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Updated: Sep 10, 2025

Comparative Study on the Polysaccharide Contents and Antioxidant Activities of Hippophae rhamnoides subsp. sinensis and Hippophae gyantsensis
Published on: August 15, 2025
Ultrasound-assisted enzyme extraction, primary structures and bioactivities of Selaginella uncinata polysaccharides
Yiru Hou1, Hui Li1, Xuxiang Zhang1
1School of Pharmacy, Zunyi Medical University, Zunyi 563000, Guizhou, China; Key Laboratory of Basic Pharmacology of Ministry of Education and Joint International Research Laboratory of Ethnomedicine of Ministry of Education, School of Pharmacy, Zunyi Medical University, Zunyi, Guizhou 563003, China.
Abstract:
In this study, polysaccharides (SUP) were extracted from Selaginella uncinata using ultrasonic-assisted enzymatic extraction (UAEE) and decoction method extraction (DME). UAEE was optimized by response surface methodology, with optimal conditions of 40 min extraction time, a 40:1 liquid-to-material ratio, cellulase to pectinase ratio of 2:1, and pH 5.0. Under these conditions, the extraction rate (2.08 ± 0.26 %) and polysaccharide content (58.78 ± 0.31 %) of UAEE-SUP were significantly higher than DME-SUP (1.63 ± 0.30 % and 38.50 ± 0.22 %, respectively). Structural analysis revealed that UAEE-SUP primarily contained Man, Glc, Gal, Xyl, and Ara, with a molar ratio of 6.96:67.48:13.08:2.50:5.61, and a molecular weight of 55,897 Da, while DME-SUP was composed of Man, Rha, GalA, Glc, Gal, Xyl, and Ara, with a molar ratio of 11.93:4.98:11.21:13.47:26.71:5.15:22.89, and a molecular weight of 13,929 Da. Both polysaccharides exhibited α and β configurations. In vitro biological activity tests indicated that UAEE-SUP exhibited good lipid-lowering, nitrite scavenging, acetylcholinesterase inhibition, and anticancer activities. Notably, in terms of lipid-lowering effects, the pancreatic lipase inhibition rate of UAEE-SUP reached 70.34 ± 1.60 %, which was significantly higher than that of DME-SUP at 52.41 ± 1.12 %. This study provides a theoretical basis for the efficient extraction of SUP and its potential pharmaceutical applications.

