Literature DB >> 1712708

Sustained release nifedipine formulations. An appraisal of their current uses and prospective roles in the treatment of hypertension, ischaemic heart disease and peripheral vascular disorders.

D Murdoch1, R N Brogden.   

Abstract

Nifedipine antagonises influx of calcium through cell membrane slow channels, and sustained release formulations of the calcium channel blocker have been shown to be effective in the treatment of mild to moderate hypertension and both stable and variant angina pectoris. Preliminary findings also indicate that these formulations are effective in the treatment of Raynaud's phenomenon and hypertension in pregnancy, and that they reduce the frequency of ischaemic episodes in some patients with silent myocardial ischaemia. The exact mechanism of action of nifedipine in all of these disorders has not been defined. However, its potent peripheral and coronary arterial dilator properties, together with improvements in oxygen supply/demand, are of particular importance. A major goal of sustained release therapy is to permit reductions in the frequency of nifedipine administration, preferably to once daily, and thus improve patient compliance. Two new once-daily formulations--the nifedipine gastrointestinal therapeutic system (GITS) and a fixed combination capsule comprising sustained release nifedipine 20 mg and atenolol 50 mg--have exhibited marked antihypertensive efficacy. The GITS preparation has also been used effectively in the treatment of stable angina pectoris, and both formulations appear to be well tolerated. Sustained release nifedipine formulations are generally better tolerated than their conventionally formulated counterparts, particularly with regard to reflex tachycardia. Adverse effects seem to be dose related, are mainly associated with the drug's potent vasodilatory action, and include headache, flushing and dizziness. Generally, these effects are mild to moderate in severity and transient, usually diminishing with continued treatment. Thus, sustained release nifedipine formulations are useful and established cardiovascular therapeutic agents which have demonstrable efficacy in various forms of angina, mild to moderate hypertension and Raynaud's phenomenon. Further, promising results shown by the nifedipine GITS formulation, with its advantage of once daily administration suggest that it is likely to become one of the preferred nifedipine formulations for the treatment of hypertension and the various forms of angina.

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Year:  1991        PMID: 1712708     DOI: 10.2165/00003495-199141050-00006

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  235 in total

1.  The effects of intravenous and oral nifedipine on ex vivo platelet function.

Authors:  T J Walley; K L Woods; D B Barnett
Journal:  Eur J Clin Pharmacol       Date:  1989       Impact factor: 2.953

2.  Calcium antagonist withdrawal syndrome.

Authors:  M Mysliwiec; A Rydzewski; W Bulhak
Journal:  Br Med J (Clin Res Ed)       Date:  1983-06-11

3.  Pharmacokinetics of nifedipine slow release tablet in Mexican subjects: further evidence for an oxidation polymorphism.

Authors:  C Hoyo-Vadillo; G Castañeda-Hernández; J E Herrera; J Vidal-Gárate; A Moreno-Ramos; F Chávez; E Hong
Journal:  J Clin Pharmacol       Date:  1989-09       Impact factor: 3.126

4.  The Nifedipine-Total Ischemia Awareness Program: a national survey of painful and painless myocardial ischemia including results of antiischemic therapy.

Authors:  P F Cohn; G W Vetrovec; R Nesto; F R Gerber
Journal:  Am J Cardiol       Date:  1989-03-01       Impact factor: 2.778

5.  Acute renal failure during nifedipine therapy in a patient with congestive heart failure.

Authors:  J C Eicher; P Morelon; J M Chalopin; Y Tanter; P Louis; G Rifle
Journal:  Crit Care Med       Date:  1988-11       Impact factor: 7.598

6.  Pharmacokinetics and metabolism of nifedipine.

Authors:  K D Raemsch; J Sommer
Journal:  Hypertension       Date:  1983 Jul-Aug       Impact factor: 10.190

7.  Pharmacokinetic studies of nifedipine tablet. Correlation with antihypertensive effects.

Authors:  A M Taburet; E Singlas; J N Colin; O Banzet; M Thibonnier; P Corvol
Journal:  Hypertension       Date:  1983 Jul-Aug       Impact factor: 10.190

8.  Nifedipine in unstable angina: a double-blind, randomized trial.

Authors:  G Gerstenblith; P Ouyang; S C Achuff; B H Bulkley; L C Becker; E D Mellits; K L Baughman; J L Weiss; J T Flaherty; C H Kallman; M Llewellyn; M L Weisfeldt
Journal:  N Engl J Med       Date:  1982-04-15       Impact factor: 91.245

9.  Antihypertensive effects at rest and during exercise of a calcium blocker, nifedipine, alone and in combination with metoprolol.

Authors:  L G Ekelund; C Ekelund; S Rössner
Journal:  Acta Med Scand       Date:  1982

10.  Pharmacokinetic and pharmacodynamic interactions between nifedipine and propranolol or betaxolol.

Authors:  P Vinceneux; M Canal; Y Domart; A Roux; B Cascio; B Orofiamma; J Larribaud; B Flouvat; C Carbon
Journal:  Int J Clin Pharmacol Ther Toxicol       Date:  1986-03
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4.  Comparison of once-daily nifedipine controlled-release with twice-daily nifedipine retard in the treatment of essential hypertension.

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Review 6.  The nifedipine gastrointestinal therapeutic system (GITS). Evaluation of pharmaceutical, pharmacokinetic and pharmacological properties.

Authors:  J S Grundy; R T Foster
Journal:  Clin Pharmacokinet       Date:  1996-01       Impact factor: 6.447

Review 7.  Nifedipine gastrointestinal therapeutic system (GITS). A review of its pharmacodynamic and pharmacokinetic properties and therapeutic efficacy in hypertension and angina pectoris.

Authors:  R N Brogden; D McTavish
Journal:  Drugs       Date:  1995-09       Impact factor: 9.546

Review 8.  [Pharmacologic importance of the combination atenolol/nifedipine in hypertensive patients].

Authors:  A Carré
Journal:  Drugs       Date:  1998       Impact factor: 9.546

Review 9.  Modified-release nifedipine: a review of the use of modified-release formulations in the treatment of hypertension and angina pectoris.

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Journal:  Drugs       Date:  2006       Impact factor: 11.431

10.  Development and validation of LC/MS/MS method for the simultaneous determination of montelukast, gliclazide, and nifedipine and its application to a pharmacokinetic study.

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