- Local anesthetics are drugs that cause reversible loss of sensation, especially pain, in a localized area of the body when applied topically or injected locally. They block the generation and conduction of nerve impulses at the site of contact without damaging neurons. - Common uses include dentistry, excision procedures, dermatology, and spinal or regional anesthesia. Local anesthetics work by inhibiting sodium influx through voltage-gated sodium channels in neurons, interrupting action potential generation and signal conduction. - Examples of side effects include central nervous system stimulation or depression in high doses, cardiovascular effects like arrhythmias and hypotension, and hypersensitivity reactions.

1. Local AnaestheticsLocal Anaesthetics
Dr. D. K. BrahmaDr. D. K. Brahma
Department of PharmacologyDepartment of Pharmacology
NEIGRIHMS, SHILLONGNEIGRIHMS, SHILLONG

2. Common Uses of LocalCommon Uses of Local
Anaesthetics:Anaesthetics:
Dentistry
Excision
Dermatology
Spinal Anaesthesia

3. Definition:Definition:
• Local anaesthetics are drugs which upon topical
application or local injection cause reversible loss of
sensory perception, especially of pain in a localized area
of the body.
– Block generation and conduction of nerve impulses at a
localized site of contact without structural damage to neurons.
• Clinically - to block pain sensation from—or sympathetic
vasoconstrictor impulses to—specific areas of the body
– Loss of sensory as well as motor impulses

4. Some Clinical Examples of theirSome Clinical Examples of their
UseUse
• Topically: Nasal mucosa and wound
margins
• Infiltration: Vicinity of peripheral nerve
endings and major nerve trunks
• Epidural or Subarachnoid spaces:
surrounding spinal nerves
• Regional anesthesia: Intravenous
injection in arm or leg (Bier block)

5. Local Vs General AnaesthesiaLocal Vs General Anaesthesia
General Local
Site of action CNS Peripheral nerves
Area Whole body Restricted areas
Consciousness Lost Unaltered
Preferential use Major surgery Minor surgery
Use in non-coperative
patients
Possible Not possible
Poor health patient Risky Safer
Care for vital functions Essential Not needed

6. History:History:
• In Western Europe between 1750 to 1850
• Chemists and physicians collected sample of coca
leaves for experiments
• Isolated active principle of coca leaf, synthesized to a
drug for patients to feel more relief of pain when taking
surgeries
• In 1860, German chemist Albert Niemann successfully
isolate the active principle of coca leaf; he named it
cocaine
• Cocaine, an ester of benzoic acid and methylecgonine

7. What are the drugs?What are the drugs?
(Classification)(Classification)
• Injectable anaesthetic:
– Low potency, short duration – Procaine and Chlorprocaine
– Intermediate potency – Lidocaine (Lignocaine) and Prilocaine
– High potency and long duration – Tetracaine, Bupivacaine,
Ropivacaine, Etidocaine, Mepivacaine and Dibucaine
(Cinchocaine)
• Surface anaesthetic:
– Soluble – Cocaine, Lidocaine, Tetracaine and Benoxinate
– Insoluble – Benzocaine, Butylaminobenzoate and Oxethazine
• Miscellaneous drugs:
– Clove oil, phenol, chlorpromazine and diphenhydramine etc.

8. Another Classification ?Another Classification ?
• Local anesthetics are also classified according
to Chemical Structure!
• What is it ?

9. AnswerAnswer
– Ester-linked
• Short acting
• Metabolized in the plasma and tissue fluids
• Excreted in urine
– Amide-linked
• Longer acting
• Metabolized by liver enzymes
• Excreted in urine
REMEMBER: All are weak Bases!

10. C
Chemistry of LA – contd. (LAs areChemistry of LA – contd. (LAs are
Weak Bases)Weak Bases)
C O
O
R N
R
R
NH
O
R N
R
R
Aromatic portion Amine portion
Intermediate chain
ESTER
AMIDE
LIPOPHILIC HYDROPHILIC

11. Chemistry of LAs – contd.Chemistry of LAs – contd.
ESTER LINKAGE AMIDE LINKAGE (2 EYES!!)
PROCAINE
procaine (Novocaine)
tetracaine (Pontocaine)
benzocaine
cocaine
LIDOCAINE
lidocaine (Xylocaine)
mepivacaine (Carbocaine)
bupivacaine (Marcaine)
etidocaine (Duranest)
ropivacaine (Naropin)

12. Chemistry of LAs (ClinicalChemistry of LAs (Clinical
significance)significance)
• Cross sensitivity (allergy with ESTER LINKAGE)
– Occurs with drugs in the same chemical class
– Esters are metabolized to common metabolite PABA
– Allergy rarely occurs with amide linkage class
• Biotransformation/duration of action
– ESTERS are rapidly metabolized in the plasma by a
cholinesterase
– AMIDES are more slowly destroyed by liver
microsomal P450 enzymes.

13. Mechanism - LAsMechanism - LAs
• As you know, entry of
Na+ is essential for
Action potential
• Two things happen:
– Rate and rise of AP and
maximum depolarization
decreases – slowing of
conduction.
– Finally, local depolarization
fails to reach threshold
potential – conduction block.

14. Mechanism of LAs – contd.Mechanism of LAs – contd.
• LAs interact with a receptor
within the voltage sensitive
Na+ channel and raise the
threshold of opening the
channel
• Na+ permeability decreased
and ultimately stopped in
response to stimulus or
impulse
• Impulse conduction is
interrupted when a critical
length of fiber is blocked (2-3
nodes of Ranvier).

15. + +
- -
+ +
--
- -
+ + + +
- -
Na+
+ ++ +
- - - -
Resting
(Closed**)
Open
(brief)
inactivated
Very slow
repolarization in
presence of LA
LA receptor
LA have highest
affinity for the
inactivated form
Refractory period
Mechanism of LA – contd.Mechanism of LA – contd.

16. Mechanism of LA – contd.Mechanism of LA – contd.
- Higher concentration of Ca++ reduces
inactivation of Na+ channel
- Blockade is not due to hyperpolarization (RMP is
unaltered as K+ channels are not blocked)
- Blockade is related to pKa of particular drug:
- 7.6 to 7.8: e.g. lidocaine - fast acting drugs
(more undissociated form)
- 8.1 to 8.9 – slow acting – slow acting (more
dissociated form)

17. Voltage gated Sodium ChannelVoltage gated Sodium Channel
Composed of (I) 2 large alpha and (II) 2 small beta-1 and beta-2
subunits

18. Voltage gated Sodium ChannelVoltage gated Sodium Channel

19. B + H +
BH+
(active form)
B + H +
BH+
B + H +
BH+
axoplasm
B
Specific
action
Non-specific action
pH = 7.4
pH = 6.9
pH = 7.4
Most LA are
in this form
at pH 7.4
Nerve sheath

20. Summary of Mechanism - LAsSummary of Mechanism - LAs
• All local anesthetics are membrane stabilizing drugs
– slows down speed of AP - ultimately stop AP generation
• Reversibly decrease the rate of depolarization and repolarization of
excitable membranes
• Act by inhibiting sodium influx through sodium-specific ion channels
in the neuronal cell - voltage-gated sodium channels
• When the influx of sodium is interrupted - action potential cannot
rise and signal conduction is inhibited
• Local anesthetic s bind (located at inner surface) more readily to
sodium channels in activated state – and slows its reversion to the
resting state – refractory period is increased - “state dependent
blockade” - no action on resting nerve.
• Blockade develops rapidly on stimulation of nerves repeatedly
(Greater the stimulation higher is the blockade)
• Many other drugs also have membrane stabilizing properties, all are
not used as LA, e.g. propranolol

21. Influencing factor of LA actionInfluencing factor of LA action
Lipid solubility
• All local anesthetics have weak bases. Increasing the lipid solubility leads
to faster nerve penetration, block sodium channels, and speed up the onset
of action.
Influence of pH
• Lower pKa (7.6 – 7.8) – faster acting (lidocaine, mepivacaine)
• Higher pKa (8.1 – 8.9) – slower acting (procaine, tetracaine, bupivacaine)
Vasoconstrictors
• Cocaine itself is vasoconstrictor
• Adrenaline
– Potential adverse effects of vasoconstrictors
• DON’T use in areas of toes, fingers, ear lobes, penis (ischemia) and necrosis
Inflammation tends to produce lower pH in tissues therefore
• LA are more ionized - don’t penetrate very well
• Blood flow
• Decreased ability of LA to produce effects

22. Actions of LA - LocalActions of LA - Local
• All LAs have effects on nerves acting via Na+ channel –
sensory endings, nerve trunks, NM junctions, ganglion
and receptors
• Injected near Mixed nerve – anaesthesia of skin and
paralysis of voluntary muscles
• Sensory and Motor fibres are equally sensitive –
depends on diameter and types of fibres (gr. C & gr A
etc.)
– Smaller fibers are more sensitive than larger ones
– Frequency dependence
– Myelinated nerves are blocked earlier than non-myelinated ones
• Autonomic fibres are more susceptible than somatic
ones

23. Functions lost with LAFunctions lost with LA
Answer
– Pain perception
– Temperature
– Touch sensation
– Proprioception
– Skeletal muscle tone
• The order of blockade:
– Initially gr.`C` fibres are
blocked – pain and
sympathetic
vasoconstrictors
– Then gr.`A` fibres
• Pain – temperature –
touch - pressure and
vibration –motor fibres
(Muscle)
• Tongue: bitter – sweet –
sour - salt

24. Undesired effects of LA – contd.Undesired effects of LA – contd.
• CNS Stimulation:
• (More sensitive than cardiac)
– Dose-related spectrum of effects
and All effects are due to
depression of neurons
• First an apparent CNS
stimulation (convulsions
most serious)
• Followed by CNS depression
(death due to respiratory
depression)
• Premonitory signs include:
ringing in ears, metallic taste,
numbness around lips
– Cocaine - euphoria (unique in its
ability to stimulate CNS)
– Lidocaine - sedation even at non-
toxic doses

25. Cardiovascular SystemCardiovascular System
• ARRHYTHMIAS: direct
effect (More resistant
than CNS)
• Decrease cardiac
excitability and contractility
• Decreased conduction
rate
• Increased refractory rate
(bupivicaine)
• ALL can cause
arrhythmias if conc. is high
enough
Note: cocaine is
exception......it
stimulates heart
• HYPOTENSION: Arteriolar
dilation is a result of:
– Direct effect (procaine and
lidocaine have most effect)
– Block of postganglionic
sympathetic fiber function
– CNS depression
– Avoid by adding
vasoconstrictor to the
preparation
– Cocaine is exception:
produces vasoconstriction,
blocks catecholamine
reuptake

26. • Methemoglobinemia
– Some LA metabolites have significant oxidizing
properties
– This may cause a significant conversion of
hemoglobin to methemoglobin and compromise ability
to carry oxygen
– May be a problem if cardiopulmonary reserve is
limited
– Treat with oxygen and methylene blue (converts
methemoglobin to hemoglobin)
• prilocaine benzocaine lidocaine have been implicated
Undesired effects of LA – contd.Undesired effects of LA – contd.

27. Undesired effects of LA – contd.Undesired effects of LA – contd.
• Hypersensitivity:
– Common with ester-linked LA
– Rashes, angio-edema, dermatitis and rare anaphylaxis
– Sometimes typical asthmatic attack
• Neurotoxicity:
– LA can cause concentration-dependent nerve damage to
central and peripheral NS
– Mechanism(s) not clear
– Permanent neurological injury is rare
– May account for transient neurological symptoms after spinal
anesthesia
• Cauda equina syndrome

28. Pharmacokinetic of LAPharmacokinetic of LA
• Absorption:
- Surface anesthetics from mucus membrane and
abraded areas
- Depends on Blood flow to the area, total dose and
specific drug characteristics
- Procaine has poor penetration in mucus membrane
- Procaine is negligibly bound to plasma protein but
amides are bound to alpha 1 acid glycoprotein
• Distribution:
- Widely distributed in the body: (lipophilic)
- Enters brain, heart, liver and kidney
- Followed by muscle and other viscera

29. Pharmacokinetic of LA – contd.Pharmacokinetic of LA – contd.
• METABOLISM
– Ester type LA
• Hydrolysis by cholinesterase in plasma to PABA derivatives
– pseudo cholinesterase or butrylcholinesterase
• Generally, short acting and low systemic toxicity
• Prolonged effects seen with genetically determined deficiency or
altered esterase (cholinesterase inhibitors)
- Amide type LA
• Bound to alpha1 acid glycoprotein
• Hydrolyzed by liver microsomal enzymes (P450)
• Longer acting & more systemic toxicity than esters
• High first pass metabolism on oral ingestion

30. Individual LA -Individual LA - CocaineCocaine
• Natural alkaloid from Erythroxylon coca
• Medical use limited to surface or topical anesthesia
(corneal or nasopharyngeal)
– Constriction of corneal vessels and sloughing and drying
• A toxic action on heart may induce rapid and lethal
cardiac failure – reuptake inhibition of Adr. And NA
• CNS: Stimulation of vasomotor, vomiting and
temperature centre etc.
– Initially euphoria followed by dysphoria (DA reuptake)
• Avoid adrenaline because cocaine already has
vasoconstrictor properties. (EXCEPTION!!!)
• A marked pyrexia is associated with cocaine overdose
• Not used presently

31. Esters – contd.Esters – contd.
Procaine (Novocaine)
– Topically ineffective - disadvantage
– Used for infiltration because of low potency and short
duration but most commonly used for spinal
anesthesia
– Short local duration ......produces significant
vasodilation. Adrenaline used to prolong effect
– Systemic toxicity negligible because rapidly destroyed
in plasma
– Procaine penicillin

32. Individual LA - AmidesIndividual LA - Amides
LIDOCAINE (Xylocaine) Most widely used and popular LA
– Effective by all routes – topical, infiltration, spinal etc.
– Faster onset (3 Vs 15 min), more intense, longer lasting (30 – 60
min.), than procaine
– Addition of Adr in 1:200,000 prolongs the action for 2 Hrs
– More potent than procaine but about equal toxicity
– Quicker CNS effects than others (drowsiness, mental clouding,
altered taste and tinnitus)
– Overdose (muscle twitching, cardiac arrhythmia, fall in BP, coma
and respiratory arrest)
– Antiarrhythmic
– Available as Injections, topical solution, jelly and ointment etc.

33. Individual LA (Amides) – contd.Individual LA (Amides) – contd.
Bupivacaine (Marcaine)
– No topical effect
– Slower onset and one of longer duration agents (8
Hrs.)
– Used for infiltration, spinal, nerve block and epidural
– Unique property analgesia without significant motor
blockade (popular drug for analgesia during labor)
– High lipid solubility, high distribution in tissues and
less in blood (benefit to fetus)
– More cardio toxic than other LA (prolong QT interval)
– not given IV
– Available as 0.25%, 0.5% inj.

34. ConclusionConclusion
Anesthetic pKa Onset Duration
(with
Adrenaline)
in minutes
Max Dose
(with
adrenaline)
Procaine 9.1 Slow 45 - 90 8mg/kg –
10mg/kg
Lidocaine 7.9 Rapid 120 - 240 4.5mg/kg –
7mg/kg
Bupivacaine 8.1 Slow 4 hours – 8
hours
2.5mg/kg –
3mg/kg

35. Individual LA (Amides) – contd.Individual LA (Amides) – contd.
EMLA = eutectic mixture of local
anesthetics
– Eutectic = two solid substances mixed
together in equal quantities by weight form a
eutectic mixture
– the melting point of the mixture is lower than
the melting points of the individual
components
• EMLA = lidocaine and prilocaine becomes
an oily mixture

36. Individual LA (Amides) – contd.Individual LA (Amides) – contd.
lidocaine/prilocaine combination is indicated for
dermal anaesthesia
– Specifically it is applied to prevent pain associated
with intravenous catheter insertion, blood sampling,
superficial surgical procedures; and topical
anaesthesia of leg ulcers for cleansing or
debridement
– it can also be used to numb the skin before tattooing.
– EMLA cream is also used in the treatment of
premature ejaculation

37. Individual LA (Amides) – contd.Individual LA (Amides) – contd.
TAC: (LET)
• tetracaine 0.5%, adrenaline1 in 2000 and
cocaine 10%
• topical anesthetic mixture found to be effective
for nonmucosal skin lacerations to the face and
scalp
• applied directly to the wound using a cotton-
tipped applicator with firm pressure that is
maintained for 20 to 40 minutes
• maximum dose for children-0.05ml/Kg
• toxicity due to cocaine

38. EMLA applicationEMLA application

39. CLINICAL APPLICATIONS (TECHNIQUES)CLINICAL APPLICATIONS (TECHNIQUES)
OF LOCAL ANAESTHESIAOF LOCAL ANAESTHESIA
1. Surface anaesthesia:
– Mucous membranes and abraded skin
– Nose, mouth, bronchial tree, cornea and urinary tracts
• Lidocaine, tetracaine
1. Infiltration anaesthesia:
– Direct injection into tissues to reach nerve branches and terminals
– Used in minor surgery = incisions, hydrocele, herniorrhaphy etc.
1. Field block:
– Injection of LA subcutaneously
– Aim is to anaesthetize the region distal to the site of injection
– Examples – forearm, anterior abdominal wall, scalp and lower extremity
1. Nerve Block:
- LA is injected around the nerve trunks or plexuses
- Area of anaesthesia is large in comparison to the amount of drug used
- Lasts longer than the field or infiltration methods
- Flooding technique for plexus block
- Examples: Trigeminal nerve blocks (face) , Ophthalmic nerve block (eyelids and scalp),
Supraorbital nerve block (forehead)

40. Clinical applications of LA – contd.Clinical applications of LA – contd.
Spinal anaesthesia:
• Site of injection – Subarachnoid space between L 2-3 or
L 3-4
• Site of action – nerve root in the cauda equina
• Level of anaesthesia – vol. & speed of injection; baricity
of drug soln. with CSF and posture of patient
• Order of anaesthesia – sympathetic > motor
• Uses – lower limbs, pelvis, lower abdomen,
prostatectomy fracture setting and obstetric procedures
• Problems - Spinal headache, hypotension, bradycardia
and respiratory depression, cauda equina syndrome and
nausea-vomiting
• Drugs - Lidocaine, tetracaine

41. Clinical applications of LA – contd.Clinical applications of LA – contd.
• Epidural and Caudal Anaesthesia:
– Site of injection – sacral hiatus (caudal) or lumber,
thoracic or cervical region
– Catheters are used for continuous infusion
– Unwanted effects similar to that of spinal except less
likely because longitudinal spread is reduced -
• Drugs - Lidocaine, bupivacaine, ropivacaine
• Regional anaesthesia (Intravenous)
- Injection of LA in a vein of a torniquet occluded limb
- Mostly limited to upper limb
- Orthopaedic procedures

43. Local AnestheticsLocal Anesthetics
DESIRABLE CHARACTERISTICSDESIRABLE CHARACTERISTICS
Rapid onset of action
Brief, reversible block of nerve conduction
Low degree of systemic toxicity
Soluble in water and stable in solution
Effective on all parts of the nervous
system, all types of nerve fibers and
muscle fibers

44. Newer Techniques of LANewer Techniques of LA
Iontophoresis: Lidocaine-soaked sponges

45. Newer Techniques of LANewer Techniques of LA
Liposomes: Liposomal Bupivacaine Formulation

46. B + H +
BH+
(active form)
B + H +
BH+
B + H +
BH+
axoplasm
B
Specific
action
Non-specific action
pH = 7.4
pH = 6.9
pH = 7.4
Most LA are
in this form
at pH 7.4
Nerve sheathThank
You
Thank
You