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首页> 外文期刊>Nanotechnology >Dual targeting of a thermosensitive nanogel conjugated with transferrin and RGD-containing peptide for effective cell uptake and drug release
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Dual targeting of a thermosensitive nanogel conjugated with transferrin and RGD-containing peptide for effective cell uptake and drug release

机译:与转铁蛋白和含RGD的肽偶联的热敏纳米凝胶的双重靶向,可有效吸收细胞并释放药物

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摘要

In this paper, both arginine-glycine-aspartic acid (RGD)-containing peptide and transferrin (Tf) were conjugated to the thermosensitive poly(N-isopropylacrylamide-co-propyl acrylic acid) (poly(NIPAAm-co-PAAc)) nanogel to prepare a dual-targeting drug carrier. The obtained nanogel was characterized in terms of fluorescence spectroscopy, UV-vis spectroscopy, dynamic light scattering (DLS) and transmission electron microscopy (TEM). In order to track the dual-ligand conjugated nanogel, fluorescein isothiocyanate (FITC) was further conjugated to the nanogel. A cell internalization experiment showed that the dual-ligand conjugated nanogel exhibited obviously enhanced endocytosis by HeLa cells as compared with non-tumorous cells (COS-7 cells). The drug-loaded dual-ligand conjugated nanogel could be transported efficiently into the target tumor cells and the anti-tumor effect was enhanced significantly, suggesting that the dual-ligand conjugated nanogel has great potential as a tumor targeting drug carrier.
机译:在本文中,精氨酸-甘氨酸-天冬氨酸(RGD)包含的肽和转铁蛋白(Tf)都与热敏性聚(N-异丙基丙烯酰胺-共-丙基丙烯酸)(聚(NIPAAm-co-PAAc))纳米凝胶偶联制备双重靶向药物载体。所获得的纳米凝胶通过荧光光谱,UV-可见光谱,动态光散射(DLS)和透射电子显微镜(TEM)表征。为了追踪双配体共轭纳米凝胶,将异硫氰酸荧光素(FITC)进一步共轭至纳米凝胶。细胞内化实验表明,与非肿瘤细胞(COS-7细胞)相比,双配体缀合的纳米凝胶具有明显增强的HeLa细胞内吞作用。载药的双配体结合的纳米凝胶可以有效地转运到靶肿瘤细胞中,并且显着增强了抗肿瘤效果,表明该双配体的结合纳米凝胶作为靶向肿瘤的药物载体具有很大的潜力。

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