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首页> 外文期刊>International Journal of Pharmaceutics >(-)-Epigallocatechin gallate (EGCG)-nanoethosomes as a transdermal delivery system for docetaxel to treat implanted human melanoma cell tumors in mice
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(-)-Epigallocatechin gallate (EGCG)-nanoethosomes as a transdermal delivery system for docetaxel to treat implanted human melanoma cell tumors in mice

机译:(-)-表没食子儿茶素没食子酸酯(EGCG)-纳米脂质体作为多西他赛的透皮递送系统治疗小鼠植入的人黑素瘤细胞肿瘤

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摘要

(-)-Epigallocatechin-3-O-gallate (EGCG), a versatile natural product in fresh tea leaves and green tea, has been investigated as a preventative treatment for cancers and cardiovascular disease. The objective of this study was to develop EGCG-nanoethosomes for transdermal delivery and to evaluate them for treating subcutaneously implanted human melanoma cell tumors. EGCG-nanoethosomes, composed of 0.2% EGCG, 2% soybean phosphatidylcholine, 30% ethanol, 1% Tween-80 and 0.1% sugar esters, were prepared and characterized using laser transmission electron microscopy. These nanoethosomes were smoother and more compact than basic-nanoethosomes with the same components except for EGCG. The effectiveness of transdermal delivery by EGCG-nanoethosomes was demonstrated in an in vitro permeability assay system using mouse skin. The inhibitory effect of docetaxel (DT) loaded in EGCG-nanoethosomes (DT-EGCG-nanoethosomes) was analyzed by monitoring growth of a subcutaneously implanted tumor from A-375 human melanoma cells in mice. Mice treated with DT-EGCG-nanoethosomes exhibited a significant therapeutic effect, with tumors shrinking, on average, by 31.5% of initial volumes after 14 d treatment. This indicated a potential for treating skin cancer. In a pharmacokinetic study, transdermal delivery by DT-EGCG-nanoethosomes enabled sufficient DT exposure to the tumor. Together, these findings indicated that EGCG-nanoethosomes have great potential as drug carriers for transdermal delivery. (C) 2016 Elsevier B.V. All rights reserved.
机译:(-)-表没食子儿茶素-3-O-没食子酸酯(EGCG)是新鲜茶叶和绿茶中的一种多用途天然产物,已被研究用作预防癌症和心血管疾病的方法。这项研究的目的是开发用于透皮递送的EGCG纳米脂质体,并评估它们用于治疗皮下植入的人黑色素瘤细胞肿瘤的能力。制备了由0.2%EGCG,2%大豆磷脂酰胆碱,30%乙醇,1%Tween-80和0.1%糖酯组成的EGCG纳米脂质体,并使用激光透射电子显微镜对其进行了表征。这些纳米脂质体比除EGCG以外具有相同成分的碱性纳米脂质体更光滑,更致密。在使用小鼠皮肤的体外渗透性测定系统中,证明了EGCG-纳米脂质体透皮递送的有效性。通过监测小鼠A-375人黑素瘤细胞皮下植入的肿瘤的生长,分析了EGCG-纳米核小体(DT-EGCG-纳米核小体)中装载的多西紫杉醇(DT)的抑制作用。用DT-EGCG-纳米核小体治疗的小鼠表现出显着的治疗效果,治疗14天后,肿瘤平均缩小初始体积的31.5%。这表明治疗皮肤癌的潜力。在药代动力学研究中,DT-EGCG-纳米脂质体透皮递送使足够的DT暴露于肿瘤。总之,这些发现表明,EGCG-纳米核小体作为透皮递送的药物载体具有巨大的潜力。 (C)2016 Elsevier B.V.保留所有权利。

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