固定策略对 Peptoids 减少铜绿假单胞菌菌株在隐形眼镜上粘附能力的影响。

IF 3 2区 医学 Q1 OPHTHALMOLOGY
Manjulatha Sara , Sudip Chakraborty , Renxun Chen , Dennis Palms , Georgio Katsifis , Zhongyan Li , Syamak Farajikhah , Vinod Massedupally , Alex Hui , Edgar H.H. Wong , Naresh Kumar , Krasimir Vasilev , David Mackenzie , Linda Losurdo , Farida Dehghani , Havard Jenssen , Kristian Sorensen , Jennifer S. Lin , Annelise E. Barron , Mark Willcox
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引用次数: 0

摘要

目的:以往的研究表明,隐形眼镜涂上抗菌阳离子肽 Mel4(美利明的衍生物)后,可减少角膜炎的发生。然而,由于 Mel4 容易被蛋白水解,其抗菌活性会随着时间的推移而减弱。低聚-N-取代的甘氨酸蛋白胨(如 TM5 和 TM18)具有抗菌特性,并能抵抗蛋白分解。本研究的重点是探索将这些类蛋白胨共价连接到隐形眼镜上的方法,以提高隐形眼镜在体外的耐用性和性能:方法:通过碳二亚胺化学(EDC/NHS)、噁唑啉等离子体和等离子体离子浸泡植入法(PIII)将类蛋白胨 TM5 和 TM18 共价连接到依他非康镜片上。使用 X 射线光电子能谱 (XPS)、表面电荷和疏水性对镜片进行了分析。评估了镜片对多重耐药铜绿假单胞菌粘附的抑制作用以及对角膜上皮细胞的细胞毒性。此外,还评估了湿热灭菌对活性的影响:XPS证实了蛋白胨与镜片的结合。蛋白胨涂层会略微增大接触角(≤23°),但不会影响整体电荷。通过碳二亚胺结合的类蛋白胨能抑制铜绿假单胞菌的粘附,每个镜片能抑制超过 5 log10 CFU,其效果优于美利明,后者需要六倍的浓度才能减少 3 log10。通过噁唑啉或 PIII 附着的蛋白胨能减少超过 5 log10 CFU 的粘附。与未经处理的镜片相比,所有共价方法都能明显减少细菌粘附(P < 0.0001)。蛋白胨结合的镜片对角膜上皮细胞无毒性。灭菌对碳化二亚胺处理的镜片没有影响,但会降低草唑啉和 PIII 表面的活性,减少 1-2 log10 CFU:Peptoids TM5 和 TM18 能有效减少铜绿假单胞菌在镜片上的粘附,与碳化二亚胺结合的表面在灭菌后仍能保持活性,为开发抗菌隐形眼镜带来了希望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The effect of immobilisation strategies on the ability of peptoids to reduce the adhesion of P. aeruginosa strains to contact lenses

Aim

Previous studies have demonstrated that contact lenses coated with the antimicrobial cationic peptide Mel4, a derivative of melimine, can reduce the occurrence of keratitis. However, the antimicrobial activity of Mel4 weakened over time due to its susceptibility to proteolytic degradation. Oligo-N-substituted glycine peptoids such as TM5 and TM18 possess antimicrobial properties and are resistant to proteolytic breakdown. This study focused on exploring methods for covalently attaching these peptoids to contact lenses to enhance their durability and performance in vitro.

Methods

The peptoids TM5 and TM18 were covalently attached to etafilcon lenses via carbodiimide chemistry (EDC/NHS), oxazoline plasma, and plasma ion immersion implantation (PIII). The lenses were analysed using X-ray photoelectron spectroscopy (XPS), surface charge, and hydrophobicity. Inhibition of adhesion of multidrug-resistant Pseudomonas aeruginosa and cytotoxicity on corneal epithelial cells were evaluated. The impact of moist heat sterilization on activity was also assessed.

Results

XPS confirmed peptoid binding to lenses. Peptoid coatings slightly increased contact angles (≤23°) without affecting overall charge. Peptoids, bound via carbodiimide, inhibited P. aeruginosa adhesion by over 5 log10 CFU per lens, outperforming melimine, which required six times the concentration for a 3 log10 reduction. Peptoids attached via oxazoline or PIII reduced adhesion by > 5 log10 CFU. All covalent methods significantly reduced bacterial adhesion compared to untreated lenses (P < 0.0001). Peptoid-bound lenses were non-toxic to corneal epithelial cells. Sterilization did not affect carbodiimide-treated lenses but reduced the activity of oxazoline and PIII surfaces by 1–2 log10 CFU.

Conclusion

Peptoids TM5 and TM18 effectively reduced P. aeruginosa adhesion on lenses, with carbodiimide-bound surfaces retaining activity post-sterilization, showing promise for the development of antimicrobial contact lenses.
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来源期刊
Experimental eye research
Experimental eye research 医学-眼科学
CiteScore
6.80
自引率
5.90%
发文量
323
审稿时长
66 days
期刊介绍: The primary goal of Experimental Eye Research is to publish original research papers on all aspects of experimental biology of the eye and ocular tissues that seek to define the mechanisms of normal function and/or disease. Studies of ocular tissues that encompass the disciplines of cell biology, developmental biology, genetics, molecular biology, physiology, biochemistry, biophysics, immunology or microbiology are most welcomed. Manuscripts that are purely clinical or in a surgical area of ophthalmology are not appropriate for submission to Experimental Eye Research and if received will be returned without review.
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