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首页> 外文期刊>Drug delivery and translational research >Tetrahydrocurcumin-loaded vaginal nanomicrobicide for prophylaxis of HIV/AIDS: in silico study, formulation development, and in vitro evaluation
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Tetrahydrocurcumin-loaded vaginal nanomicrobicide for prophylaxis of HIV/AIDS: in silico study, formulation development, and in vitro evaluation

机译:用于预防艾滋病毒/艾滋病的四氢胶质蛋白加载的阴道纳米霉病:在硅研究,配方发育和体外评估中

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摘要

A vaginal microbicide is a front-line women-dependent approach and an alternative to a condom for prevention of unprotected sexual intercourse-associated HIV. The microbicide research is still in its infancy with several products in the clinical studies being reported to have good efficacy, safe, but with poor adherence. One such molecule reported with an excellent efficacy when tested preclinically is curcumin, a natural polyphenol derived from Curcuma longa. Despite its potential HIV-1 inhibitory activity, it has intense yellow color staining properties, which would result in poor consumer compliance and adherence for vaginal application. To address this issue, tetrahydrocurcumin (THC), a colorless derivative of curcumin, was subjected to in silico screening (molecular docking and dynamics simulation studies) using homology model of gp120-CD4 binding. It was found that THC exhibited equivalent gp120-CD4 binding inhibitory activity as compared with curcumin due to its stable hydrophobic interactions with residues Asp368 and Trp427 deeper in the Phe43 cavity of CD4 receptor. Hence, it can be effectively used as a potential microbicide candidate. THC, a BCS Class II molecule exhibits poor solubility, spreadability, and intracellular uptake when used in the conventional form. Thus, it was decided to develop a lipid-based nanomicrobicide gel for delivery of THC. The developed THC-loaded o/w microemulsion gel was characterized for physicochemical properties (globule size, drug content, drug release, and permeation) and further used for in vitro cell line studies (cell viability, cellular uptake, and anti-HIV activity). The developed formulation was found to be stable with coitus-independent release profile and exhibited a rapid time-independent intracellular uptake. In addition, it exhibited a fourfold increase in efficacy as compared with conventional THC. Thus, the novel THC-loaded o/w microemulsion gel exhibited the potential for prevention of HIV-1 infection associated with unprotected sexual intercourse.
机译:阴道杀微生物是一种前线女性依赖性方法,以及用于预防未受保护性交相关的HIV的避孕套的替代品。杀微生物剂研究仍然在其婴儿期间,临床研究中的几种产品据报道,有良好的疗效,安全,但坚持不懈。当尿液蛋白尿蛋白尿蛋白测试时,源自姜黄素的姜黄素,其中一种这样的分子以优异的功效报告。尽管其潜在的HIV-1抑制活性,它具有强烈的黄色染色特性,这将导致消费者的符合性和阴道应用粘附性差。为了解决该问题,使用GP120-CD4结合的同源模型,在硅筛选(分子对接和动力学模拟研究中,四氢胶蛋白(THC),无色衍生物。发现由于其与CD4受体的PHE43腔体中的残基ASP368和TRP427更深的疏水相互作用,THC表现出相同的GP120-CD4结合抑制抑制活性。因此,它可以有效地用作潜在的微生物剂候选者。当以常规形式使用时,BCS II类分子表现出差的溶解度,铺展性和细胞内摄取。因此,决定开发一种用于递送的脂质的纳米二杀虫剂凝胶。发育的THC负载的O / W微乳液凝胶的特征在于物理化学性质(球粒大小,药物含量,药物释放和渗透),并进一步用于体外细胞系研究(细胞活力,细胞吸收和抗HIV活性) 。发现开发的制剂与肖联无关的释放型材稳定,并且表现出快速的时间依赖性细胞内摄取。此外,与常规THC相比,它表现出效力的四倍。因此,新型THC负载的O / W微乳液凝胶表现出预防与未受保护性交相关的HIV-1感染的可能性。

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