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Evaluation of the efficacy of photodynamic antimicrobial therapy using a phenothiazine compound and Laser (λ=660ηm) on the interface: macrophage vs S. aureus

机译:使用吩噻嗪化合物和激光(λ= 660mm)在界面上评价光动力抗微生物治疗的功效:巨噬细胞Vs Aureus

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Nowadays photodynamic inactivation has been proposed as an alternative treatment for localized bacterial infections as a response to the problem of antibiotic resistance. Much is already known about the photodynamic inactivation of microorganisms: both antibiotic-sensitive and -resistant strains can be successfully photoinactivated and there is the additional advantage that repeated photosensitization of bacterial cells does not induce a selection of resistant strains. Staphylococcus spp. are opportunistic microorganisms known for their capacity to develop resistance against antimicrobial agents. The emergence of resistant strains of bacteria such as methicillui-resistant Staphylococcus aureus (MRSA) poses a major challenge to healthcare. MRSA is a major cause of hospital-acquired infection throughout the world and is now also prevalent in the community as well as nursing and residential homes. The aim of this study was to evaluate the phagocytic function of macrophages J774 against S. aureus in the presence and absence of AmPDT with phenothiazine compound (12.5 μg/mL) and low level laser (λ=660nm, 12 J/cm~2). Experimental groups: Control group (L-P-), Phenothiazine group (L-P+) Laser group (L+P-), AmPDT group (L+P+).The tests presented in this study were performed in triplicate. This study showed that AmPDT induced bacterial death in about 80% as well as increasing phagocytic capacity of macrophages by approximately 20% and enhanced the antimicrobial activity by approximately 50% compared to the control group and enabling more intense oxidative burst.
机译:现今的光动力失活已被提出作为一种替代治疗用于局部细菌感染,以抗生素抗性的问题的响应。多少是已知的关于微生物的光动力失活:两个抗生素敏感性和抗性菌株可以成功photoinactivated并有附加的优点:细菌细胞的重复光敏不诱导选择抗性菌株。葡萄球菌SPP。因它们开发针对抗菌药物耐药能力称为机会主义的微生物。细菌的耐药菌株,如耐methicillui金黄色葡萄球菌(MRSA)的出现,成为医疗保健的一大挑战。 MRSA是医院获得性感染的主要原因在世界各地,现在也盛行于社会,以及护理安老院。本研究的目的是评估在对存在和不存在AmPDT与吩噻嗪化合物(12.5微克/毫升)和低强度激光的金黄色葡萄球菌的巨噬细胞J774的吞噬功能(λ= 660nm的,12J /厘米〜2) 。实验组:对照组(L-P-),吩噻嗪基(L-P +)激光组(L + P-),AmPDT基团(L + P +)在本研究中测试一式三份进行。这项研究表明,AmPDT相比于对照组和使更多的激烈氧化突发诱导约80%的细菌死亡,以及大约20%的巨噬细胞增加的吞噬能力和增强的抗微生物活性约50%。

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