Sheet 2 (Local Anesthesia 2)
Sheet 2 (Local Anesthesia 2)
Sheet 2 (Local Anesthesia 2)
Anaesthesia :
Is loss of all forms of sensation including
pain, touch, by impairment of motor
function.
Methods which induced LOCAL ANAESTHESIA
C. Quinoline :
Centbucridine
All local anesthetics posses a degree of
vasoactivity most producing dilation of the
vascular bed into which they are deposited,
although the degree of vasodilation may
vary, and some may produce
vasoconstriction. (concentration dependent)
Ester local anesthetics are also potent
voasodilating drugs.
Procaine, the most potent vasodilator
among local anesthetics.
Time to Achieve Peak Blood Level
Route Time, min
Intravenous 1
Topical 5 (approximately)
Intramuscular 5-10
Subcutaneous 30-90
ORAL ROUTE
With the exception of cocaine, local
anesthetics are absorbed poorly, if at
all, from the gastrointestinal tract
after oral administration.
TOPICAL ROUTE
Local anesthetics are absorbed at differing rates
after application to mucous membrane: In the
tracheal mucosa, absorption is almost as rapid
as with intravenous (IV) administration (indeed,
intratracheal drug administration {epinephrine,
lidocaine, atropine, naloxone and flumazenil} is
used in certain emergency situations); in the
pharyngeal mucosa, absorption is slower; and in
the esophageal or bladder mucosa, uptake is
even slower than occurs through the pharynx.
INJECTION
The rate of uptake (absorption) of
local anesthetics after parenteral
administration (subcutaneous,
intramuscular, or IV) is related to
both the vascularity of the injection
site and the vasoactivity of the drug.
Pattern of Distribution of Local
Anesthetics after absorption
Site of
Fat Slow
injection
equilibrium
B Muscle space
L
O
Brain Rapid
O
Myocardium equilibrium
D
Lungs space
Liver
ELIMINATION