Phthalocyanines Structure Versus Photodynamic Effectiveness towards Pathogenic Microorganisms: Our Recent Experience

Q3 Physics and Astronomy
V. Mantareva, I. Angelov, Meliha Syuleyman, V. Kussovski, I. Eneva, L. Avramov, E. Borisova
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引用次数: 2

Abstract

. The present review paper aims to summarize our recent experience in research and development of new phthalocyanine complexes and investigations of the main photophysical, photochemical and photobiological properties which are related to antimicrobial photodynamic therapy (aPDT) as alternative method for inactivation of the resistant pathogens. The effect of functionalization of Zn(II) phthalocyanine (ZnPc) with biologically-active natural substances such as amino acids, sugars and steroids was studied in comparison to the basic ZnPc ring molecule. The structural features of the substitution groups were chosen to facilitate the main properties responsible for PDT outcome. For example, the linkage groups of amino acids tyrosine, phenylalanine, lysine and arginine have positive charge in physiological media to the better attachment to bacterial wall and some of them have a good fluorescence for a contribution to the visualization of the infected area. Also, ZnPcs linked to sugars and steroids was expecting to possess receptor specific selectivity. The physicochemical properties of the novel functionalized ZnPcs are presented in respect to their efficiency for a number of pathogenic bacterial and fungal species. Additionally, the complexes of two heavy metal ions such as lutetium(III) (Lu(III)) and tin(IV) (Sn(IV)) were synthesized and evaluated for antimicrobial PDT. These complexes were designed with the same structural skeleton as our previous water-soluble methylpiridyloxy-substituted phthalocyanine complexes with zinc (II), silicon (IV), germanium (IV), indium (III) and gallium (III), all with relatively promising antibacterial efficiency. © 2021 Journal of Biomedical Photonics & Engineering.
酞菁结构对光动力对致病微生物的作用:我们最近的经验
本文旨在总结我们最近在新型酞菁配合物的研究和开发方面的经验,以及与抗微生物光动力疗法(aPDT)作为灭活耐药病原体的替代方法相关的主要光物理、光化学和光生物特性的研究。与碱性ZnPc环分子相比,研究了用生物活性天然物质如氨基酸、糖和类固醇对Zn(II)酞菁(ZnPc)的功能化作用。选择取代基团的结构特征是为了促进PDT结果的主要性质。例如,氨基酸酪氨酸、苯丙氨酸、赖氨酸和精氨酸的连接基团在生理介质中具有正电荷,以更好地附着在细菌壁上,其中一些具有良好的荧光,有助于感染区域的可视化。此外,与糖和类固醇连接的ZnPcs有望具有受体特异性选择性。介绍了新型功能化ZnPcs的物理化学性质及其对多种病原细菌和真菌的效率。此外,合成了两种重金属离子的络合物,如镥(III)(Lu(III))和锡(IV)(Sn(IV)),并对其抗微生物PDT进行了评价。这些配合物的结构骨架与我们以前的水溶性甲基铱氧基取代酞菁与锌(II)、硅(IV)、锗(IV),铟(III)和镓(III)的配合物相同,所有这些都具有相对有希望的抗菌效率。©2021生物医学光子与工程杂志。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Biomedical Photonics and Engineering
Journal of Biomedical Photonics and Engineering Physics and Astronomy-Acoustics and Ultrasonics
CiteScore
1.60
自引率
0.00%
发文量
17
审稿时长
8 weeks
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