Literature DB >> 2293211

Theophylline-controlled release preparations and fatty food: an in vitro study using the rotating dialysis cell method.

S K el-Arini1, G K Shiu, J P Skelly.   

Abstract

The in vitro dissolution behavior of four controlled-release theophylline products was investigated utilizing the rotating dialysis cell method. The effects of pH, oil, and enzymes on the dissolution profiles were studied. The wide range of pH values and the content of oil and enzymes in the dissolution media in the dialysis cell, which functioned as an in vitro model, were simulated to mimic physiological changes due to food along the entire gastrointestinal tract. Treatment with oil affected the dissolution behavior of Uniphyl and especially Theo-Dur Sprinkle but had little or no effect on the dissolution profiles of Theo-Dur tablets and Theo-24 capsules. The in vitro observations of the oil effect were related to the food effect obtained from published in vivo studies. The rotating dialysis cell can be a useful tool in studying factors which may be responsible for dissolution-related food effects on the absorption of controlled-release products.

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Year:  1990        PMID: 2293211     DOI: 10.1023/a:1015976108251

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  12 in total

1.  New results on an in vitro model for the study of the influence of fatty meals on the bioavailability of theophylline controlled-release formulations.

Authors:  J M Aiache; N Pierre; E Beyssac; V K Prasad; J P Skelly
Journal:  J Pharm Sci       Date:  1989-03       Impact factor: 3.534

2.  Measurement of gastrointestinal pH profiles in normal ambulant human subjects.

Authors:  D F Evans; G Pye; R Bramley; A G Clark; T J Dyson; J D Hardcastle
Journal:  Gut       Date:  1988-08       Impact factor: 23.059

3.  Relationship between rate and extent of absorption of oral theophylline from Uniphyl brand of slow-release theophylline and resulting serum concentrations during multiple dosing.

Authors:  G Milavetz; L M Vaughan; M M Weinberger; J B Harris; T A Mullenix
Journal:  J Allergy Clin Immunol       Date:  1987-11       Impact factor: 10.793

4.  Influence of a high fat breakfast on the bioavailability of theophylline controlled-release formulations: an in vitro demonstration of an in vivo observation.

Authors:  P K Maturu; V K Prasad; W N Worsley; G K Shiu; J P Skelly
Journal:  J Pharm Sci       Date:  1986-12       Impact factor: 3.534

5.  The relation of product formulation to absorption of oral theophylline.

Authors:  M Weinberger; L Hendeles; L Bighley
Journal:  N Engl J Med       Date:  1978-10-19       Impact factor: 91.245

6.  Greatly enhanced bioavailability of theophylline on postprandial administration of a sustained release tablet.

Authors:  M Lagas; J H Jonkman
Journal:  Eur J Clin Pharmacol       Date:  1983       Impact factor: 2.953

7.  Effect of food on the bioavailability and pattern of release of a sustained-release theophylline tablet.

Authors:  N H Leeds; P Gal; A A Purohit; J B Walter
Journal:  J Clin Pharmacol       Date:  1982-04       Impact factor: 3.126

8.  Food-induced changes in theophylline absorption from controlled-release formulations. Part II. Importance of meal composition and dosing time relative to meal intake in assessing changes in absorption.

Authors:  A Karim; T Burns; D Janky; A Hurwitz
Journal:  Clin Pharmacol Ther       Date:  1985-12       Impact factor: 6.875

9.  Food-induced changes in theophylline absorption from controlled-release formulations. Part I. Substantial increased and decreased absorption with Uniphyl tablets and Theo-Dur Sprinkle.

Authors:  A Karim; T Burns; L Wearley; J Streicher; M Palmer
Journal:  Clin Pharmacol Ther       Date:  1985-07       Impact factor: 6.875

10.  Food-induced "dose-dumping" from a once-a-day theophylline product as a cause of theophylline toxicity.

Authors:  L Hendeles; M Weinberger; G Milavetz; M Hill; L Vaughan
Journal:  Chest       Date:  1985-06       Impact factor: 9.410

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  4 in total

1.  Effect of destruction force on drug release from multiple unit controlled release dosage forms in humans.

Authors:  N Katori; W S Ma; N Aoyagi; S Kojima
Journal:  Pharm Res       Date:  1996-10       Impact factor: 4.200

Review 2.  Effects of food on clinical pharmacokinetics.

Authors:  B N Singh
Journal:  Clin Pharmacokinet       Date:  1999-09       Impact factor: 6.447

3.  Estimation of agitation intensity in the GI tract in humans and dogs based on in vitro/in vivo correlation.

Authors:  N Katori; N Aoyagi; T Terao
Journal:  Pharm Res       Date:  1995-02       Impact factor: 4.200

4.  Oral solid controlled release dosage forms: role of GI-mechanical destructive forces and colonic release in drug absorption under fasted and fed conditions in humans.

Authors:  M Shameem; N Katori; N Aoyagi; S Kojima
Journal:  Pharm Res       Date:  1995-07       Impact factor: 4.200

  4 in total

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