State Key Laboratory of Chemo/Bio-Sensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, China.
Tumor Hospital, Xiangya School of Medicine, Central South University, Changsha 410013, China.
ACS Appl Bio Mater. 2021 Jul 19;4(7):5566-5574. doi: 10.1021/acsabm.1c00298. Epub 2021 Jun 17.
As an efficient, noninvasive, and high spatiotemporal resolved approach, photodynamic therapy (PDT) has high therapeutic potential for cancer treatment, whereas its development still faces a number of challenges, such as the lack of efficient and stable photosensitizers (PSs) and the inadequate ability of PSs to accumulate at tumor sites and target responses. Herein, a pH-responsive calcium carbonate (CaCO)-mineralized AIEgen nanoprobe was prepared by using bovine serum albumin as the skeleton and loaded with a mitochondria-specific aggregation-induced emission (AIE)-active PS of 1-methyl-4-(4-(1,2,2-triphenylvinyl)styryl)quinolinium iodide (TPE-Qu), which exhibits superior singlet oxygen (O)-generation ability and meanwhile possesses a bright near-infrared fluorescence emission. The biomineralized nanoparticles have small sizes (100 ± 10 nm) with good water dispersion and stability. With an increase in acidity (pH = 7.4-5.0), the internal TPE-Qu molecules are released gradually and accumulated in the mitochondria due to their hydrophobicity and electropositivity and then generate fluorescence emission and PDT under an external light source. Tumor inhibition and low acute toxicity were further successfully confirmed by the intracellular uptake test and 4T1-tumor-bearing mouse model.
作为一种高效、无创且具有高时空分辨率的方法,光动力疗法(PDT)在癌症治疗方面具有很大的治疗潜力,但其发展仍然面临许多挑战,例如缺乏高效稳定的光敏剂(PS)以及 PS 在肿瘤部位积累和靶向反应的能力不足。在此,我们制备了一种 pH 响应的碳酸钙(CaCO)矿化 AIEgen 纳米探针,该探针以牛血清白蛋白为骨架,负载线粒体特异性聚集诱导发射(AIE)活性 PS,即 1-甲基-4-(4-(1,2,2-三苯基乙烯基)-苯乙烯基)-喹啉鎓碘化物(TPE-Qu),其具有优异的单线态氧(O)生成能力,同时具有明亮的近红外荧光发射。生物矿化纳米颗粒具有较小的尺寸(100±10nm),具有良好的水分散性和稳定性。随着酸度的增加(pH=7.4-5.0),内部的 TPE-Qu 分子由于其疏水性和正电性而逐渐释放并积累在线粒体中,然后在外光源下产生荧光发射和 PDT。通过细胞内摄取试验和 4T1 荷瘤小鼠模型进一步成功证实了肿瘤抑制和低急性毒性。