CN116268416A - Composition containing maltodextrin and crystalline fructose and preparation method thereof - Google Patents
Composition containing maltodextrin and crystalline fructose and preparation method thereof Download PDFInfo
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- CN116268416A CN116268416A CN202310479411.2A CN202310479411A CN116268416A CN 116268416 A CN116268416 A CN 116268416A CN 202310479411 A CN202310479411 A CN 202310479411A CN 116268416 A CN116268416 A CN 116268416A
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- crystalline fructose
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- 239000000203 mixture Substances 0.000 title claims abstract description 38
- 229930091371 Fructose Natural products 0.000 title claims abstract description 25
- 239000005715 Fructose Substances 0.000 title claims abstract description 25
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 title claims abstract description 25
- 239000005913 Maltodextrin Substances 0.000 title claims abstract description 17
- 229920002774 Maltodextrin Polymers 0.000 title claims abstract description 17
- 229940035034 maltodextrin Drugs 0.000 title claims abstract description 17
- 238000002360 preparation method Methods 0.000 title claims abstract description 8
- 235000015872 dietary supplement Nutrition 0.000 claims abstract description 18
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 23
- 239000008103 glucose Substances 0.000 claims description 23
- QAQJMLQRFWZOBN-LAUBAEHRSA-N L-ascorbyl-6-palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](O)[C@H]1OC(=O)C(O)=C1O QAQJMLQRFWZOBN-LAUBAEHRSA-N 0.000 claims description 18
- 239000011786 L-ascorbyl-6-palmitate Substances 0.000 claims description 18
- 235000010385 ascorbyl palmitate Nutrition 0.000 claims description 18
- 240000000111 Saccharum officinarum Species 0.000 claims description 15
- 235000007201 Saccharum officinarum Nutrition 0.000 claims description 15
- OENHQHLEOONYIE-UKMVMLAPSA-N all-trans beta-carotene Natural products CC=1CCCC(C)(C)C=1/C=C/C(/C)=C/C=C/C(/C)=C/C=C/C=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C OENHQHLEOONYIE-UKMVMLAPSA-N 0.000 claims description 15
- TUPZEYHYWIEDIH-WAIFQNFQSA-N beta-carotene Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)CCCC1(C)C)C=CC=C(/C)C=CC2=CCCCC2(C)C TUPZEYHYWIEDIH-WAIFQNFQSA-N 0.000 claims description 15
- 235000013734 beta-carotene Nutrition 0.000 claims description 15
- 239000011648 beta-carotene Substances 0.000 claims description 15
- 229960002747 betacarotene Drugs 0.000 claims description 15
- 150000008442 polyphenolic compounds Chemical class 0.000 claims description 15
- 235000013824 polyphenols Nutrition 0.000 claims description 15
- OENHQHLEOONYIE-JLTXGRSLSA-N β-Carotene Chemical compound CC=1CCCC(C)(C)C=1\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C OENHQHLEOONYIE-JLTXGRSLSA-N 0.000 claims description 15
- SERLAGPUMNYUCK-DCUALPFSSA-N 1-O-alpha-D-glucopyranosyl-D-mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O SERLAGPUMNYUCK-DCUALPFSSA-N 0.000 claims description 10
- 235000010439 isomalt Nutrition 0.000 claims description 10
- 239000000905 isomalt Substances 0.000 claims description 10
- HPIGCVXMBGOWTF-UHFFFAOYSA-N isomaltol Natural products CC(=O)C=1OC=CC=1O HPIGCVXMBGOWTF-UHFFFAOYSA-N 0.000 claims description 10
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 claims description 8
- PVXPPJIGRGXGCY-TZLCEDOOSA-N 6-O-alpha-D-glucopyranosyl-D-fructofuranose Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OC[C@@H]1[C@@H](O)[C@H](O)C(O)(CO)O1 PVXPPJIGRGXGCY-TZLCEDOOSA-N 0.000 claims description 5
- 235000001727 glucose Nutrition 0.000 claims description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 4
- 239000002994 raw material Substances 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 3
- NOESYZHRGYRDHS-UHFFFAOYSA-N insulin Chemical compound N1C(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(NC(=O)CN)C(C)CC)CSSCC(C(NC(CO)C(=O)NC(CC(C)C)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CCC(N)=O)C(=O)NC(CC(C)C)C(=O)NC(CCC(O)=O)C(=O)NC(CC(N)=O)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CSSCC(NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2C=CC(O)=CC=2)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2NC=NC=2)NC(=O)C(CO)NC(=O)CNC2=O)C(=O)NCC(=O)NC(CCC(O)=O)C(=O)NC(CCCNC(N)=N)C(=O)NCC(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC(O)=CC=3)C(=O)NC(C(C)O)C(=O)N3C(CCC3)C(=O)NC(CCCCN)C(=O)NC(C)C(O)=O)C(=O)NC(CC(N)=O)C(O)=O)=O)NC(=O)C(C(C)CC)NC(=O)C(CO)NC(=O)C(C(C)O)NC(=O)C1CSSCC2NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(N)CC=1C=CC=CC=1)C(C)C)CC1=CN=CN1 NOESYZHRGYRDHS-UHFFFAOYSA-N 0.000 abstract description 14
- 206010022489 Insulin Resistance Diseases 0.000 abstract description 10
- 230000002980 postoperative effect Effects 0.000 abstract description 10
- 208000001072 type 2 diabetes mellitus Diseases 0.000 abstract description 10
- 102000004877 Insulin Human genes 0.000 abstract description 7
- 108090001061 Insulin Proteins 0.000 abstract description 7
- 229940125396 insulin Drugs 0.000 abstract description 7
- 235000013305 food Nutrition 0.000 abstract description 3
- 230000035945 sensitivity Effects 0.000 abstract description 2
- 230000000052 comparative effect Effects 0.000 description 11
- 230000000694 effects Effects 0.000 description 9
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 241000700159 Rattus Species 0.000 description 7
- 210000004369 blood Anatomy 0.000 description 7
- 239000008280 blood Substances 0.000 description 7
- 238000009472 formulation Methods 0.000 description 5
- 235000016709 nutrition Nutrition 0.000 description 5
- 238000001356 surgical procedure Methods 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 239000001103 potassium chloride Substances 0.000 description 4
- 235000011164 potassium chloride Nutrition 0.000 description 4
- 238000011084 recovery Methods 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 229910001868 water Inorganic materials 0.000 description 4
- 230000003187 abdominal effect Effects 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- 206010009944 Colon cancer Diseases 0.000 description 2
- 206010058467 Lung neoplasm malignant Diseases 0.000 description 2
- 208000035965 Postoperative Complications Diseases 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 230000001133 acceleration Effects 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 150000001720 carbohydrates Chemical class 0.000 description 2
- 235000014633 carbohydrates Nutrition 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000002695 general anesthesia Methods 0.000 description 2
- 230000036737 immune function Effects 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 201000005202 lung cancer Diseases 0.000 description 2
- 208000020816 lung neoplasm Diseases 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 239000013589 supplement Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 description 1
- 206010007733 Catabolic state Diseases 0.000 description 1
- 208000001333 Colorectal Neoplasms Diseases 0.000 description 1
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- QGMRQYFBGABWDR-UHFFFAOYSA-M Pentobarbital sodium Chemical compound [Na+].CCCC(C)C1(CC)C(=O)NC(=O)[N-]C1=O QGMRQYFBGABWDR-UHFFFAOYSA-M 0.000 description 1
- FPIPGXGPPPQFEQ-BOOMUCAASA-N Vitamin A Natural products OC/C=C(/C)\C=C\C=C(\C)/C=C/C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-BOOMUCAASA-N 0.000 description 1
- 229930003268 Vitamin C Natural products 0.000 description 1
- 210000001015 abdomen Anatomy 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000002730 additional effect Effects 0.000 description 1
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 1
- 230000003064 anti-oxidating effect Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 208000029742 colonic neoplasm Diseases 0.000 description 1
- 208000002925 dental caries Diseases 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000000667 effect on insulin Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 230000002757 inflammatory effect Effects 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 230000003871 intestinal function Effects 0.000 description 1
- 239000007928 intraperitoneal injection Substances 0.000 description 1
- 238000010253 intravenous injection Methods 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 238000002690 local anesthesia Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 235000003715 nutritional status Nutrition 0.000 description 1
- 230000003204 osmotic effect Effects 0.000 description 1
- 229960002275 pentobarbital sodium Drugs 0.000 description 1
- 210000005259 peripheral blood Anatomy 0.000 description 1
- 239000011886 peripheral blood Substances 0.000 description 1
- 230000001766 physiological effect Effects 0.000 description 1
- 238000011470 radical surgery Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 238000013112 stability test Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
- 235000019155 vitamin A Nutrition 0.000 description 1
- 239000011719 vitamin A Substances 0.000 description 1
- 239000011718 vitamin C Substances 0.000 description 1
- 235000019154 vitamin C Nutrition 0.000 description 1
- 229940045997 vitamin a Drugs 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/125—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives containing carbohydrate syrups; containing sugars; containing sugar alcohols; containing starch hydrolysates
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
- A23L27/30—Artificial sweetening agents
- A23L27/33—Artificial sweetening agents containing sugars or derivatives
- A23L27/34—Sugar alcohols
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/105—Plant extracts, their artificial duplicates or their derivatives
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/15—Vitamins
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A40/00—Adaptation technologies in agriculture, forestry, livestock or agroalimentary production
- Y02A40/90—Adaptation technologies in agriculture, forestry, livestock or agroalimentary production in food processing or handling, e.g. food conservation
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Nutrition Science (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Mycology (AREA)
- Molecular Biology (AREA)
- Botany (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
The invention provides a composition containing maltodextrin and crystalline fructose and a preparation method thereof, and relates to the field of medical formula foods. The composition has excellent efficacy, good safety and high stability, and can be used for preparing preoperative nutritional supplements so as to promote the sensitivity of the body to insulin and relieve postoperative insulin resistance.
Description
Technical Field
The invention relates to the field of medical formula foods, in particular to a composition containing maltodextrin and crystalline fructose and a preparation method thereof.
Background
Usually, patients need fasted fluid before selecting general anesthesia or local anesthesia, but carbohydrate loss in the patient after water forbidding is difficult to supplement, so that about 2 hours before operation, some nutritional compositions can be supplemented, thereby being beneficial to operation development and postoperative recovery. At present, modes of intravenous injection of 10% glucose and the like are commonly used, but generally, the compliance of patients in the method is poor, urine is increased due to too fast absorption, kidney burden is caused, and compared with the oral nutritional supplement, the oral nutritional supplement is higher in acceptance and more convenient.
Related studies, such as literature: li Rong, deng Fang use of a preoperative oral nutritional supplement in rapid rehabilitation therapy of colorectal cancer patients [ J ]. Colorectal anal surgery, 2019,25 (2): 5: in the rapid rehabilitation of patients with laparoscopic colon cancer radical surgery, the oral nutritional supplement for the patients before surgery can improve the immune function and the nutritional state of the patients, reduce the level of inflammatory factors and promote the recovery of intestinal functions after surgery. Furthermore, literature: zhou Yujing the effects of the intervention time of the oral nutritional supplement on postoperative complications and nutritional indexes of patients with thoracoscopic lung cancer [ J ]. International journal of protection, 2023,42 (02): 341-344. The study also shows that the oral nutritional supplement can effectively improve the nutritional status and immune function of patients with thoracoscopic lung cancer in the perioperative period, reduce the incidence rate of the complications of the patients, promote postoperative rehabilitation of the patients, and has better effect before operation.
Besides the literature, another patent CN107692221A discloses a nutritional supplement for patients to drink before surgery, which consists of water, sodium chloride, potassium chloride, glucose and an acidic pH regulator, and is characterized in that the proportion of the sodium chloride to the potassium chloride is (4-5): 1, the proportion of the glucose to the potassium chloride is (60-210): 1, and the content of the potassium chloride in the supplement is 0.2-0.4 g/L, thereby being beneficial to postoperative recovery and reducing the risk of surgery. And patent CN108835616a discloses a nutritional supplement for pre-operative consumption by patients consisting of only water, maltodextrin, fructose and pH regulator, which provides sufficient calories while having a low osmotic pressure, and which is safer for pre-operative, especially general anesthesia, patients without other additives than pH regulator.
From the above, the applicable surface of the preoperative nutritional supplement plays a key role in reducing postoperative complications, shortening recovery time and the like. However, up to now, the use of excessive amounts of some nutritional supplement additives causes safety hazards or there is a poor product stability, which in turn results in additional effects and even further increases safety risks. In response to such problems, it is necessary to find a nutritional supplement that is excellent in efficacy, safe and stable.
Disclosure of Invention
Aiming at the problems existing in the prior art, the invention provides a composition containing maltodextrin and crystalline fructose and a preparation method thereof, and the composition has excellent efficacy, good safety and high stability, and can be used for preparing a preoperative nutritional supplement so as to relieve postoperative insulin resistance.
In order to achieve the above purpose, the technical scheme adopted by the invention is as follows:
the invention provides a composition, which comprises maltodextrin, crystalline fructose, glucose, ascorbyl palmitate, sugarcane polyphenol, isomalt and beta-carotene as raw materials.
Further, the composition comprises the following components in parts by weight: 60-90 parts of maltodextrin, 15-30 parts of crystalline fructose, 5-12 parts of glucose, 0.2-0.3 part of ascorbyl palmitate, 2-3 parts of sugarcane polyphenol, 0.1-0.2 part of isomalt and 0.1-0.3 part of beta-carotene.
Preferably, the composition comprises the following components in parts by weight: 80 parts of maltodextrin, 20 parts of crystalline fructose, 10 parts of glucose, 0.3 part of ascorbyl palmitate, 2.5 parts of sugarcane polyphenol, 0.2 part of isomalt and 0.2 part of beta-carotene.
Further, the weight ratio of the crystalline fructose to the glucose to the sugarcane polyphenol is 15-30:5-12:2-3. Preferably 20:10:2.5.
Further, the weight ratio of the ascorbyl palmitate to the isomalt to the beta-carotene is 0.2-0.3:0.1-0.2:0.1-0.3. Preferably 0.3:0.2:0.2.
Further, the invention provides a preparation method of the composition, which comprises the following steps: mixing maltodextrin, crystalline fructose, glucose, ascorbyl palmitate, sugarcane polyphenol, isomaltulose alcohol and beta-carotene.
Further, the composition provided by the invention can be used for preparing a preoperative nutritional supplement.
Further, the preoperative nutritional supplement also comprises water and other auxiliary materials which are suitable for being added in medical foods.
The invention has the technical effects that:
the product has excellent efficacy, good safety and high stability, wherein maltodextrin, crystalline fructose and glucose are used as carbohydrates and are easy to be absorbed by human bodies; the ascorbyl palmitate in the product has all the physiological activities of vitamin C, and the stability is higher; the sugarcane polyphenol can block active/passive transportation of glucose, control the rate of entering blood, reduce the blood sugar reaction after eating, and have corresponding regulation effect by matching with crystalline fructose; isomalt can adjust the taste of the nutritional agent, and has high stability, low energy and non-caries property; beta-carotene can be converted into vitamin A by human body according to the requirement, and has good antioxidation effect. Compared with additives added into other products, the product of the invention is safer and more stable, and according to research, the invention discovers that good interaction exists among crystalline fructose, glucose and sugarcane polyphenol and among ascorbyl palmitate, isomaltulose alcohol and beta-carotene, thus being capable of effectively controlling the absorption rate of the nutritional supplement, improving the sensitivity of the organism to insulin, relieving insulin resistance, improving the stability of the nutritional agent to a certain extent and prolonging the quality guarantee time; especially, the latter three materials can obtain better effect even in micro-adjustment.
Detailed Description
Other advantages and effects of the present invention will become apparent to those skilled in the art from the following disclosure, which describes the embodiments of the present invention with reference to specific examples. The invention may be practiced or carried out in other embodiments that depart from the specific details, and the details of the present description may be modified or varied from the spirit and scope of the present invention.
Before the embodiments of the invention are explained in further detail, it is to be understood that the invention is not limited in its scope to the particular embodiments described below; it is also to be understood that the terminology used in the examples of the invention is for the purpose of describing particular embodiments only, and is not intended to limit the scope of the invention.
Where numerical ranges are provided in the examples, it is understood that unless otherwise stated herein, both endpoints of each numerical range and any number between the two endpoints are significant both in the numerical range. Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs.
It should be noted that the raw materials used in the present invention are all common commercial products, and therefore the sources thereof are not particularly limited.
Examples 1 to 3 and comparative examples 1 to 5
Table 1 example formulation (Unit: parts by weight)
Raw materials | Example 1 | Example 2 | Example 3 |
Maltodextrin | 60 | 90 | 80 |
Crystalline fructose | 15 | 30 | 20 |
Glucose | 5 | 12 | 10 |
Ascorbyl palmitate | 0.2 | 0.3 | 0.3 |
Sugarcane polyphenol | 2 | 3 | 2.5 |
Isomalt | 0.1 | 0.2 | 0.2 |
Beta-carotene | 0.1 | 0.3 | 0.2 |
Table 2 comparative example formulation (Unit: parts by weight)
The preparation method of the compositions of examples 1-3 and comparative example 1 comprises the following steps: mixing maltodextrin, crystalline fructose, glucose, ascorbyl palmitate, sugarcane polyphenol, isomaltulose alcohol and beta-carotene. The compositions of comparative examples 2-5 were prepared without the addition of the corresponding starting materials.
1. Stability acceleration test
The test method comprises the following steps: the products in each example are placed for 3 months under the conditions that the temperature is 40 ℃ and the humidity is 75%, three indexes of crystalline fructose and ascorbyl palmitate are selected, the change condition of each index before and after the test is examined, and the initial detection result is taken as 100% reference.
TABLE 3 stability acceleration test results
Examples | Crystalline fructose (%) | Ascorbyl palmitate (%) |
Example 1 | 100.6 | 91.3 |
Example 2 | 99.8 | 93.5 |
Example 3 | 100.2 | 96.7 |
Comparative example 1 | 84.4 | 68.1 |
Comparative example 2 | 90.3 | 64.2 |
Comparative example 3 | 85.0 | 58.0 |
Comparative example 4 | 73.9 | 36.3 |
Comparative example 5 | 87.2 | 60.5 |
According to the table, the product provided by the invention has good stability, and can effectively promote the stability among various components. In contrast, when the formulation was adjusted, the crystalline fructose or ascorbyl palmitate had reduced component content after the accelerated stability test.
2. Effect of the compositions of the present invention on post-operative insulin resistance
Test animals: SD rats total 80, male, weight 220-240g;
the test method comprises the following steps: randomly dividing rats into 10 groups, wherein 8 rats in each group are not treated, performing abdominal operation after the rest rats are anesthetized by intraperitoneal injection of 1% pentobarbital sodium solution, and suturing after 5cm and 5min of a median incision in the abdomen; one group of rats subjected to abdominal operation was selected as a control group, the rats of the group were not preoperatively perfused with the composition of the present invention, and the remaining rats of the group subjected to abdominal operation were preoperatively perfused with the composition (5 mL, mass fraction: 10%) in each example of stomach for 1h, and 5 μl of peripheral blood samples were collected for 5h before and 1h after each operation to detect fasting blood glucose and fasting insulin content, while calculating insulin resistance index: insulin resistance index = fasting insulin x fasting blood glucose/22.5.
TABLE 4 fasting blood glucose and fasting insulin conditions
( And (3) injection: * : intra-group postoperative pre-operative comparison, p < 0.05,: comparing intra-group postoperative with preoperative comparison, wherein p is less than 0.01; #: comparing the group with the control group, p < 0.05, # #: p < 0.01 compared with the control group. )
TABLE 5 insulin resistance test results
( And (3) injection: * : intra-group postoperative pre-operative comparison, p < 0.05,: comparing intra-group postoperative with preoperative comparison, wherein p is less than 0.01; #: comparing the group with the control group, p < 0.05, # #: p < 0.01 compared with the control group. )
As is clear from the above table, the operation causes the body to undergo catabolic reaction and at the same time insulin resistance to increase, but the efficiency of insulin to promote the uptake and utilization of glucose and the like is lowered, thereby causing insulin resistance. The composition can effectively regulate insulin so as to stabilize blood sugar, and the insulin resistance index between groups and in groups is reduced; the composition in comparative example 1 was not remarkable in the regulation effect on insulin and the like due to unreasonable formulation matching, and the increment of blood sugar was also large, and the composition in the remaining comparative examples was weaker in the whole than the formulation of the present application, although having the corresponding regulation effect.
Finally, it should be noted that the above description is only for illustrating the technical solution of the present invention, and not for limiting the scope of the present invention, and that the simple modification and equivalent substitution of the technical solution of the present invention can be made by those skilled in the art without departing from the spirit and scope of the technical solution of the present invention.
Claims (10)
1. A composition characterized by: the raw materials comprise maltodextrin, crystalline fructose, glucose, ascorbyl palmitate, sugarcane polyphenol, isomaltulose and beta-carotene.
2. The composition of claim 1, wherein: the weight portion of the composition comprises: 60-90 parts of maltodextrin, 15-30 parts of crystalline fructose, 5-12 parts of glucose, 0.2-0.3 part of ascorbyl palmitate, 2-3 parts of sugarcane polyphenol, 0.1-0.2 part of isomalt and 0.1-0.3 part of beta-carotene.
3. The composition of claim 2, wherein: the weight portion of the composition comprises: 80 parts of maltodextrin, 20 parts of crystalline fructose, 10 parts of glucose, 0.3 part of ascorbyl palmitate, 2.5 parts of sugarcane polyphenol, 0.2 part of isomalt and 0.2 part of beta-carotene.
4. The composition of claim 1, wherein: the weight ratio of the crystalline fructose to the glucose to the sugarcane polyphenol is 15-30:5-12:2-3.
5. The composition of claim 4, wherein: the weight ratio of the crystalline fructose to the glucose to the sugarcane polyphenol is 20:10:2.5.
6. The composition of claim 1, wherein: the weight ratio of the ascorbyl palmitate to the isomalt to the beta-carotene is 0.2-0.3:0.1-0.2:0.1-0.3.
7. The composition of claim 6, wherein: the weight ratio of the ascorbyl palmitate to the isomalt to the beta-carotene is 0.3:0.2:0.2.
8. A method of preparing a composition according to any one of claims 1 to 7, wherein: the method comprises the following steps: mixing maltodextrin, crystalline fructose, glucose, ascorbyl palmitate, sugarcane polyphenol, isomaltulose alcohol and beta-carotene.
9. Use of a composition according to any one of claims 1-7 for the preparation of a pre-operative nutritional supplement.
10. A preoperative nutritional supplement characterized by: comprising the composition of any one of claims 1-7.
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