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Targeting and detecting cancer cells using spontaneously formed multifunctional dendrimer-stabilized gold nanoparticles

机译:使用自发形成的多功能树枝状聚合物稳定的金纳米颗粒靶向和检测癌细胞

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摘要

We develop a facile approach to fabricating multifunctional dendrimer-stabilized gold nanoparticlesn(Au DSNPs) for cancer cell targeting and imaging. In this work, amine-terminated generation 5 (G5)npoly(amidoamine) (PAMAM) dendrimers pre-functionalized with folic acid (FA) and fluoresceinnisothiocyanate (FI) are complexed with Au(III) ions, followed by acetylation of the amine groups on thendendrimer surfaces. This one-step process leads to the spontaneous formation of 6 nm-sized Aunnanoparticles stabilized by multifunctional dendrimers bearing both targeting and imagingnfunctionalities. The multifunctional Au DSNPs are characterized by UV-Vis spectrometry, 1H NMR,nand transmission electron microscopy (TEM). The formed Au DSNPs are water-soluble, stable, andnbiocompatible. Combined flow cytometry, confocal microscopy, silver staining, and inductivelyncoupled plasma-mass spectrometry (ICP-MS) analyses show that the FA- and FI-functionalized AunDSNPs can specifically target to cancer cells expressing high-affinity FA receptors in vitro. Thisnapproach to functionalizing Au DSNPs may be extended to other targeting molecules, providingna unique nanoplatform for targeting and imaging of a variety of biological systems.
机译:我们开发了一种简便的方法来制造多功能树状聚合物稳定的金纳米颗粒(Au DSNPs),用于癌细胞靶向和成像。在这项工作中,将用叶酸(FA)和荧光素异硫氰酸酯(FI)预功能化的胺终止的第5代(G5)npoly(amidoamine)(PAMAM)树状聚合物与Au(III)离子络合,然后将胺基乙酰化在树枝状聚合物表面上。这一一步过程导致由具有靶向和成像功能的多功能树枝状聚合物稳定的6 nm大小的金纳米颗粒的自发形成。通过紫外可见光谱,1 H NMR,透射电子显微镜(TEM)对Au DSNP进行了表征。所形成的Au DSNP是水溶性的,稳定的并且是非生物相容的。结合流式细胞仪,共聚焦显微镜,银染和电感耦合等离子体质谱(ICP-MS)分析显示,FA和FI功能化的AunDSNPs可以特异性靶向体外表达高亲和力FA受体的癌细胞。这种使Au DSNPs功能化的方法可以扩展到其他靶向分子,从而为多种生物系统的靶向和成像提供独特的纳米平台。

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  • 来源
    《The Analyst》 |2009年第7期|p.1373-1379|共7页
  • 作者单位

    aCollege of Chemistry, Chemical Engineering, and Biotechnology,Donghua University, Shanghai 210620, P. R. China. E-mail: xshi@dhu.edu.cn, Fax: +86-21-67792306-804bMichigan Nanotechnology Institute for Medicine and Biological Sciences,University of Michigan, Ann Arbor, MI 48109, USA. E-mail: shidasui@umich.edu, jbakerjr@umich.edu† Electronic supplementary information (ESI) available: 1H NMRspectra of the DSNPs {(Au0)7-G5.NHAc-FI} and{(Au0)7-G5.NHAc-FI-FA}. See DOI: 10.1039/b902199j,;

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