Transdermal versus subcutaneous leuprolide: a comparison of acute pharmacodynamic effect

Clin Pharmacol Ther. 1990 Oct;48(4):340-5. doi: 10.1038/clpt.1990.161.

Abstract

Transdermal administration of peptides has been limited by the barrier properties of the skin. We compared the acute luteinizing hormone (LH) response to subcutaneous and transdermal administration of an LH-releasing hormone agonist (leuprolide). Eighteen volunteers received 5 mg leuprolide added to electrically powered patches delivering a current of 0.22 microA (transdermally). One week later, they received a 5 mg subcutaneous dose. LH response was measured. The area under the curve for LH response, maximum LH response, and time to maximum LH response were similar. Time to first response was shorter (147 +/- 108 minutes [transdermally] and 73 +/- 74 minutes [subcutaneously]; p less than 0.05), and the area under the curve for the first 150 minutes was greater (3655 +/- 2246 mIU.min/ml [transdermally] and 8666 +/- 4067 mIU.min/ml [subcutaneously]; p less than 0.05) for subcutaneous delivery. No major adverse effects were seen. This electrically powered transdermal technique merits further study.

Publication types

  • Comparative Study

MeSH terms

  • Administration, Cutaneous
  • Antineoplastic Agents / administration & dosage*
  • Antineoplastic Agents / adverse effects
  • Antineoplastic Agents / pharmacology
  • Gonadotropin-Releasing Hormone / administration & dosage
  • Gonadotropin-Releasing Hormone / adverse effects
  • Gonadotropin-Releasing Hormone / analogs & derivatives*
  • Gonadotropin-Releasing Hormone / pharmacology
  • Humans
  • Injections, Subcutaneous
  • Leuprolide
  • Luteinizing Hormone / blood
  • Testosterone / blood

Substances

  • Antineoplastic Agents
  • Gonadotropin-Releasing Hormone
  • Testosterone
  • Luteinizing Hormone
  • Leuprolide