Indication | For production of local or regional anesthesia by infiltration techniques such as percutaneous injection and intravenous regional anesthesia by peripheral nerve block techniques such as brachial plexus and intercostal and by central neural techniques such as lumbar and caudal epidural blocks. |
Pharmacodynamics | Dibucaine is an amide-type local anesthetic, similar to lidocaine. |
Mechanism of action | Local anesthetics block both the initiation and conduction of nerve impulses by decreasing the neuronal membrane's permeability to sodium ions through sodium channel inhibition. This reversibly stabilizes the membrane and inhibits depolarization, resulting in the failure of a propagated action potential and subsequent conduction blockade. |
Absorption | In general, ionized forms (salts) of local anesthetics are not readily absorbed through intact skin. However, both nonionized (bases) and ionized forms of local anesthetics are readily absorbed through traumatized or abraded skin into the systemic circulation. |
Volume of distribution | Not Available |
Protein binding | Not Available |
Metabolism | Primarily hepatic. |
Route of elimination | Not Available |
Half life | Not Available |
Clearance | Not Available |
Toxicity | Subcutaneous LD50 in rat is 27 mg/kg. Symptoms of overdose include convulsions, hypoxia, acidosis, bradycardia, arrhythmias and cardiac arrest. |
Monday, October 15, 2012
Pharmacology Of Dibucaine
Labels:
Pharmacology of Drugs,
UNCLASSIFIED
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