首页> 外文期刊>International Journal of Pharmaceutics >Design and optimization of topical methotrexate loaded niosomes for enhanced management of psoriasis: Application of Box-Behnken design, in-vitro evaluation and in-vivo skin deposition study
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Design and optimization of topical methotrexate loaded niosomes for enhanced management of psoriasis: Application of Box-Behnken design, in-vitro evaluation and in-vivo skin deposition study

机译:设计和优化甲氨蝶呤局部负载纳米粒以改善牛皮癣的治疗:Box-Behnken设计的应用,体外评估和体内皮肤沉积研究

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Psoriasis, a skin disorder characterized by impaired epidermal differentiation, is regularly treated by systemic methotrexate (MTX), an effective cytotoxic drug but with numerous side effects. The aim of this work was to design topical MIX loaded niosomes for management of psoriasis to avoid systemic toxicity. To achieve this goal, MTX niosomes were prepared by thin film hydration technique. A Box-Behnken (BB) design, using Design-Expert(R) software, was employed to statistically optimize formulation variables. Three independent variables were evaluated: MTX concentration in hydration medium (X-1), total weight of niosomal components (X-2) and surfactant: cholesterol ratio (X-3). The encapsulation efficiency percent (Y-1: EE%) and particle size (Y-2: PS) were selected as dependent variables. The optimal formulation (F12) displayed spherical morphology under transmission electron microscopy (TEM), optimum particle size of 1375.00 nm and high EE% of 78.66%. In-vivo skin deposition study showed that the highest value of percentage drug deposited (22.45%) and AUC(0-10) (1.15 mg. h/cm(2)) of MIX from niosomes were significantly greater than that of drug solution (13.87% and 0.49 mg .h/cm(2), respectively). Moreover, in-vivo histopathological studies confirmed safety of topically applied niosomes. Concisely, the results showed that targeted MTX delivery might be achieved using topically applied niosomes for enhanced treatment of psoriasis. (C) 2015 Elsevier B.V. All rights reserved.
机译:牛皮癣是一种以表皮分化受损为特征的皮肤疾病,通常通过全身性甲氨蝶呤(MTX)进行治疗,后者是一种有效的细胞毒性药物,但副作用很多。这项工作的目的是设计局部用MIX负载的脂质体来治疗牛皮癣,以避免全身毒性。为了实现这一目标,通过薄膜水化技术制备了MTX脂质体。使用Design-Expert(R)软件的Box-Behnken(BB)设计用于统计优化配方变量。评价了三个独立变量:水合介质中的MTX浓度(X-1),血浆成分总重量(X-2)和表面活性剂:胆固醇比(X-3)。选择包封效率百分比(Y-1:EE%)和粒径(Y-2:PS)作为因变量。最佳配方(F12)在透射电子显微镜(TEM)下显示出球形形态,最佳粒径为1375.00 nm,高EE%为78.66%。体内皮肤沉积研究表明,从脂质体中沉积MIX的药物百分比百分比(22.45%)和AUC(0-10)(1.15 mg.h / cm(2))的最大值显着大于药物溶液( 13.87%和0.49 mg.h / cm(2)。此外,体内组织病理学研究证实了局部应用的脂质体的安全性。简而言之,结果表明,使用局部应用的脂质体可增强牛皮癣的治疗效果,可实现靶向MTX递送。 (C)2015 Elsevier B.V.保留所有权利。

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