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用于治疗寻常痤疮的载有氨苯砜的混合胶束凝胶

Dapsone-Loaded Mixed Micellar Gel for Treatment OF Acne Vulgaris.

作者信息

Rao Monica Rp, Deshpande Sushant, Deshpande Padmanabh

机构信息

Department of Pharmaceutics, AISSMS College of Pharmacy, Kennedy Road, Near R.T.O., Maharashtra, 411001, Pune, India.

Department of Pharmaceutical Quality Assurance, AISSMS College of Pharmacy, Kennedy Road, Near R.T.O., Pune, 411001, India.

出版信息

AAPS PharmSciTech. 2023 Apr 26;24(5):109. doi: 10.1208/s12249-023-02564-1.

Abstract

Mixed polymeric micelles are potential nanocarriers for topical drug delivery. Dapsone (DAP) is an antibacterial used as anti-acne agent, but challenged by low water solubility and poor skin permeability. In the present study, DAP-loaded mixed micellar gel was developed comprising Pluronics F-68 and F-127. Micelles were prepared by solvent evaporation method and particle size, ex vivo permeation, drug loading, and entrapment efficiency were determined. Central Composite Design was used to optimize formulation. Independent variables were concentration of Pluronics at three levels while micelle size and drug loading capacities were dependent variables. Droplet size ranged from 400 to 500 nm. Transmission electron microscopy revealed spherical morphology of micelles. Optimized micelles were incorporated into gel base using HPMC K100M, Sodium CMC, and Carbopol 980 as gelling agents. Gels were evaluated for pH, drug content, spreadability, rheology, syneresis, ex vivo permeation, and subacute dermal toxicity. Compared with solubility of free DAP (0.24+0.056 µg/ml), solubility in mixed micelles was 18.42±3.4 µg/ml in water at room temperature. Order of spreadability of gels was Na CMC < HPMC < Carbopol 980. Carbopol gels displayed thixotropy with index of 3.17. Syneresis for all gels from day 0 to day 30 was found to be in range of 4.2 to 15.6% w/w. Subacute dermal toxicity studies showed no signs of erythema and edema on rat skin until 21 days. These results suggest that mixed micelles can significantly increase solubility and permeability and sustain release of DAP and are suitable carriers for topical DAP delivery in anti-acne therapies.

摘要

混合聚合物胶束是局部给药的潜在纳米载体。氨苯砜(DAP)是一种用作抗痤疮药物的抗菌剂,但存在水溶性低和皮肤渗透性差的问题。在本研究中,开发了一种包含普朗尼克F - 68和F - 127的载DAP混合胶束凝胶。通过溶剂蒸发法制备胶束,并测定粒径、体外渗透、载药量和包封率。采用中心复合设计优化配方。自变量为三个水平的普朗尼克浓度,而胶束大小和载药能力为因变量。液滴大小范围为400至500nm。透射电子显微镜显示胶束呈球形形态。使用羟丙甲纤维素K100M、羧甲基纤维素钠和卡波姆980作为凝胶剂,将优化后的胶束加入凝胶基质中。对凝胶进行pH值、药物含量、铺展性、流变学、脱水收缩、体外渗透和亚急性皮肤毒性评估。与游离DAP的溶解度(0.24 + 0.056μg/ml)相比,在室温下,其在混合胶束中的水中溶解度为18.42±3.4μg/ml。凝胶铺展性顺序为羧甲基纤维素钠<羟丙甲纤维素<卡波姆980。卡波姆凝胶表现出触变性,指数为3.17。发现所有凝胶从第0天到第30天的脱水收缩率在4.2%至15.6%(w/w)范围内。亚急性皮肤毒性研究表明,直到21天,大鼠皮肤均未出现红斑和水肿迹象。这些结果表明,混合胶束可显著提高DAP的溶解度和渗透性,并实现其缓释,是抗痤疮治疗中局部递送DAP的合适载体。

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