Zobrazeno 1 - 10
of 18
pro vyhledávání: '"G. P. Tosolini"'
Publikováno v:
European Journal of Clinical Pharmacology. 10:257-262
In a pharmacokinetic study of the new analgesic and anti-inflammatory drug indoprofen, plasma levels and urinary excretion were determined in four healthy volunteers after 100 mg and 200 mg iv, and after 100 mg (capsules) and 200 mg (tablets) oral do
Publikováno v:
European Journal of Clinical Pharmacology. 15:323-327
Six healthy volunteers received single iv and oral doses of 2-[p-(1-oxo-2-isoindolinyl)phenyl] butyric acid 100 mg (indobufen; K 3920), an inhibitor of platelet aggregation. Plasma levels and urinary excretion of the drug were determined by GLC. Coll
Publikováno v:
European Journal of Clinical Pharmacology. 6:256-260
The fate of the new analgesic and anti-inflammatory agent α-[4-(1-oxo-2-iso-indolinyl)-phenyl]-propionic acid (compound K 4277) in healthy volunteers has been investigated by a radio-isotope method and gas-liquid chromatography. After oral administr
Autor:
Giuliano Nannini, Longo R, I. De Carneri, G. Meinardi, G. P. Tosolini, Pier Nicola Giraldi, E. Dradi, Gisella Monti
Publikováno v:
Biochemical Pharmacology. 20:339-349
The metabolism has been investigated in man of 1-( N - β -ethylmorpholine)-5-nitroimidazole, a new trichomonacidal agent. From the urine of patients treated with the compound, two main metabolites have been isolated, quantitatively determined and th
Publikováno v:
Journal of Heterocyclic Chemistry. 7:1429-1431
Publikováno v:
Arzneimittel-Forschung. 24(10)
Publikováno v:
International journal of clinical pharmacology and biopharmacy. 15(8)
The influence of food on the bioavailability of two oral dosage forms (100-mg capsules and 200-mg tablets) of indoprofen, a new propionic acid derivative with marked anti-inflammatory and analgesic properties, has been investigated. Plasma levels and
Publikováno v:
Thrombosis and Haemostasis.
Given by the i.v. route to healthy volunteers, indobufen has an half-life of 7-9 h. After oral administration of tablets, the drug is completely absorbed. Excretion occurs through the kidney and the drug is present in the urine as glucoronide and in
Publikováno v:
European journal of clinical pharmacology. 15(5)
The effect of food on bioavailability of indobufen tablets was investigated in 6 healthy volunteers. Subsequently, the same subjects took 100 mg b.i.d. for 7 days. Plasma levels and urinary excretion of indobufen were determined by GLC. Platelet aggr
Publikováno v:
International journal of clinical pharmacology and biopharmacy. 15(9)
The pharmacokinetics of indoprofen in healthy subjects after single oral and i.v. administrations is reviewed. During repeated administration of indoprofen to 6 normal subjects (200-mg tablet every 8 hours for 6 days) no variations in the disposition