MOE Key Laboratory of Laser Life Science & Institute of Laser Life Science, College of Biophotonics, South China Normal University, Guangzhou 510631, P. R. China.
Guangdong Provincial Key Laboratory of Laser Life Science, College of Biophotonics, South China Normal University, Guangzhou 510631, P. R. China.
ACS Appl Mater Interfaces. 2021 Mar 3;13(8):9316-9328. doi: 10.1021/acsami.0c14730. Epub 2020 Oct 22.
Biomarker-activatable theranostic formulations offer the potential for removing specific tumors with a high diagnostic accuracy and a significant pharmacological effect. Herein, we developed a novel activatable theranostic nanoformulation UAS-PD [upconversion nanophosphor (UCNP)-aptamer/ssDNA-pyropheophorbide-a (PPA)-doxyrubicin (DOX)], which can recognize specific cancer cells with sensitivity and trigger the localized photodynamic destruction and enhanced chemotherapy. UAS-PD was constructed by the conjugation of UCNPs and aptamer probes containing the photosensitizer PPA and the chemotherapeutic drug DOX. When cancer cells are present, the UAS-PD specifically binds to PTK7, an overexpressed protein present on the surface of cancer cells, through conformational recombination of the aptamer structure and switches its upconversion luminescence from 655 to 540 nm. This long-lived ratiometric optical signal provides an ultrasensitive detection limit as low as 3.9 nM for PTK7. Changes in the conformation of UAS-PD can also induce PPA to approach UCNPs, which can produce cytotoxic singlet oxygens under near-infrared excitation to destroy the cell membrane and enhance its permeability for the simultaneously released DOX that targets cellular DNA degradation, which results in a highly effective tumor-killing effect by synergistic extra-intracellular sequential damage.
生物标志物激活治疗配方具有高诊断准确性和显著药理效应的潜力,可用于特异性去除肿瘤。在此,我们开发了一种新型的激活治疗纳米制剂 UAS-PD[上转换纳米荧光粉 (UCNP)-适体/ssDNA-原卟啉 IX-阿霉素 (PPA-多柔比星 (DOX))],它可以通过适体结构的构象重组和从 655nm 到 540nm 的上转换发光来特异性识别肿瘤细胞,从而触发局部光动力破坏和增强化学疗法。UAS-PD 是通过 UCNPs 和包含光敏剂 PPA 和化疗药物 DOX 的适体探针的缀合构建的。当存在癌细胞时,UAS-PD 通过适体结构的构象重组特异性结合到癌细胞表面过表达的蛋白 PTK7 上,并将其上转换发光从 655nm 切换到 540nm。这种长寿命的比率光学信号提供了对 PTK7 的超低检测限,低至 3.9 nM。UAS-PD 构象的变化也可以诱导 PPA 接近 UCNPs,在近红外激发下产生细胞毒性单线态氧,破坏细胞膜并增强其对同时释放的靶向细胞 DNA 降解的 DOX 的通透性,从而通过协同的细胞内外顺序损伤实现高效的肿瘤杀伤作用。