贻贝启发的聚多巴胺复合介孔生物活性玻璃纳米颗粒:潜在金属离子负载平台及体外生物活性探索

Mussel-Inspired Polydopamine Composite Mesoporous Bioactive Glass Nanoparticles: An Exploration of Potential Metal-Ion Loading Platform and In Vitro Bioactivity.

作者信息

Sui Baiyan, Xu Zhiyan, Xue Zhiyu, Xiang Yong, Zhou Tian, Beltrán Ana M, Zheng Kai, Liu Xin, Boccaccini Aldo R

机构信息

Department of Dental Materials, Shanghai Biomaterials Research and Testing Center, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine; College of Stomatology, Shanghai Jiao Tong University; National Center for Stomatology; National Clinical Research Center for Oral Diseases; Shanghai Key Laboratory of Stomatology, No. 639 Zhizaoju Road, 200011 Shanghai, China.

Institute of Biomaterials, University of Erlangen-Nuremberg, Cauerstr. 6, 91058 Erlangen, Germany.

出版信息

ACS Appl Mater Interfaces. 2023 Jun 21;15(24):29550-29560. doi: 10.1021/acsami.3c03680. Epub 2023 Jun 6.

Abstract

Exploring new approaches to realize the possibility of incorporating biologically active elements into mesoporous silicate bioactive glass nanoparticles (MBG NPs) and guaranteeing their meso- structural integrity and dimensional stability has become an attractive and interesting challenge in biomaterials science. We present a postgrafting strategy for introducing different metal elements into MBG NPs. This strategy is mediated by polydopamine (PDA) coating, achieving uniform loading of copper or copper-cobalt on the particles efficiently and ensuring the stability of MBG NPs in terms of particle size, mesoporous structure, and chemical structure. However, the PDA coating reduced the ion-binding free energy of the MBG NPs for calcium and phosphate ions, resulting in the deposition of minimal CaP clusters on the PDA@MBG NP surface when immersed for 7 days in simulated body fluid, indicating the absence of hydroxyapatite mineralization.

摘要

探索新方法以实现将生物活性元素纳入介孔硅酸盐生物活性玻璃纳米颗粒(MBG NPs)并确保其介观结构完整性和尺寸稳定性,已成为生物材料科学中一个具有吸引力且有趣的挑战。我们提出了一种后接枝策略,用于将不同金属元素引入MBG NPs。该策略由聚多巴胺(PDA)涂层介导,能有效地在颗粒上实现铜或铜钴的均匀负载,并确保MBG NPs在粒径、介孔结构和化学结构方面的稳定性。然而,PDA涂层降低了MBG NPs对钙离子和磷酸根离子的离子结合自由能,导致在模拟体液中浸泡7天时,PDA@MBG NP表面仅有少量CaP簇沉积,这表明不存在羟基磷灰石矿化现象。

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