نمایش پرونده ساده آیتم

dc.contributor.authorMahkam, M
dc.contributor.authorAllahverdipoor, M
dc.contributor.authorMohammadi, R
dc.contributor.authorRanaei-Simat, SO
dc.contributor.authorRashidi, MR
dc.contributor.authorDavaran, S
dc.contributor.authorBarshan, M
dc.contributor.authorRanaei-Siadat, SE
dc.date.accessioned2018-08-26T08:30:14Z
dc.date.available2018-08-26T08:30:14Z
dc.date.issued2006
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/51941
dc.description.abstractCrosslinked 2-hydroxyethyl methacrylate (HEMA) and methacrylic acid (MAA) copolymer hydrogels were studied as drug delivery systems. Terephthalic acid was covalently linked with 2-hydroxyethyl methacrylate (HEMA), abbreviated as cross-linking agent (CA). Free radical copolymerization of HEMA and MAA with terephthetalic acid (CA) (2, 4, and 6%) as crosslinking agent were carried out at 70 degrees C. The structure of the CA was confirmed by FT-IR, (1)H-NMR and (13)C-NMR spectroscopy. The composition of the crosslinked three-dimensional polymers were determined by FTIR spectroscopy. Glass transition temperature (Tg) of the network polymers was determined calorimetrically. The effect of copolymer composition on the swelling behavior and hydrolytic degradation was studied in simulated gastric fluid (SGF, pH 1) and simulated intestinal fluid (SIF, pH 7.4). The swelling and hydrolytic behavior of the copolymers depended on the content of MAA which caused a decrease in gel swelling in SGF or an increase in gel swelling in SIR It was observed that in acidic media hydrogen bonds formed due to the protonation of the carboxylic acid groups of the MAA while in more basic or neutral conditions electrostatic repulsion occurred between the ionized carboxylic acid groups. This complex behavior affected the macroscopic swelling properties of the resultant hydrogels. The amount of drug release depended on the degree of hydrogel swelling and crosslinking.
dc.language.isoEnglish
dc.relation.ispartofJOURNAL OF BIOACTIVE AND COMPATIBLE POLYMERS
dc.subjecthydrogel
dc.subjectswelling
dc.subjectperoral
dc.subjectinsulin
dc.subjectcrosslinking
dc.subjectsimulated gastic fluids
dc.titleAn oral delivery system for insulin
dc.typeArticle
dc.citation.volume21
dc.citation.issue2
dc.citation.spage135
dc.citation.epage148
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1177/0883911506063212


فایلهای درون آیتم

فایلهاسایزفرمتنمایش

هیچ فایل مرتبطی وجود ندارد

این آیتم در مجموعه های زیر مشاهده می شود

نمایش پرونده ساده آیتم