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Section IICoredrugs in anaesthetic practiceCH 3CH 3CH 3CH 3
CH 3CH 3CH (^3) CH
3
CH 3
CH 2
CH 3
CH 3
C 4 H 9 NH
C 3 H 7
N(C 2 H 5 ) 2
C 3 H 7
C—O— CH 2 CH 2 — N(CH 3 ) 2
CCOOOONNCO NNO
HHNCH OCH 3CH 3C 4 H 9
N
NCH OHO
NCHO
NCC
HHNHMepivacaineCocaineAmethocainePrilocaineLidocaine
RopivacaineBupivacaineFigure 10.3.Structure of some local anaesthetics. Asterisk marks chiral centre.would appear more appropriate than bupivacaine for epidural infusion due to its
sensory/motor discrimination and greater clearance.Kinetics
Ropivacaine is metabolized in the liver by aromatic hydroxylation, mainly to 3-
hydroxy-ropivacaine, but also to 4-hydroxy-ropivacaine, both of which have some
local anaesthetic activity.