Method for extracting procyanidine A2 from litchi rind
A technology of proanthocyanidins and lychee skin, which is applied in the direction of organic chemistry, can solve the problem that the combined proanthocyanidins in lychee skin cannot be extracted, and achieve the effects of promoting sustainable development, simple operation, and wide application range
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Publication Date
- 2020-06-19
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Abstract
Description
technical field
[0001] The invention belongs to the technical field of plant active ingredient extraction. More specifically, it relates to a method for extracting proanthocyanidin A2 from litchi peel. Background technique
[0002] Litchi is a seasonal fruit that is a specialty in southern my country, and has the reputation of "Lingnan Fruit King". It matures in the high temperature season of midsummer, and it is difficult to store and keep fresh for a long time. Therefore, in addition to fresh food, litchi is mainly used in the deep processing industry. The industrialization of lychee is mainly based on canned food, fruit juice and fruit wine, and a large amount of lychee peel is discarded as a by-product, which has not been effectively developed and utilized. Litchi skin is rich in polyphenols, especially A-type proanthocyanidins, which are less sourced in nature. Among them, procyanidins A2 (Procyanidins A2, PCA2), a dimer of proanthocyanidins polymerized by epicatechin...
Examples
Embodiment 1
[0029] Embodiment 1 A method of extracting proanthocyanidin A2 from litchi peel
[0030] The method for extracting proanthocyanidin A2 from litchi bark specifically comprises the following steps:
[0031] S1. Freeze the lychee skin, put it into a 70% ethanol solution by volume, and pulverize it so that the weight-volume ratio of the lychee skin to the ethanol solution is 1:20g / ml, extract at 50°C for 3h, centrifuge, add the bottom residue X to the ethanol solution Use the same method to extract again to obtain the combined supernatant A and the bottom residue Y after two extractions, and store them at 4°C for later use;
[0032] S2, add the bottom layer residue Y obtained in step S1 under the protection of nitrogen gas to a 2mol / L sodium hydroxide solution with a mass volume ratio of 1:15g / ml, shake and hydrolyze for 4h, and adjust the pH to 2.0, 4 with hydrochloric acid with a concentration of 6mol / L. Centrifuge at 6000rpm for 10min at ℃ to separate supernatant B;
[0033] ...
Embodiment 2
[0035] Embodiment 2 A method of extracting proanthocyanidin A2 from litchi peel
[0036] The method for extracting proanthocyanidin A2 from litchi bark specifically comprises the following steps:
[0037] S1. Freeze the lychee skin, put it into a 70% ethanol solution by volume, and pulverize it so that the weight-volume ratio of the lychee skin to the ethanol solution is 1:20g / ml, extract at 50°C for 3h, centrifuge, add the bottom residue X to the ethanol solution Use the same method to extract again to obtain the combined supernatant A and the bottom residue Y after two extractions, and store them at 4°C for later use;
[0038] S2. Add the bottom layer residue Y obtained in step S1 under nitrogen protection to a 3mol / L sodium hydroxide solution with a mass volume ratio of 1:15g / ml, shake and hydrolyze for 3h, and adjust the pH to 2.0, 4 with hydrochloric acid with a concentration of 6mol / L. Centrifuge at 6000rpm for 10min at ℃ to separate supernatant B;
[0039] S3. Combine...
Embodiment 3
[0041] Embodiment 3 A method of extracting proanthocyanidin A2 from litchi peel
[0042] The method for extracting proanthocyanidin A2 from litchi bark specifically comprises the following steps:
[0043] S1. Freeze the lychee skin, put it into a 70% ethanol solution by volume and pulverize it so that the weight volume ratio of the lychee skin to the ethanol solution is 1:15g / ml, extract at 50°C for 3h, centrifuge, add the bottom residue X to the ethanol solution Use the same method to extract again to obtain the combined supernatant A and the bottom residue Y after two extractions, and store them at 4°C for later use;
[0044] S2, add the bottom layer residue Y obtained in step S1 under the protection of nitrogen gas to a 4mol / L sodium hydroxide solution with a mass volume ratio of 1:15g / ml, shake and hydrolyze for 2h, and adjust the pH to 2.0, 4 with hydrochloric acid with a concentration of 6mol / L. Centrifuge at 6000rpm for 10min at ℃ to separate supernatant B;
[0045] S...