Formulation of sumatriptan succinate orodispersible tablets using chitosan and sodium starch glycolate for immediate migraine relief.

IF 0.7 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Tuba Sahar, Syed Muhammad Farid Hasan, Salman Ashfaq Ahmad, Rabia Bushra, Abdur Rehman, Rabia Noor, Shahnaz Usman, Nighat Razvi, Fouzia Hassan
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Abstract

Migraine is one of the common neurological disease affecting around 23% of the Pakistani population. Prompt treatment is required to regain the functional ability of patients. The present study was designed to develop sumatriptan succinate orodispersible tablets that would quickly overcome acute migraine episodes using 22 full-factorial design. The chitosan and sodium starch glycolate were taken as independent variables; friability, disintegration, dispersion time and water absorption ratio as response variables. Eight trial formulations were generated by Design Expert® software. The main effect plots were used to check the interaction of formulations with response variables. All trial formulations showed good micromeritic properties in terms of angle of repose (19.59o-24.57°), Carr's index (17.08-24.90%) and Hausner's ratio (1.20-1.33). The tablets wetted quickly (17.1- 39 sec) in dispersion medium, showed higher water absorption ratio (188-341 sec) and disintegrated quickly (13-20 sec) with an excellent dissolution rate (94-99%). The main effect plots show interactions between the independent variables against most of the study responses. A 22 full-factorial model was found to be effective in studying the influence of formulation variables on response parameters. Both chitosan and sodium starch glycolate can be used in combination to fabricate an effective orodispersible formulation of sumatriptan succinate.

使用壳聚糖和淀粉乙醇酸钠配制琥珀酸舒马曲坦口崩片剂,用于立即缓解偏头痛。
偏头痛是常见的神经系统疾病之一,影响着巴基斯坦约 23% 的人口。需要及时治疗才能恢复患者的功能。本研究采用 22 个全因子设计,旨在开发能迅速缓解急性偏头痛发作的琥珀酸舒马曲普坦乳油分散片。将壳聚糖和淀粉乙醇酸钠作为自变量;将易碎性、崩解度、分散时间和吸水率作为响应变量。设计专家®软件生成了八个试验配方。主效应图用于检查配方与响应变量之间的相互作用。所有的试验配方都显示出良好的微粒特性,如悬浮角(19.59o-24.57°)、卡尔指数(17.08-24.90%)和豪斯纳比率(1.20-1.33)。片剂在分散介质中润湿速度快(17.1-39 秒),吸水率高(188-341 秒),崩解速度快(13-20 秒),溶解率高(94-99%)。主效应图显示了自变量与大多数研究反应之间的相互作用。在研究制剂变量对反应参数的影响时,发现 22 全因子模型是有效的。壳聚糖和淀粉乙醇酸钠可结合使用,制成有效的琥珀酸舒马曲普坦口服分散制剂。
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来源期刊
CiteScore
1.40
自引率
12.50%
发文量
211
审稿时长
4.5 months
期刊介绍: Pakistan Journal of Pharmaceutical Sciences (PJPS) is a peer reviewed multi-disciplinary pharmaceutical sciences journal. The PJPS had its origin in 1988 from the Faculty of Pharmacy, University of Karachi as a biannual journal, frequency converted as quarterly in 2005, and now PJPS is being published as bi-monthly from January 2013. PJPS covers Biological, Pharmaceutical and Medicinal Research (Drug Delivery, Pharmacy Management, Molecular Biology, Biochemical, Pharmacology, Pharmacokinetics, Phytochemical, Bio-analytical, Therapeutics, Biotechnology and research on nano particles.
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