Literature DB >> 3508541

Temperature and pH dependence of fluocinolone acetonide degradation in a topical cream formulation.

R A Kenley1, M O Lee, L Sukumar, M F Powell.   

Abstract

We investigated the degradation of fluocinolone acetonide (FA) incorporated into an oil-in-water cream base. The study examined the influence of temperature (23 to 80 degrees C) and cream pH (pH 2.3 to 6) on FA degradation rates. FA degradation followed pseudo-first-order kinetics and adhered to the Arrhenius expression over the entire temperature range investigated. At all temperatures, the pH strongly influenced the observed degradation rate constant (kobs) values, with rate minima observed near pH 4. The FA log(degradation rate)-pH profiles were consistent with a reaction mechanism requiring drug hydrolysis catalyzed by hydroxide and hydrogen ions. Taking into account both the temperature and the pH dependence of FA degradation permits calculating kobs values from the following equation: kobs = exp[22.5 - (17,200/RT)] + exp[38.7 - (22,200/RT)] x [H+] + exp[49.5 - (21,100/RT)] x [OH-] where the three bracketed terms represent Arrhenius expressions for neutral, acid-catalyzed, and base-catalyzed hydrolysis reactions. FA degradation in the cream base parallels the degradation of a related steroid (triamcinolone acetonide) in an aqueous alcohol solution. The equivalence between FA and triamcinolone acetonide kinetics in the different reaction media suggests that in the cream base, FA degradation is limited to an aqueous phase largely unperturbed by the presence of nonaqueous constituents that comprise the cream formulation.

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Year:  1987        PMID: 3508541     DOI: 10.1023/a:1016457522866

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


  8 in total

1.  FACTORS INFLUENCING STABILITY OF PREDNISOLONE IN AQUEOUS SOLUTION.

Authors:  T O OESTERLING; D E GUTTMAN
Journal:  J Pharm Sci       Date:  1964-10       Impact factor: 3.534

2.  The kinetics of the base-catalyzed degradation of prednisolone.

Authors:  D E GUTTMAN; P D MEISTER
Journal:  J Am Pharm Assoc Am Pharm Assoc       Date:  1958-11

3.  Long-term stability studies using radiopharmaceuticals: consequence of using multiply tritiated compounds, with an application to fluocinolone acetonide.

Authors:  M F Powell; A Magill; A R Becker
Journal:  Pharm Res       Date:  1986-12       Impact factor: 4.200

4.  Effect of vehicles and other active ingredients on stability of hydrocortisone.

Authors:  V D Gupta
Journal:  J Pharm Sci       Date:  1978-03       Impact factor: 3.534

5.  Kinetics and factors affecting stability of methylprednisolone in aqueous formulation.

Authors:  M I Amin; J T Bryan
Journal:  J Pharm Sci       Date:  1973-11       Impact factor: 3.534

6.  The degradation of triamcinolone acetonide in aqueous solution: influence of the cyclic ketal function.

Authors:  P Timmins; E A Gray
Journal:  J Pharm Pharmacol       Date:  1983-03       Impact factor: 3.765

7.  Stability of triamcinolone acetonide solutions as determined by high-performance liquid chromatography.

Authors:  V D Gupta
Journal:  J Pharm Sci       Date:  1983-12       Impact factor: 3.534

8.  Kinetics of decomposition and formulation of hydrocortisone butyrate in semiaqueous and gel systems.

Authors:  Y W Yip; A Li Wan Po; W J Irwin
Journal:  J Pharm Sci       Date:  1983-07       Impact factor: 3.534

  8 in total
  1 in total

1.  Influence of solute degradation on the accumulation of solutes migrating into solution from polymeric parenteral containers.

Authors:  L A Cruz; M P Jenke; R A Kenley; M J Chen; D R Jenke
Journal:  Pharm Res       Date:  1990-09       Impact factor: 4.200

  1 in total

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