Literature DB >> 8846626

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

J S Grundy1, R T Foster.   

Abstract

Nifedipine is a short-acting calcium antagonist formulated into several different oral preparations, each of which offers a distinct drug release profile. Of these, the nifedipine gastrointestinal therapeutic system (GITS) affords (rate)-controlled-release (CR) and once-daily administration. Although it is recognised that CR drug formulations may enhance the treatment compliance of patients by reducing the number of daily doses, there are several pharmaceutical, pharmacokinetic and pharmacological considerations which may influence the ultimate selection of a particular dosage form. The formulation design of the nifedipine GITS involves an osmotic pump process which provides approximately zero-order delivery of the drug. This mechanism serves to prevent the possibility of dose dumping, but more importantly allows for maintenance of the relatively constant plasma drug concentrations assumed necessary to maintain smooth control of blood pressure. The pharmacokinetic characteristics of the nifedipine GITS have been evaluated in both single- and multiple-dose studies. The GITS formulation provides drug concentrations which reach a plateau within 6 hours after administration of a single dose, and continue at that concentration until at least 24 hours after administration. In this way large fluctuations in plasma drug concentrations are avoided, which may improve the efficacy and tolerability of the drug. Although a trend showing a small increase in the 24-hour plasma nifedipine concentrations has been observed by our group from some single-dose studies, it does not appear to be clinically relevant. One potentially important disadvantage of the GITS compared with 'naturally' long-acting agents is that the 'intrinsic' pharmacokinetic properties of nifedipine may be exposed in poorly compliant patients, leading to extended periods of subtherapeutic drug concentrations. Drug delivery by the nifedipine GITS is unaffected by changes in pH and gastrointestinal (GI) motility, but the rate of drug release can increase slightly with food intake (although absolute bioavailability remains unchanged). No studies have been conducted to determine the average GI transit time of this particular dosage form, but it is possible that inadequate retention may occur in some patients, perhaps leading to less optimal clinical outcomes. For example, the median GI transit time for both oxprenolol and metoprolol Oros drug delivery systems has been reported as 27.4 hours, with individual times ranging from 5.1 to 58.3 hours. The possibility of inadequate GI retention of the nifedipine GITS is perhaps more likely in patients who have pre-existing GI motility disorders or who are taking other medications that enhance GI motility. The interaction between grapefruit juice and nifedipine is interesting, considering that the exact mechanism involved has yet to be determined. Nonetheless, inhibition of presystemic metabolic processes (probably involving liver enzymes but possibly also enzymes contained within the wall of the small intestine) is likely to be a factor in the increased bioavailability of nifedipine observed in individuals coingesting grapefruit juice. Thus, potential nifedipine formulation differences with respect to the degree of interaction with grapefruit juice may occur if a significant degree of extrahepatic metabolism is involved. The majority of clinical trials with the nifedipine GITS have assessed its efficacy in patients with mild-to-moderate essential hypertension, and have found it to be at least equivalent to other dosage forms of the drug. Since there is limited information available directly comparing the efficacy and adverse effects of the different types of nifedipine formulation, little attention has been focused on this subject. However, modifying the rate and duration of nifedipine release may profoundly affect the clinical performance of this drug. A slower rate of intravenous nifedipine infusion has been shown to reduce the incide

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Year:  1996        PMID: 8846626     DOI: 10.2165/00003088-199630010-00003

Source DB:  PubMed          Journal:  Clin Pharmacokinet        ISSN: 0312-5963            Impact factor:   6.447


  110 in total

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Journal:  Br J Clin Pharmacol       Date:  1987-10       Impact factor: 4.335

Review 5.  Pharmacokinetics as an aid to optimising compliance with medications.

Authors:  P Rudd; L Lenert
Journal:  Clin Pharmacokinet       Date:  1995-01       Impact factor: 6.447

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Authors:  H L Elliott; P A Meredith
Journal:  Lancet       Date:  1993-01-30       Impact factor: 79.321

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Authors:  D Murdoch; R N Brogden
Journal:  Drugs       Date:  1991-05       Impact factor: 9.546

8.  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

9.  Pharmacokinetics and metabolism of nifedipine.

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

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Journal:  Hypertension       Date:  1983 Jul-Aug       Impact factor: 10.190

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  11 in total

Review 1.  Pharmacokinetic and pharmacodynamic drug interactions with ethanol (alcohol).

Authors:  Lingtak-Neander Chan; Gail D Anderson
Journal:  Clin Pharmacokinet       Date:  2014-12       Impact factor: 6.447

2.  The role of oral controlled release matrix tablets in drug delivery systems.

Authors:  Ali Nokhodchi; Shaista Raja; Pryia Patel; Kofi Asare-Addo
Journal:  Bioimpacts       Date:  2012-11-04

Review 3.  The INSIGHT and NORDIL trials: Are calcium antagonists equivalent to established drug therapies for cardiovascular protection?

Authors:  M C Ruddy
Journal:  Curr Hypertens Rep       Date:  2001-08       Impact factor: 5.369

Review 4.  Clinical pharmacokinetics of nifedipine. Implications for the care of the elderly.

Authors:  H L Elliott; P A Meredith
Journal:  Drugs Aging       Date:  1997-12       Impact factor: 3.923

Review 5.  Use of in vitro and in vivo data to estimate the likelihood of metabolic pharmacokinetic interactions.

Authors:  R J Bertz; G R Granneman
Journal:  Clin Pharmacokinet       Date:  1997-03       Impact factor: 6.447

6.  Efficacy and tolerability of long-acting nifedipine GITS/OROS monotherapy or combination therapy in hypertensive patients: results of a 12-week international, prospective, multicentre, observational study.

Authors:  Kwo-Chang Ueng; Sun Ningling; Abd El Maksod; Kuan-Yu Hung; Yin Yuehui
Journal:  Clin Drug Investig       Date:  2011       Impact factor: 2.859

7.  Relative effects of dihydropyridine L-type calcium channel antagonism on biliary, duodenal, and vascular tissues: an in vivo and in vitro analysis in Australian brush-tailed possum.

Authors:  A G Craig; A Tottrup; J Toouli; G T P Saccone
Journal:  Dig Dis Sci       Date:  2002-09       Impact factor: 3.199

8.  A randomized controlled trial on the blood pressure-lowering effect of amlodipine and nifedipine-GITS in sustained hypertension.

Authors:  Qi-Fang Huang; Chang-Sheng Sheng; Yan Li; Yu Dou; Mei-Sheng Zheng; Zhi-Ming Zhu; Ji-Guang Wang
Journal:  J Clin Hypertens (Greenwich)       Date:  2019-04-11       Impact factor: 3.738

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

Authors:  Katherine F Croom; Keri Wellington
Journal:  Drugs       Date:  2006       Impact factor: 11.431

Review 10.  Review of nifedipine GITS in the treatment of high risk patients with coronary artery disease and hypertension.

Authors:  Amber Lundy; Nahla Lutfi; Cherylyn Beckey
Journal:  Vasc Health Risk Manag       Date:  2009
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