2017
DOI: 10.1002/jssc.201700471
|View full text |Cite
|
Sign up to set email alerts
|

Large‐scale isolation of high‐purity anthocyanin monomers from mulberry fruits by combined chromatographic techniques

Abstract: Anthocyanins have attracted attention over the past several decades because of their beneficial health effects. In this research, a strategy combining column chromatography and high-speed countercurrent chromatography was developed for the separation of high-purity anthocyanin monomers from mulberry fruits. After purification using Amberlite XAD-7HP column with 80% ethanol (0.1% HCl), a fraction of anthocyanins mixtures with a purity of 68.6% was obtained. High-speed countercurrent chromatography with a biphas… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
9
0

Year Published

2018
2018
2024
2024

Publication Types

Select...
6
2

Relationship

0
8

Authors

Journals

citations
Cited by 19 publications
(9 citation statements)
references
References 23 publications
0
9
0
Order By: Relevance
“…It was preliminarily proven that C3G–ACR was a mono-ACR adduct of C3G. Based on the known NMR data of C3G, , the 13 C NMR spectra of C3G–ACR showed a carbon skeleton similar to that of C3G except for three additional carbon signals at δ C 95.15, δ C 26.70, and δ C 16.32 (Table ). Additionally, it was also observed from its 1 H NMR spectrum that the proton signal of C3G at δ H 6.64 (1H, d, J = 1.9 Hz) disappeared, and additional proton signals appeared at δ H 2.81 (2H, m), δ H 2.17 (2H, m), and δ H 5.82 (1H, m), indicating that the ACR group was joined at C-6 in the A ring of C3G.…”
Section: Resultsmentioning
confidence: 94%
“…It was preliminarily proven that C3G–ACR was a mono-ACR adduct of C3G. Based on the known NMR data of C3G, , the 13 C NMR spectra of C3G–ACR showed a carbon skeleton similar to that of C3G except for three additional carbon signals at δ C 95.15, δ C 26.70, and δ C 16.32 (Table ). Additionally, it was also observed from its 1 H NMR spectrum that the proton signal of C3G at δ H 6.64 (1H, d, J = 1.9 Hz) disappeared, and additional proton signals appeared at δ H 2.81 (2H, m), δ H 2.17 (2H, m), and δ H 5.82 (1H, m), indicating that the ACR group was joined at C-6 in the A ring of C3G.…”
Section: Resultsmentioning
confidence: 94%
“…Peonidin-3-glucoside and malvidin-3-glucoside were obtained from grapes in a single step, while in a second step, cyanidin-3-glucoside was isolated [72]. In another research, the separation of anthocyanin monomers of high purity from mulberry fruits was developed [73].…”
Section: Countercurrent-chromatographymentioning
confidence: 99%
“…10,13,[19][20][21] Unrefined simple extracts or tinctures, although often colored, contain only low levels of anthocyanins and are of limited use, however approaches for the preparation of extracts containing relatively high levels of anthocyanins for large scale applications have been reported. [22][23][24] Extraction and semi-purification of polyphenols Dried blackcurrant epicarp (30 g) was immersed in mL water acidified with 0.01% v/v conc. HCl and stirred gently by magnetic follower at room temperature for 2 hours.…”
Section: Introductionmentioning
confidence: 99%