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卡波氯铵经皮给药制剂的研制。

Formulation of carbenoxolone for delivery to the skin.

机构信息

Department of Pharmaceutics, UCL School of Pharmacy, 29-39 Brunswick Square, London, WC1N 1AX, United Kingdom.

出版信息

Int J Pharm. 2013 May 20;448(2):360-5. doi: 10.1016/j.ijpharm.2013.03.045. Epub 2013 Mar 29.

Abstract

Carbenoxolone (CEX), a semi-synthetic derivative of glycyrrhetinic acid, has previously been used as a disodium salt for the management of dyspepsia and peptic ulcer because of its anti-inflammatory properties. Although glycyrrhetinic acid is available in pharmaceutical and personal care products for skin care, the topical use of the free acid form of CEX, has not previously been reported. In this work we investigated the percutaneous penetration of CEX. Solubility and permeability studies were conducted using a range of solvents or skin permeation enhancers (SPEs) commonly used for skin delivery. Binary combinations of dimethyl isosorbide (DMI) and Transcutol™ (TC) with isopropyl myristate (IPM) were effective in promoting skin permeation of CEX although individual solvents were not. Alternative fatty acid esters to IPM were subsequently investigated with the most promising formulation consisting of TC and propylene glycol laurate (PGL). Interestingly, propylene glycol monolaurate (PGML) did not demonstrate comparable efficacy when combined with TC. A ternary formulation consisting of TC, PGL and IPM demonstrated the best permeation enhancement of CEX compared with all other vehicles. The findings confirm (i) the feasibility of promoting CEX penetration across the skin (ii) the synergistic effect of combinations of solvents and SPEs on dermal and transdermal delivery (iii) the necessity for more fundamental studies to explain the differential effects of fatty acid esters on the skin barrier.

摘要

卡波氯铵(CEX)是甘草次酸的半合成衍生物,由于其抗炎特性,曾被用作治疗消化不良和消化性溃疡的二钠盐。虽然甘草次酸可用于制药和个人护理产品的皮肤护理,但 CEX 的游离酸形式的局部使用以前并未报道过。在这项工作中,我们研究了 CEX 的经皮渗透。使用一系列常用于皮肤给药的溶剂或皮肤渗透增强剂(SPE)进行了溶解度和渗透性研究。尽管单独的溶剂没有效果,但二甲基异山梨醇(DMI)和 Transcutol™(TC)与肉豆蔻酸异丙酯(IPM)的二元组合有效地促进了 CEX 的皮肤渗透。随后研究了替代 IPM 的脂肪酸酯,最有前途的配方由 TC 和丙二醇月桂酸酯(PGL)组成。有趣的是,当与 TC 结合时,丙二醇单月桂酸酯(PGML)并没有表现出相当的功效。与所有其他载体相比,由 TC、PGL 和 IPM 组成的三元配方表现出对 CEX 渗透增强的最佳效果。这些发现证实了 (i) 促进 CEX 穿透皮肤的可行性,(ii) 溶剂和 SPE 组合对皮肤和经皮给药的协同作用,(iii) 需要更基础的研究来解释脂肪酸酯对皮肤屏障的不同影响。

相似文献

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Formulation of carbenoxolone for delivery to the skin.卡波氯铵经皮给药制剂的研制。
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