辣根过氧化物酶
脱氧核酶
化学
检出限
色谱法
免疫分析
黄曲霉毒素
酶
真菌毒素
过氧化物酶
荧光
生物化学
生物
食品科学
抗体
量子力学
物理
免疫学
作者
Panting Sang,Gang Lu,Dongwei Yu,Xiaodong Song,Yahui Guo,Yunfei Xie,Weirong Yao,Qian He,Zhigang Hu
标识
DOI:10.1021/acs.jafc.2c03833
摘要
The simultaneous detection of three kinds of small-molecule contaminants (antibiotics, mycotoxins, and hormones) in milk was realized by using an 8-17 DNAzyme-based fluorescent enzyme-linked immunosorbent assay (ELISA), in which 8-17 DNAzyme was utilized as the catalytic enzyme for amplifying the signal. Compared with the conventional ELISA in which horseradish peroxidase is used as the catalyzing factor, this 8-17 DNAzyme-based ELISA could achieve multicolor signal output with lower detection limits. The linearities for chloramphenicol, 17β-estradiol, and aflatoxin M1 were in the range of 0.3 ng/mL-3 μg/mL, 3 ng/mL-3 μg/mL, and 3 pg/mL-3 ng/mL with quantitation limits of 0.3, 3, and 0.003 ng/mL, respectively. This proposed scheme demonstrated that the 8-17 DNAzyme might be an effective substitute for horseradish peroxidase in ELISA for the development of ultrasensitive and multicolor fluorescence immunoassay, which would stimulate the development of ELISA in a new orientation.
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