TOLERABILITY AND PHARMACOKINETICS OF SINGLE AND MULTIPLE DOSES OF AZELASTINE HYDROCHLORIDE IN ELDERLY VOLUNTEERS

Citation
G. Peter et al., TOLERABILITY AND PHARMACOKINETICS OF SINGLE AND MULTIPLE DOSES OF AZELASTINE HYDROCHLORIDE IN ELDERLY VOLUNTEERS, Arzneimittel-Forschung, 45(5), 1995, pp. 576-581
Citations number
14
Categorie Soggetti
Pharmacology & Pharmacy",Chemistry
Journal title
ISSN journal
00044172
Volume
45
Issue
5
Year of publication
1995
Pages
576 - 581
Database
ISI
SICI code
0004-4172(1995)45:5<576:TAPOSA>2.0.ZU;2-U
Abstract
The tolerability and pharmacokinetics of azelastine hydrochloride (CAS 73907-93-0, A-05610) after single and multiple dosing (4.4 mg as tabl et, tau = 12 h) were investigated in 14 volunteers (6 female, 8 male) older than 65 years (70 +/- 5 years, mean +/- SD). The medication was administered as tablets in the morning of days 1 and 11, and b.i.d. on days 4 to 10 in a randomized, open-labelled, uncontrolled study. Tole rance proved to be very good. Reported number of adverse events was in dependent from height of plasma levels measured, which showed pronounc ed inter- and intraindividual variation. When comparing pharmacokineti c parameters from plasma levels (determined with a radioimmunoassay (R IA)) of the elderly with those of young volunteers (26 +/- 5 years), t here is a difference in half lives (t(1/2) elderly vs young: single do se: 38.5 +/- 15.3 h vs 25.0 +/- 5.2 h; multiple dose: 35.5 +/- 16.3 h vs 55.4 +/- 24.9 h), and also after a single dose AUC and after multip le dosing AUC(tau)(ss), t(max)(ss), C-max(ss), C-min(ss) (pre dose lev els), and the ratios of accumulation R(max) and R(min) (calculated fro m C-max(ss)/C-max and C-min(ss)/C-min) are approximately twice as high in elderly as those in young volunteers. The RIA co-detects besides a zelastine the pharmacodynamically active metabolite N-demethyl-azelast ine and thus, the parameters describe the pharmacokinetic behaviour as a resultant from both compounds, i.e. the ''active principle''. N-Dem ethylated metabolites are known to have longer half-lives usually than their parent compounds and thus, accumulate in a higher degree during multiple dosing. Therefore, in this context (RIA!) it is discussed th at the N-demethyl metabolite dominates the pharmacokinetic parameters in multiple dosing more than after a single dose. The reason that the pharmacokinetic parameters mentioned above (except t(max), t(max)(ss)) in addition are elevated more in the elderly than in young volunteers after single dosing in part and after multiple dosing in general, mig ht be due to the physiological functional decline with aging. Due to t his finding patients greater than or equal to 65 years are recommended to start therapy with half the azelastine dosage, i.e. with 2.2 mg (r hinitis) or 4.4 mg (asthma) as a single daily administration in the ev ening. After 10-14 days according to the clinical picture in cases of no or insufficient action and lack of adverse drug reactions the dose may be increased. From the viewpoint of pharmacokinetics, due to the l ong terminal half-life of the ''active principle'' in plasma and the g ood tolerability of azelastine a single oral dose per day in the elder ly seems to be justified, and could be taken into account, possibly at a doubled dose level, for the young as well.