双氯芬酸钠与磺胺甲恶唑在纯剂型、颗粒剂剂型和卡波波尔凝胶剂型中的协同作用

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引用次数: 0

摘要

由于传染病与疼痛和感染有关,因此应优先治疗疼痛和感染。患有细菌感染的患者在常规使用磺胺甲恶唑治疗期间可能需要双氯芬酸钠(DS)。因此,可能需要同时或后续使用DS和SM。以聚乙二醇-6000 (PEG-6000)为原料,采用冷/热(熔融)分散法制备6种载药(DS和SM)的聚乙二醇-6000 (PEG-6000)微球制剂(MF-1-MF-6)。然后将配制好的微粒与卡波波尔凝胶(0.75和1.00% w/v)混合并进行评价。所有配制的微颗粒的收率在94.13% ~ 97.18%之间。DS和SM的药物含量均在规定范围内。粒径研究表明,无壳聚糖制备的微颗粒比有壳聚糖制备的微颗粒小。体外药物释放结果表明,与不含壳聚糖相比,含壳聚糖的微颗粒中DS和SM的释放量增加。与单独的微颗粒相比,凝胶制剂中的微颗粒表现出缓慢的药物释放。根据所获得的工作结果,可以得出结论:壳聚糖增加了颗粒大小,从而使药物释放更快。该研究还表明,当DS和SM以纯、微粒和凝胶形式一起给药时,它们会产生协同释放。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synergistic Effect of Diclofenac Sodium and Sulfamethoxazole in Pure form, Microparticle Formulation and in Carbopol Incorporated Gel Containing Microparticle Formulation
As infectious diseases are connected with pain and infections, treating pain and infection should be prioritized. Patients suffering from bacterial infection may need diclofenac sodium (DS) during the regular use of sulfamethoxazole (SM) treatment. So, simultaneous or following administration of DS and SM may be needed. The goal of this study was to prepare six microparticle formulations (MF-1-MF-6) made up of Polyethylene glycol-6000 (PEG-6000) with and without chitosan and that was loaded with two drugs (DS and SM) by cold/hot (melt) dispersion method. The formulated microparticle was then mixed with carbopol gel (0.75 and 1.00% w/v) and evaluated. The percentage yield for all the formulated microparticles was found to be between 94.13% and 97.18%. The drug content for both DS and SM is within the prescribed limits. The microparticle size studies revealed that microparticles prepared without chitosan had smaller particles than those prepared with chitosan. The in vitro drug release results illustrate that the release of DS and SM from prepared microparticles is increased for the preparation containing chitosan compared to without chitosan preparation. When compared to microparticles alone, the microparticles in gel formulations demonstrated slow drug release. Based on the obtained results of the work, it may be concluded that chitosan increases particle size, and subsequently, drugs are released more rapidly. The research also suggests that DS and SM produce synergistic drug release when administrated together in pure, microparticle, and gel form.
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