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聚β-羟基丁酸戊酸酯(PHBV)为载体的药物缓释微球的制备 被引量:5

Preparation of Micro-spheres Using PHBV as Carrier for Drug Slowly Releasing
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摘要 对用PHBV为载体,采用乳化溶剂蒸发法制备黄体酮的缓释微球进行了研究。结果表明,当选用明胶为乳化剂时,可以制得分散、较圆且表面光滑的微球;;明胶浓度及搅拌转速不但影响微球的粒径而且影响药物包埋率;;药物的包埋率还受PHSV在氯仿相中浓度、药物加入量以及制备温度的影响。研究微球体外释放行为发现,当PHBV在氯仿中浓度为0.1(w/v)、黄体酮加入量为PHBV质量的0.06(w/v)、温度为40℃时,制得的微球具有较好的缓释效果。 PHBV was used as a carrier for slowly releasing of progesterone. The emulsion solventevaporation method was applied to prepare PHBV micro-spheres containing progesterone. With gelatinas the emulsifier, the discrete and spherical micro-particles with smooth surface were obtained. It wasobserved that both the concentration of gelatin and the stirring rate took an important role for eitherparticle size or encapsulation efficiency. The encapsulation efficiency of progesterone was alsodependent upon the concentration of PHBV in chloroform, the ratio of progesterone to PHBV and thetemperature of preparation. The experimental results of drug release in vitro indicated that theappropriate preparation conditions were : 0. 1(w/v) of PHBV in chloroform, progesterone to PHBV ratioof 0.06:1 (w/w) and temperature at 40℃.
出处 《高校化学工程学报》 EI CAS CSCD 北大核心 1999年第2期129-134,共6页 Journal of Chemical Engineering of Chinese Universities
基金 轻工总会科技基金
关键词 微球 黄体酮 PHBV 药物缓释载体 Poly (3 -hydroxybutyrate-co-3-hydroxyvalerate) , Microsphere, Preparation, Progesterone,Slow release
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参考文献3

  • 1潘仁荣 易武 等.-[J].中国药学杂志,1993,28(7):405-408.
  • 2陈坚,CN 1171410A,1998年
  • 3潘仕荣,中国药学杂志,1993年,28卷,2期,405页

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