๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Preliminary evaluation of the correlation between in vitro release and in vivo bioavailability of two aminophylline slow-release tablets

โœ Scribed by Shan-Yang Lin; Yuh-Horng Kao; Hsiao-Ning Chang


Publisher
John Wiley and Sons
Year
1990
Tongue
English
Weight
462 KB
Volume
79
Category
Article
ISSN
0022-3549

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Sustained-release and swelling character
โœ T. Quinten; T. De Beer; F. O. Onofre; G. Mendez-Montealvo; Y. J. Wang; J. P. Rem ๐Ÿ“‚ Article ๐Ÿ“… 2011 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 419 KB

Sustained-release matrix tablets were developed by injection moulding using metoprolol tartrate (MPT) and ethylcellulose (EC) as sustained-release agent. Dibutyl sebacate was selected as plasticiser. The influence of matrix composition, plasticiser concentration, and drug load on drug release was ev

Comparative bioavailability of josamycin
โœ M. Skinner; I. Kanfer ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 192 KB ๐Ÿ‘ 2 views

The bioavailability of josamycin from a tablet formulation (2 ร— Josacine ยฎ 500 mg tablets) was investigated and compared with the bioavailability of a solution (containing 1 g drug and buffered at pH 4.0) following administration to six healthy human volunteers. Bioavailability profiles for the solu

Novel mucoadhesive extended release tabl
โœ J.M. Llabot; R.H. Manzo; D.A. Allemandi ๐Ÿ“‚ Article ๐Ÿ“… 2009 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 124 KB

Mucoadhesive tablets containing nystatin (10 mg) were evaluated in vivo. The assays were carried out with 12 healthy volunteers and the concentration of nystatin in saliva was determined at different times. Tablets remained attached to the buccal mucosa during 270 min +/- 30 min. No evidence of ulce

Interpretation and optimization of the d
โœ Siobhรกn Hayes; Adrian Dunne; Trevor Smart; John Davis ๐Ÿ“‚ Article ๐Ÿ“… 2004 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 138 KB

This article considers the in vivo significance attached to in vitro dissolution testing. Almost invariably, the in vitro dissolution test is interpreted in terms of bioequivalence. The literature that describes methods for setting in vitro dissolution specifications is reviewed. The most common int