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[含氯化钠的油包水微乳剂用于氟尿嘧啶的透皮给药]

[Water in oil microemulsions containing NaCl for transdermal delivery of fluorouracil].

作者信息

Xiao Yan-Yu, Liu Fang, Chen Zhi-Peng, Ping Qi-Neng

机构信息

Department of Pharmaceutics, China Pharmaceutical University, Nanjing 210009, China.

出版信息

Yao Xue Xue Bao. 2011 Jun;46(6):720-6.

Abstract

This study is to prepare the W/O microemulsion containing NaCl and fluorouracil (5-Fu) as a model drug to investigate the transdermal characteristics and skin irritation of the microemulsion in vitro. Isopropylmyristate (IPM) acting as oil phase, Aerosol-OT (AOT) as surfactant, Tween 85 as cosurfactant, NaCl solution was added dropwise to the oil phase to prepare W/O microemulsion at room temperature using magnetic stirring, and then 5-Fu powder was added. According to the area of microemulsion based on the pseudo-tertiary phase diagrams, the optimum formulation was screened initially. And the permeation flux of fluorouracil across excised mice skin was determined in vitro using Franz diffusion cells to study the influence of the amount of water and the drug loading capacity and optimize the formulation further. Refer to 5-Fu cream, the irritation of microemulsion on the rat skin was studied. The optimum formulation was composed of 0.7% (w/v) 5-Fu, 50% NaCl solution (0.05 mol x L(-1)), 20% mix-surfactant (AOT/Tween 85, K(m) = 2) and 29.3% oil (IPM). The cumulative amount of fluorouracil permeated in 12 h was (2 013.4 +/- 41.6) microg x cm(-2), 20.23 folds and 10.38 folds more than 0.7% fluorouracil aqueous solution and 2.5% (w/w) fluorouracil cream, respectively. Microemulsion exhibited some irritation, but could be reversed after drug withdrawal. The addition of NaCl significantly increased the content of water and the drug loading in microemulsion systems. The NaCl/AOT-Tween 85/IPM microemulsion system promoted the permeation of fluorouracil greatly, which may be a promising vehicle for the transdermal delivery of fluorouracil and other hydrophilic drug.

摘要

本研究以含氯化钠和氟尿嘧啶(5-氟尿嘧啶)的W/O微乳作为模型药物进行制备,以研究该微乳在体外的透皮特性及皮肤刺激性。采用肉豆蔻酸异丙酯(IPM)作为油相,气溶胶OT(AOT)作为表面活性剂,吐温85作为助表面活性剂,在室温下通过磁力搅拌将氯化钠溶液滴加到油相中制备W/O微乳,然后加入5-氟尿嘧啶粉末。根据基于拟三元相图的微乳区域,初步筛选出最佳配方。并使用Franz扩散池在体外测定氟尿嘧啶透过离体小鼠皮肤的渗透通量,以研究水量和载药量的影响并进一步优化配方。参照5-氟尿嘧啶乳膏,研究微乳对大鼠皮肤的刺激性。最佳配方由0.7%(w/v)的5-氟尿嘧啶、50%的氯化钠溶液(0.05 mol·L⁻¹)、20%的混合表面活性剂(AOT/吐温85,Kₘ = 2)和29.3%的油(IPM)组成。12小时内氟尿嘧啶的累积渗透量为(2013.4±41.6)μg·cm⁻²,分别比0.7%氟尿嘧啶水溶液和2.5%(w/w)氟尿嘧啶乳膏高20.23倍和10.38倍。微乳表现出一定刺激性,但停药后可恢复。氯化钠的加入显著增加了微乳体系中的含水量和载药量。NaCl/AOT-吐温85/IPM微乳体系极大地促进了氟尿嘧啶的渗透,可能是氟尿嘧啶及其他亲水性药物透皮给药的一种有前景的载体。

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