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RGD peptide-targeted polyethylenimine-entrapped gold nanoparticles for targeted CT imaging of an orthotopic model of human hepatocellular carcinoma

机译:用于靶向CT成像的RGD肽靶向聚乙基菊氨氨酸的金纳米颗粒的人肝细胞癌的原位模型的靶向CT成像

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We report the synthesis and characterization of arginine-glycine-aspartic acid (RGD) peptide-targeted polyethylenimine (PEI)-entrapped gold nanoparticles (RGD-Au PENPs) for targeted CT imaging of hepatic carcinomas in situ. In this work, PEI sequentially modified with polyethylene glycol (PEG), and RGD linked-PEG was used as a nanoplatform to prepare AuNPs, followed by complete acetylation of PEI surface amines. We showed that the designed RGD-Au PENPs were colloidally stable and biocompatible in the given concentration range, and could be specifically taken up by a_vβ3 integrin-overexpressing liver cancer cells in vitro. Furthermore, in vivo CT imaging results revealed that the particles displayed a great contrast enhancement of hepatic carcinomas region, and could target to hepatic carcinomas region in situ. With the proven biodistribution and histological examinations in vivo, the synthesized RGD-Au PENPs show a great formulation to be used as a contrast agent for targeted CT imaging of different a_(vβ3) integrin receptor-overexpressing tumors.
机译:我们报道了精氨酸 - 甘氨酸 - 天冬氨酸(RGD)肽靶向聚乙烯亚胺(PEI) - 基因的金纳米粒子(RGD-AU PENP)的合成和表征用于原位的肝癌的靶向CT成像。在该作品中,用聚乙二醇(PEG)顺序改性PEI和RGD LINKED-PEG作为纳米孔,以制备肛周,然后完成PEI表面胺的完全乙酰化。我们表明,设计的RGD-AU PENP在给定的浓度范围内是胶体稳定和生物相容性,并且可以在体外由A_Vβ3整合蛋白过度抑制肝癌细胞特异性地吸收。此外,在体内CT成像结果表明,颗粒呈现出肝癌区域的巨大对比度,并且可以原位靶向肝癌区域。随着体内的经过验证的生物分布和组织学检查,合成的RGD-Au Penps显示出一种伟大的配方,其用作不同A_(Vβ3)整合蛋白受体过表达肿瘤的靶向CT成像的造影剂。

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