Interspecies Comparison of Pharmacokinetic Parameters of an Oral Sustained Release Preparation of Iloprost
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry,Drug Discovery,Pharmaceutical Science,Pharmacology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03639049409038376
Reference14 articles.
1. An enzyme isolated from arteries transforms prostaglandin endoperoxides to an unstable substance that inhibits platelet aggregation
2. Schillinger E., Krais T., Stock Iloprost G. New drugs annual: Cardiovascular drugs, A. Scriabine. Raven Press, New York 1987; 209–231
3. Reduction of enzyme release from reperfused ischemic hearts by steroidal and non-steroidal prostaglandin synthesis inhibitors
4. Comparison of the vasodepressor action of ZK 36 374, a stable prostacyclin derivative, PGI2 and PGE1 with their effect on platelet aggregation and bleeding time in rats
5. Hemodynamic and Platelet Effects of Iloprost (ZK 36.374) in Patients with Peripheral Arterial Disease
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3. Pharmacokinetics and tolerability of oral iloprost in thromboangiitis obliterans patients;European Journal of Clinical Pharmacology;1997-10-02
4. In-Vitrodn-Vivo Correlation of Drug Liberation with an Extended Release Peroral Dosage form for Iloprost in Man;Drug Development and Industrial Pharmacy;1995-01
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