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首页> 外文期刊>Frontiers in Microbiology >Murine Model Imitating Chronic Wound Infections for Evaluation of Antimicrobial Photodynamic Therapy Efficacy
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Murine Model Imitating Chronic Wound Infections for Evaluation of Antimicrobial Photodynamic Therapy Efficacy

机译:模仿慢性伤口感染的鼠模型用于评估抗菌光动力疗法的疗效

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It is generally acknowledged that the age of antibiotics could come to an end, due to their widespread, and inappropriate use. Particularly for chronic wounds alternatives are being thought. Antimicrobial Photodynamic Therapy (APDT) is a potential candidate, and while approved for some indications, such as periodontitis, chronic sinusitis and other niche indications, its use in chronic wounds is not established. To further facilitate the development of APDT in chronic wounds we present an easy to use animal model exhibiting the key hallmarks of chronic wounds, based on full-thickness skin wounds paired with an optically transparent cover. The moisture-retaining wound exhibited rapid expansion of pathogen colonies up to 8 days while not jeopardizing the host survival. Use of two bioluminescent pathogens; methicillin resistant Staphylococcus aureus (MRSA) and Pseudomonas aeruginosa permits real time monitoring of the pathogens. The murine model was employed to evaluate the performance of four different photosensitizers as mediators in Photodynamic Therapy. While all four photosensitizers, Rose Bengal, porphyrin TMPyP, New Methylene Blue, and TLD1411 demonstrated good to excellent antimicrobial efficacy in planktonic solutions at 1 to 50 μM concentrations, whereas in in vivo the growth delay was limited with 24–48 h delay in pathogen expansion for MRSA, and we noticed longer growth suppression of P. aeruginosa with TLD1411 mediated Photodynamic Therapy. The murine model will enable developing new strategies for enhancement of APDT for chronic wound infections.
机译:人们普遍认为,由于抗生素的广泛使用和不当使用,抗生素的时代可能会终结。特别是对于慢性伤口,正在考虑替代方案。抗菌光动力疗法(APDT)是一种潜在的候选药物,虽然已批准用于某些适应症,例如牙周炎,慢性鼻窦炎和其他利基适应症,但尚未确定在慢性伤口中的使用。为了进一步促进APDT在慢性伤口中的发展,我们提出了一种易于使用的动物模型,该模型基于全厚度皮肤伤口与光学透明的覆盖物相结合,展现出慢性伤口的关键特征。保持水分的伤口在不损害宿主存活的情况下表现出高达8天的病原菌集快速扩增。使用两种生物发光病原体;耐甲氧西林的金黄色葡萄球菌(MRSA)和铜绿假单胞菌可实时监控病原体。鼠模型被用来评估四种不同的光敏剂在光动力疗法中作为介质的性能。尽管所有四种光敏剂(玫瑰红,卟啉TMPyP,新亚甲基蓝和TLD1411)在1至50μM浓度的浮游溶液中均表现出良好的抗菌性能,但在体内,其生长延迟受到病原体延迟24–48 h的限制MRSA的扩增,我们注意到TLD1411介导的光动力疗法对铜绿假单胞菌的生长抑制作用更长。鼠模型将有助于开发新的策略来增强针对慢性伤口感染的APDT。

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