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Volumn 92, Issue 4, 2000, Pages 993-1001

Pharmacokinetics and arteriovenous differences in clevidipine concentration following a short- and a long-term intravenous infusion in healthy volunteers

Author keywords

Arteriovenons; Context sensitive times; Decrement times

Indexed keywords

CLEVIDIPINE;

EID: 0034079587     PISSN: 00033022     EISSN: None     Source Type: Journal    
DOI: 10.1097/00000542-200004000-00016     Document Type: Article
Times cited : (52)

References (34)
  • 2
    • 0027403294 scopus 로고
    • The ideal agent for perioperative hypertension and potential cytoprotective effects
    • Levy JH: The ideal agent for perioperative hypertension and potential cytoprotective effects. Acta Anaesthesiol Scand Suppl 1993; 37:20-5
    • (1993) Acta Anaesthesiol Scand Suppl , vol.37 , pp. 20-25
    • Levy, J.H.1
  • 3
    • 0027403296 scopus 로고
    • Comperative study of isradipine and sodium nitroprusside in the control of hypertension in patients following coronary artery-bypass surgery
    • Lawrence CJ, Lestrade A, De Lange S: Comperative study of isradipine and sodium nitroprusside in the control of hypertension in patients following coronary artery-bypass surgery. Acta Anaestesiol Scand Suppl 1993; 37:48-52
    • (1993) Acta Anaestesiol Scand Suppl , vol.37 , pp. 48-52
    • Lawrence, C.J.1    Lestrade, A.2    De Lange, S.3
  • 5
    • 0002442008 scopus 로고    scopus 로고
    • Treatment of perioperative hypertension
    • Edited by Epstein M. Philadelphia, Hanely and Belfus
    • Levy JH, Huraux C, Nordlander M: Treatment of perioperative hypertension, Calcium Antagonists in Clinical Medicine. Edited by Epstein M. Philadelphia, Hanely and Belfus, 1997, pp 345-58
    • (1997) Calcium Antagonists in Clinical Medicine , pp. 345-358
    • Levy, J.H.1    Huraux, C.2    Nordlander, M.3
  • 6
    • 0032979711 scopus 로고    scopus 로고
    • In vitro hydrolysis rate and protein binding of clevidipine, a new ultrashort-acting calcium antagonist metabolised by esterases, in different animal species and man
    • Ericsson H, Tholander B, Regårdh CG: In vitro hydrolysis rate and protein binding of clevidipine, a new ultrashort-acting calcium antagonist metabolised by esterases, in different animal species and man. Eur J Pharm Sci 1999; 8:29-37
    • (1999) Eur J Pharm Sci , vol.8 , pp. 29-37
    • Ericsson, H.1    Tholander, B.2    Regårdh, C.G.3
  • 9
    • 0025782251 scopus 로고
    • Pharmacokinetics and pharmacodynamics of atracurium obtained with arterial and venous blood samples
    • Donati F, Varin F, Ducharme J, Gill SS, Theoret Y, Bevan DR: Pharmacokinetics and pharmacodynamics of atracurium obtained with arterial and venous blood samples. Clin Pharmacol Ther 1991; 49: 515-22
    • (1991) Clin Pharmacol Ther , vol.49 , pp. 515-522
    • Donati, F.1    Varin, F.2    Ducharme, J.3    Gill, S.S.4    Theoret, Y.5    Bevan, D.R.6
  • 10
    • 0032964039 scopus 로고    scopus 로고
    • Influence of arteriovenous sampling on remifentanil pharmacokinetics and pharmacodynamics
    • Hermann DJ, Egan TD, Muir KT: Influence of arteriovenous sampling on remifentanil pharmacokinetics and pharmacodynamics. Clin Pharmacol Ther 1999; 65:511-8
    • (1999) Clin Pharmacol Ther , vol.65 , pp. 511-518
    • Hermann, D.J.1    Egan, T.D.2    Muir, K.T.3
  • 11
    • 0343740040 scopus 로고    scopus 로고
    • Therapeutic dose rates and pharmacokinetics of clevidipine in patients undergoing coronary artery bypass surgery
    • Vuylsteke A, Milner QJ, Ericsson H, Mur D, Dunning J, Latimer RD: Therapeutic dose rates and pharmacokinetics of clevidipine in patients undergoing coronary artery bypass surgery (abstract). Br J Anaesth 1998; 80:A11
    • (1998) Br J Anaesth , vol.80
    • Vuylsteke, A.1    Milner, Q.J.2    Ericsson, H.3    Mur, D.4    Dunning, J.5    Latimer, R.D.6
  • 12
    • 0022336615 scopus 로고
    • Use of dodecyl sulfate as an esterase inhibitor before gas-chromatographic determination of labile β-adrenoceptor blocking drugs
    • Holm G, Hanssen K, Svensson L: Use of dodecyl sulfate as an esterase inhibitor before gas-chromatographic determination of labile β-adrenoceptor blocking drugs. Clin Chem 1985; 31:868-70
    • (1985) Clin Chem , vol.31 , pp. 868-870
    • Holm, G.1    Hanssen, K.2    Svensson, L.3
  • 13
    • 0033052775 scopus 로고    scopus 로고
    • Determination of an ultrashort-acting antihypertensive dihydropyridine, clevidipine, in blood using capillary gas chromatography mass spectrometry and of the primary metabolite using liquid chromatography and fluorescence detection
    • Fakt C, Stenhoff H: Determination of an ultrashort-acting antihypertensive dihydropyridine, clevidipine, in blood using capillary gas chromatography mass spectrometry and of the primary metabolite using liquid chromatography and fluorescence detection. J Chromatogr B Biomed Appl 1999; 723:211-9
    • (1999) J Chromatogr B Biomed Appl , vol.723 , pp. 211-219
    • Fakt, C.1    Stenhoff, H.2
  • 14
    • 0018091195 scopus 로고
    • Application of Akaiki's information criteria (AIC) in the evaluation of linear pharmacokinetic equations
    • Yamaoka K, Nakagawa T, Uno T: Application of Akaiki's information criteria (AIC) in the evaluation of linear pharmacokinetic equations. J Pharmacokinet Biopharm 1976; 6:165-75
    • (1976) J Pharmacokinet Biopharm , vol.6 , pp. 165-175
    • Yamaoka, K.1    Nakagawa, T.2    Uno, T.3
  • 16
    • 0026510602 scopus 로고
    • Context-sensitive half-time in multicompartment pharmacokinetic models for intravenous anesthetic drugs
    • Hughes M, Glass P, Jacobs J: Context-sensitive half-time in multicompartment pharmacokinetic models for intravenous anesthetic drugs. ANESTHESIOLOGY 1992; 76:334-41
    • (1992) Anesthesiology , vol.76 , pp. 334-341
    • Hughes, M.1    Glass, P.2    Jacobs, J.3
  • 17
    • 0025757077 scopus 로고
    • Pharmacokinetics, pharmacodynamics, and rational opioid selection
    • Shafer SL, Varvel JR: Pharmacokinetics, pharmacodynamics, and rational opioid selection. ANESTHESIOLOGY 1991; 74:53-63
    • (1991) Anesthesiology , vol.74 , pp. 53-63
    • Shafer, S.L.1    Varvel, J.R.2
  • 18
    • 0030743105 scopus 로고    scopus 로고
    • Myocardial circulatory and metabolic effects of clevidipine after coronary artery bypass grafting (CABG)
    • Kieler-Jensen N, Jolin-Mellgård Å, Nordlander M, Ricksten SE: Myocardial circulatory and metabolic effects of clevidipine after coronary artery bypass grafting (CABG). Br J Anaesth 1997; 78:A12
    • (1997) Br J Anaesth , vol.78
    • Kieler-Jensen, N.1    Jolin-Mellgård, Å.2    Nordlander, M.3    Ricksten, S.E.4
  • 20
    • 0020411522 scopus 로고
    • Arterial-venous nitroglycerin gradient during intravenous infusion in man
    • Armstrong PW, Moffat JA, Marks GS: Arterial-venous nitroglycerin gradient during intravenous infusion in man. Circulation 1982; 666:1273-6
    • (1982) Circulation , vol.666 , pp. 1273-1276
    • Armstrong, P.W.1    Moffat, J.A.2    Marks, G.S.3
  • 21
    • 0020411910 scopus 로고
    • Possible site of the in vivo disposition of sodium nitroprusside in the rat
    • Kreye VA, Reske SN: Possible site of the in vivo disposition of sodium nitroprusside in the rat. Naunyn-Schmiedebergs Arch Pharmacol 1982; 320:260-5
    • (1982) Naunyn-Schmiedebergs Arch Pharmacol , vol.320 , pp. 260-265
    • Kreye, V.A.1    Reske, S.N.2
  • 22
    • 0024442139 scopus 로고
    • The phenomenon and rationale of marked dependence of drug concentration on blood sampling site: I. Implications in pharmacokinetics, pharmacodynamics, toxicology and therapeutics
    • Chiou WL: The phenomenon and rationale of marked dependence of drug concentration on blood sampling site: I. Implications in pharmacokinetics, pharmacodynamics, toxicology and therapeutics Clin Pharmacokinet 1989; 17:175-99
    • (1989) Clin Pharmacokinet , vol.17 , pp. 175-199
    • Chiou, W.L.1
  • 23
    • 0024461323 scopus 로고
    • The phenomenon and rationale of marked dependence of drug concentration on blood sampling site: II. Implications in pharmacokinetics, pharmacodynamics, toxicology and therapeutics
    • Chiou WL: The phenomenon and rationale of marked dependence of drug concentration on blood sampling site: II. Implications in pharmacokinetics, pharmacodynamics, toxicology and therapeutics. Clin Pharmacokinet 1989; 17:275-90
    • (1989) Clin Pharmacokinet , vol.17 , pp. 275-290
    • Chiou, W.L.1
  • 25
    • 0030723143 scopus 로고    scopus 로고
    • Arteriovenous differences in plasma concentration of nicotine and cathecholamines and related cardiovascular effects after smoking, nicotine nasal spray, and intravenous nicotine
    • Gourley SG, Benowitz NL: Arteriovenous differences in plasma concentration of nicotine and cathecholamines and related cardiovascular effects after smoking, nicotine nasal spray, and intravenous nicotine. Clin Pharmacol Ther 1997; 62:453-63
    • (1997) Clin Pharmacol Ther , vol.62 , pp. 453-463
    • Gourley, S.G.1    Benowitz, N.L.2
  • 26
    • 0343740036 scopus 로고
    • Fundamental properties: Mechanisms, classification, sites of action
    • Norwell, MA: Kluwer Academic Publisher
    • Opie LH: Fundamental properties: Mechanisms, classification, sites of action, Clinical Use of Calcium Channel Antagonist Drugs. Norwell, MA: Kluwer Academic Publisher, 1990, pp 28-70
    • (1990) Clinical Use of Calcium Channel Antagonist Drugs , pp. 28-70
    • Opie, L.H.1
  • 27
    • 0004218743 scopus 로고
    • New York, Oxford University Press
    • Folkow B, Neil E: Circulation. New York, Oxford University Press, 1971
    • (1971) Circulation
    • Folkow, B.1    Neil, E.2
  • 30
    • 0027750786 scopus 로고
    • A mathematical model for dynamics of cardiovascular drug action: Application to intravenous dihydropyridines in healthy volunteers
    • Francheteau P, Steimer J, Merdjan H, Guerret M, Dubray C: A mathematical model for dynamics of cardiovascular drug action: Application to intravenous dihydropyridines in healthy volunteers. J Pharmacokinet Biopharm 1993; 21:489-514
    • (1993) J Pharmacokinet Biopharm , vol.21 , pp. 489-514
    • Francheteau, P.1    Steimer, J.2    Merdjan, H.3    Guerret, M.4    Dubray, C.5
  • 31
    • 0028928324 scopus 로고
    • Compartment model to describe peripheral arterial-venous drug concentration gradients with drug elimination from the venous sampling compartment
    • Jacobs JR, Nath PA: Compartment model to describe peripheral arterial-venous drug concentration gradients with drug elimination from the venous sampling compartment. J Pharm Sci 1995; 84:370-5
    • (1995) J Pharm Sci , vol.84 , pp. 370-375
    • Jacobs, J.R.1    Nath, P.A.2
  • 32
    • 0024811607 scopus 로고
    • Clinical pharmacology and the choice between theory and empiricism
    • Sheiner LB: Clinical pharmacology and the choice between theory and empiricism. Clin Pharmacol Ther 1989; 46:605-15
    • (1989) Clin Pharmacol Ther , vol.46 , pp. 605-615
    • Sheiner, L.B.1
  • 33
    • 0027968057 scopus 로고
    • Pharmacokinetic-pharmacodynamic (PK-PD) modelling in non-steady-state studies and arteriovenous drug concentration differences
    • Gumbleton M, Oie S, Verotta D: Pharmacokinetic-pharmacodynamic (PK-PD) modelling in non-steady-state studies and arteriovenous drug concentration differences. Br J Clin Pharmacol 1994; 38:389-400
    • (1994) Br J Clin Pharmacol , vol.38 , pp. 389-400
    • Gumbleton, M.1    Oie, S.2    Verotta, D.3
  • 34
    • 0030666686 scopus 로고    scopus 로고
    • The impact of arteriovenous concentration differences on pharmacodynamic parameter estimates
    • Tuk B, Danhof M, Mandema JW: The impact of arteriovenous concentration differences on pharmacodynamic parameter estimates. J Pharmacokin Biopharm 1997; 25:39-62
    • (1997) J Pharmacokin Biopharm , vol.25 , pp. 39-62
    • Tuk, B.1    Danhof, M.2    Mandema, J.W.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.