Biochemical and mechanical characterization of enzyme-digestible hydrogels
- PMID: 2235879
- DOI: 10.1023/a:1015956714669
Biochemical and mechanical characterization of enzyme-digestible hydrogels
Abstract
Albumin-cross-linked hydrogels were prepared by free radical polymerization using 1-vinyl-2-pyrrolidinone as a monomer and functionalized albumin as a crosslinking agent. The degree of chemical cross-linking was controlled by varying the degree of albumin functionality and the concentration of albumin. With emphasis placed on the potential use of these hydrogels for long-term oral drug delivery, gel characterization studies examined both the swelling and the mechanical properties in the absence and presence of pepsin. In the absence of pepsin, the equilibrium swelling ratio in simulated gastric fluid ranged from 17 to 55, depending on the degree of albumin functionality and the albumin concentration. Swelling was pH dependent at pH's greater than 7. The uptake of solvent into the dried hydrogels was determined to be Fickian. The integrity of swelling gels was dependent on the concentration of the functionalized albumin as well as on the degree of albumin functionality. In the presence of pepsin, a predominance of either surface or bulk degradation was observed, depending on the functionality of the albumin used as a cross-linker. Gel integrity during pepsin degradation also showed a marked dependence on the albumin functionality.
Similar articles
-
Enzyme-digestible swelling hydrogels as platforms for long-term oral drug delivery: synthesis and characterization.Biomaterials. 1988 Sep;9(5):435-41. doi: 10.1016/0142-9612(88)90009-9. Biomaterials. 1988. PMID: 3146993
-
Photo-cross-linked biodegradable hydrogels based on n-arm-poly(ethylene glycol), poly(ε-caprolactone) and/or methacrylic acid for controlled drug release.J Biomater Appl. 2017 Oct;32(4):511-523. doi: 10.1177/0885328217730465. Epub 2017 Sep 12. J Biomater Appl. 2017. PMID: 28899224
-
Preliminary studies on pH-sensitive hydrogels and in vitro release profiles of two model drugs.J Biomater Sci Polym Ed. 2013;24(12):1459-71. doi: 10.1080/09205063.2013.768943. Epub 2013 Feb 26. J Biomater Sci Polym Ed. 2013. PMID: 23829458
-
Synthesis and characterization of pH-sensitive dextran hydrogels as a potential colon-specific drug delivery system.J Biomater Sci Polym Ed. 1999;10(5):591-608. doi: 10.1163/156856299x00504. J Biomater Sci Polym Ed. 1999. PMID: 10357268
-
Hydrogels: swelling, drug loading, and release.Pharm Res. 1992 Mar;9(3):283-90. doi: 10.1023/a:1015887213431. Pharm Res. 1992. PMID: 1614957 Review.
Cited by
-
Hydrogels for site-specific drug delivery to the colon: in vitro and in vivo degradation.Pharm Res. 1992 Dec;9(12):1540-5. doi: 10.1023/a:1015847921435. Pharm Res. 1992. PMID: 1488395
-
Novel gastroretentive dosage forms: evaluation of gastroretentivity and its effect on levodopa absorption in humans.Pharm Res. 2003 Sep;20(9):1466-73. doi: 10.1023/a:1025770530084. Pharm Res. 2003. PMID: 14567643 Clinical Trial.
-
Novel gastroretentive dosage forms: evaluation of gastroretentivity and its effect on riboflavin absorption in dogs.Pharm Res. 2002 Oct;19(10):1516-23. doi: 10.1023/a:1020412817716. Pharm Res. 2002. PMID: 12425470
-
Novel oral drug formulations. Their potential in modulating adverse effects.Drug Saf. 1994 Mar;10(3):233-66. doi: 10.2165/00002018-199410030-00005. Drug Saf. 1994. PMID: 8043223 Review.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources