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基于金纳米簇@胃蛋白酶@鲁米诺的新型灵敏化学发光免疫分析法用于同时检测四溴双酚 A 双(2-羟乙基)醚和四溴双酚 A 单(2-羟乙基)醚。

A novel and sensitive chemiluminescence immunoassay based on AuNCs@pepsin@luminol for simultaneous detection of tetrabromobisphenol A bis(2-hydroxyethyl) ether and tetrabromobisphenol A mono(hydroxyethyl) ether.

机构信息

School of the Environment and Safety Engineering, Jiangsu University, Zhenjiang 212013, China.

School of the Environment and Safety Engineering, Jiangsu University, Zhenjiang 212013, China.

出版信息

Anal Chim Acta. 2018 Dec 4;1035:168-174. doi: 10.1016/j.aca.2018.06.039. Epub 2018 Jun 15.

DOI:10.1016/j.aca.2018.06.039
PMID:30224136
Abstract

A novel chemiluminescence immunoassay based on luminol-modified gold nanoclusters (AuNCs@Peps@luminol) was developed for simultaneous detection of tetrabromobisphenol A bis(2-hydroxyethyl) ether (TBBPA-DHEE) and tetrabromobisphenol A mono(hydroxyethyl) ether (TBBPA-MHEE), an important derivative and byproduct of tetrabromobisphenol A (TBBPA), respectively. In the system, alkaline phosphatase (ALP) was labeled on the second antibody (Ab) for signal amplification. When ALP-Ab was captured by antigen-primary antibody (Ab) complex, disodium phenyl phosphate (PPNa) generated massive phenol under the catalysis of ALP, markedly inhibiting the chemiluminescence intensity of AuNCs@Peps@luminol. Under the optimized conditions, the calculated detection of limit (LOD, 90% inhibition) was 0.078 μg/L for TBBPA-DHEE with a linear range of 0.23-9.32 μg/L, which was lower 9 times than that of conventional ELISA with the same antibody. In addition, our method showed satisfactory accuracy and precision (recoveries, 88.00-113.4%; CV, 2.75-8.14%), it can be applied to systematically investigate the concentration of the trace TBBPA-DHEE and TBBPA-MHEE in environmental and food samples.

摘要

基于鲁米诺修饰的金纳米簇(AuNCs@Peps@luminol)的新型化学发光免疫分析被开发用于同时检测四溴双酚 A 双(2-羟乙基)醚(TBBPA-DHEE)和四溴双酚 A 单(2-羟乙基)醚(TBBPA-MHEE),它们分别是四溴双酚 A(TBBPA)的重要衍生物和副产物。在该体系中,碱性磷酸酶(ALP)被标记在第二抗体(Ab)上用于信号放大。当 ALP-Ab 被抗原-一抗(Ab)复合物捕获时,在 ALP 的催化下,大量的酚被生成,显著抑制了 AuNCs@Peps@luminol 的化学发光强度。在优化条件下,TBBPA-DHEE 的计算检测限(LOD,90%抑制)为 0.078μg/L,线性范围为 0.23-9.32μg/L,比相同抗体的常规 ELISA 低 9 倍。此外,我们的方法表现出令人满意的准确性和精密度(回收率,88.00-113.4%;CV,2.75-8.14%),可用于系统地研究环境和食品样品中痕量 TBBPA-DHEE 和 TBBPA-MHEE 的浓度。

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