Competitive Protein-binding Radioassay of Thiamine in Simple Solutions and in Multivitamin Pharmaceuticals

Author:

Kozik Andrzej1,Wróabel Radoslawa1,Turyna Izabela1

Affiliation:

1. Jagiellonian University, Institute of Molecular Biology, Al. Mickiewicza 3, 31-120 Kraków, Poland

Abstract

Abstract A competitive inhibition radioassay of thiamine is described using a gel obtained by coupling a buckwheat-seed thiamine-binding protein to CNBr-activated Sepharose. The sample to be analysed is incubated with gel suspension and [14C]thiamine and after centrifugation the radioactivity of the supernatant is measured. The method is simple and specific, and applicable over a thiamine concentration range 0.5-5 μM with a coefficient of variation typically below 5%. The gel is reusable and stable for several months. Applicability of the method for direct determination of thiamine in multivitamin pharmaceuticals is demonstrated.

Publisher

Oxford University Press (OUP)

Subject

Pharmaceutical Science,Pharmacology

Reference13 articles.

1. Acid dye method for the analysis of thiamine;Das Gupta,1970

2. Evaluation of internal standards and extraction solvents in the gas chromatographic determination of thiamine;Echols;J. Chromatogr.,1985

3. Thiamin;Ellefson,1985

4. A new liquid membrane electrode for determination of vitamin B1 in multivitamin preparations;Hassan;Fraesenius Z. Anal. Chem.,1985

5. Vitamin B12 and folacin radioassays in blood serum;Herbert,1985

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