the emulsion was regulated to have a pH of 8, filtered, subpackaged and sterilized at 121° C. for 15 min. Nitrogen gas is fed for protection during the whole process.
  • composition (g) Butylphthalide 5 Soybean oil 100 Ovolecithin 12 Poloxamer 188 20 Sodium oleate 3 Water for injection Added to 1000 ml
  • the preparation process comprises the steps of: butylphthalide, ovolecithin, sodium oleate and soybean oil were weighed and mixed to form an oil phase, and the oil phase was pre-heated in a 60° C. water bath. Poloxamer 188 was weighed and dispersed in water to form an aqueous phase, and the aqueous phase was pre-heated in a 60° C. water bath. The oil phase was slowly poured into the aqueous phase, and the mixture was dispersed by using a high shear emulsifying machine under 10,000 rpm for 5 min. Then the mixture was circulated in a high pressure homogenizer for 5 times, in which the first stage pressure is 100 MPa and the second stage pressure is 10 MPa. Then the emulsion was regulated to have a pH of 8, filtered, subpackaged and sterilized at 121° C. for 15 min. Nitrogen gas is fed for protection during the whole process.

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Abstract

The present invention discloses a butylphthalide intravenous emulsion for intravenous injection or infusion, containing butylphthalide or derivatives thereof as an active ingredient in an amount of 0.01˜50 wt % and an excipient in an amount of 50˜99.99 wt %, based on the total weight of the emulsion.

Description

    CROSS-REFERENCE TO RELATED APPLICATIONS
  • This application claims priority to PCT International Application No. PCT/CN2006/003434, filed on Dec. 15, 2006, which claims priority to Chinese Patent Application No. 200510102355.2, filed on Dec. 16, 2005, hereby incorporated by reference.
    • FIELD OF INVENTION
  • The present invention relates to a butylphthalide preparation, and specifically to a butylphthalide intravenous emulsion and application thereof.
    • BACKGROUND OF THE INVENTION
  • dl-3-n-Butylphthalide (NBP) also called butylphthalide is dl-3-butylisobenzofuran-1(3H)-one, which is a raceme. 1-3-n-Butylphthalid is extracted from celery seeds. NBP acts on multiple steps of cerebral ischemia procedure, such as reducing infarct area after focal cerebral ischemia, increasing cerebral blood flow in ischemic area and improving microcirculation in cerebral ischemic area, protecting mitochondrial function, alleviating damage to nerve function, and improving cerebral energy metabolism after total cerebral ischemia. Chinese Patent Nos. 98125618.X, 03137457.3, 200310100222.2 and 200410001748.X respectively disclose the applications of butylphthalide in anti-thrombus and anti-platelet aggregation, the application of l-n-butylphthalide in prevention and treatment of dementia, cerebral infarction and in manufacture of medicaments for treatment of cerebral ischemia.
  • Currently butylphthalide preparations available in market are only soft capsules. Since butylphthalide is of an oily liquid form, it can be dissolved in an oil phase or directly processed to form an emulsion, then can be packaged in hard capsules or soft capsules, or can be orally administered directly. However, butylphthalide has a relatively apparent first pass effect which leads to a relatively low bioavailability. In addition, cerebral ischemia patients usually are companied with dysphagia or coma, so that capsules cannot meet the clinical requirements for these patients. For cerebral ischemia patients, time is life. Therefore, it is vital to develop a new delivery system suitable for clinical application.
    • SUMMARY OF THE INVENTION
  • Since butylphthalide is an oily liquid and hardly dissoluble in water, a specific manufacture technology is employed in the present invention to process butylphthalide into an emulsion for intravenous administration. The butylphthalide intravenous emulsion of the present invention has the following advantages: the drug directly enters into systemic circulation, thus resulting in quick action; the solubility of butylphthalide is improved, resulting in a reduced dosage; and/or the targeting of butylphthalide to brain tissue is improved, thus reducing its toxic side-effects.
  • The emulsion of the present invention has a particle size of between 10 and 2000 nm, and may be administered via intravenous injection or infusion in order to achieve quick action and brain targeting effect.
  • The butylphthalide intravenous emulsion of the present invention comprises butylphthalide or derivatives thereof as an active ingredient in an amount of 0.01˜50 wt %, preferably 0.01˜20 wt %, more preferably 0.01˜10 wt %, and an excipient in an amount of 50˜99.99 wt %, preferably 80˜99.9 wt %, more preferably 90˜99.5 %, based on the total weight of the emulsion. The excipient comprises an oil phase, an aqueous phase, an emulsifier, a stabilizer and/or an osmoregulation agent. Butylphthalide or derivatives thereof may be either a raceme of butylphthalide or derivatives thereof, or l-butylphthalide or derivatives thereof.
  • The excipient may comprise an oil phase in an amount of 0˜50 wt %, preferably 0.1˜40 wt %, an aqueous phase in an amount of 50˜98 wt %, preferably 60˜97 wt %, an emulsifier in an amount of 0.01˜50 wt %, preferably 0.5˜10 wt %, a stabilizer in an amount of 0˜50 wt %, preferably 0˜15 wt %, and an osmoregulation agent in an amount of 0˜10 wt %, all based on the total weight of the excipient.
  • The process for manufacture of the butylphthalide intravenous emulsion of the present invention comprises the steps of, such as preparing a primary emulsion, homogenizing, sterilizing and quality controlling. The step of preparing the primary emulsion is carried out by utilizing ultrasonic method or high-speed shearing method (FA25 Model High Shear Emulsifying Machine, FLUKO Equipment Shanghai Co., Ltd.). The step of homogenizing is carried out by utilizing a two-stage high pressure emulsifying and homogenizing method (Niro-Soavi NS1001L Model High Pressure Homogenizer and Avestin EmulsiFlex-C5 High Pressure Homogenizer) or microfluidizing technology. The step of sterilizing is carried out by using high pressure sterilizing under rotation. The quality controlling is mainly carried out by measuring particle size.
    • DETAILED DESCRIPTION OF THE INVENTION (1) Selection of Oil Phase
  • In the emulsion of the present invention, the oil phase generally has an amount in mass of 0˜50% (w/v). It is required in the present invention that a therapeutically effective amount of drug should be dissolved in a relatively small amount of oil phase, no drug precipitate occurs or no layer separation occurs under cryogenic storage condition, and in the meantime a stable emulsion is able to be formed with an aqueous phase in the presence of an emulsifier. The oil phase as used in the present invention may be a natural vegetable oil with long chain fatty acid ester groups or a vegetable oil or fatty acid ester being subjected to structure modification and hydrolysis. The examples of those may be one of or a mixture of soybean oil (especially in injection grade), castor oil, tea-seed oil, peanut oil, cottonseed oil, sesame oil, rape oil, safflower oil, olive oil, coconut oil, palm oil and cacao oil; or may be a glyceride with a chain length of C6˜C12 fatty acid, such as but not limited to Arlacel 80, Arlacel 86, Capmul MCM, Captex 200 (oil), Captex 355 (oil), Miglyol 812 (oil), Myvacet (oil), Myverol 18-92, glyceride oleate, glyceride linoleate, macrogol glyceryl laurate, ethyl oleate, ethyl linoleate, caprylocaproyl triglyceride, and a mixture thereof; or may be a mixture of the above long chain fatty acid esters and medium-chain fatty acid esters.
  • During the manufacture of an injection emulsion, a preferred oil phase has relatively little haemolysis effect and is refined. Besides generally used vegetable oils, the following oils may also be used in the present invention:
  •
    Arlacel 80 (HLB = 4.3) Sorbitan monooleate
    Arlacel 86 (HLB = 2.8) Glyceride oleate: propylene glycol (90:10)
    Capmul MCM Coconut oil C8/C10 monoglyceride
    (HLB = 5.5~6.0) or diglyceride
    Captex 200 (oil) Coconut oil C8/C10 propylene glycol diester
    Captex 355 (oil) Coconut oil C8/C10 triglyceride
    Miglyol 812 (oil) Coconut oil C8/C10 triglyceride
    Myvacet (oil) Purified and acetylated monoglyceride
    Myverol 18-92 (HLB-3~7) Purified sunflower oil monoglyceride
    (containing 90% of glyceride linoleate)
    Peceol (HLB = 3) Glyceride oleate
    Maisine (HLB = 3) Glyceride linoleate
    Gelucire 44/14 (HLB = 14) Macrogol glyceryl laurate
    • (2) Selection of Emulsifier
  • The emulsifier as used in the present invention may be one of or a mixture of nonionic surfactants and anionic surfactants.. The preferred emulsifier may be but not limited to one of or a mixture of soybean lecithin or modified soybean lecthin (natural or synthesized), ovolecithin or modified ovolecithin (natural or synthesized), Ophase 31, Poloxamer 108, Poloxamer 188, Poloxamer 407, polyoxyethylene (hydrogenated) castor oil, water soluble VE (TPGS), Solutol HS-15, PEG-400 monostearate, PEG-1750 monostearate, Tween-80, Tween-20, and Span-20. It is preferred to use a mixture of these emulsifiers. During the manufacture of an injection emulsion, the preferred emulsifier has relatively little haemolysis effect and is refined. Besides the above emulsifiers, the following may also be used in the butylphthalide emulsion of the present invention:
  •
    Ophase 31 (HLB = 4) Liquid lecithin
    Soybean lecithin (HLB = 4/7/9) Soybean lecithin
    Cremophor EL (HLB = 13.5) Polyoxyethylene castor oil
    Poloxamer 108 (HLB = 30.5) Polyoxyethylene polyoxypropylene
    ether F-38
    Poloxamer 188 (HLB = 29) Polyoxyethylene polyoxypropylene
    ether F-68
    Poloxamer 407 (HLB = 21.5) Polyoxyethylene polyoxypropylene
    ether F-127
    Tween 80 (HLB = 15) Polyoxyethylene sorbitan monoleate
    Tween 20 (HLB = 16.7) Polyoxyethylene sorbitan monolaurate
    Span 20 (HLB = 8.6) Sorbitan monolaurate
    • (3) Selection of Stabilizer
  • Suitable stabilizer as used in the present invention may be but not limited to one of or a mixture of oleic acid, sodium oleate, sodium caprylate, cholesterol, cholic acid, deoxycholic acid and sodium salt thereof, vitamin A, vitamin C, and vitamin E.
    • (4) Selection of Osmoregulation Agent
  • Suitable osmoregulation agent as used in the present invention may be but not limited to one of or a mixture of sodium chloride, glucose, sorbitol, xylitol, mannitol, and glycerol.
    • (5) Basic Formulation of Butylphthalide Intravenous Emulsion
  • In the butylphthalide intravenous emulsion of the present invention, the ratio of butylphthalide:oil phase:emulsifier:aqueous phase:stabilizer:osmoregulation agent is any ratio (by weight) within the range of 0.01˜50 wt %:0˜50 wt %:0.01˜50 wt %:50˜98 wt %:0˜50 wt %:0˜10 wt %.
  • In one embodiment, the butylphthalide intravenous emulsion of the present invention has the following composition:
  •
    Butylphthalide 10 g
    Oil phase 100 g
    Emulsifier 50 g
    Stabilizer 50 g
    Aqueous phase Added to 1000 ml
    • DESCRIPTION OF THE PREFERRED EMBODIMENTS EXAMPLE 1 Preparation of Butylphthalide Intravenous Emulsion
  • Formula composition (g)
    Butylphthalide 10
    Soybean lecithin 12
    Soybean oil 100
    Vitamin E 1
    Sorbitol 25
    Water for injection Added to 1000 ml
  • The preparation process comprises the steps of: butylphthalide, vitamin E and soybean oil were weighed and mixed to form an oil phase, and the oil phase was pre-heated in a 60° C. water bath. Soybean lecithin and sorbitol were weighed and dispersed in water to form an aqueous phase, and the aqueous phase was pre-heated in a 60° C. water bath. The oil phase was slowly poured into the aqueous phase, and the mixture was dispersed by using a high shear emulsifying machine under 10,000 rpm for 5 min. Then the mixture was circulated in a high pressure homogenizer for 5 times, in which the first stage pressure is 100 MPa and the second stage pressure is 10 MPa. Then the emulsion was regulated to have a pH of 8, filtered, subpackaged and sterilized at 121° C. for 15 min. Nitrogen gas is fed for protection during the whole process.
    • EXAMPLE 2 Preparation of Butylphthalide Intravenous Emulsion
  • Formula composition (g)
    Butylphthalide 15
    Castor oil 100
    Soybean lecithin 12
    Poloxamer 188 6
    Glycerol 25
    Oleic acid 10
    Water for injection Added to 1000 ml
  • The preparation process comprises the steps of: butylphthalide, soybean lecithin, oleic acid and castor oil were weighed and mixed to form an oil phase, and the oil phase was pre-heated in a 60° C. water bath. Poloxamer 188 and glycerol were weighed and dispersed in water to form an aqueous phase, and the aqueous phase was pre-heated in a 60° C. water bath. The oil phase was slowly poured into the aqueous phase, and the mixture was dispersed by using a high shear emulsifying machine under 10,000 rpm for 5 min. Then the mixture was circulated in a high pressure homogenizer for 5 times, in which the first stage pressure is 100 MPa and the second stage pressure is 10 MPa. Then the emulsion was regulated to have a pH of 8, filtered, subpackaged and sterilized at 121° C. for 15 min. Nitrogen gas is fed for protection during the whole process.
    • EXAMPLE 3 Preparation of Butylphthalide Intravenous Emulsion
  • Formula composition (g)
    Butylphthalide 20
    Soybean lecithin 12
    Olive oil 100
    Cholic acid 1
    Mannitol 20
    Water for injection Added to 1000 ml
  • The preparation process comprises the steps of: butylphthalide, cholic acid and olive oil were weighed and mixed to form an oil phase, and the oil phase was pre-heated in a 60° C. water bath. Soybean lecithin and mannitol were weighed and dispersed in water to form an aqueous phase, and the aqueous phase was pre-heated in a 60° C. water bath. The oil phase was slowly poured into the aqueous phase, and the mixture was treated with ultrasonic waves for 10 times (10 seconds for each time, power: 400W). Then the mixture was circulated in a high pressure homogenizer for 5 times, in which the first stage pressure is 100 MPa and the second stage pressure is 10 MPa. Then the emulsion was regulated to have a pH of 8, filtered, subpackaged and sterilized at 121° C. for 15 min. Nitrogen gas is fed for protection during the whole process.
    • EXAMPLE 4 Preparation of Butylphthalide Intravenous Emulsion
  • Formula composition (g)
    Butylphthalide 25
    Cottonseed oil 100
    Ovolecithin 12
    Poloxamer 188 20
    Glycerol 25
    Sodium oleate 10
    Water for injection Added to 1000 ml
  • The preparation process comprises the steps of: butylphthalide, ovolecithin, sodium oleate and cottonseed oil were weighed and mixed to form an oil phase, and the oil phase was pre-heated in a 60° C. water bath. Poloxamer 188 and glycerol were weighed and dispersed in water to form an aqueous phase, and the aqueous phase was pre-heated in a 60° C. water bath. The oil phase was slowly poured into the aqueous phase, and the mixture was dispersed by using a high shear emulsifying machine under 10,000 rpm for 5 min. Then the mixture was circulated in a high pressure homogenizer for 5 times, in which the first stage pressure is 100 MPa and the second stage pressure is 10 MPa. Then the emulsion was regulated to have a pH of 8, filtered, subpackaged and sterilized at 121° C. for 15 min. Nitrogen gas is fed for protection during the whole process.
    • EXAMPLE 5 Preparation of Butylphthalide Intravenous Emulsion
  • Formula composition (g)
    Butylphthalide 30
    Soybean lecithin 12
    Soybean oil 200
    Tween 80 6
    Vitamin E 8
    Xylitol 100
    Water for injection Added to 1000 ml
  • The preparation process comprises the steps of: butylphthalide, Tween 80, vitamin E and soybean oil were weighed and mixed to form an oil phase, and the oil phase was pre-heated in a 60° C. water bath. Soybean lecithin and xylitol were weighed and dispersed in water to form an aqueous phase, and the aqueous phase was pre-heated in a 60° C. water bath. The oil phase was slowly poured into the aqueous phase, and the mixture was dispersed by using a high shear emulsifying machine under 10,000 rpm for 5 min. Then the mixture was circulated in a high pressure homogenizer for 5 times, in which the first stage pressure is 100 MPa and the second stage pressure is 10 MPa. Then the emulsion was regulated to have a pH of 8, filtered, subpackaged and sterilized at 121° C. for 15 min. Nitrogen gas is fed for protection during the whole process.
    • EXAMPLE 6 Preparation of Butylphthalide Intravenous Emulsion
  • Formula composition (g)
    Butylphthalide 40
    Caprylocaproyl triglyceride 200
    Soybean lecithin 12
    Poloxamer 188 20
    Glycerol 25
    Oleic acid 10
    Water for injection Added to 1000 ml
  • The preparation process comprises the steps of: butylphthalide, soybean lecithin, oleic acid and caprylocaproyl triglyceride were weighed and mixed to form an oil phase, and the oil phase was pre-heated in a 60° C. water bath. Poloxamer 188 and glycerol were weighed and dispersed in water to form an aqueous phase, and the aqueous phase was pre-heated in a 60° C. water bath. The oil phase was slowly poured into the aqueous phase, and the mixture was dispersed by using a high shear emulsifying machine under 10,000 rpm for 5 min. Then the mixture was circulated in a high pressure homogenizer for 5 times, in which the first stage pressure is 100 MPa and the second stage pressure is 10 MPa. Then the emulsion was regulated to have a pH of 8, filtered, subpackaged and sterilized at 121° C. for 15 min. Nitrogen gas is fed for protection during the whole process.
    • EXAMPLE 7 Preparation of Butylphthalide Intravenous Emulsion
  • Formula composition (g)
    Butylphthalide 50
    Soybean lecithin 15
    Sesame oil 100
    Vitamin E 8
    Glycerol 22.5
    Water for injection Added to 1000 ml
  • The preparation process comprises the steps of butylphthalide, vitamin E and sesame oil were weighed and mixed to form an oil phase, and the oil phase was pre-heated in a 60° C. water bath. Soybean lecithin and glycerol were weighed and dispersed in water to form an aqueous phase, and the aqueous phase was pre-heated in a 60° C. water bath. The oil phase was slowly poured into the aqueous phase, and the mixture was dispersed by using a high shear emulsifying machine under 10,000 rpm for 5 min. Then the mixture was circulated in a high pressure homogenizer for 5 times, in which the first stage pressure is 100 MPa and the second stage pressure is 10 MPa. Then the emulsion was regulated to have a pH of 8, filtered, subpackaged and sterilized at 121° C. for 15 min. Nitrogen gas is fed for protection during the whole process.
    • EXAMPLE 8 Preparation of Butylphthalide Intravenous Emulsion
  • Formula composition (g)
    Butylphthalide 20
    Soybean oil 100
    Ovolecithin 12
    Poloxamer 188 20
    Glycerol 25
    Sodium oleate 10
    Water for injection Added to 1000 ml
  • The preparation process comprises the steps of butylphthalide, ovolecithin, sodium oleate and soybean oil were weighed and mixed to form an oil phase, and the oil phase was pre-heated in a 60° C. water bath. Poloxamer 188 and glycerol were weighed and dispersed in water to form an aqueous phase, and the aqueous phase was pre-heated in a 60° C. water bath. The oil phase was slowly poured into the aqueous phase, and the mixture was dispersed by using a high shear emulsifying machine under 10,000 rpm for 5 min. Then the mixture was circulated in a high pressure homogenizer for 5 times, in which the first stage pressure is 100 MPa and the second stage pressure is 10 MPa. Then the emulsion was regulated to have a pH of 8, filtered, subpackaged and sterilized at 121° C. for 15 min. Nitrogen gas is fed for protection during the whole process.
    • EXAMPLE 9 Preparation of Butylphthalide Intravenous Emulsion
  • Formula composition (g)
    Butylphthalide 100
    Ovolecithin 20
    Poloxamer 188 20
    Glycerol 25
    Sodium oleate 30
    Water for injection Added to 1000 ml
  • The preparation process comprises the steps of: butylphthalide, ovolecithin and sodium oleate were weighed and mixed to form an oil phase, and the oil phase was pre-heated in a 60° C. water bath. Poloxamer 188 and glycerol were weighed and dispersed in water to form an aqueous phase, and the aqueous phase was pre-heated in a 60° C. water bath. The oil phase was slowly poured into the aqueous phase, and the mixture was dispersed by using a high shear emulsifying machine under 10,000 rpm for 5 min. Then the mixture was circulated in a high pressure homogenizer for 5 times, in which the first stage pressure is 100 MPa and the second stage pressure is 10 MPa. Then the emulsion was regulated to have a pH of 8, filtered, subpackaged and sterilized at 121° C. for 15 min. Nitrogen gas is fed for protection during the whole process.
    • EXAMPLE 10 Preparation of Butylphthalide Intravenous Emulsion
  • Formula composition (g)
    Butylphthalide 0.1
    Soybean oil 100
    Ovolecithin 19
    Poloxamer 188 25
    Glycerol 25
    Water for injection Added to 1000 ml
  • The preparation process comprises the steps of butylphthalide, ovolecithin and soybean oil were weighed and mixed to form an oil phase, and the oil phase was pre-heated in a 60° C. water bath. Poloxamer 188 and glycerol were weighed and dispersed in water to form an aqueous phase, and the aqueous phase was pre-heated in a 60° C. water bath. The oil phase was slowly poured into the aqueous phase, and the mixture was dispersed by using a high shear emulsifying machine under 10,000 rpm for 5 min. Then the mixture was circulated in a high pressure homogenizer for 5 times, in which the first stage pressure is 100 MPa and the second stage pressure is 10 MPa. Then the emulsion was regulated to have a pH of 8, filtered, subpackaged and sterilized at 121° C. for 15 min. Nitrogen gas is fed for protection during the whole process.
    • EXAMPLE 11 Preparation of Butylphthalide Intravenous Emulsion
  • Formula composition (g)
    Butylphthalide 5
    Soybean oil 100
    Ovolecithin 12
    Poloxamer 188 20
    Sodium oleate 3
    Water for injection Added to 1000 ml
  • The preparation process comprises the steps of: butylphthalide, ovolecithin, sodium oleate and soybean oil were weighed and mixed to form an oil phase, and the oil phase was pre-heated in a 60° C. water bath. Poloxamer 188 was weighed and dispersed in water to form an aqueous phase, and the aqueous phase was pre-heated in a 60° C. water bath. The oil phase was slowly poured into the aqueous phase, and the mixture was dispersed by using a high shear emulsifying machine under 10,000 rpm for 5 min. Then the mixture was circulated in a high pressure homogenizer for 5 times, in which the first stage pressure is 100 MPa and the second stage pressure is 10 MPa. Then the emulsion was regulated to have a pH of 8, filtered, subpackaged and sterilized at 121° C. for 15 min. Nitrogen gas is fed for protection during the whole process.

Claims (10)

1. A butylphthalide intravenous emulsion comprising butylphthalide or derivatives thereof as an active ingredient in an amount of 0.01˜50 wt % and an excipient in an amount of 50˜99.99 wt %, based on the total weight of the emulsion.
2. The butylphthalide intravenous emulsion according to claim 1, wherein the butylphthalide or derivatives thereof is a raceme of butylphthalide or derivatives thereof, or l-butylphthalide or derivatives thereof.
3. The butylphthalide intravenous emulsion according to claim 1 or 2, wherein the excipient comprises an oil phase in an amount of 0˜50 wt %, an aqueous phase in an amount of 50˜98 wt %, an emulsifier in an amount of 0.01˜50 wt %, a stabilizer in an amount of 0˜50 wt %, and an osmoregulation agent in an amount of 0˜10 wt %, based on the total weight of the excipient.
4. The butylphthalide intravenous emulsion according to claim 3, wherein the oil phase comprises a natural vegetable oil with long chain fatty acid ester groups, or a vegetable oil or fatty acid ester being subjected to structure modification and hydrolysis, or glyceride with a chain length of C6˜C12 fatty acid, or a mixture thereof.
5. The butylphthalide intravenous emulsion according to claim 4, wherein the oil phase is one of or a mixture of soybean oil, castor oil, tea-seed oil, peanut oil, cottonseed oil, sesame oil, rape oil, safflower oil, olive oil, coconut oil, palm oil, cacao oil, Arlacel 80, Arlacel 86, Capmul MCM, Captex 200 (oil), Captex 355 (oil), Miglyol 812 (oil), Myvacet (oil), Myverol 18-92, glyceride oleate, glyceride linoleate, macrogol glyceryl laurate, ethyl oleate, ethyl linoleate, and caprylocaproyl triglyceride,.
6. The butylphthalide intravenous emulsion according to claim 3, wherein the emulsifier comprises one of or a mixture of nonionic surfactants and anionic surfactants.
7. The butylphthalide intravenous emulsion according to claim 6, wherein the emulsifier is one of or a mixture of soybean lecithin or modified soybean lecthin, ovolecithin or modified ovolecithin, Ophase 31, Poloxamer 108, Poloxamer 188, Poloxamer 407, polyoxyethylene (hydrogenated) castor oil, water soluble VE (TPGS), Solutol HS-15, PEG-400 monostearate, PEG-1750 monostearate, Tween-80, Tween-20, and Span-20.
8. The butylphthalide intravenous emulsion according to claim 3, wherein the stabilizer is one of or a mixture of oleic acid, sodium oleate, sodium caprylate, cholesterol, cholic acid, deoxycholic acid and sodium salt thereof, vitamin A, vitamin C, and vitamin E.
9. The butylphthalide intravenous emulsion according to claim 3, wherein the osmoregulation agent is one of or a mixture of sodium chloride, glucose, sorbitol, xylitol, mannitol, and glycerol.
10. The butylphthalide intravenous emulsion according to claim 1, which is administered by intravenous injection or infusion.
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* Cited by examiner, † Cited by third party
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TWI547280B (en) * 2014-04-24 2016-09-01 長弘生物科技股份有限公司 Stable pharmaceutical composition
US9504751B2 (en) 2014-04-24 2016-11-29 Everfront Biotech Inc. Stable pharmaceutical composition
CN114886848A (en) * 2022-05-20 2022-08-12 山东泰合医药科技有限公司 Preparation method of nano-micelle composition and prepared nano-micelle composition
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WO2024250546A1 (en) * 2023-06-08 2024-12-12 华北制药集团新药研究开发有限责任公司 7-hydroxy-butylphthalide nano-emulsion formulation, preparation method therefor and use thereof

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Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4647586A (en) * 1984-08-10 1987-03-03 Lederle (Japan), Ltd. Pharmaceutical oil-in-water type micro-emulsion
US5364632A (en) * 1989-04-05 1994-11-15 Yissum Research Development Company Of The Hebrew University Of Jerusalem Medicinal emulsions
US20070265336A1 (en) * 2004-06-18 2007-11-15 Yipu Feng Application of L-N-Butylphthalide in Preventing and Treating Dementia

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4950567A (en) 1988-01-15 1990-08-21 E. I. Du Pont De Nemours And Company Holographic optical combiners for head-up displays
JPH01226807A (en) * 1988-03-04 1989-09-11 Tsumura & Co Fat emulsion and production thereof
DE4015108A1 (en) * 1990-05-11 1991-11-14 Leopold Pharma Gmbh STABLE EMULSION FOR APPLICATION OF PHARMACOLOGICALLY ACTIVE ACTIVE SUBSTANCES
CN1029293C (en) * 1993-01-01 1995-07-12 浙江省中医院 Coix Seed Neutral Oil Emulsion
CN1048158C (en) * 1993-09-09 2000-01-12 中国医学科学院药物研究所 Apiolin-A use in preparation of medicine for prevention and treatment of diseases caused by cerebral ischemia
JP2000128786A (en) * 1998-10-28 2000-05-09 Kobayashi Seiyaku Kogyo Kk Miconazole-containing aqueous injection and its production
CN1086942C (en) 1998-12-18 2002-07-03 中国医学科学院药物研究所 Application of butyl phthalide in preparing medicines curing thrombosis and thrombocyte coagulation
JP2003277281A (en) * 2002-03-20 2003-10-02 Kumamoto Technology & Industry Foundation Medicine for preventing and curing phlebitis
CN1375288A (en) * 2002-05-13 2002-10-23 周桂荣 Composite medicine for treating cerebrovascular diseases
ATE489972T1 (en) 2002-08-21 2010-12-15 Shijiazhuang Pharma Group Zhongqi Pharmaceutical Technology Shijiazhuang Co Ltd INCLUSION COMPLEXES OF BUTYLPHTHALIDE AND CYCLODEXTRIN DERIVATIVES AND METHOD FOR THE PRODUCTION THEREOF
CN1565441B (en) 2003-06-20 2010-05-26 中国医学科学院药物研究所 Use of L-n-butylphthalide in the preparation of drugs for preventing or treating dementia
US7115230B2 (en) * 2003-06-26 2006-10-03 Intel Corporation Hydrodynamic focusing devices
US20050049209A1 (en) * 2003-08-06 2005-03-03 Chen Andrew Xian Pharmaceutical compositions for delivering macrolides
CN1254245C (en) * 2003-08-26 2006-05-03 曹永强 Hydroxy camptothecin emulsion and its preparation method
CN1605336A (en) 2003-10-10 2005-04-13 中国医学科学院药物研究所 Application of L-butylphthalide in the process for preparing cerebral infarction preventing and treating medicine
CN1647796A (en) 2004-01-20 2005-08-03 中奇制药技术（石家庄）有限公司 Application of L-butylphthalide in the preparation of drugs for the prevention and treatment of cerebral ischemic diseases
CN100361656C (en) * 2004-08-27 2008-01-16 石药集团中奇制药技术（石家庄）有限公司 Butylbenzene phthalein self emulsifying releasing medicine system, preparation method and application
CN1290491C (en) 2004-09-20 2006-12-20 周桂荣 Medicine for treating acute ischemic cerebral apoplexy and its preparing method

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4647586A (en) * 1984-08-10 1987-03-03 Lederle (Japan), Ltd. Pharmaceutical oil-in-water type micro-emulsion
US5364632A (en) * 1989-04-05 1994-11-15 Yissum Research Development Company Of The Hebrew University Of Jerusalem Medicinal emulsions
US20070265336A1 (en) * 2004-06-18 2007-11-15 Yipu Feng Application of L-N-Butylphthalide in Preventing and Treating Dementia

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI547280B (en) * 2014-04-24 2016-09-01 長弘生物科技股份有限公司 Stable pharmaceutical composition
US9504751B2 (en) 2014-04-24 2016-11-29 Everfront Biotech Inc. Stable pharmaceutical composition
CN115177614A (en) * 2021-04-01 2022-10-14 长春藤生物科技股份有限公司 Application of n-butylphthalide
CN114886848A (en) * 2022-05-20 2022-08-12 山东泰合医药科技有限公司 Preparation method of nano-micelle composition and prepared nano-micelle composition
CN116459224A (en) * 2023-05-15 2023-07-21 济南大学 Butylphthalide nano liposome freeze-dried powder injection and preparation method thereof
WO2024250546A1 (en) * 2023-06-08 2024-12-12 华北制药集团新药研究开发有限责任公司 7-hydroxy-butylphthalide nano-emulsion formulation, preparation method therefor and use thereof

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