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Lethal photosensitisation of bacteria using a tin chlorin e6-glutathione-gold nanoparticle conjugate

机译:锡二氢卟酚e6-谷胱甘肽-金纳米颗粒偶联物对细菌的致死性光敏作用

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摘要

Because of the increasing resistance of bacteria to antibiotics there is considerable interest in light-activated antimicrobial agents (LAAAs) as alternatives to antibiotics for treating localized infections. In this paper we report that covalently coupling the LAAA tin-chlorin e6 to a gold nanoparticle via glutathione results in a potent antimicrobial agent when activated by white light. On a molar basis, the tin chlorin e6-nanogold conjugate was a hundred times more effective at killing Staphylococcus aureus than free tin chlorin e6. The conjugate also displayed antibacterial activity against mcthicillin-resistant S. aureus and Streptococcus pyogenes. This potent new LAAA may be useful for the treatment of topical infections or could be incorporated into coatings that could be used to reduce the microbial load in sensitive environments such as hospitals and food processing facilities.
机译:由于细菌对抗生素的抵抗力不断增强,因此人们对光活化抗菌剂(LAAAs)产生了极大的兴趣,这些光敏抗菌剂可以替代抗生素来治疗局部感染。在本文中,我们报告说,当被白光激活时,通过谷胱甘肽将LAAA锡-二氢卟酚e6与金纳米颗粒共价偶联会产生有效的抗菌剂。以摩尔计,锡二氢卟酚e6-纳米金偶联物杀死金黄色葡萄球菌的效率是游离锡二氢卟酚e6的一百倍。该结合物还显示出对耐甲氧西林的金黄色葡萄球菌和化脓性链球菌的抗菌活性。这种有效的新型LAAA可用于治疗局部感染,或者可掺入可用于降低敏感环境(如医院和食品加工设施)中微生物负荷的涂层中。

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