Development of a Highly Sensitive Biotin-Streptavidin Amplified Enzyme-Linked Immunosorbent Assay for Determination of Progesterone in Milk Samples
Autor: | Xiping Cui, Yingying Zhong, Jinfeng Yan, Suqing Zhao, Junkang Pan, Jinlong Ding, Tiantian Wang, Lu Minglei, Liang Minting, Chunguo Zhang |
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Rok vydání: | 2021 |
Předmět: |
Detection limit
Streptavidin Chromatography medicine.diagnostic_test Chemistry Coefficient of variation Contamination Tandem mass spectrometry Applied Microbiology and Biotechnology Analytical Chemistry chemistry.chemical_compound Biotin Linear range Immunoassay medicine Safety Risk Reliability and Quality Safety Research Food Science |
Zdroj: | Food Analytical Methods. 15:541-551 |
ISSN: | 1936-976X 1936-9751 |
Popis: | Agricultural product contamination by endocrine-disrupting compounds (EDCs) residues is an international public health issue and requires continuously stringent administration. A high-throughput biotin-streptavidin-amplified enzyme-linked immunosorbent assay (BA-ELISA) for detection of progesterone (P4) has been established to be applied in determining milk samples. Under experimental optimization, BA-ELISA based on anti-P4-specific antibody (P4-pAb-based BA-ELISA) showed a linear range from 0.44 to 31.06 ng/mL. The IC50 was 3.68 ng/mL, and the limit of detection (LOD) was 1.25 × 10−1 ng/mL, with negligible cross-reactivities on structural P4 analogues. The signal amplification system enhanced sensitivity on account of strongly supramolecular affinity between biotin and streptavidin. Good recoveries ranged from 87.81 to 113.11%, and low coefficient of variation (below 9.75%) of the immunoassay validated the feasibility and applicability to monitor P4 in milk samples. Milk samples with different spiked levels were tested by both the established P4-pAb-based BA-ELISA and liquid chromatography-electrospray tandem mass spectrometry (LC-MS/MS). Our results, combined with the advantages of specific antibodies, elucidated that P4-pAb-based BA-ELISA is an applicable method for routine screening analysis of P4. |
Databáze: | OpenAIRE |
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