首页> 外文期刊>Acta biomaterialia >Functionalised nanoscale coatings using layer-by-layer assembly for imparting antibacterial properties to polylactide-co-glycolide surfaces
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Functionalised nanoscale coatings using layer-by-layer assembly for imparting antibacterial properties to polylactide-co-glycolide surfaces

机译:使用逐层组装的功能化纳米级涂料,可赋予聚丙交酯-共-乙交酯表面抗菌性能

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In order to achieve high local biological activity and reduce the risk of side effects of antibiotics in the treatment of periodontal and bone infections, a localised and temporally controlled delivery system is desirable. The aim of this research was to develop a functionalised and resorbable surface to contact soft tissues to improve the antibacterial behaviour during the first week after its implantation in the treatment of periodontal and bone infections. Solvent-cast poly(D,L-lactide-co-glycolide acid) (PLGA) films were aminolysed and then modified by Layer-by-Layer technique to obtain a nano-layered coating using poly(sodium4-styrenesulfonate) (PSS) and poly(allylamine hydrochloride) (PAH) as polyelectrolytes. The water-soluble antibiotic, metronidazole (MET), was incorporated from the ninth layer. Infrared spectroscopy showed that the PSS and PAH absorption bands increased with the layer number. The contact angle values had a regular alternate behaviour from the ninth layer. X-ray Photoelectron Spectroscopy evidenced two distinct peaks, N-1s, and S-2p, indicating PAH and PSS had been introduced. Atomic Force Microscopy showed the presence of polyelectrolytes on the surface with a measured roughness about 10 nm after 20 layers' deposition. The drug release was monitored by Ultraviolet-visible spectroscopy showing 80% loaded-drug delivery in 14 days. Finally, the biocompatibility was evaluated in vitro with L929 mouse fibroblasts and the antibacterial properties were demonstrated successfully against the keystone periodontal bacteria Poiphyromonas gingivalis, which has an influence on implant failure, without compromising in vitro biocompatibility. In this study, PLGA was successfully modified to obtain a localised and temporally controlled drug delivery system, demonstrating the potential value of LbL as a coating technology for the manufacture of medical devices with advanced functional properties. (C) 2015 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
机译:为了获得高的局部生物活性并减少在治疗牙周和骨感染中抗生素副作用的风险,需要局部和时间控制的递送系统。这项研究的目的是开发一种功能化且可吸收的表面,使其接触软组织,以改善其植入牙周和骨骼感染后第一周的抗菌性能。将溶剂流延的聚(D,L-丙交酯-乙交酯共聚物)(PLGA)薄膜进行氨解,然后通过逐层技术进行改性,以使用聚(4-苯乙烯磺酸钠)(PSS)和聚(烯丙胺盐酸盐)(PAH)作为聚电解质。从第九层开始加入水溶性抗生素甲硝唑(MET)。红外光谱表明,随着层数的增加,PSS和PAH的吸收带增加。接触角值从第九层开始有规律的交替行为。 X射线光电子能谱显示两个不同的峰N-1s和S-2p,表明已引入PAH和PSS。原子力显微镜显示在沉积20层后,表面上存在聚电解质,测量的粗糙度约为10 nm。通过紫外线-可见光谱法监测药物释放,显示在14天内80%的载药量。最后,在体外用L929小鼠成纤维细胞对生物相容性进行了评估,并成功证明了其对梯形牙周病菌牙龈线虫(Poiphyromonas gingivalis)的抗菌性能,该细菌对植入失败具有影响,而不会损害体外生物相容性。在这项研究中,成功​​地对PLGA进行了改进,以获得局部和时间控制的药物输送系统,证明了LbL作为涂层技术用于制造具有先进功能特性的医疗设备的潜在价值。 (C)2015 Acta Materialia Inc.,由Elsevier Ltd.发行。保留所有权利。

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