Gren T, Bjerre C, Camber O, "In vitro drug release from porous cellulose matrices", Int J Pharm, 1996,141, 53-62.Gren T., Bjerre C., Camber O., Ragnarsson G., In vitro drug release from porous cellulose matrices, Int. J. Pharm., 1996, 141, 53-62....
The kinetics of the drug release was studied in order to ascertain the type of release mechanism. Because the release of drugs from drug-intercalated montmorillonite was controllable, these new materials have a great potential as a delivery host in the pharmaceutical field. Highlights ► Chitosan ...
By altering the composition of composite hydrogel, sol-gel-sol transition behavior and in vitro drug release behavior of the prepared composite hydrogel could be controlled, which was of great importance for their further application as injectable in situ gel-forming drug release system....
In vitro drug release and antibacterial activity evaluation of silk fibroin coated vancomycin hydrochloride loaded poly (lactic-co-glycolic acid) (PLGA) su... In vitro drug release and antibacterial activity evaluation of silk fibroin coated vancomycin hydrochloride loaded poly (lactic-co-glycolic acid...
Release characteristics and in vitro-in vivo correlation of pulsatile pattern for a pulsatile drug delivery system activated by membrane rupture via osmoti... This study attempted to characterize the influence of core and coating formulations on the release profiles to establish in vitro/in vivo corr...
网络释义 1. 体外药物释放 体外药物释放,Drug release in... ... )Drug release in vitro体外药物释放) drug delivery systems 药物释放体系 ... www.dictall.com|基于2个网页 2. 体外释药 体外释药... ... ) In vitro drug release 体外释药 )drug release in vitro体外释药) Vitro Drug Release Ra...
ID: ALA1909046 Title: DrugMatrix in vitro pharmacology data Authors: Scott S. Auerbach, DrugMatrix¨ and ToxFX¨ Coordinator National Toxicology Program Abstract: The DrugMatrix Pharmacology data is a subset of the data freely available from the National Toxicology Program. For more details see:htt...
Of these, drug release kinetics provides critical information about dosage form behavior and is a key parameter used to assess product safety and efficacy. Due to the expense, time, labor, and need for human subjects/animals when performing in vitro measurements of drug release kinetics, in ...
Another approach to preclinical in vitro drug testing is to use genetically characterized cell lines to assess drug effects against cells containing known specific DNA mutations. For example, the National Cancer Institute (NCI) has been studying the use of genetically defined yeast strains as a ...
In vitro – in vivo correlation (IVIVC) allows prediction of the in vivo performance of a pharmaceutical product based on its in vitro drug release profiles and can be used to optimize formulations, set dissolution limits, reduce the number of bioequivalence studies during product development, and...