Reaction cell inductively coupled plasma mass spectrometry-based immunoassay using ferrocene tethered hydroxysuccinimide ester as label for the determination of 2,4-dichlorophenoxyacetic acid
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Deng, AP
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机构:Natl Sun Yat Sen Univ, Dept Chem, Kaohsiung 80424, Taiwan
Deng, AP
Liu, HT
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机构:Natl Sun Yat Sen Univ, Dept Chem, Kaohsiung 80424, Taiwan
Liu, HT
Jiang, SJ
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Natl Sun Yat Sen Univ, Dept Chem, Kaohsiung 80424, TaiwanNatl Sun Yat Sen Univ, Dept Chem, Kaohsiung 80424, Taiwan
Jiang, SJ
[1
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Huang, HJ
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机构:Natl Sun Yat Sen Univ, Dept Chem, Kaohsiung 80424, Taiwan
Huang, HJ
Ong, CW
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机构:Natl Sun Yat Sen Univ, Dept Chem, Kaohsiung 80424, Taiwan
Ong, CW
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[1] Natl Sun Yat Sen Univ, Dept Chem, Kaohsiung 80424, Taiwan
[2] Lanzhou Univ, Dept Chem, Lanzhou 730000, Peoples R China
The high sensitive dynamic reaction cell inductively coupled plasma mass spectrometry (DRC ICP-MS)-based immunoassay using ferrocene (Fc) tethered hydroxysuccinimide ester as label for the determination of 2,4-dichlorophenoxyacetic acid (2,4-D) was presented. Ferrocene tethered hydroxysuccinimide ester was directly or via horse radish peroxidase (HRP) as a bridge coupled to monoclonal antibody (mAb) of 2,4-D. Competitive immumoreactions were completed in microtiter plate and the signal of Fe-56 in the bound ferrocene labeled conjugate was detected by DRC ICP-MS. The potentially interfering (ArO+)-Ar-40-O-16 at the iron mass m/z 56 was reduced in intensity significantly by using NH3 as the reaction gas. The optimization process of the inummoassay was greatly simplified in the aid of enzyme linked immunosorbent assay (ELISA) procedure. The 2,4-D was determined in the dynamic range of 0.1-1000 ng/ml and the detection limits of the assays using the two ferrocene labeled conjugates were found to be 0.044 and 0.055 ng/ml, respectively. The relative standard deviation for six measurements were within 5.5-15.3%. (C) 2002 Elsevier Science B.V.(C) 2002 Elsevier Science B.V. All rights reserved.