Pharmacokinetics, bioavailability and opioid effects of liquid versus tablet buprenorphine

Drug Alcohol Depend. 2006 Mar 15;82(1):25-31. doi: 10.1016/j.drugalcdep.2005.08.005. Epub 2005 Sep 6.

Abstract

Aims: Two tablet formulations of buprenorphine (a buprenorphine mono-product, Subutex, and a buprenorphine/naloxone combination product, Suboxone) are available for use in the treatment of opioid addiction; however, the bulk of the clinical studies supporting its approval by the US Food and Drug Administration (FDA) were conducted with a sublingual liquid preparation. To assist the clinician in interpreting the relevant literature in establishing dosing parameters for prescription of tablet buprenorphine, this study was designed to compare the steady state: (1) pharmacokinetics and bioavailability, and (2) physiological, subjective and objective opiate effects of two 8 mg buprenorphine tablets (16 mg) to those of 1 ml (8 mg/ml) buprenorphine solution based upon early reports suggesting that the bioavailability of the tablet was approximately 50% of that of the liquid.

Design: Randomized, open-label, two-way crossover study.

Setting: Inpatient hospitalization for 21 days.

Participants: Twenty-four male and females in general good health and meeting DSM-IV criteria for opiate dependence.

Intervention: Subjects received one of the two buprenorphine formulations in the first 10-day period, and the other for the second 10-day period with no washout.

Measurements: Pharmacokinetic analyses, opiate effects and adverse events.

Findings: Drug steady state was reached by Day 7 of each 10-day period, area under the curve for 16 mg (two 8 mg) tablets was higher than the solution. The only non-kinetic statistically significant difference observed between the formulations was in changes in total opioid agonist score.

Conclusions: The serum concentration achieved by 16 mg of tablet buprenorphine is higher than that of the 8 mg solution, although differences between physiologic, subjective and objective opioid effects were not noted. The relative bioavailability of tablet versus solution is estimated to be 0.71; thus, with respect to dosing parameters for the tablet, clinicians should consider using less than 16 mg to achieve bioequivalence to the 8 mg solution.

Publication types

  • Randomized Controlled Trial
  • Research Support, N.I.H., Extramural

MeSH terms

  • Adult
  • Biological Availability
  • Buprenorphine / administration & dosage
  • Buprenorphine / pharmacokinetics*
  • Buprenorphine / therapeutic use*
  • Cross-Over Studies
  • Dosage Forms
  • Drug Administration Routes
  • Female
  • Humans
  • Male
  • Narcotic Antagonists / administration & dosage
  • Narcotic Antagonists / pharmacokinetics*
  • Narcotic Antagonists / therapeutic use*
  • Opioid-Related Disorders / drug therapy*

Substances

  • Dosage Forms
  • Narcotic Antagonists
  • Buprenorphine