CAS Key Laboratory of Soft Matter Chemistry, Hefei National Laboratory for Physical Sciences at the Microscale, and National Synchrotron Radiation Laboratory, iChEM, University of Science and Technology of China, Jinzai Road 96#, Hefei, 230026, Anhui, P. R. China.
Biomater Sci. 2016 Oct 18;4(11):1638-1645. doi: 10.1039/c6bm00581k.
Near infrared (NIR) imaging-guided photodynamic therapy (PDT) is attractive, especially the utilization of one dye as both a photosensitizer and fluorescent probe, and the as-synthesized BODIPY-Br molecule is a candidate. Here, a galactose targeted amphiphilic copolymer of a polypeptide was synthesized and its micelles work as nanocarriers for BODIPY for targeting the NIR imaging-guided PDT of hepatoma cancer cells. At the same time, BODIPY could light up the cytoplasm for real-time imaging and kill cancer cells when the light was switched on. In vitro tests performed on both HepG2 and HeLa cells confirmed that the as-prepared PMAGP-POEGMA-PLys-B micelles showed efficient cell suppression of the cells with galactose receptors in the presence of light under an extremely low energy density (6.5 J cm). This protocol highlights the potential of polypeptides as biodegradable carriers for NIR image-guided and confined targeting photodynamic therapy.
近红外(NIR)光成像引导的光动力疗法(PDT)很有吸引力,尤其是将一种染料同时用作光敏剂和荧光探针的应用,所合成的 BODIPY-Br 分子就是一个候选物。在这里,合成了一种靶向半乳糖的多肽两亲性共聚物,其胶束可用作 BODIPY 的纳米载体,用于肝癌细胞的 NIR 光成像引导 PDT。同时,当打开光时,BODIPY 可以点亮细胞质,实现实时成像并杀死癌细胞。在 HepG2 和 HeLa 细胞上进行的体外测试证实,所制备的 PMAGP-POEGMA-PLys-B 胶束在极低的能量密度(6.5 J cm)下,在有光照的条件下,对具有半乳糖受体的细胞表现出高效的细胞抑制作用。该方案突出了多肽作为 NIR 图像引导和受限靶向光动力治疗的生物可降解载体的潜力。