» Articles » PMID: 39103612

A Sequential Dual-locked Luminescent Copper Nanocluster Probe for Tumor Cell Imaging and Killing

Overview
Journal Mikrochim Acta
Specialties Biotechnology
Chemistry
Date 2024 Aug 5
PMID 39103612
Authors
Affiliations
Soon will be listed here.
Abstract

A sequential dual-locked luminescent copper nanoclusters (CuNCs) probe was designed and synthesized for the specific imaging and selective killing of tumor cells. This nanoprobe was prepared by first forming a Fe-coupled tannic acid (TA)-stabilized CuNCs (CuNCs-Fe), which is in quenching state due to the electron transfer between CuNCs and Fe, and then coating a protectable layer of hyaluronic acid (HA) on the surface of CuNCs-Fe to form the final dual-locked nanoprobe (CuNCs-Fe@HA). When the nanoprobe of CuNCs-Fe@HA target enter the tumor cells through CD44-HA receptor, HAase will first digest the HA layer of the nanoprobes, and then, GSH over-expressed in tumor cells will reduce Fe to Fe, thus restoring the fluorescence emission of CuNCs and at the same time killing the tumor cells with the hydroxyl free radicals (∙OH) produced by the Fenton reaction between Fe and HO. This sequential dual-locked luminescent nanoprobe of CuNCs-Fe@HA has been successfully used for the specific imaging and selective killing of tumor cells.

References
1.
Fidler I, Yano S, Zhang R, Fujimaki T, Bucana C . The seed and soil hypothesis: vascularisation and brain metastases. Lancet Oncol. 2002; 3(1):53-7. DOI: 10.1016/s1470-2045(01)00622-2. View

2.
Adams A, Okagbare P, Feng J, Hupert M, Patterson D, Gottert J . Highly efficient circulating tumor cell isolation from whole blood and label-free enumeration using polymer-based microfluidics with an integrated conductivity sensor. J Am Chem Soc. 2008; 130(27):8633-41. PMC: 2526315. DOI: 10.1021/ja8015022. View

3.
Anderson N, Simon M . The tumor microenvironment. Curr Biol. 2020; 30(16):R921-R925. PMC: 8194051. DOI: 10.1016/j.cub.2020.06.081. View

4.
Michiels C, Tellier C, Feron O . Cycling hypoxia: A key feature of the tumor microenvironment. Biochim Biophys Acta. 2016; 1866(1):76-86. DOI: 10.1016/j.bbcan.2016.06.004. View

5.
Hu Q, Katti P, Gu Z . Enzyme-responsive nanomaterials for controlled drug delivery. Nanoscale. 2014; 6(21):12273-86. PMC: 4425417. DOI: 10.1039/c4nr04249b. View