Graduate Institute of Biomedical Materials and Engineering, College of Oral Medicine, Taipei Medical University, Taipei 110, Taiwan.
Antimicrob Agents Chemother. 2011 May;55(5):1883-90. doi: 10.1128/AAC.00550-10. Epub 2011 Jan 31.
Antimicrobial photodynamic inactivation (PDI) was shown to be a promising treatment modality for microbial infections. This study explores the effect of chitosan, a polycationic biopolymer, in increasing the PDI efficacy against Gram-positive bacteria, including Staphylococcus aureus, Staphylococcus epidermidis, Streptococcus pyogenes, and methicillin-resistant S. aureus (MRSA), as well as the Gram-negative bacteria Pseudomonas aeruginosa and Acinetobacter baumannii. Chitosan at <0.1% was included in the antibacterial process either by coincubation with hematoporphyrin (Hp) and subjection to light exposure to induce the PDI effect or by addition after PDI and further incubation for 30 min. Under conditions in which Hp-PDI killed the microbe on a 2- to 4-log scale, treatment with chitosan at concentrations of as low as 0.025% for a further 30 min completely eradicated the bacteria (which were originally at ∼10(8) CFU/ml). Similar results were also found with toluidine blue O (TBO)-mediated PDI in planktonic and biofilm cells. However, without PDI treatment, chitosan alone did not exert significant antimicrobial activity with 30 min of incubation, suggesting that the potentiated effect of chitosan worked after the bacterial damage induced by PDI. Further studies indicated that the potentiated PDI effect of chitosan was related to the level of PDI damage and the deacetylation level of the chitosan. These results indicate that the combination of PDI and chitosan is quite promising for eradicating microbial infections.
抗菌光动力灭活(PDI)被证明是一种有前途的治疗微生物感染的方法。本研究探讨了壳聚糖(一种聚阳离子生物聚合物)在提高PDI 对革兰氏阳性菌(包括金黄色葡萄球菌、表皮葡萄球菌、化脓性链球菌和耐甲氧西林金黄色葡萄球菌(MRSA))以及革兰氏阴性菌铜绿假单胞菌和鲍曼不动杆菌的疗效方面的作用。壳聚糖在抗菌过程中以<0.1%的浓度存在,要么与血卟啉(Hp)共同孵育并暴露于光线下诱导 PDI 效应,要么在 PDI 后加入并进一步孵育 30 分钟。在 Hp-PDI 将微生物杀死 2-4 个对数级的条件下,用浓度低至 0.025%的壳聚糖进一步处理 30 分钟即可完全消灭细菌(最初的细菌浓度约为 10(8)CFU/ml)。在浮游和生物膜细胞中,甲苯胺蓝 O(TBO)介导的 PDI 也得到了类似的结果。然而,如果没有 PDI 处理,单独的壳聚糖在孵育 30 分钟时不会表现出显著的抗菌活性,这表明壳聚糖的增效作用是在 PDI 诱导的细菌损伤之后发挥的。进一步的研究表明,壳聚糖增强 PDI 效应与 PDI 损伤的程度和壳聚糖的脱乙酰化水平有关。这些结果表明,PDI 和壳聚糖的联合使用对于消除微生物感染具有很大的潜力。