Enantioselective immunoaffinity extraction for simultaneous determination of optically active bufuralol and its metabolites in human plasma by HPLC
Autor: | Ni Made Ria Isriyanthi, Youichi Kawashima, Kenji Matsuura, Takehiro Sato, Junichi Goto, Shinichi Miyairi, Hideo Takashina, Shigeo Ikegawa, Toshifumi Niwa |
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Rok vydání: | 1998 |
Předmět: |
Metabolite
Adrenergic beta-Antagonists Clinical Biochemistry Serum albumin Pharmaceutical Science High-performance liquid chromatography Chromatography Affinity Analytical Chemistry chemistry.chemical_compound Drug Discovery Humans Chromatography High Pressure Liquid Spectroscopy Chromatography biology Elution Immune Sera Bufuralol Extraction (chemistry) Reproducibility of Results Stereoisomerism chemistry Ethanolamines biology.protein Quantitative analysis (chemistry) Ammonium acetate |
Zdroj: | Journal of Pharmaceutical and Biomedical Analysis. 17:1-9 |
ISSN: | 0731-7085 |
DOI: | 10.1016/s0731-7085(97)00147-7 |
Popis: | A combined method of immunoaffinity extraction with high-performance liquid chromatography has been developed for the enantioselective determination of bufuralol and its metabolites in human plasma. The antibodies having high affinity toward the asymmetric center at the C-1 position of bufuralol and its 1′-oxidized metabolites and low affinity to their antipodes were elicited by immunization of rabbits with immunogens, (1 R )- and (1 S )-1′-oxobufuralol O -carboxymethyl oxime-bovine serum albumin conjugates, respectively. 0.5 ml Of the immunoaffinity adsorbent (7.6 mg·ml −1 for anti-(1 S )-antibody and 28.8 mg·ml −1 for anti-(1 R )-antibody) prepared by immobilization of an antibody was capable of retaining up to 1 μg of ( R )- and ( S )-bufuralol and up to 500 ng of other metabolites. The adsorbates were recovered quantitatively by elution with methanol–10 mM ammonium acetate buffer (pH 5) (95:5, v/v) without any interfering peaks on the high-performance liquid chromatogram. The proposed method was evaluated to be useful for the simultaneous determination of optically active bufuralol and its metabolite in plasma with acceptable recovery and precision. |
Databáze: | OpenAIRE |
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