Maisch T, Bosl C, Szeimies R-M, Love B, Abels C
Department of Dermatology, University of Regensburg, Klinik und Poliklinik für Dermatologie, Franz-Josef-Strauss-Allee 11, 93053, Regensburg, Germany.
Photochem Photobiol Sci. 2007 May;6(5):545-51. doi: 10.1039/b614770d. Epub 2007 Feb 23.
Following extensive in vitro screening of new photosensitizers the purpose of the present study was to examine penetration as well as antibacterial efficacy of a lead photosensitizer against MRSA using an ex vivo porcine skin model. Two different applications were performed: (i) preincubation of bacteria in solution with a porphyrin-based photosensitizer XF73 and subsequent application on the ex vivo porcine skin; (ii) application of pure bacteria on the explants followed by an incubation with XF73 in a water-ethanol formulation for up to 60 min under occlusion. The localisation of XF73 was restricted to the stratum corneum. Different concentrations (0-10 microM) of XF73 and different incubation times (5-60 min) were used to determine phototoxicity against methicillin-resistant and methicillin-sensitive S. aureus, which was applied on the explants. Preincubation of S. aureus with 0.1 microM XF73 in solution prior to the application of these XF73-incubated bacteria on the skin demonstrates a higher efficacy (>3 log10) after irradiation. Antibacterial photodynamic inactivation resulted in a approximately 1 log10 (0.1 microM)-3.64+/-0.035 (10 microM) log10 growth reduction independently of the antibiotic resistance pattern of used S. aureus strains. Irradiation of applied bacteria without photosensitizer incubation did not show any marked decrease (<1 log10) of bacteria cell number, indicating a significant phototoxicity of the XF73. Histological evaluations of untreated and treated skin areas upon irradiation within 24 h showed no significant degree of necrosis or apoptosis determined by TUNEL-assay indicating that the porcine skin is still vital. This study demonstrates that this XF73 porphyrin-based photosensitizer had concentration-dependent differences in killing efficacy of MRSA in comparison to skin cells using an ex vivo porcine skin model. The results described here imply that topical delivery of XF73 may be considered as a possible treatment in patients with superficial infections of the skin.
在对新型光敏剂进行广泛的体外筛选之后,本研究的目的是使用离体猪皮肤模型,研究一种先导光敏剂对耐甲氧西林金黄色葡萄球菌(MRSA)的渗透作用以及抗菌效果。进行了两种不同的应用方式:(i)将基于卟啉的光敏剂XF73与细菌在溶液中预孵育,随后应用于离体猪皮肤上;(ii)将纯细菌应用于外植体上,然后在封闭条件下,用XF73的水 - 乙醇制剂孵育长达60分钟。XF73的定位局限于角质层。使用不同浓度(0 - 10 microM)的XF73和不同孵育时间(5 - 60分钟)来确定对应用于外植体的耐甲氧西林和甲氧西林敏感金黄色葡萄球菌的光毒性。在将用0.1 microM XF73在溶液中预孵育过的金黄色葡萄球菌应用于皮肤之前,对这些经XF73孵育的细菌进行照射后显示出更高的效力(> 3 log10)。抗菌光动力灭活导致细菌生长减少约1 log10(0.1 microM) - 3.64±0.035(10 microM)log10,这与所用金黄色葡萄球菌菌株的抗生素耐药模式无关。对未用光敏剂孵育而直接照射的细菌进行照射后,细菌细胞数量没有明显减少(<1 log10),这表明XF73具有显著的光毒性。在24小时内对未处理和处理过的皮肤区域进行照射后的组织学评估显示,通过TUNEL检测确定没有明显程度的坏死或凋亡,表明猪皮肤仍然具有活力。本研究表明,使用离体猪皮肤模型,与皮肤细胞相比,这种基于XF73卟啉的光敏剂在杀灭MRSA方面具有浓度依赖性差异。此处描述的结果表明,XF73的局部递送可能被认为是皮肤浅表感染患者的一种可能治疗方法。