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聚(3-羟基丁酸酯)纳米颗粒中游离和包封的酞菁铟(III)对细菌和生物分子的光动力灭活作用:香豆素基团位置的影响

Photodynamic Inactivation of and Biomolecules by Free and Encapsulated Indium(III) Phthalocyanines in PHB Nanoparticles: The Influence of the Position of the Coumarin Group.

作者信息

Ferreira Julyana Noval de Souza, Figueiredo Barbara Silva, Vasconcelos Vannyla Viktória Viana, de Abreu Antony Luca Luna Vieira, Ribeiro Sheila Souza da Silva, Kaya Esra Nur, Bulut Mustafa, Ribeiro Joselito Nardy, Durmuş Mahmut, Romero da Silva André

机构信息

Graduate Program in Biochemistry and Pharmacology, Federal University of Espírito Santo, Campus Maruípe, 29047-105 Vitória, Espírito Santo, Brazil.

Federal Institute of Education, Science and Technology of Espírito Santo, Campus Vitória, 29040-780 Vitória, Espírito Santo, Brazil.

出版信息

Biomacromolecules. 2025 Apr 14;26(4):2076-2094. doi: 10.1021/acs.biomac.4c00862. Epub 2025 Mar 31.

Abstract

Antimicrobial photodynamic therapy (APDT) is a promising alternative to inactivating resistant microorganisms. Metallic phthalocyanines (Pc) substituted with coumarin groups exhibit favorable photophysical properties for APDT; however, their hydrophobicity limits administration. This study investigates indium(III) Pc substituted with 7-oxy-3-(3',4',5'-trimethoxyphenyl)coumarin at nonperipheral () and peripheral () positions, both in their free form and encapsulated in polyhydroxybutyrate nanoparticles, for the photodynamic inactivation of methicillin-resistant (MRSA) and methicillin-susceptible (MSSA) bacteria. The photodynamic activity was also assessed through the photooxidation of tryptophan and bovine serum albumin. Theoretical calculations and molecular docking were performed to corroborate the experimental results, investigating the influence of molecular structure on the photodynamic and antimicrobial performance of Pc-loaded nanoparticles as well as their nanoparticulate properties. Overall, both free and encapsulated Pc were capable of photooxidizing biomolecules and exhibited moderate antimicrobial activity, with demonstrating superior efficacy, achieving an average reduction of 2 logs (99%) in MSSA and MRSA colonies.

摘要

抗菌光动力疗法(APDT)是一种使耐药微生物失活的有前景的替代方法。被香豆素基团取代的金属酞菁(Pc)对APDT表现出良好的光物理性质;然而,它们的疏水性限制了给药。本研究调查了在非周边()和周边()位置被7-氧基-3-(3',4',5'-三甲氧基苯基)香豆素取代的铟(III)酞菁,以游离形式以及封装在聚羟基丁酸酯纳米颗粒中的形式,用于耐甲氧西林金黄色葡萄球菌(MRSA)和甲氧西林敏感金黄色葡萄球菌(MSSA)的光动力灭活。还通过色氨酸和牛血清白蛋白的光氧化来评估光动力活性。进行了理论计算和分子对接以证实实验结果,研究分子结构对负载Pc的纳米颗粒的光动力和抗菌性能及其纳米颗粒性质的影响。总体而言,游离和封装的Pc都能够光氧化生物分子并表现出适度的抗菌活性,其中显示出优异的效果,使MSSA和MRSA菌落平均减少2个对数(99%)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03d8/12004533/22dff6c5be4f/bm4c00862_0001.jpg

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