FORMULATION OF ENTERIC GRANULES CONTAINING GREEN TEA (CAMELLIA SINENSIS) EXTRACT USING EUDRAGIT L100-55 AS A DELAYED RELEASE MATRIX

  • EFFIONORA ANWAR Laboratory of Pharmaceutics and Pharmaceutical Technology Development, Faculty of Pharmacy, Universitas Indonesia, Depok, Indonesia
  • JESSICA RAMADHANTY VALENSYA SHERMAN Laboratory of Pharmaceutics and Pharmaceutical Technology Development, Faculty of Pharmacy, Universitas Indonesia, Depok, Indonesia

Abstract

Objective: Epigallocatechin gallate (EGCG) inhibits glucose absorption into the blood by inhibiting small intestinal α-glucosidase but is unstable in
gastric fluid. Hence, we formulated EGCG into enteric preparations that prevent release in gastric fluid.
Methods: Granules were prepared using a wet granulation method and were formulated into polyvinylpyrrolidone (PVP)-Eudragit L100-55 (5:1; F1),
PVP-Eudragit L100-55 (1:1; F2), and Eudragit L100-55 (F3) preparations using 30% w/w Eudragit L100-55 as a matrix. EGCG contents of granules
were evaluated and dissolution tests were performed at pH 1.2 and 6.8.
Results: F1–3 formulas had good flow properties and contained EGCG at 24.05%±0.15%–24.96%±0.28%. Dissolution tests showed that F1 and F2
formulas released EGCG at 50.53%±0.04% and 17.80%±0.55%, respectively, after 2 h in HCl medium at pH 1.2. Cumulative drug release from F1 and
F2 formulations after 2 h under these conditions (pH 1.2) and 1 h in phosphate buffer (pH 6.8) was 94.40%±1.58% and 93.70%±1.08%, respectively.
Conclusion: As the optimal formula, F3 granules limited drug release to 7.03%±0.22% in HCl at pH 1.2 over 2 h and cumulative drug release in HCl
medium (pH 1.2) followed by phosphate buffer (pH 6.8) of 86.13%±0.20%.

Keywords: Delayed release, Enteric, Epigallocatechin gallate, Eudragit L100-55, Granules, Green tea (Camellia sinensis) extract

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ANWAR, E., & SHERMAN, J. R. V. (2020). FORMULATION OF ENTERIC GRANULES CONTAINING GREEN TEA (CAMELLIA SINENSIS) EXTRACT USING EUDRAGIT L100-55 AS A DELAYED RELEASE MATRIX. International Journal of Applied Pharmaceutics, 12(1), 126-129. https://doi.org/10.22159//ijap.2020.v12s1.FF028
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