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                                (2017.02.21) 
                           
                            
                       
                     
                    
                     
                        
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                      121[±¹¼Ò¸¶ÃëÁ¦                                                      ] 
                     
                    
                      
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657401251  [ºñ±Þ¿©]
                         
                        
						     
						     
                         
                      
                     
                       
                     
                     
                    
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                      Lidocaine  / N01BB02 
                     
                    
                    
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      Pharmacokinetics 
      
       
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    DUR (ÀǾàǰ»ç¿ëÆò°¡) 
    º´¿ë±Ý±â :
     
	 °í½ÃµÈ º´¿ë±Ý±â ³»¿ëÀº ¾ø½À´Ï´Ù.
	 
	 [»óÈ£ÀÛ¿ë/º´¿ë±Ý±â°Ë»ö]  										
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    Mechanism of Action 
    
      Lidocaine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸  Lidocaine stabilizes the neuronal membrane by inhibiting the ionic fluxes required for the initiation and conduction of impulses thereby effecting local anesthetic action. 
     
   
  
   
    Pharmacology 
     
      Lidocaine¿¡ ´ëÇÑ Pharmacology Á¤º¸  Lidocaine is an anesthetic agent indicated for production of local or regional anesthesia and in the treatment of ventricular tachycardia occurring during cardiac manipulation, such as surgery or catheterization, or which may occur during acute myocardial infarction, digitalis toxicity, or other cardiac diseases. The mode of action of the antiarrhythmic effect of Lidocaine appears to be similar to that of procaine, procainamide and quinidine. Ventricular excitability is depressed and the stimulation threshold of the ventricle is increased during diastole. The sinoatrial node is, however, unaffected. In contrast to the latter 3 drugs, Lidocaine in therapeutic doses does not produce a significant decrease in arterial pressure or in cardiac contractile force. In larger doses, lidocaine may produce circulatory depression, but the magnitude of the change is less than that found with comparable doses of procainamide. 
     
   
  
   
    Metabolism 
    
      Lidocaine¿¡ ´ëÇÑ Metabolism Á¤º¸  # Phase_1_Metabolizing_Enzyme:Cytochrome P450 1A2 (CYP1A2)Cytochrome P450 2D6 (CYP2D6) 
     
   
  
   
    Protein Binding 
    
      Lidocaine¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸  60-80% 
     
   
  
   
    Half-life 
    
      Lidocaine¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸  109 minutes 
     
   
  
   
    Absorption 
    
      Lidocaine¿¡ ´ëÇÑ Absorption Á¤º¸  Information derived from diverse formulations, concentrations and usages reveals that lidocaine is completely absorbed following parenteral administration, its rate of absorption depending, for example, upon various factors such as the site of administration and the presence or absence of a vasoconstrictor agent. 
     
   
  
   
    Pharmacokinetics 
    
      LidocaineÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á  
	È¿°ú¹ßÇö½Ã°£ (1ȸ bolus ¿ë·®À¸·Î¼) : 45-90ÃÊ
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	 ´Ü¹é°áÇÕ : 60-80%, ¥á1 -acid glycoprotein°ú °áÇÕ
	 ´ë»ç : °£¿¡¼ 90% ´ë»ç  
	
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	 ¹Ý°¨±â (biphasic) : ¿ïÇ÷¼º ½ÉºÎÀü, °£Áúȯ, ¼îÅ©, ÁßÁõÀÇ ½ÅÁúȯ¿¡¼ Áõ°¡
	
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    Biotransformation 
    
      Lidocaine¿¡ ´ëÇÑ Biotransformation Á¤º¸  Primarily hepatic. 
     
   
  
   
    Toxicity 
    
      Lidocaine¿¡ ´ëÇÑ Toxicity Á¤º¸  The oral LD 50 of lidocaine HCl in non-fasted female rats is 459 (346-773) mg/kg (as the salt) and 214 (159-324) mg/kg (as the salt) in fasted female rats. Symptoms of overdose include convulsions, hypoxia, acidosis, bradycardia, arrhythmias and cardiac arrest. 
     
   
  
   
    Drug Interactions 
    
      Lidocaine¿¡ ´ëÇÑ Drug_Interactions Á¤º¸  Not Available 
     
   
  
   
    CYP450  Drug Interaction 
    
      [CYP450 TableÁ÷Á¢Á¶È¸]  
     
   
  
   
    Food Interaction 
    
      Lidocaine¿¡ ´ëÇÑ Food Interaction Á¤º¸  Not Available 
     
   
  
   
    Drug Target 
    
      
      [Drug Target]  
     
   
  
   
    Description 
    
      Lidocaine¿¡ ´ëÇÑ Description Á¤º¸  A local anesthetic and cardiac depressant used as an antiarrhythmia agent. Its actions are more intense and its effects more prolonged than those of procaine but its duration of action is shorter than that of bupivacaine or prilocaine. [PubChem] 
     
   
  
   
    Dosage Form 
    
      Lidocaine¿¡ ´ëÇÑ Dosage_Form Á¤º¸  Aerosol	TopicalAerosol, metered	TopicalCream	TopicalGel	TopicalJelly	TopicalJelly	UrethralLiquid	BuccalLiquid	DentalLiquid	InfiltrationLiquid	IntravenousLiquid	OralLiquid	TopicalLotion	TopicalOintment	TopicalSolution	InfiltrationSolution	IntramuscularSolution	IntravenousSolution	OralSolution	TopicalSpray	TopicalSwab	Topical 
     
   
  
   
    Drug Category 
    
      Lidocaine¿¡ ´ëÇÑ Drug_Category Á¤º¸  AnestheticsAnesthetics, LocalAnti-Arrhythmia AgentsAntiarrhythmic Agents 
     
   
  
   
    Smiles String Canonical 
    
      Lidocaine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸  CCN(CC)CC(=O)NC1=C(C)C=CC=C1C 
     
   
  
   
    Smiles String Isomeric 
    
      Lidocaine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸  CCN(CC)CC(=O)NC1=C(C)C=CC=C1C 
     
   
  
   
    InChI Identifier 
    
      Lidocaine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸  InChI=1/C14H22N2O/c1-5-16(6-2)10-13(17)15-14-11(3)8-7-9-12(14)4/h7-9H,5-6,10H2,1-4H3,(H,15,17)/f/h15H 
     
   
  
   
    Chemical IUPAC Name 
    
      Lidocaine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸  2-diethylamino-N-(2,6-dimethylphenyl)acetamide 
     
   
  
   
    Drug-Induced Toxicity Related Proteins 
    
      DOCA   ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸Replated Protein  :Aquaporin-2Drug  :DOCA Toxicity  :hypertension. [¹Ù·Î°¡±â] LIDOCAINE   ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸Replated Protein  :glucose-regulated protein Drug  :lidocaine Toxicity  :intestinal disorder. [¹Ù·Î°¡±â] Replated Protein  :Alkaline phosphataseDrug  :lidocaine  Toxicity  :lidocaine induced hepatitis. [¹Ù·Î°¡±â] Replated Protein  :C-reactive proteinDrug  :lidocaine  Toxicity  :fever. [¹Ù·Î°¡±â] Replated Protein  :C-reactive proteinDrug  :lidocaine  Toxicity  :lidocaine induced hepatitis. [¹Ù·Î°¡±â] Replated Protein  :Alpha-1-acid glycoproteinDrug  :lidocaine  Toxicity  :lidocaine tolerance. [¹Ù·Î°¡±â] Replated Protein  :Gamma-glutamyltranspeptidase Drug  :lidocaine  Toxicity  :fever. [¹Ù·Î°¡±â] Replated Protein  :Alkaline phosphataseDrug  :lidocaine  Toxicity  :fever. [¹Ù·Î°¡±â] Replated Protein  :Gamma-glutamyltranspeptidase Drug  :lidocaine  Toxicity  :lidocaine induced hepatitis. [¹Ù·Î°¡±â]  
     
   
    
 
	  
	   
	
	  
       
	    
	      
	        
            
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