Related Experiment Video
Updated: Aug 13, 2026

Coherent anti-Stokes Raman Scattering (CARS) Microscopy Visualizes Pharmaceutical Tablets During Dissolution
Published on: July 4, 2014
[Theophylline semi-solid matrices containing polyethyleneglycols. 3--Mechanism of release]
1Laboratoire de Pharmacie Galénique, Pharmacotechnie et Biopharmacie, Faculté de Pharmacie, Montpellier.
Abstract:
Some rheologic mesures made on a PEG range ranking from PEG 300 to PEG 6000 and containing, as a theophylline plot indicate an expected result: the viscosity increases with the molecular mass of the polymer. These same measures made on a binary mixture of PEG composed of 95% PEG 300, liquid, and 5% of solid, thickening, make appear the peculiarity of the binary mixtures of PEG: the viscosity of the binary mixture of PEG is higher than the one of the solid PEG. This "paradoxical" viscosity results, apparently, on one side from the concomitant translation and opposed of the respective points of vitrous transition of the vehicle (liquid PEG) and of the thickening (solid PEG); and on the other side, of the different solidifications of the chains of different polymers forming the binary mixture.
More Related Videos
10:53Anionic Polymerization of an Amphiphilic Copolymer for Preparation of Block Copolymer Micelles Stabilized by π-π Stacking Interactions
Published on: October 10, 2016
07:32Preparation and Characterization of Individual and Multi-drug Loaded Physically Entrapped Polymeric Micelles
Published on: August 28, 2015
Related Concept Videos
Antiasthma Drugs: Methylxanthines
Theophylline is thought to inhibit phosphodiesterase enzymes, increasing intracellular levels of cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP). This rise in cAMP and cGMP concentrations stimulates cardiac function,...
Oral Drug Delivery Systems: Continuous-Release Systems
IV Infusion to Oral Dosing: Conversion Methods
Modified-Release Drug Delivery Systems: Rate-Programmed II
Drug Delivery Systems: Different Types
Modified-Release Drug Delivery Systems: Influencing Factors