光敏剂
膜
部分
化学
单线态氧
光动力疗法
卟啉
分子
脂质体
自由基
组合化学
光化学
生物物理学
立体化学
有机化学
生物化学
氧气
盐(化学)
生物
作者
Daria A. Polivanovskaia,Anna N. Konstantinova,Kirill P. Birin,Valerij S. Sokolov,Oleg V. Batishchev,Yulia G. Gorbunova
出处
期刊:Membranes
[MDPI AG]
日期:2022-08-30
卷期号:12 (9): 846-846
标识
DOI:10.3390/membranes12090846
摘要
Photodynamic therapy (PDT) is a widely used technique for skin cancer treatment and antimicrobial therapy. An improvement in PDT efficiency requires not only an increase in quantum yield of photosensitizer (PS) molecules but also their applicability for biological systems. Recently, we demonstrated that the activity of porphyrin-based PSs in the lipid membrane environment depends on the nature of the cation in the macrocycle due to its interactions with the lipid phosphate moiety, as well as the orientation of the PS molecules inside the membrane. Here, we report the synthesis, membrane binding properties and photodynamic efficiency of novel dicationic free-base, Ni(II) and Zn(II) pyrazinoporphyrins with terminal tetraalkylammonium units (2H-1, Ni-1 and Zn-1), to show the possibility to enhance the membrane binding of PS molecules, regardless of the central cation. All of these substances adsorb at the lipid membrane, while free-base and Zn(II) porphyrins actively generate singlet oxygen (SO) in the membranes. Thus, this study reveals a new way to tune the PDT activity of PSs in biological membranes through designing the structure of the peripheral groups in the macrocyclic photosensitizer.
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