A method of separating and purifying quercetagetin from tagetes erecta

A technology for separation and purification of quercetin marigold, which is applied in the direction of organic chemistry, can solve the problems of unsuitable separation and purification of substances with complex components, unsuitable for industrialized large-scale production, and lack of repeatability, so as to shorten the preparation time and batch High degree of consistency between times and the effect of reducing column elution time

Active Publication Date: 2016-06-22
TIANJIN YAOYU BIOLOGICAL TECH
View PDF3 Cites 17 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] The paper "Isolation and Structural Identification of Tagetin and Quercetin Tagetin" (Journal of Guangzhou Medical College, Volume 18, No. 1, 1990) proposed that quercetin tagetin crystals could be obtained by organic solvent extraction and recrystallization. However, the crystallization is obtained through multiple extractions and multiple recrystallizations. Not only is the operation complicated, the workload is heavy, and the cost is high. More importantly, this method is not repeatable and is not suitable for industrialized large-scale production.
[0005] The Chinese invention patent with the publication number CN102190646B also discloses a preparation method of quercetin tagetin, which proposes to use a preparative high-speed countercurrent chromatography for extraction, and the purity of the quercetin tagetin obtained can reach more than 95%, but the The method has limited separation components and low separation efficiency, and is not suitable for the separation and purification of substances with complex components such as whole marigold flowers

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
  • A method of separating and purifying quercetagetin from tagetes erecta
  • A method of separating and purifying quercetagetin from tagetes erecta
  • A method of separating and purifying quercetagetin from tagetes erecta

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0036] The method for separating and purifying quercetin tagetin from marigold in this embodiment comprises the following steps:

[0037] Take dried marigold flowers as raw materials, grind them into powder, extract and rotary steam with ethanol to obtain dried marigold coarse powder, weigh 5g, dissolve in 50mL of 95% methanol-water solution, and prepare a marigold extract solution with a concentration of 100mg / mL, passed through a 0.45 μm microporous membrane, and prepared by one-dimensional liquid chromatography. One-dimensional liquid chromatography using reversed-phase column DAISOC 18 (250mm×20mmi.d., 8μm), the mobile phase is a mixture of organic phase and water phase, wherein phase A is water, phase B is methanol, isocratic elution method: concentration of phase B is 53% isocratic for 20min. Using UV detector 210nm and 260nm as dual selective absorption wavelengths, preparation temperature is room temperature, injection volume is 500μL / needle, mobile phase flow rate i...

Embodiment 2

[0040] The method for separating and purifying quercetin tagetin from marigold in this embodiment comprises the following steps:

[0041] Take dried marigold flowers as raw materials, grind them into powder, extract and rotary steam with ethanol to obtain dry marigold coarse powder, weigh 5g, dissolve in 100mL95% methanol-water solution, and prepare marigold extract solution with a concentration of 25mg / mL, passed through a 0.45 μm microporous membrane, and prepared by one-dimensional liquid chromatography. One-dimensional liquid chromatography using reversed-phase column DAISOC 18 (250mm×20mmi.d., 8μm), the mobile phase is a mixture of organic phase and water phase, wherein A phase is water, B phase is methanol, isocratic elution method: B phase concentration 55% isocratic 20min, 0 % isocratic for 10 min. Adopting ultraviolet detector 210nm and 260nm as dual selective absorption wavelengths, preparation temperature is room temperature, injection volume is 500 μ L / needle, m...

Embodiment 3

[0044] Take dried marigold flowers as raw materials, grind them into powder, extract and rotary steam with ethanol to obtain dried marigold coarse powder, weigh 5g, dissolve in 25mL of 95% methanol-water solution, and obtain a marigold extract solution with a concentration of 200mg / mL, passed through a 0.45 μm microporous membrane, and prepared by one-dimensional liquid chromatography. One-dimensional liquid chromatography using reversed-phase column DAISOC 18 (250mm×20mmi.d., 8μm), the mobile phase is a mixture of organic phase and water phase, wherein A phase is water, B phase is methanol, isocratic elution method: B phase concentration 50% isocratic 20min, 100 % isocratic for 10 min. Adopting ultraviolet detector 210nm and 260nm as dual selective absorption wavelengths, preparation temperature is room temperature, injection volume is 500 μ L / needle, mobile phase flow rate is 12mL / min, according to ultraviolet absorption spectrum ( Figure 7 As shown), the fractions colle...

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
diameteraaaaaaaaaa
particle diameteraaaaaaaaaa
diameteraaaaaaaaaa
Login to view more

Abstract

A method of separating and purifying quercetagetin from tagetes erecta is provided. The method includes a step of drying tagetes erecta dry flowers, grinding into powder, dipping with ethanol or performing reflux extraction, subjecting a filtrate after filtration to rotary evaporation until a product is dry and dissolving the product to a methanol-water mixed solvent; a step of performing one-dimensional liquid chromatogram, wherein DAISO C18 is adopted as a chromatographic column, a mobile phase adopting water as an A phase and methanol as a B phase is adopted, isocratic elution is performed for 20 min with the concentration of the B phase in the mobile phase being 50-55%, eluate from the 6 min to the 12 min is collected according to an ultraviolet absorption spectrum, adopted as a target component, and subjected to rotary evaporation until a product is dry, and the product of the rotary evaporation is dissolved into the methanol-water mixed solution again; and a step of performing two-dimensional liquid chromatogram, wherein Acchrom X-Amide is adopted as a chromatographic column, a mobile phase adopting water as an A phase and acetonitrile as a B phase is adopted, isocratic elution is performed for 40 min with the concentration of the B phase in the mobile phase being 92-98%, and eluate from the 27 min to the 33 min is collected according to an ultraviolet absorption spectrum, adopted as the target component, and subjected to rotary evaporation until a product is dry to obtain quercetagetin the purity of which is 99% or above.

Description

technical field [0001] The invention relates to the technical field of extraction of effective plant components, in particular to a method for separating and purifying quercetin tagetes from marigolds. Background technique [0002] Marigold, also known as Chrysanthemum chrysanthemum, scientific name Tageteserecta, belongs to the genus Marigold of Compositae, is an annual herbaceous plant, in addition to having ornamental value, it also has good medicinal value. Quercetagetin contained in marigold flowers is a flavonoid compound unique to marigolds, which has anti-inflammatory, anti-allergic, blood pressure-lowering, anti-arrhythmic, anti-platelet aggregation, and anti-oxidation effects. Its molecular formula is C 15 h 10 o 8 , the molecular weight is 318.237, and the structural formula is as follows: [0003] [0004] The paper "Isolation and Structural Identification of Tagetin and Quercetin Tagetin" (Journal of Guangzhou Medical College, Volume 18, No. 1, 1990) prop...

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): C07D311/30C07D311/40
Inventor 张耀洲陆洪
Owner TIANJIN YAOYU BIOLOGICAL TECH
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products