改良钙三醇外用制剂治疗银屑病

M. Kumari, M. Sachdeva, V. Agarwal
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引用次数: 0

摘要

本课题旨在通过掺入抗炎剂、角化剂、保湿剂、表面活性剂、增稠剂制备治疗银屑病的钙化三醇改进型外用制剂,并对其进行评价。在这些不同的乳液制剂中,羧甲基纤维素钠被用作不同浓度的增粘剂。这种非甾体制剂是通过添加茶树油来制备的,以避免与甾体制剂相关的副作用,并避免长期使用类固醇引起的萎缩问题。对各制剂进行涂敷性、黏度、药含量测定、pH、体外释放度等评价,选择最佳制剂。根据ICH指南进行稳定性研究,检查所制制剂在室温下3个月的稳定性(如外观、pH、粘度、药物含量等参数)。采用透析扩散法对CT5制剂进行体外释药研究。CT5制剂在210min内的累积释药率为85.10%。通过评价,发现CT5配方在所有配方中效果较好。对所制备的钙化三醇制剂和市售钙化三醇制剂的抗银屑病活性进行了评价。采用咪喹莫特诱导的银屑病皮肤模型进行体内抗银屑病治疗。本研究的结果表明,所制备的制剂(CT5)在治疗银屑病的局部给药方面具有很大的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
IMPROVED TOPICAL PREPARATION OF CALCIPOTRIOL IN THE TREATMENT OF PSORIASIS
This research project is aimed to prepare improved topical preparation of Calcipotriol in the treatment of psoriasis by incorporation of an anti-inflammatory agent, keratolytic agent, humectants, surfactant, thickener & to perform its evaluation. In these different preparations of lotions sodium carboxymethylcellulose is used as a viscosity-enhancing agent in varying concentrations. This non-steroidal formulation is prepared by adding tea tree oil to avoid side effects associated with steroidal preparation and to avoid the issue of atrophy with long-term use of steroids. Evaluation of all the formulations such as spreadability, viscosity, drug content determination, pH, in-vitro release study, to choose the optimized formulation was carried out. According to ICH guidelines, stability studies were carried out to check the stability (parameters such as appearance, pH, viscosity, drug content) of prepared formulations for 3 months at room temperature. In-vitro drug release study CT5 formulation was carried by dialysis diffusion method. The cumulative% drug release of CT5 formulation in 210minutes was 85.10%. Based on the evaluation, formulation (CT5) was found to be better among all the formulations. The prepared calcipotriol formulation and a commercial formulation of calcipotriol were evaluated for anti-psoriatic activity. In-vivo anti-psoriatic was performed by using the Imiquimod Induced Psoriasis skin model. The results obtained in this study have been concluded that the prepared formulation (CT5) has great potential for topical delivery in the treatment of psoriasis.
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