Abstract
The antianginal effectiveness of isosorbide dinitrate (ISDN) has been demonstrated in many studies [1, 4, 5, 9, 10, 13, 14, 15, 17, 18]. Since the bioavailability of ISDN after oral application is negligible, its long-acting effects on the angina pectoris syndrome (APS) are related to the main metabolites isosorbide-2-mononitrate (IS-2-MN) and isosorbide-5-mononitrate (IS-5-MN) which show a prolonged half-life period [1, 8, 11, 13]. In contrast to ISDN, orally taken IS-5-MN has a bioavailability of 100% without any first-pass effect [1, 8, 11]. Because of these different pharmacodynamic properties, it was of interest to investigate the so-far open question of the equieffective oral dosage of ISDN and IS-5-MN.
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Schoeller, R. et al. (1985). Comparison of Changes on Exercise-Induced Ischemia After a Single Oral Dose of IS-5-MN and ISDN. In: Cohn, J.N., Rittinghausen, R. (eds) Mononitrates. International Boehringer Mannheim Symposia. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-70234-1_25
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DOI: https://doi.org/10.1007/978-3-642-70234-1_25
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