Plant-extracted weight-loss and anti-aging vitamin tablet and preparation method thereof

Abstract

The present invention belongs to the field of vitamin tablet preparation, and particularly relates to a plant-extracted weight-loss and anti-aging vitamin tablet and its preparation method. The crushed fat synthesis-inhibiting powder is mixed with a monascus extract obtained by ultrasonic crushing and filtration, and the weight-loss components are subjected to a cross-linking reaction, and then loaded onto a thermosensitive polymer material with a high specific surface area. The resulting weight-loss complex can be efficiently released into the body. Boric acid reacts with galactomannan molecules to form borate ester bonds, and the resulting viscous substance that promotes cell absorption fully absorbs the anti-aging solution. The resulting anti-aging agent can have a significant anti-aging effect. The vitamin stabilizer can maintain the stability of the effective components for a long time. The weight-loss and anti-aging complex is mixed and tableted. The resulting plant-extracted weight-loss and anti-aging vitamin tablet has significant and long-lasting weight-loss and anti-aging effects, is highly stable, and is conducive to long-term storage.

Description

Technical Field

[0001] The invention belongs to the field of vitamin tablet preparation, and specifically relates to a plant-extracted weight-loss and anti-aging vitamin tablet and a preparation method thereof. Background Art

[0002] Plant extract vitamin tablets are nutritional supplements primarily based on natural plant extracts and vitamins. Plant extracts are biologically active compounds extracted from various natural plants, including vitamins, polyphenols, and carotenoids. These extracts are combined with vitamins and processed through scientific formulas and processes to create tablets for easy administration and absorption. Plant extract vitamin tablets can also serve as a dietary supplement, helping people obtain adequate nutrition and promoting overall health, meeting consumer demand for natural, green, and environmentally friendly products.

[0003] Plant-derived vitamin tablets can supplement the body with a variety of vitamins and phytonutrients, helping to alleviate nutritional deficiencies caused by an unbalanced diet. Ingredients like vitamin C and vitamin E can enhance the immune system, improve resistance, and prevent colds and other illnesses. Polyphenols and carotenoids in plant extracts have potent antioxidant properties, neutralizing free radicals, reducing cell damage, and delaying aging. Some plant extracts, such as lycopene and grape seed extract, have skin-whitening, antioxidant, and anti-aging effects. They also promote energy metabolism and help maintain normal physiological functions.

[0004] Currently, the preparation technology of existing weight loss and anti-aging preparations has the following problems: First, the existing weight loss and anti-aging preparations have low production efficiency, poor bioavailability, and insignificant weight loss and anti-aging effects; second, the existing weight loss and anti-aging preparations are effective when used, but will rebound after discontinuation, and the effect is not long-lasting; third, the existing weight loss and anti-aging preparations have poor stability and are not conducive to long-term storage. Summary of the Invention

[0005] In view of the above situation, in order to overcome the defects of the prior art, the present invention provides a plant-extracted weight loss and anti-aging vitamin tablet and a preparation method thereof. In order to solve the problems that the existing weight loss and anti-aging preparations have no significant weight loss and anti-aging effects, the weight loss and anti-aging effects are not long-lasting, the product stability is poor, and it is not conducive to long-term storage, the present invention uses a weight loss complex, an anti-aging agent, and a vitamin-containing stabilizer to mix. The prepared plant-extracted weight loss and anti-aging vitamin tablet has significant and long-lasting weight loss and anti-aging effects, is stable, and is conducive to long-term storage.

[0006] In order to achieve the above-mentioned object, the technical solution adopted by the present invention is as follows: the present invention provides a plant-extracted weight loss and anti-aging vitamin tablet and a preparation method thereof. The raw materials for preparing the plant-extracted weight loss and anti-aging vitamin tablet specifically include the following components in parts by weight:

[0007] 16-22 parts of slimming complex, 15-17 parts of anti-aging agent, 2-3 parts of vitamin C, 2-3 parts of vitamin E, 2-3 parts of vitamin B6, 1.5-1.8 parts of ergothioneine, and 1.3-1.7 parts of sodium benzoate.

[0008] Preferably, the raw materials for preparing the weight loss compound include the following components in parts by weight: 4-6 parts of Camellia ternata, 3-5 parts of Rhizoma Alismatis, 3-4 parts of Astragalus sinensis, 6-7 parts of Garcinia, 1.2-1.4 parts of Monascus, 3.5-4.8 parts of N-vinylcaprolactam, 2.6-3.4 parts of glucose, and 4.2-5.7 parts of water-soluble silk fibroin;

[0009] Preferably, the raw materials for preparing the anti-aging agent include the following components in parts by weight: 2.2-2.6 parts of cyanidin-3-galactoside, 2.5-3 parts of meadowsweet extract, 1.8-2.5 parts of limonene, 1.4-1.7 parts of rutin, 1.8-2.3 parts of boric acid, and 2.8-3.6 parts of galactomannan.

[0010] Preferably, the method for preparing the weight loss compound comprises the following steps:

[0011] S1. Place Camellia ternata, Rhizoma Alismatis, Astragalus sinensis, and Garcinia gamboge in a 10-13 kW grinder and grind at a temperature of 25-28° C. for 35-45 minutes to obtain a fat synthesis inhibiting powder.

[0012] S2. Inoculate Monascus into a 5% sterile glucose solution, place the solution in a constant temperature shaking incubator with a power of 2.2-2.6 kW, set the constant temperature shaking incubation temperature to 33°C, the constant temperature shaking incubation time to 24-30 h, and the constant temperature shaking incubation speed to 270 r / min. After constant temperature shaking incubation, place the solution in an ultrasonic cell disruptor with a power of 1.2-1.5 kW, set the ultrasonic disruption frequency to 20 kHz, set the ultrasonic disruption temperature to 0°C, and set the ultrasonic disruption time to 10-13 min. After disruption, filter the solution through a 0.22 mm sterile filter membrane to obtain a Monascus extract.

[0013] S3. Place N-vinylcaprolactam, glucose, water-soluble silk fibroin, and ultrapure water into a 2.4 kW reactor at a reaction temperature of 60°C, a reaction rate of 300 r / min, and a reaction time of 24 h, and mix and perform a cross-linking reaction to obtain a thermosensitive polymer material.

[0014] S4. Place the fat synthesis inhibiting powder prepared in S1 and the Monascus extract prepared in S2 into a stirring tank with a power of 1.2-1.5 kW, stir at a temperature of 25-28° C., stir for 10-15 minutes, and stir at a speed of 110-130 r / min to obtain a weight loss component;

[0015] S5. Add the thermosensitive polymer material prepared by S3 to the weight loss component prepared by S4, stir at a temperature of 25-28°C, stir for 20-25 min, and stir at a speed of 300 r / min, perform stirring adsorption, place in a freeze dryer with a power of 2.3-2.8 kW, freeze-dry at a temperature of -40°C, freeze-dry for 4 h, and perform freeze-drying to obtain a weight loss complex.

[0016] Furthermore, in S2, the Monascus was purchased from the China General Microbiological Culture Collection Center with a collection number of CGMCC3.7183, and the solid-liquid ratio of the Monascus to 5% sterile glucose solution was 1:100 g / mL.

[0017] Furthermore, in S3, the mass fraction of the glucose in the ultrapure water is 12%.

[0018] Preferably, the preparation method of the anti-aging agent specifically comprises the following steps:

[0019] L1. Place cyanidin-3-galactoside, meadowsweet extract, limonene, rutin, and 70% ethanol solution in a 1.2-1.5 kW stirrer at 60°C for 15-20 min at a stirring speed of 130-160 r / min to mix and dissolve to obtain an anti-aging solution;

[0020] L2. Boric acid, galactomannan, and ultrapure water were placed in a 2.4 kW reactor at a reaction temperature of 70°C, a reaction rate of 300 r / min, and a reaction time of 4 h, and mixed to undergo a cross-linking reaction to obtain a viscous substance that promotes cell absorption;

[0021] L3. Add the cell absorption promoting viscous substance prepared in L2 into the anti-aging solution prepared in L1, stir at a temperature of 25-30°C, a stirring time of 20-30 min, a stirring speed of 500 r / min, and stir to mix to obtain an anti-aging agent.

[0022] Furthermore, in L1, the mass fraction of cyanidin-3-galactoside in the 70% ethanol solution is 2%.

[0023] Furthermore, in L2, the mass fraction of the boric acid in ultrapure water is 5%.

[0024] The present invention also provides a method for preparing a plant-extracted weight-loss and anti-aging vitamin tablet, which specifically comprises the following steps:

[0025] Step 1, vitamin C, vitamin E, vitamin B6, thioneine, sodium benzoate are put into a stirring tank with a power of 1.8 kW, the stirring temperature is 28 ° C, the stirring time is 15-20 min, and the stirring speed is 300 r / min, and mixed to obtain a vitamin-containing stabilizer;

[0026] Step 2: Place the weight loss compound and the anti-aging agent into a stirring tank with a power of 1.8 kW, stir at a temperature of 28° C., stir for 30 minutes, and stir at a speed of 600 r / min, and mix to obtain a weight loss and anti-aging compound;

[0027] Step 3: Place the weight loss and anti-aging complex prepared in step 2 into the vitamin-containing stabilizer prepared in step 1, with a stirring temperature of 26°C, a stirring time of 25-35 min, and a stirring speed of 600 r / min. After mixing, place it in a tablet press with a power of 1.8-2.2kW, a tableting temperature of 20-25°C, a tableting time of 18-22 min, and a tablet diameter of 8-10 mm. After tableting, place it at a temperature of 25-28°C for 2-2.5 h, and air-dry to obtain plant-extracted weight loss and anti-aging vitamin tablets.

[0028] The beneficial effects achieved by the present invention are as follows:

[0029] The present invention grinds Camellia ternata, Rhizoma Alismatis, Astragalus sinensis and Garcinia to obtain a fat synthesis inhibiting powder which can inhibit the proliferation and differentiation of fat cells, reduce the formation of triglycerides, and increase the level of adiponectin in serum, thereby inhibiting appetite. The hydroxycitric acid contained in the powder can also inhibit an enzyme called citrate lyase, which plays a key role in the process of converting carbohydrates into fat. The powder contains dietary fiber and plant protein, etc., which can promote intestinal peristalsis, increase satiety and help regulate the body's metabolic function. Monascus is connected to a 5% sterile glucose solution for constant temperature shaking culture, and then ultrasonically crushed and filtered to obtain a Monascus extract containing monacolin K, which can inhibit HMG-CoA reductase in the liver and reduce It can promote the synthesis of cholesterol and increase the clearance of low-density lipoprotein cholesterol, thereby reducing the cholesterol level in the blood, helping to reduce the deposition of fat in the blood vessel walls, improving blood lipid metabolism, and thus reducing the accumulation of fat in the body. N-vinyl caprolactam, glucose, water-soluble silk protein and ultrapure water are mixed, and N-vinyl caprolactam undergoes free radical polymerization to obtain poly N-vinyl caprolactam with thermosensitive properties. The hydroxyl groups of glucose undergo esterification reaction with the amide groups on the poly N-vinyl caprolactam chain, and undergo cross-linking reaction with the amino or carboxyl groups in the silk protein to form stable chemical bonds. The formed thermosensitive polymer material has a network structure and a high specific surface area. It is mixed with the weight loss components, and the obtained weight loss complex enters the body. The body can release the weight loss components efficiently and protect them from degradation such as enzymatic hydrolysis and oxidation in the body, thereby prolonging the half-life of the effective ingredients; cyanidin-3-galactoside, meadowsweet extract, limonene, rutin, and 70% ethanol solution are mixed and dissolved to obtain an anti-aging solution that can scavenge free radicals, reduce the damage of oxidative stress to cells, and delay cell aging. Meadowsweet extract can inhibit the expression of collagenase MMP-1 and elastase MMP-12 in skin fibroblasts, reduce the decomposition of collagen and elastin, and also reduce inflammatory response, maintaining skin elasticity and firmness. Boric acid is mixed with galactomannan and ultrapure water to react. Boric acid can partially dissociate in water to form borate ions, which react with galactomannan molecular chains. The cis-vicinal hydroxyl groups on the surface undergo cross-linking reaction to form borate bonds, forming a gel with a three-dimensional network structure and temperature-sensitive properties, which promotes cell absorption of the viscous substance and full adsorption of the anti-aging solution. The obtained anti-aging agent can significantly have anti-aging effects and can adhere to the inner wall of the gastrointestinal tract and exert its effect for a long time; Vitamin C and Vitamin E both have strong antioxidant properties and can effectively scavenge free radicals and prevent other ingredients from being oxidized. They work together with vitamin B6, ergothioneine, and sodium benzoate to obtain a vitamin-containing stabilizer that can maintain the stability of the effective components for a long time. The mixed weight loss and anti-aging complex is tableted to obtain plant-extracted weight loss and anti-aging vitamin tablets with significant weight loss and anti-aging effects, long-lasting weight loss and anti-aging effects, high product stability, and conducive to long-term storage. BRIEF DESCRIPTION OF THE DRAWINGS

[0030] In order to more clearly illustrate the present invention or the technical solutions in the prior art, the following will be described in a clear and easy-to-understand manner with reference to the accompanying drawings. Obviously, the drawings described below are only for the present invention. For ordinary technicians in this field, other drawings can be obtained based on these drawings without paying any creative work.

[0031] Figure 1 This is a graph showing the results of promoting collagen synthesis as described in Experimental Example 1 of the present invention;

[0032] Figure 2 This is a graph showing the skin elasticity growth rate results described in Experimental Example 1 of the present invention;

[0033] Figure 3 This is the DPPH clearance result diagram described in Experimental Example 1 of the present invention;

[0034] Figure 4 This is a graph showing the skin moisture content growth rate results described in Experimental Example 1 of the present invention. DETAILED DESCRIPTION

[0035] The technical solutions in the embodiments of the present invention will be clearly and completely described below in conjunction with the drawings in the present invention. Obviously, the described embodiments are only part of the embodiments of the present invention, rather than all the embodiments; based on the embodiments of the present invention, all other embodiments obtained by ordinary technicians in this field without making creative work are within the scope of protection of the present invention.

[0036] Unless otherwise defined, all technical and scientific terms used herein have the same meanings as those familiar to those skilled in the art. Furthermore, any methods and materials similar or equivalent to those described herein can be applied to the present invention. The preferred embodiments and materials described herein are for illustrative purposes only and are not intended to limit the scope of this application.

[0037] The experimental methods in the following examples, unless otherwise specified, are conventional methods; the test materials and test strains used in the following examples, unless otherwise specified, are purchased from commercial channels.

[0038] Example 1: This example provides a plant-extracted weight loss and anti-aging vitamin tablet and a preparation method thereof. The plant-extracted weight loss and anti-aging vitamin tablet comprises the following components in parts by weight:

[0039] 16 parts of slimming complex, 15 parts of anti-aging agent, 2 parts of vitamin C, 2 parts of vitamin E, 2 parts of vitamin B6, 1.5 parts of ergothioneine, and 1.3 parts of sodium benzoate.

[0040] The raw materials for preparing the weight loss compound include the following components in parts by weight: 4 parts of Camellia ternata, 3 parts of Rhizoma Alismatis, 3 parts of Astragalus sinensis, 6 parts of Garcinia cambogia, 1.2 parts of Monascus, 3.5 parts of N-vinylcaprolactam, 2.6 parts of glucose, and 4.2 parts of water-soluble silk fibroin;

[0041] The raw materials for preparing the anti-aging agent include the following components in parts by weight: 2.2 parts of cyanidin-3-galactoside, 2.5 parts of meadowsweet extract, 1.8 parts of limonene, 1.4 parts of rutin, 1.8 parts of boric acid, and 2.8 parts of galactomannan.

[0042] The preparation method of the weight loss compound specifically comprises the following steps:

[0043] S1. Place Camellia ternata, Rhizoma Alismatis, Astragalus sinensis, and Garcinia gamboge in a 10 kW grinder and grind at a temperature of 25° C. for 35 minutes to obtain a fat synthesis inhibiting powder.

[0044] S2. Inoculate Monascus into a 5% sterile glucose solution and place it in a constant temperature shaking incubator with a power of 2.2 kW. The constant temperature shaking incubation temperature is 33°C, the constant temperature shaking incubation time is 24 h, and the constant temperature shaking incubation speed is 270 r / min. After constant temperature shaking incubation, place it in an ultrasonic cell disruptor with a power of 1.2 kW, the ultrasonic disruption frequency is 20 kHz, the ultrasonic disruption temperature is 0°C, and the ultrasonic disruption time is 10 min. After disruption, filter using a 0.22 mm sterile filter membrane to obtain a Monascus extract;

[0045] S3. Place N-vinylcaprolactam, glucose, water-soluble silk fibroin, and ultrapure water into a 2.4 kW reactor at a reaction temperature of 60°C, a reaction rate of 300 r / min, and a reaction time of 24 h, and mix and perform a cross-linking reaction to obtain a thermosensitive polymer material.

[0046] S4. Place the fat synthesis inhibiting powder prepared in S1 and the Monascus extract prepared in S2 into a stirring tank with a power of 1.2 kW, stir at a temperature of 25° C., stir for 10 minutes, and stir at a speed of 110 r / min, and mix to obtain a weight loss component;

[0047] S5. Add the thermosensitive polymer material prepared by S3 to the weight loss component prepared by S4, stir at 25°C, stir for 20 min, and stir at 300 r / min for adsorption, place in a freeze dryer with a power of 2.3 kW, freeze-dry at -40°C, freeze-dry for 4 h, and freeze-dry to obtain a weight loss complex.

[0048] In S2, the Monascus was purchased from the China General Microbiological Culture Collection Center with a collection number of CGMCC3.7183. The material-liquid ratio of the Monascus to 5% sterile glucose solution was 1:100 g / mL.

[0049] In S3, the mass fraction of the glucose in the ultrapure water is 12%.

[0050] The preparation method of the anti-aging agent specifically comprises the following steps:

[0051] L1. Place cyanidin-3-galactoside, meadowsweet extract, limonene, rutin, and 70% ethanol solution in a 1.2 kW stirrer at 60°C for 15 min and a stirring speed of 130 r / min to mix and dissolve to obtain an anti-aging solution;

[0052] L2. Boric acid, galactomannan, and ultrapure water were placed in a 2.4 kW reactor at a reaction temperature of 70°C, a reaction rate of 300 r / min, and a reaction time of 4 h, and mixed to undergo a cross-linking reaction to obtain a viscous substance that promotes cell absorption;

[0053] L3. Add the cell absorption promoting viscous substance prepared in L2 into the anti-aging solution prepared in L1, stir at a temperature of 25°C, a stirring time of 20 min, a stirring speed of 500 r / min, and stir to mix to obtain an anti-aging agent.

[0054] In L1, the mass fraction of cyanidin-3-galactoside in the 70% ethanol solution is 2%.

[0055] In L2, the mass fraction of the boric acid in ultrapure water is 5%.

[0056] This embodiment also provides a method for preparing plant-extracted weight-loss and anti-aging vitamin tablets, which specifically comprises the following steps:

[0057] Step 1, vitamin C, vitamin E, vitamin B6, thioneine, sodium benzoate are put into the stirring tank of power being 1.8 kW, and stirring temperature is 28 DEG C, stirring time is 15 min, and stirring speed is 300 r / min, is mixed, and obtains containing vitamin stabilizer;

[0058] Step 2: Place the weight loss compound and the anti-aging agent into a stirring tank with a power of 1.8 kW, stir at a temperature of 28° C., stir for 30 minutes, and stir at a speed of 600 r / min, and mix to obtain a weight loss and anti-aging compound;

[0059] Step 3: Place the weight loss and anti-aging complex prepared in step 2 into the vitamin-containing stabilizer prepared in step 1, with a stirring temperature of 26°C, a stirring time of 25 min, and a stirring speed of 600 r / min. After mixing, place it in a tablet press with a power of 1.8 kW, a tableting temperature of 20°C, a tableting time of 18 min, and a tablet diameter of 8 mm. After tableting, place it at a temperature of 25°C for 2 h, and air-dry to obtain plant-extracted weight loss and anti-aging vitamin tablets.

[0060] Example 2: This example provides a plant-extracted weight loss and anti-aging vitamin tablet and a preparation method thereof. The plant-extracted weight loss and anti-aging vitamin tablet comprises the following components in parts by weight:

[0061] 20 parts of slimming complex, 16 parts of anti-aging agent, 2.5 parts of vitamin C, 2.5 parts of vitamin E, 2.5 parts of vitamin B6, 1.6 parts of ergothioneine, and 1.5 parts of sodium benzoate.

[0062] The raw materials for preparing the weight loss compound include the following components in parts by weight: 5 parts of Camellia ternata, 4 parts of Rhizoma Alismatis, 3.5 parts of Astragalus sinensis, 6.5 parts of Garcinia cambogia, 1.3 parts of Monascus, 4.2 parts of N-vinylcaprolactam, 3.1 parts of glucose, and 5 parts of water-soluble silk fibroin;

[0063] The raw materials for preparing the anti-aging agent include the following components in parts by weight: 2.5 parts of cyanidin-3-galactoside, 2.8 parts of meadowsweet extract, 2.2 parts of limonene, 1.6 parts of rutin, 2.1 parts of boric acid, and 3.2 parts of galactomannan.

[0064] The preparation method of the weight loss compound specifically comprises the following steps:

[0065] S1. Place Camellia ternata, Rhizoma Alismatis, Astragalus sinensis, and Garcinia gamboge in an 11 kW grinder and grind at a temperature of 26° C. for 40 minutes to obtain a fat synthesis inhibiting powder;

[0066] S2. Inoculate Monascus into a 5% sterile glucose solution and place it in a constant temperature shaking incubator with a power of 2.3 kW. The constant temperature shaking incubation temperature is 33°C, the constant temperature shaking incubation time is 28 h, and the constant temperature shaking incubation speed is 270 r / min. After constant temperature shaking incubation, place it in an ultrasonic cell disruptor with a power of 1.3 kW, the ultrasonic disruption frequency is 20 kHz, the ultrasonic disruption temperature is 0°C, and the ultrasonic disruption time is 12 min. After disruption, filter using a 0.22 mm sterile filter membrane to obtain a Monascus extract;

[0067] S3. Place N-vinylcaprolactam, glucose, water-soluble silk fibroin, and ultrapure water into a 2.4 kW reactor at a reaction temperature of 60°C, a reaction rate of 300 r / min, and a reaction time of 24 h, and mix and perform a cross-linking reaction to obtain a thermosensitive polymer material.

[0068] S4. Place the fat synthesis inhibiting powder prepared in S1 and the Monascus extract prepared in S2 into a stirring tank with a power of 1.3 kW, stir at a temperature of 26° C., stir for 13 minutes, and stir at a speed of 120 r / min, and mix to obtain a weight loss component;

[0069] S5. Add the thermosensitive polymer material prepared by S3 to the weight loss component prepared by S4, stir at 26°C, stir for 23 min, and stir at 300 r / min for adsorption, place in a freeze dryer with a power of 2.5 kW, freeze-dry at -40°C, freeze-dry for 4 h, and freeze-dry to obtain a weight loss complex.

[0070] In S2, the Monascus was purchased from the China General Microbiological Culture Collection Center with a collection number of CGMCC3.7183. The material-liquid ratio of the Monascus to 5% sterile glucose solution was 1:100 g / mL.

[0071] In S3, the mass fraction of the glucose in the ultrapure water is 12%.

[0072] The preparation method of the anti-aging agent specifically comprises the following steps:

[0073] L1. Place cyanidin-3-galactoside, meadowsweet extract, limonene, rutin, and 70% ethanol solution in a 1.3 kW stirrer at 60°C for 18 min and a stirring speed of 150 r / min to mix and dissolve to obtain an anti-aging solution;

[0074] L2. Boric acid, galactomannan, and ultrapure water were placed in a 2.4 kW reactor at a reaction temperature of 70°C, a reaction rate of 300 r / min, and a reaction time of 4 h, and mixed to undergo a cross-linking reaction to obtain a viscous substance that promotes cell absorption;

[0075] L3. Add the cell absorption promoting viscous substance prepared in L2 into the anti-aging solution prepared in L1, stir at a temperature of 28°C, a stirring time of 25 min, a stirring speed of 500 r / min, and stir to mix to obtain an anti-aging agent.

[0076] In L1, the mass fraction of cyanidin-3-galactoside in the 70% ethanol solution is 2%.

[0077] In L2, the mass fraction of the boric acid in ultrapure water is 5%.

[0078] This embodiment also provides a method for preparing plant-extracted weight-loss and anti-aging vitamin tablets, which specifically comprises the following steps:

[0079] Step 1, vitamin C, vitamin E, vitamin B6, thioneine, sodium benzoate are put into the stirring tank of power being 1.8 kW, and stirring temperature is 28 DEG C, stirring time is 16 min, and stirring speed is 300 r / min, is mixed, and obtains the vitamin-containing stabilizer;

[0080] Step 2: Place the weight loss compound and the anti-aging agent into a stirring tank with a power of 1.8 kW, stir at a temperature of 28° C., stir for 30 minutes, and stir at a speed of 600 r / min, and mix to obtain a weight loss and anti-aging compound;

[0081] Step 3: Place the weight loss and anti-aging complex prepared in step 2 into the vitamin-containing stabilizer prepared in step 1, with a stirring temperature of 26°C, a stirring time of 30 min, and a stirring speed of 600 r / min. After mixing, place it in a tablet press with a power of 2.1 kW, a tableting temperature of 23°C, a tableting time of 20 min, and a tablet diameter of 9 mm. After tableting, place it at a temperature of 26°C for 2.3 h, and air-dry to obtain plant-extracted weight loss and anti-aging vitamin tablets.

[0082] Example 3: This example provides a plant-extracted weight loss and anti-aging vitamin tablet and a preparation method thereof. The plant-extracted weight loss and anti-aging vitamin tablet comprises the following components in parts by weight:

[0083] 22 parts of slimming complex, 17 parts of anti-aging agent, 3 parts of vitamin C, 3 parts of vitamin E, 3 parts of vitamin B6, 1.8 parts of ergothioneine, and 1.7 parts of sodium benzoate.

[0084] The raw materials for preparing the weight loss compound include the following components in parts by weight: 6 parts of Camellia ternata, 5 parts of Rhizoma Alismatis, 4 parts of Astragalus sinensis, 7 parts of Garcinia cambogia, 1.4 parts of Monascus, 4.8 parts of N-vinylcaprolactam, 3.4 parts of glucose, and 5.7 parts of water-soluble silk fibroin;

[0085] The raw materials for preparing the anti-aging agent include the following components in parts by weight: 2.6 parts of cyanidin-3-galactoside, 3 parts of meadowsweet extract, 2.5 parts of limonene, 1.7 parts of rutin, 2.3 parts of boric acid, and 3.6 parts of galactomannan.

[0086] The preparation method of the weight loss compound specifically comprises the following steps:

[0087] S1. Place Camellia ternata, Rhizoma Alismatis, Astragalus sinensis, and Garcinia gamboge in a 13 kW grinder and grind at a temperature of 28° C. for 45 minutes to obtain a fat synthesis inhibiting powder.

[0088] S2. Inoculate Monascus into a 5% sterile glucose solution and place it in a constant temperature shaking incubator with a power of 2.6 kW, the constant temperature shaking incubation temperature is 33°C, the constant temperature shaking incubation time is 30 h, and the constant temperature shaking incubation speed is 270 r / min. After constant temperature shaking incubation, place it in an ultrasonic cell disruptor with a power of 1.5 kW, the ultrasonic disruption frequency is 20 kHz, the ultrasonic disruption temperature is 0°C, and the ultrasonic disruption time is 13 min. After disruption, filter using a 0.22 mm sterile filter membrane to obtain a Monascus extract;

[0089] S3. Place N-vinylcaprolactam, glucose, water-soluble silk fibroin, and ultrapure water into a 2.4 kW reactor at a reaction temperature of 60°C, a reaction rate of 300 r / min, and a reaction time of 24 h, and mix and perform a cross-linking reaction to obtain a thermosensitive polymer material.

[0090] S4. Place the fat synthesis inhibiting powder prepared in S1 and the Monascus extract prepared in S2 into a stirring tank with a power of 1.5 kW, stir at a temperature of 28° C., stir for 15 minutes, and stir at a speed of 130 r / min, and mix to obtain a weight loss component;

[0091] S5. Add the thermosensitive polymer material prepared by S3 to the weight loss component prepared by S4, stir at 28°C, stir for 25 min, and stir at 300 r / min for adsorption, place in a freeze dryer with a power of 2.8 kW, freeze-dry at -40°C, freeze-dry for 4 h, and freeze-dry to obtain a weight loss complex.

[0092] In S2, the Monascus was purchased from the China General Microbiological Culture Collection Center with a collection number of CGMCC3.7183. The material-liquid ratio of the Monascus to 5% sterile glucose solution was 1:100 g / mL.

[0093] In S3, the mass fraction of the glucose in the ultrapure water is 12%.

[0094] The preparation method of the anti-aging agent specifically comprises the following steps:

[0095] L1. Place cyanidin-3-galactoside, meadowsweet extract, limonene, rutin, and 70% ethanol solution in a 1.5 kW stirrer at 60°C for 20 min at a stirring speed of 160 r / min to mix and dissolve to obtain an anti-aging solution;

[0096] L2. Boric acid, galactomannan, and ultrapure water were placed in a 2.4 kW reactor at a reaction temperature of 70°C, a reaction rate of 300 r / min, and a reaction time of 4 h, and mixed to undergo a cross-linking reaction to obtain a viscous substance that promotes cell absorption;

[0097] L3. Add the cell absorption promoting viscous substance prepared in L2 into the anti-aging solution prepared in L1, stir at a temperature of 30°C, a stirring time of 30 min, a stirring speed of 500 r / min, and stir to mix to obtain an anti-aging agent.

[0098] In L1, the mass fraction of cyanidin-3-galactoside in the 70% ethanol solution is 2%.

[0099] In L2, the mass fraction of the boric acid in ultrapure water is 5%.

[0100] This embodiment also provides a method for preparing plant-extracted weight-loss and anti-aging vitamin tablets, which specifically comprises the following steps:

[0101] Step 1, vitamin C, vitamin E, vitamin B6, thioneine, sodium benzoate are put into the stirring tank of power being 1.8 kW, stirring temperature is 28 DEG C, stirring time is 20 min, and stirring speed is 300 r / min, is mixed, and obtains the vitamin-containing stabilizer;

[0102] Step 2: Place the weight loss compound and the anti-aging agent into a stirring tank with a power of 1.8 kW, stir at a temperature of 28° C., stir for 30 minutes, and stir at a speed of 600 r / min, and mix to obtain a weight loss and anti-aging compound;

[0103] Step 3: Place the weight loss and anti-aging complex prepared in step 2 into the vitamin-containing stabilizer prepared in step 1, with a stirring temperature of 26°C, a stirring time of 35 min, and a stirring speed of 600 r / min. After mixing, place it in a tablet press with a power of 2.2 kW, a tableting temperature of 25°C, a tableting time of 22 min, and a tablet diameter of 10 mm. After tableting, place it at a temperature of 28°C for 2.5 h, and air-dry to obtain plant-extracted weight loss and anti-aging vitamin tablets.

[0104] Comparative Example 1: This comparative example provides a weight loss and anti-aging tablet and a preparation method thereof. The only difference from Example 1 is that the added weight loss compound does not contain a thermosensitive polymer material, and the remaining components, component contents, and method steps are the same as those in Example 1.

[0105] Comparative Example 2: This comparative example provides a weight loss and anti-aging tablet and a preparation method thereof. The only difference from Example 1 is that the added anti-aging agent does not contain a viscous substance that promotes cell absorption. The remaining components, component contents, and method steps are the same as those in Example 1.

[0106] Experimental Example 1: Weight loss and anti-aging effect measurement test.

[0107] The test steps for determining the weight loss and anti-aging effects of the plant extract weight loss and anti-aging vitamin tablets prepared in Examples 1-3 of the present invention are as follows:

[0108] (1) Sixty 8-week-old SPF mice weighing 25 g were selected (purchased from Chengdu Dashuo Animal Co., Ltd.) and randomly divided into 6 groups of 10 mice each. The mice were housed in separate cages, kept clean and dry, at a temperature of 24°C and a humidity of 50%, with free access to food and water.

[0109] (2) After feeding for 1 week, the mice in Example 1-3 groups were fed with a high-fat diet and gavage, and were fed 0.25 g of the plant extract weight loss and anti-aging vitamin tablets prepared in Example 1-3 groups respectively every day. The mice in Comparative Example 1-2 groups were fed with a high-fat diet and gavage, and were fed 0.25 g of the weight loss and anti-aging tablets prepared in Comparative Example 1-2 groups respectively every day. The mice in the control group were fed with a high-fat diet and gavage, and were fed 0.25 g of the commercially available weight loss and anti-aging preparation (purchased from Zhangshu Jiaqi Health Products Co., Ltd.) in the control group every day. After continuous feeding for 9 weeks, the mice were anesthetized and blood was collected from the eyeballs. The mice were killed by cervical dislocation, and the liver, colon, and white fat (epididymal fat, perirenal fat, and mesenteric fat) tissues were dissected and the contents of the cecum were collected aseptically. Parts of the liver, colon, and epididymal adipose tissue were fixed with fixative, and the remaining tissues were snap-frozen in liquid nitrogen and stored at −80°C. Mice were weighed once on day 0 and at the end of the experiment, and the weight gain rate was calculated according to the formula. During dissection, the liver and white fat of the mice were removed, washed, and quickly weighed to calculate the organ index: weight gain rate = (weight at the end of the experiment - weight on day 0) / weight at the end of the experiment - weight on day 0 × 100%. Organ index = organ wet mass / mouse body mass × 100%. The results are recorded in Table 1.

[0110] (3) The content of collagen type I, III and IV in fibroblasts was determined by enzyme-linked immunosorbent assay. The fibroblasts were digested with trypsin and transferred to a 96-well culture plate. The edge wells were filled with sterile phosphate buffer solution and moved into an incubator for continued culture. When the cells were completely attached to the wall and grew, a micropipette was used to sequentially add the plant extract weight loss and anti-aging vitamin tablets prepared in Examples 1-3, the weight loss and anti-aging tablets prepared in Comparative Example 1-2, and the commercially available weight loss and anti-aging preparation (purchased from Zhangshu Jiaqi Health Products Co., Ltd.) in the control group at 20 mg / well. After 48 hours of adding the samples, the content of type I, type III and type IV collagen was determined according to the instructions of the kit. Three replicates were added to each group, and the results were recorded.

[0111] (4) 30 healthy volunteers aged between 30 and 40 were selected and divided into 6 groups with 5 volunteers in each group. The skin elasticity test values ​​of each volunteer before taking the drug were measured and recorded using a skin elasticity meter, Cutometer MPA580. The volunteers in each group took the plant extract weight loss and anti-aging vitamin tablets prepared in Examples 1-3 and the weight loss and anti-aging tablets prepared in Comparative Examples 1-2 every day. The control group took a commercial weight loss and anti-aging preparation twice a day, taking 2 g. During the experiment, the subjects were not allowed to apply any other cosmetics on the experimental area.

[0112] (5) After the volunteers of Example 1-3, Comparative Example 1-2, and Control Group in step (2) took the medicine for 2 consecutive weeks, the skin conditions of the volunteers in the first week, the second week, and the fourth week after stopping the medicine were tested using a skin elasticity meter, Cutometer MPA580. The test site was the zygomatic region. The probe was used to repeat the measurement 3 times in the same tested area. The average value was taken and calculated according to the formula: Skin elasticity growth rate (%) = [(elasticity test value during the T period after taking the medicine - skin elasticity test value before taking the medicine) / skin elasticity test value before taking the medicine] × 100%, and the results were recorded;

[0113] (6) Prepare a DPPH solution with a concentration of 0.2 mmol / L using 95% ethanol and store it in the dark. Take 20 mg of the plant-extracted weight loss and anti-aging vitamin tablets prepared in Examples 1-3, the weight loss and anti-aging tablets prepared in Comparative Examples 1-2, and the commercial weight loss and anti-aging preparation in the control group as samples of each group, add 2 mL of DPPH solution, shake and mix, react in a dark environment for 30 minutes, centrifuge at 6000 r / min for 10 minutes, measure the absorbance at 517 nm and record it as the absorbance value (A1) after the reaction of the sample solution with DPPH, take 2 mL of the plant-extracted weight loss and anti-aging vitamin tablets prepared in Examples 1-3, the weight loss and anti-aging tablets prepared in Comparative Examples 1-2, and the commercial weight loss and anti-aging preparation in the control group, add 2 mL of 95% ethanol, measure the absorbance at 517 nm and record it as the absorbance value (A2) of the sample solution and ethanol, and add 2 mL of anhydrous ethanol and 2 mL of 0.1 mmol / L DPPH solution. The reaction between 10 mL and 20 mL was used as a comparison, and its absorbance value was recorded as the absorbance value of the blank group (A0). The DPPH clearance rate (%) was calculated according to the formula: (blank group absorbance value - absorbance value after the reaction of the sample solution with DPPH / blank group absorbance value - absorbance value of the sample solution with ethanol) × 100%. The measurement was repeated three times, and the average value was recorded.

[0114] (7) 30 healthy volunteers aged between 30 and 40 were selected and divided into 6 groups with 5 volunteers in each group. The skin moisture content of each volunteer before taking the medicine was measured and recorded using a capacitive skin moisture meter Corneometer CM825. The volunteers in each group took the plant extract weight loss and anti-aging vitamin tablets prepared in Examples 1-3 and the weight loss and anti-aging tablets prepared in Comparative Examples 1-2 every day. The control group took a commercial weight loss and anti-aging preparation twice a day, taking 2 g. The subjects were not allowed to apply any other cosmetics on the experimental area.

[0115] (8) In step (7), each group of volunteers took the drug for 7 consecutive days and then stopped taking it. At 4 h, 8 h, 16 h, and 48 h after stopping taking the drug, the skin moisture content of the test parts of each group of volunteers was measured using a capacitive skin moisture meter Corneometer CM825 probe. The average value of each group at the corresponding time point was calculated. The skin moisture content growth rate (%) = (skin moisture content at time t after taking the drug - skin moisture content before taking the drug / skin moisture content before taking the drug) × 100%.

[0116] Table 1. Weight loss effect measurement table

[0117]

[0118] Result analysis:

[0119] As shown in Table 1, the plant-extracted weight-loss and anti-aging vitamin tablets prepared in Examples 1-3 of the present invention can significantly reduce the body weight, white fat and liver index of mice; Figure 1 This is a graph showing the results of promoting collagen synthesis as described in Experimental Example 1 of the present invention. As shown in the figure, the plant-extracted weight loss and anti-aging vitamin tablets prepared in Examples 1-3 were added to the fibroblasts digested with trypsin, and after incubation for 48 hours, the synthesis amounts of type I, type III, and type IV collagen in Group 3 of Example 3 reached 189.23%, 190.80%, and 183.21%, respectively. The weight loss and anti-aging tablets prepared in Comparative Example 1 were added to the fibroblasts digested with trypsin, and after incubation for 48 hours, the synthesis amounts of type I, type III, and type IV collagen in Group 1 of Comparative Example 1 reached 173.24%, 175.11%, and 168.82%, respectively. The weight loss and anti-aging tablets prepared in Comparative Example 2 were added to the fibroblasts digested with trypsin, and after incubation for 48 hours, the synthesis amounts of type I, type III, and type IV collagen in Group 2 of Comparative Example 2 reached 158.29%, 166.09%, and 155.21%, respectively. The commercially available weight loss and anti-aging preparation in the control group was added to the fibroblasts digested with trypsin, and after incubation for 48 hours, the synthesis amounts of type h later, the synthesis of type I, type III, and type IV collagen in the control group reached 121.57%, 127.21%, and 119.46%, respectively; Figure 2 This is a graph showing the skin elasticity growth rate results of Experimental Example 1 of the present invention. As shown in the figure, the volunteers in the Example 3 group took the plant extract weight loss and anti-aging vitamin tablets prepared in Example 3 every day. The skin elasticity growth rate was 22.14% in the first week of taking the tablets, 25.59% in the second week of taking the tablets, and 6.88% in the fourth week after stopping taking the tablets. The volunteers in the Comparative Example 1 group took the weight loss and anti-aging tablets prepared in Comparative Example 1 every day, and the skin elasticity growth rate was 16.27% in the first week of taking the tablets, 19.02% in the second week of taking the tablets, and 5.14% in the fourth week after stopping taking the tablets. The volunteers in the Comparative Example 2 group took the weight loss and anti-aging tablets prepared in Comparative Example 2 every day, and the skin elasticity growth rate was 13.61% in the first week of taking the tablets, 15.36% in the second week of taking the tablets, and 3.11% in the fourth week after stopping taking the tablets. The volunteers in the control group took the commercially available weight loss and anti-aging preparation of the control group every day, and the skin elasticity growth rate was 4.17% in the first week of taking the tablets, 8.67% in the second week of taking the tablets, and 0.98% in the fourth week after stopping taking the tablets. Figure 3This is a graph showing the DPPH clearance results described in Experimental Example 1 of the present invention. As shown in the figure, the plant-extracted weight loss and anti-aging vitamin tablets prepared in Examples 1-3, after reacting with DPPH, had DPPH clearance rates of 96.95%, 97.29%, and 98.05%, respectively. The weight loss and anti-aging tablets prepared in Comparative Examples 1-2, after reacting with DPPH, had DPPH clearance rates of 90.09% and 79.75%, respectively. The commercially available weight loss and anti-aging preparation in the control group, after reacting with DPPH, had a DPPH clearance rate of 49.14%. Figure 4 This is a graph showing the skin moisture content growth rate results of Experimental Example 1 of the present invention. As shown in the figure, the volunteers in Example 3 group took the plant extract weight loss and anti-aging vitamin tablets prepared in Example 3 every day, and stopped taking them after taking them for 7 consecutive days. The skin moisture content growth rate was 97.24% 4 hours after stopping taking them, the skin moisture content growth rate was 88.37% 8 hours later, the skin moisture content growth rate was 57.43% 16 hours later, and the skin moisture content growth rate was 38.93% 48 hours later. The volunteers in Comparative Example 1 group took the weight loss and anti-aging tablets prepared in Comparative Example 1 every day, and stopped taking them after taking them for 7 consecutive days. The skin moisture content growth rate was 87.27% 4 hours after stopping taking them, the skin moisture content growth rate was 68.04% 8 hours later, the skin moisture content growth rate was 38.92% 16 hours later, and the skin moisture content growth rate was 20.14% 48 hours later. The volunteers in Comparative Example 2 group took the weight loss and anti-aging tablets prepared in Comparative Example 2 every day, and stopped taking them after taking them for 7 consecutive days. The skin moisture content growth rate was 77.62% 4 hours after stopping taking them, 87.62% 8 hours later, and 77.62% 16 hours later. The skin moisture content growth rate was 63.15% after 1 h, 22.18% after 16 h, and 13.56% after 48 h. The volunteers in the control group took the commercially available weight loss and anti-aging preparation of the control group every day for 7 consecutive days and then stopped taking it. The skin moisture content growth rate was 28.14% 4 hours after stopping taking it, the skin moisture content growth rate was 22.06% after 8 hours, the skin moisture content growth rate was 12.69% after 16 hours, and the skin moisture content growth rate was 7.61% after 48 hours. This shows that the plant-extracted weight loss and anti-aging vitamin tablets prepared by the present invention can effectively and permanently promote the synthesis of collagen, restore skin elasticity, have the ability to scavenge free radicals, protect the skin from oxidative damage, and can significantly increase the elasticity of the skin, make the skin firmer, achieve significant weight loss and anti-aging effects, and can maintain the efficacy for a long time.

[0120] Experimental Example 2: Effect stability test after storage.

[0121] The test steps for determining the stability of the plant-extracted weight loss and anti-aging vitamin tablets after storage prepared in Examples 1-3 of the present invention are as follows:

[0122] (1) The plant extract weight loss and anti-aging vitamin tablets prepared in Examples 1-3, the weight loss and anti-aging tablets prepared in Comparative Examples 1-2, and a control group commercial weight loss and anti-aging preparation (purchased from Zhangshu Jiaqi Health Products Co., Ltd.) were stored for 48 days at a temperature of 36°C and a humidity of 85% to obtain the plant extract weight loss and anti-aging vitamin tablets prepared in Examples 1-3 after storage, the weight loss and anti-aging tablets prepared in Comparative Examples 1-2 after storage, and the control group commercial weight loss and anti-aging preparation after storage;

[0123] (2) Sixty 8-week-old SPF mice weighing 25 g were selected (purchased from Chengdu Dashuo Animal Co., Ltd.) and randomly divided into 6 groups of 10 mice each. The mice were housed in separate cages, kept clean and dry, at a temperature of 24°C and a humidity of 50%, with free access to food and water.

[0124] (2) After feeding for 1 week, the mice in Example 1-3 groups were fed with a high-fat diet and gavage, and were fed 0.25 g of the plant-extracted weight loss and anti-aging vitamin tablets prepared in Example 1-3 groups after storage every day. The mice in Comparative Example 1-2 groups were fed with a high-fat diet and gavage, and were fed 0.25 g of the weight loss and anti-aging tablets prepared in Comparative Example 1-2 groups after storage every day. The mice in the control group were fed with a high-fat diet and gavage, and were fed 0.25 g of the commercially available weight loss and anti-aging preparation prepared in the control group after storage every day. After continuous feeding for 9 weeks, the mice were anesthetized and blood was collected from their eyeballs. The mice were killed by cervical dislocation, and their liver, colon, and white fat (epididymal fat, perirenal fat, and mesenteric fat) tissues were dissected and the contents of the cecum were collected aseptically. Part of the liver, colon, and epididymal adipose tissue was fixed with fixative, and the remaining tissues were snap-frozen in liquid nitrogen and stored at −80°C. During the experiment, mice were weighed once on day 0 and at the end of the experiment, and the weight gain rate was calculated according to the formula. During dissection, the liver and white fat of the mice were removed, washed, and quickly weighed to calculate the organ index: weight gain rate = (weight at the end of the experiment - weight on day 0) / weight at the end of the experiment - weight on day 0 × 100%. Organ index = organ wet weight / mouse body weight × 100%. The results are recorded in Table 2.

[0125] Table 2. Weight loss effect after storage

[0126]

[0127] Result analysis:

[0128] As can be seen from Table 2, after storing the plant extract weight loss and anti-aging vitamin tablets prepared in Examples 1-3 for 48 days at a temperature of 36°C and a humidity of 85%, the weight of mice can still be significantly reduced, and the white fat and liver indexes can be reduced. This shows that the plant extract weight loss and anti-aging vitamin tablets prepared by the present invention have a significant weight loss effect, high product stability, and are conducive to long-term storage.

[0129] While embodiments of the present invention have been shown and described, it will be appreciated by those skilled in the art that various changes, modifications, substitutions, and variations may be made to these embodiments without departing from the principles and spirit of the invention, and that the scope of the invention is defined by the appended claims and their equivalents.

[0130] The present invention and its embodiments are described above. Such description is not restrictive. The drawings show only one embodiment of the present invention, and actual applications are not limited thereto. In short, if a person skilled in the art is inspired by the above, and does not deviate from the purpose of the present invention, any method and embodiment similar to the technical solution without creative design shall fall within the scope of protection of the present invention.

Claims

1. A plant-extracted weight-loss and anti-aging vitamin tablet, characterized in that: The plant-extracted weight-loss and anti-aging vitamin tablets specifically include the following components in parts by weight: 16-22 parts of slimming compound, 15-17 parts of anti-aging agent, 2-3 parts of vitamin C, 2-3 parts of vitamin E, 2-3 parts of vitamin B6, 1.5-1.8 parts of ergothioneine, 1.3-1.7 parts of sodium benzoate; The raw materials for preparing the weight loss compound include the following components in parts by weight: 4-6 parts of Camellia ternata, 3-5 parts of Rhizoma Alismatis, 3-4 parts of Chinese Milkvetch, 6-7 parts of Garcinia, 1.2-1.4 parts of Monascus, 3.5-4.8 parts of N-vinylcaprolactam, 2.6-3.4 parts of glucose, and 4.2-5.7 parts of water-soluble silk fibroin; The raw materials for preparing the anti-aging agent include the following components in parts by weight: 2.2-2.6 parts of cyanidin-3-galactoside, 2.5-3 parts of meadowsweet extract, 1.8-2.5 parts of limonene, 1.4-1.7 parts of rutin, 1.8-2.3 parts of boric acid, and 2.8-3.6 parts of galactomannan; The method for preparing the weight loss compound specifically comprises the following steps: S1. Grinding Camellia ternata, Rhizoma Alismatis, Astragalus sinensis, and Garcinia to obtain a fat synthesis inhibiting powder; S2. Inoculate Monascus into 5% sterile glucose solution for cultivation, disrupt with ultrasound, and filter using a 0.22 mm sterile filter membrane to obtain a Monascus extract; S3, mixing N-vinylcaprolactam, glucose, water-soluble silk fibroin, and ultrapure water to react to obtain a temperature-sensitive polymer material; S4, mixing the fat synthesis inhibiting powder prepared in S1 with the Monascus extract prepared in S2, to obtain a weight loss component; S5, adding the thermosensitive polymer material prepared in S3 to the weight loss component prepared in S4, stirring and adsorbing, and freeze-drying to obtain a weight loss complex; The preparation method of the anti-aging agent specifically comprises the following steps: L1. Mix and dissolve cyanidin-3-galactoside, meadowsweet extract, limonene, rutin, and 70% ethanol solution to obtain an anti-aging solution; L2. mixing boric acid, galactomannan, and ultrapure water to react and obtain a viscous substance that promotes cell absorption; L3. Add the cell absorption promoting viscous substance prepared in L2 into the anti-aging solution prepared in L1, stir and mix, and obtain an anti-aging agent.

2. A method for preparing the plant-extracted weight-loss and anti-aging vitamin tablets according to claim 1, characterized in that: The specific steps include: Step 1: Mix vitamin C, vitamin E, vitamin B6, ergothioneine, and sodium benzoate to obtain a vitamin-containing stabilizer; Step 2: Mix the weight loss compound with the anti-aging agent to obtain a weight loss and anti-aging compound; Step 3: Add the weight loss and anti-aging complex prepared in step 2 to the vitamin-containing stabilizer prepared in step 1, mix evenly, press into tablets, place at 25-28°C for 2-2.5 hours, and air-dry to obtain plant-extracted weight loss and anti-aging vitamin tablets.

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