๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Comparative physiological disposition of two nitrofuran anti-microbial agents

โœ Scribed by J. P. Labaune; J. P. Moreau; R. Byrne


Publisher
John Wiley and Sons
Year
1986
Tongue
English
Weight
538 KB
Volume
7
Category
Article
ISSN
0142-2782

No coin nor oath required. For personal study only.

โœฆ Synopsis


The physiological disposition of two nitrofuran derivatives used as antimicrobial agents for the treatment of acute infectious diarrhoea was evaluated in humans and animals. Upon administration of a single oral dose (600mg) of nifurzide or nifuroxazide, no unchan ed parent drug was detected in human blood or urine. In rats cent of the dose of nifurzide and nifuroxazide, respectively, were excreted in urine over a 48-hour period. None of this radioactivity was present as unchanged drug, indicating that renal excretion of both drugs occurs as metabolites. In the faeces 20 per cent of the radioactivity recovered was associated with unchanged nifuroxazide as compared with 100 per cent for nifurzide. Whole body autoradiography using rats showed that after oral administration of I4C-nifurzide and "C-nifuroxazide, most of the radioactivity remained in the gastrointestinal lumen.

K ~Y WOKI)S

Nifurzidc Nifuroxazidc Infcctious diarrhoca

given "C-nifurzide and ' 5 '

C-nifuroxazide at a dose of lOmg kg-', 5 per cent and 17 per


๐Ÿ“œ SIMILAR VOLUMES


Comparative study of two anti-scale agen
โœ S.A. Al-Saleh; A.R. Khan ๐Ÿ“‚ Article ๐Ÿ“… 1994 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 694 KB

The performance of MSF distiller depends on scale formation inside the condenser tubes since scale impairs heat transfer and adversely affects the production of the main utility. In the past three decades a great deal of research activity has focus& on the development and testing of anti-scale agent

Comparative effects of (SBE)7m-ฮฒ-CD and
โœ David Q. MA; Roger A. Rajewski; David Vander Velde; Valentino J. Stella ๐Ÿ“‚ Article ๐Ÿ“… 2000 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 376 KB

The purpose of this study was to evaluate and compare the potential use of two parenterally safe โค-cyclodextrins derivatives, (SBE) 7m -โค-CD and HP-โค-CD, as solubilizers and stabilizers for melphalan and carmustine, two very unstable antineoplastic agents. Phase solubility and chemical stability of