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基于交替氧化还原合成的脉冲电化学驱动聚多巴胺和羟基磷灰石纳米薄膜逐层快速组装用于骨再生

Pulse Electrochemical Driven Rapid Layer-by-Layer Assembly of Polydopamine and Hydroxyapatite Nanofilms via Alternative Redox Synthesis for Bone Regeneration.

作者信息

Xie Chaoming, Lu Xiong, Wang Kefeng, Yuan Huipin, Fang Liming, Zheng Xiaotong, Chan Chunwai, Ren Fuzeng, Zhao Cancan

机构信息

Key Lab of Advanced Technologies of Materials, Ministry of Education, School of Materials Science and Engineering, Southwest Jiaotong University, Chengdu, Sichuan 610031, China.

National Engineering Research Center for Biomaterials, Genome Research Center for Biomaterials, Sichuan University, Chengdu, Sichuan 610064, China.

出版信息

ACS Biomater Sci Eng. 2016 Jun 13;2(6):920-928. doi: 10.1021/acsbiomaterials.6b00015. Epub 2016 May 12.

Abstract

Polydopamine (PDA) is an important candidate material for the surface modification of biomedical devices because of its good adhesiveness and biocompatibility. However, PDA nanofilms lack osteoinductivity, limiting their applications in bone tissue engineering. Hydroxyapatite nanoparticles (HA-NPs) are the major component of natural bone, which can be used to effectively enhance the osteoinductivity of PDA nanofilms. Herein, we developed a pulse electrochemical driven layer-by-layer (PED-LbL) assembly process to rapidly deposit HA-NPs and PDA (HA-PDA) multilayer nanofilms. In this process, PDA and HA-NPs are synthesized in two sequential oxidative and reductive pulses in each electrochemical deposition cycle and alternately deposited on the substrate surfaces. PDA assists the synthesis of HA-NPs by working as a template, which avoids the noncontrollable HA nucleation and aggregation. The HA-PDA multilayer nanofilms serve as a tunable reservoir to deliver bone morphogenetic protein-2 and exhibit high osteoinductivity both and . This PED-LbL assembly process breaks the limitation of traditional LbL assembly, allowing not only the rapid assembly of oppositely charged polyelectrolytes but also the synthesis of organic/inorganic NPs that are uniformly incorporated in the nanofilm. It has broad applications in the preparation of versatile surface coatings on various biomedical devices.

摘要

聚多巴胺(PDA)因其良好的粘附性和生物相容性,是生物医学设备表面改性的重要候选材料。然而,PDA纳米薄膜缺乏骨诱导性,限制了它们在骨组织工程中的应用。羟基磷灰石纳米颗粒(HA-NPs)是天然骨的主要成分,可用于有效增强PDA纳米薄膜的骨诱导性。在此,我们开发了一种脉冲电化学驱动的逐层(PED-LbL)组装工艺,以快速沉积HA-NPs和PDA(HA-PDA)多层纳米薄膜。在这个过程中,PDA和HA-NPs在每个电化学沉积循环中通过两个连续的氧化和还原脉冲合成,并交替沉积在基底表面。PDA作为模板辅助HA-NPs的合成,避免了HA的不可控成核和聚集。HA-PDA多层纳米薄膜作为一个可调谐的储存库来递送骨形态发生蛋白-2,并且在体内和体外均表现出高骨诱导性。这种PED-LbL组装工艺打破了传统LbL组装的限制,不仅允许快速组装带相反电荷的聚电解质,还允许合成均匀掺入纳米薄膜中的有机/无机NP。它在各种生物医学设备上制备多功能表面涂层方面具有广泛的应用。

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