Formulation Development and Release Profile of Levomilnacipran Extended Release Capsules using Principles of Quality by Design

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Abstract

The study’s goal was to use Quality By Design (QbD) principles to design an Extended Release dosage form of levomilnacipran and evaluate its in vitro release profile. Doses of levomilnacipran extended release capsules (LERC) ranging from 20 mg to 120 mg. QbD was employed in this work to design LERC capsule formulation and production, which ensures LERC safety and efficacy. To create the LERC, wurster coating was applied to non-pariel seeds, which were then filled with capsules. To provide prolonged absorption, a polymer derived from ethylcellulose was chosen. Extensive release capsules are made up of four main components: (1) Drug layering, (2) extended release coating, (3) lubricant application, and finally (4) capsule filling. Results revealed that there was no significant difference in release profile LERC in different doses; however, the highest release of drug was seen at 120 mg, that is, 93%. The present formulation may be used as an effective treatment therapy against major depressive disorder.
采用质量设计原则的左旋美那西普兰缓释胶囊的配方开发及释放特性研究
本研究的目的是利用质量设计(QbD)原则来设计左旋美那西普兰的缓释剂型,并评估其体外释放谱。左旋美那西普兰缓释胶囊(LERC)的剂量从20毫克到120毫克不等。本工作采用QbD对LERC胶囊的配方和生产进行设计,保证了LERC的安全性和有效性。为了制造LERC,将wurster涂层涂在非颗粒种子上,然后用胶囊填充种子。为了延长吸收时间,选择了一种从乙基纤维素中提取的聚合物。缓释胶囊由四个主要部分组成:(1)药物分层,(2)缓释涂层,(3)润滑剂应用,最后(4)胶囊填充。结果显示,不同剂量下的释放谱无显著差异;120 mg时释药率最高,释药率为93%。本发明可作为治疗重度抑郁症的有效方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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