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  • [Study of the bioequivalence of a new isosorbide dinitrate tablet formulation compared with the standard preparation].

[Study of the bioequivalence of a new isosorbide dinitrate tablet formulation compared with the standard preparation].

Arzneimittel-Forschung (1997-06-01)
J E Metzner, D Buchberger, N Häring, J Läuter
摘要

An investigation in the bioequivalence of a new tablet formulation with 5 mg isosorbide dinitrate (CAS 87-33-2, ISDN 5 von ct) was performed in a two-way cross-over study with 18 subjects. The relative bioavailability with respect to a reference preparation for AUC related to isosorbide dinitrate was 107.5% and for Cmax 112.5%. A positive decision for bioequivalence derived from the usual confidence intervals for both parameters related to isosorbide dinitrate and the metabolites isosorbide-2-nitrate and isosorbide-5-nitrate, respectively. The difference in tmax showed no clinical relevance. The new formulation was bioequivalent to the reference.

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2-硝酸异山梨酯, European Pharmacopoeia (EP) Reference Standard
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