Interactions of sulfonylureas with plasma proteins
β Scribed by Par-Lin Hsu; K. H. Joseph; Louis A. Luzzi
- Book ID
- 102408863
- Publisher
- John Wiley and Sons
- Year
- 1974
- Tongue
- English
- Weight
- 399 KB
- Volume
- 63
- Category
- Article
- ISSN
- 0022-3549
No coin nor oath required. For personal study only.
β¦ Synopsis
expressed as micrograms per milliliter, uersus time in hours showed that the disappearance of I from plasma was biphasic.
The half-life for the terminal phase, as estimated graphically from the data between 6 and 24 hr after drug administration, was 6.2 hr. The combined results from these, investigations showed that the GLC method could be used for: (a) evaluating the pharmacokinetics, (b) evaluating drug availability from various dosage formulations, and (c) selecting an optimum dosage regimen for I administration to humans.
π SIMILAR VOLUMES
Data on the binding of imipramine, desipramine, and 3-chlorodesmethylimipramine to plasma proteins have been obtained over a wide range of ligand concentration using a modified equilibrium dialysis technique. Plasma proteins other than albumin do not appreciably contribute to complex formation with
## Abstract During the investigation of fibrin deposition onto hydrophobic polymers in contact with human blood, a model was developed in which fibrinogen was denatured and irreversibly coated onto a polyethylene surface by heating to 70Β°C for 10 min. The denatured fibrinogenβpolyethylene surface i
The interactions of serum proteins are diverse, complex and can lead to dramatic effects on liposome stability and in vivo behavior; conversely lipids can modify the biological activities of serum proteins. Serum lipoproteins can potentially destabilize bilayer membranes leading to vesicle disruptio