CN110973634A - Nutritional composition for improving hypoevolutism and preparation method thereof - Google Patents
Nutritional composition for improving hypoevolutism and preparation method thereof Download PDFInfo
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- CN110973634A CN110973634A CN201911354955.6A CN201911354955A CN110973634A CN 110973634 A CN110973634 A CN 110973634A CN 201911354955 A CN201911354955 A CN 201911354955A CN 110973634 A CN110973634 A CN 110973634A
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- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
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- A—HUMAN NECESSITIES
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- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
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Abstract
The invention belongs to the technical field of nutritional food, and particularly relates to a nutritional composition for improving hypoevolutism, which comprises, by weight, 30-80 parts of plant seed oil microcapsule powder containing α -linolenic acid, 20-100 parts of animal and vegetable oil microcapsule powder containing DHA, 0.001-0.008 part of phosphatidylserine, 0.001-0.005 part of (6S) -5-methyltetrahydrofolate, 1-5 parts of vitamin composition premix, 5-35 parts of calcium carbonate, 0.2-25 parts of magnesium carbonate, 0.5-6 parts of ferrous gluconate, 0.1-3 parts of zinc gluconate, 0.01-0.1 part of retinyl palmitate, 0.01-0.05 part of vitamin D3, 0.1-2 parts of D- α -tocopherol, 0.1-5 parts of taurine and 5-25 parts of soybean protein isolate powder.
Description
Technical Field
The invention belongs to the technical field of nutritional foods, and particularly relates to a nutritional composition for improving hypoevolutism and a preparation method thereof.
Background
Growth retardation (stunting) refers to the phenomenon of slowing down or abnormal sequence in the process of growth and development. The incidence rate is between 6% and 8%. Developmental delays are implicated by a number of factors, such as nutritional deficiencies, systemic disease, familial inheritance, congenital disease or mental factors. Fetal intrauterine growth restriction (FGR) is an obstetrical disorder that seriously compromises fetal life quality and affects childhood and pubertal growth, even leading to a variety of long-term complications, with 80% to 90% of children with developmental delay resulting from intrauterine dysplasia and congenital genetic factors. Some diseases are caused by pathological factors such as chromosome abnormality, bone diseases, metabolic diseases, chronic diseases or chronic malnutrition, endocrine diseases, etc., which can cause growth retardation of children. Pregnant women are the basic source of nutrient substances of fetuses, and the growth and development of the fetuses are influenced by malnutrition of the pregnant women, particularly insufficient supply of protein and energy. In addition, the combination of trace elements essential to human body with amino acids, proteins, etc. can form enzymes and hormones with high biochemical effect and special physiological function, and the deficiency of trace elements and vitamins can affect the growth and development of fetus. For example, zinc deficiency in pregnant women can affect nucleic acid and protein synthesis, decrease the total area of placental villi, affect fetal development, and lead to IUGR and fetal malformation. The enzyme deficiency or insufficient supply of vitamin B6, B12 or folic acid can cause hyperhomocysteinemia, affect fetal placental development, and induce obstetrical complications such as abortion, pregnancy-induced hypertension, IUGR, teratogenesis and early placental stripping. The invention discloses a nutritional composition which has a remarkable effect on both intrauterine growth retardation of a fetus and growth and development retardation of an infant, and provides a new method from the aspects of nutrition absorption and metabolism, so that the nutritional composition has an effect of improving the intrauterine growth retardation of the fetus and the growth and development retardation of the infant.
α -linolenic acid is essential fatty acid of human body, which can be converted into eicosapentaenoic acid and docosahexaenoic acid in human body, α -linolenic acid can increase brain transmission medium (Neurotransmitter), enhance brain activity function, make brain operation more effective and make learning and thinking ability better, α -linolenic acid has most important function for pregnant and lying-in women, which is to control gene expression, optimize genetic gene, transport cell material raw material, control nutrient to enter cells, influence growth and development of brain cells of baby, α -linolenic acid is also brain gold DHA, which can be converted into DHA in baby body, α -linolenic acid is very important for health development of brain, retina, skin and kidney function of baby and baby.
DHA is an important constituent of brain cell membrane, participates in the formation and development of brain cells, plays an important role in the extension of nerve cell axons and the formation of new processes, can maintain the normal physiological activity of nerve cells, and participates in the process of brain thinking and memory formation. May be related to promoting the protein synthesis of nerve cells and promoting the growth of nerve cells. DHA is very closely related to brain health. Increasing DHA content in food, and improving DHA level in brain, so as to enhance learning and memory function, promote brain and nerve health development, and prevent and treat visual deterioration.
Phosphatidylserine forms the cell membrane of nerve cells, activates Protein Kinase C (PKC), and the activated protein kinase C can phosphorylate serine and threonine residues, so that biological information conduction is influenced, and the phosphatidylserine can help repair the cell membrane of the nerve cells of the brain, not only bring nutrients into the cells and discharge waste, but also help the brain cells to be normalized. Phosphatidylserine can help repair the cell membrane, especially for the cranial nerve cell, and not only can bring nutrients into the cell and discharge wastes, but also can help the brain cell to be normalized.
Folic acid is a water-soluble B vitamin essential for maintaining normal life activities of human body, and its main biological function is to provide methyl for methylation reaction in cells and synthesis of deoxyribonucleic acid. Research shows that various birth defects such as neural tube deformity and cleft lip and palate are related to folic acid deficiency in the early pregnancy of women, folic acid is an indispensable nutrient for fetal growth and development, the folic acid deficiency of pregnant women can cause low body weight, cleft lip and palate, heart defect and the like during the birth of the fetus, and the folic acid deficiency in the first 3 months of pregnancy can cause the neural tube development defect of the fetus to cause deformity. In contrast to folic acid, (6S) -5-methyltetrahydrofolate, glucosamine salt is used as a folate with metabolic activity, which is not affected by MTHFR enzyme (methylenetetrahydrofolate reductase) gene polymorphism, can be directly utilized without any metabolic 'finished product' folic acid, and 5-methyltetrahydrofolate is ingested to ensure that Hcy can complete methionine circulation, reduce the content of Hcy in blood, and avoid spontaneous abortion, birth defects and the like caused by Hcy increase in the early pregnancy; relieve the occlusion and angiosclerosis of three-level chorion small blood vessels of placenta and even the thrombosis of the circulatory system of a fetus caused by the increase of Hcy in the middle and late pregnancy, and further cause the adverse effects of oligohydramnios, limited growth and development of the fetus, pregnancy-induced hypertension, premature birth and the like.
The vitamin E can enhance the activity of brain nerve cells of the baby and maintain the normal immune function of the baby, in particular to the function of T lymphocytes. Protecting nervous system, bone marrow muscle, and retina from oxidative damage. Adequate vitamin E is also required for normal development of the human neuromuscular system and maintenance of retinal function. Calcium is a nutrient that maintains heart health, hemostasis, nerve health, muscle contraction, and skin, bone, and tooth health. Zinc is a component of more than 200 enzymes, DNA and RNA in vivo, and is an essential substance for growth and development.
Vitamin D can promote absorption of calcium and phosphorus by small intestinal mucosa, effectively promote growth of osteoclast and new osteocyte of bone, maintain calcium concentration, promote calcium deposition in bone, and harden bone. In addition, vitamin D is also involved in the proliferation and differentiation of various cells and in the regulation of immune function.
The vitamins and minerals are important substances which are indispensable for maintaining the life of the body, and the vitamins participate in a plurality of important life processes of the body and have great health relationship with the human body, because the infants are in the period of vigorous growth and development, the required amount of various vitamins is large, and the vitamins and the minerals should be supplemented. Minerals, also known as inorganic salts, are present in small amounts in the human body, but some are essential for the body tissue and some are involved in maintaining enzymatic and hormonal activities. It is therefore more important to ingest sufficient minerals during the vigorous growth and development period of the infant. The demand of the pregnant women for nutrients is increased because more nutrients are needed for blood circulation of the fetus, development of organs and skeletons of the fetus, growth of placenta, and the like, and the workload of important organs of the mothers is increased. Therefore, during pregnancy, enough multivitamin minerals are needed to be taken, so as to avoid the lack of nutrition in the diet, ensure the body to be in the optimal state and ensure that the blood of the user contains enough nutrients required by the fetus.
Taurine is a nerve inhibitor, and can promote the growth and development of nervous system, and the proliferation and differentiation of nerve cells, and the deficiency of taurine can make the developing cerebellum abnormal, and affect the development of brain and intelligence. In addition, the synthesis of DNA and RNA of brain cells can be promoted, and the content of phosphatidylethanolamine of membranes and the utilization rate of the brain cells to protein are increased, so that the development of the brain cells, particularly the structure and the function of hippocampal cells, is promoted. At present, no comprehensive and targeted nutritional composition exists on the market, and a nutritional preparation for improving the hypoevolutism has single component, is mainly a medicinal preparation for being matched with physical therapy, and the single component is easy to cause poor absorption, so the treatment effect is not ideal.
Disclosure of Invention
The present invention has been made to solve the above problems, and an object of the present invention is to provide a nutritional composition for improving developmental delay and a method for producing a nutritional composition for improving developmental delay, which are aimed at comprehensively improving the nutritional absorption and nutritional metabolism of a mother during embryonic development and a child during growth.
The invention provides a nutritional composition for improving developmental retardation, which has the following specific technical scheme:
the nutritional composition for improving hypoevolutism comprises, by weight, 30-80 parts of plant seed oil microcapsule powder containing α -linolenic acid, 20-100 parts of animal and plant oil microcapsule powder containing DHA, 0.001-0.008 part of phosphatidylserine, 0.001-0.005 part of (6S) -5-methyltetrahydrofolate, 1-5 parts of vitamin composition premix, 5-35 parts of calcium carbonate, 0.2-25 parts of magnesium carbonate, 0.5-6 parts of ferrous gluconate, 0.1-3 parts of zinc gluconate, 0.01-0.1 part of retinyl palmitate, 0.01-0.05 part of vitamin D3, 0.1-2 parts of D- α -tocopherol, 0.1-5 parts of taurine and 5-25 parts of soybean protein isolate powder.
In some embodiments, the α -linolenic acid-containing plant seed oil microcapsule powder comprises linseed oil microcapsule powder and walnut oil microcapsule powder, wherein the weight ratio of the linseed oil microcapsule powder to the walnut oil microcapsule powder is 2:3-5: 1.
In some embodiments, the DHA-containing animal and vegetable oil microcapsule powder is DHA algal oil microcapsule powder, fish oil microcapsule powder, and/or lecithin DHA yolk microcapsule powder.
In some embodiments, the vitamin composition premix is a compound nutrient supplement premix, and each 1000 parts of the compound nutrient supplement premix comprises 10-15 parts of thiamine hydrochloride, 10-15 parts of riboflavin, 10-15 parts of pyridoxine hydrochloride, 1-5 parts of cobalamin, 65-80 parts of nicotinamide, 740-753 parts of L-ascorbic acid, 47-55 parts of D-calcium pantothenate and the balance of starch.
In certain embodiments, the (6S) -5-methyltetrahydrofolate is glucosamine (6S) -5-methyltetrahydrofolate or a combination of calcium (6S) -5-methyltetrahydrofolate and (6S) -5-methyltetrahydrofolate.
In certain embodiments, 30 parts of linseed oil microcapsule powder, 20 parts of walnut oil microcapsule powder, 20 parts of DHA algae oil microcapsule powder, 0.005 part of phosphatidylserine, 0.003 part of (6S) -5-methyltetrahydrofolate glucosamine salt, 3 parts of a compound nutrient supplement premix, 5 parts of calcium carbonate, 2 parts of magnesium carbonate, 1 part of ferrous gluconate, 0.1 part of zinc gluconate, 0.01 part of retinyl palmitate, 0.02 part of vitamin D3, and 0.2 part of D- α -tocopherol.
The invention also provides a preparation method of the nutritional composition for improving hypoevolutism, which is used for preparing the nutritional composition and is characterized by comprising the following steps:
(1) sieving plant seed oil microcapsule powder containing α -linolenic acid, animal and vegetable oil microcapsule powder containing DHA, phosphatidylserine, 6S-5-methyltetrahydrofolate, vitamin composition premix, calcium carbonate, magnesium carbonate, ferrous gluconate, zinc gluconate, retinyl palmitate, vitamin D3, D- α -tocopherol, taurine and soybean protein isolate powder respectively;
(2) placing the sieved phosphatidylserine, (6S) -5-methyltetrahydrofolate, vitamin composition premix, calcium carbonate, magnesium carbonate, ferrous gluconate, zinc gluconate, retinyl palmitate, vitamin D3, D- α -tocopherol and taurine into a powder mixer, and uniformly mixing to obtain a mixture A;
(3) placing the sieved plant seed oil microcapsule powder containing α -linolenic acid, animal and plant oil microcapsule powder containing DHA, soybean protein isolate powder and the mixture A in the step (2) into a vacuum drying mixer to be uniformly mixed to obtain the nutritional composition for improving the hypoevolutism;
(4) and (4) preparing the nutrient composition for improving the hypoevolutism in the step (3) into powder, tablets or capsules.
The nutritional composition for improving the hypoevolutism contains abundant nutritional substances such as α -linolenic acid, DHA, (6S) -5-methyltetrahydrofolic acid, multiple vitamin minerals and the like, the nutritional substances can be mutually promoted and absorbed, so that the absorption rate is enhanced, and the nutritional composition can be combined with the traditional physical treatment method, is convenient to eat, has an obvious effect and does not have any obvious side effect.
Drawings
Fig. 1 is a flow chart of a method of preparing a nutritional composition for ameliorating stunted development according to the present invention.
Detailed Description
In order to make the objects, technical solutions and advantages of the present invention more apparent, the present invention is described in further detail below with reference to the accompanying drawings 1 in conjunction with specific embodiments.
Example 1
Weighing 20 parts of linseed oil microcapsule powder, 25 parts of walnut oil microcapsule powder, 100 parts of DHA algae oil microcapsule powder, 0.001 part of phosphatidylserine, (6S) -5-methyltetrahydrofolic acid glucosamine salt, 0.005 part of compound nutrient enhancer premix, 5 parts of calcium carbonate, 0.2 part of magnesium carbonate, 0.5 part of ferrous gluconate, 3 parts of zinc gluconate, 0.1 part of retinyl palmitate, 30.05 parts of vitamin D, 2 parts of D- α -tocopherol, 0.1 part of taurine and 5 parts of soybean protein isolate according to the parts by weight, wherein the compound nutrient enhancer is prepared by processing and uniformly mixing 13 parts of thiamine hydrochloride, 13 parts of riboflavin, 12 parts of pyridoxine hydrochloride, 3 parts of cobalamin, 70 parts of nicotinamide, 745 parts of L-ascorbic acid, 50 parts of D-calcium pantothenate and the balance of starch in a vacuum drying mixer to prepare the nutrient enhancer of tablets, capsules or capsules.
Respectively sieving the weighed materials with a 60-mesh sieve, mixing phosphatidylserine, (6S) -5-methyltetrahydrofolic acid glucosamine salt, a compound nutrient enhancer premix, calcium carbonate, magnesium carbonate, ferrous gluconate, zinc gluconate, retinyl palmitate, vitamin D3, D- α -tocopherol and taurine for 30min by a powder mixer according to the formula amount to prepare a mixture A, and uniformly mixing linseed oil microcapsule powder, walnut oil microcapsule powder, DHA algal oil microcapsule powder, soybean protein isolate powder and the mixture A for 20-40min by a vacuum drying mixer to prepare the powdery nutrient composition for improving the stunting.
Example 2
The compound nutrient enhancer premix is prepared as follows: every 1000 parts of premix comprises 10 parts of thiamine hydrochloride, 10 parts of riboflavin, 10 parts of pyridoxine hydrochloride, 1 part of cobalamin, 65 parts of nicotinamide, 740 parts of L-ascorbic acid, 47 parts of D-calcium pantothenate and the balance of starch, the raw materials are processed and then are mixed uniformly in a vacuum drying mixer, and the compound nutrient enhancer premix of tablets, powder or capsules is prepared.
The rest of the raw materials for preparing the nutritional composition for improving hypoevolutism in parts by weight and the preparation method are the same as those of example 1.
Example 3
The compound nutrient enhancer premix is prepared as follows: each 1000 parts of premix comprises 15 parts of thiamine hydrochloride, 15 parts of riboflavin, 15 parts of pyridoxine hydrochloride, 5 parts of cobalamin, 80 parts of nicotinamide, 753 parts of L-ascorbic acid, 55 parts of D-calcium pantothenate and the balance of starch, the raw materials are processed and mixed uniformly in a vacuum drying mixer, and the compound nutrient enhancer premix of tablets, powder or capsules is prepared.
The rest of the raw materials for preparing the nutritional composition for improving hypoevolutism in parts by weight and the preparation method are the same as those of example 1.
Example 4
Weighing 50 parts of linseed oil microcapsule powder, 30 parts of walnut oil microcapsule powder, 45 parts of DHA algae oil microcapsule powder, 0.001 part of phosphatidylserine, (6S) -5-methyl tetrahydrofolic acid glucosamine salt, 0.008 part of compound nutrient enhancer premix, 1 part of calcium carbonate, 25 parts of magnesium carbonate, 6 parts of gluconic acid, 0.1 part of zinc gluconate, 0.1 part of retinyl palmitate, 30.01 parts of vitamin D, 0.03 part of D- α -tocopherol, 5 parts of taurine and 25 parts of soybean protein isolate according to the parts by weight, wherein the compound nutrient enhancer is prepared by processing 13 parts of thiamine hydrochloride, 13 parts of riboflavin, 12 parts of pyridoxine hydrochloride, 3 parts of cobalamin, 70 parts of nicotinamide, 745 parts of L-ascorbic acid, 50 parts of D-calcium pantothenate and the balance of starch in each 1000 parts of the premix, and then uniformly mixing the processed raw materials in a vacuum drying mixer to prepare the compound nutrient enhancer of tablets, powder or capsules.
Respectively sieving the weighed materials with a 60-mesh sieve, mixing phosphatidylserine, (6S) -5-methyltetrahydrofolic acid glucosamine salt, a compound nutrient enhancer premix, calcium carbonate, magnesium carbonate, ferrous gluconate, zinc gluconate, retinyl palmitate, vitamin D3, D- α -tocopherol and taurine for 30min by a powder mixer according to the formula amount to prepare a mixture A, and uniformly mixing linseed oil microcapsule powder, walnut oil microcapsule powder, DHA algal oil microcapsule powder, soybean protein isolate powder and the mixture A for 20-40min by a vacuum drying mixer to prepare the capsule nutritional composition for improving the stunting.
Example 5
The compound nutrient enhancer premix is prepared as follows: every 1000 parts of premix comprises 10 parts of thiamine hydrochloride, 10 parts of riboflavin, 10 parts of pyridoxine hydrochloride, 1 part of cobalamin, 65 parts of nicotinamide, 740 parts of L-ascorbic acid, 47 parts of D-calcium pantothenate and the balance of starch, the raw materials are processed and then are mixed uniformly in a vacuum drying mixer, and the compound nutrient enhancer premix of tablets, powder or capsules is prepared.
The rest of the raw materials for preparing the nutritional composition for improving hypoevolutism in parts by weight and the preparation method are the same as those of example 4.
Example 6
The compound nutrient enhancer premix is prepared as follows: each 1000 parts of premix comprises 15 parts of thiamine hydrochloride, 15 parts of riboflavin, 15 parts of pyridoxine hydrochloride, 5 parts of cobalamin, 80 parts of nicotinamide, 753 parts of L-ascorbic acid, 55 parts of D-calcium pantothenate and the balance of starch, the raw materials are processed and mixed uniformly in a vacuum drying mixer, and the compound nutrient enhancer premix of tablets, powder or capsules is prepared.
The rest of the raw materials for preparing the nutritional composition for improving hypoevolutism in parts by weight and the preparation method are the same as those of example 4.
Example 7
Weighing 30 parts of linseed oil microcapsule powder, 20 parts of walnut oil microcapsule powder, 20 parts of DHA algae oil microcapsule powder, 0.005 part of phosphatidylserine, (6S) -5-methyltetrahydrofolic acid glucosamine salt, 0.003 part of compound nutrient enhancer premix, 3 parts of calcium carbonate, 2 parts of magnesium carbonate, 1 part of gluconic acid, 0.1 part of zinc gluconate, 0.1 part of retinyl palmitate, 30.02 parts of vitamin D, 0.02 part of D- α -tocopherol, 2 parts of taurine and 15 parts of soybean protein isolate according to the parts by weight, wherein the compound nutrient enhancer is prepared by processing 13 parts of thiamine hydrochloride, 13 parts of riboflavin, 12 parts of pyridoxine hydrochloride, 3 parts of cobalamin, 70 parts of nicotinamide, 745 parts of L-ascorbic acid, 50 parts of D-calcium pantothenate and the balance of starch in each 1000 parts of premix, and then uniformly mixing the processed raw materials in a vacuum drying mixer to prepare the compound nutrient enhancer of tablets, powder or capsules.
Respectively sieving the weighed materials with a 60-mesh sieve, mixing phosphatidylserine, (6S) -5-methyltetrahydrofolic acid glucosamine salt, a compound nutrient enhancer premix, calcium carbonate, magnesium carbonate, ferrous gluconate, zinc gluconate, retinyl palmitate, vitamin D3, D- α -tocopherol and taurine for 30min by a powder mixer according to the formula amount to prepare a mixture A, and uniformly mixing linseed oil microcapsule powder, walnut oil microcapsule powder, DHA algal oil microcapsule powder, soybean protein isolate powder and the mixture A for 20-40min by a vacuum drying mixer to prepare the tablet nutritional composition for improving the stunting.
Example 8
The compound nutrient enhancer premix is prepared as follows: every 1000 parts of premix comprises 10 parts of thiamine hydrochloride, 10 parts of riboflavin, 10 parts of pyridoxine hydrochloride, 1 part of cobalamin, 65 parts of nicotinamide, 740 parts of L-ascorbic acid, 47 parts of D-calcium pantothenate and the balance of starch, the raw materials are processed and then are mixed uniformly in a vacuum drying mixer, and the compound nutrient enhancer premix of tablets, powder or capsules is prepared.
The rest of the raw materials for preparing the nutritional composition for improving hypoevolutism in parts by weight and the preparation method are the same as those of example 7.
Example 9
The compound nutrient enhancer premix is prepared as follows: each 1000 parts of premix comprises 15 parts of thiamine hydrochloride, 15 parts of riboflavin, 15 parts of pyridoxine hydrochloride, 5 parts of cobalamin, 80 parts of nicotinamide, 753 parts of L-ascorbic acid, 55 parts of D-calcium pantothenate and the balance of starch, the raw materials are processed and mixed uniformly in a vacuum drying mixer, and the compound nutrient enhancer premix of tablets, powder or capsules is prepared.
The rest of the raw materials for preparing the nutritional composition for improving hypoevolutism in parts by weight and the preparation method are the same as those of example 7.
Example 10
Weighing 45 parts of linseed oil microcapsule powder, 10 parts of walnut oil microcapsule powder, 20 parts of DHA algae oil microcapsule powder, 0.005 part of phosphatidylserine, (6S) -5-methyltetrahydrofolic acid glucosamine salt, 0.045 part of compound nutrient enhancer premix, 3 parts of calcium carbonate, 2 parts of magnesium carbonate, 1 part of ferrous gluconate, 0.3 part of zinc gluconate, 0.01 part of retinyl palmitate, 30.01 parts of vitamin D, 0.1 part of D- α -tocopherol, 0.2 part of taurine and 15 parts of soybean protein isolate according to parts by weight, wherein the compound nutrient enhancer premix is prepared by 10-14 parts of thiamine hydrochloride, 10-15 parts of riboflavin, 10-15 parts of pyridoxine hydrochloride, 1-5 parts of cobalamin, 65-80 parts of nicotinamide, 740-ascorbic acid and 753 parts of D-calcium pantothenate and the balance of starch in each 1000 parts of premix, and drying the raw materials in a vacuum mixer to prepare a uniform nutrient premix or a compound premix.
The weighed materials are respectively sieved by a 60-mesh sieve, phosphatidylserine, (6S) -5-methyltetrahydrofolic acid glucosamine salt, a compound nutrient enhancer premix, calcium carbonate, magnesium carbonate, ferrous gluconate, zinc gluconate, retinyl palmitate, vitamin D3, D- α -tocopherol and taurine are mixed for 30min by a powder mixer according to the formula amount to prepare a mixture A, and linseed oil microcapsule powder, walnut oil microcapsule powder, DHA algal oil microcapsule powder, soybean protein isolate and the mixture A are uniformly mixed for 20-40min by a vacuum drying mixer to prepare the powdery nutrient composition for improving the stunting, wherein each bag is 20 g and the dosage is 90 g per day.
48 pregnant women with 8-city intrauterine fetal growth retardation in obstetrical department are selected, wherein the pregnant women are 24-42 years old and 29 years old on average; after 25-35 weeks of pregnancy, 48 pregnant women have 28 vaginal deliveries and 20 cesarean deliveries, and all newborns survive. The weight of the newborn is more than or equal to 2500g and 40 cases, the weight of the newborn is more than or equal to 3000g and 5 cases, wherein the number of delivery weeks of 3 pregnant women is 34-36 weeks, and the weight of the newborn is more than or equal to 2200 g. The effect is remarkable.
Example 11
Weighing 20 parts of linseed oil microcapsule powder, 10 parts of walnut oil microcapsule powder, 45 parts of DHA algae oil microcapsule powder, 0.006 part of phosphatidylserine, (6S) -5-methyl calcium tetrahydrofolate, 2 parts of compound nutrient enhancer premix, 12 parts of calcium carbonate, 2 parts of magnesium carbonate, 3 parts of ferrous gluconate, 0.9 part of zinc gluconate, 0.06 part of retinyl palmitate, 30.02 parts of vitamin D, 0.03 part of D- α -tocopherol, 0.25 part of taurine and 12 parts of soybean protein isolate.
The compound nutrient enhancer premix is prepared by the following steps: every 1000 parts of premix contains 13 parts of thiamine hydrochloride, 13 parts of riboflavin, 12 parts of pyridoxine hydrochloride, 3 parts of cobalamin, 75 parts of nicotinamide, 745 parts of L-ascorbic acid, 50 parts of D-calcium pantothenate and the balance of starch, the raw materials are processed and then are mixed uniformly in a vacuum drying mixer, and the compound nutrient enhancer premix of tablets, powder or capsules is prepared.
The raw materials are respectively sieved by a 60-mesh sieve, phosphatidylserine, (6S) -5-methyltetrahydrofolate calcium, a compound nutrient enhancer premix, calcium carbonate, magnesium carbonate, ferrous gluconate, zinc gluconate, retinyl palmitate, vitamin D3, D- α -tocopherol and taurine are mixed for 30min by a powder mixer according to the formula amount to prepare a mixture A, and linseed oil microcapsule powder, walnut oil microcapsule powder, DHA algal oil microcapsule powder, soybean protein isolate and the mixture A are uniformly mixed for 20-40min by a vacuum drying mixer to prepare the powdery nutrient composition for improving the hypoevolutism, wherein each bag is 20 g, and the daily dose is 60 g.
298 children of 20 months to 5 years old with short stature and different language and motor ability from the same age are selected, the children are diagnosed as children with hypoevolutism in a children hospital, and after the children are taken for 6 months to 12 months, the physique development index, the language and the motor ability evaluation index of 260 children are close to the level of the same age or have no difference with the level of the same age.
The above description is only for the purpose of illustrating preferred embodiments of the present invention and is not to be construed as limiting the invention, and the present invention is not limited to the above examples, and those skilled in the art should also be able to make various changes, modifications, additions or substitutions within the spirit and scope of the present invention.
Claims (7)
1. The nutritional composition for improving the hypoevolutism is characterized by comprising, by weight, 30-80 parts of plant seed oil microcapsule powder containing α -linolenic acid, 20-100 parts of animal and vegetable oil microcapsule powder containing DHA, 0.001-0.008 part of phosphatidylserine, 0.001-0.005 part of (6S) -5-methyltetrahydrofolate, 1-5 parts of vitamin composition premix, 5-35 parts of calcium carbonate, 0.2-25 parts of magnesium carbonate, 0.5-6 parts of ferrous gluconate, 0.1-3 parts of zinc gluconate, 0.01-0.1 part of retinyl palmitate, 0.01-0.05 part of vitamin D3, 0.1-2 parts of D- α -tocopherol, 0.1-5 parts of taurine and 5-25 parts of soybean protein isolate powder.
2. The nutritional composition for improving developmental delay of claim 1, wherein the plant seed oil microcapsule powder containing α -linolenic acid comprises linseed oil microcapsule powder and walnut oil microcapsule powder, and the weight ratio of the linseed oil microcapsule powder to the walnut oil microcapsule powder is 2:3-5: 1.
3. The nutritional composition for improving developmental delay according to claim 2, wherein the DHA-containing animal and vegetable oil microcapsule powder is DHA algae oil microcapsule powder, fish oil microcapsule powder and/or lecithin DHA yolk microcapsule powder.
4. The nutritional composition for improving developmental delay according to claim 3, wherein the vitamin composition premix is a compound nutrient supplement premix, and each 1000 parts of the compound nutrient supplement premix comprises 10-15 parts of thiamine hydrochloride, 10-15 parts of riboflavin, 10-15 parts of pyridoxine hydrochloride, 1-5 parts of cobalamin, 65-80 parts of nicotinamide, 740-.
5. A nutritional composition for improving developmental delay according to claim 1 wherein the salt of (6S) -5-methyltetrahydrofolate is glucosamine (6S) -5-methyltetrahydrofolate or a mixture of calcium (6S) -5-methyltetrahydrofolate and (6S) -5-methyltetrahydrofolate.
6. The nutritional composition for improving hypoevolutism according to claim 4, wherein the amount of the linseed oil microcapsule powder is 30 parts, the amount of the walnut oil microcapsule powder is 20 parts, the amount of the DHA algal oil microcapsule powder is 20 parts, the amount of the phosphatidylserine is 0.005 part, the amount of the (6S) -5-methyltetrahydrofolate glucosamine salt is 0.003 part, the amount of the compound nutrient premix is 3 parts, the amount of the calcium carbonate is 5 parts, the amount of the magnesium carbonate is 2 parts, the amount of the ferrous gluconate is 1 part, the amount of the zinc gluconate is 0.1 part, the amount of the retinyl palmitate is 0.01 part, the amount of the vitamin D3 is 0.02 part, and the amount of the D- α -tocopherol is 0.2 part.
7. A process for the preparation of a nutritional composition for the amelioration of developmental delay according to any of claims 1-6, comprising the steps of:
(1) sieving plant seed oil microcapsule powder containing α -linolenic acid, animal and vegetable oil microcapsule powder containing DHA, phosphatidylserine, 6S-5-methyltetrahydrofolate, vitamin composition premix, calcium carbonate, magnesium carbonate, ferrous gluconate, zinc gluconate, retinyl palmitate, vitamin D3, D- α -tocopherol, taurine and soybean protein isolate powder respectively;
(2) placing the sieved phosphatidylserine, (6S) -5-methyltetrahydrofolate, vitamin composition premix, calcium carbonate, magnesium carbonate, ferrous gluconate, zinc gluconate, retinyl palmitate, vitamin D3, D- α -tocopherol and taurine into a powder mixer, and uniformly mixing to obtain a mixture A;
(3) placing the sieved plant seed oil microcapsule powder containing α -linolenic acid, animal and plant oil microcapsule powder containing DHA, soybean protein isolate powder and the mixture A in the step (2) into a vacuum drying mixer to be uniformly mixed to obtain the nutritional composition for improving the hypoevolutism;
(4) and (4) preparing the nutrient composition for improving the hypoevolutism in the step (3) into powder, tablets or capsules.
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CN107348480A (en) * | 2017-05-19 | 2017-11-17 | 云南雪域印象生物科技有限公司 | Walnut oil microcapsule albumen powder |
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US20060217386A1 (en) * | 2005-03-10 | 2006-09-28 | Edwards John B | Nutritional preparations |
CN102458150A (en) * | 2009-06-02 | 2012-05-16 | 雀巢产品技术援助有限公司 | Nutritional composition for supporting brain development and function of toddlers |
CN107348480A (en) * | 2017-05-19 | 2017-11-17 | 云南雪域印象生物科技有限公司 | Walnut oil microcapsule albumen powder |
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