Departament de Farmacologia, Toxicologia i Química Terapèutica, Universitat de Barcelona, Avda. Joan XXIII 27-31, 08028 Barcelona, Spain; Institut de Nanociència i Nanotecnologia UB (IN2UB), Universitat de Barcelona, Avda. Joan XXIII 27-31, 08028 Barcelona, Spain.
Departament de Biologia Cel·lular, Fisiologia i Immunologia, Universitat Autònoma de Barcelona, Spain.
Colloids Surf B Biointerfaces. 2017 Oct 1;158:602-609. doi: 10.1016/j.colsurfb.2017.07.033. Epub 2017 Jul 18.
Zn-containing porphyrins are intensely investigated for their ability to form reactive oxygen species and thereby being potent photosensitizers for use in photodynamic therapy (PDT). Some of the drawbacks of the PDT approach, such as unspecific distribution, could be addressed by means of photosensitizer drug delivery systems. In this work, we synthesize and characterize new water-soluble gold nanoparticles (GNP) stabilized by a mixture of a polyethyleneglycol-containing thiol (to improve water solubility) and a new amphiphilic gemini-type pyridinium salt, which also acts as promotor of the incorporation of the anionic photosensitizer Na-ZnTCPP into the GNP. The obtained GNP have sizes between 7 and 10nm, as observed by Transmission Electron Microscopy. The incorporation of the photosensitizer caused an increase in the hydrodynamic size, detected by Dynamic Light Scattering, as well as a shift in the Surface Plasmon Resonance peak on the GNP UV-vis absorption spectra. The presence of the photosensitizer in the GNP was corroborated using Fluorescence Spectroscopy. The amount of Na-ZnTCPP was found to be 327 molecules per GNP. The porphyrin-containing Na-ZnTCPP-1·GNP showed good enhanced ability to produce singlet oxygen, compared to free Na-ZnTCPP. Their cytotoxicity and phototoxicity were investigated in vitro using two different human breast cell lines, one of tumoral origin (SKBR-3) and another of normal epithelium origin (MCF-10A). SKBR-3 cells showed higher sensitivity to Na-ZnTCCP and Na-ZnTCPP-1·GNP in dark conditions. After irradiation, no significant differences were observed between both cell lines except for 1μM Na-ZnTCCP-1·GNP where SKBR-3 cells were also more sensitive.
含锌卟啉因其能够形成活性氧物种而被强烈研究,从而成为光动力疗法 (PDT) 的有效光敏剂。 PDT 方法的一些缺点,如非特异性分布,可以通过光敏剂药物传递系统来解决。在这项工作中,我们合成并表征了新的水溶性金纳米粒子 (GNP),由含有巯基的聚乙二醇混合物(以提高水溶性)和新的两亲性Gemini 型吡啶盐稳定,后者还可以促进阴离子光敏剂 Na-ZnTCPP 掺入 GNP。通过透射电子显微镜观察到,所得 GNP 的尺寸在 7 到 10nm 之间。通过动态光散射检测到,光敏剂的掺入导致水动力尺寸增加,并且在 GNP 的紫外可见吸收光谱中的表面等离子体共振峰发生位移。荧光光谱证实了 GNP 中存在光敏剂。发现每个 GNP 中含有 327 个 Na-ZnTCPP 分子。与游离的 Na-ZnTCPP 相比,含卟啉的 Na-ZnTCPP-1·GNP 显示出更好的增强产生单线态氧的能力。在体外使用两种不同的人乳腺细胞系,一种是肿瘤来源的 (SKBR-3),另一种是正常上皮来源的 (MCF-10A),研究了它们的细胞毒性和光毒性。在黑暗条件下,SKBR-3 细胞对 Na-ZnTCCP 和 Na-ZnTCPP-1·GNP 的敏感性更高。照射后,除了 1μM Na-ZnTCCP-1·GNP 外,两种细胞系之间没有观察到显著差异,而 SKBR-3 细胞对其更为敏感。