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用于5-氟尿嘧啶经皮给药的新型离子液体基微乳制剂的研发。

Development of novel ionic liquid-based microemulsion formulation for dermal delivery of 5-Fluorouracil.

作者信息

Goindi Shishu, Arora Prabhleen, Kumar Neeraj, Puri Ashana

机构信息

University Institute of Pharmaceutical Sciences, Panjab University, Chandigarh, 160014, India,

出版信息

AAPS PharmSciTech. 2014 Aug;15(4):810-21. doi: 10.1208/s12249-014-0103-1. Epub 2014 Mar 26.

Abstract

The present study was aimed at synthesizing an imidazole-based ionic liquid 1-butyl-3-methylimidazolium bromide (BMIMBr) and subsequent development of a novel ionic liquid-in-oil (IL/o) microemulsion (ME) system for dermal delivery of a poorly permeating drug 5-fluorouracil (5-FU). A significant enhancement in the solubility of 5-FU was observed in BMIMBr. IL/o MEs of 5-FU were prepared using isopropyl myristate, Tween 80/Span 20, and BMIMBr. Results of ex vivo skin permeation studies through mice skin indicated that the selected IL/o ME exhibited 4-fold enhancement in percent drug permeation as compared to aqueous solution, 2.3-fold as compared to hydrophilic ointment, and 1.6-fold greater permeation than water in oil (w/o) ME. The results of in vivo studies against dimethylbenz(a)anthracene (DMBA)/12-O-tetradecanoylphorbol-13-acetate (TPA)-induced mice skin carcinogenesis demonstrated that the IL/o ME could effectively treat skin cancer in 4 weeks. In addition, the side effects such as erythema and irritation associated with the conventional formulations were not observed. Histopathological studies showed that the use of IL/o ME caused no anatomic and pathological changes in the skin structure of mice. These studies suggest that the use of IL-based ME system can efficiently enhance the solubility and permeability of 5-FU and hence its therapeutic efficacy.

摘要

本研究旨在合成一种基于咪唑的离子液体1-丁基-3-甲基咪唑溴盐(BMIMBr),并随后开发一种新型的油包离子液体(IL/o)微乳液(ME)系统,用于皮肤递送渗透性差的药物5-氟尿嘧啶(5-FU)。在BMIMBr中观察到5-FU的溶解度显著提高。使用肉豆蔻酸异丙酯、吐温80/司盘20和BMIMBr制备了5-FU的IL/o微乳液。通过小鼠皮肤进行的离体皮肤渗透研究结果表明,与水溶液相比,所选的IL/o微乳液的药物渗透百分比提高了4倍,与亲水软膏相比提高了2.3倍,比油包水(w/o)微乳液的渗透率高1.6倍。针对二甲基苯并(a)蒽(DMBA)/12-O-十四酰佛波醇-13-乙酸酯(TPA)诱导的小鼠皮肤癌发生的体内研究结果表明,IL/o微乳液可在4周内有效治疗皮肤癌。此外,未观察到与传统制剂相关的红斑和刺激等副作用。组织病理学研究表明,使用IL/o微乳液不会引起小鼠皮肤结构的解剖学和病理学变化。这些研究表明,基于离子液体的微乳液系统的使用可以有效地提高5-FU的溶解度和渗透率,从而提高其治疗效果。

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