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1) ¾Ï·ÎµðÇÉÀº Ƽ¾ÆÁöµå°è ÀÌ´¢Á¦, ¾ËÆÄÂ÷´ÜÁ¦, º£Å¸Â÷´ÜÁ¦, ACEÀúÇØÁ¦, ÀÛ¿ë½Ã°£ÀÌ ±ä Áú»ê¿°Á¦Á¦, ´ÏÆ®·Î±Û¸®¼¼¸° ¼³ÇÏÁ¤, ºñ½ºÅ×·ÎÀ̵强 ¼Ò¿°Á¦, Ç×»ýÁ¦, °æ±¸ Ç÷´ç°ÇÏÁ¦¿Í º´¿ë ½Ã ¾ÈÀüÇÏ¿´´Ù.
2) »ç¶÷Ç÷ÀåÀ» ÀÌ¿ëÇÑ ½ÇÇè½ÇÀûÀÚ·á´Â ¾Ï·ÎµðÇÉÀÌ µð°î½Å, Æä´ÏÅäÀÎ, ¿ÍÆÄ¸°, Àεµ¸ÞŸ½ÅÀÇ ´Ü¹é°áÇÕ¿¡ ¿µÇâÀ» ¹ÌÄ¡Áö ¾Ê´Â ´Ù´Â °ÍÀ» ¾Ë·ÁÁØ´Ù.
3) ÀÚ¸ùÁ꽺: 20¸íÀÇ °Ç°ÇÑ Áö¿øÀÚ¿¡¼ 240 mLÀÇ ÀÚ¸ùÁ꽺¿Í ¾Ï·ÎµðÇÉ 10 mgÀÇ ´Üȸº´¿ëÅõ¿©´Â ¾Ï·ÎµðÇÉÀÇ ¾àµ¿Çп¡ À¯ÀÇÇÑ ¿µÇâÀ» ¹ÌÄ¡Áö ¾Ê¾Ò´Ù. ÀÌ ½ÃÇè¿¡¼ ¾Ï·ÎµðÇÉÀÇ ÁÖ ´ë»ç°æ·ÎÀÎ CYP3A4¿¡¼ÀÇ À¯ÀüÀû ´ÙÇü¼º (genetic polymorphism) ¿¡ ´ëÇÑ ¿µÇâÆò°¡´Â ÀÌ·ç¾îÁöÁö ¾Ê¾Ò´Ù. µû¶ó¼, ¾Ï·ÎµðÇÉÀº ÀÚ¸ùÀ̳ª ÀÚ¸ùÁ꽺¿Í º´¿ë½Ã ÀϺΠȯÀÚ¿¡¼ »ýüÀÌ¿ë·ü Áõ°¡·Î ÀÎÇÑ Ç÷¾Ð°ÇÏ È¿°úÀÇ Áõ°¡°¡ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¹Ç·Î, º´¿ëÅõ¿©¸¦ ±ÇÀåÇÏÁö ¾Ê´Â´Ù.
4) ´ÜÆ®·Ñ·» (ÁÖÀÔ): IV¸¦ ÅëÇØ º£¶óÆÄ¹Ð, ´ÜÆ®·Ñ·»À» Åõ¿©ÇÏ´Â µ¿¹°½ÇÇè¿¡¼ Ä¡¸íÀûÀÎ ½É½Ç¿¬ÃàÀÌ Áö¼ÓÀûÀ¸·Î °üÂûµÇ¾ú´Ù. ¾Ï·ÎµðÇɰú ´ÜÆ®·Ñ·»ÀÇ µ¿½ÃÅõ¿©´Â ÇÇÇØ¾ß ÇÑ´Ù.
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6) Ŭ·¡¸®Æ®·Î¸¶À̽Å: Ŭ·¡¸®Æ®·Î¸¶À̽ÅÀº ½ÃÅäÅ©·Ò P3A4 ÀúÇØÁ¦ÀÌ´Ù. Ŭ·¡¸®Æ®·Î¸¶À̽ÅÀ» ÀÌ ¾à°ú º´¿ëÅõ¿©½Ã ÀúÇ÷¾ÐÀÇ À§ÇèÀÌ Áõ°¡ÇÏ¿´´Ù.
ÀÌ ¾à°ú Ŭ·¡¸®Æ®·Î¸¶À̽ÅÀ» º´¿ëÅõ¿©½Ã ȯÀÚ¸¦ ÁÖÀDZí°Ô °üÂûÇÏ´Â °ÍÀÌ ±ÇÀåµÈ´Ù.
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(2) ¾Ë·ç¹Ì´½/¸¶±×³×½· (Á¦»êÁ¦): ¾Ë·ç¹Ì´½/¸¶±×³×½· Á¦»êÁ¦¿Í ´Üȸ¿ë·®ÀÇ ¾Ï·ÎµðÇɰú º´¿ëÅõ¿© ½Ã ¾Ï·ÎµðÇÉÀÇ ¾àµ¿Çп¡ À¯ÀÇÀûÀÎ ¿µÇâÀÌ ¾ø¾ú´Ù.
(3) ½Çµ¥³ªÇÊ: ¿ø¹ß¼º °íÇ÷¾ÐȯÀÚ¿¡ ½Çµ¥³ªÇÊ 100 mg ´Üȸ¿ë·®ÀÇ Åõ¿©´Â ¾Ï·ÎµðÇÉÀÇ ¾àµ¿ÇÐÀû ÆÄ¶ó¸ÞŸ¿¡ ¿µÇâÀ» ¹ÌÄ¡Áö ¾Ê¾Ò´Ù. ¾Ï·ÎµðÇɰú ½Çµ¥³ªÇÊÀ» º´¿ëÅõ¿© ½Ã, °¢ ¾à¹°Àº ´Üµ¶ÀûÀ¸·Î °¢°¢ÀÇ Ç÷¾ÐÀúÇÏÈ¿°ú¸¦ ¹ßÈÖÇÑ´Ù.
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(5) CYP3A4 À¯µµÁ¦: CYP3A4 À¯µµÁ¦ (¿¹, ¸®ÆÊÇǽÅ, ¼¼ÀÎÆ® Á¸½º ¿öÆ® (hypericum perforatum))¿ÍÀÇ º´¿ëÅõ¿©´Â ¾Ï·ÎµðÇÉÀÇ Ç÷Àå³óµµ¸¦ º¯È½Ãų ¼ö ÀÖ´Ù. ±×·¯¹Ç·Î ƯÈ÷ °·ÂÇÑ CYP3A4 À¯µµÁ¦¿Í º´¿ëÅõ¿©ÇÏ´Â ±â°£ ¹× ±× ÀÌÈÄ¿¡ Ç÷¾ÐÀ» ¸ð´ÏÅ͸µÇÏ°í ¿ë·® Á¶ÀýÀ» °í·ÁÇØ¾ß ÇÑ´Ù.
8) ¾Ï·ÎµðÇÉÀÌ ´Ù¸¥ ¾à¹°µé¿¡ ¹ÌÄ¡´Â ¿µÇâ
(1) ¾ÆÅ丣¹Ù½ºÅ¸Æ¾: ¾ÆÅ丣¹Ù½ºÅ¸Æ¾ 80 mg°ú ¾Ï·ÎµðÇÉ 10 mg ´Ùȸ¿ë·®À» º´¿ëÅõ¿©½Ã ¾ÆÅ丣¹Ù½ºÅ¸Æ¾ÀÇ Ç×Á¤ ¾àµ¿ÇÐÀû ÆÄ¶ó¸ÞÅÍ¿¡ À¯ÀÇÀûÀÎ º¯È°¡ ¾ø¾ú´Ù.
(2) µð°î½Å: °Ç°ÇÑ Áö¿øÀÚ¿¡°Ô ¾Ï·ÎµðÇɰú µð°î½ÅÀ» º´¿ëÅõ¿© ½Ã Ç÷ûµð°î½ÅÀÇ ¼öÄ¡ ȤÀº µð°î½ÅÀÇ ½ÅÀå Ŭ¸®¾î·±½º¿¡ º¯È°¡ ¾ø¾ú´Ù.
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(6) Ÿũ·Î¸®¹«½º: ÀÌ ¾à°ú º´¿ëÅõ¿© ½Ã Ÿũ·Î¸®¹«½ºÀÇ Ç÷Áß³óµµ Áõ°¡ À§ÇèÀÌ ÀÖÀ¸¹Ç·Î Ÿũ·Î¸®¹«½º·Î Ä¡·á ¹Þ´Â ȯÀÚ¿¡°Ô ÀÌ ¾à Åõ¿© ½Ã Ÿũ·Î¸®¹«½ºÀÇ Ç÷Á߳󵵸¦ ¸ð´ÏÅ͸µÇϰí, Ÿũ·Î¸®¹«½ºÀÇ Åõ¿©·®À» ÀûÀýÈ÷ Á¶ÀýÇÏ¿© Ÿũ·Î¸®¹«½º µ¶¼ºÀ» ÇÇÇϵµ·Ï ÇØ¾ß ÇÑ´Ù
(7) mTOR ¾ïÁ¦Á¦: mTOR ¾ïÁ¦Á¦(¿¹, ½Ã·Ñ¸®¹«½º, Å۽÷Ѹ®¹«½º, ¿¡º£·Î¸®¹«½º)´Â CYP3AÀÇ ±âÁúÀÌ´Ù. ¾Ï·ÎµðÇÉÀº ¾àÇÑ CYP3A ÀúÇØÁ¦À̸ç, mTOR ¾ïÁ¦Á¦¿Í º´¿ëÅõ¿©½Ã ¾Ï·ÎµðÇÉÀÌ mTOR ¾ïÁ¦Á¦¿¡ ´ëÇÑ ³ëÃâÀ» Áõ°¡½Ãų ¼ö ÀÖ´Ù.
(8) ½É¹Ù½ºÅ¸Æ¾: ¾Ï·ÎµðÇÉ 10 mg°ú ½É¹Ù½ºÅ¸Æ¾ 80 mgÀÇ ´Ùȸ¿ë·® º´¿ëÅõ¿©´Â ½É¹Ù½ºÅ¸Æ¾ ´Üµ¶Åõ¿©½Ã¿Í ºñ±³ÇÏ¿© ½É¹Ù½ºÅ¸Æ¾ÀÇ ³ëÃâÀ» 77%Á¤µµ Áõ°¡½ÃÄ×´Ù. ¾Ï·ÎµðÇÉÀ» Åõ¿©¹Þ´Â ȯÀÚ¿¡¼ ½É¹Ù½ºÅ¸Æ¾ 1ÀÏ ÃÖ´ë Åõ¿©¿ë·®Àº 20 mg±îÁöÀÌ´Ù. |
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| Mechanism of Action |
Amlodipine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Amlodipine is a calcium channel blocking agent. It inhibits the influx of extracellular calcium across the myocardial and vascular smooth muscle cell membranes. The decrease in intracellular calcium inhibits the contractile processes of the myocardial smooth muscle cells, causing dilation of the coronary and systemic arteries, increased oxygen delivery to the myocardial tissue, decreased total peripheral resistance, decreased systemic blood pressure, and decreased afterload. Another possible mechanism is that amlodipine inhibits vascular smooth muscle carbonic anhydrase I activity with consecutive pH increase which may be involved in intracelluar calcium influx through calcium channels.
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| Pharmacology |
Amlodipine¿¡ ´ëÇÑ Pharmacology Á¤º¸ Amlodipine, a calcium-channel blocker, is used alone or with benazepril, an angiotensin-converting enzyme inhibitor, to treat hypertension, chronic stable angina pectoris, and Prinzmetal's variant angina. Amlodipine is similar to the peripheral vasodilator nifedipine and other members of the dihydropyridine class.
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| Metabolism |
Amlodipine¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 3A4 (CYP3A4)
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| Protein Binding |
Amlodipine¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ 97.5%
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| Half-life |
Amlodipine¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 30-50 hours
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| Absorption |
Amlodipine¿¡ ´ëÇÑ Absorption Á¤º¸ Amlodipine is slowly and almost completely absorbed from the gastrointestinal tract.
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| Pharmacokinetics |
Amlodipine besylateÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- ÀÛ¿ë¹ßÇö½Ã°£ : 30~50ºÐ
- ÃÖ°íÈ¿°ú ¹ßÇö½Ã°£ : 6~12½Ã°£
- ÀÛ¿ëÁö¼Ó½Ã°£ : 24½Ã°£
- Èí¼ö : °æ±¸ : Èí¼ö ÀßµÊ
- ´Ü¹é°áÇÕ : 93%
- ´ë»ç : 90% ÀÌ»óÀº ºñȰ¼ºÇüÀ¸·Î, °£´ë»ç
- »ýü³»ÀÌ¿ëÀ² : 64%~90%
- ¹Ý°¨±â : 30~50½Ã°£
- ¼Ò½Ç : ´ë»çü ¹× ¹Ìº¯Èü·Î¼ ½Å¹è¼³
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| Biotransformation |
Amlodipine¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hepatic.
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| Toxicity |
Amlodipine¿¡ ´ëÇÑ Toxicity Á¤º¸ Gross overdosage could result in excessive peripheral vasodilatation and possibly reflex tachycardia. Marked and probably prolonged systemic hypotension up to an including shock with fatal outcome have been reported.
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| Drug Interactions |
Amlodipine¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Diltiazem Diltiazem increases the effect and toxicity of amlodipineQuinupristin This combination presents an increased risk of toxicity
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸] Amlodipine¿¡ ´ëÇÑ P450 table
SUBSTRATES
CYP 3A4/3A5/3A7
Macrolide antibiotics:
clarithromycin
erythromycin
NOT azithromycin
telithromycin
Anti-arrhythmics:
quinidine
Benzodiazepines:
alprazolam
diazepam
midazolam
triazolam
Immune Modulators:
cyclosporine
tacrolimus (FK506)
HIV Protease Inhibitors:
indinavir
ritonavir
saquinavir
Prokinetic:
cisapride
Antihistamines:
astemizole
chlorpheniramine
Calcium Channel Blockers:
**amlodipine**
diltiazem
felodipine
nifedipine
nisoldipine
nitrendipine
verapamil
HMG CoA Reductase Inhibitors:
atorvastatin
cerivastatin
lovastatin
NOT pravastatin
simvastatin
aripiprazole
buspirone
gleevec
haloperidol (in part)
methadone
pimozide
quinine
NOT rosuvastatin
sildenafil
tamoxifen
trazodone
vincristine
INHIBITORS
CYP 3A4/3A5/3A7
HIV Protease Inhibitors:
indinavir
nelfinavir
ritonavir
amiodarone
NOT azithromycin
cimetidine
clarithromycin
diltiazem
erythromycin
fluvoxamine
grapefruit juice
itraconazole
ketoconazole
mibefradil
nefazodone
troleandomycin
verapamil
INDUCERS
CYP 3A4/3A5/3A7
carbamazepine
phenobarbital
phenytoin
rifabutin
rifampin
St. John's wort
troglitazone
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| Food Interaction |
Amlodipine¿¡ ´ëÇÑ Food Interaction Á¤º¸ Take without regard to meals.Grapefruit can significantly increase serum levels of this product.Avoid taking grapefruit or grapefruit juice throughout treatment.Avoid natural licorice.
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| Drug Target |
[Drug Target]
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| Description |
Amlodipine¿¡ ´ëÇÑ Description Á¤º¸ A long-acting dihydropyridine calcium channel blocker. It is effective in the treatment of angina pectoris and hypertension. [PubChem]
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| Drug Category |
Amlodipine¿¡ ´ëÇÑ Drug_Category Á¤º¸ AntianginalsAntihypertensive AgentsCalcium Channel BlockersVasodilator Agents
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| Smiles String Canonical |
Amlodipine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CCOC(=O)C1=C(COCCN)NC(C)=C(C1C1=CC=CC=C1Cl)C(=O)OC
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| Smiles String Isomeric |
Amlodipine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CCOC(=O)C1=C(COCCN)NC(C)=C([C@@H]1C1=CC=CC=C1Cl)C(=O)OC
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| InChI Identifier |
Amlodipine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C20H25ClN2O5/c1-4-28-20(25)18-15(11-27-10-9-22)23-12(2)16(19(24)26-3)17(18)13-7-5-6-8-14(13)21/h5-8,17,23H,4,9-11,22H2,1-3H3
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| Chemical IUPAC Name |
Amlodipine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ O3-ethyl O5-methyl 2-(2-aminoethoxymethyl)-4-(2-chlorophenyl)-6-methyl-1,4-dihydropyridine-3,5-dicarboxylate
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º» ¼öÁ¤ÀÏ Á¤º¸´Â Çã°¡Á¤º¸ ÀÌ¿ÜÀÇ ±âŸÁ¤º¸ ¼öÁ¤ÀÏÀ» ÀǹÌÇϹǷÎ, Çã°¡Á¤º¸¼öÁ¤ÀÏÀº º»¹®¿¡ Ç¥±âµÈ ³¯Â¥¸¦ ÂüÁ¶ÇϽñ⠹ٶø´Ï´Ù.
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»ó¼¼Á¤º¸´Â ½ÄǰÀǾàǰ¾ÈÀüóÀÇ Á¦Ç°Çã°¡»çÇ×À» Åä´ë·Î ÀÛ¼ºµÇ¾úÀ¸¸ç ¿ä¾àÁ¤º¸´Â »ó¼¼Á¤º¸ ¹× ±âŸ¹®ÇåÀ» ±â¹ÝÀ¸·Î µå·°ÀÎÆ÷¿¡¼ ÆíÁýÇÑ ³»¿ëÀÔ´Ï´Ù. Á¦Ç°Çã°¡»çÇ×ÀÇ ¸ñÂ÷¿Í ´Ù¼Ò »óÀÌÇÒ ¼ö ÀÖ½À´Ï´Ù. |
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µå·°ÀÎÆ÷ ÀǾàÇмúÁ¤º¸´Â ½ÄǰÀǾàǰ¾ÈÀüóÀÇ Á¦Ç°Çã°¡»çÇ×, Çмú¹®Çå, Á¦¾àȸ»ç Á¦°øÁ¤º¸ µîÀ» ±Ù°Å·Î ÀÛ¼ºµÈ Âü°í Á¤º¸ÀÔ´Ï´Ù.
Á¤º¸ÀÇ Á¤È®¼ºÀ» À§ÇØ ³ë·ÂÇϰí ÀÖÀ¸³ª ÆíÁý»óÀÇ ¿À·ù, Çã°¡»çÇ× º¯°æ, Ãß°¡ÀûÀÎ Çмú¿¬±¸ ¶Ç´Â Àӻ󿬱¸ ¹ßÇ¥ µîÀ¸·Î ÀÎÇØ ¹ß»ýÇÏ´Â ¹®Á¦¿¡ ´ëÇØ µå·°ÀÎÆ÷´Â
Ã¥ÀÓÀ» ÁöÁö ¾Ê½À´Ï´Ù. ÀÚ¼¼ÇÑ ³»¿ëÀº ¡°Ã¥ÀÓÀÇ ÇÑ°è ¹× ¹ýÀû°íÁö¡±¸¦ ÂüÁ¶ÇØ ÁֽʽÿÀ.
¹Ýµå½Ã Á¦Á¶¡¤¼öÀÔ»ç, ÆÇ¸Å»ç, ÀÇ»ç, ¾à»ç¿¡°Ô ÃÖÁ¾ÀûÀ¸·Î È®ÀÎÇϽñ⠹ٶø´Ï´Ù.
ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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