𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Absorption, metabolism, and excretion of the ephedrines in man II. Pharmacokinetics

✍ Scribed by G. R. Wilkinson; A. H. Beckett


Publisher
John Wiley and Sons
Year
1968
Tongue
English
Weight
514 KB
Volume
57
Category
Article
ISSN
0022-3549

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Pharmacokinetic model for nalidixic acid
✍ G. A. Portmann; E. W. McChesney; H. Stander; W. E. Moore πŸ“‚ Article πŸ“… 1966 πŸ› John Wiley and Sons 🌐 English βš– 532 KB

a two-step protonation. As a check of the method, the pKa of o-iodobenzoic acid was determined concurrently, yielding the value of -7.4 which is in good agreement with previously published data ( 12). A first protonation of compound I could lead to structures Ib, Id, Ic, or If; loss of water from I

Pharmacokinetics, metabolism and renal e
✍ T. B. Vree; T. B. Vree; Y. A. Hekster; M. W. Tijhuis; E. F. S. Termond; J. F. M. πŸ“‚ Article πŸ“… 1986 πŸ› John Wiley and Sons 🌐 English βš– 535 KB

Hydroxylation is the predominant pathway of metabolism for sulfatroxazole in the body, accounting for 70 per cent of the dose. Fifteen per cent of the dose is acetylated unimodally and 10 per cent is excreted unchanged. The half-lives of sulfatroxazole and its metabolites 5-hydroxysulfatroxazole and

The pharmacokinetics and metabolism of 1
✍ John E. Ray; Denis N. Wade πŸ“‚ Article πŸ“… 1982 πŸ› John Wiley and Sons 🌐 English βš– 510 KB

## Abstract Three healthy male subjects received single 100mg oral doses of carprofen containing 20 ΞΌCi of ^14^C‐carprofen. Venous blood samples were drawn during the first 48 h after the dose and urine and feces were collected for 120h. Concentrations of carprofen and its metabolites in body fluid

Absorption, distribution, metabolism, an
✍ Gerald J. Yakatan; Dale D. Maness; Jean Scholler; Wm. J. Novick Jr.; James T. Do πŸ“‚ Article πŸ“… 1976 πŸ› John Wiley and Sons 🌐 English βš– 598 KB

35S-Furosemide was administered to beagle dogs and rhesus monkeys in an oral solution on a single and a 20 repeated 5-mg/kg/day dosing regimen. Following the single dose, 25.0% (dogs) and 24.0% (monkeys) of the dose were excreted in the urine in 24 hr. TLC analysis demonstrated that both species had