首页> 外文期刊>The international journal of artificial organs >Photodynamic action of Tri-meso (N-methyl-pyridyl), meso (N-tetradecyl-pyridyl) porphine on Staphylococcus epidermidis biofilms grown on Ti6Al4V alloy.
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Photodynamic action of Tri-meso (N-methyl-pyridyl), meso (N-tetradecyl-pyridyl) porphine on Staphylococcus epidermidis biofilms grown on Ti6Al4V alloy.

机译:三内消旋(N-甲基-吡啶基),内消旋(N-十四烷基-吡啶基)卟啉对在Ti6Al4V合金上生长的表皮葡萄球菌生物膜的光动力作用。

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Staphylococcus epidermidis is a leading cause of nosocomial infections, and its virulence is attributable to formation of biofilm, especially on implanted devices. Photodynamic treatment (PDT) has been actively investigated for the eradication of bacterial biofilm growing on dental plaques and oral implants. In this study, we used Tri-meso (N-methyl-pyridyl), meso (N-tetradecyl-pyridyl) porphine (C14) for inactivation of two structurally distinct S. epidermidis biofilms grown on Ti6Al4V alloy and compared its photosensitizing efficiency with that of the parent molecule, tetra-substituted N-methyl-pyridyl-porphine (C1). A more significant reduction in bacterial survival was observed when both bacterial biofilms were exposed to a lower dose of C14, and simultaneously to visible light in comparison with C1. The different responses of both staphylococcal biofilms to C1- or C14-treatment appeared to depend on photosensitizer endocellular concentration. C14 bound to both biofilms to a greater extent than C1. Moreover, C14 penetrates deeper into the bacterial membranes, as determined by fluorescence quenching experiments with methylviologen, allowing for better bacterial killing photoefficiency. Confocal laser scanning microscope (CLSM) analysis indicated damage to bacterial cell membranes in both photodynamically treated biofilms, while disruption of PDT-treated biofilm was confirmed by scanning electron microscopy (SEM). In summary, C14 may be a potential photosensitizer for the inactivation of staphylococcal biofilms for many device-related infections which are accessible to visible light.
机译:表皮葡萄球菌是医院感染的主要原因,其毒力可归因于生物膜的形成,尤其是在植入设备上。为了消除在牙菌斑和口腔植入物上生长的细菌生物膜,光动力治疗(PDT)已被积极研究。在这项研究中,我们使用Tri-meso(N-甲基-吡啶基),meso(N-十四烷基-吡啶基)卟啉(C14)灭活了在Ti6Al4V合金上生长的两种结构不同的表皮葡萄球菌生物膜,并将其光敏效率与母体分子中的四取代的N-甲基-吡啶基-卟啉(C1)。与C1相比,当两个细菌生物膜都暴露于较低剂量的C14并同时暴露于可见光时,观察到细菌存活率的下降更为显着。两种葡萄球菌生物膜对C1或C14处理的不同反应似乎取决于光敏剂的细胞内浓度。 C14与C1的结合程度更大。而且,通过用甲基紫精进行荧光猝灭实验确定,C14可以更深地渗透到细菌膜中,从而可以更好地杀死细菌。共聚焦激光扫描显微镜(CLSM)分析表明,两种光动力处理过的生物膜均对细菌细胞膜造成了损害,而PDT处理过的生物膜的破坏则由扫描电子显微镜(SEM)证实。总之,对于可见光可及的许多与设备有关的感染,C14可能是用于灭活葡萄球菌生物膜的潜在光敏剂。

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