The Determination of Labetalol in Plasma by High-performance Liquid Chromatography Using Fluorescence Detection
Overview
Toxicology
Authors
Affiliations
A sensitive and specific assay for labetalol is described. The method employed is reverse phase high-performance liquid chromatography (HPLC) with fluorescence detection. Using 1 ml of plasma, the limit of detection of the assay was 8 ng/ml and the coefficient of variation over a typical calibration range is 5.5%. Various drugs that might be coadministered with labetalol are shown not to interfere in the assay. The method has been employed to study the pharmacokinetics of labetalol following intravenous and oral administration.
Labetalol disposition and concentration-effect relationships during pregnancy.
Rubin P, Butters L, Kelman A, Fitzsimons C, Reid J Br J Clin Pharmacol. 1983; 15(4):465-70.
PMID: 6849783 PMC: 1427790. DOI: 10.1111/j.1365-2125.1983.tb01531.x.
McAreavey D, Ramsey L, Latham L, McLAREN A, LORIMER A, Reid J Br Med J (Clin Res Ed). 1984; 288(6411):106-11.
PMID: 6419809 PMC: 1443950. DOI: 10.1136/bmj.288.6411.106.
Elliott H, MEREDITH P, Sumner D, Reid J Br J Clin Pharmacol. 1984; 17(5):573-8.
PMID: 6145441 PMC: 1463447. DOI: 10.1111/j.1365-2125.1984.tb02392.x.
Elliott H, McLean K, MEREDITH P, Sumner D, Reid J Br J Clin Pharmacol. 1984; 17(5):565-72.
PMID: 6145440 PMC: 1463449. DOI: 10.1111/j.1365-2125.1984.tb02391.x.