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Effect of size on in vitro release of water insoluble drug from polilactofate microspheres

机译:大小对多聚乳酸微球水不溶性药物体外释放的影响

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The release rate of a drug from polymer microspheres is of tremendous importance in formulating and developing appropriate and effective drug delivery systems. It is difficult to conduct a drug release study that occurs over prolonged periods of time. Drug release studies that can be completed in a single day to provide relevant information regarding the formulation and influence key decisions to be made relatively quickly are required. Also, it is difficult to quantify a drug that is insoluble in an aqueous or other medium. A proper release medium must be able to solubilize released drug in real time whiel not dissolving the formulation matrix. To achieve these goals, we have developed a medium (GPI-X buffer) that contains a solubility-enhancing agent to study the release of an insoluble drug substance from a polyphosphoester polymer microspheres formulation.
机译:药物从聚合物微球中的释放速率在制定和开发适当而有效的药物输送系统中具有极其重要的意义。很难进行长时间的药物释放研究。需要在一天之内完成的药物释放研究,以提供有关制剂的相关信息,并影响相对迅速做出的关键决策。另外,难以定量不溶于水性或其他介质的药物。适当的释放介质必须能够实时溶解释放的药物,而不会溶解制剂基质。为实现这些目标,我们开发了一种包含溶解度增强剂的介质(GPI-X缓冲液),以研究不溶性药物从聚磷酸酯聚合物微球制剂中的释放。

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