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首页> 外文期刊>Journal of drug targeting >Non-ionic surfactant vesicles as a carrier system for dermal delivery of (t)-Catechin and their antioxidant effects
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Non-ionic surfactant vesicles as a carrier system for dermal delivery of (t)-Catechin and their antioxidant effects

机译:非离子表面活性剂囊泡作为(t)-儿茶素真皮递送的载体系统及其抗氧化作用

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摘要

Numerous skin disorders and diseases are related to oxidative stress. The application of an antioxidant, serving as a strong defense agent against oxidation, is of great interest in dermatology yet remains challenging for delivery. This paper aimed to develop a niosome carrier system to deliver the antioxidant (t) Catechin into the skin. (t) Catechin-loaded niosomes were prepared using film hydration technique and the physicochemical properties of drug-loaded niosomes were characterised and investigated by a series of in vitro and ex vivo studies. The optimised formulation displayed an acceptable size in nanoscale (204 nm), high drug entrapment efficiency (49) and amorphous state of drug in niosomes. It was found that (t) Catechin-loaded niosomes could effectively prolong the drug release. Drug deposition in the viable layers of human skin was significantly enhanced when niosomal carriers were applied (p<0.05). Compared to the pure drug, the niosomal formulation had a greater protective effect on the human skin fibroblasts (Fbs). This is consistent with the observation of internalisation of niosomes by Fbs which was concentration-, time- and temperature-dependent, via an energy-dependent process of endocytosis. The research highlighted that niosomes are potential topical carriers for dermal delivery of antioxidants in skin-care and pharmaceutical products.
机译:许多皮肤病和疾病都与氧化应激有关。抗氧化剂作为抗氧化的强力防御剂,在皮肤病学中引起了极大的兴趣,但在输送方面仍然具有挑战性。本文旨在开发一种铌体载体系统,将抗氧化剂(t)儿茶素输送到皮肤中。(t) 使用薄膜水合技术制备了载药儿茶素的铌小体,并通过一系列体外和离体研究表征和研究了载药黌小体的物理化学性质。优化后的配方在纳米级 (204 nm) 中显示出可接受的尺寸、高药物捕获效率 (49%) 和药物在 niosome 中的无定形状态。研究发现,(t)儿茶素负载的锌骨体可以有效延长药物释放。当应用niosom载体时,药物在人体皮肤活层中的沉积显着增强(p<0.05)。与纯药物相比,niosomal制剂对人体皮肤成纤维细胞(Fbs)具有更大的保护作用。这与 Fbs 对 niosome 内化的观察一致,Fbs 通过能量依赖性内吞过程对浓度、时间和温度依赖。该研究强调,niosomes 是皮肤护理和药品中抗氧化剂皮肤递送的潜在局部载体。

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