Development of an Enzyme-Linked Immunosorbent Assay for the Quantification of Amiodarone

A sensitive and specific enzyme-linked immunosorbent assay for an antiarrhythmic drug, amiodarone (AMI), was developed, which is capable of measuring levels as low as 16 ng/ml. Anti-AMI antibody was obtained by immunizing rabbits with an antigen conjugated with bovine serum albumin using diazotized...

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Veröffentlicht in:Biological & pharmaceutical bulletin 2002, Vol.25(8), pp.954-958
Hauptverfasser: Saita, Tetsuya, Fujito, Hiroshi, Mori, Masato
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Fujito, Hiroshi
Mori, Masato
description A sensitive and specific enzyme-linked immunosorbent assay for an antiarrhythmic drug, amiodarone (AMI), was developed, which is capable of measuring levels as low as 16 ng/ml. Anti-AMI antibody was obtained by immunizing rabbits with an antigen conjugated with bovine serum albumin using diazotized 4-amino-1-(2-diethylaminoethoxy)-2,6-diiodobenzene. Enzyme labeling of AMI with β-D-galactosidase was similarly performed using a diazotized 4-amino-1-(2-diethylaminoethoxy)-2,6-diiodobenzene. This enzyme-linked immunosorbent assay was specific for AMI and showed a very slight cross-reactivity (1.25%) with its major metabolite, mono-N-desethylamiodarone. The values of the AMI concentrations measured by this assay were in good correlation to those by HPLC. Its analytical applicability was demonstrated by a kinetic study with human liver microsomes. The enzyme-linked immunosorbent assay should be a valuable tool in therapeutic drug monitoring and pharmacokinetic studies of AMI.
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Anti-AMI antibody was obtained by immunizing rabbits with an antigen conjugated with bovine serum albumin using diazotized 4-amino-1-(2-diethylaminoethoxy)-2,6-diiodobenzene. Enzyme labeling of AMI with β-D-galactosidase was similarly performed using a diazotized 4-amino-1-(2-diethylaminoethoxy)-2,6-diiodobenzene. This enzyme-linked immunosorbent assay was specific for AMI and showed a very slight cross-reactivity (1.25%) with its major metabolite, mono-N-desethylamiodarone. The values of the AMI concentrations measured by this assay were in good correlation to those by HPLC. Its analytical applicability was demonstrated by a kinetic study with human liver microsomes. The enzyme-linked immunosorbent assay should be a valuable tool in therapeutic drug monitoring and pharmacokinetic studies of AMI.</description><subject>amiodarone</subject><subject>Amiodarone - analysis</subject><subject>Amiodarone - chemistry</subject><subject>Amiodarone - metabolism</subject><subject>Analysis</subject><subject>Animals</subject><subject>antiarrhythmic drug</subject><subject>Antiarythmic agents</subject><subject>Biological and medical sciences</subject><subject>Cardiovascular system</subject><subject>ELISA</subject><subject>Enzyme-Linked Immunosorbent Assay - methods</subject><subject>Evaluation Studies as Topic</subject><subject>Female</subject><subject>General pharmacology</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Microsomes, Liver</subject><subject>Pharmacology. 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subjects amiodarone
Amiodarone - analysis
Amiodarone - chemistry
Amiodarone - metabolism
Analysis
Animals
antiarrhythmic drug
Antiarythmic agents
Biological and medical sciences
Cardiovascular system
ELISA
Enzyme-Linked Immunosorbent Assay - methods
Evaluation Studies as Topic
Female
General pharmacology
Humans
Medical sciences
Microsomes, Liver
Pharmacology. Drug treatments
Rabbits
title Development of an Enzyme-Linked Immunosorbent Assay for the Quantification of Amiodarone
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