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A Novel In Vitro Pulmonary Dissolution Testing Method for Controlled ReleaseInhalation Formulations

机译:一种新的对脱裂性配方的体外肺溶出试验方法

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摘要

A standardized in vitro dissolution method was designed to predict the in vivo dissolution rate of inhaled active ingredients. A commercial dissolution tester (USP apparatus 1, Basket) was modified as a testing apparatus. Each basket was modified with a polycarbonate membrane having 15-50 nm pore size (to approximate the tight junction of an alveolar epithelial surface).
机译:设计了一种标准化的体外溶解方法,以预测吸入活性成分的体内溶解速率。将商业溶解测试仪(USP装置1,篮筐)被修改为测试装置。用具有15-50nm孔径的聚碳酸酯膜改性每个篮子(以近似肺泡上皮表面的紧密结)。

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