用Raft技术研究肉桂碱-盐酸缓释口服混悬液配方中的缓释聚合物

Tabinda Islam, Nusrat Hossain, Mohsina Rahman, Sadia Shabnam, Eyasmin Chowdhury, Syeda Tahsin Nahar, Zarin Tasnim Gias, H. Reza
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引用次数: 2

摘要

本研究的主要目的是利用筏形法制备盐酸肉桂利嗪缓释混悬液。这种创新的方法已被用于配制一系列以羟丙基纤维素(HPC)为缓释剂的悬浮液配方。以不同浓度的HPC、柠檬酸钠、糖精钠、碳酸钙、海藻酸钠、羟苯甲酸甲酯和羟苯甲酸丙酯为混配剂,采用物理混合法制备肉桂嗪嗪缓释混悬液。对配方进行了漂浮时间、漂浮滞后时间、筏体重量、物理外观和体外溶出度的测定。在0.1N pH为1.2的盐酸介质中,通过USP仪器2(桨式)进行溶解。该研究的主要发现表明,可以使用筏形方法配制稳定的肉桂碱缓释液,以提高生物利用度和患者的便利性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Study of Release-Retardant Polymers in Formulation Development of Cinnarizine-HCl Sustained-release Oral Suspension Using Raft Technology
The main objective of this research was to develop a sustained-release suspension of cinnarizine hydrochloride using raft-forming technique. This innovative approach has been utilized to formulate a series of suspension formulations using hydroxypropyl cellulose (HPC) as a release-retardant polymeric agent. Cinnarizine sustained-release suspensions were prepared by physical mixing method with varying concentrations and combinations of HPC, sodium citrate, sodium saccharin, calcium carbonate, sodium alginate, methyl hydroxybenzoate and propyl hydroxybenzoate. The formulations were subjected for determination of floating time, floating lag time, weight of the raft, physical appearance and in-vitro dissolution. The dissolution was conducted through USP apparatus 2 (paddle type) in 0.1N hydrochloric acid medium having pH 1.2. The key findings of the study demonstrate that a stable sustained-release suspension of cinnarizine can be formulated using raft-forming approach for increased bioavailability and patient-convenience.
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