Kidney tonifying tablet and preparation method thereof
By using kidney-tonifying tablets made of ingredients such as oyster peptide, crocodile peptide and sea cucumber peptide, the problem that existing nutritional and health foods are difficult to effectively alleviate physical fatigue, and the effects of multiple nutritional effects are achieved, meeting consumer needs.
Patent Information
- Application Number
- CN202510636753.X
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Filing Date
- 2025-05-17
- Publication Date
- 2025-06-20
AI Technical Summary
Existing nutritional and health foods are difficult to effectively alleviate physical fatigue, and they are diverse in shape and difficult to meet the needs of consumers.
Oyster peptide, crocodile peptide and sea cucumber peptide are used as the main raw materials, combined with sorbitol and a variety of powder ingredients, kidney-tonifying tablets are made through specific preparation methods, which have the effects of enhancing immunity, improving sleep, nourishing kidneys and blood.
Through the use of Shenshen tablets, it can effectively relieve physical fatigue, improve immunity, and improve energy. It also has a variety of nutritional effects to meet consumer needs.
Abstract
Description
Technical Field
[0001] The present invention relates to the technical field of nutritional health foods. Specifically, it relates to a kidney-tonifying tablet and a preparation method thereof. Background Art
[0002] Fatigue, once an enemy that people didn't pay much attention to, mercilessly threatens everyone who works hard and nervously. That is to say, fatigue has brought undeniable helplessness to people at different levels in all walks of life. The intense work and life rhythm will cause physical and mental fatigue. Often feeling exhausted is a typical "sub-healthy state". Fatigue is a physiological warning reaction of the human body, indicating that people should rest. Fatigue is generally caused by overloading physical work, such as the training of soldiers and athletes, heavy physical labor, etc. When the body is in an over-fatigued state, it will cause a series of physiological and even pathological changes, such as a decline in immune function, being prone to infection or an increase in the incidence of various chronic diseases. Therefore, relieving physical fatigue, reducing the discomfort caused by fatigue to the human body, and enabling people to work more energetically are of great significance for maintaining good health. At present, most of the functional foods with the function of relieving physical fatigue are developed using traditional nourishing foods in our country or medicinal and edible plants with the effects of nourishing yin and tonifying the kidney, and tonifying both qi and blood. And most of them appear in the forms of capsules, oral liquids, granules, etc., which are difficult to meet the needs of the vast number of consumers. There is a need for a kidney-tonifying tablet and a preparation method to solve this problem. Summary of the Invention
[0003] The purpose of the present invention is to provide a kidney-tonifying tablet and a preparation method thereof to solve the problems raised in the above background art.
[0004] To achieve the above purpose, the present invention provides the following technical solution: A kidney-tonifying tablet and a preparation method thereof, including raw material components and by weight: 3 - 6 parts of oyster peptide, 4 - 7 parts of crocodile peptide, 2 - 5 parts of sea cucumber peptide, 0.5 - 1 part of sorbitol, 0.2 - 0.4 part of deer penis powder, 0.3 - 0.5 part of astragalus membranaceus powder, 0.2 - 0.3 part of codonopsis pilosula powder, 0.1 - 0.2 part of cistanche deserticola powder, 0.2 - 0.5 part of dendrobium officinale powder, 0.3 - 0.6 part of american ginseng powder, 0.1 - 0.3 part of ganoderma lucidum powder, 0.1 - 0.2 part of cornel powder, 0.2 - 0.4 part of gastrodia elata powder, 0.3 - 0.5 part of eucommia ulmoides leaf powder, 0.1 - 0.3 part of polygonatum sibiricum powder, 0.2 - 0.3 part of okra powder, 0.3 - 0.5 part of mulberry powder, 0.4 - 0.7 part of eucommia male flower powder, 0.3 - 0.5 part of semen myristicae powder, 0.4 - 0.6 part of raspberry powder, 0.1 - 0.3 part of ginseng powder, 0.2 - 0.4 part of bull penis powder, 0.2 - 0.5 part of maca powder, 1 - 2 parts of calcium carbonate, 1 - 3 parts of magnesium stearate.
[0005] As a preferred technical solution of the present invention, 3 parts of oyster peptides, 4 parts of crocodile peptides, 2 parts of sea cucumber peptides, 0.5 part of sorbitol, 0.2 part of deer penis powder, 0.3 part of astragalus powder, 0.2 part of codonopsis powder, 0.1 part of cistanche powder, 0.2 part of dendrobium officinale powder, 0.3 part of american ginseng powder, 0.1 part of ganoderma lucidum powder, 0.1 part of cornel powder, 0.2 part of gastrodia elata powder, 0.3 part of eucommia ulmoides leaf powder, 0.1 part of polygonatum sibiricum powder, 0.2 part of okra powder, 0.3 part of mulberry powder, 0.4 part of eucommia male flower powder, 0.3 part of alpinia oxyphylla powder, 0.4 part of raspberry powder, 0.1 part of ginseng powder, 0.2 part of bull penis powder, 0.2 part of maca powder, 1 part of calcium carbonate, and 1 part of magnesium stearate.
[0006] As a preferred technical solution of the present invention, 6 parts of oyster peptides, 7 parts of crocodile peptides, 5 parts of sea cucumber peptides, 1 part of sorbitol, 0.4 part of deer penis powder, 0.5 part of astragalus powder, 0.3 part of codonopsis powder, 0.2 part of cistanche powder, 0.5 part of dendrobium officinale powder, 0.6 part of american ginseng powder, 0.3 part of ganoderma lucidum powder, 0.2 part of cornel powder, 0.4 part of gastrodia elata powder, 0.5 part of eucommia ulmoides leaf powder, 0.3 part of polygonatum sibiricum powder, 0.3 part of okra powder, 0.5 part of mulberry powder, 0.7 part of eucommia male flower powder, 0.5 part of alpinia oxyphylla powder, 0.6 part of raspberry powder, 0.3 part of ginseng powder, 0.4 part of bull penis powder, 0.5 part of maca powder, 2 parts of calcium carbonate, and 3 parts of magnesium stearate.
[0007] As a preferred technical solution of the present invention, the calcium carbonate is a calcium supplement, and the magnesium stearate is a lubricant.
[0008] As a preferred technical solution of the present invention, the sorbitol is a white crystalline powder, and the sorbitol is a compound.
[0009] A kidney-tonifying tablet and its preparation method, characterized by the following steps: S1. Select a certain amount of oyster peptides, crocodile peptides, and sea cucumber peptides and conduct inspections on them. Take appropriate weights of the qualified oyster peptides, crocodile peptides, and sea cucumber peptides by weighing with an electronic scale and put them into a mixing and stirring container to mix them evenly; S2. Add pure water to the materials mixed in step S1 until the raw materials are completely submerged, then add the corresponding weight parts of sorbitol and stir, and soak for 2 - 3 hours to obtain a new mixed solution; S3. Add deer penis powder, astragalus powder, codonopsis powder, cistanche powder, dendrobium officinale powder, american ginseng powder, ganoderma lucidum powder, cornel powder, gastrodia elata powder, eucommia ulmoides leaf powder, polygonatum sibiricum powder, okra powder, mulberry powder, eucommia male flower powder, alpinia oxyphylla powder, raspberry powder, ginseng powder, bull penis powder, and maca powder to the mixed solution prepared in step S2 in sequence according to the corresponding mass fractions, and repeat stirring and mixing to obtain a primary solution; S4. Put the primary liquid obtained in step S3 into a dryer. The baking time is 40 - 50 min, and the baking temperature is 40°C - 80°C until the primary liquid is dried to a water content of 8%. Then, granulate it and mix it with magnesium stearate and calcium carbonate. Next, place the granules in a tabletting machine at a temperature of 50 - 60°C and spray 3% of sterilized water to press out the primary product of Bushen tablets; S5. Sterilize the primary product of Bushen tablets obtained in step S4 by irradiating with 200 nm ultraviolet light for 5 - 8 min to obtain the finished product of Bushen tablets; S6. Pack and seal the finished product of Bushen tablets inside and outside, and transport it to the designated location.
[0010] Compared with the prior art, the present invention has the following beneficial effects: (1) The present invention relates to a Bushen tablet and its preparation method. The Bushen tablet provided by the present invention selects oyster peptide, crocodile peptide and sea cucumber peptide as the main raw materials, which have the effects of enhancing immunity, improving sleep, tonifying the kidney and nourishing blood, promoting blood circulation, regulating endocrine and protecting the liver. Supplementary sorbitol can assist in improving blood sugar, lubricating the intestines and relieving constipation, diuresis, increasing appetite, and can stimulate the sensitivity of taste buds, having the effect of relieving anorexia. Adding various powders further has the effects of clearing heat and detoxifying, tonifying the kidney and consolidating essence, beautifying the face and enhancing immunity, thereby thoroughly improving the symptoms caused by kidney deficiency, and can also achieve the effects of improving immunity and strengthening the body. Specific Embodiments
[0011] Next, in combination with specific embodiments, the invention will be further described: Example 1
[0012] Example 1 includes the raw material composition and weight parts as follows: oyster peptide 3 - 6 parts, crocodile peptide 4 - 7 parts, sea cucumber peptide 2 - 5 parts, sorbitol 0.5 - 1 part, deer penis powder 0.2 - 0.4 part, astragalus powder 0.3 - 0.5 part, codonopsis powder 0.2 - 0.3 part, cistanche powder 0.1 - 0.2 part, dendrobium officinale powder 0.2 - 0.5 part, american ginseng powder 0.3 - 0.6 part, ganoderma lucidum powder 0.1 - 0.3 part, cornel powder 0.1 - 0.2 part, gastrodia elata powder 0.2 - 0.4 part, eucommia ulmoides leaf powder 0.3 - 0.5 part, polygonatum sibiricum powder 0.1 - 0.3 part, okra powder 0.2 - 0.3 part, mulberry powder 0.3 - 0.5 part, eucommia male flower powder 0.4 - 0.7 part, semen coicis powder 0.3 - 0.5 part, raspberry powder 0.4 - 0.6 part, ginseng powder 0.1 - 0.3 part, bull penis powder 0.2 - 0.4 part, maca powder 0.2 - 0.5 part, calcium carbonate 1 - 2 parts, magnesium stearate 1 - 3 parts; In this embodiment, calcium carbonate is a calcium supplement, magnesium stearate is a kind of lubricant, sorbitol is a white crystalline powder, and sorbitol is a kind of compound. Among them, sorbitol can assist in improving blood sugar, moistening the intestines and relieving constipation, diuresis, increasing appetite, and can stimulate the sensitivity of taste buds, and has the effect of relieving anorexia. Example 2
[0013] Example 2. This embodiment further illustrates Example 1 and includes the following steps: S1. Select a certain amount of oyster peptides, crocodile peptides and sea cucumber peptides and conduct inspections on them. Weigh an appropriate amount of the qualified oyster peptides, crocodile peptides and sea cucumber peptides by an electronic scale and put them into a mixing and stirring container to mix them evenly; S2. Add pure water to the mixture in step S1 until the raw materials are completely submerged, then add the corresponding weight parts of sorbitol, stir, and soak for 2 - 3 hours to obtain a new mixture; S3. Add deer penis powder, astragalus powder, codonopsis powder, cistanche powder, dendrobium officinale powder, american ginseng powder, ganoderma lucidum powder, cornel powder, gastrodia elata powder, eucommia ulmoides leaf powder, polygonatum sibiricum powder, okra powder, mulberry powder, eucommia male flower powder, alpinia oxyphylla powder, raspberry powder, ginseng powder, bull penis powder and maca powder to the mixture prepared in step S2 in sequence according to the corresponding mass fractions, and repeat stirring and mixing to obtain a primary liquid; S4. Put the primary liquid prepared in step S3 into a dryer, bake for 40 - 50 minutes at a baking temperature of 40°C - 80°C until the water content of the primary liquid is dried to 8%, then granulate after sizing, mix with magnesium stearate and calcium carbonate, and then place the granules in a tablet press at a temperature of 50 - 60°C and spray 3% of sterilized water to press into primary kidney - tonifying tablets; S5. Sterilize the primary kidney - tonifying tablets in step S4 by irradiating with 200nm ultraviolet light for 5 - 8 minutes to obtain the finished kidney - tonifying tablets; S6. Package the finished kidney - tonifying tablets in inner and outer packages, seal them, and transport them to the designated location.
[0014] Finally, it should be noted that the above are only the preferred embodiments of the present invention and are not used to limit the present invention. Although the present invention has been described in detail with reference to the foregoing embodiments, for those skilled in the art, they can still modify the technical solutions recorded in the foregoing embodiments, or perform equivalent replacements for some of the technical features. Any modifications, equivalent replacements, improvements, etc. made within the spirit and principle of the present invention shall be included within the protection scope of the present invention.
Claims
1. A kidney-tonifying tablet and a preparation method, characterized in that: The raw material composition and weight parts are as follows: 3-6 parts of oyster peptide, 4-7 parts of crocodile peptide, 2-5 parts of sea cucumber peptide, 0.5-1 parts of sorbitol, 0.2-0.4 parts of deer penis powder, 0.3-0.5 parts of astragalus powder, 0.2-0.3 parts of codonopsis powder, 0.1-0.2 parts of cistanche powder, 0.2-0.5 parts of dendrobium officinale powder, 0.3-0.6 parts of American ginseng powder, 0.1-0.3 parts of ganoderma lucidum powder, 0.1-0.2 parts of cornus powder, and 0.1-0.2 parts of gastrodia elata. Powder 0.2-0.4 parts, eucommia leaf powder 0.3-0.5 parts, polygonatum powder 0.1-0.3 parts, okra powder 0.2-0.3 parts, mulberry powder 0.3-0.5 parts, eucommia male pollen 0.4-0.7 parts, Alpinia oxyphylla powder 0.3-0.5 parts, raspberry powder 0.4-0.6 parts, ginseng powder 0.1-0.3 parts, bull whip powder 0.2-0.4 parts, maca powder 0.2-0.5 parts, calcium carbonate 1-2 parts, magnesium stearate 1-3 parts.
2. A kidney-tonifying tablet and preparation method according to claim 1, characterized in that: The invention discloses 3 parts of oyster peptide, 4 parts of crocodile peptide, 2 parts of sea cucumber peptide, 0.5 parts of sorbitol, 0.2 parts of deer penis powder, 0.3 parts of astragalus powder, 0.2 parts of codonopsis pilosula powder, 0.1 parts of cistanche powder, 0.2 parts of dendrobium officinale powder, 0.3 parts of American ginseng powder, 0.1 parts of ganoderma lucidum powder, 0.1 parts of cornus officinalis powder, 0.2 parts of gastrodia elata powder, 0.3 parts of eucommia leaf powder, 0.1 parts of polygonatum powder, 0.2 parts of okra powder, 0.3 parts of mulberry powder, 0.4 parts of eucommia male pollen, 0.3 parts of alkyl oxyphylla powder, 0.4 parts of raspberry powder, 0.1 parts of ginseng powder, 0.2 parts of bull penis powder, 0.2 parts of maca powder, 1 parts of calcium carbonate and 1 parts of magnesium stearate.
3. A kidney-tonifying tablet and preparation method according to claim 1, characterized in that: The invention discloses 6 parts of oyster peptide, 7 parts of crocodile peptide, 5 parts of sea cucumber peptide, 1 part of sorbitol, 0.4 parts of deer penis powder, 0.5 parts of astragalus powder, 0.3 parts of codonopsis pilosula powder, 0.2 parts of cistanche powder, 0.5 parts of dendrobium officinale powder, 0.6 parts of American ginseng powder, 0.3 parts of ganoderma lucidum powder, 0.2 parts of cornus officinalis powder, 0.4 parts of gastrodia elata powder, 0.5 parts of eucommia leaf powder, 0.3 parts of polygonatum sibiricum powder, 0.3 parts of okra powder, 0.5 parts of mulberry powder, 0.7 parts of eucommia male pollen, 0.5 parts of alkyl oxyphylla powder, 0.6 parts of raspberry powder, 0.3 parts of ginseng powder, 0.4 parts of bull penis powder, 0.5 parts of maca powder, 2 parts of calcium carbonate and 3 parts of magnesium stearate.
4. A kidney-tonifying tablet and preparation method according to claim 1, characterized in that: The calcium carbonate is a calcium supplement and the magnesium stearate is a lubricant.
5. A kidney-tonifying tablet and preparation method according to claim 1, characterized in that: The sorbitol is a white crystalline powder, and sorbitol is a kind of compound.
6. A kidney-tonifying tablet and a preparation method, characterized in that: Follow these steps: S1, purchasing a certain amount of oyster peptide, crocodile peptide and sea cucumber peptide and inspecting them, weighing the qualified oyster peptide, crocodile peptide and sea cucumber peptide by electronic scale, taking an appropriate amount of weight and putting them into a mixing and stirring container to mix them evenly; S2, adding purified water to the mixed materials in step S1 until the raw materials are completely submerged, then adding sorbitol in corresponding parts by weight, stirring, and soaking for 2-3 hours to obtain a new mixed solution; S3, add deer penis powder, astragalus powder, codonopsis powder, cistanche powder, dendrobium officinale powder, American ginseng powder, ganoderma lucidum powder, cornus officinalis powder, gastrodia powder, eucommia leaf powder, polygonatum powder, okra powder, mulberry powder, eucommia male pollen, alkyl oxyphylla powder, raspberry powder, ginseng powder, bull penis powder and maca powder to the mixed solution prepared in step S2 in corresponding mass fractions, and repeatedly stir and mix to obtain an initial solution; S4, putting the initial liquid prepared in step S3 into a dryer, baking for 40-50 minutes at a temperature of 40°C-80°C, until the initial liquid is dried to a water content of 8%, and then granulating it into granules, mixing it with magnesium stearate and calcium carbonate, and then placing the granules in a tablet press at a temperature of 50-60°C, spraying 3% sterilized water, and pressing them into initial kidney-tonifying tablets; S5, sterilizing the primary Bushen Bu Tablets in step S4 by irradiating with 200nm ultraviolet light for 5-8 min to obtain the finished Bushen Bu Tablets; S6. Bag and seal the inner and outer packaging of the finished kidney-tonifying tablets and transport them to the designated location.