Quan Chang-Yun, Chang Cong, Wei Hua, Chen Chang-Sheng, Xu Xiao-Ding, Cheng Si-Xue, Zhang Xian-Zheng, Zhuo Ren-Xi
Key Laboratory of Biomedical Polymers of Ministry of Education & Department of Chemistry, Wuhan University, Wuhan 430072, People's Republic of China.
Nanotechnology. 2009 Aug 19;20(33):335101. doi: 10.1088/0957-4484/20/33/335101. Epub 2009 Jul 28.
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.
在本文中,含精氨酸-甘氨酸-天冬氨酸(RGD)的肽和转铁蛋白(Tf)均与热敏性聚(N-异丙基丙烯酰胺-共-丙基丙烯酸)(聚(NIPAAm-共-PAAc))纳米凝胶偶联,以制备双靶向药物载体。通过荧光光谱、紫外可见光谱、动态光散射(DLS)和透射电子显微镜(TEM)对所得纳米凝胶进行了表征。为了追踪双配体偶联的纳米凝胶,将异硫氰酸荧光素(FITC)进一步偶联到纳米凝胶上。细胞内化实验表明,与非肿瘤细胞(COS-7细胞)相比,双配体偶联的纳米凝胶对HeLa细胞的内吞作用明显增强。载药的双配体偶联纳米凝胶能够有效地转运到靶肿瘤细胞中,且抗肿瘤效果显著增强,这表明双配体偶联纳米凝胶作为肿瘤靶向药物载体具有巨大潜力。