Controlled drug release from gels using surfactant aggregates: I. Effect of lipophilic interactions for a series of uncharged substances
✍ Scribed by Paulsson, Mattias (author);Edsman, Katarina (author)
- Publisher
- John Wiley and Sons Inc.
- Year
- 2001
- Tongue
- English
- Weight
- 187 KB
- Volume
- 90
- Category
- Article
- ISSN
- 0022-3549
- DOI
- 10.1002/jps.1075
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✦ Synopsis
Gels are often used for the delivery of drugs because they have rheological properties that will give a long residence time. Most pharmaceutical gels consist of 99% water and a polymer matrix that will not hinder the release of drugs with a small molecular weight. To fully take advantage of the residence time, it is necessary to have a sustained drug release. In this paper it is suggested that surfactant micelles can be used to control the release from gels. The in vitro release under physiological conditions of ®ve parabens from four different poly(acrylic acid) gels (Carbopol 934, 940, 1342) and one gellan gum (Gelrite) gel was measured using a USP dissolution bath modi®ed for gels, and the diffusion coef®cients were calculated. The diffusion coef®cient of uncharged parabens was generally lower in gels with lipophilic modi®cations, such as C1342, and the greatest effect was seen for butylparaben, with a diffusion that was 25% lower than that in C934 (lacking lipophilic modi®cation). Addition of surfactant micelles to gels delayed the release of all the uncharged drugs in all types of gels studied. The slowest release was seen for butylparaben in a lipophilically modi®ed gel with micelles present. The diffusion coef®cient in such a system was almost 30 times smaller than that in C934 without micelles.
📜 SIMILAR VOLUMES
The aim of this article was to study interactions between different gel forming polymers and amphiphilic drugs and surfactants with the intention of finding interactions that can be used for designing controlled release formulations. The release from gels was measured by detecting the UV-absorbance