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体外和体内展示超高效广谱抗菌剂用于光动力抗菌化疗。

In Vitro and In Vivo Demonstration of Ultraefficient and Broad-Spectrum Antibacterial Agents for Photodynamic Antibacterial Chemotherapy.

机构信息

School of Pharmaceutical Sciences (Shenzhen), Sun Yat-Sen University, Shenzhen 518107, P. R. China.

School of Chinese Medicine, The Chinese University of Hong Kong, Hong Kong, China.

出版信息

ACS Appl Mater Interfaces. 2021 Mar 17;13(10):11588-11596. doi: 10.1021/acsami.0c20837. Epub 2021 Mar 3.

Abstract

Increasing threats from both pathogenic infections and antibiotic resistance highlight the pressing demand for nonantibiotic agents and alternative therapies. Herein, we report several new phenothiazinium-based derivatives, which could be readily synthesized via fragment-based assembly, which exhibited remarkable bactericidal activities both in vitro and in vivo. Importantly, in contrast to numerous clinically and preclinically used antibacterial photosensitizers, these compounds were able to eliminate various types of microorganisms, including Gram-(+) (), Gram-(-) , multidrug-resistant , and their associated biofilms, at low drug and light dosages (e.g., 0.21 ng/mL in vitro and 1.63 ng/cm in vivo to eradicate at 30 J/cm). This study thus unveils the potential of these novel phenothiaziniums as potent antimicrobial agents for highly efficient photodynamic antibacterial chemotherapy.

摘要

越来越多的致病感染和抗生素耐药性的威胁凸显了对抗生素替代品和替代疗法的迫切需求。在此,我们报告了几种新的吩噻嗪基衍生物,这些化合物可以通过基于片段的组装方法很容易地合成,在体外和体内都表现出显著的杀菌活性。重要的是,与许多临床和临床前使用的抗菌光敏剂不同,这些化合物能够在低药物和光照剂量下消除各种类型的微生物,包括革兰氏阳性菌()、革兰氏阴性菌、多药耐药菌及其相关生物膜,例如,在体外低至 0.21 ng/mL 和体内低至 1.63 ng/cm 时就可以消除 30 J/cm 光照下的 。因此,这项研究揭示了这些新型吩噻嗪作为高效光动力抗菌化疗的潜在强效抗菌剂的潜力。

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