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PHARMACOLOGY OF LOCAL
     ANESTHESIA


    Dr. Hesham El-Hawary
       Assistant Professor OMFS
Pharmacology of Local Anesthesia
CONSTITUENTS OF THE ANESTHETIC CARPULE
Anesthesia
          with V.C.

1.   Local anesthetic agent
     ( L.A.)
2.   Vasoconstrictor agent
     ( V.C.)
3.   Preservative for V.C.
     agent
     (anti- oxidant)
4.   Vehicle to make solution
     isotonic
     ( 0.9%NaCl)
Anesthesia                  Plain Anesthesia
          with V.C.                   (without V.C.)

1.   Local anesthetic agent     1. Local anesthetic agent
     ( L.A.)                       ( L.A.)
2.   Vasoconstrictor agent      2. Vehicle to make solution
     ( V.C.)                       isotonic
3.   Preservative for V.C.         ( 0.9%NaCl)
     agent
     (anti- oxidant)
4.   Vehicle to make solution
     isotonic
     ( 0.9%NaCl)
Keep in mind

•    The main agent in the carpule is the L.A. agent

•    The other ingredients of the local anesthetic
     carpule are added :

    1. To potentiate the action of the L.A. agent
    2. To prevent deterioration of the contents
Pharmacology of Local Anesthesia

THE LOCAL ANESTHETIC DRUG
Local anesthetic drugs

• Drugs temporary interrupt nerve conduction when
  absorbed into it and have little or no irritating
  effect when injected



• They are all synthetic compounds except the
  cocaine
Properties of ideal anesthetic agent
1. Reversible action
2. Nonirritant
3. Produce no secondary local reaction (No allergic reaction)
4. No systemic toxicity
5. Rapid onset
6. Sufficient duration
7. Potent
8. Sufficient penetrating properties
9. Stable in solution and undergo biotransformation in body
10. Can be sterilized without deterioration
11. Not interfere with healing of local tissues
12. Have vasoconstrictor action or compatible with V.C.
13. Not expensive
Common properties of injectable LA
                Agents
1. Form salts with strong acids which is water soluble
2. When injected in the body (alkali)
     •   Hydrolyzed by plasma proteins to free the alkaloid base which is lipid
         soluble
     •   Undergo biotransformation
3.   Affect the nerve conduction and have reversible action
4.   Compatible with vasoconstrictors
5.   Not or slightly irritant to the tissue in the concentration used
6.   Capable of producing toxic effect when sufficient high
     plasma concentration is reached
Mode of Action Of Local
  Anesthetic Drugs
 Mechanical or Reversible coagulation theory
 Physiological theory
 Acetyl choline and enzyme system theory
 Electrical potential theory
 Displacing calcium ions from receptor sites
Pharmacokinetics of local
      anesthetics
             Uptake
             Potency
             Duration
        Biotransformation
            Excretion
Uptake
•   Most L.A. agents producing vasodilatation
•   Procaine is the most potent vasodilator
•   Cocaine is the only L.A. agents that produces
    vasoconstriction
•   Vasodilatation results in
    –   ↑ rate of absorption
    –   ↓ duration of action of anesthesia
    –   ↑ anesthetic blood level & risk for toxicity
Potency
• The majority of local anesthetics are tertiary
  amines
• Few local anesthetics are secondary amines as
  Procaine
• NH3 → NR3
• Local anesthetic agent is prepared in the carpule in
  the form of hydrochloride salt of tertiary amine
  ( NR3 ̶ HCL)
•   The free base (NR3) of the hydrochloride salt of
    tertiary amine ( NR3 ̶ HCL) is liberated from its
    salt (HCL) by interaction with alkaline
    medium, alkaline PH, ( body fluids, NaHCO3 )

•   (NR3 ̶ HCL) + NaHCO3 → NR3 + Na CL + H2 CO3
• In presence of tissue infection or inflammation
  (Acidic PH)
    The free base (NR3) of the hydrochloride salt of tertiary
    amine ( NR3 ̶ HCL) fail to liberated from its salt
    (HCL) & failure of anesthesia occurs


• (NR3 ̶ HCL) + Acidic PH → (NR3 ̶ HCL)
Duration
The following factors affect both duration & depth of
   anesthetic action :

1. Factors related to the anesthesitic agent
  –   Lipid solubility
  –   Concentration and type of the drug
  –   Presence or absence of vaconstrictor or vasoconstriction effect
  –   Duration of exposure
Duration
The following factors affect both duration & depth of
   anesthetic action :

2. Factors related to the injection technique
  –   Technique ( infiltration vs. nerve block)
  –   Volume of the solution
  –   Accuracy of the technique
  –   Anatomical variation
Duration
The following factors affect both duration & depth of
   anesthetic action :

3. Factors related to the site of injection
   –   Alkalinity; Affect the ionization of the drug and the rate of liberation
       of free base
   –   Vascularity of tissue
Duration
The following factors affect both duration & depth of
   anesthetic action :

4. Factors related to the individual to be injected
  –   Individual variation in response
Biotransformation
                         (metabolism)

•       Ester group
    –     Metabolized in
         • Plasma by plasma pseudo-cholinesterase enzyme
         • Liver by the estrase enzyme
    –     Toxicity (high toxic blood level) occurs in patients with plasma
          pseudo-cholinesterase enzyme deficiency ( 1 out of 2500)


•       Amide group
    –     Metabolized in
    –     Liver by the liver microsomal enzymes
    –     Toxicity (high toxic blood level) occurs in patients with impaired
          liver function (liver dysfunction)
Excretion

•   Both groups of local anesthetics & their metabolites are
    excreted by kidneys

•   Patients with renal dysfunction may be unable to eliminate
    local anesthetics & their metabolites from the blood with
    increase risk of toxicity
Local Anesthetic Agents
Local
         anesthetic
          agents


Ester Group      Amide Group
Esters
• Esters of benzoic acid
   –   Cocaine
   –   Butacaine
   –   Tetracaine
   –   Benzocaine
   –   Hexylcaine
• Esters of Para-aminobenzoic acid
   –   Procaine
   –   Chloroprocaine
   –   Ravocaine
   –   Propoxycaine
• Esters of Meta - amino benzoic acid
   – Unacaine
   – Primcaine
• Esters of Para - ethyox benzoic acid
   – Intracaine
Amides
•   Lidocaine
•   Bupivacaine
•   Articaine
•   Mepivacaine
•   Prilocaine
•   Etidocaine
•   Ropivacaine
Biotransformation of LA Drugs

• Ester group undergo biotransformation in
  – Liver by the estrase enzyme
  – Plasma by the cholinesterase enzyme




• Amide group undergo biotransformation in the liver
Contrast between ester & amide groups

   Features         Esters          Amides

 Chemical bond    Ester bond      Amide bond

                   Procaine         Lidocaine
Common example
                 ( Novocaine)     ( Xylocaine)

    Allergy           Low          Very low

                    Plasma
                                     Liver
 Metabolism in      pseudo-
                                  microsomal
                 cholinesterase
                                   enzymes
                    enzyme
Keep in mind
•   Type: ester - amide
•   Onset of action: rapid – slow
•   Duration of action: Long – short
•   Vasodilatation properties: VD – VC- Non
•   Topical anesthetic properties: yes - no
•   Metabolized in: plasma – liver
•   Excreted by: kidney
•   Allergy: allergic – non allergic
•   Available forms: with or without VC
unacaine
tetracaine
 buycaine
 procaine
 articaine
 marcaine
mepivicaine
 Lidocaine




                                                       Metabolism

                                                                    Excretion
                             duration




                                             Topical




                                                                                Allergy
                     Onset




                                                                                          forms
              Type




                                        VD
Maximum doses of L.A. agents
L.A. agent   Max. dose   Normal dose


 Lidocaine     300 mg      4.4 mg / kg


Mepivacaine    400 mg      6.6 mg / kg


 Marcaine      90 mg       1.3 mg / kg


 Articaine     400 mg      6 mg / kg


 Prilocaine    500 mg      7 mg / kg
Dilution of L.A. agents
• The dilution of L.A. agent as 2 % means that there is
  two grams (2000 mg) of the L.A. agent in 100 ml of
  the solution
• The dilution of L.A. agent as 2 % means that there is
  two grams (2000 mg) of the L.A. agent in 100 ml of
  the solution

• 2 % means 2 g / 100 ml
• 2 % means 2000 mg / 100 ml
• The dilution of L.A. agent as 2 % means that there is
  two grams (2000 mg) of the L.A. agent in 100 ml of
  the solution

• 2 % means 2 g / 100 ml
• 2 % means 2000 mg / 100 ml

• 2000 mg – 100 ml
• ? mg - 1.8 ml
• The dilution of L.A. agent as 2 % means that there is
  two grams (2000 mg) of the L.A. agent in 100 ml of
  the solution

• 2 % means 2 g / 100 ml
• 2 % means 2000 mg / 100 ml

• 2000 mg – 100 ml
• ? mg - 1.8 ml
• ? = 1.8 x 2000 / 100
• The dilution of L.A. agent as 2 % means that there is
  two grams (2000 mg) of the L.A. agent in 100 ml of
  the solution

• 2 % means 2 g / 100 ml
• 2 % means 2000 mg / 100 ml

•   2000 mg – 100 ml
•   ? mg - 1.8 ml
•   ? = 1.8 x 2000 / 100 = 36 mg
•   Therefore carpule of 1.8 ml contains 36 mg solution
The Vasoconstrictor
Advantages
                      It causes V.C. of B.V. that
1.    Aid in producing local ischemia by vasocntricting the
      blood vessels leading to:
     1.   Aids positively in producing anesthesia
     2.   Decreases bleeding caused by the surgical procedure
2.    Decreases absorption rate of the anesthetic drug
      leading to:
     1.   Increases duration of action of the L.A.
     2.   Decreases the volume of local anesthetic solution needed
     3.   Decreases the toxicity of the anesthetic drug
3.    It stimulate the heart
          Thus counteract the depressant effect of the local anesthetic agent
          on the heart
Advantages
                      It causes V.C. of B.V. that
1.    Aid in producing local ischemia by vasocntricting the
      blood vessels leading to:
     1.   Aids positively in producing anesthesia
     2.   Decreases bleeding caused by the surgical procedure
2.    Decreases absorption rate of the anesthetic drug
      leading to:
     1.   Increases duration of action of the L.A.
     2.   Decreases the volume of local anesthetic solution needed
     3.   Decreases the toxicity of the anesthetic drug
3.    It stimulate the heart
          Thus counteract the depressant effect of the local anesthetic agent
          on the heart
Advantages
                      It causes V.C. of B.V. that
1.    Aid in producing local ischemia by vasocntricting the
      blood vessels leading to:
     1.   Aids positively in producing anesthesia
     2.   Decreases bleeding caused by the surgical procedure
2.    Decreases absorption rate of the anesthetic drug
      leading to:
     1.   Increases duration of action of the L.A.
     2.   Decreases the volume of local anesthetic solution needed
     3.   Decreases the toxicity of the anesthetic drug
3.    It stimulate the heart
          Thus counteract the depressant effect of the local anesthetic agent
          on the heart
Advantages
                      It causes V.C. of B.V. that
1.    Aid in producing local ischemia by vasocntricting the
      blood vessels leading to:
     1.   Aids positively in producing anesthesia
     2.   Decreases bleeding caused by the surgical procedure
2.    Decreases absorption rate of the anesthetic drug
      leading to:
     1.   Increases duration of action of the L.A.
     2.   Decreases the volume of local anesthetic solution needed
     3.   Decreases the toxicity of the anesthetic drug
3.    It stimulate the heart
          Thus counteract the depressant effect of the local anesthetic agent
          on the heart
Contra-Indications
1.   Diabetics:
       As V.C. counteract the action of insulin
       i.e. ( increase blood glucose level)


2.   Hypertensive pt:
       As V.C. raises patient’s blood pressure


3.   Cardiac pt.:
       As V.C. stimulate the heart, produce tachycardia & increase H.R.
       ( this is doubtful because of the small amount used which is about
       0.04 mg if 2 ml of 1:50 000 solution is used & this is about 1/5
       permissible dose that can be given to cardiac pt without ill effect)
Contra-Indications Cont.
4.   Pregnancy:
     Because the V.C. causes uterine contraction & may causes abortion


5.   Extraction of teeth with chronic peri-apical sepsis:
     Because V.C. decrease blood flow to the tissues & may lead to dry
     socket


5.   Hyperthyroidism (toxic goiter):
     Because V.C. specially adrenaline may cause thyroid crisis & sudden
     death
Types of V.C.
1. Epinephrine ( adrenaline)

2. Nor- Epinephrine ( nor - adrenaline)

3. Neo- cobefrin (levonordefrin)

4. Phenylephrine (neosynephrine)

5. Felypressin (octapressin)
Dilution of V.C. Cont.

The dilution of V.C. 1: 1000
means that there is one gram
(1000 mg) of the V.C. in 1000 ml
( 1 liter) of the solution, or in other
words 1.0 mg/ml of the solution
• Examples
1: 50 000 means
• Examples
1: 50 000 means
      1 gm : 50 000 ml
• Examples
1: 50 000 means
      1 gm : 50 000 ml
      1000 mg : 50 000 ml
• Examples
1: 50 000 means
      1 gm : 50 000 ml
      1000 mg : 50 000 ml
      (1000/50 000) mg : (50 000/50 000) ml
• Examples
1: 50 000 means
      1 gm : 50 000 ml
      1000 mg : 50 000 ml
      (1000/50 000) mg : (50 000/50 000) ml
      (1/50) mg : (1/1) ml
• Examples
1: 50 000 means
      1 gm : 50 000 ml
      1000 mg : 50 000 ml
      (1000/50 000) mg : (50 000/50 000) ml
      (1/50) mg : (1/1) ml
      0.02 mg: 1 ml or 0.02mg/ml
• Examples
1: 50 000 means 0.02mg/ml
      1 gm : 50 000 ml
      1000 mg : 50 000 ml
      (1000/50 000) mg : (50 000/50 000) ml
      (1/50) mg : (1/1) ml
      0.02 mg: 1 ml or 0.02mg/ml
A & B adrenergic receptors
• A receptors
  – Vasodilatation of cardiac coronaries
  – Peripheral vasoconstriction
• B1 receptors
  – Increase cardiac output
  – Increase heart rate
• B2 receptors
  – Broncho-dilatation
Epinephrine       Nor          Levo       Phenyl    Felypressen
                          Epinephrine    nordefrine   ephrine

Action         A&B           A&B         A more B       A          ADH
CVS            A&B           A&B

RS           Broncho      Mild broncho
             dilatation    dilatation
CNS             Mild          Mild
            stimulation   stimulation
Potency      Very high       25%           15%          5%

Toxicity       High          Less         Lesser

Stability      Less          More          Higher     Highest


CI            Cardiac       Cardiac       Cardiac     Cardiac    pregnant
              thyroid       thyroid       thyroid     thyroid
Maximum Doses Of V.C.
     V.C.          Max. dose       Concentration

 epinephrine      0.2mg     20ml    1 : 100 000

nor epinephrine   0.34mg    10ml    1 : 100 000

levonordefrin     1.0mg     20ml     1 : 20 000

Phenylephrine     4.0mg     20ml     1 : 2 500

  felypressin     0.27 IU   9ml       0.03 IU
Vehicle
•   The vehicle to make the local anesthetic solution
    isotonic

•   The isotonicity of the local anesthetic solution is
    important to produce the desired anesthetic
    effect

•   It may be:
    –   Saline solution ( 0.9 % Na CL)
    –   Ringer’s solution (0.5 % Na CL , 0.04 % Ca CL and
        0.02 % K CL)
•        If the injected anesthetic solution is hypotonic:
         water will pass from the injected anesthetic
         solution to inside the tissue cells until equilibrium
         occurs between the intercellular & the
         intracellular fluids & this results in:

1.       Postoperative pain & delayed healing:
         As water escapes from the injected solution intercellularly:
     •     Increases the volume of intercellular fluid
     •     Rupture of the cells in the area occurs

2.       Less profound anesthesia:
           As viscosity of the injected solution increased due to
           loss of water & thus the power of diffusion of the
           injected solution in the area is reduced
•        If the injected anesthetic solution is hypotonic:
         water will pass from the injected anesthetic
         solution to inside the tissue cells until equilibrium
         occurs between the intercellular & the
         intracellular fluids & this results in:

1.       Postoperative pain & delayed healing:
         As water escapes from the injected solution intercellularly:
     •     Increases the volume of intercellular fluid
     •     Rupture of the cells in the area occurs

2.       Less profound anesthesia:
           As viscosity of the injected solution increased due to
           loss of water & thus the power of diffusion of the
           injected solution in the area is reduced
•        If the injected anesthetic solution is hypotonic:
         water will pass from the injected anesthetic
         solution to inside the tissue cells until equilibrium
         occurs between the intercellular & the
         intracellular fluids & this results in:

1.       Postoperative pain & delayed healing:
         As water escapes from the injected solution intercellularly:
     •     Increases the volume of intercellular fluid
     •     Rupture of the cells in the area occurs

2.       Less profound anesthesia:
           As viscosity of the injected solution increased due to
           loss of water & thus the power of diffusion of the
           injected solution in the area is reduced
•    If the injected anesthetic solution is hypertonic:
     water will escape from the intracellular fluids to
     outside towards the injected anesthetic solution
     until equilibrium occurs between the intercellular
     & the intracellular fluids & this results in:

1.   Postoperative pain & delayed healing:
     As water escapes from the cells, the volume of
     intercellular fluid decreases & shrinkage of the cells in the
     area occurs
2.   Less profound anesthesia:
     As concentration of the injected solution decreased due
     gain of water ( dilution of the injected solution in the area)
•    If the injected anesthetic solution is hypertonic:
     water will escape from the intracellular fluids to
     outside towards the injected anesthetic solution
     until equilibrium occurs between the intercellular
     & the intracellular fluids & this results in:

1.   Postoperative pain & delayed healing:
     As water escapes from the cells, the volume of
     intercellular fluid decreases & shrinkage of the cells in the
     area occurs
2.   Less profound anesthesia:
     As concentration of the injected solution decreased due
     gain of water ( dilution of the injected solution in the area)
•    If the injected anesthetic solution is hypertonic:
     water will escape from the intracellular fluids to
     outside towards the injected anesthetic solution
     until equilibrium occurs between the intercellular
     & the intracellular fluids & this results in:

1.   Postoperative pain & delayed healing:
     As water escapes from the cells, the volume of
     intercellular fluid decreases & shrinkage of the cells in the
     area occurs
2.   Less profound anesthesia:
     As concentration of the injected solution decreased due
     gain of water ( dilution of the injected solution in the area)
Preservative
•   Na bisulphite (0.5mg/ml)
    –   It is added to local anesthetic carpule to prevent
        oxidation of the V.C. agent


•   Methylparaben ( 1mg/ml)
    –   It is added to local anesthetic carpule as preservative to
        L.A. agent as Articaine
    –   It may cause allergic reactions
    –   Patients with para -group allergy (sulfa & procaine)
        should not take local anesthetic carpule that contains
        this preservative
Topical anesthetics
1. Topical anesthetics that produce their effect by the
    chemical action on the free nerve endings
    ( spray, gel, or ointment):
   – Xylocaine (5-10%)
   – Benzocaine (10-20%)

2. Topical anesthetics that produce their effect by the
   means of the refrigerant action:
  –   Application of cold on the surface of mucous membranes
      ( ice bags or crushed ice)
  –   Topical use of ethyl chloride
Name:     Hesham El-Hawary
Email:    hesham@elhawarydentalclinic.com
Website: www.elhawarydentalclini.com
Twitter:  @elhawary_hesham
Facebook: Hesham El-Hawary

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Pharmacology of Dental local anesthesia

  • 1.
  • 2. PHARMACOLOGY OF LOCAL ANESTHESIA Dr. Hesham El-Hawary Assistant Professor OMFS
  • 3. Pharmacology of Local Anesthesia CONSTITUENTS OF THE ANESTHETIC CARPULE
  • 4. Anesthesia with V.C. 1. Local anesthetic agent ( L.A.) 2. Vasoconstrictor agent ( V.C.) 3. Preservative for V.C. agent (anti- oxidant) 4. Vehicle to make solution isotonic ( 0.9%NaCl)
  • 5. Anesthesia Plain Anesthesia with V.C. (without V.C.) 1. Local anesthetic agent 1. Local anesthetic agent ( L.A.) ( L.A.) 2. Vasoconstrictor agent 2. Vehicle to make solution ( V.C.) isotonic 3. Preservative for V.C. ( 0.9%NaCl) agent (anti- oxidant) 4. Vehicle to make solution isotonic ( 0.9%NaCl)
  • 6. Keep in mind • The main agent in the carpule is the L.A. agent • The other ingredients of the local anesthetic carpule are added : 1. To potentiate the action of the L.A. agent 2. To prevent deterioration of the contents
  • 7. Pharmacology of Local Anesthesia THE LOCAL ANESTHETIC DRUG
  • 8. Local anesthetic drugs • Drugs temporary interrupt nerve conduction when absorbed into it and have little or no irritating effect when injected • They are all synthetic compounds except the cocaine
  • 9. Properties of ideal anesthetic agent 1. Reversible action 2. Nonirritant 3. Produce no secondary local reaction (No allergic reaction) 4. No systemic toxicity 5. Rapid onset 6. Sufficient duration 7. Potent 8. Sufficient penetrating properties 9. Stable in solution and undergo biotransformation in body 10. Can be sterilized without deterioration 11. Not interfere with healing of local tissues 12. Have vasoconstrictor action or compatible with V.C. 13. Not expensive
  • 10. Common properties of injectable LA Agents 1. Form salts with strong acids which is water soluble 2. When injected in the body (alkali) • Hydrolyzed by plasma proteins to free the alkaloid base which is lipid soluble • Undergo biotransformation 3. Affect the nerve conduction and have reversible action 4. Compatible with vasoconstrictors 5. Not or slightly irritant to the tissue in the concentration used 6. Capable of producing toxic effect when sufficient high plasma concentration is reached
  • 11. Mode of Action Of Local Anesthetic Drugs Mechanical or Reversible coagulation theory Physiological theory Acetyl choline and enzyme system theory Electrical potential theory Displacing calcium ions from receptor sites
  • 12. Pharmacokinetics of local anesthetics Uptake Potency Duration Biotransformation Excretion
  • 13. Uptake • Most L.A. agents producing vasodilatation • Procaine is the most potent vasodilator • Cocaine is the only L.A. agents that produces vasoconstriction • Vasodilatation results in – ↑ rate of absorption – ↓ duration of action of anesthesia – ↑ anesthetic blood level & risk for toxicity
  • 14. Potency • The majority of local anesthetics are tertiary amines • Few local anesthetics are secondary amines as Procaine • NH3 → NR3 • Local anesthetic agent is prepared in the carpule in the form of hydrochloride salt of tertiary amine ( NR3 ̶ HCL)
  • 15. The free base (NR3) of the hydrochloride salt of tertiary amine ( NR3 ̶ HCL) is liberated from its salt (HCL) by interaction with alkaline medium, alkaline PH, ( body fluids, NaHCO3 ) • (NR3 ̶ HCL) + NaHCO3 → NR3 + Na CL + H2 CO3
  • 16. • In presence of tissue infection or inflammation (Acidic PH) The free base (NR3) of the hydrochloride salt of tertiary amine ( NR3 ̶ HCL) fail to liberated from its salt (HCL) & failure of anesthesia occurs • (NR3 ̶ HCL) + Acidic PH → (NR3 ̶ HCL)
  • 17. Duration The following factors affect both duration & depth of anesthetic action : 1. Factors related to the anesthesitic agent – Lipid solubility – Concentration and type of the drug – Presence or absence of vaconstrictor or vasoconstriction effect – Duration of exposure
  • 18. Duration The following factors affect both duration & depth of anesthetic action : 2. Factors related to the injection technique – Technique ( infiltration vs. nerve block) – Volume of the solution – Accuracy of the technique – Anatomical variation
  • 19. Duration The following factors affect both duration & depth of anesthetic action : 3. Factors related to the site of injection – Alkalinity; Affect the ionization of the drug and the rate of liberation of free base – Vascularity of tissue
  • 20. Duration The following factors affect both duration & depth of anesthetic action : 4. Factors related to the individual to be injected – Individual variation in response
  • 21. Biotransformation (metabolism) • Ester group – Metabolized in • Plasma by plasma pseudo-cholinesterase enzyme • Liver by the estrase enzyme – Toxicity (high toxic blood level) occurs in patients with plasma pseudo-cholinesterase enzyme deficiency ( 1 out of 2500) • Amide group – Metabolized in – Liver by the liver microsomal enzymes – Toxicity (high toxic blood level) occurs in patients with impaired liver function (liver dysfunction)
  • 22. Excretion • Both groups of local anesthetics & their metabolites are excreted by kidneys • Patients with renal dysfunction may be unable to eliminate local anesthetics & their metabolites from the blood with increase risk of toxicity
  • 24. Local anesthetic agents Ester Group Amide Group
  • 25. Esters • Esters of benzoic acid – Cocaine – Butacaine – Tetracaine – Benzocaine – Hexylcaine • Esters of Para-aminobenzoic acid – Procaine – Chloroprocaine – Ravocaine – Propoxycaine • Esters of Meta - amino benzoic acid – Unacaine – Primcaine • Esters of Para - ethyox benzoic acid – Intracaine
  • 26. Amides • Lidocaine • Bupivacaine • Articaine • Mepivacaine • Prilocaine • Etidocaine • Ropivacaine
  • 27. Biotransformation of LA Drugs • Ester group undergo biotransformation in – Liver by the estrase enzyme – Plasma by the cholinesterase enzyme • Amide group undergo biotransformation in the liver
  • 28. Contrast between ester & amide groups Features Esters Amides Chemical bond Ester bond Amide bond Procaine Lidocaine Common example ( Novocaine) ( Xylocaine) Allergy Low Very low Plasma Liver Metabolism in pseudo- microsomal cholinesterase enzymes enzyme
  • 29. Keep in mind • Type: ester - amide • Onset of action: rapid – slow • Duration of action: Long – short • Vasodilatation properties: VD – VC- Non • Topical anesthetic properties: yes - no • Metabolized in: plasma – liver • Excreted by: kidney • Allergy: allergic – non allergic • Available forms: with or without VC
  • 30. unacaine tetracaine buycaine procaine articaine marcaine mepivicaine Lidocaine Metabolism Excretion duration Topical Allergy Onset forms Type VD
  • 31. Maximum doses of L.A. agents
  • 32. L.A. agent Max. dose Normal dose Lidocaine 300 mg 4.4 mg / kg Mepivacaine 400 mg 6.6 mg / kg Marcaine 90 mg 1.3 mg / kg Articaine 400 mg 6 mg / kg Prilocaine 500 mg 7 mg / kg
  • 34. • The dilution of L.A. agent as 2 % means that there is two grams (2000 mg) of the L.A. agent in 100 ml of the solution
  • 35. • The dilution of L.A. agent as 2 % means that there is two grams (2000 mg) of the L.A. agent in 100 ml of the solution • 2 % means 2 g / 100 ml • 2 % means 2000 mg / 100 ml
  • 36. • The dilution of L.A. agent as 2 % means that there is two grams (2000 mg) of the L.A. agent in 100 ml of the solution • 2 % means 2 g / 100 ml • 2 % means 2000 mg / 100 ml • 2000 mg – 100 ml • ? mg - 1.8 ml
  • 37. • The dilution of L.A. agent as 2 % means that there is two grams (2000 mg) of the L.A. agent in 100 ml of the solution • 2 % means 2 g / 100 ml • 2 % means 2000 mg / 100 ml • 2000 mg – 100 ml • ? mg - 1.8 ml • ? = 1.8 x 2000 / 100
  • 38. • The dilution of L.A. agent as 2 % means that there is two grams (2000 mg) of the L.A. agent in 100 ml of the solution • 2 % means 2 g / 100 ml • 2 % means 2000 mg / 100 ml • 2000 mg – 100 ml • ? mg - 1.8 ml • ? = 1.8 x 2000 / 100 = 36 mg • Therefore carpule of 1.8 ml contains 36 mg solution
  • 40. Advantages It causes V.C. of B.V. that 1. Aid in producing local ischemia by vasocntricting the blood vessels leading to: 1. Aids positively in producing anesthesia 2. Decreases bleeding caused by the surgical procedure 2. Decreases absorption rate of the anesthetic drug leading to: 1. Increases duration of action of the L.A. 2. Decreases the volume of local anesthetic solution needed 3. Decreases the toxicity of the anesthetic drug 3. It stimulate the heart Thus counteract the depressant effect of the local anesthetic agent on the heart
  • 41. Advantages It causes V.C. of B.V. that 1. Aid in producing local ischemia by vasocntricting the blood vessels leading to: 1. Aids positively in producing anesthesia 2. Decreases bleeding caused by the surgical procedure 2. Decreases absorption rate of the anesthetic drug leading to: 1. Increases duration of action of the L.A. 2. Decreases the volume of local anesthetic solution needed 3. Decreases the toxicity of the anesthetic drug 3. It stimulate the heart Thus counteract the depressant effect of the local anesthetic agent on the heart
  • 42. Advantages It causes V.C. of B.V. that 1. Aid in producing local ischemia by vasocntricting the blood vessels leading to: 1. Aids positively in producing anesthesia 2. Decreases bleeding caused by the surgical procedure 2. Decreases absorption rate of the anesthetic drug leading to: 1. Increases duration of action of the L.A. 2. Decreases the volume of local anesthetic solution needed 3. Decreases the toxicity of the anesthetic drug 3. It stimulate the heart Thus counteract the depressant effect of the local anesthetic agent on the heart
  • 43. Advantages It causes V.C. of B.V. that 1. Aid in producing local ischemia by vasocntricting the blood vessels leading to: 1. Aids positively in producing anesthesia 2. Decreases bleeding caused by the surgical procedure 2. Decreases absorption rate of the anesthetic drug leading to: 1. Increases duration of action of the L.A. 2. Decreases the volume of local anesthetic solution needed 3. Decreases the toxicity of the anesthetic drug 3. It stimulate the heart Thus counteract the depressant effect of the local anesthetic agent on the heart
  • 44. Contra-Indications 1. Diabetics: As V.C. counteract the action of insulin i.e. ( increase blood glucose level) 2. Hypertensive pt: As V.C. raises patient’s blood pressure 3. Cardiac pt.: As V.C. stimulate the heart, produce tachycardia & increase H.R. ( this is doubtful because of the small amount used which is about 0.04 mg if 2 ml of 1:50 000 solution is used & this is about 1/5 permissible dose that can be given to cardiac pt without ill effect)
  • 45. Contra-Indications Cont. 4. Pregnancy: Because the V.C. causes uterine contraction & may causes abortion 5. Extraction of teeth with chronic peri-apical sepsis: Because V.C. decrease blood flow to the tissues & may lead to dry socket 5. Hyperthyroidism (toxic goiter): Because V.C. specially adrenaline may cause thyroid crisis & sudden death
  • 46. Types of V.C. 1. Epinephrine ( adrenaline) 2. Nor- Epinephrine ( nor - adrenaline) 3. Neo- cobefrin (levonordefrin) 4. Phenylephrine (neosynephrine) 5. Felypressin (octapressin)
  • 47. Dilution of V.C. Cont. The dilution of V.C. 1: 1000 means that there is one gram (1000 mg) of the V.C. in 1000 ml ( 1 liter) of the solution, or in other words 1.0 mg/ml of the solution
  • 48. • Examples 1: 50 000 means
  • 49. • Examples 1: 50 000 means 1 gm : 50 000 ml
  • 50. • Examples 1: 50 000 means 1 gm : 50 000 ml 1000 mg : 50 000 ml
  • 51. • Examples 1: 50 000 means 1 gm : 50 000 ml 1000 mg : 50 000 ml (1000/50 000) mg : (50 000/50 000) ml
  • 52. • Examples 1: 50 000 means 1 gm : 50 000 ml 1000 mg : 50 000 ml (1000/50 000) mg : (50 000/50 000) ml (1/50) mg : (1/1) ml
  • 53. • Examples 1: 50 000 means 1 gm : 50 000 ml 1000 mg : 50 000 ml (1000/50 000) mg : (50 000/50 000) ml (1/50) mg : (1/1) ml 0.02 mg: 1 ml or 0.02mg/ml
  • 54. • Examples 1: 50 000 means 0.02mg/ml 1 gm : 50 000 ml 1000 mg : 50 000 ml (1000/50 000) mg : (50 000/50 000) ml (1/50) mg : (1/1) ml 0.02 mg: 1 ml or 0.02mg/ml
  • 55. A & B adrenergic receptors • A receptors – Vasodilatation of cardiac coronaries – Peripheral vasoconstriction • B1 receptors – Increase cardiac output – Increase heart rate • B2 receptors – Broncho-dilatation
  • 56. Epinephrine Nor Levo Phenyl Felypressen Epinephrine nordefrine ephrine Action A&B A&B A more B A ADH CVS A&B A&B RS Broncho Mild broncho dilatation dilatation CNS Mild Mild stimulation stimulation Potency Very high 25% 15% 5% Toxicity High Less Lesser Stability Less More Higher Highest CI Cardiac Cardiac Cardiac Cardiac pregnant thyroid thyroid thyroid thyroid
  • 57. Maximum Doses Of V.C. V.C. Max. dose Concentration epinephrine 0.2mg 20ml 1 : 100 000 nor epinephrine 0.34mg 10ml 1 : 100 000 levonordefrin 1.0mg 20ml 1 : 20 000 Phenylephrine 4.0mg 20ml 1 : 2 500 felypressin 0.27 IU 9ml 0.03 IU
  • 59. The vehicle to make the local anesthetic solution isotonic • The isotonicity of the local anesthetic solution is important to produce the desired anesthetic effect • It may be: – Saline solution ( 0.9 % Na CL) – Ringer’s solution (0.5 % Na CL , 0.04 % Ca CL and 0.02 % K CL)
  • 60. If the injected anesthetic solution is hypotonic: water will pass from the injected anesthetic solution to inside the tissue cells until equilibrium occurs between the intercellular & the intracellular fluids & this results in: 1. Postoperative pain & delayed healing: As water escapes from the injected solution intercellularly: • Increases the volume of intercellular fluid • Rupture of the cells in the area occurs 2. Less profound anesthesia: As viscosity of the injected solution increased due to loss of water & thus the power of diffusion of the injected solution in the area is reduced
  • 61. If the injected anesthetic solution is hypotonic: water will pass from the injected anesthetic solution to inside the tissue cells until equilibrium occurs between the intercellular & the intracellular fluids & this results in: 1. Postoperative pain & delayed healing: As water escapes from the injected solution intercellularly: • Increases the volume of intercellular fluid • Rupture of the cells in the area occurs 2. Less profound anesthesia: As viscosity of the injected solution increased due to loss of water & thus the power of diffusion of the injected solution in the area is reduced
  • 62. If the injected anesthetic solution is hypotonic: water will pass from the injected anesthetic solution to inside the tissue cells until equilibrium occurs between the intercellular & the intracellular fluids & this results in: 1. Postoperative pain & delayed healing: As water escapes from the injected solution intercellularly: • Increases the volume of intercellular fluid • Rupture of the cells in the area occurs 2. Less profound anesthesia: As viscosity of the injected solution increased due to loss of water & thus the power of diffusion of the injected solution in the area is reduced
  • 63. If the injected anesthetic solution is hypertonic: water will escape from the intracellular fluids to outside towards the injected anesthetic solution until equilibrium occurs between the intercellular & the intracellular fluids & this results in: 1. Postoperative pain & delayed healing: As water escapes from the cells, the volume of intercellular fluid decreases & shrinkage of the cells in the area occurs 2. Less profound anesthesia: As concentration of the injected solution decreased due gain of water ( dilution of the injected solution in the area)
  • 64. If the injected anesthetic solution is hypertonic: water will escape from the intracellular fluids to outside towards the injected anesthetic solution until equilibrium occurs between the intercellular & the intracellular fluids & this results in: 1. Postoperative pain & delayed healing: As water escapes from the cells, the volume of intercellular fluid decreases & shrinkage of the cells in the area occurs 2. Less profound anesthesia: As concentration of the injected solution decreased due gain of water ( dilution of the injected solution in the area)
  • 65. If the injected anesthetic solution is hypertonic: water will escape from the intracellular fluids to outside towards the injected anesthetic solution until equilibrium occurs between the intercellular & the intracellular fluids & this results in: 1. Postoperative pain & delayed healing: As water escapes from the cells, the volume of intercellular fluid decreases & shrinkage of the cells in the area occurs 2. Less profound anesthesia: As concentration of the injected solution decreased due gain of water ( dilution of the injected solution in the area)
  • 67. Na bisulphite (0.5mg/ml) – It is added to local anesthetic carpule to prevent oxidation of the V.C. agent • Methylparaben ( 1mg/ml) – It is added to local anesthetic carpule as preservative to L.A. agent as Articaine – It may cause allergic reactions – Patients with para -group allergy (sulfa & procaine) should not take local anesthetic carpule that contains this preservative
  • 69. 1. Topical anesthetics that produce their effect by the chemical action on the free nerve endings ( spray, gel, or ointment): – Xylocaine (5-10%) – Benzocaine (10-20%) 2. Topical anesthetics that produce their effect by the means of the refrigerant action: – Application of cold on the surface of mucous membranes ( ice bags or crushed ice) – Topical use of ethyl chloride
  • 70. Name: Hesham El-Hawary Email: hesham@elhawarydentalclinic.com Website: www.elhawarydentalclini.com Twitter: @elhawary_hesham Facebook: Hesham El-Hawary