TY - JOUR
T1 - Tablet Formulation Containing Chitosan-Alginate Microparticles
T2 - Characterization and Release Profile of Xanthones
AU - Krisanti, Elsa Anisa
AU - Lazuardi, David
AU - Kiresya, Kianti Kasya
AU - Mulia, Kamarza
N1 - Publisher Copyright:
© 2020. All Rights Reserved.
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2020/11/20
Y1 - 2020/11/20
N2 - Mangosteen pericarp extract contains a high amount of xanthones, which are secondary plant metabolites that exhibit high antioxidant activities as well as beneficial pharmacological properties, but low bioavailabilities. In this study, xanthones extracted from the pericarp of soursop fruit were encapsulated in chitosan-alginate microparticles by ionic gelation, and the microparticles were subsequently formulated into antioxidant supplement tablets by direct compression. One of the tablet formulations satisfied the requirements for weight and size uniformity as well as friability, but not hardness. Dissolution test results revealed similar release profiles characterized by a burst release that occurs in the first 60 min of immersion in simulated gastrointestinal fluids and a complete release of xanthones in 120 min. The results obtained herein demonstrated the potential of the tested tablet formulations for the delivery of xanthones into the gastrointestinal tract. If a targeted release to a specific area in the gastrointestinal tract is desirable, the composition of the excipients in the present formulation should be modified.
AB - Mangosteen pericarp extract contains a high amount of xanthones, which are secondary plant metabolites that exhibit high antioxidant activities as well as beneficial pharmacological properties, but low bioavailabilities. In this study, xanthones extracted from the pericarp of soursop fruit were encapsulated in chitosan-alginate microparticles by ionic gelation, and the microparticles were subsequently formulated into antioxidant supplement tablets by direct compression. One of the tablet formulations satisfied the requirements for weight and size uniformity as well as friability, but not hardness. Dissolution test results revealed similar release profiles characterized by a burst release that occurs in the first 60 min of immersion in simulated gastrointestinal fluids and a complete release of xanthones in 120 min. The results obtained herein demonstrated the potential of the tested tablet formulations for the delivery of xanthones into the gastrointestinal tract. If a targeted release to a specific area in the gastrointestinal tract is desirable, the composition of the excipients in the present formulation should be modified.
KW - Alginate
KW - Chitosan
KW - Mangosteen
KW - Mangostin
KW - Xanthone
UR - http://www.scopus.com/inward/record.url?scp=85097681490&partnerID=8YFLogxK
U2 - 10.14716/ijtech.v11i5.4338
DO - 10.14716/ijtech.v11i5.4338
M3 - Article
AN - SCOPUS:85097681490
SN - 2086-9614
VL - 11
SP - 900
EP - 909
JO - International Journal of Technology
JF - International Journal of Technology
IS - 5
ER -