Study on bioequivalence of domestic bambuterol capsules and imported tablets by high performance capillary zone electrophoresis / 药学学报
Yao Xue Xue Bao
; (12): 942-945, 2003.
Article
de Zh
| WPRIM
| ID: wpr-301169
Bibliothèque responsable:
WPRO
ABSTRACT
<p><b>AIM</b>To study bioequivalences of bambuterol and its metabolites terbutaline in 20 healthy male volunteers.</p><p><b>METHODS</b>A single oral dose of domestic bambuterol capsule or imported bambuterol tablet was given according to a randomized 2-way cross-over design. The plasma bambuterol and terbutaline concentrations were determined by high performance capillary zone electrophoresis (HPCZE).</p><p><b>RESULTS</b>The pharmacokinetic parameters of the capsule and tablet of bambuterol: AUC0-1 were (72 +/- 18) and (72 +/- 13) microgram.h.L-1, Cmax were (8.1 +/- 1.8) and (9.2 +/- 2.3) microgram.L-1, Tmax were (3.6 +/- 1.3) and (3.7 +/- 1.0) h, respectively; terbutaline: AUC0-t were (129 +/- 32) and (130 +/- 34) microgram.h.L-1, Cmax were (7.8 +/- 2.2) and (8.5 +/- 2.9) microgram.L-1, Tmax were (5.4 +/- 0.8) and (5.6 +/- 1.1) h, respectively. The bioavaiability of the capsule was (100 +/- 16)% (bambuterol) and (101 +/- 13)% (terbutaline).</p><p><b>CONCLUSION</b>The results demonstrated that the two preparations of bambuterol and terbutaline were bioequivalent by analysis of variance, with two-one sided test at 90% confidential level.</p>
Texte intégral:
1
Indice:
WPRIM
Sujet Principal:
Comprimés
/
Terbutaline
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Sang
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Capsules
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Pharmacocinétique
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Biodisponibilité
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Équivalence thérapeutique
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Administration par voie orale
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Chromatographie en phase liquide à haute performance
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Études croisées
Type d'étude:
Clinical_trials
/
Prognostic_studies
Limites du sujet:
Adult
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Humans
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Male
langue:
Zh
Texte intégral:
Yao Xue Xue Bao
Année:
2003
Type:
Article