Determination of thyroxine enantiomers in pharmaceutical formulation by high-performance liquid chromatography-mass spectrometry with precolumn derivatization |
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Authors: | Dongri Jin Avvaru Praveen Kumar Yong-Ill Lee |
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Affiliation: | a Department of Chemistry, Changwon National University, Changwon 641-773, South Korea b Key Laboratory of Organism Functional Factors of the Changbai Mountain (Yanbian University), Ministry of Education, Yanji 133002, China |
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Abstract: | A sensitive and specific liquid chromatography-electrospray ionization-mass spectrometry (LC-ESI-MS) method for the separation and analysis of d- and l-thyroxine was developed using R(−)/S(+)-4-(3-isothiocyanatopyrrolidin-1-yl)-7-(N,N-dimethylaminosulfonyl-2,1,3-benzoxadiazole, [R(−)/S(+)-DBD-PyNCS] as a chiral derivatization reagents. The T4 derivatives with R(−)-DBD-PyNCS were efficiently separated on a reversed-phase column with water-acetonitrile containing 0.1% formic acid (41:59, v/v) as the eluent and analyzed using ESI-MS with negative selected ion monitoring (SIM) mode. The calibration curves of both the d-T4 and l-T4 were linear over the concentration range of 0.13-13 μg/ml. The detection limits (S/N = 3) were 28 ng/ml for d-T4 and 40 ng/ml for l-T4, respectively. The relative standard deviations (RSD, n = 5) were less than 3.6% at 1.3 μg/ml for both T4 enantiomers. The proposed method was applied to the determination of l-T4 enantiomer in a pharmaceutical formulation. |
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Keywords: | Chiral tagging reagent Precolumn derivatization Thyroxine enantiomers LC-ESI-MS |
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