Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Method for separating and preparing petunidin 3-galactoside chloride

A technology for petunin and galactoside, which is applied in the field of separation and preparation of petunin-3-O-galactoside, and can solve the problem of separation and preparation of petunin-3-O-galactoside that has not been found. Issues such as body research and reporting, to achieve the effect of large sample processing volume and good repeatability

Active Publication Date: 2018-09-11
ZHEJIANG UNIV
View PDF6 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0013] However, there is no research and report on the isolation and preparation of petunienin-3-O-galactoside monomers from blueberries

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Method for separating and preparing petunidin 3-galactoside chloride
  • Method for separating and preparing petunidin 3-galactoside chloride
  • Method for separating and preparing petunidin 3-galactoside chloride

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0069] (1) Wash 1000g of fresh blueberries, add 70% ethanol aqueous solution containing 0.1% (v / v) hydrochloric acid (volume of ethanol and water) according to the ratio of solid to liquid 1:7 (w / v, g / mL) Ratio of 70:30) was fully mixed, ultrasonically extracted for 90 minutes, (45°C, protected from light), vacuum filtered, the filter residue was extracted twice according to the above conditions, the filtrate was combined, and ethanol was removed by vacuum rotary evaporation at 48°C to obtain crude anthocyanins extract;

[0070] (2) The AB-8 macroporous resin soaked in ethanol for 24h is packed into a chromatographic column, washed with deionized water until there is no alcohol smell, washed with 4% hydrochloric acid solution for 1h at a flow rate of 2BV / h, and then deionized Wash with ionized water until the effluent is neutral; wash with 4% sodium hydroxide solution at a flow rate of 2BV / h for 1 hour, and then wash with deionized water until neutral. Inject the crude anthoc...

Embodiment 2

[0076] (1) Wash 3kg of fresh blueberries, add 80% ethanol aqueous solution containing 1.0% (v / v) hydrochloric acid according to the ratio of solid to liquid 1:9 (w / v) and mix thoroughly, ultrasonically extract for 120min, (45°C hereinafter, protected from light), filtered under reduced pressure, and the filter residue was repeatedly extracted 3 times according to the above conditions, and the filtrate was combined, and the ethanol was removed by vacuum rotary evaporation at 46°C to obtain a crude anthocyanin extract;

[0077] (2) The AB-8 macroporous resin soaked in ethanol for 24h is packed into a chromatographic column, washed with deionized water until there is no alcohol smell, washed with 4% hydrochloric acid solution for 1h at a flow rate of 2BV / h, and then deionized Wash with ionized water until the effluent is neutral; wash with 4% sodium hydroxide solution at a flow rate of 2BV / h for 1 hour, and then wash with deionized water until neutral. Inject the crude anthocyani...

Embodiment 3

[0082] (1) Wash 5kg of fresh blueberries, add 90% ethanol aqueous solution containing 1.5% (v / v) hydrochloric acid according to the ratio of material to liquid (w / v) of 1:8 (w / v), mix thoroughly, and extract by ultrasonic for 200min, (45°C hereinafter, protected from light), filtered under reduced pressure, and the filter residue was repeatedly extracted 4 times according to the above conditions, the filtrates were combined, and the ethanol was removed by vacuum rotary evaporation at 47°C to obtain a crude anthocyanin extract;

[0083] (2) The AB-8 macroporous resin soaked in ethanol for 24h is packed into a chromatographic column, washed with deionized water until there is no alcohol smell, washed with 4% hydrochloric acid solution for 1h at a flow rate of 2BV / h, and then deionized Wash with ionized water until the effluent is neutral; wash with 4% sodium hydroxide solution at a flow rate of 2BV / h for 1 hour, and then wash with deionized water until neutral. Inject the crude an...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
wavelengthaaaaaaaaaa
Login to View More

Abstract

The invention provides a method for separating and preparing petunidin 3-galactoside chloride. The method comprises alcohol extraction and concentration, macroporous resin adsorption, preparative liquid chromatography purification and high-speed counter-current chromatography separation, and a high-purity petunidin 3-galactoside chloride monomer is isolated and prepared from blueberry raw materials with complicated composition of anthocyanin. The method combines preparative liquid chromatography and high-speed counter-current chromatography technologies for the first time, the high-purity petunidin 3-galactoside chloride monomer is isolated and obtained from blueberries by optimizing process parameters, and the purity is up to 99%.

Description

technical field [0001] The invention relates to the field of separation and purification of natural products, in particular to a method for the separation and preparation of petunienin-3-O-galactoside. Background technique [0002] Anthocyanin is a water-soluble pigment widely present in plants. It is a polyphenol compound formed by combining anthocyanin with one or more sugar groups, such as glucose, galactose, and arabinose, through glycosidic bonds. There are mainly 6 kinds of anthocyanins commonly found in nature, namely Pelargonidin, Cyaniain, Delphinidin, Peonidin, Petunidin and Malva pigment (Malvidin). In recent years, a large number of studies have confirmed that anthocyanins from natural sources have biological activities such as anti-oxidation, anti-tumor, prevention of cardiovascular diseases, alleviation of diabetes and obesity control. With the continuous improvement of people's living standards, people's calls for functional components from natural sources w...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): C07H17/065C07H1/08
CPCC07H1/08C07H17/065
Inventor 陈卫徐阳谢佳宏
Owner ZHEJIANG UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products