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Release Characteristics of Quetiapine Fumarate Extended Release Tablets Under Biorelevant Stress Test Conditions

机译:生物相关压力测试条件下富马酸喹硫平缓释片的释放特性

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摘要

The aim of the present work was the investigation of robustness and reliability of drug release from 50 to 400 mg quetiapine extended release HPMC matrix tablets towards mechanical stresses of biorelevant intensity. The tests were performed under standard conditions (USP apparatus II) as well as under simulated gastrointestinal stress conditions. Mechanical stresses including pressure and agitation were applied by using the biorelevant dissolution stress test apparatus as it has been introduced recently. Test algorithms already established in previous studies were applied to simulate fasting gastrointestinal conditions. The dissolution experiments demonstrated striking differences in the product performance among standard and stress test conditions as well as dose strengths. In USP apparatus II, dissolution profiles were affected mainly by media pH. The dissolution experiments performed in biorelevant dissolution stress test device demonstrated that stress events of biorelevant intensity provoked accelerated drug release from the tablets.Electronic supplementary materialThe online version of this article (doi:10.1208/s12249-013-0050-2) contains supplementary material, which is available to authorized users.
机译:本工作的目的是研究从50到400 mg喹硫平缓释HPMC基质片剂对生物相关强度的机械应力释放药物的稳健性和可靠性。在标准条件下(USP装置II)以及模拟胃肠道压力条件下进行测试。如最近所介绍的那样,通过使用生物相关的溶解应力测试装置施加包括压力和搅动的机械应力。在先前研究中已经建立的测试算法被用于模拟禁食胃肠道状况。溶出度实验表明,标准和压力测试条件以及剂量强度之间的产品性能差异显着。在USP设备II中,溶出曲线主要受培养基pH值的影响。在生物相关溶出应力测试设备中进行的溶出实验表明,生物相关强度的应力事件引起了片剂的药物释放加速。电子补充材料本文的在线版本(doi:10.1208 / s12249-013-0050-2)包含补充材料,可供授权用户使用。

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