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2
pH-activated nanoparticles for controlled topical delivery of farnesol to disrupt oral biofilm virulence.用于将法尼醇可控局部递送以破坏口腔生物膜毒力的pH激活纳米颗粒。
ACS Nano. 2015 Mar 24;9(3):2390-404. doi: 10.1021/nn507170s. Epub 2015 Feb 13.
3
Effect of divalent cation removal on the structure of gram-negative bacterial outer membrane models.去除二价阳离子对革兰氏阴性菌外膜模型结构的影响。
Langmuir. 2015;31(1):404-12. doi: 10.1021/la504407v. Epub 2014 Dec 19.
4
Iron-regulated expression of alginate production, mucoid phenotype, and biofilm formation by Pseudomonas aeruginosa.铜绿假单胞菌藻酸盐产生、黏液样表型及生物膜形成的铁调节表达
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5
Pseudomonas aeruginosa adapts its iron uptake strategies in function of the type of infections.铜绿假单胞菌会根据感染类型调整其铁摄取策略。
Front Cell Infect Microbiol. 2013 Nov 14;3:75. doi: 10.3389/fcimb.2013.00075. eCollection 2013.
6
Ferrous iron is a significant component of bioavailable iron in cystic fibrosis airways.亚铁是囊性纤维化气道中生物可利用铁的重要组成部分。
mBio. 2013 Aug 20;4(4):e00557-13. doi: 10.1128/mBio.00557-13.
7
Mini-review: Lactoferrin: a bioinspired, anti-biofilm therapeutic.综述:乳铁蛋白:一种仿生、抗生物膜的治疗方法。
Biofouling. 2013;29(4):443-55. doi: 10.1080/08927014.2013.773317.
8
Stealth properties to improve therapeutic efficacy of drug nanocarriers.改善药物纳米载体治疗效果的隐身特性。
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Targeting iron uptake to control Pseudomonas aeruginosa infections in cystic fibrosis.靶向铁摄取以控制囊性纤维化中的铜绿假单胞菌感染。
Eur Respir J. 2013 Dec;42(6):1723-36. doi: 10.1183/09031936.00124012. Epub 2012 Nov 8.
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用于抑制细菌生物膜形成的三联吡啶胶束

Terpyridine-Micelles for Inhibiting Bacterial Biofilm Development.

作者信息

Qiao Jing, Purro Max, Liu Zhi, Xiong May P

机构信息

Department of Pharmaceutical and Biomedical Sciences, College of Pharmacy , University of Georgia , 250 W. Green Street , Athens , Georgia 30602-2352 , United States.

Pharmaceutical Sciences Division, School of Pharmacy , University of Wisconsin-Madison , 777 Highland Avenue , Madison , Wisconsin 53705-2222 , United States.

出版信息

ACS Infect Dis. 2018 Sep 14;4(9):1346-1354. doi: 10.1021/acsinfecdis.8b00091. Epub 2018 Jul 31.

DOI:10.1021/acsinfecdis.8b00091
PMID:29974746
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6138535/
Abstract

Iron plays a critical role in bacterial infections and is especially critical for supporting biofilm formation. Until recently, Fe(III) was assumed to be the most relevant form of iron to chelate in therapeutic antimicrobial strategies due to its natural abundance under normal oxygen and physiologic conditions. Recent clinical data obtained from cystic fibrosis (CF) patients found that there is actually quite an abundance of Fe(II) present in sputum and that there exists a significant relationship between sputum Fe(II) concentration and severity of the disease. A biocompatible mixed micelle formed from the self-assembly of poly(lactic- co-glycolic acid)- block-methoxy poly(ethylene glycol) (PLGA- b-mPEG) and poly(lactic- co-glycolic acid)- block-poly(terpyridine) [PLGA- b-p(Tpy)] polymers was prepared to chelate Fe(II) (Tpy-micelle). Tpy-micelles showed high selectivity for Fe(II) over Fe(III), decreased biofilm mass more effectively under anaerobic conditions at >4 μM Tpy-micelles, reduced bacteria growth in biofilms by >99.9% at 128 μM Tpy-micelles, effectively penetrated throughout a 1-day old biofilm, and inhibited biofilm development in a concentration-dependent manner. This study reveals that Fe(II) chelating Tpy-micelles are a promising addition to Fe(III) chelating strategies to inhibit biofilm formation in CF lung infections.

摘要

铁在细菌感染中起着关键作用,对支持生物膜形成尤为重要。直到最近,由于在正常氧气和生理条件下铁(III)天然丰富,所以在治疗性抗菌策略中,它被认为是最需要螯合的铁的形式。从囊性纤维化(CF)患者获得的最新临床数据发现,痰液中实际上存在相当大量的亚铁(Fe(II)),并且痰液中亚铁浓度与疾病严重程度之间存在显著关系。由聚(乳酸-共-乙醇酸)-嵌段-甲氧基聚(乙二醇)(PLGA-b-mPEG)和聚(乳酸-共-乙醇酸)-嵌段-聚(三联吡啶)[PLGA-b-p(Tpy)]聚合物自组装形成的生物相容性混合胶束被制备用于螯合亚铁(Tpy-胶束)。Tpy-胶束对亚铁的选择性高于铁(III),在>4 μM Tpy-胶束的厌氧条件下能更有效地降低生物膜质量,在128 μM Tpy-胶束时生物膜中的细菌生长减少>99.9%,能有效穿透1天龄的生物膜,并以浓度依赖的方式抑制生物膜形成。这项研究表明,螯合亚铁的Tpy-胶束有望成为铁(III)螯合策略的补充,以抑制CF肺部感染中的生物膜形成。