Chirality and anaesthetic drugs: A review and an update

Many molecules can exist as right-handed and left-handed forms that are non-superimposable mirror images of each other. They are known as enantiomers or substances of opposite shape. Such compounds are also said to be chiral (Greek chiros meaning ′hand′). Such chiral molecules are of great relevance...

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Main Authors: Sukanya Mitra, Puneet Chopra
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2011-01-01
Series:Indian Journal of Anaesthesia
Subjects:
Online Access:http://www.ijaweb.org/article.asp?issn=0019-5049;year=2011;volume=55;issue=6;spage=556;epage=562;aulast=Mitra
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spelling doaj-6b27c7366a0f4177b8622e079cc0f22f2020-11-25T00:25:28ZengWolters Kluwer Medknow PublicationsIndian Journal of Anaesthesia0019-50492011-01-0155655656210.4103/0019-5049.90608Chirality and anaesthetic drugs: A review and an updateSukanya MitraPuneet ChopraMany molecules can exist as right-handed and left-handed forms that are non-superimposable mirror images of each other. They are known as enantiomers or substances of opposite shape. Such compounds are also said to be chiral (Greek chiros meaning ′hand′). Such chiral molecules are of great relevance to anaesthetic theory and practice. This review summarizes the basic concepts, pharmacokinetic and pharmacodynamic aspects of chirality, and some specific examples of their application in anaesthesia, along with recent advances to elucidate the anaesthetic mechanisms. Chirality is relevant to anaesthesia, simply because more than half of the synthetic agents used in anaesthesia practice are chiral drugs. Almost all these synthetic chiral drugs are administered as racemic mixture, rather than as single pure enantiomers. These mixtures are not drug formulations containing two or more therapeutic substances, but combination of isomeric substances, with the therapeutic activity residing mainly in one of the enantiomer. The other enantiomer can have undesirable properties, have different therapeutic activities or be pharmacologically inert. Specific examples of application of chirality in anaesthetic drugs include inhalational general anaesthetics (e.g. isoflurane), intravenous anaesthetics (e.g. etomidate, thiopentone), neuromuscular blocking agents (e.g. cisatracurium), local anaesthetics (e.g. ropivacaine and levobupivacaine) and other agents (e.g. levosimendan, dexmedetomidine, L-cysteine). In the recent advances, chirality study has not only helped new drug development as mentioned above, but has also contributed in a more profound way to the understanding of the mechanism of anaesthesia and anaesthetic drugs.http://www.ijaweb.org/article.asp?issn=0019-5049;year=2011;volume=55;issue=6;spage=556;epage=562;aulast=MitraAnaesthesiaanaesthetic drugschiralityenantiomers
collection DOAJ
language English
format Article
sources DOAJ
author Sukanya Mitra
Puneet Chopra
spellingShingle Sukanya Mitra
Puneet Chopra
Chirality and anaesthetic drugs: A review and an update
Indian Journal of Anaesthesia
Anaesthesia
anaesthetic drugs
chirality
enantiomers
author_facet Sukanya Mitra
Puneet Chopra
author_sort Sukanya Mitra
title Chirality and anaesthetic drugs: A review and an update
title_short Chirality and anaesthetic drugs: A review and an update
title_full Chirality and anaesthetic drugs: A review and an update
title_fullStr Chirality and anaesthetic drugs: A review and an update
title_full_unstemmed Chirality and anaesthetic drugs: A review and an update
title_sort chirality and anaesthetic drugs: a review and an update
publisher Wolters Kluwer Medknow Publications
series Indian Journal of Anaesthesia
issn 0019-5049
publishDate 2011-01-01
description Many molecules can exist as right-handed and left-handed forms that are non-superimposable mirror images of each other. They are known as enantiomers or substances of opposite shape. Such compounds are also said to be chiral (Greek chiros meaning ′hand′). Such chiral molecules are of great relevance to anaesthetic theory and practice. This review summarizes the basic concepts, pharmacokinetic and pharmacodynamic aspects of chirality, and some specific examples of their application in anaesthesia, along with recent advances to elucidate the anaesthetic mechanisms. Chirality is relevant to anaesthesia, simply because more than half of the synthetic agents used in anaesthesia practice are chiral drugs. Almost all these synthetic chiral drugs are administered as racemic mixture, rather than as single pure enantiomers. These mixtures are not drug formulations containing two or more therapeutic substances, but combination of isomeric substances, with the therapeutic activity residing mainly in one of the enantiomer. The other enantiomer can have undesirable properties, have different therapeutic activities or be pharmacologically inert. Specific examples of application of chirality in anaesthetic drugs include inhalational general anaesthetics (e.g. isoflurane), intravenous anaesthetics (e.g. etomidate, thiopentone), neuromuscular blocking agents (e.g. cisatracurium), local anaesthetics (e.g. ropivacaine and levobupivacaine) and other agents (e.g. levosimendan, dexmedetomidine, L-cysteine). In the recent advances, chirality study has not only helped new drug development as mentioned above, but has also contributed in a more profound way to the understanding of the mechanism of anaesthesia and anaesthetic drugs.
topic Anaesthesia
anaesthetic drugs
chirality
enantiomers
url http://www.ijaweb.org/article.asp?issn=0019-5049;year=2011;volume=55;issue=6;spage=556;epage=562;aulast=Mitra
work_keys_str_mv AT sukanyamitra chiralityandanaestheticdrugsareviewandanupdate
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