Drug-protein binding studies New trends in analytical and experimental methodology
スポンサーリンク
概要
- 論文の詳細を見る
- 1996-02-23
著者
-
Lindner Wolfgang
Institute Of Analytical Chemistry And Food Chemistry University Of Vienna
-
Lindner Wolfgang
Institute Of Pharmaceutical Chemistry Karl-franzens-university Of Graz
-
ORAVCOVA Jana
Institute of Pharmaceutical Chemistry, Karl-Franzens-University of Graz
-
BOHS Barbara
Institute of Pharmaceutical Chemistry, Karl-Franzens-University of Graz
-
Bohs Barbara
Institute Of Pharmaceutical Chemistry Karl-franzens-university Of Graz
-
Oravcova Jana
Institute Of Pharmaceutical Chemistry Karl-franzens-university Of Graz
-
LINDNER Wolfgang
Institute of Pharmaceutical Chemistry, Karl-Franzens-University of Graz
関連論文
- Automated and simultaneous two-dimensional micro-high-performance liquid chromatographic determination of proline and hydroxyproline enantiomers in mammals
- Drug-protein binding studies New trends in analytical and experimental methodology
- Computerized optimization of the high-performance liquid chromatographic enantioseparation of a mixture of 4-dinitrophenyl amino acids on a quinine carbamate-type chiral stationary phase using DRYLAB
- Optimization of a ligand immobilization and azide group endcapping concept via "Click-Chemistry" for the preparation of adsorbents for antibody purification
- Kinetics of binding properties of 5'-GMP with cisplatin under simulated physiological conditions by capillary electrophoresis
- Changes in peptic digestibility of bovine β-lactoglobulin as a result of food processing studied by capillary electrophoresis and immunochemical methods
- Molecularly imprinted polymer-assisted sample clean-up of ochratoxin A from red wine : merits and limitations
- Direct separation and quantitative analysis of thyroxine and triiodothyronine enantiomers in pharmaceuticals by high-performance liquid chromatography
- Comparison of the Hummel-Dreyer method in high-performance liquid chromatography and capillary electrophoresis conditions for study of the interaction of (RS)-, (R)- and (S)-carvedilol with isolated plasma proteins