Sevoflurane
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Systematic (IUPAC) name | |
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1,1,1,3,3,3-Hexafluoro-2-(fluoromethoxy)propane
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Clinical data | |
Trade names | Sojourn, Ultane, Sevorane |
AHFS/Drugs.com | Consumer Drug Information |
Legal status | |
Routes of administration |
inhaled |
Identifiers | |
CAS Number | 28523-86-6 ![]() |
ATC code | N01AB08 (WHO) |
PubChem | CID: 5206 |
IUPHAR/BPS | 7296 |
DrugBank | DB01236 ![]() |
ChemSpider | 5017 ![]() |
UNII | 38LVP0K73A ![]() |
KEGG | D00547 ![]() |
ChEBI | CHEBI:9130 ![]() |
ChEMBL | CHEMBL1200694 ![]() |
Chemical data | |
Formula | C4H3F7O |
Molecular mass | 200.055 g/mol |
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Sevoflurane (1,1,1,3,3,3-hexafluoro-2-(fluoromethoxy)propane; synonym, fluoromethyl hexafluoroisopropyl ether), is a sweet-smelling, nonflammable, highly fluorinated methyl isopropyl ether used as an inhalational anaesthetic for induction and maintenance of general anesthesia. After desflurane, it is the volatile anesthetic with the fastest onset and offset.[1]
It is one of the most commonly used volatile anesthetic agents, particularly for outpatient anesthesia,[2] and including in anesthesia of children and infants, and in veterinary medicine. Together with desflurane, sevoflurane is replacing isoflurane and halothane in modern anesthesiology. It is often administered in a mixture of nitrous oxide and oxygen.
Sevoflurane "has an excellent safety record",[2] but is under review for potential neurotoxicity, especially relevant to administration in infants and children, and rare reports similar to halothane hepatotoxicity.[2] Sevoflurane is the preferred agent for mask induction due to its lesser irritation to mucous membranes.
Sevoflurane was discovered by Ross Terrell[3] and independently by Bernard M Regan. A detailed report of its development and properties appeared in 1975 in a paper authored by Richard Wallin, Bernard Regan, Martha Napoli and Ivan Stern it was introduced into clinical practice initially in Japan in 1990. The rights for sevoflurane in the US and other countries were held by Abbott Laboratories; it is available as a generic drug. Sevoflurane's name derives from the seven fluorine atoms in its substituents, alongside a standard suffix for such agents.
Contents
Medical uses
Sevoflurane is an inhaled anaesthetic that is often used to put children asleep for surgery.[4] During the process of waking up from the medication, it has been known to cause agitation and delirium.[4] It is not clear if this can be prevented.[4]
Adverse effects
Sevoflurane raises intracranial pressure and can cause respiratory depression.[5]
Studies examining a current significant health concern, anesthetic-induced neurotoxicity (including with sevoflurane, and especially with children and infants) are "fraught with confounders, and many are underpowered statistically", and so are argued to need "further data... to either support or refute the potential connection".[6]
Concern regarding the safety of anaesthesia is especially acute with regard to children and infants, where preclinical evidence from relevant animal models suggest that common clinically important agents, including sevoflurane, may be neurotoxic to the developing brain, and so cause neurobehavioural abnormalities in the long term; two large-scale clinical studies (PANDA and GAS) were ongoing as of 2010, in hope of supplying "significant [further] information" on neurodevelopmental effects of general anaesthesia in infants and young children, including where sevoflurane is used.[7]
Pharmacology
The exact mechanism of the action of general anaesthetics have not been delineated.[8] Sevoflurane is thought to potentially acts as a positive allosteric modulator of the GABAA receptor.[9] However, it also acts as an NMDA receptor antagonist,[10] potentiates glycine receptor currents,[9] and inhibits nACh[11] and 5-HT3 receptor currents.[9][12][13]
Physical properties
Boiling point: | 58.6 °C | (at 101.325 kPa) | |
Density: | 1.517–1.522 g/cm³ | (at 20 °C) | |
MAC : | 2.1 vol % | ||
Molecular weight: | 200 u | ||
Vapor pressure: | 157 mmHg (22.9 kPa) | (at 20 °C) | |
197 mmHg (26.3 kPa) | (at 25 °C) | ||
317 mmHg (42.3 kPa) | (at 36 °C) | ||
Blood:Gas partition coefficient: | 0.68 | ||
Oil:Gas partition coefficient: | 47 |
Bispectral index
Lua error in package.lua at line 80: module 'strict' not found. Sevoflurane has lower values of controversial bispectral index than desflurane.[14][15][verification needed]
Veterinary medicine
Sevoflurane had "become a popular inhalation anesthetic in veterinary practice" with a rapid induction and recovery from anesthesia due to a relatively low blood/gas solubility coefficient. [16]
References
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Further reading
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External links
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- ↑ Lua error in package.lua at line 80: module 'strict' not found.
- ↑ 2.0 2.1 2.2 Livertox: Clinical and Research Information on Drug-Induced Liver Injury (2014) "Drug Record: Sevoflurane", U.S. National Library of Medicine, 2 July 2014 update, see [1], accessed 15 August 2014.
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- ↑ 4.0 4.1 4.2 Lua error in package.lua at line 80: module 'strict' not found.
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- ↑ http://www.scientificamerican.com/article/how-does-anesthesia-work/
- ↑ 9.0 9.1 9.2 Lua error in package.lua at line 80: module 'strict' not found. Cite error: Invalid
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- Pages with reference errors
- Articles in need of cleanup
- Chemical articles having calculated molecular weight overwritten
- Infobox drug articles without a structure image
- Wikipedia articles needing factual verification from July 2015
- General anesthetics
- Ethers
- Organofluorides
- GABAA receptor positive allosteric modulators
- Glycine receptor agonists
- Nicotinic antagonists
- 5-HT3 antagonists