Patent Application
20210289827
This application relates to food production, and more particularly to a food containing a vitamin D2 mushroom oil.
Vitamin D is an essential vitamin for a human body, and a lack of the vitamin D will cause rickets in children and osteomalacia in adults. The vitamin D can be used for treatments of vitamin D deficiency, chronic hypocalcemia, hypophosphatemia, rickets, osteomalacia with chronic renal insufficiency, familial hypophosphatemia, hypoparathyroidism, acute, chronic and potential postoperative tetany and idiopathic tetany.
The vitamin D is ingested by the human body through food supplements and sunbathing. However, natural foods usually contain a low content of the vitamin D, lean meat, milk, and nuts contain trace amounts of the vitamin D, and vegetables, grains, fruits and their products contain little or no vitamin D. In addition, people with skin diseases and nightlife fail to supplement the vitamin D through sunbathing.
The vitamin D mainly comprises vitamin D2 (ergocalciferol) and vitamin D3 (cholecalciferol), where the vitamin D2 is obtained from plants and the vitamin D3 is obtained from animals. The existing vitamin D supplements mainly contain the vitamin D3 from animals. The vitamin D2 and the vitamin D3 have similar structures and similar metabolites, whose active metabolites are calcifediol and calcitriol, respectively. Animal pharmacology and toxicology studies show that there is no significant difference between the vitamin D2 and the vitamin D3 in stimulating the intestinal absorption of calcium and phosphorus in rats, while a median lethal dose (LD50) of the vitamin D2 in the rats is about 5-15 times higher than that of the vitamin D3. Such studies indicate that the vitamin D2 is safer than the vitamin D3.
Mushrooms also contain the vitamin D2, which are processed into mushroom powder for food or medicine in recent years. The mushroom powder has a particle size with 100-200 mesh through drying and crushing by a grinder. However, the mushrooms themselves have lignified fibers and are subjected to the drying process, causing the obtained mushroom powder is solid, insoluble powder. Such mushroom powder can only be applied in solid products and is not easily absorbed by the human body. At the same time, the vitamin D2 in the mushrooms is fat-soluble vitamin with a low self-dissolution rate, which is not easily absorbed and utilized by the human body through a conventional eating method.
An object of this application is to provide a food to solve problems in the prior art that the vitamin D2 in mushroom powder is not easy to be absorbed and has a low dissolution rate. The food provided herein contains a vitamin D2 mushroom oil, which is prepared by dissolving the mushroom vitamin D2 in an edible oil, facilitating promoting the absorption of vitamin D2 in human body.
Technical solutions of this application are described as follows.
This application provides a food, comprising a vitamin D2 mushroom oil.
In an embodiment, the vitamin D2 mushroom oil is used as an ingredient of the food; and a content of vitamin D2 in unit dose of the food is not less than 0.5 μg, preferably not less than 5 μg, and more preferably not less than 10 μg.
In an embodiment, the vitamin D2 mushroom oil has a peroxide value less than or equal to 15 meq/kg and an acid value less than or equal to 3 mg/g.
In an embodiment, the vitamin D2 mushroom oil is prepared through a step of:
subjecting a vitamin D2-containing mushroom powder to extraction with an edible oil.
In an embodiment, the vitamin D2 mushroom oil is added with an antioxidant; the antioxidant is selected from the group consisting of: vitamin E, lecithin, rosemary, sodium L-ascorbate and a combination thereof; and an addition amount of the antioxidant is 800-1500 ppm based on a total amount of the vitamin D2 mushroom oil.
In an embodiment, the edible oil is selected from the group consisting of: sunflower oil, rapeseed oil, soybean oil, olive oil, corn oil, peanut oil, coconut oil, tea seed oil and a combination thereof; a weight ratio of the vitamin D2-containing mushroom powder to the edible oil is 1:(0.5-30); and the extraction is performed at 10-85° C. for 8-120 h.
In an embodiment, the vitamin D2-containing mushroom powder is prepared through steps of:
(1) slicing an ergosterol-containing mushroom raw material to obtain mushroom slices; and irradiating the mushroom slices with ultraviolet light for 8-150 min to convert ergosterol into vitamin D2; and
(2) crushing irradiated mushroom slices to obtain the vitamin D2-containing mushroom powder with a particle size of 80-150 mesh.
In an embodiment, the food further comprises a nutrient;
wherein the nutrient is selected from the group consisting of perilla oil, walnut oil, linseed oil, peanut oil, olive oil, arachidonic acid (ARA), docosahexaenoic acid (DHA), vitamin A, calcium alginate and a combination thereof.
In an embodiment, the food is a health food or a functional food in a form of a soft capsule, a drop, a spray, a soft candy and a gelatinous candy.
Compared to the prior art, this disclosure has the following beneficial effects.
(1) In this application, the vitamin D2-containing mushroom powder is replaced with the vitamin D2 mushroom oil to be added to the food. The vitamin D2 in the vitamin D2 mushroom oil is dissolved in the edible oil, improving the dissolution rate of the vitamin D2 and promoting the absorption of vitamin D2 in human body.
(2) The vitamin D2 mushroom oil instead of the vitamin D2-containing mushroom powder can be applied in the food in forms of the drop and the spray. In addition, the vitamin D2 mushroom oil does not clog a nozzle, which is more convenient to use the drop and the spray.
(3) The vitamin D2 mushroom oil of this application is clear and transparent by filtration. Therefore, the vitamin D2 mushroom oil can be applied in the food in forms of the soft capsule and the gelatinous candy with some degree of transparency, so that their materials inside the gelatin shell are evenly distributed without layering precipitation or eccentricity.
(4) In this application, plant-derived vitamin D2 is selected to add to the food to supplement vitamin D necessary for the human body instead of animal-derived vitamin D3, so as to ensure there is no residual solvent or toxic by-product caused by industrial production of the food and a high food safety.
(5) In this application, the vitamin D2 mushroom oil and the calcium alginate are composited to add to the food, which can provide the human body with vitamin D2, and also promote the absorption of calcium and growth of bones in children and adolescents and prevent osteoporosis in the elderly.
The endpoint values and any values of the range disclosed herein are not limited to the precise range or value, and these ranges or values should be understood to include values close to these ranges or values. For numerical ranges, one or more new numerical ranges may be obtained between the endpoint values of each of the ranges, between the endpoint values of each of the ranges and intermediate values, and between intermediate values. These new numerical ranges shall be considered as specifically disclosed herein.
This application provides a food, containing a vitamin D2 mushroom oil. An addition amount of the vitamin D2 mushroom oil is determined according to a content of the vitamin D2 in the food that meets daily physiological needs of the human body.
In an embodiment, the vitamin D2 mushroom oil is used as an ingredient of the food. A content of vitamin D2 in unit dose of the food is not less than 0.5 μg (20 IU), preferably not less than 5 μg (200 IU), and more preferably not less than 10 μg (400 IU). Unit dose of the food represents a measurement value of the smallest package or smallest monomer of the food. For example, the unit dose in a soft capsule is one capsule. The unit dose in a gelatinous candy and a soft candy is one grain. The unit dose in a drop is a single drawing volume of a dropper and the unit dose in a spray is a single spraying volume of a spray nozzle.
In an embodiment, the vitamin D2 mushroom oil has a peroxide value less than or equal to 15 meq/kg and an acid value less than or equal to 3 mg/g.
In an embodiment, the vitamin D2 mushroom oil is prepared through a step of:
subjecting a vitamin D2-containing mushroom powder to extraction with an edible oil.
The vitamin D2-containing mushroom powder can be obtained by a method provided herein or commercially available. In an embodiment, the vitamin D2-containing mushroom powder is prepared through the following steps.
(1) An ergosterol-containing mushroom raw material is sliced to obtain mushroom slices. The mushroom slices are irradiated with ultraviolet light for 8-150 min to convert ergosterol into vitamin D2.
(2) The irradiated mushroom slices are crushed to obtain the vitamin D2-containing mushroom powder with a particle size of 80-150 mesh. In the step (1), the ultraviolet light is a combination of ultraviolet B (UVB) radiation of 280-315 nm and ultraviolet C (UVC) radiation of 200-280 nm.
The edible oil is edible grease. The edible oil is selected from the group consisting of: sunflower oil, rapeseed oil, soybean oil, olive oil, corn oil, peanut oil, coconut oil, tea seed oil and a combination thereof, where an extraction efficiency of the vitamin D2 is optimal using the high oleic sunflower oil as an extractant.
An extraction condition only needs to meet that the vitamin D2 in the vitamin D2-containing mushroom powder can be extracted and dissolved in the edible oil. In an embodiment, in order to ensure that the vitamin D2 can be extracted into the edible oil in large quantities, a weight ratio of the vitamin D2-containing mushroom powder to the edible oil is 1:(0.5-30), preferably 1:(1-10). The extraction temperature is 10-85° C. for 8-120 h, preferably 35-55° C. for 24-72 h. An extraction reaction is preferably carried out under a stirring condition.
The extraction reaction is carried out under an inert gas environment after an extraction tank is vacuumed to protect the vitamin D2 from being oxidized. The inert gas is preferably nitrogen, more preferably nitrogen with a purity of more than 99.9%. An introduction amount of the inert gas is determined to meet that a tank pressure of the extraction tank is 0.02-0.1 MPa. After the extraction reaction is completed, a solid-liquid separation of the edible oil and the vitamin D2-containing mushroom powder is performed by filtration, where a filtration method is pressure filtration or suction filtration.
In this application, the vitamin D2 mushroom oil is added with an antioxidant after the filtration is completed to prevent the vitamin D2 in the vitamin D2 mushroom oil from being oxidized. The antioxidant is a commonly used antioxidant in the food. The antioxidant is preferably selected from the group consisting of: vitamin E, lecithin, rosemary, sodium L-ascorbate and a combination thereof, more preferably vitamin E and lecithin. In an embodiment, an addition amount of the antioxidant is 800-1500 ppm based on a total amount of the vitamin D2 mushroom oil.
The food further contains a nutrient, where the nutrient is selected from the group consisting of perilla oil, walnut oil, linseed oil, peanut oil, olive oil, arachidonic acid (ARA), docosahexaenoic acid (DHA), vitamin A, calcium alginate and a combination thereof to promote mental development of children and adolescents. The vitamin D2 mushroom oil and the calcium alginate are composited to add to the food, which can promote absorption of calcium by the human body through the vitamin D2 of the vitamin D2 mushroom oil.
The food can be various types of food. The food is a health food or a functional food in a form of the soft capsule, the soft candy, the drop, the spray and the gelatinous candy.
A method of preparing the soft capsule containing the vitamin D2 mushroom oil is performed through the following steps.
(1) Water, gelatin powder and glycerin are mixed and peptized to obtain a sol mixture.
(2) The vitamin D2 mushroom oil and other components are evenly mixed to obtain a feed liquid and the feed liquid is poured into the sol mixture to obtain the soft capsule.
In an embodiment, an ambient temperature for mixing the vitamin D2 mushroom oil and other components is preferably lower than 25° C. and a relative humidity is less than 65%. A temperature of the obtained feed liquid is lower than 30° C. In addition, the vitamin D2 mushroom oil and other components are evenly stirred for 70-80 min. In an embodiment, the obtained feed liquid is preferably subjected to vacuum degassing to avoid excessive contact with oxygen, and the obtained feed liquid should not be stored for more than 2 h under the protection of the inert gas, where the inert gas can be nitrogen. The obtained feed liquid is prepared when it is in need, so as to shorten its exposure time in the air.
In an embodiment, a peptizing temperature is 60-85° C., preferably 70-77° C., a vapor pressure is less than 0.2 MPa and a peptizing time is 40-50 min. A temperature of the sol mixture is controlled at 58-62° C. during discharge and a discharge pressure is less than 0.05 MPa and the sol mixture is filtered through a double-layer bag. In addition, the peroxide value and the acid value of the vitamin D2 mushroom oil is reduced to reduce the exposure time of the obtained sol mixture in the air, thereby reducing the degree of oxidation and inhibiting the color change of the capsule. The obtained sol mixture should not be stored for more than 48 h, preferably more than 40 h. The obtained sol mixture is more preferably prepared when it is in need.
A method described in step (2) for pouring the feed liquid into the sol mixture can be that for preparing the soft capsule in the prior art, which is not particularly limited in this application.
In a method for preparing the gelatinous candy, a reducing sugar is added to the sol mixture, which is different from the method for preparing the soft capsule.
The soft candy containing the vitamin D2 mushroom oil is prepared by an existing process, which is not particularly limited in this application.
This application is described in detail with reference to the embodiments below.
In the following preparation methods, the content of the vitamin D2 in the vitamin D2 mushroom oil is measured using a high performance liquid chromatograph (L-7000) produced by Hitachi Co., Ltd. according to a GB 5009.82 method. The peroxide value is measured by a GB 5009.227-2016 method, and the acid value is measured by a GB5009.229-2016 method.
The rapeseed oil, the olive oil, the soybean oil and the high oleic sunflower oil are all commercially available products of China Oil And Foodstuffs Corporation. The vitamin E, the rosemary and the sodium L-ascorbate are all commercially available. The perilla oil, the walnut oil, the linseed oil, the peanut oil, the lecithin, the ARA, the DHA, the vitamin A and the calcium alginate are all commercially available, preferably self-made. Agaricus bisporus and Lentinus edodes are commercially available products of Shandong Deze Agricultural Technology Co., Ltd.
The high-purity nitrogen used herein has a purity of more than 99.9%.
(1) 20 kg of freshly-harvested Agaricus bisporus was cleaned to remove the culture medium and cut into slices with a thickness of 1.2 mm. Both sides of the Agaricus bisporus slices were irradiated with UVB with a wavelength of 280 nm at an irradiation dose of 1.5 J/cm2 for 120 min and then irradiated with UVC with a wavelength of 200 nm at an irradiation dose of 80 mJ/cm2 for 30 min, and then the slices were ground to obtain Agaricus bisporus powder with a particle size of 80-150 mesh.
(2) 20 kg of high oleic acid sunflower oil was fed into an extraction tank under vacuum, to which 2 kg of the Agaricus bisporus powder was sucked. The extraction tank was vacuumized to a micro-positive pressure of 0.06 MPa, and then the high-purity nitrogen was introduced. The Agaricus bisporus powder and the high oleic acid sunflower oil were stirred evenly in the extraction tank and heated to 45° C. The extraction was performed at 45° C. for 72 h, and then extraction mixture was filtered to obtain a filtrate.
(3) The filtrate was added with 14.4 g of vitamin E and 9.6 g of lecithin as antioxidants, evenly stirred and cooled to 25° C. to obtain vitamin D2 mushroom oil.
(1) 20 kg of freshly-harvested Agaricus bisporus was cleaned to remove the culture medium and cut into slices with a thickness of 1.5 mm. Both sides of the Agaricus bisporus slices were irradiated with UVB with a wavelength of 300 nm at an irradiation dose of 4 J/cm2 for 80 min and then irradiated with UVC with a wavelength of 240 nm at an irradiation dose of 100 mJ/cm2 for 25 min, and then the slices were ground to obtain Agaricus bisporus powder with a particle size of 80-150 mesh.
(2) 1 kg of rapeseed oil was fed into an extraction tank under vacuum, to which 2 kg of the Agaricus bisporus powder was sucked. The extraction tank was vacuumized to a micro-positive pressure of 0.03 MPa, and then the high-purity nitrogen was introduced. The Agaricus bisporus powder and the rapeseed oil were stirred evenly in the extraction tank and cooled to 10° C. The extraction was performed at 10° C. for 8 h, and then extraction mixture was filtered to obtain a filtrate.
(3) The filtrate was added with 0.48 g of vitamin E and 0.32 g of rosemary as antioxidants, evenly stirred and cooled to 25° C. to obtain vitamin D2 mushroom oil.
(1) 20 kg of freshly-harvested Lentinus edodes was cleaned to remove the culture medium and cut into slices with a thickness of 0.8 mm. Both sides of the Lentinus edodes slices were irradiated with UVB with a wavelength of 315 nm at an irradiation dose of 6.5 J/cm2 for 8 min and then irradiated with UVC with a wavelength of 280 nm at an irradiation dose of 120 mJ/cm2 for 20 min, and then the slices were ground to obtain Agaricus bisporus powder with a particle size of 80-150 mesh.
(2) 30 kg of soybean oil and 30 kg of olive oil were fed into an extraction tank under vacuum, to which 2 kg of the Lentinus edodes powder was sucked. The extraction tank was vacuumized to a micro-positive pressure of 0.1 MPa, and then the high-purity nitrogen was introduced. The Lentinus edodes powder and the soybean oil and the olive oil were stirred evenly in the extraction tank and heated to 80° C. The extraction was performed at 80° C. for 120 h, and then extraction mixture was filtered to obtain a filtrate.
(3) The filtrate was added with 90 g of sodium L-ascorbate as antioxidants, evenly stirred and cooled to 25° C. to obtain vitamin D2 mushroom oil.
Parameters of the vitamin D2 mushroom oil prepared by the above examples are shown in Table 1.
(1) A gelatin melter and feed and discharge pipelines were sterilized by steam for 15-30 min before production. 11.88 kg of water was boiled and sucked into the gelatin melter. At the same time, 5.6 kg of glycerin, 0.64 kg of microcrystalline cellulose and 11.88 kg of gelatin powder were sucked into the gelatin melter and mixed under stirring. The gelatin melting was performed at a temperature of 75° C. and a vapor pressure of 0.2 MPa for 45 min. After the melting process was completed, the mixture was cooled to 60° C., filtered and subjected to vacuum degassing to obtain a sol for use, where the storage time should not exceed 48 h.
(2) 16.95 kg of the vitamin D2 mushroom oil prepared in Example 1 was added to a mixing container at an ambient temperature of less than 25° C. and a relative humidity of less than 65%. 4.25 kg of peanut oil, 9.5 kg of linseed oil, 10.5 kg of walnut oil and 8.8 kg of perilla oil were mixed and poured into the mixing container. The mixture in the mixing container was stirred for 75 min and then subjected to vacuum degassing to obtain a feed liquid for use, where the feed liquid should not be stored for more than 2 h.
(3) The feed liquid prepared in step (2) was poured into the sol prepared in step (1) in a pelleter and pelletized at a temperature of 20° C. and a relative humidity of 65% to obtain the soft capsules with a gelatin shell thickness of 0.65-0.8 mm, where a shaping temperature of the gelatin shell was 10° C. An average weight of the gelatin shell of the soft capsules was 300 mg; an average weight of the material inside the gelatin shell was 500 mg; and each soft capsule contained 400 IU of vitamin D2 and 57 mg of linolenic acid.
The soft capsules were dried at a humidity of 65% and a temperature of 30° C. for 6 h, then dried at a humidity of 30% and a temperature of 32° C. for 6 h and cleaned with food-grade petroleum ether to obtain finished soft capsules. A unit dose of the finished soft capsules was one capsule and the recommended dose was one capsule per day.
(1) A gelatin melter and feed and discharge pipelines were sterilized by steam for 15-30 min before production. 11.68 kg of water was boiled and sucked into the gelatin melter. At the same time, 6 kg of glycerin, 0.64 kg of microcrystalline cellulose and 11.68 kg of gelatin powder were sucked into the gelatin melter and mixed under stirring. The gelatin melting was performed at a temperature of 75° C. and a vapor pressure of 0.2 MPa for 45 min. After the melting process was completed, the mixture was cooled to 60° C., filtered and subjected to vacuum degassing to obtain a sol for use, where the storage time should not exceed 48 h.
(2) 8.48 kg of the vitamin D2 mushroom oil prepared in Example 1 was added to a mixing container at an ambient temperature of less than 25° C. and a relative humidity of less than 65%. 15 kg of peanut oil, 3.02 kg of olive oil, 25 mg of vitamin A and 23.5 kg of calcium alginate were mixed and poured into the mixing container. The mixture in the mixing container was stirred for 75 min and then subjected to vacuum degassing to obtain a feed liquid for use, where the feed liquid should not be stored for more than 2 h.
(3) The feed liquid prepared in step (2) was poured into the sol prepared in step (1) in a pelleter and pelletized at a temperature of 20° C. and a relative humidity of 65% to obtain the soft capsules with a gelatin shell thickness of 0.65-0.8 mm, where a shaping temperature of the gelatin shell was 10° C. An average weight of the gelatin shell of the soft capsules was 300 mg; an average weight of the material inside the gelatin shell was 500 mg; and each soft capsule contained 200 IU of vitamin D2, 100 IU of vitamin A and 80 mg of calcium.
The soft capsules were dried at a humidity of 65% and a temperature of 30° C. for 6 h, then dried at a humidity of 30% and a temperature of 32° C. for 6 h and cleaned with food-grade petroleum ether to obtain finished soft capsules. A unit dose of the finished soft capsules was one capsule and the recommended dose was two capsules per day.
(1) A gelatin melter and feed and discharge pipelines were sterilized by steam for 15-30 min before production. 6.2 kg of water was boiled and sucked into the gelatin melter. At the same time, 2.9 kg of crystalline fructose, 1.2 kg of xylitol, 0.6 kg of microcrystalline cellulose, 4.6 kg of glycerinum and 14.5 kg of gelatin powder were sucked into the gelatin melter and mixed under stirring. The gelatin melting was performed at a temperature of 75° C. and a vapor pressure of 0.2 MPa for 45 min. After the melting process was completed, the mixture was cooled to 60° C., filtered and subjected to vacuum degassing to obtain a sol for use, where the storage time should not exceed 48 h.
(2) 0.226 kg of the vitamin D2 mushroom oil prepared in Example 2 was added to a mixing container at an ambient temperature of less than 25° C. and a relative humidity of less than 65%. 23.2 kg of DHA, 15.574 kg of peanut oil and 11 kg of walnut oil were mixed and poured into the mixing container. The mixture in the mixing container was stirred for 75 min and then subjected to vacuum degassing to obtain a feed liquid for use, where the feed liquid should not be stored for more than 2 h.
(3) The feed liquid prepared in step (2) was poured into the sol prepared in step (1) in a pelleter and pelletized at a temperature of 20° C. and a relative humidity of 65% to obtain the gelatinous candies with a gelatin shell thickness of 0.65-0.8 mm, where a shaping temperature of the gelatin shell was 10° C. An average weight of the gelatin shell of the gelatinous candies was 300 mg; an average weight of the material inside the gelatin shell was 500 mg; and each gelatinous candy contained 200 IU of vitamin D2 and 100 IU of DHA.
The gelatinous candies were dried at a humidity of 65% and a temperature of 30° C. for 6 h, then dried at a humidity of 30% and a temperature of 32° C. for 6 h and cleaned with food-grade petroleum ether to obtain finished gelatinous candies. A unit dose of the finished gelatinous candies was one grain and the recommended dose was two grains per day.
27.07 L of the vitamin D2 mushroom oil prepared in Example 3 was added to a mixing container at an ambient temperature of less than 25° C. and a relative humidity of less than 65%, to which 22.93 L of walnut oil was added. The mixture was mixed for 25 min and poured into food-grade polyester bottles each for 50 mL, where the polyester bottles were provided with a spray nozzle. Single spray dose of the spray nozzle was about 0.5 mL, in which a content of vitamin D2 was about 400 IU. The unit dose of the spray was a single spraying volume of the spray nozzle, and the recommended dose was 0.5 mL, i.e., the single spraying volume of the spray nozzle.
18.39 L of the vitamin D2 mushroom oil prepared in Example 1 was added to a mixing container at an ambient temperature of less than 25° C. and a relative humidity of less than 65%, to which 18.7 L of walnut oil and 12.91 L of perilla oil were added. The mixture was mixed for 25 min and poured into food-grade polyester bottles each for 50 mL, where the polyester bottles were provided with a dropper. Single drop dose of the dropper was about 0.5 mL, in which a content of vitamin D2 was about 400 IU. The unit dose of the drop was the volume drawn by the dropper each time, and the recommended dose was 0.5 mL, i.e., the single drawing volume of the dropper.
9.2 L of the vitamin D2 mushroom oil prepared in Example 1 was added to a mixing container at an ambient temperature of less than 25° C. and a relative humidity of less than 65%, to which 21.84 L of walnut oil and 18.96 L of ARA were added. The mixture was mixed for 25 min and poured into food-grade polyester bottles each for 50 mL, where the polyester bottles were provided with a dropper. Single drop dose of the dropper was about 0.5 mL, in which a content of vitamin D2 was about 200 IU and a content of ARA was 75 mg. The unit dose of the drop was the volume drawn by the dropper each time, and the recommended dose was the volume drawn by the dropper twice, i.e., 1 mL.
(1) 2 kg of agar, 2 kg of carrageenan and 5 kg of white granulated sugar were evenly mixed, to which 20 kg of water was added. The mixture was soaked for 20 min and then heated for complete dissolution to obtain a sol.
(2) 5 kg of white granulated sugar, 5 kg of malt syrup and 6.76 kg of water were mixed, heated, boiled and stirred to form a sugar solution. When the sugar solution was not easy to break off after picked up, the sugar solution was added with the sol prepared in step (1), evenly stirred and then boiled at 104-107° C. When a moisture content of the system dropped to 22-24%, the heating was stopped, and the system was cooled to 70° C., added with 4.24 kg of the vitamin D2 mushroom oil prepared in Example 1 and evenly stirred to obtain syrup.
(3) The syrup prepared in step (2) was poured into a mold while it was hot. The syrup was cooled and solidified to form a molded sugar body, which was dried by hot air drying at 45° C. for 8-10 h to enable the moisture content to drop to 14-18%. The dried sugar body was cooled to room temperature to obtain the soft candy. An average weight of each soft candy was 500 mg and a content of vitamin D2 in each soft candy was 100 IU. A unit dose of the soft candies was one grain, and the recommended dose was four grains per day.
The above are only preferred embodiments of this application, which are not intended to limit this application. It should be understood that changes, modifications and replacements made by those skilled in the art without departing from the spirit of this application shall fall within the scope of this application.
| Number | Date | Country | Kind |
|---|---|---|---|
| 201811506528.0 | Dec 2018 | CN | national |
This application is a continuation of International Patent Application No. PCT/CN2019/101025, filed on Aug. 16, 2019, which claims the benefit of priority from Chinese patent application No. 201811506528.0, filed on Dec. 10, 2018. The content of the aforementioned applications, including any intervening amendments thereto, are incorporated herein by reference.
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/CN2019/101025 | Aug 2019 | US |
| Child | 17343034 | US |
