State Key Laboratory of Food Science and Technology, National Centre for Technology Innovation on Fast Biological Detection of Grain Quality and Safety, School of Food Science and Technology, Jiangnan University, Wuxi 214122, China.
Safety & Quality Management Department, Inner Mongolia Mengniu Dairy (group) CO., LTD, Hohhot 011500, China.
J Agric Food Chem. 2022 Oct 5;70(39):12681-12688. doi: 10.1021/acs.jafc.2c03833. Epub 2022 Aug 29.
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 M 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.
通过使用基于 8-17 DNA zyme 的荧光酶联免疫吸附测定(ELISA),同时检测牛奶中的三种小分子污染物(抗生素、真菌毒素和激素)成为可能,其中 8-17 DNA zyme 被用作放大信号的催化酶。与传统 ELISA 中使用辣根过氧化物酶作为催化因子相比,基于 8-17 DNA 酶的 ELISA 可以实现多色信号输出,具有更低的检测限。氯霉素、17β-雌二醇和黄曲霉毒素 M 的线性范围分别为 0.3ng/mL-3μg/mL、3ng/mL-3μg/mL 和 3pg/mL-3ng/mL,定量限分别为 0.3ng/mL、3ng/mL 和 0.003ng/mL。该方案表明,8-17 DNA 酶可能是 ELISA 中辣根过氧化物酶的有效替代品,用于开发超灵敏和多色荧光免疫分析,这将刺激 ELISA 朝着新的方向发展。