Literature DB >> 8331541

Kinetics of absorption of a new once-a-day formulation of theophylline in the presence and absence of food.

L I Harrison1, A K Mitra, C R Kehe, N M Klinger, K A Wick, S E McCarville, K M Cooper, S F Chang, P J Roddy, S M Berge.   

Abstract

Two three-way crossover studies were done to characterize the drug release characteristics of Monospan (3M Pharmaceuticals, St. Paul, MN) capsules, a new once-a-day theophylline formulation. In the first study, 22 healthy males received single 450-mg doses of Monospan in the presence and absence of a high-fat breakfast; the same dose of Somophyllin (Fisons, Rochester, NY) immediate-release liquid was given to fasted subjects as a reference. The second study involved 29 healthy males given a single dose of 900 mg of Monospan in the presence and absence of the same high-fat meal; Theo-24 (G. D. Searle and Co., Skokie, IL) capsules were given to fasted subjects as a reference. The results of both studies showed that food did not affect the absorption of theophylline from Monospan; peak concentration, to and area under the serum concentration-time curve were all unchanged. The absorption rates were similar with both strengths and dietary conditions and showed that theophylline was absorbed slowly from Monospan at a constant rate (approximately 3.2%/h) over 24 h. Absorption continued past 24 h, and the extent of absorption from Monospan compared with that from each reference averaged 88% or higher. A good correlation (r > 0.980) was observed for Monospan between the amount absorbed in vivo and the amount released in the in vitro dissolution test, a result that demonstrates the precise rate control of Monospan. We conclude that Monospan is a suitable once-a-day formulation that can be taken without regard to food.

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Year:  1993        PMID: 8331541     DOI: 10.1002/jps.2600820620

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  2 in total

Review 1.  Food-drug interactions.

Authors:  Lars E Schmidt; Kim Dalhoff
Journal:  Drugs       Date:  2002       Impact factor: 9.546

2.  Acceleration of in vitro dissolution studies of sustained release dosage form of theophylline and in vitro-in vivo evaluations in terms of correlations.

Authors:  Gökhan Ertan; Ercüment Karasulu; Işık Ozgüney; Yeşim Karasulu; Sebnem Apaydın; Gülten Kantarcı; Aysu Yurdasiper; Mehmet Ali Ege
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2011-07-08       Impact factor: 2.441

  2 in total

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