Publication:
Preparation of poly (N-isopropylacrylamide/itaconic acid) copolymeric hydrogels and their drug release behavior

dc.contributor.authorKAYAMAN APOHAN, NİLHAN
dc.contributor.authorsTasdelen, B; Kayaman-Apohan, N; Guven, O; Baysal, BM
dc.date.accessioned2022-03-12T17:17:49Z
dc.date.accessioned2026-01-10T20:22:44Z
dc.date.available2022-03-12T17:17:49Z
dc.date.issued2004
dc.description.abstractN-isopropylacrylamide/itaconic acid copolymeric hydrogels were prepared by irradiation of the ternary mixtures of N-isopropylacrylamide/itaconic acid/water by gamma-rays at ambient temperature. The effect of comonomer concentration, irradiation dose and pH on the swelling equilibria were studied. Lidocaine was used as a model drug for the investigation of drug release behaviour of hydrogels. Lidocaine adsorption capacity of the hydrogels were found to increase from 3.6 to 862.1 (mg lidocame/g dry gel) with increasing amount of itaconic acid in the gel structure. Adsorption and release processes were followed at 4 and 37 degreesC, respectively. The release studies showed that the basic parameters affecting the drug release behaviour of the hydrogels were pH and temperature of the solution and cross-link density of the gels. (C) 2004 Elsevier B.V. All rights reserved.
dc.identifier.doi10.1016/j.ijpharm.2004.03.017
dc.identifier.eissn1873-3476
dc.identifier.issn0378-5173
dc.identifier.pubmed15196639
dc.identifier.urihttps://hdl.handle.net/11424/227899
dc.identifier.wosWOS:000222536200014
dc.language.isoeng
dc.publisherELSEVIER
dc.relation.ispartofINTERNATIONAL JOURNAL OF PHARMACEUTICS
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjecthydrogel
dc.subjectN-isopropylacrylamide
dc.subjectitaconic acid
dc.subjectlidocaine
dc.subjectdrug release
dc.titlePreparation of poly (N-isopropylacrylamide/itaconic acid) copolymeric hydrogels and their drug release behavior
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage351
oaire.citation.issue2
oaire.citation.startPage343
oaire.citation.titleINTERNATIONAL JOURNAL OF PHARMACEUTICS
oaire.citation.volume278

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