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在紫外光下从封装的 S-亚硝基谷胱甘肽向人体皮肤递送一氧化氮:一项体外和离体研究。

Delivering nitric oxide into human skin from encapsulated S-nitrosoglutathione under UV light: An in vitro and ex vivo study.

机构信息

Center for Natural and Human Sciences, Universidade Federal do ABC, Santo André, Brazil.

Medical Research Council Centre for Inflammation Research, University of Edinburgh, Queen's Medical Research Institute, UK.

出版信息

Nitric Oxide. 2020 Jan 1;94:108-113. doi: 10.1016/j.niox.2019.11.003. Epub 2019 Nov 21.

Abstract

Nitric oxide (NO) is a crucial molecule in the human body. The encapsulation of exogenous NO donors into chitosan nanoparticles (CS NPs) has been widely used to overcome NO drawbacks in pharmacological applications, such as, its short half-life. The NO donor, S-nitrosoglutathione (GSNO), was encapsulated into CS NPs (GSNO-CS NPs) and characterized by AFM and DLS measurements. The nanoparticles presented a hydrodynamic size of 123.3 ± 1.5 nm and a polydispersity of 0.25 ± 0.01. The ability of GSNO-CS NPs, combined with UV irradiation, to deliver NO was evaluated using ex vivo human skin. The human skin was pre-treated with GSNO-CS NPs, in the presence and absence of UV irradiation. The results showed that the combined treatment significantly increased the NO and S-nitrosothiol levels in human skin. This effect can emulate the cardiovascular benefits related to NO without negative side effects of skin exposure to UV light.

摘要

一氧化氮(NO)是人体内至关重要的分子。将外源性 NO 供体包封到壳聚糖纳米粒子(CS NPs)中已广泛用于克服药理学应用中 NO 的缺点,例如半衰期短。NO 供体 S-亚硝基谷胱甘肽(GSNO)被包封到 CS NPs(GSNO-CS NPs)中,并通过 AFM 和 DLS 测量进行了表征。纳米粒子的水动力直径为 123.3 ± 1.5nm,多分散性为 0.25 ± 0.01。使用离体人体皮肤评估了 GSNO-CS NPs 与紫外线照射相结合输送 NO 的能力。在存在和不存在紫外线照射的情况下,将 GSNO-CS NPs 预处理人体皮肤。结果表明,联合处理显著增加了人体皮肤中的 NO 和 S-亚硝基硫醇水平。这种作用可以模拟与 NO 相关的心血管益处,而不会对皮肤暴露于紫外线产生负面影响。

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