dc.contributor.author | Hossieni-Aghdam, SJ | |
dc.contributor.author | Foroughi-Nia, B | |
dc.contributor.author | Zare-Akbari, Z | |
dc.contributor.author | Mojarad-Jabali, S | |
dc.contributor.author | Motasadizadeh, H | |
dc.contributor.author | Farhadnejad, H | |
dc.date.accessioned | 2018-08-26T04:55:48Z | |
dc.date.available | 2018-08-26T04:55:48Z | |
dc.date.issued | 2018 | |
dc.identifier.uri | http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/38405 | |
dc.description.abstract | The main aim of the present study was to design pH-sensitive bionanocomposite hydrogel beads based on CMC and HNT-AT nanohybrid and evaluate whether prepared bionanocomposite beads have the potential to be used in drug delivery applications. Atenolol (AT), as a model drug, was incorporated into the lumen of HA nanotubes via the co-precipitation technique. HNT/AT nanohybrid and CMC/HNT-AT beads were characterized via XRD, SEM, TGA, and FT-IR techniques. Drug loading and encapsulation efficiency was found to be high for CMC/HNT3 beads. Moreover, the swelling and drug release properties of the prepared CMC/HA-AT beads were investigated, and showed a pH sensitive swelling behavior with maximum its content at pH 6.8. Also, it was found that the swelling ratio of CMC/HNT beads was lower than that of pristine CMC beads. Drug release behavior of CMC/HNT-AT bionanocomposite hydrogel beads were investigated. A more sustained and controlled drug releases were observed for CMC/HNT-AT beads. | |
dc.language.iso | English | |
dc.relation.ispartof | International journal of biological macromolecules | |
dc.subject | Aluminum Silicates | |
dc.subject | Atenolol | |
dc.subject | Carboxymethylcellulose Sodium | |
dc.subject | Drug Delivery Systems | |
dc.subject | Drug Liberation | |
dc.subject | Humans | |
dc.subject | Hydrogel, Polyethylene Glycol Dimethacrylate | |
dc.subject | Hydrogen-Ion Concentration | |
dc.subject | Nanocomposites | |
dc.title | Facile fabrication and characterization of a novel oral pH-sensitive drug delivery system based on CMC hydrogel and HNT-AT nanohybrid. | |
dc.type | article | |
dc.citation.volume | 107 | |
dc.citation.issue | Pt B | |
dc.citation.spage | 2436 | |
dc.citation.epage | 2449 | |
dc.citation.index | Pubmed | |
dc.identifier.DOI | https://doi.org/10.1016/j.ijbiomac.2017.10.128 | |