Isolation of highly polar galloyl glucoside tautomers from Saxifraga tangutica through preparative chromatography and assessment of their in vitro antioxidant activity.

ABSTRACT: In this work, the rapid and efficient preparation of isolated galloyl glucoside tautomer free radical inhibitors was investigated using Saxifraga tangutica as a raw material. Four highly polar galloyl glucoside tautomers, 3-O-galloyl-α-D-glucose ⇌ 3-O-galloyl-β-D-glucose (Fr2-1-1), 2-O-galloyl-α-D-glucose ⇌ 2-O-galloyl-β-D-glucose (Fr2-1-2/2-1-3), 1-O-galloyl-β-D-glucose (Fr2-2-1), and 6-O-galloyl-α-D-glucose ⇌ 6-O-galloyl-β-D-glucose (Fr2-3-1/Fr2-3-2), were obtained via two-step medium-pressure liquid chromatography (with solid loading instead of conventional liquid injection) and one-step high-performance chromatography coupled with on-line RPLC-DPPH techniques for targeted isolation. This separation integration technique not only increases sample intake and reduces time cost but also vi

SUBMITTER: Tong Y 

PROVIDER: S-EPMC11549745 | biostudies-literature | 2024 Nov

REPOSITORIES: biostudies-literature