Literature DB >> 10799813

A five way crossover human volunteer study to compare the pharmacokinetics of paracetamol following oral administration of two commercially available paracetamol tablets and three development tablets containing paracetamol in combination with sodium bicarbonate or calcium carbonate.

T Grattan1, R Hickman, A Darby-Dowman, M Hayward, M Boyce, S Warrington.   

Abstract

This report concerns a single dose randomized five way crossover study to compare the pharmacokinetics of paracetamol from two commercially available paracetamol (500 mg) tablets and three different development paracetamol (500 mg) tablet formulations containing either sodium bicarbonate (400 mg), sodium bicarbonate (630 mg) or calcium carbonate (375 mg). The results demonstrated that addition of sodium bicarbonate (630 mg) to paracetamol tablets, increased the rate of absorption of paracetamol relative to conventional paracetamol tablets and soluble paracetamol tablets. Addition of sodium bicarbonate (400 mg) to paracetamol tablets increased the absorption rate of paracetamol relative to conventional paracetamol tablets, but there was no difference in the rate of absorption compared to soluble paracetamol tablets. Inclusion of calcium carbonate (375 mg) to paracetamol tablets had no effect on absorption kinetics compared to the conventional paracetamol tablet. The faster absorption observed for the sodium bicarbonate formulations may be as a result of an increase in gastric emptying rate leading to faster transport of paracetamol to the small intestine where absorption takes place.

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Year:  2000        PMID: 10799813     DOI: 10.1016/s0939-6411(00)00081-3

Source DB:  PubMed          Journal:  Eur J Pharm Biopharm        ISSN: 0939-6411            Impact factor:   5.571


  5 in total

1.  Comparison of the rates of disintegration, gastric emptying, and drug absorption following administration of a new and a conventional paracetamol formulation, using gamma scintigraphy.

Authors:  Kilian Kelly; Bridget O'Mahony; Blythe Lindsay; Tamara Jones; Tim J Grattan; Amin Rostami-Hodjegan; Howard N E Stevens; Clive G Wilson
Journal:  Pharm Res       Date:  2003-10       Impact factor: 4.200

Review 2.  Why is the therapeutic effect of acute antimigraine drugs delayed? A review of controlled trials and hypotheses about the delay of effect.

Authors:  Peer Tfelt-Hansen; Karl Messlinger
Journal:  Br J Clin Pharmacol       Date:  2019-09-04       Impact factor: 4.335

Review 3.  The Role of Functional Excipients in Solid Oral Dosage Forms to Overcome Poor Drug Dissolution and Bioavailability.

Authors:  Jannes van der Merwe; Jan Steenekamp; Dewald Steyn; Josias Hamman
Journal:  Pharmaceutics       Date:  2020-04-25       Impact factor: 6.321

4.  Bioavailability of the Common Cold Medicines in Jellies for Oral Administration.

Authors:  Ki Hyun Kim; Minju Jun; Mi-Kyung Lee
Journal:  Pharmaceutics       Date:  2020-11-10       Impact factor: 6.321

5.  Does a hot drink provide faster absorption of paracetamol than a tablet? A pharmacoscintigraphic study in healthy male volunteers.

Authors:  Lee Ann Hodges; Alison Hughes; Darren Targett; Michael J Durcan
Journal:  Pharm Res       Date:  2014-02-21       Impact factor: 4.200

  5 in total

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