Beta-cyclodextrin Grafted with Poly (ε-caprolactone) for Ibuprofen Delivery System | ||||
Egyptian Journal of Chemistry | ||||
Article 4, Volume 62, Issue 5, May 2019, Page 827-835 PDF (1.7 MB) | ||||
Document Type: Original Article | ||||
DOI: 10.21608/ejchem.2018.5125.1455 | ||||
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Authors | ||||
Ahmed Haroun 1; Ali Osman2; Sayed Ahmed2; Ahmed Elghandour2 | ||||
1National research centre | ||||
2Department of organic chemistry, Faculty of science, Beni-suef University, 62514, Egypt. | ||||
Abstract | ||||
The aim of this study is to synthesize a polymeric composite based on grafted beta-cyclodextrin (β-CD) with poly (ε-caprolactone) using ring-opening polymerization (ROP) technique, in presence of ethylene glycol dimethacrylate (EGDMA) and benzoyl peroxide (BP) as crosslinker and initiator, respectively, for drug delivery system (ß-CD-PCL). The obtained ß-CD-PCL composites were characterized by nuclear magnetic resonance (1HNMR), Fourier transform infrared spectroscopy (FT-IR) and transmission electron microscope (TEM). Ibuprofen (IBU) was used as anti-inflammatory drug model. IBU was loaded onto the resulting materials during the preparation process at different drug concentrations (400, 516, 600, 700 and 1000) mg/L. On the other hand, the kinetics study of the copolymerization was carried out in terms of grafting yields (GY%), grafting efficiency (GE%), and monomer conversion (%). Moreover, in vitro IBU release study was investigated in phosphate buffer of pH 7.4 at 37°C. The results indicated that the prepared composites based on grafted β-CD with PCL could be used as a potential hydrophobic drug delivery carrier with sustained release property. Besides, due to the sustained release of IBU from the cavity of the β-CD, it was possible to maintain a constant desired IBU concentration over a period of 24 h, as confirmed by the release steady. | ||||
Keywords | ||||
β-cyclodextrin; ε-caprolactone; Ibuprofen; ring-opening polymerization; in vitro drug release | ||||
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