首页> 外文会议>International Conference on Frontiers of Design and Manufacturing(ICFDM'2006) vol.2; 20060619-22; Guangzhou(CN) >DESIGN OF NEW CONTROLLED DRUG RELEASE MICRO-CARRIERS BASED ON MEMS AND STUDY OF ITS DRUG RELEASE TRAITS
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DESIGN OF NEW CONTROLLED DRUG RELEASE MICRO-CARRIERS BASED ON MEMS AND STUDY OF ITS DRUG RELEASE TRAITS

机译:基于MEMS的新型可控药物释放微载体的设计及其药物释放性状的研究

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摘要

The objective of this work is to design and fabricate a novel poly(lactic-co-glycolic acid)(PLGA) biodegradable carrier with multi-chambers by solvent-casting technique on a poly(dimethylsiloxane)(PDMS) mold, for controlled drug release system. Three types of PLGA films, as follow single PLGA film, multiple molar ratios PLGA mixed film and porous film, are fabricated to encapsulate the carriers loading with paracetamol, a conventional low molecular weight water-soluble drug. After the carriers encapsulated to form three kinds of capsules, we study the capsules in vitro tests to evaluate the kinetics of drug release. The results show that the capsules can't achieve sustained drug release only by diffusion, but the carriers with porous film have realized preferable linear release of sample representing a suitable dosage form for implantable long-term controlled drug release system.
机译:这项工作的目的是在聚二甲基硅氧烷(PDMS)模具上通过溶剂浇铸技术设计和制造一种新型的具有多腔室的聚乳酸-乙醇酸共聚物(PLGA)可生物降解的载体。系统。制备了三种类型的PLGA膜,分别是单个PLGA膜,多个摩尔比的PLGA混合膜和多孔膜,以用对乙酰氨基酚(一种传统的低分子量水溶性药物)封装载有载体的载体。载体包封形成三种胶囊后,我们研究了这些胶囊的体外试验,以评估药物释放的动力学。结果表明,胶囊不能仅通过扩散来实现持续的药物释放,但是带有多孔膜的载体已经实现了优选的线性释放样品,代表了可植入的长期控制药物释放系统的合适剂型。

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