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Lipid Membrane Adsorption Determines Photodynamic Efficiency of β-Imidazolyl-Substituted Porphyrins

机译:脂质膜吸附决定了β-咪唑基取代卟啉的光动力学效率

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摘要

Photosensitizers (PSs) represent a group of molecules capable of generating reactive oxygen species (ROS), such as singlet oxygen (SO); thus, they are considered to be promising agents for anti-cancer therapy. The enhancement of the photodynamic efficiency of these compounds requires increasing the PS activity in the cancer cell milieu and exactly at the target cells. In the present work, we report the synthesis, lipid membrane binding and photodynamic activity of three novel cationic PSs based on β-imidazolyl-substituted porphyrin and its Zn(II) and In(III) complexes (1H2, 1Zn and 1In). Comparison of the behavior of the investigated porphyrins at the bilayer lipid membrane (BLM) demonstrated the highest adsorption for the 1In complex and the lowest one for 1Zn. The photodynamic efficiency of these porphyrins was evaluated by determining the oxidation rate of the styryl dye, di-4-ANEPPS, incorporated into the lipid membrane. These rates were proportional to the surface density (SD) of the porphyrin molecules at the BLM and were roughly the same for all three porphyrins. This indicates that the adsorption of these porphyrins at the BLM determines their photodynamic efficiency rather than the extinction or quantum yield of singlet oxygen.
机译:光敏剂(PSs)代表一组能够产生活性氧(ROS)的分子,例如单线态氧(SO);因此,它们被认为是抗癌治疗的有前途的药物。这些化合物的光动力效率的提高要求增加癌细胞环境中以及确切地靶细胞处的PS活性。在本工作中,我们报告了三种新型的基于β-咪唑基取代的卟啉及其Zn(II)和In(III)配合物(1H2、1Zn和1In)的阳离子PS的合成,脂质膜结合和光动力活性。比较研究的卟啉在双层脂质膜(BLM)上的行为,结果表明1In复合物的吸附最高,而1Zn的最低。这些卟啉的光动力效率是通过确定脂质膜中苯乙烯基染料di-4-ANEPPS的氧化速率来评估的。这些比率与BLM上卟啉分子的表面密度(SD)成正比,并且对于所有三种卟啉都大致相同。这表明这些卟啉在BLM上的吸附决定了其光动力效率,而不是单线态氧的消光或量子产率。

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