Literature DB >> 10434405

Stability and bioequivalence studies of two marketed formulations of coenzyme Q10 in beagle dogs.

T R Kommuru1, M Ashraf, M A Khan, I K Reddy.   

Abstract

Coenzyme Q10 (CoQ10), a highly lipophilic compound present in the inner mitochondrial membrane, is essential for production of cellular energy in the form of ATP. CoQ10 is used as an antioxidant and also in the treatment of various cardiovascular disorders. The relative bioavailabilities of powder filled capsule (I) and oil-based formulation (II) of CoQ10 were compared in beagle dogs in an open, randomized, multiple dose, cross-over design. Poor and slow absorption characteristics were observed for both the formulations. The AUC, Cmax, and Tmax for formulation I and II are comparable (p < 0.05) where the values for formulation I are 22.84 +/- 6.3 micrograms ml-1 h, 0.51 +/- 0.11 microgram/ml, and 6.1 +/- 2.0 h whereas the values for formulation II are 24.32 +/- 5.6 micrograms ml-1 h, 0.55 +/- 0.16 microgram/ml, and 6.6 +/- 2.3 h, respectively. Stability of CoQ10 at various temperature and humidity conditions and its photostability were studied. Various antioxidants were evaluated to determine the type and amount of antioxidant(s) required to improve the stability of CoQ10. Large extent of degradation was observed at 45 degrees C and 55 degrees C. The effect of humidity conditions on degradation was insignificant. Among the various antioxidants studied, mixture of ascorbic acid (5%) and EDTA (0.1%) offered better protection than phenolic antioxidants such as butylated hydroxy anisole (BHA), butylated hydroxy toluene (BHT), or propyl gallate (PG). Further, increasing concentrations of phenolic antioxidants (from 0.1 to 0.3%) accelerated the degradation.

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Year:  1999        PMID: 10434405     DOI: 10.1248/cpb.47.1024

Source DB:  PubMed          Journal:  Chem Pharm Bull (Tokyo)        ISSN: 0009-2363            Impact factor:   1.645


  4 in total

1.  Protective effect of coenzyme Q10-loaded liposomes on the myocardium in rabbits with an acute experimental myocardial infarction.

Authors:  Daya D Verma; William C Hartner; Vineet Thakkar; Tatyana S Levchenko; Vladimir P Torchilin
Journal:  Pharm Res       Date:  2007-07-27       Impact factor: 4.200

2.  Solid-state nuclear magnetic resonance determination of the physical form of BHA on common pharmaceutical excipients.

Authors:  Julius F Remenar; Robert Wenslow; Drazen Ostovic; Andrey Peresypkin
Journal:  Pharm Res       Date:  2004-01       Impact factor: 4.200

3.  Stability of Reduced and Oxidized Coenzyme Q10 in Finished Products.

Authors:  Žane Temova Rakuša; Albin Kristl; Robert Roškar
Journal:  Antioxidants (Basel)       Date:  2021-02-27

4.  Coenzyme Q10 Reduces Infarct Size in Animal Models of Myocardial Ischemia-Reperfusion Injury: A Meta-Analysis and Summary of Underlying Mechanisms.

Authors:  Kamal Awad; Ahmed Sayed; Maciej Banach
Journal:  Front Cardiovasc Med       Date:  2022-04-15
  4 in total

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