Biomimetic recognition strategy for efficient capture and release of circulating tumor cells

被引:4
|
作者
Zheng, Ji [1 ]
Li, Dayong [1 ]
Jiao, Jin [1 ]
Duan, Chengjie [1 ]
Gong, Youjing [1 ]
Shi, Hai [1 ]
Wang, Zhongyun [2 ]
Xiang, Yang [1 ]
机构
[1] Nanjing Univ, Sch Life Sci, State Key Lab Pharmaceut Biotechnol, Nanjing 210023, Peoples R China
[2] Nanjing Med Univ, Dept Anesthesiol, Affiliated Hosp 1, Nanjing 210029, Peoples R China
基金
中国国家自然科学基金;
关键词
Gold-coated magnetic nanomaterials; Biomimetic tentacles; Rolling circle amplification; Multivalent aptamer; PERIPHERAL-BLOOD; BREAST-CANCER; NANOPARTICLES; QUANTITATION;
D O I
10.1007/s00604-021-04856-4
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Efficient capture and release of circulating tumor cells play an important role in cancer diagnosis, but the limited affinity of monovalent adhesion molecules in existing capture technologies leads to low capture efficiency, and the captured cells are difficult to be separated. Inspired by the phenomenon that the long tentacles of jellyfish contain multiple adhesion domains and can effectively capture moving food, we have constructed a biomimetic recognition strategy to capture and release tumor cells. In details, gold-coated magnetic nanomaterials (Au@Fe3O4 NPs) were first prepared and characterized by scanning electron microscopy, UV-vis absorption spectra, and Zeta potential. Then, the DNA primers modified on Au@Fe3O4 nanoparticles can be extended to form many radialized DNA products by rolling circle amplification. These long DNA products resemble jellyfish tentacles and contain multivalent aptamers that can be extended into three dimensions to increase the accessibility of target cells, resulting in efficient, simple, rapid, and specific cells capture. The capture efficiencies are no less than 92% in PBS buffer and 77% in blood. Subsequently, DNase I was selected to degrade biomimetic tentacles to release the captured tumor cells with high viability. This release strategy can not only improve cell viability, but also reduce a tedious release process and unnecessary costs. We believe that the proposed method can be expanded for the capture and release of various tumor cells and will inspire the development of circulating tumor cells analysis.
引用
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页数:7
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