Correlation of Serum and Saliva Theophylline Concentration After Administration of a Sustained Release Preparation
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The correlation between serum and saliva levels of theophylline was investigated in seven healthy volunteers after multiple dose administration of a low dose (300 mg/day) and a high dose (900 mg/day) of a sustained release theophylline preparation (Theo-Dur). Tablets were taken for five days, at 8 a. m. and 8 p. m. and a last dose was taken on Day 6 at 8 a. m. Fourteen serum and saliva samples were collected simultaneously during the dosing period and for up to 32 h after the last dose. On the 300 mg/day regimen the level in saliva was 55.3% of the serum level, with an overall variability of 6.7% and an intrasubject variability of 10.5%. After 900 mg/day, the saliva concentration was 55.5% of the serum concentration, with an overall variability of 7.6% and an intrasubject variability of 12.7%. A good correlation was found between both determinations (r = 0.99), which suggests that saliva levels could be used to monitor theophylline after administration of a sustained release tablet.
Pharmacokinetics of sustained release theophylline in low and high multidose regimens.
Koeter G, Jonkman J, de Vries K, Schoenmaker R, Greving J, de Zeeuw R Br J Clin Pharmacol. 1981; 12(5):647-51.
PMID: 7332728 PMC: 1401956. DOI: 10.1111/j.1365-2125.1981.tb01283.x.
Jackson A, Edwards C, Cope A, Stockley R, Purkiss R Br J Clin Pharmacol. 1983; 15(4):407-10.
PMID: 6849775 PMC: 1427805. DOI: 10.1111/j.1365-2125.1983.tb01522.x.
ELLIS E Clin Rev Allergy. 1983; 1(1):73-85.
PMID: 6367926 DOI: 10.1007/BF02991318.
Takagi K, Yamaki K, Nadai M, Kuzuya T, Hasegawa T Antimicrob Agents Chemother. 1991; 35(6):1137-41.
PMID: 1929255 PMC: 284300. DOI: 10.1128/AAC.35.6.1137.