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Gender Differences in Labetalol Kinetics: Importance of Determining Stereoisomer Kinetics for Racemic Drugs
Author(s) -
Johnson Julie A.,
Akers Wendell S.,
Herring Vanessa L.,
Wolfe Michael S.,
Sullivan Jay M.
Publication year - 2000
Publication title -
pharmacotherapy: the journal of human pharmacology and drug therapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.227
H-Index - 109
eISSN - 1875-9114
pISSN - 0277-0008
DOI - 10.1592/phco.20.7.622.35180
Subject(s) - labetalol , pharmacokinetics , crossover study , high performance liquid chromatography , dose , pharmacology , medicine , ambulatory , chemistry , blood pressure , chromatography , alternative medicine , pathology , placebo
Study Objective . To evaluate the impact of gender on labetalol kinetics. Design . Part of a randomized, crossover study. Setting . Academic medical center. Patients . Nineteen hypertensive patients (14 men, 5 women; 6 blacks, 13 whites). Interventions . Participants had labetalol dosages titrated to a specific antihypertensive response, then underwent ambulatory blood pressure monitoring (ABPM) and a pharmacokinetic study. Labetalol plasma concentrations were measured by high‐performance liquid chromatography (HPLC) and labetalol stereoisomer ratios were determined in a single plasma sample by chiral HPLC, both with fluorescence detection. Measurements and Main Results . Labetalol concentrations were 80% higher in women (area under the concentration‐time curve [AUC]/dose•1000: 6.79 ± 2.11 in women vs 3.82 ± 1.37 hr/L in men, p<0.05), yet both genders had a similar antihypertensive response by 24‐hour ABPM. Dose‐corrected AUC (AUC/dose•1000) for labetalol's stereoisomers in women and men, respectively, were S,R‐labetalol 7.55 ± 1.47 and 4.83 ± 1.54 hr/L (p<0.05), S,S‐labetalol 8.23 ± 2.93 and 4.65 ± 1.78 hr/L (p<0.05), R,S‐labetalol 6.99 ± 3.30 and 4.25 ± 2.35 hr/L (p= 0.11), and R,R‐labetalol 3.91 ± 2.57 and 3.55 ± 3.08 hr/L (NS). Conclusion . The higher labetalol concentration in women than in men was explained largely by differences in inactive and α 1 ‐blocking stereoisomers. However, concentrations were similar between genders for the (β‐blocking stereoisomer (R,R‐labetalol), possibly explaining the similarity in antihypertensive response to the drug. This study highlights the importance of determining stereoisomer kinetics for agents administered as racemates, particularly when relating concentrations to pharmacologic response.