Alcohol Exposure Rate Control Through Physiologically Based Pharmacokinetic Modeling

Martin H. Plawecki, Ulrich S. Zimmermann, Victor Vitvitskiy, Peter C. Doerschuk, David Crabb, Sean O'Connor

Research output: Contribution to journalArticle

10 Citations (Scopus)

Abstract

Background: The instantaneous rate of change of alcohol exposure (slope) may contribute to changes in measures of brain function following administration of alcohol that are usually attributed to breath alcohol concentration (BrAC) acting alone. To test this proposition, a 2-session experiment was designed in which carefully prescribed, constant-slope trajectories of BrAC intersected at the same exposure level and time since the exposure began. This paper presents the methods and limitations of the experimental design. Methods: Individualized intravenous infusion rate profiles of 6% ethanol (EtOH) that achieved the constant-slope trajectories for an individual were precomputed using a physiologically based pharmacokinetic model. Adjusting the parameters of the model allowed each infusion profile to account for the subject's EtOH distribution and elimination kinetics. Sessions were conducted in randomized order and made no use of feedback of BrAC measurements obtained during the session to modify the precalculated infusion profiles. In one session, an individual's time course of exposure, BrAC(t), was prescribed to rise at a constant rate of 6.0 mg% per minute until it reached 68 mg% and then descend at -1.0 mg% per minute; in the other, to rise at a rate of 3.0 mg% per minute. The 2 exposure trajectories were designed to intersect at a BrAC (t = 20 minutes) = 60 mg% at an experimental time of 20 minutes. Results: Intersection points for 54 of 61 subjects were within prescribed deviations (range of ±3 mg% and ±4 minutes from the nominal intersection point). Conclusions: Results confirmed the feasibility of applying the novel methods for achieving the intended time courses of the BrAC, with technical problems limiting success to 90% of the individuals tested.

Original languageEnglish
Pages (from-to)530-542
Number of pages13
JournalAlcoholism: Clinical and Experimental Research
Volume36
Issue number6
DOIs
StatePublished - Jun 2012

Fingerprint

Pharmacokinetics
Alcohols
Trajectories
Intravenous Infusions
Design of experiments
Brain
Research Design
Ethanol
Feedback
Kinetics

Keywords

  • Acute Tolerance
  • Alcohol
  • Biphasic Effects
  • Brain Exposure
  • Physiologically Based Pharmacokinetic Models
  • Rate of Change

ASJC Scopus subject areas

  • Medicine (miscellaneous)
  • Psychiatry and Mental health
  • Toxicology

Cite this

Alcohol Exposure Rate Control Through Physiologically Based Pharmacokinetic Modeling. / Plawecki, Martin H.; Zimmermann, Ulrich S.; Vitvitskiy, Victor; Doerschuk, Peter C.; Crabb, David; O'Connor, Sean.

In: Alcoholism: Clinical and Experimental Research, Vol. 36, No. 6, 06.2012, p. 530-542.

Research output: Contribution to journalArticle

Plawecki, Martin H. ; Zimmermann, Ulrich S. ; Vitvitskiy, Victor ; Doerschuk, Peter C. ; Crabb, David ; O'Connor, Sean. / Alcohol Exposure Rate Control Through Physiologically Based Pharmacokinetic Modeling. In: Alcoholism: Clinical and Experimental Research. 2012 ; Vol. 36, No. 6. pp. 530-542.
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abstract = "Background: The instantaneous rate of change of alcohol exposure (slope) may contribute to changes in measures of brain function following administration of alcohol that are usually attributed to breath alcohol concentration (BrAC) acting alone. To test this proposition, a 2-session experiment was designed in which carefully prescribed, constant-slope trajectories of BrAC intersected at the same exposure level and time since the exposure began. This paper presents the methods and limitations of the experimental design. Methods: Individualized intravenous infusion rate profiles of 6{\%} ethanol (EtOH) that achieved the constant-slope trajectories for an individual were precomputed using a physiologically based pharmacokinetic model. Adjusting the parameters of the model allowed each infusion profile to account for the subject's EtOH distribution and elimination kinetics. Sessions were conducted in randomized order and made no use of feedback of BrAC measurements obtained during the session to modify the precalculated infusion profiles. In one session, an individual's time course of exposure, BrAC(t), was prescribed to rise at a constant rate of 6.0 mg{\%} per minute until it reached 68 mg{\%} and then descend at -1.0 mg{\%} per minute; in the other, to rise at a rate of 3.0 mg{\%} per minute. The 2 exposure trajectories were designed to intersect at a BrAC (t = 20 minutes) = 60 mg{\%} at an experimental time of 20 minutes. Results: Intersection points for 54 of 61 subjects were within prescribed deviations (range of ±3 mg{\%} and ±4 minutes from the nominal intersection point). Conclusions: Results confirmed the feasibility of applying the novel methods for achieving the intended time courses of the BrAC, with technical problems limiting success to 90{\%} of the individuals tested.",
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