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DOI 10.1021/acsabm.4c01049

Медицинская библиотека · ACS applied bio materials · 2024

Photoinactivation of Multidrug-Resistant mcr-1-Positive E. coli Using PCPDTBT Conjugated Polymer Nanoparticles under White Light.

Caires Cynthia S A, Lima Thalita H N, Nascimento Rafael C, Araujo Leandro O, Aguilera Laís F, Caires Anderson R L, Oliveira Samuel L

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

The issue of antimicrobial resistance is an escalating concern within the scope of global health. It is predicted that the existence of antibiotic-resistant bacteria might result in an estimated annual death of up to 10 million by 2050, along with possible economic losses ranging from 100 to 210 trillion. This study reports the production of poly[2,6-(4,4-bis(2-ethylhexyl)-4H-cyclopenta[2,1-b;3,4-b']dithiophene)-alt-4,7(2,1,3-benzothiadiazole)] nanoparticles (PCPDTBT-NPs) by nanoprecipitation as an alternative to tackle this problem. The size, shape, and optical features of these conjugated polymer NPs were analyzed. Their efficacy as photosensitizers against nonresistant (ATCC) and multidrug-resistant mcr-1-positive Escherichia coli was assessed under white light doses of 250 and 375 J·cm-2. PCPDTBT-NPs inactivated both E. coli strains exposed to white light at an intensity of 375 J·cm-2, while no antimicrobial effect was observed in the group not exposed to white light. Reactive oxygen species and singlet oxygen were detected using DCFH-DA and DPBF probes, allowing the investigation of the photoinactivation pathways. This work showcases PCPDTBT-NPs as photosensitizers to eliminate multidrug-resistant bacteria through photodynamic inactivation employing visible light.

Для цитирования: Caires Cynthia S A, Lima Thalita H N, Nascimento Rafael C, Araujo Leandro O, Aguilera Laís F, Caires Anderson R L, Oliveira Samuel L. Photoinactivation of Multidrug-Resistant mcr-1-Positive E. coli Using PCPDTBT Conjugated Polymer Nanoparticles under White Light.. ACS applied bio materials. 2024. DOI: 10.1021/acsabm.4c01049.

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