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首页> 外文期刊>European journal of pharmaceutics and biopharmaceutics: official journal of Arbeitsgemeinschaft fuer Pharmazeutische Verfahrenstechnik e.V >The clinical efficacy of cosmeceutical application of liquid crystalline nanostructured dispersions of alpha lipoic acid as anti-wrinkle
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The clinical efficacy of cosmeceutical application of liquid crystalline nanostructured dispersions of alpha lipoic acid as anti-wrinkle

机译:药妆应用α硫辛酸液晶纳米结构分散体作为抗皱的临床功效

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摘要

Topical 5% alpha lipoic acid (ALA) has shown efficacy in treatment of photo-damaged skin. The aim of this work was to evaluate the potential of poloxamer (P407) gel as a vehicle for the novel lipid base particulate system (cubosome dispersions) of ALA. Cubosome dispersions were formulated by two different approaches, emulsification of glyceryl monoolein (GMO) and poloxamer (P407) in water followed by ultrasonication, and the dilution method using a hydrotrope. Three different concentrations of GMO were used to formulate the cubosome dispersions using the first method, 5% (D1), 10% (D2) and 15% w/w (D3). In the second technique an isotropic liquid was produced by combining GMO with ethanol, and this isotropic liquid was then diluted with a P407 solution (D4). The dispersions were characterized by zeta potential, light scattering techniques, optical and transmission electron microscopy, encapsulation efficiency and in vitro drug release. Results showed that D4 was not a uniform dispersion and that D1, D2 and D3 were uniform dispersions, in which by increasing the GMO content in the dispersion, the size of the cubosomes decreased, zeta potential became more negative, encapsulation efficiency increased up to 86.48% and the drug release rate was slower. P407 gels were prepared using the cold method. Two concentrations of P407 gel were fabricated, 20 and 30% w/w. P407 gels were loaded with either ALA or dispersions containing ALA cubosomes. P407 gels were characterized by critical gelation temperature, rheological measurements and in vitro drug release studies. Results suggested that by increasing P407 concentration, the gelation temperature decreases and viscosity increases. Drug release in both cases was found to follow the Higuchi square root model. Gel loaded with ALA cubosomes provided a significantly lower release rate than the gel loaded with the un-encapsulated ALA. A double blinded placebo controlled clinical study was conducted, aiming to evaluate the efficacy as an anti-wrinkle agent and volunteer's satisfaction upon application of topical 30% P407 gel loaded with ALA cubosomes. Results indicated reduction in facial lines, almost complete resolution of fine lines in the periorbital region and upper lip area and overall improvement in skin color and texture in most volunteers. There were no instances of irritation, peeling or other apparent adverse side effects.
机译:局部用5%α硫辛酸(ALA)已显示出对光损伤皮肤的治疗功效。这项工作的目的是评估泊洛沙姆(P407)凝胶作为ALA新型脂质基础颗粒系统(立方体分散体)的媒介物的潜力。通过两种不同的方法配制立方微粒分散体:甘油单油精(GMO)和泊洛沙姆(P407)在水中的乳化,然后进行超声处理,以及使用水溶助长剂的稀释方法。使用第一种方法,使用三种不同浓度的GMO配制立方微粒分散体:5%(D1),10%(D2)和15%w / w(D3)。在第二种技术中,通过将GMO与乙醇混合生产各向同性液体,然后用P407溶液(D4)稀释该各向同性液体。通过ζ电位,光散射技术,光学和透射电子显微镜,包封效率和体外药物释放来表征分散体。结果表明,D4不是均匀分散体,D1,D2和D3是均匀分散体,其中通过增加分散体中GMO的含量,使小立方体的尺寸减小,ζ电势变得更负,包封效率提高至86.48。 %和药物释放速率较慢。使用冷方法制备P407凝胶。制备两种浓度的P407凝胶,分别为20%和30%w / w。 P407凝胶上装有ALA或含有ALA cubosomes的分散体。通过临界胶凝温度,流变学测量和体外药物释放研究来表征P407凝胶。结果表明,通过增加P407的浓度,胶凝温度降低,粘度增加。两种情况下的药物释放均遵循Higuchi平方根模型。载有ALA cubosomes的凝胶的释放速率显着低于未包封的ALA的凝胶。进行了双盲安慰剂对照临床研究,旨在评估应用局部载有ALA cubicsomes的30%P407凝胶作为抗皱剂的功效和志愿者的满意度。结果表明,大多数志愿者的脸部线条减少,眼眶周围区域和上唇区域的细纹几乎完全消除,皮肤颜色和质地总体得到改善。没有刺激,脱皮或其他明显不良副作用的情况。

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