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基于组群分类的中药物质成分与药性关系研究进展 被引量:1
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作者 陈晨 王鹏 谢欢欢 《甘肃中医药大学学报》 2018年第2期90-93,共4页
查阅近10年相关文献,从思路与方法、科属分类、药性分类、功效分类4个方面对基于组群分类的中药物质成分与药性关系的研究进行归纳与总结,认为基于组群分类的中药物质成分与药性关系的研究方式是可行的,通过结合中医的整体认知模式,做... 查阅近10年相关文献,从思路与方法、科属分类、药性分类、功效分类4个方面对基于组群分类的中药物质成分与药性关系的研究进行归纳与总结,认为基于组群分类的中药物质成分与药性关系的研究方式是可行的,通过结合中医的整体认知模式,做到宏观与微观并重,为中药理论的现代化提供依据。 展开更多
关键词 中药药性 组群分类 物质成分 药性关系 综述
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Structure-Property Relationships and Models of Controlled Drug Delivery of Biodegradable Poly (D, L-lactic acid) Microspheres 被引量:8
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作者 潘吉铮 章莉娟 钱宇 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2004年第6期869-876,共8页
An oil-in-water (O/W) solvent evaporation method was used to prepare biodegradable microspheresbased on poly(D,L-lactic acid) (PLA). Nifedipine, a hydrophobic drug, was chosen as a model molecule in the studyof drug e... An oil-in-water (O/W) solvent evaporation method was used to prepare biodegradable microspheresbased on poly(D,L-lactic acid) (PLA). Nifedipine, a hydrophobic drug, was chosen as a model molecule in the studyof drug entrapment and release. Effect of preparation conditions on the size, morphology, drug loading, and releaseprofiles of micropheres was investigated. Based on in vitro release experimental findings, a diffusion/dissolutionmodel was presented for quantitative description of the resulting release behaviors and drug release kinetics fromPLA microspheres analyzed. The mathematical models were used to predict the effect of microstructure on theresulting drug release. It provided an approach to determine the suitable structure parameters for microspheres toachieve desired drug release behaviors. 展开更多
关键词 MICROSPHERES drug delivery NIFEDIPINE controlled release solventevaporation structure-property relationships MODEL
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