A rapid, sensitive, precise and accurate high-performance liquid chromatographic assay with ultraviolet detection was developed for the determination of nalbuphine in human, rabbit, pig and dog plasma. It is comprised of only a one-step extraction procedure with hexane-isoamyl alcohol at pH 9.25 and reversed-phase chromatography on a μPorasil column. The recoveries of nalbuphine and ethylmorphine (internal standard) were greater than 86%. Calibration graphs were linear over the concentration range 0.75-150 ng/ml with a coefficient of variation, both within-day and between-day, of less than 10% at any level. The limit of quantitation was 0.75 ng/ml of plasma based on a signal-to-noise ratio of 3. Seven other clinically used analgesics were investigated to check for potential interferences and their analytical conditions. The specificity of this assay was checked with a metabolite of nalbuphine (noroxymorphine). Nalbuphine in plasma did not decompose significantly at -20°C for six weeks. Pharmacokinetic application in three surgical patients and four rabbits revealed that nalbuphine followed a linear three-compartment model with two distribution phases. The two distribution and one elimination half-lives and the plasma clearance of nalbuphine were 0.9, 5.8 and 157 min and 370 ml/min in human, and 3.5, 28 and 117 min and 21 166 ml/min in rabbits.
|頁（從 - 到）||289-296|
|期刊||Journal of Chromatography B: Biomedical Applications|
|出版狀態||已發佈 - 四月 12 1996|
ASJC Scopus subject areas
Ho, S. T., Wang, J. J., Hu, O. Y. P., Chiang, P. S., & Lee, S. C. (1996). Determination of nalbuphine by high-performance liquid chromatography with ultraviolet detection: Application to human and rabbit pharmacokinetic studies. Journal of Chromatography B: Biomedical Applications, 678(2), 289-296. https://doi.org/10.1016/0378-4347(95)00477-7