负载银和氨砜的niosome共给药的制备、表征和利什曼尼毒性评估:硅内和体外研究。

IF 3.1 Q2 PHARMACOLOGY & PHARMACY
Advanced pharmaceutical bulletin Pub Date : 2024-12-30 Epub Date: 2024-12-05 DOI:10.34172/apb.42740
Anna Etemadifar, Sina Bahraminejad, Abbas Pardakhty, Iraj Sharifi, Alireza Keyhani, Mehdi Ranjbar
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引用次数: 0

摘要

目的:目前,迫切需要制定控制利什曼病的替代战略,它威胁着全世界10亿多人。同时使用联合治疗和纳米结构脂质载体,目的是评估银和氨砜颗粒体在体外和硅体内共同给药的利什曼尼杀灭活性。方法:采用膜水合法制备氨苯砜和银的乳质体制剂后,以7/3的摩尔比选择Span 40和Tween 40/胆固醇为最佳配方。因此,我们进行了一系列的实验方法来比较ready ni质体与两性霉素B抗利什曼病的功效,并对它们可能的作用机制有了更深入的了解。结果:我们的研究结果显示,与阳性对照组两性霉素B相比,负载银和负载氨砜的niosome共同给药的效力更高。等线图和联合指数(CI)分析结果证实了该合剂的增效潜力。这种组合触发巨噬细胞的抗利什曼通路,促进Th1细胞相关基因的表达水平,下调Th2细胞相关表型的表达。此外,高水平的抗氧化和细胞凋亡谱为皮肤利什曼病提供了合理的基础和潜在的药物组合。此外,分子对接结果显示氨苯砜与iNOS具有高结合亲和力,刺激Th1方向的免疫应答。结论:总的来说,氨砜与银粒体共给药的多功能利什曼尼杀灭活性值得进一步的体内和临床研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preparation, Characterization, and Leishmanicidal Assessment of Silver- and Dapsone-Loaded Niosomes Co-administration: In Silico and In Vitro Study.

Purpose: Currently, there is a crucial need for alternative strategies to control leishmaniasis, which threatens more than 1 billion people worldwide. The simultaneous use of combination therapy and nanostructured lipid carriers aimed to assess the leishmanicidal activity of silver and dapsone niosomes co-administration in vitro and in silico.

Methods: After preparing the niosomal formulations of dapsone and silver using the film hydration method, Span 40 and Tween 40/cholesterol with a 7/3 molar ratio was selected as the optimal formulation. Consequently, the arrays of experimental approaches were conducted to compare the anti-leishmaniasis efficacy of ready niosomes with amphotericin B and obtain a deeper understanding of their possible mechanisms of action.

Results: Our findings showed higher potency of silver-loaded and dapsone-loaded niosomes co-administration compared to amphotericin B as a positive control group. The results of isobologram and combination index (CI) analyses confirmed the synergic potential of this mixture. This combination triggered anti-leishmanial pathways of macrophages, which promoted the expression level of Th1 cell-related genes, and the downregulated expression of the phenotypes related to Th2 cells. Furthermore, a high level of antioxidant and apoptotic profiles against the parasite provides a rational basis and potential drug combination for cutaneous leishmaniasis. Moreover, the outcomes of the molecular docking showed a high binding affinity between dapsone and iNOS, stimulating the immune response in Th1 direction.

Conclusion: In general, the multifunctional leishmanicidal activity of dapsone and silver-niosomes co-administration should be considered for further in vivo and clinical studies.

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来源期刊
Advanced pharmaceutical bulletin
Advanced pharmaceutical bulletin PHARMACOLOGY & PHARMACY-
CiteScore
6.80
自引率
2.80%
发文量
51
审稿时长
12 weeks
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