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用于治疗银屑病的甲氨蝶呤包载脂质体与水杨酸局部凝胶的研制。

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

作者信息

Chandra Akhilesh, Aggarwal Geeta, Manchanda Satish, Narula Akshay

机构信息

Department of Pharmaceutics, Delhi Pharmaceutical Sciences and Research University, Pushp Vihar Sec III, New Delhi-110017, India.

Institute of Nuclear Medicine & Allied Sciences, Defence Research and Development Organisation, New Delhi-110054, India.

出版信息

Pharm Nanotechnol. 2019;7(5):362-374. doi: 10.2174/2211738507666190906123643.

Abstract

BACKGROUND

There is an unmet need for optimized drug delivery system of psoriasis therapy because of various issues like adverse reaction, permeation problem associated with convention treatment (oral and topical) available for psoriasis.

OBJECTIVE

The goal was to develop an ethosomal gel of methotrexate (MTX)-incorporated ethosomes and salicylic acid (SA) and to evaluate and study its ethosomal gel potential in Imiquimod-induced psoriasis animal model to treat symptoms of psoriasis.

METHODS

MTX-SA ethosomal gel was prepared by the cold method given by Touitou et al. and optimized by comparing it with MTX ethosomal gel and drug solution. Particle size, zeta potential, entrapment efficiency, and ex-vivo study were selected as the critical quality checking attributes. Psoriatic Area and Severity Index (PASI) score & histopathological examination were done for checking Antipsoriatic potential of MTX-SA ethosomal gel by using the imiquimod-induced psoriasis model.

RESULTS

Optimized MTX-SA exhibited a particle size of 376.04 ± 3.47nm, EE(Entrapment efficiency) of 91.77 ± 0.02%. At the end of 24h, MTX-SA ethosomal gel exhibited a slow and prolonged release of MTX (26.13 ± 1.61% versus 6.97 ± 0.06%) compared to MTX drug 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 the mice's skin, while the MTX-SA gel displayed indications of gentle hyper and parakeratosis toward the completion of investigation when contrasted with the blank gel.

CONCLUSION

The developed MTX-SA ethosomal gel formulation can be a promising alternative to existing MTX formulation in topically treating psoriasis.

摘要

背景

由于银屑病传统治疗方法(口服和外用)存在不良反应、渗透问题等各种问题,对优化的银屑病治疗药物递送系统存在未满足的需求。

目的

开发一种含有甲氨蝶呤(MTX)的乙醇脂质体和水杨酸(SA)的乙醇脂质体凝胶,并在咪喹莫特诱导的银屑病动物模型中评估和研究其治疗银屑病症状的乙醇脂质体凝胶潜力。

方法

采用Touitou等人给出的冷法制备MTX-SA乙醇脂质体凝胶,并与MTX乙醇脂质体凝胶和药物溶液进行比较优化。选择粒径、zeta电位、包封率和体外研究作为关键质量检查属性。通过使用咪喹莫特诱导的银屑病模型,进行银屑病面积和严重程度指数(PASI)评分和组织病理学检查,以检查MTX-SA乙醇脂质体凝胶的抗银屑病潜力。

结果

优化后的MTX-SA粒径为376.04±3.47nm,包封率(EE)为91.77±0.02%。在24小时结束时,与MTX药物溶液相比,MTX-SA乙醇脂质体凝胶显示出MTX的缓慢和持续释放(26.13±1.61%对6.97±0.06%)。与药物溶液(13%)相比,它还具有43%的保留率。此外,它基本上降低了PASI评分,使小鼠皮肤恢复正常,而与空白凝胶相比,MTX-SA凝胶在研究结束时显示出轻度角化过度和角化不全的迹象。

结论

所开发的MTX-SA乙醇脂质体凝胶制剂在局部治疗银屑病方面可能是现有MTX制剂的一个有前途的替代品。

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