Literature DB >> 3834065

The in vitro development of extended-release solid oral dosage forms.

L J Leeson, D Adair, J Clevenger, N Chiang.   

Abstract

A system is described for developing extended-release products, based upon predicting or simulating the entire plasma level-time curve to be expected from the administration of a controlled-release oral dosage form. Termed "biorelevant dissolution," it employs the product's in vitro dissolution behavior and the drug's pharmacokinetic parameters in conjunction with a classical pharmacokinetic model. The basic system is described along with some pertinent examples.

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Year:  1985        PMID: 3834065     DOI: 10.1007/bf01059332

Source DB:  PubMed          Journal:  J Pharmacokinet Biopharm        ISSN: 0090-466X


  18 in total

1.  A dissolution rate apparatus for the prediction of initial drug absorption patterns in beagles: tolbutamide tablets.

Authors:  D L Simmons; A A Legore; P Picotte; K S Lee; N N Joshi
Journal:  J Pharmacokinet Biopharm       Date:  1975-02

2.  Per cent absorbed time plots derived from blood level and/or urinary excretion data.

Authors:  J G WAGNER; E NELSON
Journal:  J Pharm Sci       Date:  1963-06       Impact factor: 3.534

3.  Simple transformation method for predicting plasma drug profiles from dissolution rates.

Authors:  D P Vaughan; R H Leach
Journal:  J Pharm Sci       Date:  1976-04       Impact factor: 3.534

4.  Comparative bioavailability: a new type of in vitro--in vivo correlation exemplified by prednisone.

Authors:  T J Sullivan; E Sakmar; J G Wagner
Journal:  J Pharmacokinet Biopharm       Date:  1976-04

5.  Use of in vitro dissolution data to predict plasma drug profiles.

Authors:  L J Aarons; M Rowland
Journal:  J Pharm Sci       Date:  1977-09       Impact factor: 3.534

6.  Determination of time course of in vivo pharmacological effects from in vitro drug-release testing.

Authors:  V F Smolen
Journal:  J Pharm Sci       Date:  1971-06       Impact factor: 3.534

7.  In vitro dissolution rates of aminorex dosage forms and their correlation with in vivo availability.

Authors:  W A Cressman; C A Janicki; P C Johnson; J T Doluisio; G A Braun
Journal:  J Pharm Sci       Date:  1969-12       Impact factor: 3.534

8.  Rotating-flask method for dissolution-rate determinations of aspirin from various dosage forms.

Authors:  H Weintraub; M Gibaldi
Journal:  J Pharm Sci       Date:  1970-12       Impact factor: 3.534

9.  Linearization of dissolution rate curves by the Weibull distribution.

Authors:  F Langenbucher
Journal:  J Pharm Pharmacol       Date:  1972-12       Impact factor: 3.765

10.  Acetaminophen. 3. Dissolution studies of commercial tablets of acetaminophen and comparison with in vivo absorption parameters.

Authors:  G L Mattok; I J McGilveray; C A Mainville
Journal:  J Pharm Sci       Date:  1971-04       Impact factor: 3.534

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  1 in total

Review 1.  Various administration forms of nitrates and their possibilities.

Authors:  U E Jonsson
Journal:  Drugs       Date:  1987       Impact factor: 9.546

  1 in total

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