首页> 外文期刊>Pharmaceutical Nanotechnology >Development of Topical Gel of Methotrexate Incorporated Ethosomes and Salicylic Acid for the Treatment of Psoriasis
【24h】

Development of Topical Gel of Methotrexate Incorporated Ethosomes and Salicylic Acid for the Treatment of Psoriasis

机译:甲氨蝶呤局部凝胶的研制掺入血管基体和水杨酸治疗牛皮癣

获取原文
获取原文并翻译 | 示例
       

摘要

Background: There is an unmet need for optimized drug delivery system ofpsoriasis therapy because of various issues like adverse reaction, permeation problem associatedwith convention treatment (oral and topical) available for psoriasis.Objective: The goal was to develop an ethosomal gel of methotrexate (MTX)-incorporatedethosomes and salicylic acid (SA) and to evaluate and study its ethosomal gel potential inImiquimod-induced psoriasis animal model to treat symptoms of psoriasis.Methods: MTX-SA ethosomal gel was prepared by the cold method given by Touitou etal. and optimized by comparing it with MTX ethosomal gel and drug solution. Particlesize, zeta potential, entrapment efficiency, and ex-vivo study were selected as the criticalquality checking attributes. Psoriatic Area and Severity Index (PASI) scoreandhistopathologicalexamination were done for checking Antipsoriatic potential of MTX-SA ethosomalgel by using the imiquimod-induced psoriasis model.Results: Optimized MTX-SA exhibited a particle size of 376.04 ± 3.47nm, EE(Entrapmentefficiency) of 91.77 ± 0.02%. At the end of 24h, MTX-SA ethosomal gel exhibited a slowand prolonged release of MTX (26.13 ± 1.61% versus 6.97 ± 0.06%) compared to MTXdrug solution. It also attributes of 43% retention study as compared to drug solution (13%).Besides, it essentially decreased the PASI score with the recuperation of normalcy of themice's skin, while the MTX-SA gel displayed indications of gentle hyper and parakeratosistoward the completion of investigation when contrasted with the blank gel.Conclusion: The developed MTX-SA ethosomal gel formulation can be a promising alternativeto existing MTX formulation in topically treating psoriasis.
机译:背景:未经综合治疗的优化药物递送系统有未满足的需求,因为不同的问题,如不良反应,渗透问题,与牛皮癣可用的惯例治疗(口腔和局部)相关。目标是开发甲氨蝶呤的祖传肠凝胶(MTX “-INCHERATEDINOSOMES和水杨酸(SA)并评估并研究其对咪喹啉诱导的牛皮癣动物模型以治疗牛皮癣的症状。方法:通过Touitou etal给出的冷法制备MTX-SA乙基凝胶。通过将其与MTX乙基凝胶和药物溶液进行比较来优化。将颗粒化,Zeta电位,熵效率和前体内研究选择为毫无疑问的检查属性。使用咪喹莫特诱导的牛皮癣模型来检查MTX-SA Ethosomalgel的抗血压潜力的牛肝区和严重程度指数91.77±0.02%。与MTXDRUG溶液相比,MTX-SA的Ethosomal凝胶表现出慢性的MTX延长释放(26.13±1.61%的6.97±0.06%)。与药物溶液相比,它还属于43%的保留研究(13%)。此外,它基本上降低了对实时皮肤的恢复的PASI得分,而MTX-SA凝胶显示出平缓超级和帕拉克浴池的适应症完成与坯料凝胶对比时的调查。结论:发育的MTX-SA乙糖体凝胶制剂可以是局部处理牛皮癣的有前途的替代性MTX制剂。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号