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Suxethonium chloride

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Suxethonium chloride
Identifiers
  • 2,2’-[(1,4-Dioxo-1,4-butanediyl)bis(oxy)]bis(N-ethyl-N,N-dimethylethanaminium) dichloride
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.053.581Edit this at Wikidata
Chemical and physical data
FormulaC16H34Cl2N2O4
Molar mass389.36 g·mol−1
3D model (JSmol)
  • CC[N+](C)(C)CCOC(=O)CCC(=O)OCC[N+](C)(C)CC.[Cl-].[Cl-]
  • 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 depolarisingmuscle relaxant which is presented as a dry powder in an ampoule. This is re-constituted with sterile water prior to use. It is available inAustralia as a schedule 4 drug,[1] and the US.[2]

Advantages

[edit]

It has some advantages oversuxamethonium:

  • 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

[edit]

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

[edit]
  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 fromthe original(PDF) on May 18, 2005.
Peripherally acting
(primarilyantinicotinic,
NMJ block)
Non-depolarizing
Curarealkaloids
4° ammonium agents
Depolarizing
ACh release inhibitors
Centrally acting
Carbamic acid esters
Benzodiazepines
Nonbenzodiazepines
Thienodiazepines
Quinazolines
Anticholinergics
(Antimuscarinics)
Other
Directly acting
nAChRsTooltip Nicotinic acetylcholine receptors
Agonists
(andPAMsTooltip positive allosteric modulators)
Antagonists
(andNAMsTooltip negative allosteric modulators)
Precursors
(andprodrugs)
Retrieved from "https://en.wikipedia.org/w/index.php?title=Suxethonium_chloride&oldid=1330112440"
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