Biomimetic immunomagnetic gold hybrid nanoparticles coupled with inductively coupled plasma mass spectrometry for the detection of circulating tumor cells. Issue 23 (12th May 2020)

• Record Type: Journal Article
• Authors: Chang, Zhi-min; Zhou, Hang; Yang, Chao; Zhang, Rui; You, Qiannan; Yan, Ruhong; Li, Li; Ge, Mingfeng; Tang, Yuguo; Dong, Wen-fei; Wang, Zheng
• Is Part Of: Journal of materials chemistry. Volume 8:Issue 23(2020)
• Page Start: 5019
• Page End: 5025
• Publication Date: 2020-05-12
• Subjects: Materials -- Periodicals; Chemistry, Analytic -- Periodicals; Biomedical materials -- Research -- Periodicals; 543.0284
• DOI: 10.1039/d0tb00403k
• Languages: English
• ISSNs: 2050-750X

Abstract

Abstract : Immunomagnetic beads are important tools for the isolation and detection of circulating tumor cells (CTCs). Abstract : Immunomagnetic beads are important tools for the isolation and detection of circulating tumor cells (CTCs). However, the current immunomagnetic bead technique provides poor CTC separation purity due to nonspecific binding of background cells. Furthermore, immunomagnetic beads have not been appropriately functionalized for enabling CTC analysis and quantification. In this work, bimetallic magnetic gold nanoparticles were prepared and coated with leukocyte membranes to form leukocyte membrane-camouflaged nanoparticles. After conjugation with the antibody of epithelial cell adhesion molecule (EpCAM), the biomimetic immunomagnetic gold nanoparticles (CM-Fe3 O4 @Au-Ab) showed a high specific recognition ability on mock (EpCAM-positive) CTCs and a reduced interaction with leukocytes. We subsequently optimized the conditions for CTC separation, including the concentration of nanoparticles and the incubation time. Under the optimized conditions, CM-Fe3 O4 @Au-Ab exhibited high CTC capture efficiency with negligible background cell binding in mock clinical blood samples. More importantly, gold probes were tagged on the surface of these separated CTCs. When coupled with ICP-MS analysis, the number of CTCs and gold signals exhibited a good linear relationship, and a low limit of detection was obtained, enabling us to estimate the number of CTCs in blood samples. Hence, we expected that CM-Fe3 O4 @Au-Ab could provide an opportunity to surmount the limitations of current CTC detection.