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共轭聚合物纳米粒子的生物功能化用于肿瘤细胞的靶向成像和光动力杀伤。

Biological Functionalization of Conjugated Polymer Nanoparticles for Targeted Imaging and Photodynamic Killing of Tumor Cells.

机构信息

School of Chemistry and Chemical Engineering, Shanxi University , Taiyuan 030006, P. R. China.

Department of Chemistry, Changzhi University , Changzhi 046011, P. R. China.

出版信息

ACS Appl Mater Interfaces. 2016 Aug 3;8(30):19364-70. doi: 10.1021/acsami.6b06642. Epub 2016 Jul 20.

Abstract

Conjugated polymer nanoparticles composed of PFT/PS as a core and PEG-COOH on the surface were prepared by a reprecipitating method. The CPNs diaplay excellet properties such as good photostability, low cytotoxicity, and strong brightness, etc. The average diamater of CPNs is 30 nm with a spherical morphology. To realize specific imaging in different parts of tumor cells, the bare CPNs with the carboxyls on the surface were conjugated with antibody or peptide by a covalent mode. Studies display that CPNs modified with anti-EpCAM can recognize MCF-7 tumor cells and locate on the membrane, while CPNs conjugated with transcriptional activator protein (Tat) specifically locate in the cytoplasm of MCF-7 cells. On the basis of the ability of CPNs for producing reactive oxygen species (ROS) under light irradiation, photodynamic therapy for tumor cells was investigated. Due to the long distance and wide diffusion range, MCF-7 tumor cells with CPNs/anti-EpCAM have no obvious change with or without white light irradiation. However, CPNs/Tat exhibits higher killing ability for MCF-7 cells. Noticeably, multifunctional CPNs linked with anti-EpCAM and Tat simultaneously not only can specifically target MCF-7 tumor cells, but also may inhibit and kill these cells. This work develops a potential application platform for multifunctional CPNs in locating imaging, photodynamic therapy, and other aspects.

摘要

由 PFT/PS 作为核和 PEG-COOH 表面的共轭聚合物纳米粒子通过再沉淀方法制备。CPNs 显示出良好的光稳定性、低细胞毒性和强亮度等优异性能。CPNs 的平均直径为 30nm,呈球形形态。为了在肿瘤细胞的不同部位实现特异性成像,表面带有羧基的裸 CPNs 通过共价方式与抗体或肽偶联。研究表明,修饰有抗 EpCAM 的 CPNs 可识别 MCF-7 肿瘤细胞并定位于细胞膜上,而与转录激活蛋白 (Tat) 偶联的 CPNs 则特异性定位于 MCF-7 细胞的细胞质中。基于 CPNs 在光照射下产生活性氧 (ROS) 的能力,研究了 CPNs 对肿瘤细胞的光动力治疗。由于距离长且扩散范围广,具有 CPNs/抗 EpCAM 的 MCF-7 肿瘤细胞在有或没有白光照射下没有明显变化。然而,CPNs/Tat 对 MCF-7 细胞具有更高的杀伤能力。值得注意的是,同时连接有抗 EpCAM 和 Tat 的多功能 CPNs 不仅可以特异性靶向 MCF-7 肿瘤细胞,而且可能抑制和杀死这些细胞。这项工作为多功能 CPNs 在定位成像、光动力治疗和其他方面的潜在应用平台的发展提供了基础。

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