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Theaflavin product rich in tea catechin

A technology of tea catechins and theaflavins, applied in the field of theaflavins rich in tea catechins, can solve the problems of ineffective synthesis of diester-type theaflavins and excessive consumption of tea catechins , to achieve the effect of increasing the conversion generation rate and reducing the loss rate

Active Publication Date: 2017-07-18
HANGZHOU TEA RES INST CHINA COOP
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0007] In the process of repeating the above experiments, the present inventors found that under the condition of the two-liquid phase composed of ethyl acetate and water as the reaction system, although theaflavins can be synthesized relatively well, the tea catechins are excessively consumed, and both Ester-type theaflavins cannot be effectively synthesized

Method used

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  • Theaflavin product rich in tea catechin
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  • Theaflavin product rich in tea catechin

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0038]Accurately weigh 0.7257 g of crushed and ground tender stems and place them in a 100 mL flat-bottomed Erlenmeyer flask, add 20 mL of water-saturated ethyl acetate, shake at room temperature (15 °C) for 5 min, and filter quickly with filter paper under reduced pressure to obtain the filtrate. After fully concentrating the filtrate at a vacuum degree of -0.07 MPa to -0.1 MPa and a temperature below 50 °C, add 20 mL of 5% ethanol aqueous solution, fully oscillate to extract the target substance and set the volume in a 25 mL volumetric flask, shake well before adding 10 μL of the sample was analyzed by HPLC (results in figure 1 Example-1 and Table 1), the rest of the solution was concentrated and dried to obtain theaflavin products rich in tea catechins.

[0039] Table 1 The integral area of ​​each component in the HPLC analysis diagram

[0040] Element caffeine EC EGCG ECG TF TF-3-G TF-3′-G + TF-3, 3′-G Integral area 2238262 157493 1370645 ...

Embodiment 2

[0042] Accurately weigh 0.7023 g of crushed and ground tender stems and place them in a 100 mL flat-bottomed Erlenmeyer flask, add 20 mL of water-saturated ethyl acetate, shake in a water bath (35 °C) for 120 min, and quickly filter with filter paper under reduced pressure to obtain the filtrate. After fully concentrating the filtrate at a vacuum degree of -0.07 MPa to -0.1 MPa and a temperature below 50 °C, add 20 mL of 5% ethanol aqueous solution, fully oscillate to extract the target substance and set the volume in a 25 mL volumetric flask, shake well before adding 10 μL of the sample was analyzed by HPLC (results in figure 1 Example-2 and Table 2), the rest of the solution was concentrated and dried to obtain a theaflavin product rich in tea catechins.

[0043] Table 2 The integral area of ​​each component in the HPLC analysis diagram

[0044] Element caffeine EC EGCG ECG TF TF-3-G TF-3′-G + TF-3, 3′-G Integral area 2076222 43586 522939 3...

Embodiment 3

[0046] Accurately weigh 0.6411 g of crushed and ground tender stems and 0.2170 g of crushed and ground tea tree leaves into a 100 mL flat-bottomed Erlenmeyer flask, add 20 mL of water-saturated ethyl acetate, shake in a water bath (35 °C) for 120 min, and quickly Filter the filter paper under reduced pressure to obtain the filtrate. After fully concentrating the filtrate at a vacuum degree of -0.07 MPa to -0.1 MPa and a temperature below 50 °C, add 20 mL of 5% ethanol aqueous solution, shake fully to extract the target substance and set the volume to 25 mL volumetric flask, shake well and inject 10 μL for HPLC analysis (results in figure 1 Example-3 and Table 3), the rest of the solution was concentrated and dried to obtain a theaflavin product rich in tea catechins.

[0047] Table 3 Integral area of ​​each component in the HPLC analysis diagram

[0048] Element caffeine EC EGCG ECG TF TF-3-G TF-3′-G + TF-3, 3′-G Integral area 2749060 not dete...

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Abstract

The invention discloses a theaflavin product rich in tea catechin. The theaflavin product rich in tea catechin is prepared according to the following steps: fully grinding and crushing Camellia sinensis fresh leaves or tender stems, then mixing with ethyl acetate saturated with water at a certain ratio, and performing water bath vibration for enzymatic reaction.

Description

technical field [0001] The invention relates to a theaflavin product, in particular to a theaflavin product rich in tea catechin. Background technique [0002] Fresh Tea Tree Leaves ( Camellia sinensis (L.) O. Ktze) contains tea catechin polyphenols and their corresponding polyphenol oxidase, under the action of moderate temperature and oxygen, the contact reaction can generate theaflavins (Theaflavins) polyphenols compound. That is, Epi-Catechin (EC) combined with Epigallo-Catechin (EGC), EC combined with Epigallo-Catechin Gallate (Epigallo-Catechin Gallate, EGCG), epicatechin gallate Epi-Catechin Gallate (ECG) combined with EGC, and the composition of ECG combined with EGCG were enzymatically oxidized and polycondensed by polyphenol oxidase (TPPO) to form theaflavins. Theaflavins polyphenolic compounds usually include simple theaflavins (TF) and ester-type theaflavins, among which the main component of ester-type theaflavins is theaflavin-3-monogallate (TF-3- G), thea...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12P17/16C07D311/62
CPCC07D311/62C12P17/162
Inventor 涂云飞
Owner HANGZHOU TEA RES INST CHINA COOP