UCL Division of Surgery and Interventional Science , University College London , Charles Bell House, 43-45 Foley Street , London W1W 7TS , U.K.
Materials Chemistry Research Centre, Department of Chemistry , University College London , 20 Gordon Street , London WC1H 0AJ , U.K.
ACS Appl Mater Interfaces. 2019 Apr 3;11(13):12367-12378. doi: 10.1021/acsami.9b02109. Epub 2019 Mar 21.
The rising incidence of antibiotic-resistant infections from contaminated surfaces in hospitals or implanted medical devices has led to increasing interest in new antibacterial surfaces. Photoactivatable surfaces that can generate cytotoxic reactive oxygen species under exposure to ambient light is a promising approach to inactivation of surface-borne microorganisms. There is growing interest in the use of quantum dots (QDs) as light-harvesting agents for photobactericidal applications, but the cadmium in commonly used QDs will restrict clinical application. Herein, the photobactericidal activity of novel polyurethane substrates containing cadmium-free QDs was tested against clinical multidrug-resistant Gram-positive and Gram-negative bacterial strains: methicillin-resistant Staphylococcus aureus (MRSA) and a carbapenemase-producing strain of Escherichia coli ( E. coli). To enhance the capacity for reactive oxygen species generation, QDs were incorporated into the polymer with a photosensitizing dye, crystal violet. Close proximity between the QD and dye enables electron and energy transfer processes leading to generation of cytotoxic singlet oxygen and superoxide radicals. A QD solution in cyclohexane was premixed with a solution of CV in the more polar solvent, dichloromethane, to promote the formation of QD-CV nanocomposite complexes via CV adsorption. This solution was then used to embed the QDs and crystal violet into medical grade polyurethane via swell-encapsulation. The combination of QD and CV elicited significant synergistic antibacterial activity under visible light against MRSA within 1 h (99.98% reduction) and E. coli within 4 h (99.96% reduction). Photoluminescence lifetime and singlet oxygen phosphorescence measurements demonstrated that interaction between the QDs and the crystal violet occurs within the polymer and leads to enhanced generation of reactive oxygen species. Strong inhibition of kill was observed using the superoxide scavenger, superoxide dismutase. The efficacy of these QD-CV polymer substrates, that can harvest light across the visible spectrum, against multidrug-resistant bacteria demonstrates the feasibility of this approach.
医院或植入式医疗设备表面污染导致抗生素耐药感染的发病率上升,这使得人们对新型抗菌表面越来越感兴趣。光激活表面在暴露于环境光下可以产生细胞毒性活性氧物质,这是一种很有前途的表面携带微生物失活方法。人们越来越感兴趣地将量子点 (QD) 用作光杀菌应用的光捕获剂,但常用 QD 中的镉会限制临床应用。本文测试了含有无镉 QD 的新型聚氨酯基质的光杀菌活性,以对抗临床多药耐药革兰氏阳性和革兰氏阴性细菌菌株:耐甲氧西林金黄色葡萄球菌 (MRSA) 和产碳青霉烯酶的大肠杆菌 (E. coli) 。为了增强活性氧生成能力,将 QD 与光敏染料结晶紫一起掺入聚合物中。QD 与染料的近距离使电子和能量转移过程得以进行,从而产生细胞毒性单线态氧和超氧自由基。将 QD 在环己烷中的溶液与 CV 在更极性溶剂二氯甲烷中的溶液预混合,以通过 CV 吸附促进 QD-CV 纳米复合材料复合物的形成。然后将该溶液用于通过溶胀包封将 QD 和结晶紫嵌入医用级聚氨酯中。QD 和 CV 的组合在可见光下对 MRSA (减少 99.98%)和大肠杆菌(减少 99.96%)在 1 小时内表现出显著的协同抗菌活性。光致发光寿命和单线态氧磷光测量表明,QD 与结晶紫之间的相互作用发生在聚合物内,导致活性氧物质的生成增强。超氧化物清除剂超氧化物歧化酶观察到强烈抑制杀灭作用。这些可以在可见光谱范围内收集光的 QD-CV 聚合物基质对多药耐药细菌的功效证明了这种方法的可行性。