In vitro sodium salicylate release from chitosan films
β Scribed by M. M. Bonvin; M. M. Bertorello
- Publisher
- Springer
- Year
- 1993
- Tongue
- English
- Weight
- 176 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0170-0839
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The in vitro release of physostigmine salicylate (PS) from a submicron emulsion and an aqueous solution was studied using the dialysis bag method. These formulations were then perfused to various locations along the rat small intestine (proximal, mid, and distal jejunum), and two lengths (10 and 55
The bioavailability and pharmacokinetics of salicylic acid (SA) were studied after single and multiple doses of a new slow-release formulation, based on porous membrane diffusion of sodium salicylate (NaSA). A solution of NaSA and an enteric-coated tablet of NaSA were used for comparison. Dissolutio