𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Absorption and bioavailability of captopril in mice and rats after administration by gavage and in the diet

✍ Scribed by S. M. Singhvi; K. J. Kripalani; A. V. Dean; G. R. Keim; J. S. Kulesza; F. S. Meeker Jr.; J. J. Ross Jr.; J. M. Shaw; B. H. Migdalof


Publisher
John Wiley and Sons
Year
1981
Tongue
English
Weight
517 KB
Volume
70
Category
Article
ISSN
0022-3549

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Absorption of iothalamate after oral adm
✍ Thomayant Prueksaritanont; Myung G. Lee; Fung-Hwa Hsu; Win L. Chiou πŸ“‚ Article πŸ“… 1986 πŸ› John Wiley and Sons 🌐 English βš– 773 KB

The oral absorption of iothalamate and the effect of amino acids on its absorption were studied in 6 dogs and 6 rats using a simple HPLC assay. The results showed that iothalamate was absorbed in dogs. averaging 9.9, 8.5. and 10.0 per cent following the administration of 40 and 100mg kg-' of iothala

Species and gender differences in the me
✍ Susan C. J. Sumner; Derek B. Janszen; Bahman Asgharian; Timothy A. Moore; Horace πŸ“‚ Article πŸ“… 2003 πŸ› John Wiley and Sons 🌐 English βš– 390 KB

Tertiary amyl methyl ether (TAME) is a gasoline fuel additive used to reduce emissions. Understanding the metabolism and distribution of TAME is needed to assess potential human health issues. The effect of dose level, duration of exposure and route of administration on the metabolism and distributi

Enhancement of oral bioavailability of p
✍ Jing Jin; Huichang Bi; Jinqing Hu; Guoping Zhong; Lizi Zhao; Zhiying Huang; Min πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons 🌐 English βš– 90 KB πŸ‘ 2 views

## Abstract Paclitaxel is a substrate of the efflux transporters such as P‐glycoprotein, and is mainly metabolized by the liver. Schisandrol B (Sch B), one of the active components in Schisandra, has been reported to be able to inhibit the activity of P‐gp and CYP3A. It might be possible that Sch B

Pharmacokinetics of ethopropazine in the
✍ Mojdeh Maboudian-Esfahani; Dion R. Brocks πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 115 KB πŸ‘ 2 views

The pharmacokinetics of the anticholinergic drug ethopropazine (ET) have been studied in the rat after intravenous (i.v.) and oral administration. After i.v. doses of 5 and 10 mg/kg ET HCl, mean +/- S.D. plasma AUC were 9836 +/- 2129 (n = 4 rats) and 13096 +/- 4186 ng h/mL (n = 5 rats), respectively