Abstract
A sensitive and reliable HPLC method with fluorescence detection based on the precolumn derivatization of glucosamine with 6‐aminoquinolyl–N–hydroxylsuccinimidyl carbamate (AQC) was established for the quantitative determination of glucosamine in rat plasma. The plasma protein was precipitated by acetonitrile, followed by vortex mixing and centrifugation. The supernatant was divided into the organic layer and aqueous layer by adding sodium chloride, and then the aqueous layer was derivatized with AQC in 0.2 m borate buffer of pH 8.8 before the HPLC analysis. An amino acid analysis column (3.9 × 150 mm, 4 µm) was applied, with 140 mm sodium acetate buffer (pH = 5.25) and acetonitrile as mobile phase at a flow rate of 1 mL/min. A linear correlation coefficient of 0.9987 was calculated within the range of 0.1–30 µg/mL of the standard curve for glucosamine. The limit of detection was 30 ng/mL. The intra‐ and inter‐day precisions (as RSD) were less than 7.38 and 12.72%, respectively. The intra‐ and inter‐day accuracy ranged from 91.8 to 110.0%. Extraction recoveries of glucosamine in plasma were more than 90%. The validated method was successfully applied for the quantitative determination of glucosamine in rat plasma and evaluation for pharmacokinetic study of glucosamine. It was also possible to be applied for the quantitative determination of other compounds containing amino group in biological samples. Copyright © 2008 John Wiley & Sons, Ltd.