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用于局部皮肤病药物产品体外释放的测试系统评估。

Evaluation of the test system used for in vitro release of drugs for topical dermatological drug products.

作者信息

Shah V P, Elkins J S, Williams R L

机构信息

Office of Pharmaceutical Science, Food and Drug Administration, Rockville, Maryland 20852, USA.

出版信息

Pharm Dev Technol. 1999 Aug;4(3):377-85. doi: 10.1081/pdt-100101373.

Abstract

The purpose of this research was to evaluate different parameters that can influence in vitro drug release from topical dermatological drug products such as creams, gels, and ointments. In vitro release from topical dermatological drug products was carried out by using a static diffusion cell, a synthetic membrane, and an appropriate receptor medium. The receptor medium was mixed by means of a magnetic bar rotated at 400 rpm. Experiments were designed to evaluate the influence of (i) receptor media, (ii) different lots of synthetic membranes, and (iii) agitation on drug release. Release experiments were also carried out to study inter- and intralot variability. The in vitro release test was used to evaluate the marketed glucocorticoid products. Among the parameters studied, the receptor medium was found to be the most important and critical variable that influenced drug release. The release rate ranged between 0.61 and 2.68 micrograms/cm2/min0.5 for betamethasone dipropionate, depending on the percentage of ethanol in the receptor medium. The drug release was not influenced by agitation or by different lots of synthetic membranes. Very small inter- and intralot variability was observed. These experiments establish the ruggedness of the in vitro diffusion cell test system used for the drug release measurements.

摘要

本研究的目的是评估不同参数对乳膏、凝胶和软膏等局部皮肤科药品体外药物释放的影响。通过使用静态扩散池、合成膜和合适的受体介质来进行局部皮肤科药品的体外释放实验。受体介质通过以400转/分钟旋转的磁棒进行搅拌。实验旨在评估(i)受体介质、(ii)不同批次的合成膜以及(iii)搅拌对药物释放的影响。还进行了释放实验以研究批次间和批次内的变异性。体外释放试验用于评估市售糖皮质激素产品。在所研究的参数中,发现受体介质是影响药物释放的最重要和关键变量。根据受体介质中乙醇的百分比,丙酸倍他米松的释放速率在0.61至2.68微克/平方厘米/分钟0.5之间。药物释放不受搅拌或不同批次合成膜的影响。观察到批次间和批次内的变异性非常小。这些实验证实了用于药物释放测量的体外扩散池测试系统的耐用性。

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