1983
DOI: 10.1111/j.1365-2710.1983.tb00897.x
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The Comparative Bioavailability of Slow Release Oral Theophylline Preparations

Abstract: SUMMARY Plasma concentrations of theophylline were determined in healthy volunteers following a single oral dose of six slow release preparations, immediately following a standard breakfast. There were no significant differences between the different preparations. The time taken to reach maximum plasma concentration, tmax, was found to be longer than in previous studies in which the drug was administered on an empty stomach.

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Cited by 3 publications
(3 citation statements)
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References 17 publications
(13 reference statements)
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“…where D is the diffusion coefficient (cm 2 /s) at the given temperature and x is the membrane thick- 3 2.5 1.75 0.050 (IA) 1 2.5 0.75 0.025 (IA) 2 2.5 1.25 0.040 (IA) 3 2.5 1.75 0.050…”
Section: Diffusion Measurementsmentioning
confidence: 99%
See 1 more Smart Citation
“…where D is the diffusion coefficient (cm 2 /s) at the given temperature and x is the membrane thick- 3 2.5 1.75 0.050 (IA) 1 2.5 0.75 0.025 (IA) 2 2.5 1.25 0.040 (IA) 3 2.5 1.75 0.050…”
Section: Diffusion Measurementsmentioning
confidence: 99%
“…The use of polymers as vehicles for controlled release of drugs is a young, vigorous field. 1–3 Polymers release drugs by four general mechanisms: diffusion, chemical control, solvent activation, and magnetism. 4 The most common mechanism is diffusion consisting of matrix or reservoir (membrane) systems.…”
Section: Introductionmentioning
confidence: 99%
“…The bioavailability of six different slow release oral theophylline preparations designed for 12-hourly administration has been shown to be identical, suggesting that none has advantage over the others (42). There have been no clinical studies to show that there is any synergy between beta-2 agonists and theophylline when both are given in optimal doses to those with stable asthma or acute severe asthma (43).…”
Section: T H E O P H Y L L I N Ementioning
confidence: 99%