Alginate beads as a carrier for omeprazole/SBA-15 inclusion compound: A step towards the development of personalized

Pasquale Del Gaudio1, Felicetta De Cicco1, Francesca Sansone1

  • 1Department of Pharmacy, University of Salerno, via Giovanni Paolo II, 132, 84084 Fisciano, SA, Italy.

Carbohydrate Polymers
|September 8, 2015
PubMed

Insights

New enteric alginate beads offer personalized omeprazole (OME) dosages for pediatric gastro-esophageal reflux disease (GERD). These beads provide controlled drug release, improving treatment compared to market products.

Area of Science:

  • Pharmaceutical Technology
  • Drug Delivery Systems
  • Pediatric Medicine

Background:

  • Gastro-esophageal reflux disease (GERD) treatment in children presents challenges with current dosage forms.
  • Need for age- and weight-appropriate medication delivery in pediatric patients.

Purpose of the Study:

  • To formulate enteric alginate beads loaded with omeprazole (OME) for personalized pediatric GERD treatment.
  • To evaluate the drug loading, release kinetics, and in vitro performance of these novel beads.

Main Methods:

  • Omeprazole (OME) was entrapped within SBA-15 mesoporous silica and subsequently loaded into alginate beads via prilling.
  • Characterization of beads for size, morphology, drug loading, and distribution.
  • In vitro release studies were conducted in simulated gastric fluid (SGF) and simulated intestinal fluid (SIF).

Main Results:

  • Alginate beads exhibited homogeneous size, spherical morphology, and consistent drug loading and distribution.
  • Limited swelling and drug release (<10%) were observed in SGF within 2 hours.
  • Prolonged drug release occurred in SIF over 6 hours, indicating suitability for intestinal delivery.
  • The novel beads demonstrated superior performance compared to a marketed product, particularly in SIF release.

Conclusions:

  • The developed enteric alginate beads are a promising novel tool for personalized GERD treatment in children.
  • Uniformity and controlled release properties support their potential for improved pediatric pharmacotherapy.
  • This formulation addresses limitations of existing treatments for pediatric GERD.

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