Cheng Chi-Hui, Liu Han-Cheng, Lin Jui-Che
Department of Pediatrics, College of Medicine, Chang Gung University, aoyuan 33305, Taiwan.
Department of Pediatrics, Chang Gung Memorial Hospital, Taoyuan 33305, Taiwan.
Polymers (Basel). 2021 Jul 15;13(14):2321. doi: 10.3390/polym13142321.
Reducing microbial infections associated with biomedical devices or articles/furniture noted in a hospital or outpatient clinic remains a great challenge to researchers. Due to its stability and low toxicity, the N-halamine compound has been proposed as a potential antimicrobial agent. It can be incorporated into or blended with the FDA-approved biomaterials. Surface grafting or coating of N-halamine was also reported. Nevertheless, the hydrophobic nature associated with its chemical configuration may affect the microbial interactions with the chlorinated N-halamine-containing substrate. In this study, a polymerizable N-halamine compound was synthesized and grafted onto a polyurethane surface via a surface-initiated atom transfer radical polymerization (SI-ATRP) scheme. Further, using the sequential SI-ATRP reaction method, different hydrophilic monomers, namely poly (ethylene glycol) methacrylate (PEGMA), hydroxyethyl methacrylate (HEMA), and [2-(methacryloyloxy) ethyl] dimethyl-(3-sulfopropyl) ammonium hydroxide (SBMA), were also grafted onto the polyurethane (PU) substrate before the N-halamine grafting reaction to change the surface properties of the N-halamine-modified substrate. It was noted that the chains containing the hydrophilic monomer and the polymerizable N-halamine compound were successfully grafted onto the PU substrate. The degree of chlorination was improved with the introduction of a hydrophilic monomer, except the HEMA. All of these hydrophilic monomer-containing N-halamine-modified PU substrates demonstrated a more than 2 log CFU reduction after microbial incubation. In contrast, the surface modified with N-halamine only exhibited significantly less antimicrobial efficacy instead. This is likely due to the synergistic effects caused by the reduced chlorine content, as well as the reduced surface interactions with the microbes.
减少医院或门诊诊所中与生物医学设备、物品或家具相关的微生物感染,对研究人员来说仍然是一个巨大的挑战。由于其稳定性和低毒性,N-卤胺化合物已被提议作为一种潜在的抗菌剂。它可以被并入FDA批准的生物材料中或与之混合。也有报道对N-卤胺进行表面接枝或涂层处理。然而,与其化学结构相关的疏水性可能会影响微生物与含氯N-卤胺底物的相互作用。在本研究中,合成了一种可聚合的N-卤胺化合物,并通过表面引发的原子转移自由基聚合(SI-ATRP)方案将其接枝到聚氨酯表面。此外,使用顺序SI-ATRP反应方法,在N-卤胺接枝反应之前,还将不同的亲水性单体,即聚(乙二醇)甲基丙烯酸酯(PEGMA)、甲基丙烯酸羟乙酯(HEMA)和[2-(甲基丙烯酰氧基)乙基]二甲基-(3-磺丙基)氢氧化铵(SBMA)接枝到聚氨酯(PU)基材上,以改变N-卤胺改性基材的表面性质。值得注意的是,含有亲水性单体和可聚合N-卤胺化合物的链成功地接枝到了PU基材上。除了HEMA外,随着亲水性单体的引入,氯化程度得到了提高。所有这些含亲水性单体的N-卤胺改性PU基材在微生物培养后均表现出超过2个对数CFU的减少。相比之下,仅用N-卤胺改性的表面抗菌效果明显较差。这可能是由于氯含量降低以及与微生物的表面相互作用减少所导致的协同效应。