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Development of multiple emulsion to deliver drugs

Development of multiple emulsion to deliver drugs
开发多重乳剂来输送药物
批准号:
07557296
负责人:
NAKANO Masahiro
金额:
$0.64万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B)
财政年份:
1995
资助国家:
日本
项目状态:
已结题
起止时间:
1995 至 1996

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中文摘要
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英文摘要
In this study, we selected the w/o/w multiple emulsion as a carrier of water-soluble drugs and studied on preparation, evaluation of pharmaceutical properties and applications for drug delivery system (DDS). For the oily phase of multiple emulsion, an oil mixture of Lipiodol and vegetable oil or isopropyl myristate were used to minimize the difference in specific gravity between oily phase and aqueous phase. HCO-40 or HCO-50 and Pluronic F-88 were used as hydrophobic and hydrophilic surfactants, respectively. For entrapping water-soluble drugs, vancomycin, cytarabine, doxorubicin and ACNU were used. Multiple emulsions were prepared with stirring or membrane emulsification methods.Multiple emulsions prepared by both methods were stable during storage at 4゚C.Particle size of the multiple emulsion was controlled by both methods. Especially, particle distribution of multiple emulsion prepared with membrane method showed homogeneousness. It however took too much time to prepare much multipl … More e emulsion in this method. Although the entrapment efficiency and the release property of drug were different among products, they could be controlled by formulations and preparations of the multiple emulsion.When the multiple emulsion (particle size being 3 mum) entrapping vancomycin was injected intravenously, the serum concentration of the drug was prolonged. When the multiple emulsions entrapping cytarabine whose particle sizes were 3 and 30 mum injected intraperitoneally, these emulsions were useful for treatments of lymphatic metastasis of cancer and peritoneal carcinomatosis, respectively. When the multiple emulsion entrapping doxorubicin, whose particle size was 30 mum, was injected into hepatic artery of rat bearing Waker 256, and when the emulsion whose particle size was 3 mum, was injected into the portal vein of rat bearing AH109A,survival times of the treated groups were prolonged. When the multiple emulsion entrapping ACNU was injected intrathecally to the meningeal gliomatosis, the survival time of the treated group was prolonged.The results of this study showed that the multiple emulsion was useful for a carrier of water-soluble drugs and sustained release of drugs. Therefore it can be applied to DDS by controlling the particle size of the emulsion. Less
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大河内秀昭,中野眞汎: "各種水溶性薬物封入w/o/w emulsionの製剤学的性質と体内動態" Drug Delivery System. 11(1). 37-42 (1996)
Hideaki Okochi、Masahiro Nakano:“包封各种水溶性药物的 w/o/w 乳液的药物特性和药代动力学”药物输送系统 11(1)。
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通讯作者:
H.Okochi and M.Nakano: "Studies of pharmaceutical properties and disposition kinetics of w/o/w emulsions containing some water-soluble drugs" Drug Delivery System. 11. 37-42 (1996)
H.Okochi 和 M.Nakano:“含有某些水溶性药物的 w/o/w 乳液的药物特性和处置动力学研究”药物输送系统。
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通讯作者:
大河内秀昭,中野眞汎: "各種水溶性薬物封入w/o/w emulsionの乳剤学的性質と体内動態" Drug Delivery System. 11(1). 37-42 (1996)
Hideaki Okochi、Masahiro Nakano:“包封各种水溶性药物的 w/o/w 乳液的乳液特性和药代动力学”药物输送系统 11(1)。
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通讯作者:
H.Okochi and M.Nakano: "Basic studies on formulation,method of preparation and characterization of water-in-oil-in-water type multiple emulsions containing vancomycin" Chemical and Pharmaceutical Bulletin. 44(1). 180-186 (1996)
H.Okochi 和 M.Nakano:“含有万古霉素的水包油包水型多重乳剂的配方、制备方法和表征的基础研究”化学和药物通报。
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Development of an automatic safety property prover with lemma discovery based on test
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    1994
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