A multifunctional probe for ICP-MS determination and multimodal imaging of cancer cells

被引:34
|
作者
Yang, Bin [1 ]
Zhang, Yuan [1 ]
Chen, Beibei [1 ]
He, Man [1 ]
Yin, Xiao [1 ]
Wang, Han [1 ]
Li, Xiaoting [1 ]
Hu, Bin [1 ]
机构
[1] Wuhan Univ, Dept Chem, Minist Educ, Key Lab Analyt Chem Biol & Med, Wuhan 430072, Peoples R China
关键词
Cancer cell; Inductively coupled plasma mass spectrometry; Upconversion nanoparticles; Multifunctional probe; Upconversion luminescence imaging; Fluorescence imaging; PLASMA-MASS SPECTROMETRY; CARCINOEMBRYONIC ANTIGEN; MAGNETIC IMMUNOASSAY; SELECTIVE COLLECTION; ALPHA-FETOPROTEIN; LABELING STRATEGY; NANOPARTICLES; ASSAY; MULTIPLEX; QUANTIFICATION;
D O I
10.1016/j.bios.2017.04.041
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Inductively coupled plasma-mass spectrometry (ICP-MS) based bioassay and multimodal imaging have attracted increasing attention in the current development of cancer research and theranostics. Herein, a sensitive, simple, timesaving, and reliable immunoassay for cancer cells counting and dual-modal imaging was proposed by using ICP-MS detection and down-conversion fluorescence (FL)/upconversion luminescence (UCL) with the aid of a multifunctional probe for the first time. The probe consisted of a recognition unit of goat anti-mouse IgG to label the anti-EpCAM antibody attached cells, a fluorescent dye (Cy3) moiety for FL imaging as well as upconversion nanoparticles (UCNPs) tag for both ICP-MS quantification and UCL imaging of cancer cells. Under the optimized conditions, an excellent linearity and sensitivity were achieved owing to the signal amplification effect of nanoparticles and low spectral interference. Accordingly, a limit of detection (3s) of 1x10(2) HepG2 cells and a relative standard deviation of 7.1% for seven replicate determinations of 1x10(3) HepG2 cells were obtained. This work proposed a method to employ UCNPs with highly integrated functionalities enabling us not only to count but also to see the cancer cells, opening a promising avenue for biological research and clinical theranostics.
引用
收藏
页码:77 / 83
页数:7
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