GABAA Receptor‐Specific Carbon Dots for High‐Contrast Hepatocellular Carcinoma Imaging and Differentiation

Author:

Guo Yifei1,Sun Yuanqiang1,Geng Xin1,Wang Junli1,Hu Jingyu1,Song Rong‐Bin12ORCID,Yang Ran1,Qu Lingbo1,Li Zhaohui13

Affiliation:

1. Zhengzhou Key Laboratory of Functional Nanomaterial and Medical Theranostic Institute of Analytical Chemistry for Life Science College of Chemistry Zhengzhou University Zhengzhou 450001 P. R. China

2. School of Ecology and Environment Zhengzhou University Zhengzhou 450001 P. R. China

3. The First Affiliated Hospital of Zhengzhou University Zhengzhou University Zhengzhou 450052 P. R. China

Abstract

AbstractTargeted fluorescence probes for imaging and differentiation of hepatocellular carcinoma (HCC) are highly desirable from its scientific research and clinical applications. However, most of the current targeted fluorescence probes focus on the variation of intracellular microenvironment caused by the cancerization of hepatocyte, which causes a fluorescence intensity alteration but fails to produce a spatial differentiation due to the lack of robust parameters for further improving accuracy. Herein, the study develops a new fluorescent carbon dot (CTF‐CDs) that can target the overexpressed GABAA receptor (GABAAR) on cell membrane for accurate and high‐contrast imaging of HCC and differentiation. The competition response between CTF‐CDs and typical receptor‐binding ligands reveals their affinity toward the picrotoxin‐binding site of GABAAR. Based on this GABAAR‐targeting ability, accurate imaging of HCC cells is realized by lighting their membranes, along with a big difference from the intracellular fluorescence of normal liver cells and other cancer cells. In addition, the CTF‐CDs have also been used to visualize the anticancer drug‐induced variations on HCC cell membrane and fluorescent imaging in HCC tissue. This work extends the targeting object of fluorescence probes from intracellular microenvironment to membrane protein, adding a new dimension to the imaging and differentiation of HCC.

Funder

Natural Science Foundation of Henan Province

National Natural Science Foundation of China

Publisher

Wiley

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