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The Potential of Epigallocatechin-3-gallate (EGCG) as Complementary Medicine for the Treatment of Inflammatory Bowel Disease

ORCID
0000-0003-3500-6819
Affiliation
Department of Pharmacy, Biopharmaceutics and Pharmaceutical Technology, Saarland University, 66123 Saarbrücken, Germany;(S.S.);(M.S.)
Schnur, Sabrina;
Affiliation
Department of Pharmacy, Biopharmaceutics and Pharmaceutical Technology, Saarland University, 66123 Saarbrücken, Germany;(S.S.);(M.S.)
Hans, Fabian;
Affiliation
Department of Drug Delivery, PharmBioTec Research and Development GmbH, 66123 Saarbrücken, Germany
Dehne, Annika;
Affiliation
Department of Drug Delivery, PharmBioTec Research and Development GmbH, 66123 Saarbrücken, Germany
Osti, Janina;
Affiliation
Department of Drug Delivery, PharmBioTec Research and Development GmbH, 66123 Saarbrücken, Germany
Schneemann, Malte-Ole;
ORCID
0000-0002-9260-7357
Affiliation
Department of Pharmacy, Biopharmaceutics and Pharmaceutical Technology, Saarland University, 66123 Saarbrücken, Germany;(S.S.);(M.S.)
Schneider, Marc;
Affiliation
Department of Pharmacy, Biopharmaceutics and Pharmaceutical Technology, Saarland University, 66123 Saarbrücken, Germany;(S.S.);(M.S.)
Hittinger, Marius

Complementary and alternative medicine has the potential to enrich conventional therapy to improve the treatment of various diseases. Patients that suffer from inflammatory bowel disease, which requires a constant need for medication, have to deal with the adverse effects of repeated application. Natural products such as Epigallocatechin-3-gallate (EGCG) possess the potential to improve symptoms of inflammatory diseases. We investigated the efficacy of EGCG on an inflamed co-culture model simulating IBD and compared it to the efficacies of four commonly applied active pharmaceutical ingredients. EGCG (200 µg/mL) strongly stabilized the TEER value of the inflamed epithelial barrier to 165.7 ± 4.6% after 4 h. Moreover, the full barrier integrity was maintained even after 48 h. This corresponds to the immunosuppressant 6-Mercaptopurin and the biological drug Infliximab. The EGCG treatment significantly decreased the release of the pro-inflammatory cytokines IL-6 (to 0%) and IL-8 (to 14.2%), similar to the effect of the corticosteroid Prednisolone. Therefore, EGCG has a high potential to be deployed as complementary medicine in IBD. In future studies, the improvement of EGCG stability is a key factor in increasing the bioavailability in vivo and fully harnessing the health-improving effects of EGCG.

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