Astaxanthin-loaded alginate-chitosan gel beads activate Nrf2 and pro-apoptotic signalling pathways against oxidative stress

نویسندگانGoshtasbi H. - Abdolahinia E.D. - Fathi M. - Movafeghi A. - Omidian H. - Barar J. - Omidi Y
نشریهJournal of Microencapsulation
ارائه به نام دانشگاهUniversity of Tabriz
شماره صفحات140–156
شماره سریال41
شماره مجلد2
ضریب تاثیر (IF)3.9
نوع مقالهFull Paper
تاریخ انتشار2024-05-01
رتبه نشریهISI (WOS)
نوع نشریهچاپی
کشور محل چاپبریتانیا
نمایه نشریهJCR, SCImago (SJR), Scopus

چکیده مقاله

Oxidative stress (OS) plays a crucial role in disease development. Astaxanthin (ATX), a valuable natural compound, may reduce OS and serve as a treatment for diseases like neurodegenerative disorders and cancer. Nuclear factor-erythroid 2-related factor 2 (Nrf2) regulates antioxidant enzymes and OS management. We evaluated ATX’s antioxidant activity via Alg-CS/ATX gel beads in vitro. ATX-encapsulated alginate-chitosan (Alg-CS/ATX) gel beads were synthesized and structurally/morphologically characterized by SEM, FT-IR, and XRD. Their biological effects were examined in human umbilical vein endothelial cells (HUVECs) treated with H2O2 through MTT assay, Annexin V/PI, cell cycle studies, and western blotting. Alg-CS effectively carried ATX, with high capacity and reduced pore size. Alg-CS/ATX displayed an 84% encapsulation efficiency, maintaining stability for 30 days. In vitro studies showed a 1.4-fold faster release at pH 5.4 than at neutral pH, improving ATX’s therapeutic potential. HUVECs treated with Alg-CS/ATX showed enhanced viability via increased Nrf2 expression. Alg-CS gel beads exhibit significant potential as a biocompatible vehicle for delivering ATX to combat OS with considerable opportunity for clinical applications.

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