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Building a polysaccharide hydrogel capsule delivery system for control release of ibuprofen.

Authors :
Chen, Zhi
Wang, Ting
Yan, Qing
Source :
Journal of Biomaterials Science -- Polymer Edition. Feb2018, Vol. 29 Issue 3, p309-324. 16p. 1 Black and White Photograph, 3 Diagrams, 8 Graphs.
Publication Year :
2018

Abstract

Development of a delivery system which can effectively carry hydrophobic drugs and have pH response is becoming necessary. Here we demonstrate that through preparation of β-cyclodextrin polymer (β-CDP), a hydrophobic drug molecule of ibuprofen (IBU) was incorporated into our prepared β-CDP inner cavities, aiming to improve the poor water solubility of IBU. A core-shell capsule structure has been designed for achieving the drug pH targeted and sustained release. This delivery system was built with polysaccharide polymer of Sodium alginate (SA), sodium carboxymethylcellulose (CMC) and hydroxyethyl cellulose (HEC) by physical cross-linking. The drug pH-response control release is this hydrogel system’s chief merit, which has potential value for synthesizing enteric capsule. Besides, due to our simple preparing strategy, optimal conditions can be readily determined and the synthesis process can be accurately controlled, leading to consistent and reproducible hydrogel capsules. In addition, phase-solubility method was used to investigate the solubilization effect of IBU by β-CDP. SEM was used to prove the forming of core and shell structure. FT-IR and1H-NMR were also used to perform structural characteristics. By the technique of UV determination, the pH targeted and sustained release study were also performed. The results have proved that our prepared polysaccharide hydrogel capsule delivery system has potential applications as oral drugs delivery in the field of biomedical materials. [ABSTRACT FROM PUBLISHER]

Details

Language :
English
ISSN :
09205063
Volume :
29
Issue :
3
Database :
Academic Search Index
Journal :
Journal of Biomaterials Science -- Polymer Edition
Publication Type :
Academic Journal
Accession number :
126975310
Full Text :
https://doi.org/10.1080/09205063.2017.1415583