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阿昔洛韦明胶微球的制备及体外释放度考察
引用本文:吴国际.阿昔洛韦明胶微球的制备及体外释放度考察[J].亚太传统医药,2011,7(4):36-38.
作者姓名:吴国际
作者单位:庐江县中医院,安徽,庐江,231500
摘    要:目的:制备阿昔洛韦明胶微球,并考察其体外释放性能。方法:采用乳化交联法制备阿昔洛韦明胶微球,通过考察其粒径、包封率、载药量优化处方工艺。结果:该工艺制备的微球光滑圆整,其平均粒径为21μm,粒径分布均匀。载药量、包封率分别为15.3%、80.5%。12min体外累积释药量达95.2%。结论:采用乳化交联法制备的明胶微球具有很好的缓释效果。

关 键 词:阿昔洛韦  明胶  微球  乳化交联法

Study on Preparation and Release Behavior of Aciclovir Microspheres
Wu Guoji.Study on Preparation and Release Behavior of Aciclovir Microspheres[J].Asia-Pacific Traditional Medicine,2011,7(4):36-38.
Authors:Wu Guoji
Affiliation:Wu Guoji(Lujiang County Hospital of Traditional Chinese Medicine,Anhui 231500,China)
Abstract:Objective:Study on Preparation and Release Behavior of aciclovir Microspheres.Methods:The way of emulsion cross-linked was used to prepare microspheres of acyclovir and the size,encapsulation efficiency,drug loading formulation and process optimization were examined,respectively.Results:Result:Microspheres prepared by the process were smooth and round,the average particle size was 21μm,with narrow size distribution.Drug loading,encapsulation efficiency was 15.3%,80.5%,respectively.The cumulative release in vitro on 12h reached 95.2%.Conclusion:The gelatin microspheres prepared by emulsion cross-linked were with good slow-release effect.
Keywords:Aciclovir  Gelatin  Microspheres  Emulsion Cross-linked  
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