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Bioconjugated Pluronic Triblock-Copolymer Micelle-Encapsulated Quantum Dots for Targeted Imaging of Cancer: In Vitro and In Vivo Studies

机译:生物共轭多元醇三嵌段共聚物胶束封装的量子点用于癌症的靶向成像:体内和体外研究

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摘要

Early in this study, CdTe/ZnS core/shell quantum dots (QDs) were encapsulated in carboxylated Pluronic F127 triblock polymeric micelle, to preserve the optical and colloidal stability of QDs in biological fluids. Folic acid (FA) was then conjugated to the surface of QDs for the targeted delivery of the QD formulation to the tumor site, by exploiting the overexpressed FA receptors (FARs) on the tumor cells. Cytotoxicity study demonstrated that the QD formulation has negligible in vitro toxicity. The in vitro study showed that the bioconjugated micelle-encapsulated QDs, but not the unconjugated QDs, were able to efficiently label Panc-1 cancer cells. In vivo imaging study showed that bioconjugated QDs were able to target tumor site after intravenous injection of the formulation in tumor-bearing mice.
机译:在这项研究的早期,将CdTe / ZnS核/壳量子点(QD)封装在羧化的Pluronic F127三嵌段聚合物胶束中,以保持QD在生物流体中的光学和胶体稳定性。然后,通过利用肿瘤细胞上过表达的FA受体(FAR),将叶酸(FA)偶联至QD表面,以将QD制剂靶向递送至肿瘤部位。细胞毒性研究表明,量子点制剂的体外毒性可忽略不计。体外研究表明,生物缀合的胶束封装的量子点,而非未缀合的量子点,能够有效标记Panc-1癌细胞。体内成像研究表明,在荷瘤小鼠中静脉注射制剂后,生物共轭QD能够靶向肿瘤部位。

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