Suxethonium chloride

Chemical compound
Suxethonium chloride
Identifiers
  • 2,2’-[(1,4-Dioxo-1,4-butanediyl)bis(oxy)]bis(N-ethyl-N,N-dimethylethanaminium) dichloride
PubChem CID
  • 71732
ChemSpider
  • 64776
CompTox Dashboard (EPA)
  • DTXSID20218004 Edit this at Wikidata
ECHA InfoCard100.053.581 Edit this at Wikidata
Chemical and physical data
FormulaC16H34Cl2N2O4
Molar mass389.36 g·mol−1
3D model (JSmol)
  • Interactive image
  • CC[N+](C)(C)CCOC(=O)CCC(=O)OCC[N+](C)(C)CC.[Cl-].[Cl-]
InChI
  • InChI=1S/C16H34N2O4.2ClH/c1-7-17(3,4)11-13-21-15(19)9-10-16(20)22-14-12-18(5,6)8-2;;/h7-14H2,1-6H3;2*1H/q+2;;/p-2
  • Key:BHCKTCGQZMCGAB-UHFFFAOYSA-L

Suxethonium (trade name: Brevidil-E) is a depolarising muscle relaxant which is presented as a dry powder in an ampoule. This is re-constituted with sterile water prior to use. It is available in Australia as a schedule 4 drug,[1] and the US.[2]

Advantages

It has some advantages over suxamethonium:

  • Less K+[3]
  • Possibly less muscle pain after use
  • Storage does not require refrigeration

The last advantage was what keeps it in occasional use.

Previous use

In the UK, it was used by the Obstetric Flying Squads at patient's homes to resuscitate mothers during major obstetric complications (mostly major haemorrhage) during home births.

In Australia, it was included in "Resuscitation drugs packs" in hospitals. These packs were sealed boxes containing all the drugs required for an in-hospital resuscitation. They were prepared by the hospital pharmacy and because these were sealed (usually just sticky tape) the drug contents were guaranteed to be there for use in a cardiac arrest. These packs contained ampoules of powdered suxethonium so a relaxant was available to facilitate intubation. Suxamethonium could not be used in these packs because of the requirement for refrigeration. This was certainly an issue in Queensland as it could be quite warm and hospitals wards were in the past generally not air-conditioned.

It can still be used where the storage issue is a concern (e.g. by the military, rural locations, 3rd world countries). The most recent reference to it in Medline is 1976, but it is occasionally mentioned in passing in other journals.[4]

References

  1. ^ [1][dead link]
  2. ^ "Suxethonium Chloride". Drugs.com.
  3. ^ Day S (October 1976). "Plasma potassium changes following suxamethonium and suxethonium in normal patients and in patients in renal failure". British Journal of Anaesthesia. 48 (10): 1011–5. doi:10.1093/bja/48.10.1011. PMID 791307.
  4. ^ Shrestha BM (2003). "Muscle Relaxant in the 21st Century" (PDF). Kathmandu University Medical Journal. 1 (1): 60–65. PMID 16340268. Archived from the original (PDF) on May 18, 2005.
  • v
  • t
  • e
Skeletal muscle relaxants (M03)
Peripherally acting
(primarily antinicotinic,
NMJ block)
Non-depolarizing
Curare alkaloids
4° ammonium agents
Depolarizing
ACh release inhibitors
Centrally acting
Carbamic acid esters
Benzodiazepines
Nonbenzodiazepines
Thienodiazepines
Quinazolines
Anticholinergics
(Antimuscarinics)
Other
Directly acting
  • v
  • t
  • e
nAChRsTooltip Nicotinic acetylcholine receptors
Agonists
(and PAMsTooltip positive allosteric modulators)
Antagonists
(and NAMsTooltip negative allosteric modulators)
Precursors
(and prodrugs)
See also
Receptor/signaling modulators
Muscarinic acetylcholine receptor modulators
Acetylcholine metabolism/transport modulators