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Influence of Ispaghula and Zein Coating on Ibuprofen-Loaded Alginate Beads Prepared by Vibration Technology: Physicochemical Characterization and Release Studies. | LitMetric

AI Article Synopsis

  • The study aimed to create alginate beads that enhance drug loading and prolong drug release, using ispaghula to boost loading and zein for extended release.
  • Ibuprofen served as the model drug, and the results showed better loading (42%) and entrapment efficiency (84%) when ispaghula was included in the formulation.
  • Techniques like Fourier-transform infrared spectroscopy and scanning electron microscopy confirmed the structural improvements and smoother surfaces of the ispaghula-enhanced beads, leading to a drug release period extended to 6 hours with the zein coating.

Article Abstract

The purpose behind the work was to fabricate alginate beads with better drug loading and extended drug release. Ispaghula was used to enhance the drug loading while zein was employed to extend the drug release. Ibuprofen was employed as a model drug in this study. Ibuprofen-loaded alginate beads with and without ispaghula were prepared using vibration technology and coated with zein. The beads prepared with alginate alone were shown to have loading and entrapment efficiencies of 35% and 70% , respectively. Addition of ispaghula in alginate showed a significant increase ( < 0.05) in the drug loading (42% ) and entrapment efficiency (84% ). Fourier-transform infrared spectroscopy confirmed the presence of ispaghula and zein coating in the alginate beads as well as the ibuprofen loading. Scanning electron microscopy revealed better spherical geometry in the beads with ispaghula. The surface morphology of the uncoated beads was rough due to crystalline and surface drug. The zein coating has produced a smoother surface and particle adhesion. Differential scanning calorimetry has shown a reduction in drug crystallinity. Alginate beads extended the drug release for 4 h and the presence of zein extended the release for 6 h.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6027688PMC
http://dx.doi.org/10.3390/scipharm86020024DOI Listing

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