感染控制中的协同模式:光动力治疗作为抗生素辅助策略的综述。

IF 3.8 2区 医学 Q2 CHEMISTRY, MEDICINAL
Jennifer Machado Soares, Thaila Quatrini Corrêa, Claudia Patricia Barrera Patiño, Isabella Salgado Gonçalves, Gabriel Grube Dos Santos, Gabriela Gomes Guimarães, Rebeca Vieira de Lima, Thalita Hellen Nunes Lima, Bruna Carolina Corrêa, Taina Cruz de Souza Cappellini, Maria Vitória Silva Pereira, Anna Luiza França de Oliveira Resende, Vladislav V Yakovlev, Kate Cristina Blanco, Vanderlei Salvador Bagnato
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引用次数: 0

摘要

抗菌素耐药性的威胁日益增加,需要开发新的策略来提高现有抗生素的疗效。本文综述了抗菌光动力疗法(aPDT)作为抗生素治疗辅助手段的潜力。系统检索了各大科学数据库的文献,重点检索了近十年来发表的关于aPDT与抗生素协同作用的研究。选取的文章根据其实验方法、细菌靶点、光动力学参数和报道的治疗结果进行分析。aPDT通过产生活性氧(ROS)、增强抗生素敏感性和减少所需剂量诱导细菌细胞损伤。此外,综述强调了优化治疗参数和抗生素联合策略以最大化治疗效果的有前途的研究。尽管aPDT具有潜力,但在治疗标准化、细菌反应的可变性和临床实施方面仍面临障碍。这些挑战需要标准化的方案、进一步的体内研究和监管进展,以将aPDT整合到主流抗菌治疗中。结论:aPDT与抗生素的协同作用为细菌感染的控制提供了一种更安全、更有效、耐药减轻的策略,是一个有前景的前沿。未来的研究应侧重于完善治疗参数,评估长期临床影响,并促进aPDT作为一种补充抗菌方法的广泛采用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synergistic Paradigms in Infection Control: A Review on Photodynamic Therapy as an Adjunctive Strategy to Antibiotics.

The increasing threat of antimicrobial resistance necessitates developing novel strategies to enhance the efficacy of existing antibiotics. This review explores the potential of antimicrobial photodynamic therapy (aPDT) as an adjunctive approach to antibiotic therapy. A systematic literature search was conducted in major scientific databases, focusing on studies published in the past decade investigating the synergistic effects of aPDT with antibiotics. Selected articles were analyzed based on their experimental approaches, bacterial targets, photodynamic parameters, and reported treatment outcomes. aPDT induces bacterial cell damage by generating reactive oxygen species (ROS), enhancing antibiotic susceptibility, and reducing required dosages. Furthermore, the review highlights promising research on optimizing treatment parameters and antibiotic combination strategies to maximize therapeutic outcomes. Despite its potential, aPDT faces obstacles to treatment standardization, variability in bacterial responses, and clinical implementation hurdles. These challenges require standardized protocols, further in vivo studies, and regulatory advancements to integrate aPDT into mainstream antimicrobial therapy. Conclusion: The synergy between aPDT and antibiotics represents a promising frontier in infection control, offering a safer, more effective, and resistance-mitigating strategy for bacterial infections. Future research should focus on refining treatment parameters, assessing long-term clinical impacts, and facilitating the widespread adoption of aPDT as a complementary antimicrobial approach.

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来源期刊
ACS Infectious Diseases
ACS Infectious Diseases CHEMISTRY, MEDICINALINFECTIOUS DISEASES&nb-INFECTIOUS DISEASES
CiteScore
9.70
自引率
3.80%
发文量
213
期刊介绍: ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to: * Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials. * Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets. * Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance. * Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents. * Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota. * Small molecule vaccine adjuvants for infectious disease. * Viral and bacterial biochemistry and molecular biology.
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