Abstract
A simple and rapid high-performance liquid chromatographic method has been developed for determination in human plasma of isepamicin (ISP), an aminoglycoside antibiotic agent. After protein precipitation and clean-up procedure to remove lipophilic contaminants, ISP is derivatized pre-column with 6-aminoquinolyl-N-hydroxysuccinimidyl-carbamate for fluorescence detection. Chromatographic separations are achieved using C18 column and mobile phase consisting of 20 mm KH2PO4 containing 8 mm triethylamine (pH 7.0) and acetonitrile (78/22, v/v). Amikacin was used as an internal standard. The calibration curve was linear over a concentration range of 0.5-50 μg/ml. The limit of quantification was 0.5 μg/ml. The intra- and inter-day variabilities of ISP were both less than 17.5%. Both derivatives were stable for at least a week at ambient condition. This assay procedure should have useful application in therapeutic drug monitoring of ISP. © 2008 Pharmaceutical Society of Japan.
Author supplied keywords
Cite
CITATION STYLE
Hosokawa, S., Nakamura, K., Fujita, Y., Horiuchi, R., & Yamamoto, K. (2008). Determination of isepamicin in human plasma by HPLC with fluorescence detection after derivatization using 6-aminoquinolyl/-N-hydroxysuccinimidyl- carbamate. Biological and Pharmaceutical Bulletin, 31(10), 1866–1869. https://doi.org/10.1248/bpb.31.1866
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.