TY - JOUR
T1 - A novel bioassay based on aptamer-functionalized magnetic nanoparticle for the detection of zearalenone using time resolved-fluorescence NaYF4
T2 - Ce/Tb nanoparticles as signal probe
AU - Niazi, Sobia
AU - Wang, Xiaole
AU - Pasha, Imran
AU - Khan, Imran Mahmood
AU - Zhao, Sen
AU - Shoaib, Muhammad
AU - Wu, Shijia
AU - Wang, Zhouping
N1 - Publisher Copyright:
© 2018 Elsevier B.V.
PY - 2018/8/15
Y1 - 2018/8/15
N2 - Zearalenone (ZEN) is a non-steroidal estrogenic mycotoxin produced by fungi on stored grains. The earlier detection methods used for ZEN rely on expensive equipment, time-consuming sample preparation and temperature sensitive antibodies. The current work, proposed a novel strategy based on ZEN aptamer labeled with amine-functionalized magnetic nanoparticle (MNPs) as a capture probe and time-resolved fluorescence (TRFL) nanoparticles labeled with complementary DNA (cDNA) as a signal probe. Under the optimized conditions, TRFL intensity at 544 nm was used to measure ZEN (R2 = 0.9920) in the range of 0.001–10 ng mL−1 and limits of detection (LOD) for proposed method was 0.21 pg mL−1. The specificity of bioassay was also determined by using other mycotoxins (OTA, AFB2, DON and Patulin) and results showed that the aptamer are specific to recognize only ZEN. The analytical applications of the present bioassay in maize and wheat samples were also examined and results were compared with existing methods. Based on these findings, it is suggested to use current rapid and simple bioassay for the determination of ZEN in food and agricultural products.
AB - Zearalenone (ZEN) is a non-steroidal estrogenic mycotoxin produced by fungi on stored grains. The earlier detection methods used for ZEN rely on expensive equipment, time-consuming sample preparation and temperature sensitive antibodies. The current work, proposed a novel strategy based on ZEN aptamer labeled with amine-functionalized magnetic nanoparticle (MNPs) as a capture probe and time-resolved fluorescence (TRFL) nanoparticles labeled with complementary DNA (cDNA) as a signal probe. Under the optimized conditions, TRFL intensity at 544 nm was used to measure ZEN (R2 = 0.9920) in the range of 0.001–10 ng mL−1 and limits of detection (LOD) for proposed method was 0.21 pg mL−1. The specificity of bioassay was also determined by using other mycotoxins (OTA, AFB2, DON and Patulin) and results showed that the aptamer are specific to recognize only ZEN. The analytical applications of the present bioassay in maize and wheat samples were also examined and results were compared with existing methods. Based on these findings, it is suggested to use current rapid and simple bioassay for the determination of ZEN in food and agricultural products.
KW - Aptamer
KW - Bioassay
KW - Magnetic nanoparticles
KW - Time-resolved fluorescence nanoparticles
KW - Zearalenone
UR - http://www.scopus.com/inward/record.url?scp=85046162794&partnerID=8YFLogxK
U2 - 10.1016/j.talanta.2018.04.013
DO - 10.1016/j.talanta.2018.04.013
M3 - Article
C2 - 29784425
AN - SCOPUS:85046162794
SN - 0039-9140
VL - 186
SP - 97
EP - 103
JO - Talanta
JF - Talanta
ER -