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Porous Starch-inulin Loaded Quercetin Microcapsules: Characterization, Antioxidant Activity, in-vitro Release, and Storage Stability.
Davoudi, Zahra; Azizi, Mohammad Hossein; Barzegar, Mohsen; Bernkop-Schnürch, Andreas.
Afiliação
  • Davoudi Z; Department of Food Science and Technology, Faculty of Agriculture, Tarbiat Modares University, Tehran, Iran; Department of Pharmaceutical Technology, University of Innsbruck, Institute of Pharmacy, Center for Chemistry and Biomedicine, Innrain 80-82, 6020 Innsbruck, Austria.
  • Azizi MH; Department of Food Science and Technology, Faculty of Agriculture, Tarbiat Modares University, Tehran, Iran. Electronic address: azizit_m@modares.ac.ir.
  • Barzegar M; Department of Food Science and Technology, Faculty of Agriculture, Tarbiat Modares University, Tehran, Iran.
  • Bernkop-Schnürch A; Department of Pharmaceutical Technology, University of Innsbruck, Institute of Pharmacy, Center for Chemistry and Biomedicine, Innrain 80-82, 6020 Innsbruck, Austria. Electronic address: andreas.bernkop@uibk.ac.at.
J Pharm Sci ; 113(5): 1228-1238, 2024 May.
Article em En | MEDLINE | ID: mdl-37992869
ABSTRACT
Quercetin (Q) has many potential health benefits, but its low stability limits its use in functional foods and pharmaceuticals. The low stability of quercetin is a challenge that needs to be addressed to fully realize its therapeutic potential. The purpose of this study was therefore to design a proper carrier based on porous starch (PS) and inulin (IN) in order to improve the stability of Q. The scanning electron microscopy (SEM) images denoted that the Q molecules were adsorbed in the PS pores and partially adhered to the surface of the granules. Both types of the wall material could remarkably enhance the protection of Q against thermal and light degradation. The retention index of Q under different environmental conditions was higher for the PSIN-Q than PS-Q. The results of Fourier transform infrared spectroscopy (FT-IR) revealed that Q interacted with the wall materials through non-covalent bonds. X-ray diffraction (XRD) also confirmed the encapsulation of Q in the wall materials. The bonding between Q and the hydrogen groups of starch compacted the crystalline regions and increased the relative crystallinity in PS-Q and PSIN-Q. The DPPH and ABTS scavenging activities of the microcapsules containing the PS and IN were higher than those of free Q. Examination of the in-vitro release profile indicated that the Q release rate was lower from the PSIN-Q microcapsules (21.6%) than from the PS-Q ones (33.7%). Our findings highlight the significant potential of this novel biopolymer mixture (PS/IN) as a promising wall material for the protection and delivery of bioactive compounds.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Quercetina / Antioxidantes Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Quercetina / Antioxidantes Idioma: En Ano de publicação: 2024 Tipo de documento: Article