Placental transfer of rosiglitazone in the ex vivo human perfusion model

Am J Obstet Gynecol. 2006 Dec;195(6):1715-9. doi: 10.1016/j.ajog.2006.03.054. Epub 2006 May 16.

Abstract

Objective: The objective of the study was to determine transplacental passage of rosiglitazone (Avandia) using the ex vivo human placental model.

Study design: Perfusion studies were performed on 10 placentas from term, uncomplicated deliveries. Concentrations typical for an 8-mg oral dose (216 to 692 ng/mL) as well as 2- to 3-fold increased concentrations were tested (734 to 1261 ng/mL). Transfer of rosiglitazone was assessed and accumulation was determined using the 14C-antipyrine reference method.

Results: The clearance index for low and high concentrations were 0.14 +/- 0.04 and 0.20 +/- 0.08, suggesting that the drug passes through the placenta at a relatively low rate. Fetal accumulation occurred in only 1 of 5 placentas at 16.4 ng/mL (5%) for the 8-mg dose and in 2 of 5 placentas ranging from 0 to 74 ng/mL (5% to 8%) at higher concentrations.

Conclusion: There is minimal transfer and fetal accumulation of rosiglitazone according to the ex vivo human perfusion model.

MeSH terms

  • Administration, Oral
  • Dose-Response Relationship, Drug
  • Female
  • Fetus / metabolism
  • Humans
  • Hypoglycemic Agents / administration & dosage
  • Hypoglycemic Agents / pharmacokinetics*
  • In Vitro Techniques
  • Models, Biological
  • Osmolar Concentration
  • Placenta / metabolism*
  • Pregnancy
  • Rosiglitazone
  • Thiazolidinediones / administration & dosage
  • Thiazolidinediones / pharmacokinetics*

Substances

  • Hypoglycemic Agents
  • Thiazolidinediones
  • Rosiglitazone