CN107373272B - Soybean isoflavone effervescent tablet and preparation method thereof - Google Patents

Soybean isoflavone effervescent tablet and preparation method thereof Download PDF

Info

Publication number
CN107373272B
CN107373272B CN201710589036.1A CN201710589036A CN107373272B CN 107373272 B CN107373272 B CN 107373272B CN 201710589036 A CN201710589036 A CN 201710589036A CN 107373272 B CN107373272 B CN 107373272B
Authority
CN
China
Prior art keywords
soybean isoflavone
parts
vitamin
effervescent
composition
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
CN201710589036.1A
Other languages
Chinese (zh)
Other versions
CN107373272A (en
Inventor
胡晓娟
张荣培
许阳
许平辉
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bokai Pharmaceutical Co ltd
Original Assignee
Bokai Pharmaceutical Co ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Bokai Pharmaceutical Co ltd filed Critical Bokai Pharmaceutical Co ltd
Priority to CN201710589036.1A priority Critical patent/CN107373272B/en
Publication of CN107373272A publication Critical patent/CN107373272A/en
Application granted granted Critical
Publication of CN107373272B publication Critical patent/CN107373272B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L2/00Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
    • A23L2/385Concentrates of non-alcoholic beverages
    • A23L2/39Dry compositions
    • A23L2/395Dry compositions in a particular shape or form
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L2/00Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
    • A23L2/40Effervescence-generating compositions
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L2/00Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
    • A23L2/52Adding ingredients
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L2/00Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
    • A23L2/52Adding ingredients
    • A23L2/68Acidifying substances
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L33/00Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/10Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
    • A23L33/105Plant extracts, their artificial duplicates or their derivatives
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L33/00Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/10Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
    • A23L33/15Vitamins
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23PSHAPING OR WORKING OF FOODSTUFFS, NOT FULLY COVERED BY A SINGLE OTHER SUBCLASS
    • A23P10/00Shaping or working of foodstuffs characterised by the products
    • A23P10/20Agglomerating; Granulating; Tabletting
    • A23P10/28Tabletting; Making food bars by compression of a dry powdered mixture
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23VINDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2002/00Food compositions, function of food ingredients or processes for food or foodstuffs

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Food Science & Technology (AREA)
  • Polymers & Plastics (AREA)
  • Health & Medical Sciences (AREA)
  • Nutrition Science (AREA)
  • Mycology (AREA)
  • Botany (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

The invention provides a soybean isoflavone effervescent tablet and a preparation method thereof, which relate to the technical field of health care products and are mainly prepared from the following raw materials in parts by mass: 45-55 parts of soybean isoflavone composition, 3-7 parts of vitamin E, 45-55 parts of vitamin C, 1000 parts of acid agent 900-: (5-200): (1-100): (10-50), the technical problem that most of the existing medicines for supplementing estrogen on the market are artificial estrogen, and have toxic and side effects after long-term administration is solved, and the technical effects that the medicine dependence on human bodies cannot be formed, the effects of resisting oxidation and removing free radicals are strong, and the diseases such as hypertension and hyperlipidemia can be effectively prevented are achieved.

Description

Soybean isoflavone effervescent tablet and preparation method thereof
Technical Field
The invention relates to the technical field of health care products, in particular to a soybean isoflavone effervescent tablet and a preparation method thereof.
Background
With the acceleration of life rhythm, the pressure of life of women is getting bigger and worse, and especially women after age 35 have decreased estrogen secretion and decreased immunity, and are more likely to have diseases such as osteoporosis, breast cancer, uterine cancer and the like. Therefore, there is a need to supplement estrogen to women, especially those aged 35 years and older, to improve their physical condition and enhance their immunity, thereby reducing their chances of developing a disease. However, most of the drugs for supplementing estrogen on the market are artificial estrogen, and the drugs have great toxic and side effects even cause drug dependence after being taken for a long time, thereby affecting the health of women.
In view of the above, the present invention is particularly proposed.
Disclosure of Invention
The invention aims to provide a soybean isoflavone effervescent tablet to solve the technical problems that most of the existing medicines for supplementing estrogen on the market are artificial estrogen, and the long-term administration of the medicines can cause great toxic and side effects and even cause medicine dependence to influence the health of women.
The soybean isoflavone effervescent tablet provided by the invention is mainly prepared from the following raw materials in parts by mass: 45-55 parts of soybean isoflavone composition, 3-7 parts of vitamin E, 45-55 parts of vitamin C, 1000 parts of acid agent 900-: (5-200): (1-100): (10-50), preferably (4-6): (9-11): (4-6): (2-4).
Furthermore, the soybean isoflavone effervescent tablet is mainly prepared from the following raw materials in parts by mass: 48-52 parts of soybean isoflavone, 4-6 parts of vitamin E, 48-52 parts of vitamin C, 980 parts of acid agent 940-: (9-11): (4-6): (2-4).
Further, the soybean isoflavone composition is a mixture of daidzin, daidzein, genistein and genistin, and the mass ratio of the daidzin, the daidzein, the genistein and the genistin is 5:10:5:3
Further, the acid agent is selected from at least one of tartaric acid, malic acid, fumaric acid, citric acid or sodium citrate; preferably, the acid agent is a mixture of malic acid and citric acid, and the mass ratio of the two is 1: (5-6).
Further, the alkaline agent is selected from at least one of potassium carbonate, sodium carbonate, calcium carbonate, potassium bicarbonate, sodium bicarbonate and calcium bicarbonate; preferably, the alkaline agent is sodium bicarbonate.
Further, the lubricant is selected from at least one of sodium dodecyl sulfate, magnesium stearate, talcum powder and silicon dioxide; preferably, the lubricant is magnesium stearate.
The invention also aims to provide a preparation method of the soybean isoflavone effervescent tablet, so as to relieve the technical problems that most of the existing medicines for supplementing estrogen on the market are artificial estrogen, and the long-term administration of the medicines can cause great toxic and side effects, even cause medicine dependence and influence the health of women.
The preparation method of the soybean isoflavone effervescent tablet provided by the invention comprises the following steps:
(a) mixing daidzin, daidzein, genistein and genistin uniformly to obtain soybean isoflavone composition;
(b) mixing soybean isoflavone composition, vitamin E, vitamin C, acid agent and alkali agent, and mixing with ethanol to obtain soybean isoflavone effervescent granule;
(c) drying the soybean isoflavone effervescent granules, adding a lubricant, uniformly mixing, and tabletting to obtain the soybean isoflavone effervescent tablets.
Further, the preparation method of the soybean isoflavone effervescent tablet further comprises a step(s), wherein the step(s) is arranged before the step (a) and the step (b), and the step(s) is to pulverize the soybean isoflavone composition, the vitamin E, the vitamin C, the acid agent, the alkali agent and the lubricant and to pass through a 80-mesh sieve.
Further, in the step (c), the temperature for drying is 60 to 70 ℃, preferably 65 ℃.
Further, in the step (b), the prepared soybean isoflavone effervescent granule has a particle size of 14-18 meshes, preferably 16 meshes.
The soybean isoflavone effervescent tablet provided by the invention can supplement female estrogen, improve the immunity of the organism, delay aging, prevent diseases such as osteoporosis, breast cancer, uterine cancer and the like by the synergistic cooperation of the soybean isoflavone composition, the vitamin E, the vitamin C, the acid agent, the alkali agent and the lubricant, has no toxic or side effect on a human body, does not cause drug dependence on the human body, has strong effects of resisting oxidation and removing free radicals, and can effectively prevent diseases such as hypertension, hyperlipidemia and the like.
The preparation method of the soybean isoflavone effervescent tablet provided by the invention has the advantages of simple process, convenience in operation, easiness in large-scale industrial production, reduction in preparation cost and improvement in preparation efficiency.
Detailed Description
Embodiments of the present invention will be described in detail below with reference to examples, but it will be understood by those skilled in the art that the following examples are only illustrative of the present invention and should not be construed as limiting the scope of the present invention. The examples, in which specific conditions are not specified, were conducted under conventional conditions or conditions recommended by the manufacturer. The reagents or instruments used are not indicated by the manufacturer, and are all conventional products available commercially.
According to one aspect of the invention, the invention provides a soybean isoflavone effervescent tablet which is mainly prepared from the following raw materials in parts by weight: 45-55 parts of soybean isoflavone composition, 3-7 parts of vitamin E, 45-55 parts of vitamin C, 1000 parts of acid agent 900-: (5-200): (1-100): (10-50), preferably (4-6): (9-11): (4-6): (2-4).
The soybean isoflavone effervescent tablet provided by the invention can supplement female estrogen, improve the immunity of the organism, delay aging and prevent diseases such as osteoporosis, breast cancer, uterine cancer and the like by the synergistic cooperation of the soybean isoflavone composition, the vitamin E, the vitamin C, the acid agent, the alkali agent and the lubricant.
In the present invention, the typical but non-limiting mass fraction of the soy isoflavone composition is, for example, 45.5, 46, 46.5, 47, 47.5, 48, 48.5, 49, 49.5, 50, 50.5, 51, 51.5, 52, 52.5, 53, 53.5, 54 or 54.5.
The soybean isoflavone composition is a mixture of daidzin, daidzein, genistein and genistin, and the daidzin, the daidzein, the genistein and the genistin are all extracted from natural plants, so that the composition has no toxic or side effect on human bodies, does not cause drug dependence on human bodies, can effectively supplement estrogen in female bodies by means of synergistic cooperation of the daidzin, the daidzein, the genistein and the genistin, has strong effects of resisting oxidation and removing free radicals, and can effectively prevent diseases such as hypertension and hyperlipidemia.
Daidzin is a compound extracted from plants, and has effects in scavenging free radicals, inhibiting oxidation of esters in serum, reducing cholesterol and triglyceride content in blood, inhibiting growth of tumor cells, destroying tumor cell structure or inhibiting DNA synthesis, enhancing immunity, inhibiting growth of tumor cells, resisting oxidation, scavenging free radicals, and reducing lipid peroxide.
Daidzein is one of phytoestrogens, is a nonsteroidal compound which is extracted from plants and has estrogen-like function, has the effects of dilating blood vessels, increasing coronary blood flow, reducing blood pressure, slowing down heart rhythm, reducing myocardial oxygen consumption and resisting arrhythmia, has obvious antibacterial effect on staphylococcus aureus and escherichia coli, and can also treat climacteric syndrome and osteoporosis, resist estrogen activity, prevent and treat breast cancer, endometritis and the like.
Genistein is also called phytoestrogen, can be extracted from soybean, clover, alfalfa and oat, has a structure similar to estrogen, can competitively bind with estrogen receptor to play an estrogen-like role, obviously increases the weight of uterus, increases bone density, and simultaneously has the effects of resisting tumor, resisting diabetes and preventing cardiovascular and cerebrovascular diseases.
The genistin is derived from natural plants, has phytoestrogen bidirectional regulation effect, has good effect in inhibiting vascular proliferation, has effects of delaying or preventing malignant tumor from becoming cancer cells in the development process, simultaneously can prevent cholesterol oxidation and hemolysis, can inhibit platelet aggregation, prevent smooth muscle cell proliferation, and can inhibit and assist in treating diseases caused by lipid peroxidation in vivo.
Typical but not limiting parts by mass of vitamin E in the present invention are e.g. 3.2, 3.4, 3.6, 3.8, 4, 4.2, 4.4, 4.6, 4.8, 5, 5.2, 5.4, 5.6, 5.8, 6, 6.2, 6.4, 6.6 or 6.8.
Vitamin E is a fat-soluble vitamin, the hydrolysis product of which is tocopherol, which is one of the most important antioxidants, and the tocopherol can promote the secretion of sex hormones, increase the female estrogen concentration, improve the fertility, inhibit the peroxidation ester reaction in the lens of eyes, expand peripheral blood vessels and improve blood circulation. Vitamin E has a wide role in preventing cardiovascular and cerebrovascular diseases, tumors, diabetes and other complications, central nervous system diseases, motor system diseases, skin diseases and the like.
Typical but not limiting mass fractions of vitamin C are e.g. 45.5, 46, 46.5, 47, 47.5, 48, 48.5, 49, 49.5, 50, 50.5, 51, 51.5, 52, 52.5, 53, 53.5, 54 or 54.5.
Vitamin C is a water-soluble vitamin, and has effects of promoting collagen synthesis, treating scurvy, preventing gingival atrophy and hemorrhage, preventing arteriosclerosis, preventing free radical injury to human body, treating anemia and preventing cancer.
In a preferred embodiment of the present invention, when the soy isoflavone composition is a mixture of daidzin, daidzein, genistein and genistin, and the mass ratio of the daidzin, the daidzein, the genistein and the genistin is 5:10:5:3, the effect of mutual synergy of the daidzin, the daidzein, the genistein and the genistin is better, so that the soy isoflavone has better effects in cancer prevention and treatment, body immunity improvement and aging delay.
In a preferred embodiment of the present invention, the acid agent is at least one selected from tartaric acid, malic acid, fumaric acid, citric acid and sodium citrate, and preferably, the acid agent is a mixture of malic acid and citric acid, and the mass ratio of the two is 1: (5-6).
When the acid agent is a mixture of malic acid and citric acid, the mass ratio of the two is 1: (5-6), the prepared soybean isoflavone effervescent tablet has good tablet shape, no sticky impact and higher disintegration speed.
In a preferred embodiment of the present invention, the alkaline agent is at least one selected from the group consisting of potassium carbonate, sodium carbonate, calcium carbonate, potassium bicarbonate, sodium bicarbonate and calcium bicarbonate, and preferably, the alkaline agent is sodium bicarbonate.
When the alkaline agent is sodium bicarbonate, the prepared soybean isoflavone effervescent tablet has good tablet shape, no sticky impact and higher disintegration speed.
In a preferred embodiment of the invention, the lubricant is selected from at least one of sodium lauryl sulfate, magnesium stearate, talc, silicon dioxide; preferably, the lubricant is magnesium stearate.
When the lubricant is magnesium stearate, the preparation efficiency is higher, and the dosage form of the prepared tablet is more regular.
According to another aspect of the present invention, the present invention also provides a preparation method of the above soybean isoflavone effervescent tablet, comprising the steps of:
(a) mixing daidzin, daidzein, genistein and genistin to obtain soybean isoflavone composition;
(b) mixing soybean isoflavone composition, vitamin E, vitamin C, acid agent and alkali agent, and mixing with ethanol to obtain soybean isoflavone effervescent granule;
(c) drying the soybean isoflavone effervescent granules, adding a lubricant, uniformly mixing, and tabletting to obtain the soybean isoflavone effervescent tablets.
The preparation method of the soybean isoflavone effervescent tablet provided by the invention has the advantages of simple process, convenience in operation, easiness in large-scale industrial production, reduction in preparation cost and improvement in preparation efficiency.
In a preferred embodiment of the present invention, the method for preparing the effervescent tablet of soybean isoflavone further comprises the step(s) of pulverizing the soybean isoflavone composition, vitamin E, vitamin C, acid agent, alkali agent and lubricant and sieving the pulverized product with a 80-mesh sieve, which is disposed before the steps (a) and (b).
The soybean isoflavone composition, the vitamin E, the vitamin C, the acid agent and the alkali agent are crushed and sieved by a 80-mesh sieve, so that the soybean isoflavone composition, the vitamin E, the vitamin C, the acid agent and the alkali agent are mixed more uniformly, and the drug effect difference among different tablets of the prepared soybean isoflavone effervescent tablet is reduced.
In a preferred embodiment of the invention, in step (c), the temperature of drying is 60-70 ℃, preferably 65 ℃.
By controlling the drying temperature at 60-70 ℃, the drug effect of each raw material is ensured while the ethanol is evaporated, and the phenomena of caking and the like can be avoided, especially when the drying temperature is 65 ℃, the soybean isoflavone effervescent granule has better drying effect and higher drying effect.
In a preferred embodiment of the present invention, in step (b), the prepared effervescent granule of soybean isoflavone has a particle size of 14-18 mesh, preferably 16 mesh.
By controlling the particle size of the soybean isoflavone effervescent granules in the step (b) to be 14-18 meshes, the mixing is more uniform when the subsequent tabletting process is carried out, and the tabletting process is more convenient to carry out.
In a preferred embodiment of the present invention, the preparation method of the soybean isoflavone effervescent tablet comprises the following steps:
(a) mixing daidzin, daidzein, genistein and genistin to obtain soybean isoflavone composition;
(s) respectively crushing the soybean isoflavone composition, the vitamin E, the vitamin C, the acid agent, the alkali agent and the lubricant, and sieving by a sieve of 80 meshes;
(b) dissolving the sieved soybean isoflavone composition, vitamin E, acid agent and alkali agent in ethanol, fully stirring and mixing for 30 minutes to ensure more full and uniform mixing, then granulating to prepare soybean isoflavone effervescent granules, and sieving the soybean isoflavone effervescent granules with a 16-mesh sieve for later use;
(c) drying the sieved soybean isoflavone effervescent granules at 65 ℃, grading, sieving by a 18-mesh sieve, adding a lubricant, uniformly mixing, and tabletting to obtain the soybean isoflavone effervescent tablets.
In order to facilitate understanding of the technical solutions provided by the present invention, the technical solutions provided by the present invention are further described below with reference to the embodiments.
Example 1
The embodiment provides a soybean isoflavone effervescent tablet which is prepared from the following raw materials in parts by mass: 45 parts of soybean isoflavone composition, 3 parts of vitamin E, 55 parts of vitamin C, 835 parts of citric acid, 155 parts of malic acid, 657 parts of sodium bicarbonate and 20 parts of magnesium stearate, wherein the soybean isoflavone composition is a mixture of daidzin, daidzein, genistein and genistin, and the mass ratio of the four is 4:11:6: 2.
Example 2
The embodiment provides a soybean isoflavone effervescent tablet which is prepared from the following raw materials in parts by mass: 55 parts of soybean isoflavone composition, 7 parts of vitamin E, 45 parts of vitamin C, 780 parts of citric acid, 135 parts of malic acid, 657 parts of sodium bicarbonate and 20 parts of magnesium stearate, wherein the soybean isoflavone composition is a mixture of daidzin, daidzein, genistein and genistin, and the mass ratio of the four is 6:9:4: 2.
Example 3
The embodiment provides a soybean isoflavone effervescent tablet which is prepared from the following raw materials in parts by mass: 48 parts of soybean isoflavone composition, 4 parts of vitamin E, 52 parts of vitamin C, 805 parts of citric acid, 155 parts of malic acid, 668 parts of sodium bicarbonate and 18 parts of magnesium stearate, wherein the soybean isoflavone composition is a mixture of daidzin, daidzein, genistein and genistin, and the mass ratio of the four is 5:10:5: 3.
Example 4
The embodiment provides a soybean isoflavone effervescent tablet which is prepared from the following raw materials in parts by mass: the soybean isoflavone composition comprises 52 parts of soybean isoflavone composition, 6 parts of vitamin E, 48 parts of vitamin C, 798 parts of citric acid, 150 parts of malic acid, 680 parts of sodium bicarbonate and 16 parts of magnesium stearate, wherein the soybean isoflavone composition is a mixture of daidzin, daidzein, genistein and genistin, and the mass ratio of the four is 5:10:5: 3.
Example 5
The embodiment provides a soybean isoflavone effervescent tablet which is prepared from the following raw materials in parts by mass: 50 parts of soybean isoflavone composition, 5 parts of vitamin E, 50 parts of vitamin C, 810 parts of citric acid, 150 parts of malic acid, 667.5 parts of sodium bicarbonate and 17.5 parts of magnesium stearate, wherein the soybean isoflavone composition is a mixture of daidzin, daidzein, genistein and genistin, and the mass ratio of the four is 5:10:5: 3.
The preparation method of the soybean isoflavone effervescent tablets provided in examples 1 to 5 is carried out according to the following steps:
(a) mixing daidzin, daidzein, genistein and genistin to obtain soybean isoflavone composition;
(s) respectively crushing the soybean isoflavone composition, the vitamin E, the vitamin C, the acid agent, the alkali agent and the lubricant, and sieving by a sieve of 80 meshes;
(b) dissolving the sieved soybean isoflavone composition, vitamin E, acid agent and alkali agent in ethanol, fully stirring and mixing for 30 minutes to ensure more full and uniform mixing, then granulating to prepare soybean isoflavone effervescent granules, and sieving the soybean isoflavone effervescent granules with a 16-mesh sieve for later use;
(c) drying the sieved soybean isoflavone effervescent granules at 65 ℃, grading, sieving by a 18-mesh sieve, adding a lubricant, uniformly mixing, and tabletting to obtain the soybean isoflavone effervescent tablets.
Comparative example 1
The comparative example provides a soybean isoflavone effervescent tablet which is prepared from the following raw materials in parts by weight: 68 parts of soybean isoflavone composition, 2 parts of vitamin E, 35 parts of vitamin C, 810 parts of citric acid, 150 parts of malic acid, 660 parts of sodium bicarbonate and 25 parts of magnesium stearate, wherein the soybean isoflavone composition is a mixture of daidzin, daidzein, genistein and genistin, and the mass ratio of the four is 5:10:5: 3.
Comparative example 2
The comparative example provides a soybean isoflavone effervescent tablet which is prepared from the following raw materials in parts by weight: 35 parts of soybean isoflavone composition, 10 parts of vitamin E, 75 parts of vitamin C, 800 parts of citric acid, 150 parts of malic acid, 670 parts of sodium bicarbonate and 10 parts of magnesium stearate, wherein the soybean isoflavone composition is a mixture of daidzin, daidzein, genistein and genistin, and the mass ratio of the four is 5:10:5: 3.
Comparative example 3
This comparative example provides a soy isoflavone effervescent tablet which differs from example 5 in that no daidzin is added to the soy isoflavone composition.
Comparative example 4
This comparative example provides a soy isoflavone effervescent tablet, which is different from example 5 in that daidzein was not added to the soy isoflavone composition.
Comparative example 5
This comparative example provides a soy isoflavone effervescent tablet, which is different from example 5 in that genistein was not added to the soy isoflavone composition.
Comparative example 6
This comparative example provides a soy isoflavone effervescent tablet which differs from example 5 in that genistin is not added to the soy isoflavone composition.
Comparative example 7
The comparative example provides a soy isoflavone effervescent tablet, which is different from example 5 in that the soy isoflavone composition is a mixture of daidzin, daidzein, genistein and genistin, and the mass ratio of the four is 1:50:4: 1.
The preparation method of the soybean isoflavone effervescent tablets provided in comparative examples 1 to 7 is the same as that of example 5, and is not repeated herein.
The soybean isoflavone effervescent tablets provided in the above examples 1 to 5 and comparative examples 1 to 7 were tested for their correlation properties, and the test results are shown in the following table:
TABLE 1 table for testing soybean isoflavone effervescent tablet properties
Figure BDA0001354281960000111
Figure BDA0001354281960000121
As can be seen from Table 1, the soybean isoflavone effervescent tablets provided in examples 1 to 5 of the present invention have a good tablet shape, no sticky punch, clear and transparent solution after dissolution, pH of 4.1 to 4.3, rapid disintegration, disintegration time of 81 to 85s, substantially unchanged weight and taste within 3 months, and good stability.
As can be seen from the comparison of examples 1-5 with comparative examples 1-2, when the soy isoflavone composition, vitamin E, vitamin C, acid agent, alkali agent and sodium citrate are in a specific mass portion range, the raw materials are synergistically matched, and the obtained soy isoflavone effervescent tablet has a good tablet shape, is free from sticky flushing and is more reliable for drinkers.
In addition, the isoflavone effervescent tablets provided in examples 1 to 5 and comparative examples 1 to 7 were each subjected to a microbial test in months 1, 2 and 3, respectively, and no microbial presence was found.
To verify that the soybean isoflavone effervescent tablets provided in examples 1 to 5 and comparative examples 1 to 7 were subjected to clinical trials, 1300 women of 40 to 50 years old were randomly drawn and divided into 13 groups of 100 persons each, and each of the groups was a group a to M, wherein the group a to E were administered with the soybean isoflavone effervescent tablets provided in examples 1 to 5, the group F to L were administered with the soybean isoflavone effervescent tablets provided in comparative examples 1 to 7, the group P was a blank control group, the group a to L were administered with 3.5g of soybean isoflavone effervescent tablets per day, and the group M was not administered with the soybean isoflavone effervescent tablets, and the results were counted after 6 months, as shown in the following table:
TABLE 2 clinical examination table for soybean isoflavone effervescent tablets
Figure BDA0001354281960000131
The comparison between the groups A-E and the group M shows that after the group A-E women take the soybean isoflavone for 6 months, the proportion of the climacteric discomfort people and the proportion of the menstrual discomfort people is obviously reduced, which shows that the soybean isoflavone provided by the embodiments 1-5 of the invention can supplement estrogen for the women, effectively relieve the climacteric and menstrual discomfort symptoms and improve the immunity of the organism.
The comparison between the groups A-E and F-G shows that when the soybean isoflavone composition, the vitamin E, the vitamin C, the acid agent, the alkali agent and the sodium citrate are in a specific mass part range, all the raw materials are cooperated with one another, so that the discomfort of the female in menopause and menstrual period can be obviously reduced, and the immunity of the female organism can be improved; comparing the groups A-E with the groups H-L, the soybean isoflavone composition is a mixture of daidzin, daidzein, genistein and genistin, and the mass ratio of the four is (3-4): (18-20): (3-4): (1-2), the soybean isoflavone effervescent tablet prepared by the method has better effect on relieving female menstrual discomfort and climacteric discomfort symptoms.
In addition, by tracking the daily work and rest conditions of the 13 groups of people, the A-E group women have higher sleep quality, fewer sicknesses, stronger immunity, redder complexion and more vigorous energy.
Finally, it should be noted that: the above embodiments are only used to illustrate the technical solution of the present invention, and not to limit the same; while the invention has been described in detail and with reference to the foregoing embodiments, it will be understood by those skilled in the art that: the technical solutions described in the foregoing embodiments may still be modified, or some or all of the technical features may be equivalently replaced; and the modifications or the substitutions do not make the essence of the corresponding technical solutions depart from the scope of the technical solutions of the embodiments of the present invention.

Claims (7)

1. A soybean isoflavone effervescent tablet is characterized in that,
the composite material is prepared from the following raw materials in parts by weight: 48-52 parts of soybean isoflavone composition, 4-6 parts of vitamin E, 48-52 parts of vitamin C, 980 parts of acid agent 940-;
the acid agent is a mixture of malic acid and citric acid, and the mass ratio of the malic acid to the citric acid is 1: (5-6);
the alkaline agent is sodium bicarbonate;
the lubricant is magnesium stearate.
2. The method for preparing soybean isoflavone effervescent tablets of claim 1, which comprises the following steps:
(a) mixing daidzin, daidzein, genistein and genistin uniformly to obtain soybean isoflavone composition;
(b) mixing soybean isoflavone composition, vitamin E, vitamin C, acid agent and alkali agent, and mixing with ethanol to obtain soybean isoflavone effervescent granule;
(c) drying the soybean isoflavone effervescent granules, adding a lubricant, uniformly mixing, and tabletting to obtain the soybean isoflavone effervescent tablets.
3. The method for preparing soybean isoflavone effervescent tablets of claim 2, further comprising a step(s) of pulverizing the soybean isoflavone composition, vitamin E, vitamin C, acid agent, alkali agent and lubricant and sieving the pulverized product with a 80-mesh sieve, wherein the step(s) is performed before the step (a) and the step (b).
4. The method for preparing effervescent tablet of soybean isoflavone as claimed in claim 2, wherein the drying temperature in step (c) is 60-70 ℃.
5. The method for preparing effervescent tablet of soybean isoflavone as claimed in claim 4, wherein the drying temperature in step (c) is 65 ℃.
6. The method for preparing soybean isoflavone effervescent tablets according to claim 2, wherein the soybean isoflavone effervescent granules prepared in the step (b) have a particle size of 14 to 18 meshes.
7. The method for preparing soybean isoflavone effervescent tablets according to claim 6, wherein the prepared soybean isoflavone effervescent granules have a particle size of 16 meshes in the step (b).
CN201710589036.1A 2017-07-19 2017-07-19 Soybean isoflavone effervescent tablet and preparation method thereof Active CN107373272B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201710589036.1A CN107373272B (en) 2017-07-19 2017-07-19 Soybean isoflavone effervescent tablet and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201710589036.1A CN107373272B (en) 2017-07-19 2017-07-19 Soybean isoflavone effervescent tablet and preparation method thereof

Publications (2)

Publication Number Publication Date
CN107373272A CN107373272A (en) 2017-11-24
CN107373272B true CN107373272B (en) 2020-11-06

Family

ID=60339283

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201710589036.1A Active CN107373272B (en) 2017-07-19 2017-07-19 Soybean isoflavone effervescent tablet and preparation method thereof

Country Status (1)

Country Link
CN (1) CN107373272B (en)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1589786A (en) * 2003-09-01 2005-03-09 郑州博凯医药保健品有限公司 Composite effervescent preparation containing soya isoflavone
CN103110687A (en) * 2011-11-17 2013-05-22 胡晓娟 Compound effervescent preparation containing soy isoflavone

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1589786A (en) * 2003-09-01 2005-03-09 郑州博凯医药保健品有限公司 Composite effervescent preparation containing soya isoflavone
CN103110687A (en) * 2011-11-17 2013-05-22 胡晓娟 Compound effervescent preparation containing soy isoflavone

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
博凯维康 康伊丽大豆异黄酮维生素C维生素E泡腾片1.75g/片*20片;博凯维康品牌专卖店;《非彤小可商城》;20150803;第1-8页 *
博凯维康品牌专卖店.博凯维康 康伊丽大豆异黄酮维生素C维生素E泡腾片1.75g/片*20片.《非彤小可商城》.2015, *

Also Published As

Publication number Publication date
CN107373272A (en) 2017-11-24

Similar Documents

Publication Publication Date Title
CN1956734B (en) Multi-vitamin and mineral nutritional supplements
CN107929313B (en) Natural oyster calcium carbonate preparation for preventing and treating calcium deficiency and preparation method thereof
CN105567771A (en) Pigskin small peptide chelate and preparation method and application thereof
CN107232611A (en) A kind of nutrient composition being made up of vitamin D, K and folic acid
CN1327838C (en) Vitamin C oral disintegration tablet and its preparing method
CN104664370A (en) Chewable flax tablet
CN106418545A (en) Functional food with balanced nutrients
CN102742658B (en) Goat milk tablet for maintaining beauty and keeping young and preparation method of goat milk tablet
CN103735556A (en) Multivitamin mineral composite effervescent tablet and preparation method thereof
KR20140017977A (en) Vita hybrid tablet for senior and manufacturing method thereof
CN107373272B (en) Soybean isoflavone effervescent tablet and preparation method thereof
KR20080090808A (en) Composition of healthy food for a skin
CN107373273B (en) Adult type multivitamin mineral effervescent tablet and preparation method thereof
CN106901378A (en) A kind of health food suitable for women
CN112370430A (en) Calcium and vitamin K2 tablet and preparation method thereof
WO2013074046A1 (en) Pharmaceutical formulations comprising isoflavone
JP2004315455A (en) Agent for ameliorating or treating backache, pelvic pain or pain derived from varicosis in pregnancy or leg cramp
CN101366777B (en) Medicament composition for preventing birth defection and improving memory
CN101274006B (en) Pharmaceutical combination of prepotency for preventing birth-defect and improving memory
CN106912929A (en) A kind of health food nutritional agents and preparation method with anti-fatigue effect
CN113952447A (en) Multi-taste calcium chewable tablet and production and manufacturing process thereof
UA148151U (en) METHOD OF PREPARATION OF PREPARATIVE PHARMACEUTICAL FORM FOR ORAL USE FOR DELIVERY OF DAILY DOSE OF VITAMIN C
CN112137113A (en) Formula of vitamin E tablets and preparation method thereof
CN109418809A (en) A kind of prune chewable tablets and preparation method thereof
CN101274002B (en) Pharmaceutical combination of prepotency for preventing birth-defect and improving memory

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
CB02 Change of applicant information

Address after: No.1302, No.7, Dongqing street, high tech Industrial Development Zone, Zhengzhou City, Henan Province 450001

Applicant after: Bokai Pharmaceutical Co., Ltd

Address before: 450000 No. 5 Acacia Street, hi tech Development Zone, Henan, Zhengzhou

Applicant before: Zhengzhou Bokai Medicine &. Health-Care Products Co., Ltd.

CB02 Change of applicant information
GR01 Patent grant
GR01 Patent grant