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Population Pharmacokinetics of Intravenous Methadone Enantiomers in Adults: A Comprehensive Model.

Publication ,  Journal Article
Henthorn, TK; Kharasch, ED
Published in: Clinical pharmacology and therapeutics
March 2026

Methadone is a utilitarian opioid with growing use for anesthesia and postoperative pain. Methadone pharmacokinetic models have evolved over time; however, there is no comprehensive population pharmacokinetic model. This investigation developed a population model for R(-)- and S(+)-enantiomers of methadone and the primary metabolite 2-ethyl-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP) in plasma and urine, incorporating enantiomeric disposition, metabolism, genetics, renal elimination, and frequent and long-duration sampling, to adequately describe both distribution and elimination. In this secondary analysis of previously obtained data from 64 adults sampled for 96 hours, a compartmental model utilizing eight distinct measurement categories of drug and metabolite concentration that unified enantiomer kinetics was developed using nonlinear mixed effects techniques. Potential model covariates for weight, race, sex, CYP2B6 genetics, and CYP2C19 genetics were tested. The final unified three-compartment population model accounted for significant and systematic enantiomer-specific differences in volumes of distribution, intercompartmental and elimination clearances between R(-)- and S(+)-methadone, by estimating S(+)/R(-) ratios. The model incorporated weight and CYP2B6 genotype but not CYP2C19 genotype, sex or race as covariates. Intersubject variability was consistent with that of other intravenous opioids. S(+)/R(-) ratios were consistent with known enantiomeric differences in α1-acid glycoprotein binding and in vitro biotransformation, and disposition was explainable by enantiomeric restrictive plasma protein binding effects on drug distribution, pharmacokinetic flow, and intrinsic hepatic clearance (CYP2B6-catalyzed metabolism). The population model may be applicable to pharmacokinetically guided intravenous methadone dosing and CYP2B6-mediated drug interactions in perioperative and critical care settings.

Duke Scholars

Published In

Clinical pharmacology and therapeutics

DOI

EISSN

1532-6535

ISSN

0009-9236

Publication Date

March 2026

Volume

119

Issue

3

Start / End Page

739 / 750

Related Subject Headings

  • Young Adult
  • Stereoisomerism
  • Pyrrolidines
  • Pharmacology & Pharmacy
  • Models, Biological
  • Middle Aged
  • Methadone
  • Male
  • Humans
  • Genotype
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Henthorn, T. K., & Kharasch, E. D. (2026). Population Pharmacokinetics of Intravenous Methadone Enantiomers in Adults: A Comprehensive Model. Clinical Pharmacology and Therapeutics, 119(3), 739–750. https://doi.org/10.1002/cpt.70147
Henthorn, Thomas K., and Evan D. Kharasch. “Population Pharmacokinetics of Intravenous Methadone Enantiomers in Adults: A Comprehensive Model.Clinical Pharmacology and Therapeutics 119, no. 3 (March 2026): 739–50. https://doi.org/10.1002/cpt.70147.
Henthorn TK, Kharasch ED. Population Pharmacokinetics of Intravenous Methadone Enantiomers in Adults: A Comprehensive Model. Clinical pharmacology and therapeutics. 2026 Mar;119(3):739–50.
Henthorn, Thomas K., and Evan D. Kharasch. “Population Pharmacokinetics of Intravenous Methadone Enantiomers in Adults: A Comprehensive Model.Clinical Pharmacology and Therapeutics, vol. 119, no. 3, Mar. 2026, pp. 739–50. Epmc, doi:10.1002/cpt.70147.
Henthorn TK, Kharasch ED. Population Pharmacokinetics of Intravenous Methadone Enantiomers in Adults: A Comprehensive Model. Clinical pharmacology and therapeutics. 2026 Mar;119(3):739–750.
Journal cover image

Published In

Clinical pharmacology and therapeutics

DOI

EISSN

1532-6535

ISSN

0009-9236

Publication Date

March 2026

Volume

119

Issue

3

Start / End Page

739 / 750

Related Subject Headings

  • Young Adult
  • Stereoisomerism
  • Pyrrolidines
  • Pharmacology & Pharmacy
  • Models, Biological
  • Middle Aged
  • Methadone
  • Male
  • Humans
  • Genotype