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FePt-Au磁性等离子体纳米颗粒核壳结构的形成与应用

Formation and Application of Core-Shell of FePt-Au Magnetic-Plasmonic Nanoparticles.

作者信息

Wei Da-Hua, Lin Tei-Kai, Liang Yuan-Chang, Chang Huang-Wei

机构信息

Department of Mechanical Engineering, Institute of Manufacturing Technology, National Taipei University of Technology (TAIPEI TECH), Taipei, Taiwan.

Department of Optoelectronics and Materials Technology, National Taiwan Ocean University, Keelung, Taiwan.

出版信息

Front Chem. 2021 Apr 27;9:653718. doi: 10.3389/fchem.2021.653718. eCollection 2021.

Abstract

Monodispersed FePt core and FePt-Au core-shell nanoparticles (NPs) have been chemically synthesized in liquid solution and with controllable surface-functional properties. The NP size was increased from 2.5 nm for FePt to 6.5 nm for FePt-Au, which could be tuned by the initial concentration of gold acetate coated onto FePt seeding NPs via a seed-mediated formation of self-assembled core-shell nanostructures. The analyses of the interplanar spacing obtained from the high-resolution transmission electron microscopy (HRTEM), selective electron diffraction pattern (SAED), and x-ray diffraction (XRD) confirmed that both FePt core and Au shell belong to the face-centered cubic (fcc) structure. FePt-Au NPs have a surface plasmon resonance (SPR) peak at 528 nm in the visible optical band region, indicating the red shift compared with the typical theoretical value of 520 nm of pure Au NPs. The surface modification and ligand exchange of FePt-Au was using mercaptoacetic acid (thiol) as a phase transfer reagent that turned the NPs hydrophilic due to the functional carboxyl group bond on the surface of presented multifunctional magnetic-plasmonic NPs. The water-dispersible FePt-based NPs conjugated with biomolecules could reach the different biocompatibility requirements and also provide enough heating response that acted as a potential agent for magnetic fluid hyperthermia in biomedical engineering research fields.

摘要

单分散的FePt核和FePt-Au核壳纳米颗粒(NPs)已在液相溶液中通过化学合成得到,且具有可控的表面功能特性。NP尺寸从FePt的2.5 nm增加到FePt-Au的6.5 nm,这可以通过经由种子介导的自组装核壳纳米结构形成,在FePt种子纳米颗粒上包覆醋酸金的初始浓度来调节。从高分辨率透射电子显微镜(HRTEM)、选区电子衍射图(SAED)和X射线衍射(XRD)获得的晶面间距分析证实,FePt核和Au壳均属于面心立方(fcc)结构。FePt-Au NPs在可见光波段区域的528 nm处有一个表面等离子体共振(SPR)峰,表明与纯Au NPs的典型理论值520 nm相比发生了红移。FePt-Au的表面改性和配体交换使用巯基乙酸(硫醇)作为相转移试剂,由于多功能磁等离子体NPs表面存在的功能性羧基键,使NPs具有亲水性。与生物分子共轭的水分散性FePt基NPs可以满足不同的生物相容性要求,并且还提供足够的热响应,在生物医学工程研究领域中作为磁流体热疗的潜在试剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/709e/8112197/81d2be4fd36e/fchem-09-653718-g0001.jpg

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