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本文引用的文献

1
Improved photodynamic inactivation of gram-positive bacteria using hematoporphyrin encapsulated in liposomes and micelles.使用包裹在脂质体和胶束中的血卟啉改善革兰氏阳性菌的光动力失活。
Lasers Surg Med. 2009 Apr;41(4):316-22. doi: 10.1002/lsm.20754.
2
Photodynamic therapy in the treatment of microbial infections: basic principles and perspective applications.光动力疗法在微生物感染治疗中的应用:基本原理与前景展望
Lasers Surg Med. 2006 Jun;38(5):468-81. doi: 10.1002/lsm.20361.
3
Protease-stable polycationic photosensitizer conjugates between polyethyleneimine and chlorin(e6) for broad-spectrum antimicrobial photoinactivation.用于广谱抗菌光灭活的聚乙烯亚胺与二氢卟吩(e6)之间的蛋白酶稳定型聚阳离子光敏剂缀合物。
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Correlation between Reduced Daptomycin Susceptibility and Vancomycin Resistance in Vancomycin-Intermediate Staphylococcus aureus.万古霉素中度敏感金黄色葡萄球菌中达托霉素敏感性降低与万古霉素耐药性之间的相关性
Antimicrob Agents Chemother. 2006 Mar;50(3):1079-82. doi: 10.1128/AAC.50.3.1079-1082.2006.
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Synthesis and antibacterial activity of new poly-S-lysine-porphyrin conjugates.新型聚-S-赖氨酸-卟啉共轭物的合成及其抗菌活性
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Photodynamic therapy: a new antimicrobial approach to infectious disease?光动力疗法:一种治疗传染病的新型抗菌方法?
Photochem Photobiol Sci. 2004 May;3(5):436-50. doi: 10.1039/b311900a. Epub 2004 Feb 12.
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Chitosan as antimicrobial agent: applications and mode of action.壳聚糖作为抗菌剂:应用与作用方式。
Biomacromolecules. 2003 Nov-Dec;4(6):1457-65. doi: 10.1021/bm034130m.
8
Crosslinked collagen/chitosan matrix for artificial livers.用于人工肝脏的交联胶原/壳聚糖基质
Biomaterials. 2003 Aug;24(19):3213-20. doi: 10.1016/s0142-9612(03)00170-4.
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Formulation of benzoporphyrin derivatives in Pluronics.苯并卟啉衍生物在普朗尼克中的制剂。
Photochem Photobiol. 2003 Mar;77(3):299-303. doi: 10.1562/0031-8655(2003)077<0299:fobdip>2.0.co;2.
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Chitosan dispersed system for colon-specific drug delivery.用于结肠特异性药物递送的壳聚糖分散体系。
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壳聚糖增强了阳性菌和阴性菌的光动力灭活效果。

Chitosan augments photodynamic inactivation of gram-positive and gram-negative bacteria.

机构信息

Graduate Institute of Biomedical Materials and Engineering, College of Oral Medicine, Taipei Medical University, Taipei 110, Taiwan.

出版信息

Antimicrob Agents Chemother. 2011 May;55(5):1883-90. doi: 10.1128/AAC.00550-10. Epub 2011 Jan 31.

DOI:10.1128/AAC.00550-10
PMID:21282440
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3088195/
Abstract

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.

摘要

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。