% IMPORTANT: The following is UTF-8 encoded. This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.
@ARTICLE{Li:1005796,
author = {Li, Yongqiang and Shi, Zhifeng and Shang, Liuyang and Tao,
Quan and Tang, Qisheng and Krause, Hans-Joachim and Yang,
Siwei and Ding, Guqiao and Dong, Hui},
title = {{G}raphene quantum dots-based magnetic relaxation switch
involving magnetic separation for enhanced performances of
endoglin detection using ultra-low-field nuclear magnetic
resonance relaxometry},
journal = {Sensors and actuators / B},
volume = {380},
issn = {0925-4005},
address = {Amsterdam [u.a.]},
publisher = {Elsevier Science},
reportid = {FZJ-2023-01641},
pages = {133389 -},
year = {2023},
abstract = {Magnetic relaxation switches (MRS) based on target-induced
state changes of magnetic nanoparticles are vital approaches
for biomolecule detection in in vitro diagnosis. Recently,
magnetic graphene quantum dots have been employed as
magnetic probes instead of iron oxide nanoparticles and
showed high sensitivity. Introducing magnetic separation
into an MRS assay before the relaxometry measurements can
enhance the sensitivity, elevateaccuracy, and expand the
linear region. In this work, magnetic separation-assisted
MRS was developed to detect endoglin utilizing iron oxide as
the magnetic carrier and magnetic graphene quantum dots as
the magnetic probe. The assay possesses a broad linear
region from 5 ng/mL to 50 μg/mL and a sensitive limit of
detection of 1.3 ng/mL, which is two orders of magnitude
lower than that of MRS without magnetic separation. The high
accuracy and consistency have been proved for endoglin
(CD105) detection in real samples. This graphene quantum
dotbased MRS involving magnetic separation provides a new
route for enhancing the sensitivity and accuracy of
biomolecule detection.},
cin = {IBI-3},
ddc = {620},
cid = {I:(DE-Juel1)IBI-3-20200312},
pnm = {5241 - Molecular Information Processing in Cellular Systems
(POF4-524)},
pid = {G:(DE-HGF)POF4-5241},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000979418700001},
doi = {10.1016/j.snb.2023.133389},
url = {https://juser.fz-juelich.de/record/1005796},
}