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Visualising Tablet Dissolution: Measurement of Hydration and Drug Release

机译:可视化片剂溶解度:水化和药物释放的测量

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摘要

Magnetic Resonance Imaging (MRI) measures the hydration of tablets during dissolution by non-invasively mapping ~(1)H nuclei associated with "mobile" water. Images acquired on the PharmaSense Tablet Dissolution Imager with integrated US Pharmacopeia 4 apparatus, provide key data for the formulation chemist. Furthermore, simultaneous measurement of the drug concentration in the outflow by on-line UV analysis allows comparison of the drug release profile against the rate of water ingress. Most studies of tablet dissolution are characterised by a drug release profile which is determined by collecting aliquots of the outflow, usually analysed off-line for the active pharmaceutical ingredient (API). However, controlled release pharmaceuticals are being developed with an increasing degree of complexity and are difficult to characterise using API analyses alone. They are typically a composite and therefore the rate of drug release could be dependent on a number of different factors including the excipients and coatings used as well as the geometry of the tablet.
机译:磁共振成像(MRI)通过非侵入性绘制与“流动”水相关的〜(1)H核来测量溶解过程中片剂的水合作用。在带有集成的美国药典4装置的PharmaSense片剂溶出度成像仪上采集的图像为制剂化学家提供了关键数据。此外,通过在线紫外线分析同时测量流出液中的药物浓度,可以比较药物释放曲线与进水速率。片剂溶解的大多数研究都以药物释放曲线为特征,该曲线由收集流出物的等分试样确定,通常对活性药物成分(API)进行离线分析。但是,控释药物的开发越来越复杂,难以单独使用API​​分析来表征。它们通常是复合材料,因此药物的释放速率可能取决于许多不同的因素,包括所用的赋形剂和包衣以及片剂的几何形状。

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