gastrointestinal drug release

Freeze-dried nanocomposite gel beads for oral drug delivery. In vitro simulation of gastro-intestinal drug release

We investigated entrapment efficiency, swelling and drug release from freeze-dried gel beads prepared with Gellan gum and a synthetic clay, Laponite. Polymeric beads loaded with two model molecules having different molecular weights were prepared and subjected to in vitro release studies in simulated gastric and intestinal fluids. The experimental observations confirm that laponite may be an effective additive for fabricating sustained drug delivery systems from gellan gum by means of ionotropic gelation and freeze-drying.

Gellan gum/laponite beads for the modified release of drugs: experimental and modeling study of gastrointestinal release

In this study, gellan gum (GG), a natural polysaccharide, was used to fabricate spherical porous beads suitable as sustained drug delivery systems for oral administration. GG was cross-linked with calcium ions to prepare polymeric beads. Rheological studies and preliminary experiments of beads preparation allowed to identify the GG and the CaCl2 concentrations suitable for obtaining stable and spherical particles. GG beads were formed, through ionotropic gelation technique, with and without the presence of the synthetic clay laponite.

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