TY - JOUR
T1 - Enhanced carbon quantum dots-based chemiluminescence probes for copper ion detection in human plasma and urine
AU - Lee, Seul Yi
AU - Sim, Nicole
AU - Gautam, Jagadis
AU - Kim, Young Teck
AU - Park, Soo Jin
AU - Lee, Ji Hoon
N1 - Publisher Copyright:
© 2025
PY - 2025/9/20
Y1 - 2025/9/20
N2 - Nitrogen-doped carbon quantum dots (N-CQDs), synthesized via the rapid pyrolysis of ammonium citrate dibasic and ethylenediamine dihydrochloride, demonstrate remarkable chemiluminescence capabilities, emitting a vibrant blue-green light in peroxyoxalate chemiluminescence (PO-CL) reactions. Among these, a distinct variant of N-CQDs is an exceptionally sensitive biosensor, facilitating the swift detection of copper ions (Cu2+) within human plasma and urine samples. Upon rapid binding of N-CQDs and Cu2+, non-emissive complex forms due to intra-chemiluminescence resonance energy transfer (intra-CRET) initiated by the PO-CL reaction. Consequently, the brightness of the biosensor diminishes proportionally with increasing Cu2+ concentrations in human samples. Featuring a low sensing limit of 19.5 nM and an expansive dynamic range spanning from 0.05 to 3.8 µM, this biosensor empowers the rapid and precise quantification of trace Cu2+ levels with exceptional accuracy and recovery rates. In alignment with copper quantification guidelines set forth by the Environmental Protection Agency (EPA) and the National Institutes of Health (NIH), this selective biosensor stands as a cutting-edge monitoring tool, poised to advance analytical capabilities in various fields.
AB - Nitrogen-doped carbon quantum dots (N-CQDs), synthesized via the rapid pyrolysis of ammonium citrate dibasic and ethylenediamine dihydrochloride, demonstrate remarkable chemiluminescence capabilities, emitting a vibrant blue-green light in peroxyoxalate chemiluminescence (PO-CL) reactions. Among these, a distinct variant of N-CQDs is an exceptionally sensitive biosensor, facilitating the swift detection of copper ions (Cu2+) within human plasma and urine samples. Upon rapid binding of N-CQDs and Cu2+, non-emissive complex forms due to intra-chemiluminescence resonance energy transfer (intra-CRET) initiated by the PO-CL reaction. Consequently, the brightness of the biosensor diminishes proportionally with increasing Cu2+ concentrations in human samples. Featuring a low sensing limit of 19.5 nM and an expansive dynamic range spanning from 0.05 to 3.8 µM, this biosensor empowers the rapid and precise quantification of trace Cu2+ levels with exceptional accuracy and recovery rates. In alignment with copper quantification guidelines set forth by the Environmental Protection Agency (EPA) and the National Institutes of Health (NIH), this selective biosensor stands as a cutting-edge monitoring tool, poised to advance analytical capabilities in various fields.
KW - Biosensor
KW - Chemiluminescence resonance energy transfer (CRET)
KW - Nitrogen-doped carbon quantum dots (N-CQDs)
KW - Peroxyoxalate chemiluminescence (PO-CL)
KW - Photoluminescence
UR - https://www.scopus.com/pages/publications/86000358946
U2 - 10.1016/j.jmst.2025.02.005
DO - 10.1016/j.jmst.2025.02.005
M3 - Article
AN - SCOPUS:86000358946
SN - 1005-0302
VL - 230
SP - 177
EP - 185
JO - Journal of Materials Science and Technology
JF - Journal of Materials Science and Technology
ER -