Literature DB >> 3334452

A critical appraisal of drug stability testing methods.

R B Taylor1, A S Shivji.   

Abstract

The determination of potency or shelf life, impurity limit testing, and study of reaction mechanisms are considered as different aspects of drug stability. These aspects traditionally have been treated in isolation. The current criterion for a stability-indicating assay is criticized and the merits of choosing reactant or decomposition product for monitoring decomposition are discussed. The initial-rate method of determining reaction order and rate constants by analysis of decomposition product is described and its potential advantages over traditional integral methods are discussed. Examples of the application of the initial-rate method to simple and complex drug decomposition systems for the determination of decomposition rate constants are given. Applications to limit testing and study of reaction mechanisms are outlined and the dependence of the initial-rate method and decomposition product analysis on modern chromatographic methods is emphasized.

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Year:  1987        PMID: 3334452     DOI: 10.1023/a:1016491608328

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


  16 in total

1.  AN ACCELERATED STORAGE TEST WITH PROGRAMMED TEMPERATURE RISE.

Authors:  A R ROGERS
Journal:  J Pharm Pharmacol       Date:  1963-12       Impact factor: 3.765

2.  A slope-ratio design for accelerated storage tests.

Authors:  J P TOOTILL
Journal:  J Pharm Pharmacol       Date:  1961-12       Impact factor: 3.765

3.  Prediction of stability in pharmaceutical preparations. II. Vitamin stability in liquid multivitamin preparations.

Authors:  E R GARRETT
Journal:  J Am Pharm Assoc Am Pharm Assoc       Date:  1956-03

4.  An h.p.l.c. study of the initial stages of dextrose decomposition in neutral solution.

Authors:  R B Taylor; V C Sood
Journal:  J Pharm Pharmacol       Date:  1978-08       Impact factor: 3.765

5.  Kinetics of concomitant degradation of tetracycline to epitetracycline, anhydrotetracycline, and epianhydrotetracycline in acid phosphate solution.

Authors:  P H Yuen; T D Sokoloski
Journal:  J Pharm Sci       Date:  1977-11       Impact factor: 3.534

Review 6.  Stability of pharmaceuticals.

Authors:  J A Mollica; S Ahuja; J Cohen
Journal:  J Pharm Sci       Date:  1978-04       Impact factor: 3.534

7.  Equilibrium phenomena in solid dosage forms.

Authors:  J T Carstensen; J B Johnson; D C Spera; M J Frank
Journal:  J Pharm Sci       Date:  1968-01       Impact factor: 3.534

8.  The kinetics of atropine and apoatropine in aqueous solutions.

Authors:  W Lund; T Waaler
Journal:  Acta Chem Scand       Date:  1968

9.  Stability studies ofphenylbutazone and phenylbutazone--antacid oral formulations.

Authors:  F Matsui; D L Roberston; P Lafontaine; H Kolasinski; E G Lovering
Journal:  J Pharm Sci       Date:  1978-05       Impact factor: 3.534

10.  Development of a stability-indicating assay for nafimidone [1-(2-naphthoylmethyl)imidazole hydrochloride] by high-performance liquid chromatography.

Authors:  R B Taylor; D G Durham; A S Shivji; R Reid
Journal:  J Chromatogr       Date:  1986-02-26
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  3 in total

1.  Kinetics of drug decomposition by heat conduction calorimetry.

Authors:  L D Hansen; E A Lewis; D J Eatough; R G Bergstrom; D DeGraft-Johnson
Journal:  Pharm Res       Date:  1989-01       Impact factor: 4.200

2.  Interpretation of drug stability testing.

Authors:  L Chafetz
Journal:  Pharm Res       Date:  1988-04       Impact factor: 4.200

3.  Chemical stability of ecomustine, a new antitumor agent in aqueous and biological media as assessed by high-performance liquid chromatography.

Authors:  I el Abed; P Roger; C Gosse; G Atassi; A Gouyette
Journal:  Cancer Chemother Pharmacol       Date:  1991       Impact factor: 3.333

  3 in total

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