Radix puerariae and hovenia dulcis thunb tablet candy and preparation method thereof

Abstract

The invention discloses a radix puerariae and hovenia dulcis thunb tablet candy which is prepared from the following raw materials: 25.13% of white granulated sugar, 16.67% of radix puerariae, 16.67% of hovenia dulcis thunb, 8.34% of fructus gardeniae, 1.67% of ginseng, 1.67% of lucid ganoderma, 1.67% of dendrobium officinale, 1.67% of poria cocos, 1.67% of honeysuckle, 1.67% of fructus lycii, 1.67% of liquorice, 0.50% of magnesium stearate, 1.00% of a compound coating agent and 20% of edible ethanol. Comprising the following steps: extraction and concentration, granulation and total mixing, and coating. The invention belongs to the technical field of tableted candies, and particularly provides a radix puerariae and hovenia dulcis thunb tableted candy which solves the problems of inconvenience in drinking and poor hangover alleviating effect of hangover alleviating tea and has the functions of alleviating hangover toxicity, soothing liver-gallbladder, helping produce saliva and slake thirst, tonifying qi and tonifying kidney and restoring consciousness, and a preparation method of the radix puerariae and hovenia dulcis thunb tableted candy.

Description

Technical Field

[0001] The invention belongs to the technical field of tablet candies, and in particular relates to kudzu root and hovenia dulcis tablet candies and a preparation method thereof. Background Art

[0002] Excessive drinking can inhibit the respiratory center of the brain, causing respiratory arrest, and also inhibit the decomposition of liver glycogen, so that liver glycogen cannot be converted into glucose in time, resulting in a drop in blood sugar and endangering life. There are many alcohol relieving drugs on the market to relieve symptoms such as dizziness and vomiting caused by high alcohol concentration. These drugs have large side effects and will bring additional burdens to liver and kidney metabolism. Therefore, a new type of Pueraria root and Hovenia dulcis tablet candy and its preparation method are urgently needed to solve the above problems. Summary of the invention

[0003] In order to solve the above-mentioned existing problems, the present invention provides a Pueraria root and Hovenia dulcis fruit tablet candy which can solve the problems of inconvenience in drinking hangover tea and poor hangover-detoxification effect, and has the functions of detoxifying alcohol, soothing the liver and promoting bile secretion, promoting the production of body fluid and quenching thirst, invigorating qi and tonifying the kidney, and refreshing the brain, and a preparation method thereof.

[0004] The technical scheme adopted by the present invention is as follows: the kudzu root and hovenia dulcis pressed candy of the present invention comprises the following raw materials: 25.13% of white granulated sugar, 16.67% of kudzu root, 16.67% of hovenia dulcis, 8.34% of gardenia, 1.67% of ginseng, 1.67% of ganoderma lucidum, 1.67% of dendrobium officinale, 1.67% of tuckahoe, 1.67% of honeysuckle, 1.67% of wolfberry, 1.67% of liquorice, 0.50% of magnesium stearate, 1.00% of compound coating agent and 20% of edible ethanol.

[0005] Furthermore, the white sugar is food grade white sugar with 100 meshes, the Pueraria root is a Pueraria root with a puerarin content greater than 3.2%, the Hovenia dulcis fruit is a Hovenia dulcis fruit with a dihydromyricetin content greater than 0.5%, the Gardenia jasminoides fruit is a Gardenia jasminoides fruit with a gardenoside content greater than 2%, the ginseng is artificially grown ginseng of less than 5 years old, the compound coating agent is a transparent compound coating agent, and the edible ethanol is 95% edible ethanol.

[0006] The preparation method of the kudzu root and Hovenia dulcis fruit tablet candy comprises the following steps:

[0007] S1. Put kudzu root, Hovenia dulcis, Gardenia jasminoides, ginseng, ganoderma lucidum, Dendrobium candidum, Poria cocos, and wolfberry in an extraction tank and extract twice. For the first extraction, add water 8 times the total weight of the above raw materials and extract for 1.5 hours; for the second extraction, add water 6 times the total weight of the above raw materials and extract for 1.5 hours. Filter the filtrate for later use.

[0008] S2, put honeysuckle and liquorice in an extraction tank, add 15 times the total weight of the above raw materials of water, extract for 1 hour, filter the filtrate for later use;

[0009] S3. Combine all the above filtrates and concentrate the filtrates into a density of 1.26-1.3 g / cm 3 of extract;

[0010] S4, weighing white sugar according to the formula amount and placing it in a wet mixer, starting the wet mixer, adding concentrated extract to granulate, passing the wet granules through a 16-mesh sieve to a drying fluidized bed, drying at a temperature of 60° C. until the moisture content is less than 7%, and releasing the granules;

[0011] S5, the granules are placed in an 18-mesh sieve of an oscillating granulator, the granules after granulation are placed in a three-dimensional mixer, magnesium stearate is added according to the formula amount, and the mixture is mixed for 30 minutes to obtain tableting granules;

[0012] S6. The compound coating agent is prepared into a coating liquid to coat the compressed tablet granules.

[0013] Furthermore, the weight of the compressed tablet particles is 0.6±0.03 g, and the average weight of the compressed tablet particles is greater than 0.6 g.

[0014] The beneficial effects achieved by the present invention using the above structure are as follows: the Pueraria root and Hovenia dulcis pressed candy proposed in this scheme solves the problem that the hangover tea is inconvenient to drink and has a poor hangover-relieving effect, and has the functions of detoxifying alcohol, soothing the liver and promoting bile secretion, promoting the production of body fluids and quenching thirst, invigorating qi and tonifying the kidney, and refreshing the brain. DETAILED DESCRIPTION

[0015] Various exemplary embodiments of the present invention will now be described in detail. This detailed description should not be considered as limiting the present invention, but should be understood as a more detailed description of certain aspects, features, and embodiments of the present invention.

[0016] It should be understood that the terms described in the present invention are only for describing special embodiments and are not intended to limit the present invention. In addition, for the numerical range in the present invention, it should be understood that each intermediate value between the upper and lower limits of the scope is also specifically disclosed. Each smaller range between the intermediate value in any stated value or stated range and any other stated value or intermediate value in the described range is also included in the present invention. The upper and lower limits of these smaller ranges can be independently included or excluded in the scope.

[0017] Unless otherwise indicated, all technical and scientific terms used herein have the same meanings as those generally understood by those skilled in the art. Although the present invention describes only preferred methods and materials, any methods and materials similar or equivalent to those described herein may also be used in the implementation or testing of the present invention. All documents mentioned in this specification are incorporated by reference to disclose and describe the methods and / or materials associated with the documents. In the event of a conflict with any incorporated document, the content of this specification shall prevail.

[0018] It will be apparent to those skilled in the art that various modifications and variations may be made to the specific embodiments of the present invention description without departing from the scope or spirit of the present invention. Other embodiments derived from the present invention description will be apparent to those skilled in the art. The present application description and examples are exemplary only.

[0019] Example 1

[0020] Pueraria root and Hovenia dulcis fruit compressed candy includes the following raw materials: 25.13% white sugar, 16.67% Pueraria root, 16.67% Hovenia dulcis fruit, 8.34% Gardenia jasminoides, 1.67% Ginseng, 1.67% Ganoderma lucidum, 1.67% Dendrobium officinale, 1.67% Poria cocos, 1.67% Honeysuckle, 1.67% Lycium barbarum, 1.67% Licorice, 0.50% Magnesium stearate, 1.00% Compound coating agent, and 20% Edible ethanol.

[0021] The white sugar is food grade white sugar with 100 meshes, the kudzu root uses a kudzu root with a puerarin content greater than 3.2%, the hovenia dulcis uses a hovenia dulcis with a dihydromyricetin content greater than 0.5%, the gardenia uses a gardenia with a gardenia glycoside content greater than 2%, the ginseng uses artificially grown ginseng less than 5 years old, the compound coating agent uses a transparent compound coating agent, and the edible ethanol uses edible ethanol with a concentration of 95%.

[0022] The preparation method of the kudzu root and Hovenia dulcis fruit tablet candy comprises the following steps:

[0023] S1. Put kudzu root, Hovenia dulcis, Gardenia jasminoides, ginseng, ganoderma lucidum, Dendrobium candidum, Poria cocos, and wolfberry in an extraction tank and extract twice. For the first extraction, add water 8 times the total weight of the above raw materials and extract for 1.5 hours; for the second extraction, add water 6 times the total weight of the above raw materials and extract for 1.5 hours. Filter the filtrate for later use.

[0024] S2, put honeysuckle and liquorice in an extraction tank, add 15 times the total weight of the above raw materials of water, extract for 1 hour, filter the filtrate for later use;

[0025] S3. Combine all the above filtrates and concentrate the filtrates into a density of 1.26-1.3 g / cm 3 of extract;

[0026] S4, weighing white sugar according to the formula amount and placing it in a wet mixer, starting the wet mixer, adding concentrated extract to granulate, passing the wet granules through a 16-mesh sieve to a drying fluidized bed, drying at a temperature of 60° C. until the moisture content is less than 7%, and releasing the granules;

[0027] S5, the granules are placed in an 18-mesh sieve of an oscillating granulator, the granules after granulation are placed in a three-dimensional mixer, magnesium stearate is added according to the formula amount, and the mixture is mixed for 30 minutes to obtain tableting granules;

[0028] S6. The compound coating agent is prepared into a coating liquid to coat the compressed tablet granules.

[0029] The weight of the compressed tablet particles is 0.6±0.03 g, and the average weight of the compressed tablet particles is greater than 0.6 g.

[0030] The embodiments described above are preferred embodiments of the present invention, rather than all embodiments. The detailed description of the embodiments of the present invention is not intended to limit the scope of the invention claimed for protection, but merely represents selected embodiments of the present invention. Based on the embodiments of the present invention, all other embodiments obtained by ordinary technicians in this field without creative work are within the scope of protection of the present invention.

Claims

1. Pueraria root and Hovenia dulcis fruit tablet candy, characterized by: It includes the following raw materials: 25.13% white sugar, 16.67% kudzu root, 16.67% hovenia dulcis, 8.34% gardenia, 1.67% ginseng, 1.67% ganoderma lucidum, 1.67% dendrobium officinale, 1.67% poria, 1.67% honeysuckle, 1.67% wolfberry, 1.67% licorice, 0.50% magnesium stearate, 1.00% compound coating agent, and 20% edible ethanol.

2. The kudzu root and Hovenia dulcis pressed candy according to claim 1, characterized in that: The white sugar is food grade white sugar with 100 meshes, the kudzu root uses a kudzu root with a puerarin content greater than 3.2%, the hovenia dulcis uses a hovenia dulcis with a dihydromyricetin content greater than 0.5%, the gardenia uses a gardenia with a gardenia glycoside content greater than 2%, the ginseng uses artificially grown ginseng less than 5 years old, the compound coating agent uses a transparent compound coating agent, and the edible ethanol uses edible ethanol with a concentration of 95%.

3. The method for preparing the Pueraria lobata and Hovenia dulcis tablet candy according to claim 2, characterized in that: S1. Put kudzu root, Hovenia dulcis, Gardenia jasminoides, ginseng, ganoderma lucidum, Dendrobium candidum, Poria cocos, and wolfberry in an extraction tank and extract twice. For the first extraction, add water 8 times the total weight of the above raw materials and extract for 1.5 hours; for the second extraction, add water 6 times the total weight of the above raw materials and extract for 1.5 hours. Filter the filtrate for later use. S2, put honeysuckle and liquorice in an extraction tank, add 15 times the total weight of the above raw materials of water, extract for 1 hour, filter the filtrate for later use; S3. Combine all the above filtrates and concentrate the filtrates into a density of 1.26-1.3 g / cm 3 of extract; S4, weighing white sugar according to the formula amount and placing it in a wet mixer, starting the wet mixer, adding concentrated extract to granulate, passing the wet granules through a 16-mesh sieve to a drying fluidized bed, drying at a temperature of 60° C. until the moisture content is less than 7%, and releasing the granules; S5, the granules are placed in an 18-mesh sieve of an oscillating granulator, the granules after granulation are placed in a three-dimensional mixer, magnesium stearate is added according to the formula amount, and the mixture is mixed for 30 minutes to obtain tableting granules; S6. The compound coating agent is prepared into a coating liquid to coat the compressed tablet granules.

4. The kudzu root and Hovenia dulcis pressed candy and its preparation method according to claim 3, characterized in that: The weight of the compressed tablet particles is 0.6±0.03 g, and the average weight of the compressed tablet particles is greater than 0.6 g.