Journal of Immunoassay · 2000 · 45 citations · 17 references
PharmacyBiochemistryPharmacologyBiosensorsMolecular RecognitionMonoclonal AntibodiesAntibody CharacterizationAntibody ConjugatesAntibody ConjugationAntibody-antigen RecognitionAntibody-drug ConjugatesEnzyme-linked Immunosorbent AssayAntibody - Enzyme ConjugatesCross-reactivity Of Anti-drug AntibodiesCross-reactivity ScreeningEnzyme ImmunoassaysImmunoassay Cross-reactivityImmunoassaysPhosphate Buffer SystemReactivity
Antibody generated from ractopamine-hemiglutarate-KLH was used to develop a ractopamine ELISA. The antibody showed good sensitivity in phosphate buffer, with an IC50 of 4.2 ng/ml (ppb) toward ractopamine and 16.2 ng/ml toward glucuronides of ractopamine conjugated to the phenethanolamine phenol of ractopamine. Phenylbutylamine phenol glucuronides of the (RS, SR) ractopamine diastereoisomers showed about 4% cross-reactivity, but the glucuronide of the (RR, SS) diastereoisomers conjugated at the same phenolic group showed no detectable reactivity with the antibody. The antibody generally had cross-reactivity towards compounds with bis-phenylalkyl amine structures rather than compounds with simple branched N-alkyl substituents. For example, the antibody showed little or no cross reactivity towards clenbuterol, isoproterenol, metaproterenol, and salbutamol, but cross-reacted with dobutamine. The system demonstrated a matrix effect similar to other enzyme immunoassays, dilution of urine decreased but did not eliminate the matrix effect.
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Clenbuterol residues in non-liver containing meat as a cause of collective food poisoning.
V Sporano, Laura Grasso, Mauro Esposito et al. · PubMed · 1998 · 81 citations
Pharmacy, Pharmacology, Toxicology +13
Determination of fenoterol and ractopamine in urine by enzyme immunoassay
Willem Haasnoot, Piet Stouten, Arjen Lommen et al. · The Analyst · 1994 · 68 citations