DARK Classics in Chemical Neuroscience: Fentanyl

ACS Chem Neurosci. 2018 Oct 17;9(10):2428-2437. doi: 10.1021/acschemneuro.8b00174. Epub 2018 Jun 12.

Abstract

Fentanyl rose to prominence as an alternative analgesic to morphine nearly 50 years ago; today, fentanyl has re-emerged as a dangerous recreational substance. The increased potency and analgesic effect of fentanyl are advantageous in the treatment of pain but are also responsible for the rise in unintentional opioid overdose deaths. In response to this crisis, fentanyl, its analogues, and even precursors are under heightened regulatory scrutiny. Despite this controversial history, derivatization of fentanyl has resulted in numerous synthetic analogues that provide valuable insights into opioid receptor binding and signaling events. In this review, the impact of fentanyl on chemical neuroscience is shown through its synthesis and properties, manufacturing, metabolism, pharmacology, approved and off-label indications, adverse effects, and the responsibility it has in the opioid epidemic.

Keywords: Fentanyl; analgesic; designer drug; opioid; pain.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Analgesics, Opioid / chemistry*
  • Analgesics, Opioid / pharmacology*
  • Analgesics, Opioid / therapeutic use
  • Anesthesia, General
  • Drug Industry
  • Drug Overdose / mortality
  • Epidemics
  • Fentanyl / chemistry*
  • Fentanyl / pharmacology*
  • Fentanyl / therapeutic use
  • Humans
  • Off-Label Use
  • Opioid-Related Disorders / epidemiology
  • Pain / drug therapy

Substances

  • Analgesics, Opioid
  • Fentanyl