Bravo Angélica R, Fuentealba Felipe Alejandro, González Iván A, Palavecino Christian Erick
Laboratorio de Microbiología Celular, Centro de Ciencias Médicas aplicadas, Facultad de Medicina y Ciencias de la Salud, Universidad Central de Chile, Lord Cochrane 418, Santiago 8330546, Chile.
Departamento de Química, Facultad de Ciencias Naturales, Matemáticas y del Medio Ambiente, Universidad Tecnológica Metropolitana, Las Palmeras 3360, Ñuñoa, Santiago 7800003, Chile.
Pharmaceutics. 2024 Dec 23;16(12):1626. doi: 10.3390/pharmaceutics16121626.
is a Gram-negative bacillus responsible for a wide variety of potentially fatal infections and, in turn, constitutes a critical agent of healthcare-associated infections. Moreover, is characterized by multi-drug-resistant (MDR) bacteria, such as extended-spectrum beta-lactamases (ESBL) and carbapenemase (KPC) producer strains, representing a significant health problem. Because resistances make it difficult to eradicate using antibiotics, antimicrobial photodynamic therapy (aPDT) promises to be a favorable approach to complementing conventional therapy against MDR bacteria. This study aims to provide relevant bibliographic information on the state of the art of application of aPDT against and MDR . Our methodology follows a protocol using the PRISMA extension for scoping reviews (PRISMA-ScR) guidelines, and the search consults the PubMed (MESH), Google Scholar, and Scopus databases from January 2012 to September 2024. The eligibility criteria were (1) original articles after 2012 referring to antimicrobial photodynamic activity in in vitro and in vivo: clinical applications and synergism with antibiotics, other antimicrobial drugs, or PS coupled to other particles, (2) articles in English, and (3) articles peer-reviewed. Results. Following two independent searches in databases, 298 records were found. After applying eligibility criteria and various filters, such as removing duplicates, 25 studies were included in this review. The evidence demonstrates the effectiveness of aPDT in vitro in eradicating sensitive or MDR- strains, including strains producing biofilms, ESBL, and KPC. Finally, it is concluded that aPDT is a recommended antimicrobial therapy, but more research in vivo is needed to support studies in humans.
是一种革兰氏阴性杆菌,可导致多种潜在致命感染,进而构成医疗保健相关感染的关键病原体。此外,其特征是具有多重耐药(MDR)细菌,例如超广谱β-内酰胺酶(ESBL)和碳青霉烯酶(KPC)产生菌株,这是一个重大的健康问题。由于耐药性使得使用抗生素难以根除,抗菌光动力疗法(aPDT)有望成为补充针对MDR细菌的传统疗法的有利方法。本研究旨在提供有关aPDT针对和MDR应用的最新技术状态的相关文献信息。我们的方法遵循使用PRISMA扩展进行范围综述(PRISMA-ScR)指南的方案,搜索查询了2012年1月至2024年9月的PubMed(MESH)、谷歌学术和Scopus数据库。纳入标准为:(1)2012年后的原创文章,涉及体外和体内的抗菌光动力活性:临床应用以及与抗生素、其他抗菌药物或与其他颗粒偶联的光敏剂的协同作用;(2)英文文章;(3)经过同行评审的文章。结果。在数据库中进行两次独立搜索后,共找到298条记录。应用纳入标准和各种筛选条件,如去除重复项后,本综述纳入了25项研究。证据表明aPDT在体外根除敏感或MDR菌株(包括产生生物膜、ESBL和KPC的菌株)方面有效。最后得出结论,aPDT是一种推荐的抗菌疗法,但需要更多的体内研究来支持人体研究。