Literature DB >> 22454918

Biological availability and in vitro dissolution of oxytetracycline dihydrate tablets.

H E Barber1, T N Calvey, K Muir, A Hart.   

Abstract

1 The concentration of oxytetracycline in plasma was studied by microbiological assay after oral administration of four different preparations of oxytetracycline dihydrate tablets. 2 There were statistically significant differences in biological availability between the four preparations, as assessed by the peak plasma level, the area under the plasma concentration-time curve, or the cumulative fraction of the dose excreted in urine at 405 minutes. In contrast, differences between the subjects were not statistically significant. 3 The differences in biological availability were not predictably related to the in vitro dissolution of the tablets.

Entities:  

Year:  1974        PMID: 22454918      PMCID: PMC1402476          DOI: 10.1111/j.1365-2125.1974.tb00277.x

Source DB:  PubMed          Journal:  Br J Clin Pharmacol        ISSN: 0306-5251            Impact factor:   4.335


  5 in total

1.  Correlation of dissolution rate and griseofulvin absorption in man.

Authors:  B Katchen; S Symchowicz
Journal:  J Pharm Sci       Date:  1967-09       Impact factor: 3.534

2.  Fluorometric estimation of oxytetracycline in blood and plasma.

Authors:  B Scales; D A Assinder
Journal:  J Pharm Sci       Date:  1973-06       Impact factor: 3.534

Review 3.  In vitro evaluation of physiological availability of compressed tablets.

Authors:  J H Wood
Journal:  Pharm Acta Helv       Date:  1967-03

4.  Therapeutic non-equivalence of digoxin tablets in the United Kingdom: correlation with tablet dissolution rate.

Authors:  T R Shaw; K Raymond; M R Howard; J Hamer
Journal:  Br Med J       Date:  1973-12-29

5.  Therapeutic nonequivalence of oxytetracycline capsules.

Authors:  G W Brice; H F Hammer
Journal:  JAMA       Date:  1969-05-19       Impact factor: 56.272

  5 in total

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