Pancuronium
Clinical data
AHFS/Drugs.comMonograph
Pregnancy
category
  • AU: B2
Routes of
administration		Intravenous
ATC code
Legal status
Legal status
  • AU: S4 (Prescription only)
  • UK: POM (Prescription only)
  • US: ℞-only
Pharmacokinetic data
BioavailabilityNA
Protein binding77 to 91%
MetabolismHepatic
Elimination half-life1.5 to 2.7 hours
ExcretionRenal and biliary
Identifiers
  • [(2S,3S,5S,8R,9S,10S,13S,14S,16S,17R)-17-Acetyloxy-10,13-dimethyl-2,16-bis(pyridin-1-yl)-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.035.923 Edit this at Wikidata
Chemical and physical data
FormulaC35H60N2O4
Molar mass572.875 g·mol−1
  • InChI=1S/C35H60N2O4.2BrH/c1-24(38)40-32-21-26-13-14-27-28(35(26,4)23-31(32)37(6)19-11-8-12-20-37)15-16-34(3)29(27)22-30(33(34)41-25(2)39)36(5)17-9-7-10-18-36;;/h26-33H,7-23H2,1-6H3;2*1H/q+2;;/p-2/t26-,27+,28-,29-,30-,31-,32-,33-,34-,35-;;/m0../s1 ☒N
  • Key:NPIJXCQZLFKBMV-YTGGZNJNSA-L ☒N
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Pancuronium (trademarked as Pavulon) is an aminosteroid muscle relaxant with various medical uses.[1] It is used in euthanasia and is used in some states as the second of three drugs administered during lethal injections in the United States.

Mechanism of action

Pancuronium is a typical non-depolarizing curare-mimetic muscle relaxant. It competitively inhibits the nicotinic acetylcholine receptor at the neuromuscular junction by blocking the binding of acetylcholine. It has slight vagolytic activity, causing an increase in heart rate, but no ganglioplegic (i.e., blocking ganglions) activity. It is a very potent muscle relaxant drug, with an ED95 (i.e., the dose that causes 95% depression of muscle twitch response) of only 60 µg/kg body weight. Onset of action is relatively slow compared to other similar drugs, in part due to its low dose: an intubating dose takes 3–6 minutes for full effect. Clinical effects (muscle activity lower than 25% of physiological) last for about 100 minutes. The time needed for full (over 90% muscle activity) recovery after single administration is about 120–180 minutes in healthy adults.

The effects of pancuronium can be at least partially reversed by anticholinesterasics, such as neostigmine, pyridostigmine, and edrophonium.

Development

Workers at Organon were inspired by the structure of the aminosteroid alkaloid malouetine to develop a series of aminosteroid neuromuscular blockers based on an androstane nucleus, culminating in the development of pancuronium bromide.[2][3][4]

Pancuronium is designed to mimic the action of two molecules of acetylcholine with the quaternary nitrogen atoms spaced rigidly apart by the steroid rings at a distance of ten atoms (interonium distance). Decamethonium and suxamethonium also have this same interonium distance.

Uses in medicine

Pancuronium is used with general anesthesia in surgery for muscle relaxation and as an aid to intubation or ventilation. It does not have sedative or analgesic effects.

Side-effects include moderately raised heart rate and thereby arterial pressure and cardiac output, excessive salivation, apnea and respiratory depression, rashes, flushing, and sweating.[medical citation needed] The muscular relaxation can be dangerous in the seriously ill and it can accumulate leading to extended weakness. Pancuronium is not preferable in long-term use in ICU-ventilated patients.

In Belgium and the Netherlands, pancuronium is recommended in the protocol for euthanasia. After administering sodium thiopental to induce coma, pancuronium is delivered in order to stop breathing.[5]

Uses in execution and suicide

Procedure

Pancuronium is also used as one component of a lethal injection in administration of the death penalty in some parts of the United States.[6]

Controversy

Like all non-depolarising muscle relaxants, pancuronium has no effect on level of consciousness. Therefore, if the anaesthetic used is insufficient, the individual may be awake but unable to cry out or move due to the effect of the pancuronium. There have been several civil lawsuits alleging similar failures of adequate anaesthesia during general surgical procedures. These have been largely due to improper or insufficient dosages of anaesthetic in concert with normal dosages of muscle relaxants such as pancuronium.

In 2007, Michael Munro, a Scottish neonatologist at Aberdeen Maternity Hospital, was cleared of malpractice by the General Medical Council Fitness to Practice panel after giving 23 times the standard dose of pancuronium to two dying neonates. Terminally ill, both dying babies were suffering from agonal gasping and violent body spasms, which was highly distressing for the parents to witness. Munro then administered pancuronium to the babies after advising the parents that this would ease their suffering and could also hasten death.[7][8] It was on record that neither of the children's parents were unhappy with Munro's treatment.[9]

Amnesty International has objected to its use in lethal injections on the grounds that it "may mask the condemned prisoner's suffering during the execution,"[10] thereby leading observers to conclude that lethal injection is painless, or less cruel than other forms of execution.

Export limitations

The United Kingdom bans the export of pancuronium bromide to the United States due to its use in lethal injections, but not to the Netherlands or Belgium.[11]

Uses in crime

Pancuronium was used in Efren Saldivar's killing spree.[12] It was also used by the Skin Hunters to kill patients in the Polish city of Łódź. Pavulon was also used by Richard Angelo in 1987 to kill at least ten patients under his care at the Good Samaritan Hospital in New York.

References

  1. ^ Das GN, Sharma P, Maani CV (January 2021). "Pancuronium". StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing. PMID 30855929.
  2. ^ Lewis JJ, Martin-Smith M, Muir TC, Ross HH (August 1967). "Steroidal monoquaternary ammonium salts with non-depolarizing neuromuscular blocking activity". The Journal of Pharmacy and Pharmacology. 19 (8): 502–508. doi:10.1111/j.2042-7158.1967.tb09579.x. PMID 4382437. S2CID 2938040.
  3. ^ Buckett WR, Hewett CL, Savage DS (October 1973). "Pancuronium bromide and other steroidal neuromuscular blocking agents containing acetylcholine fragments". Journal of Medicinal Chemistry. 16 (10): 1116–1124. doi:10.1021/jm00268a011. PMID 4356139.
  4. ^ McKenzie AG (June 2000). "Prelude to pancuronium and vecuronium". Anaesthesia. 55 (6): 551–556. doi:10.1046/j.1365-2044.2000.01423.x. PMID 10866718. S2CID 22476701.
  5. ^ "Administration and Compounding Of Euthanasic Agents". The Hague: Royal Dutch Society for the Advancement of Pharmacy. Archived from the original on 7 June 2008. Retrieved 15 July 2008 – via ERGO!.
  6. ^ "US court backs lethal injection". BBC News. 16 April 2008.
  7. ^ "Baby doctor cleared of misconduct". BBC News. 11 July 2007. Retrieved 2010-05-21.
  8. ^ "Doctor cleared over baby deaths". The Guardian. 11 July 2007.
  9. ^ "Doctor felt babies were suffering". BBC News. 9 July 2007. Retrieved 2010-05-21.
  10. ^ "UA 44/04 Death penalty". Amnesty International. 6 February 2004. Archived from the original on 17 May 2004.
  11. ^ "Provisions supplementing "the torture Regulation"". Article 4A of Export Control Order 2008, UK Statutory Instruments 2008 No. 3231 PART 2 Article 9. UK Legislation.
  12. ^ Ramsland K (9 April 2005). "Dark Rumors". Crimelibrary. Archived from the original on 9 April 2005.
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