Literature DB >> 2778094

Effect of altering small bowel transit time on sustained release theophylline absorption.

J C Bryson1, G E Dukes, M G Kirby, W D Heizer, J R Powell.   

Abstract

The relationship between variations in small bowel transit time (SBTT) and the absorption of theophylline from a sustained-release product was evaluated in a three-way, randomized, crossover study in 12 healthy male nonsmokers. Subjects received sustained-release theophylline (600 mg) with loperamide (8 mg every 6 hour x 8 doses). metoclopramide (15 mg every 6 hour x 8 doses) or placebo (every 6 hour x 8 doses). Theophylline solution (400 mg) was used as a reference standard. Serum samples were collected periodically for 72 hours for theophylline concentration determinations. SBTT was measured by the lactulose hydrogen breath test. Compared with placebo (98 +/- 53 min), SBTT was increased with loperamide (211 +/- 87 min; P less than 0.001) and decreased with metoclopramide (55 +/- 18 min; P less than 0.001). Loperamide decreased the rate, but not the extent of theophylline absorption from this product. This was evident from the reduced Cmax, the prolonged Tmax, and the decreased fraction of the dose absorbed at 24 hours, while the area under the curves remained the same. In contrast, metoclopramide had no effect either on rate or extent of absorption. The data suggest that the effect of loperamide on these absorption parameters was due to an increase in the dissolution time of this sustained-release product.

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Year:  1989        PMID: 2778094     DOI: 10.1002/j.1552-4604.1989.tb03408.x

Source DB:  PubMed          Journal:  J Clin Pharmacol        ISSN: 0091-2700            Impact factor:   3.126


  8 in total

Review 1.  Drug, meal and formulation interactions influencing drug absorption after oral administration. Clinical implications.

Authors:  D Fleisher; C Li; Y Zhou; L H Pao; A Karim
Journal:  Clin Pharmacokinet       Date:  1999-03       Impact factor: 6.447

2.  Absorption of theophylline from a new theophylline controlled-release capsule.

Authors:  C Kehe; K Wick; S McCarville; K Rhode; B C Meakin; D Porter; L Harrison
Journal:  Eur J Clin Pharmacol       Date:  1991       Impact factor: 2.953

3.  Meta-analysis of oro-cecal transit time in fasting subjects.

Authors:  Tohru Kokubo; Shigeyuki Matsui; Makio Ishiguro
Journal:  Pharm Res       Date:  2012-09-28       Impact factor: 4.200

Review 4.  Pharmacokinetic drug interactions with gastrointestinal motility modifying agents.

Authors:  J M Greiff; D Rowbotham
Journal:  Clin Pharmacokinet       Date:  1994-12       Impact factor: 6.447

5.  Effect of pancreatico-biliary secretions and GI transit time on the absorption and pharmacokinetic profile of ranitidine in humans.

Authors:  K S Reynolds; M H Song; W D Heizer; C B Burns; D A Sica; K L Brouwer
Journal:  Pharm Res       Date:  1998-08       Impact factor: 4.200

Review 6.  Pharmacokinetic considerations in gastrointestinal motor disorders.

Authors:  G S Hebbard; W M Sun; F Bochner; M Horowitz
Journal:  Clin Pharmacokinet       Date:  1995-01       Impact factor: 6.447

7.  Effect of metoclopramide and loperamide on the pharmacokinetics of didanosine in HIV seropositive asymptomatic male and female patients.

Authors:  C A Knupp; R L Milbrath; R H Barbhaiya
Journal:  Eur J Clin Pharmacol       Date:  1993       Impact factor: 2.953

Review 8.  Loperamide. Survey of studies on mechanism of its antidiarrheal activity.

Authors:  F Awouters; A Megens; M Verlinden; J Schuurkes; C Niemegeers; P A Janssen
Journal:  Dig Dis Sci       Date:  1993-06       Impact factor: 3.199

  8 in total

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