Transdermal delivery of heparin: Physical enhancement techniques

Int J Pharm. 2015 Dec 30;496(2):240-9. doi: 10.1016/j.ijpharm.2015.11.023. Epub 2015 Nov 29.

Abstract

Thromboembolic complications are the most common preventable cause of mortality and morbidity in trauma patients. Thrombosis is also the common cause of ischemic heart disease (acute coronary syndrome), stroke, and venous thromboembolism. Heparin, as a potent anticoagulant, has been used in clinical practice for more than five decades and remains the major medicine for the prevention and treatment of venous thromboembolism. However it binds to the endothelium and has a high affinity for plasma proteins resulting in a short half-life and unpredictable bioavailability. Transdermal drug delivery can address the problems of short half-life and unpredictable bioavailability. Other advantages of transdermal drug delivery include convenience, improved patient compliance, prompt termination of dosing and avoidance of the first-pass effect. This review focuses on different approaches used for transdermal delivery of heparin.

Keywords: Drug delivery; Electroporation; Heparin; Iontophoresis; Sonophoresis; Transdermal.

Publication types

  • Review

MeSH terms

  • Administration, Cutaneous
  • Animals
  • Anticoagulants / administration & dosage
  • Anticoagulants / metabolism*
  • Drug Delivery Systems / methods
  • Drug Delivery Systems / trends*
  • Heparin / administration & dosage
  • Heparin / metabolism*
  • Humans
  • Skin / drug effects
  • Skin / metabolism*
  • Thrombosis / drug therapy
  • Thrombosis / metabolism
  • Transdermal Patch / trends*

Substances

  • Anticoagulants
  • Heparin