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Äĺñº¥Æ®¿¡¾î·Î¼Ö COMBIVENT AERO.[Ipratropium Bromide , Salbutamol sulfate]
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Àü¹®ÀǾàǰ | »èÁ¦
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µå·°ÀÎÆ÷¿¡¼´Â ÀǾàǰ ÀÎÅÍ³Ý ÆÇ¸Å¸¦ ÇÏÁö ¾Ê½À´Ï´Ù. |
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À¯·áȸ¿ø °áÀç½Ã¿¡´Â º¸´Ù ´Ù¾çÇÑ ¾à¹°Á¤º¸¸¦
ÀÌ¿ëÇÏ½Ç ¼ö ÀÖ½À´Ï´Ù.
À¯·áÁ¤º¸¸ñ·ÏÀº Àü¹®È¸¿øÀ¸·Î
·Î±×ÀÎ ÇϽøé È®ÀÎ °¡´ÉÇÕ´Ï´Ù.
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| Ç׸ñ |
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û±¸ÄÚµå(KDÄÚµå) ºñ±Þ¿©Á¡°ËÄÚµå »óÇÑ±Ý¾× |
653500690[E04260101]
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\0 ¿ø/10ml/1Åë(2015.11.01)(ÇöÀç¾à°¡)
\7,175 ¿ø/10ml/1Åë(2014.02.01)(º¯°æÀü¾à°¡)
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ÀÏÁ¤·®¾¿ ºÐ¹«µÇ´Â º§ºê°¡ ºÎÂøµÈ ¾Ë·ç¹Ì´½ ³»¾Ð¿ë±â¿¡ À¯¹é»ö Çöʾ×ÀÌ µç ¿¡¾î·Î¼ÖÁ¦
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10ml
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| 10¹Ð¸®¸®ÅÍ |
1 Åë |
8806535006904 |
8806535006911 |
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334800CAE
[µ¿ÀÏÇÑ ÁÖ¼ººÐÄڵ带 °¡Áø ¿À¸®Áö³¯ ¶Ç´Â Á¦³×¸¯ ÀǾàǰ Á¶È¸]
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8806535006904 |
| º¸°ü¹æ¹ý |
±â¹Ð¿ë±â, ½Ç¿Âº¸°ü |
| ¾à¸®ÀÛ¿ë |
[Á¶È¸]
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[ÀûÀÀÁõ º° °Ë»ö]
´ÜÀÏ ±â°üÁö Ä¡·áÁ¦·Î½á ÃæºÐÇÑ Ä¡·áÈ¿°ú¸¦ ¾òÁö ¸øÇÑ ¸¸¼º Æó¼â¼º ÆóÁúȯÀÇ °¡¿ªÀû ±â°üÁö °æ·ÃÀÇ ¿ÏÈ
[Drugbank ÀÇ ¼ººÐÁ¤º¸¿¶÷] [Ipratropium]
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* Àý´ë ÀÓÀǺ¹¿ëÇÏÁö ¸¶½Ã°í ¹Ýµå½Ã ÀÇ»ç ¶Ç´Â ¾à»ç¿Í »ó´ãÇϽñ⠹ٶø´Ï´Ù.
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[ÁÖ¼ººÐÄÚµå:334800CAE ¿¡ µû¸¥ ½É»çÁöħ¿¶÷]
º¸Å뼺ÀÎÀÇ °æ¿ì 1ÀÏ 4ȸ,1ȸ 2¹ø¾¿ ºÐ¹«ÇÑ´Ù. 1ÀÏ ÃÑ 12¹øÀ» ÃʰúÇÏ¿© ºÐ¹«ÇÏÁö ¸»°Í.
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3)15¼¼ ¹Ì¸¸ÀÇ ¼Ò¾Æ
4)Æó¼â¼º½É±Ùºñ´ëÁõ ȯÀÚ ¶Ç´Â ºÎÁ¤ºó¸Æ ȯÀÚ
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| Related FDA Approved Drug |
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 FDA : Cµî±Þ
(salbutamol )
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| * |
»ó±â ÀÓºÎÅõ¿©¿¡ ´ëÇÑ Á¤º¸´Â Àü»êó¸® µÇ¸é¼ ÀÔ·Â ¿À·ù °¡´É¼ºÀÌ Á¸ÀçÇÕ´Ï´Ù. ¿À·ù °¡´É¼ºÀ» ÃÖ¼ÒÈÇϱâ À§ÇÏ¿© ¸¹Àº ³ë·ÂÀ» ±â¿ïÀ̰í ÀÖÀ¸³ª, ±× Á¤È®¼º¿¡ ´ëÇÏ¿© È®½ÅÀ» µå¸± ¼ö ¾ø½À´Ï´Ù. ÀÌ¿¡ ´ëÇØ ȸ»ç´Â Ã¥ÀÓÀ» ÁöÁö ¾Ê½À´Ï´Ù.
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| Pharmacokinetics |
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| Mechanism of Action |
Ipratropium¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Ipratropium bromide is an anticholinergic agent. It blocks muscarinic cholinergic receptors, without specificity for subtypes, resulting in a decrease in the formation of cyclic guanosine monophosphate (cGMP). Most likely due to actions of cGMP on intracellular calcium, this results in decreased contractility of smooth muscle.
Salbutamol¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Salbutamol is a beta(2)-adrenergic agonist and thus it stimulates beta(2)-adrenergic receptors. Binding of albuterol to beta(2)-receptors in the lungs results in relaxation of bronchial smooth muscles. It is believed that salbutamol increases cAMP production by activating adenylate cyclase, and the actions of salbutamol are mediated by cAMP. Increased intracellular cyclic AMP increases the activity of cAMP-dependent protein kinase A, which inhibits the phosphorylation of myosin and lowers intracellular calcium concentrations. A lowered intracellular calcium concentration leads to a smooth muscle relaxation. Increased intracellular cyclic AMP concentrations also cause an inhibition of the release of mediators from mast cells in the airways.
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| Pharmacology |
Ipratropium¿¡ ´ëÇÑ Pharmacology Á¤º¸ Ipratropium bromide, a synthetic ammonium compound structurally similar to atropine, is used as a bronchodilator in the management of cholinergic-mediated bronchospasm associated with chronic obstructive pulmonary disease and in the treatment of rhinorrhea associated with the common cold or with allergic or nonallergic seasonal rhinitis.
Salbutamol¿¡ ´ëÇÑ Pharmacology Á¤º¸ Salbutamol (INN) or albuterol (USAN), a moderately selective beta(2)-receptor agonist similar in structure to terbutaline, is widely used as a bronchodilator to manage asthma and other chronic obstructive airway diseases. The R-isomer, levalbuterol, is responsible for bronchodilation while the S-isomer increases bronchial reactivity. The R-enantiomer is sold in its pure form as Levalbuterol. The manufacturer of levalbuterol, Sepracor, has implied (although not directly claimed) that the presence of only the R-enantiomer produces fewer side-effects.
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| Metabolism |
Ipratropium¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 2D6 (CYP2D6)Cytochrome P450 3A4 (CYP3A4)
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| Protein Binding |
Ipratropium¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ Minimally (0 to 9% in vitro) bound to plasma albumin and a1-acid glycoproteins
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| Half-life |
Ipratropium¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ Approximately 2 hours
Salbutamol¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 1.6 hours
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| Absorption |
Ipratropium¿¡ ´ëÇÑ Absorption Á¤º¸ Inhalation (local)-minimal; Nasal-rapid and minimal
Salbutamol¿¡ ´ëÇÑ Absorption Á¤º¸ Systemic absorption is rapid following aerosol administration.
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| Pharmacokinetics |
Ipratropium BromideÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- ±â°üÁöÈ®ÀåÈ¿°ú ¹ßÇö½Ã°£ : 1-3ºÐ
- ÃÖ´ëÈ¿°ú ¹ßÇö½Ã°£ : 1.5-2 ½Ã°£ À̳»
- ÀÛ¿ëÁö¼Ó½Ã°£ : 4-6 ½Ã°£±îÁö
- Èí¼ö : ÆóÀÇ Ç¥¸éÀ̳ª À§Àå°üÀ¸·ÎºÎÅÍ Àü½Å¼øÈ¯À¸·ÎÀÇ Èí¼ö´Â °ÅÀÇ ¾øÀ½.
- ºÐÆ÷ : ÈíÀÔ : ¿ë·®ÀÇ 15%°¡ Çϱ⵵¿¡ µµ´Þ
Salbutamol sulfateÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- ÃÖ°íÈ¿°ú ¹ßÇö½Ã°£
- °æ±¸ : 2-3½Ã°£
- ºÐ¹«/°æ±¸ ÈíÀÔ : 0.5-2½Ã°£ À̳»
- ÀÛ¿ëÁö¼Ó½Ã°£
- °æ±¸ : 4-6½Ã°£
- ºÐ¹«/°æ±¸ ÈíÀÔ : 3-4½Ã°£
- ´ë»ç : °£¿¡¼ ºñȰ¼º sulfate·Î ´ë»ç
- ¹Ý°¨±â
- ÈíÀÔ : 3.8½Ã°£
- °æ±¸ : 3.7-5½Ã°£
- ¼Ò½Ç : ¹Ìº¯Èü·Î 30% ½Å¹è¼³
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| Biotransformation |
Ipratropium¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hepatic
Salbutamol¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hydrolyzed by esterases in tissue and blood to the active compound colterol. The drug is also conjugatively metabolized to salbutamol 4'-O-sulfate.
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| Toxicity |
Ipratropium¿¡ ´ëÇÑ Toxicity Á¤º¸ LD50=1001mg/kg (orally in mice)
Salbutamol¿¡ ´ëÇÑ Toxicity Á¤º¸ LD50=1100 mg/kg (orally in mice)
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| Drug Interactions |
Ipratropium¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available
Salbutamol¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Food Interaction |
Ipratropium¿¡ ´ëÇÑ Food Interaction Á¤º¸ Not Available
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| Drug Target |
[Drug Target]
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| Description |
Ipratropium¿¡ ´ëÇÑ Description Á¤º¸ A muscarinic antagonist structurally related to atropine but often considered safer and more effective for inhalation use. It is used for various bronchial disorders, in rhinitis, and as an antiarrhythmic. [PubChem]
Salbutamol¿¡ ´ëÇÑ Description Á¤º¸ A racemic mixture with a 1:1 ratio of the r-isomer, levalbuterol, and s-albuterol. It is a short-acting beta2-adrenergic agonist with its main clinical use in asthma. [PubChem]
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| Dosage Form |
Ipratropium¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Aerosol, metered NasalAerosol, metered Respiratory (inhalation)Liquid NasalLiquid Respiratory (inhalation)Solution NasalSolution Respiratory (inhalation)Spray, metered Nasal
Salbutamol¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Aerosol, metered Respiratory (inhalation)Liquid OralPowder Respiratory (inhalation)Solution IntramuscularSolution IntravenousSolution OralSolution Respiratory (inhalation)Tablet Oral
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| Drug Category |
Ipratropium¿¡ ´ëÇÑ Drug_Category Á¤º¸ AntimuscarinicsAntispasmodicsBronchodilator AgentsCholinergic Antagonists
Salbutamol¿¡ ´ëÇÑ Drug_Category Á¤º¸ Adrenergic beta-AgonistsBronchodilator AgentsTocolytic Agents
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| Smiles String Canonical |
Ipratropium¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC(C)[N+]1(C)C2CCC1CC(C2)OC(=O)C(CO)C1=CC=CC=C1
Salbutamol¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC(C)(C)NCC(O)C1=CC(CO)=C(O)C=C1
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| Smiles String Isomeric |
Ipratropium¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CC(C)[N+]1(C)[C@@H]2CC[C@@H]1CC(C2)OC(=O)C(CO)C1=CC=CC=C1
Salbutamol¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CC(C)(C)NC[C@H](O)C1=CC(CO)=C(O)C=C1
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| InChI Identifier |
Ipratropium¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C20H30NO3/c1-14(2)21(3)16-9-10-17(21)12-18(11-16)24-20(23)19(13-22)15-7-5-4-6-8-15/h4-8,14,16-19,22H,9-13H2,1-3H3/q+1/t16-,17-,18?,19?,21?/m1/s1
Salbutamol¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C13H21NO3/c1-13(2,3)14-7-12(17)9-4-5-11(16)10(6-9)8-15/h4-6,12,14-17H,7-8H2,1-3H3
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| Chemical IUPAC Name |
Ipratropium¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ [(1R,5R)-8-methyl-8-propan-2-yl-8-azoniabicyclo[3.2.1]octan-3-yl] 3-hydroxy-2-phenylpropanoate
Salbutamol¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 4-[2-(tert-butylamino)-1-hydroxyethyl]-2-(hydroxymethyl)phenol
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| Drug-Induced Toxicity Related Proteins |
SALBUTAMOL ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸ Replated Protein:Beta-2 adrenergic receptor Drug:Salbutamol Toxicity:desensitization, cardiovascular effects. [¹Ù·Î°¡±â]
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ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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