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在钛表面构建聚(乙烯醇)/聚(丙交酯-乙交酯)/万古霉素纳米颗粒以增强表面自抗菌活性和细胞相容性。

Construction of poly (vinyl alcohol)/poly (lactide-glycolide acid)/vancomycin nanoparticles on titanium for enhancing the surface self-antibacterial activity and cytocompatibility.

作者信息

Liu Zehui, Zhu Yizhou, Liu Xiangmei, Yeung K W K, Wu Shuilin

机构信息

Hubei Collaborative Innovation Center for Advanced Organic Chemical Materials, Ministry-of-Education Key Laboratory for the Green Preparation and Application of Functional Materials, Hubei Key Laboratory of Polymer Materials, School of Materials Science & Engineering, Hubei University, Wuhan 430062, China.

Department of Orthopaedics & Traumatology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.

出版信息

Colloids Surf B Biointerfaces. 2017 Mar 1;151:165-177. doi: 10.1016/j.colsurfb.2016.12.016. Epub 2016 Dec 15.

Abstract

Comparing with traditional drug dosage form, controlled release systems offer more effective and favorable route to deliver drugs in optimum dose to specific sites with long term release duration. In this work, an effective drug delivery system composed of poly (vinyl alcohol) (PVA)/poly (lactide-glycolide acid) (PLGA) nanoparticles (NPs) with encapsulated vancomycin (Van), is constructed on the surface of biomedical titanium. The PVA/PLGA/Van NPs synthesized via double emulsion route are grafted onto the surface of titanium plates modified by alkaline-heat treatment and subsequent aminopropyltriethoxysilane (APTES) deposition. In vitro tests disclose that NPs can release a small amount of drugs continuously due to the slow swelling or hydrolysis of polymer chain segments as the immersion time increases. As the pH value reduces, the ester bonds rupture with releasing more drugs, which is why this drug delivery system exhibits the highest antibacterial efficiency at the lowest pH value of 4.5 in this work. Cell culture results reveal that this smart surface system on titanium facilitates the cell attachment and proliferation on implants. Hence, this pH controlled drug delivery system can be successfully applied as a bio-platform for improving both the osteoblasts adhesion and antibacterial activity of metallic implants.

摘要

与传统药物剂型相比,控释系统提供了一种更有效且有利的途径,能够以最佳剂量将药物递送至特定部位,并具有长期释放持续时间。在这项工作中,一种由聚(乙烯醇)(PVA)/聚(丙交酯-乙交酯)(PLGA)纳米颗粒(NPs)与包裹的万古霉素(Van)组成的有效药物递送系统,被构建在生物医学钛的表面。通过双乳液法合成的PVA/PLGA/Van NPs被接枝到经碱热处理和随后的氨丙基三乙氧基硅烷(APTES)沉积修饰的钛板表面。体外试验表明,随着浸泡时间的增加,由于聚合物链段的缓慢溶胀或水解,纳米颗粒能够持续释放少量药物。随着pH值降低,酯键断裂并释放更多药物,这就是为什么在这项工作中该药物递送系统在最低pH值4.5时表现出最高的抗菌效率。细胞培养结果表明,钛表面的这种智能系统促进了植入物上细胞的附着和增殖。因此,可以成功地将这种pH控释药物递送系统用作生物平台,以提高金属植入物的成骨细胞粘附和抗菌活性。

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