LU504846B1 - Golden spherical membrane protein factor for regulating immune function of human body - Google Patents
Golden spherical membrane protein factor for regulating immune function of human body Download PDFInfo
- Publication number
- LU504846B1 LU504846B1 LU504846A LU504846A LU504846B1 LU 504846 B1 LU504846 B1 LU 504846B1 LU 504846 A LU504846 A LU 504846A LU 504846 A LU504846 A LU 504846A LU 504846 B1 LU504846 B1 LU 504846B1
- Authority
- LU
- Luxembourg
- Prior art keywords
- solution
- spherical membrane
- deep
- human body
- protein factor
- Prior art date
Links
- 108010052285 Membrane Proteins Proteins 0.000 title claims abstract description 34
- 102000018697 Membrane Proteins Human genes 0.000 title claims abstract description 33
- 230000001105 regulatory effect Effects 0.000 title claims abstract description 29
- 230000036737 immune function Effects 0.000 title claims abstract description 28
- 108090000765 processed proteins & peptides Proteins 0.000 claims abstract description 61
- 241000283690 Bos taurus Species 0.000 claims abstract description 59
- 239000012528 membrane Substances 0.000 claims abstract description 56
- 241001046595 Mora moro Species 0.000 claims abstract description 53
- 238000003756 stirring Methods 0.000 claims abstract description 50
- 239000005862 Whey Substances 0.000 claims abstract description 41
- 108010046377 Whey Proteins Proteins 0.000 claims abstract description 41
- 102000007544 Whey Proteins Human genes 0.000 claims abstract description 41
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 40
- 108010046075 Thymosin Proteins 0.000 claims abstract description 36
- 102000007501 Thymosin Human genes 0.000 claims abstract description 32
- LCJVIYPJPCBWKS-NXPQJCNCSA-N thymosin Chemical compound SC[C@@H](N)C(=O)N[C@H](CO)C(=O)N[C@H](CC(O)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)N[C@H](C(C)C)C(=O)N[C@H](CC(O)=O)C(=O)N[C@H](C(C)C)C(=O)N[C@H](CO)C(=O)N[C@H](CO)C(=O)N[C@H](CCC(O)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@H]([C@H](C)O)C(=O)N[C@H](C(C)C)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CC(O)=O)C(=O)N[C@H](CC(C)C)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CCC(O)=O)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CCC(O)=O)C(=O)N[C@H](C(C)C)C(=O)N[C@H](C(C)C)C(=O)N[C@H](CCC(O)=O)C(=O)N[C@H](CCC(O)=O)C(=O)N[C@@H](C)C(=O)N[C@H](CCC(O)=O)C(O)=O LCJVIYPJPCBWKS-NXPQJCNCSA-N 0.000 claims abstract description 32
- 238000001914 filtration Methods 0.000 claims abstract description 29
- 239000006228 supernatant Substances 0.000 claims abstract description 17
- 235000013336 milk Nutrition 0.000 claims abstract description 15
- 239000008267 milk Substances 0.000 claims abstract description 15
- 210000004080 milk Anatomy 0.000 claims abstract description 15
- 239000000706 filtrate Substances 0.000 claims abstract description 10
- 239000000243 solution Substances 0.000 claims description 103
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 57
- 102000008186 Collagen Human genes 0.000 claims description 44
- 108010035532 Collagen Proteins 0.000 claims description 44
- 229920001436 collagen Polymers 0.000 claims description 44
- 238000010438 heat treatment Methods 0.000 claims description 30
- 210000001541 thymus gland Anatomy 0.000 claims description 30
- 238000000227 grinding Methods 0.000 claims description 24
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 24
- 238000010411 cooking Methods 0.000 claims description 21
- 230000007062 hydrolysis Effects 0.000 claims description 21
- 238000006460 hydrolysis reaction Methods 0.000 claims description 21
- 238000002360 preparation method Methods 0.000 claims description 21
- 239000002994 raw material Substances 0.000 claims description 18
- 238000005406 washing Methods 0.000 claims description 18
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 14
- 239000000084 colloidal system Substances 0.000 claims description 14
- 238000005086 pumping Methods 0.000 claims description 14
- 238000002791 soaking Methods 0.000 claims description 14
- 238000005554 pickling Methods 0.000 claims description 12
- 239000007864 aqueous solution Substances 0.000 claims description 10
- 239000007788 liquid Substances 0.000 claims description 10
- 239000012141 concentrate Substances 0.000 claims description 8
- 102000004190 Enzymes Human genes 0.000 claims description 7
- 108090000790 Enzymes Proteins 0.000 claims description 7
- 239000005909 Kieselgur Substances 0.000 claims description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 7
- 239000002253 acid Substances 0.000 claims description 7
- 239000003513 alkali Substances 0.000 claims description 7
- 238000001816 cooling Methods 0.000 claims description 7
- 230000007071 enzymatic hydrolysis Effects 0.000 claims description 7
- 238000006047 enzymatic hydrolysis reaction Methods 0.000 claims description 7
- 238000000605 extraction Methods 0.000 claims description 7
- 238000004108 freeze drying Methods 0.000 claims description 7
- 230000002779 inactivation Effects 0.000 claims description 7
- 230000007935 neutral effect Effects 0.000 claims description 7
- 238000001556 precipitation Methods 0.000 claims description 7
- 238000001694 spray drying Methods 0.000 claims description 7
- 230000001954 sterilising effect Effects 0.000 claims description 7
- 238000004659 sterilization and disinfection Methods 0.000 claims description 7
- 239000003929 acidic solution Substances 0.000 claims description 4
- 239000012670 alkaline solution Substances 0.000 claims description 4
- 238000007710 freezing Methods 0.000 claims description 2
- 230000008014 freezing Effects 0.000 claims description 2
- 239000007902 hard capsule Substances 0.000 claims description 2
- 239000002893 slag Substances 0.000 claims description 2
- 239000007901 soft capsule Substances 0.000 claims description 2
- 239000003826 tablet Substances 0.000 claims description 2
- 238000001035 drying Methods 0.000 claims 1
- 235000013402 health food Nutrition 0.000 abstract description 2
- 238000006243 chemical reaction Methods 0.000 description 25
- 210000003491 skin Anatomy 0.000 description 21
- 235000018102 proteins Nutrition 0.000 description 18
- 102000004169 proteins and genes Human genes 0.000 description 18
- 108090000623 proteins and genes Proteins 0.000 description 18
- 208000024891 symptom Diseases 0.000 description 18
- 206010022000 influenza Diseases 0.000 description 15
- 239000000047 product Substances 0.000 description 15
- 108010088751 Albumins Proteins 0.000 description 7
- 102000009027 Albumins Human genes 0.000 description 7
- 239000000843 powder Substances 0.000 description 7
- 230000000694 effects Effects 0.000 description 6
- 230000036039 immunity Effects 0.000 description 6
- 230000002378 acidificating effect Effects 0.000 description 5
- 239000002775 capsule Substances 0.000 description 5
- 239000000306 component Substances 0.000 description 5
- 230000002255 enzymatic effect Effects 0.000 description 5
- 230000036541 health Effects 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 238000012856 packing Methods 0.000 description 5
- 239000002244 precipitate Substances 0.000 description 5
- 230000035484 reaction time Effects 0.000 description 5
- 230000003068 static effect Effects 0.000 description 5
- 238000001291 vacuum drying Methods 0.000 description 5
- 238000009777 vacuum freeze-drying Methods 0.000 description 5
- 206010061218 Inflammation Diseases 0.000 description 4
- 230000006872 improvement Effects 0.000 description 4
- 230000004054 inflammatory process Effects 0.000 description 4
- 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 description 4
- 238000004806 packaging method and process Methods 0.000 description 4
- 102000004196 processed proteins & peptides Human genes 0.000 description 4
- 230000036772 blood pressure Effects 0.000 description 3
- 235000005911 diet Nutrition 0.000 description 3
- 230000000378 dietary effect Effects 0.000 description 3
- 201000010099 disease Diseases 0.000 description 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 238000011160 research Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 208000001072 type 2 diabetes mellitus Diseases 0.000 description 3
- 108060003951 Immunoglobulin Proteins 0.000 description 2
- 206010022004 Influenza like illness Diseases 0.000 description 2
- 102000004877 Insulin Human genes 0.000 description 2
- 108090001061 Insulin Proteins 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 description 2
- 102000010445 Lactoferrin Human genes 0.000 description 2
- 108010063045 Lactoferrin Proteins 0.000 description 2
- ROHFNLRQFUQHCH-UHFFFAOYSA-N Leucine Natural products CC(C)CC(N)C(O)=O ROHFNLRQFUQHCH-UHFFFAOYSA-N 0.000 description 2
- XUMBMVFBXHLACL-UHFFFAOYSA-N Melanin Chemical compound O=C1C(=O)C(C2=CNC3=C(C(C(=O)C4=C32)=O)C)=C2C4=CNC2=C1C XUMBMVFBXHLACL-UHFFFAOYSA-N 0.000 description 2
- 206010033307 Overweight Diseases 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- 230000000975 bioactive effect Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000036760 body temperature Effects 0.000 description 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
- 230000003750 conditioning effect Effects 0.000 description 2
- 230000001186 cumulative effect Effects 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- 230000002708 enhancing effect Effects 0.000 description 2
- 230000003203 everyday effect Effects 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 230000002496 gastric effect Effects 0.000 description 2
- 230000012010 growth Effects 0.000 description 2
- JYGXADMDTFJGBT-VWUMJDOOSA-N hydrocortisone Chemical compound O=C1CC[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 JYGXADMDTFJGBT-VWUMJDOOSA-N 0.000 description 2
- 210000000987 immune system Anatomy 0.000 description 2
- 102000018358 immunoglobulin Human genes 0.000 description 2
- 229940125396 insulin Drugs 0.000 description 2
- CSSYQJWUGATIHM-IKGCZBKSSA-N l-phenylalanyl-l-lysyl-l-cysteinyl-l-arginyl-l-arginyl-l-tryptophyl-l-glutaminyl-l-tryptophyl-l-arginyl-l-methionyl-l-lysyl-l-lysyl-l-leucylglycyl-l-alanyl-l-prolyl-l-seryl-l-isoleucyl-l-threonyl-l-cysteinyl-l-valyl-l-arginyl-l-arginyl-l-alanyl-l-phenylal Chemical compound C([C@H](N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CS)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)N[C@@H](C)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CO)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CS)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C)C(=O)N[C@@H](CC=1C=CC=CC=1)C(O)=O)C1=CC=CC=C1 CSSYQJWUGATIHM-IKGCZBKSSA-N 0.000 description 2
- 235000021242 lactoferrin Nutrition 0.000 description 2
- 229940078795 lactoferrin Drugs 0.000 description 2
- 235000012054 meals Nutrition 0.000 description 2
- 230000003020 moisturizing effect Effects 0.000 description 2
- 235000016709 nutrition Nutrition 0.000 description 2
- 235000008935 nutritious Nutrition 0.000 description 2
- 230000001717 pathogenic effect Effects 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 108010074051 C-Reactive Protein Proteins 0.000 description 1
- 102100032752 C-reactive protein Human genes 0.000 description 1
- 206010008479 Chest Pain Diseases 0.000 description 1
- 208000035473 Communicable disease Diseases 0.000 description 1
- 206010011224 Cough Diseases 0.000 description 1
- 102000004127 Cytokines Human genes 0.000 description 1
- 108090000695 Cytokines Proteins 0.000 description 1
- 208000035240 Disease Resistance Diseases 0.000 description 1
- 208000000059 Dyspnea Diseases 0.000 description 1
- 206010013975 Dyspnoeas Diseases 0.000 description 1
- 206010014970 Ephelides Diseases 0.000 description 1
- 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 description 1
- 206010019233 Headaches Diseases 0.000 description 1
- 208000022559 Inflammatory bowel disease Diseases 0.000 description 1
- 102000007330 LDL Lipoproteins Human genes 0.000 description 1
- 108010007622 LDL Lipoproteins Proteins 0.000 description 1
- 208000002720 Malnutrition Diseases 0.000 description 1
- 208000003351 Melanosis Diseases 0.000 description 1
- 208000000112 Myalgia Diseases 0.000 description 1
- 206010028735 Nasal congestion Diseases 0.000 description 1
- 208000012902 Nervous system disease Diseases 0.000 description 1
- 208000008589 Obesity Diseases 0.000 description 1
- 206010068319 Oropharyngeal pain Diseases 0.000 description 1
- 201000007100 Pharyngitis Diseases 0.000 description 1
- 229940100389 Sulfonylurea Drugs 0.000 description 1
- 208000037063 Thinness Diseases 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 230000001195 anabolic effect Effects 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 230000002929 anti-fatigue Effects 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- 230000003064 anti-oxidating effect Effects 0.000 description 1
- 230000002155 anti-virotic effect Effects 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 230000004596 appetite loss Effects 0.000 description 1
- 230000003796 beauty Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 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 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 230000036765 blood level Effects 0.000 description 1
- 150000005693 branched-chain amino acids Chemical class 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 230000007969 cellular immunity Effects 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 230000001684 chronic effect Effects 0.000 description 1
- 208000037976 chronic inflammation Diseases 0.000 description 1
- 230000006020 chronic inflammation Effects 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 239000008358 core component Substances 0.000 description 1
- 230000002354 daily effect Effects 0.000 description 1
- 230000001934 delay Effects 0.000 description 1
- 210000004207 dermis Anatomy 0.000 description 1
- 235000018823 dietary intake Nutrition 0.000 description 1
- 235000015872 dietary supplement Nutrition 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940029980 drug used in diabetes Drugs 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 235000012631 food intake Nutrition 0.000 description 1
- 230000037406 food intake Effects 0.000 description 1
- 210000001035 gastrointestinal tract Anatomy 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 239000003102 growth factor Substances 0.000 description 1
- 231100000869 headache Toxicity 0.000 description 1
- 235000021083 high saturated fats Nutrition 0.000 description 1
- 235000020256 human milk Nutrition 0.000 description 1
- 230000004727 humoral immunity Effects 0.000 description 1
- 229960000890 hydrocortisone Drugs 0.000 description 1
- 230000002519 immonomodulatory effect Effects 0.000 description 1
- 229940088592 immunologic factor Drugs 0.000 description 1
- 239000000367 immunologic factor Substances 0.000 description 1
- 230000002757 inflammatory effect Effects 0.000 description 1
- 230000028709 inflammatory response Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000003834 intracellular effect Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 108010058587 lactokinins Proteins 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 208000019017 loss of appetite Diseases 0.000 description 1
- 235000021266 loss of appetite Nutrition 0.000 description 1
- 230000001071 malnutrition Effects 0.000 description 1
- 235000000824 malnutrition Nutrition 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 235000020124 milk-based beverage Nutrition 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 210000003205 muscle Anatomy 0.000 description 1
- 230000037257 muscle growth Effects 0.000 description 1
- 208000013465 muscle pain Diseases 0.000 description 1
- 210000002569 neuron Anatomy 0.000 description 1
- 230000000324 neuroprotective effect Effects 0.000 description 1
- 230000035764 nutrition Effects 0.000 description 1
- 208000015380 nutritional deficiency disease Diseases 0.000 description 1
- 235000003715 nutritional status Nutrition 0.000 description 1
- 235000020824 obesity Nutrition 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 230000001766 physiological effect Effects 0.000 description 1
- 230000035790 physiological processes and functions Effects 0.000 description 1
- 229920001184 polypeptide Polymers 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 230000000291 postprandial effect Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 230000008458 response to injury Effects 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 230000001502 supplementing effect Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 229940126680 traditional chinese medicines Drugs 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 206010048828 underweight Diseases 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23J—PROTEIN COMPOSITIONS FOR FOODSTUFFS; WORKING-UP PROTEINS FOR FOODSTUFFS; PHOSPHATIDE COMPOSITIONS FOR FOODSTUFFS
- A23J3/00—Working-up of proteins for foodstuffs
- A23J3/04—Animal proteins
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23J—PROTEIN COMPOSITIONS FOR FOODSTUFFS; WORKING-UP PROTEINS FOR FOODSTUFFS; PHOSPHATIDE COMPOSITIONS FOR FOODSTUFFS
- A23J1/00—Obtaining protein compositions for foodstuffs; Bulk opening of eggs and separation of yolks from whites
- A23J1/20—Obtaining protein compositions for foodstuffs; Bulk opening of eggs and separation of yolks from whites from milk, e.g. casein; from whey
- A23J1/205—Obtaining protein compositions for foodstuffs; Bulk opening of eggs and separation of yolks from whites from milk, e.g. casein; from whey from whey, e.g. lactalbumine
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23J—PROTEIN COMPOSITIONS FOR FOODSTUFFS; WORKING-UP PROTEINS FOR FOODSTUFFS; PHOSPHATIDE COMPOSITIONS FOR FOODSTUFFS
- A23J3/00—Working-up of proteins for foodstuffs
- A23J3/04—Animal proteins
- A23J3/08—Dairy proteins
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23J—PROTEIN COMPOSITIONS FOR FOODSTUFFS; WORKING-UP PROTEINS FOR FOODSTUFFS; PHOSPHATIDE COMPOSITIONS FOR FOODSTUFFS
- A23J3/00—Working-up of proteins for foodstuffs
- A23J3/30—Working-up of proteins for foodstuffs by hydrolysis
- A23J3/32—Working-up of proteins for foodstuffs by hydrolysis using chemical agents
- A23J3/34—Working-up of proteins for foodstuffs by hydrolysis using chemical agents using enzymes
- A23J3/341—Working-up of proteins for foodstuffs by hydrolysis using chemical agents using enzymes of animal proteins
- A23J3/342—Working-up of proteins for foodstuffs by hydrolysis using chemical agents using enzymes of animal proteins of collagen; of gelatin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
- A61K35/12—Materials from mammals; Compositions comprising non-specified tissues or cells; Compositions comprising non-embryonic stem cells; Genetically modified cells
- A61K35/20—Milk; Whey; Colostrum
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
- A61K35/56—Materials from animals other than mammals
- A61K35/60—Fish, e.g. seahorses; Fish eggs
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/22—Hormones
- A61K38/2292—Thymosin; Related peptides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P39/00—General protective or antinoxious agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
- C07K14/461—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from fish
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
- C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
- C07K14/4701—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals not used
- C07K14/4702—Regulators; Modulating activity
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/76—Albumins
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Zoology (AREA)
- Organic Chemistry (AREA)
- Biochemistry (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Veterinary Medicine (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Toxicology (AREA)
- Gastroenterology & Hepatology (AREA)
- Animal Behavior & Ethology (AREA)
- Polymers & Plastics (AREA)
- Pharmacology & Pharmacy (AREA)
- Food Science & Technology (AREA)
- Public Health (AREA)
- Biophysics (AREA)
- Nutrition Science (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Immunology (AREA)
- General Chemical & Material Sciences (AREA)
- Biotechnology (AREA)
- Marine Sciences & Fisheries (AREA)
- Cell Biology (AREA)
- Developmental Biology & Embryology (AREA)
- Biomedical Technology (AREA)
- Virology (AREA)
- Endocrinology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Abstract
The present invention is applicable to the technical field of health food, and provides a golden spherical membrane protein factor for regulating immune function of human body, which comprises: 30-56 parts of deep-sea cod peptide, 10-20 parts of special whey spherical membrane, and 10-44 parts of bovine thymosin; wherein, the special whey spherical membrane is obtained by adding 15-25% volume of absolute ethanol to milk, stirring evenly, and then filtering after standing for 30-60 min, adding the absolute ethanol to the obtained filtrate to make the absolute ethanol content reach 35% volume, continuously adding the absolute ethanol until the content gradually reaches 55% volume, stirring evenly, standing for 30-60min, centrifuging at 3000-5000 rpm, and pouring out the supernatant.
Description
DESCRIPTION LU504846
GOLDEN SPHERICAL MEMBRANE PROTEIN FACTOR FOR REGULATING IMMUNE
FUNCTION OF HUMAN BODY
The present invention relates to the technical field of health food, and in particular to a golden spherical membrane protein factor for regulating immune function of human body.
With the acceleration of the pace of life in the global society and the increase of work and psychological pressure, sub-health problems have gradually become the focus of attention.
Sub-health means that the human body is in a state between health and disease. Sub-health state is characterized by decreased vitality, function and adaptability for a period of time, but it does not meet the clinical or subclinical diagnostic criteria of diseases in modern medicine, among which decreased immune function is one of the most common manifestations of sub-health state. Immune system is an important part of the body to resist external pathogenic factors, including specific immunity and non-specific immunity. Under the same conditions, there are differences in resistance among individuals, and individuals with poor resistance are easily affected by pathogenic factors and get sick. Age, constitution and living habits are the main factors that affect the body's immunity. In addition, malnutrition, obesity, underweight and unbalanced dietary intake also significantly affects the function of human immune system.
Therefore, the individual's nutritional status is considered as an important index to evaluate the body's immunity, and good dietary nutrition intake is a key step to promote the body's immunity. At present, research shows that immunoglobulin and lactoferrin are ideal raw materials for immune-enhancing peptides. These raw materials have a variety of biological activities, including broad-spectrum antibacterial effects, enhancing the body's anti-virus, anti-oxidation and immune capabilities, comprehensively preventing and treating infectious diseases, maintaining the balance of gastrointestinal flora, and promoting the transfer and absorption of iron. In view of this sub-health symptom, many health-care and nutritious foods have appeared in the market one after another. Although most of the product formulas até/504846 based on immune-enhancing peptide raw materials such as immunoglobulin and lactoferrin, they still can't effectively improve sub-health symptoms because of the unscientific types and contents of ingredients in the formulas.
Embodiments of the present invention provide a golden spherical membrane protein factor for regulating immune function of human body, which aims to solve a problem that the existing health-care nutritious food cannot effectively improve sub-health symptoms due to unscientific formula component types and contents. The embodiment of the invention is realized as follows, a golden spherical membrane protein factor for regulating immune function of human body, comprises raw materials of the following parts by weight: 30-56 parts of deep-sea cod peptide, 10-20 parts of special whey spherical membrane, and 10-44 parts of bovine thymosin; wherein, a preparation method of the special whey spherical membrane is as follows: adding 15-25% volume of absolute ethanol to milk, stirring evenly, and then filtering after standing for 30-60min, adding the absolute ethanol to the obtained filtrate to make the absolute ethanol content reach 35% volume, continuously adding the absolute ethanol until the content gradually reaches 55% volume, stirring evenly, standing for 30-60min, centrifuging at 3000-5000 rpm, and pouring out the supernatant, and obtaining the special whey spherical membrane.
In an embodiment of the present application, the golden spherical membrane protein factor is prepared by deep-sea cod peptide, special whey spherical membrane and bovine thymosin according to a specific ratio, wherein the core component, special whey spherical membrane is prepared by adding 15-25% volume of absolute ethanol to milk, stirring evenly, and then filtering after standing for 30-60min, adding the absolute ethanol to the obtained filtrate to make the absolute ethanol content reach 35% volume, continuously adding the absolute ethanol until the content gradually reaches 55% volume, stirring evenly, standing for 30-60min, centrifuging at 3000-5000 rpm, and pouring out the supernatant. By adding the special deep-sea cod peptide and the bovine thymosin in proportion, the present applicatid 504846 has a scientific and reasonable formula, high nutritional value, a good curative effect on sub-health conditioning, is safe for using, and has no toxic and side effects on the body, which has positive effects on immune prevention, gastrointestinal tract health and exercise ability improvement of middle-aged and elderly people.
Hereinafter, in order to make the purpose, technical solutions and advantages of the present invention more clearly, the present invention will be further described in detail with specific embodiments. It should be understood that the specific embodiments described herein are only used to explain the present invention, and are not used to limit the present invention.
The embodiments of the present application provide a golden spherical membrane protein factor for regulating immune function of human body, comprises raw material of the following parts by weight: 30-56 parts of deep-sea cod peptide, 10-20 parts of special whey spherical membrane, and 10-44 parts of bovine thymosin; wherein, a preparation method of the special whey spherical membrane is as follows: adding 15-25% volume of absolute ethanol to milk, stirring evenly, and then filtering after standing for 30-60min, adding the absolute ethanol to the obtained filtrate to make the absolute ethanol content reach 35% volume, continuously adding the absolute ethanol until the content gradually reaches 55% volume, stirring evenly, standing for 30-60min, centrifuging at 3000-5000 rpm, and pouring out the supernatant, and obtaining the special whey spherical membrane.
Optionally, selecting fresh milk from pasture; adding 15-25% anhydrous ethanol into milk, stirring evenly, and then filtering after standing for 30-60min, adding the absolute ethanol to the obtained filtrate to make the absolute ethanol content reach 35%, continuously adding the absolute ethanol until the content gradually reaches 55%, stirring evenly, standing for 30-60min, centrifuging at 3000-5000 rpm, and pouring out the supernatant, and vacuum drying or freeze drying the obtained precipitate, grinding it to 140-180 mesh with a universal pulverizer, and making into capsules or tablets; and removing residual products, packing and storing tHé/504846 qualified ones.
Wherein, the deep-sea cod peptide is obtained by soaking deep-sea cod skin in an alkaline solution, an aqueous solution, an acidic solution, and an aqueous solution, followed by colloid grinding, enzymatic hydrolysis by heating, high temperature and high pressure, and freeze-drying.
Preferably, a preparation method of the deep-sea cod peptide is: sequentially placing the deep-sea cod skin in alkaline solution, aqueous solution, acidic solution, and aqueous solution for soaking treatment; grinding the deep-sea cod skin soaked in the aqueous solution with a colloid mill to obtain a crude collagen solution; placing the crude collagen solution at a temperature of 85-95°C with the enzymolysis liquid for stirring, heating and enzymolysis treating, and then standing for precipitation after stirring to obtain a collagen peptide solution; placing the collagen peptide solution at a temperature of 140-150°C and a pressure of 0.4-0.5mpa for high-temperature and high-pressure treatment; and freezing the collagen peptide solution after high-temperature and high-pressure treatment at -30°C for not less than 6 hours.
Optionally, selecting high-quality deep-sea cod in high-quality sea areas and cooperate with two sets of driving devices to place the deep-sea cod skin in the alkaline pool, pool, acid pool, and pool in turn; grinding: washing the deep-sea cod skin from the pool with clean water into the colloid mill and grinding into a crude collagen solution; heating and enzymatic hydrolysis: transporting the crude collagen solution to the upper reaction furnace and mixing with the enzymatic solution at 85-95°C, and after stirring, the collagen peptide solution is obtained by static precipitation; filtrating: filtering the collagen peptide solution into the lower reaction furnace; high-temperature and high-pressure treatment: the temperature in the lower reaction furnace is 140-150°C, and the pressure is 0.4-0.5mpa for high-temperature and high-pressure treatment; freeze-drying: the collagen peptide solution after high-temperature and high-pressure treatment is frozen below -30°C for more than 6 hours; the soaking time in the alkaline pool, the soaking time in the acidic pool, the grinding time of the colloid mill, tH&)504846 reaction time of the upper reaction furnace and the lower reaction furnace are all the same, which can be 30-80min, namely the deep sea cod peptide.
Wherein, the bovine thymosin is obtained by acid washing and aqueous treatment of bovine thymus, followed by cooking, slag removal, hydrolysis, concentration and spray drying.
Preferably, a preparation method of the bovine thymosin is as follows: sequentially pickling the bovine thymus with acetic acid solution and washing the bovine thymus with the water solution; adding water into a cooking tank, heating up while stirring, adding the washed bovine thymus and edible acetic acid at the same time, raising the temperature to 55°C in a lower part of the cooking pot and 65°C in an upper part thereof, keeping it warm for 60min, stopping stirring, letting stand for 0.5-1.5h, and supernatant is primary solution; immediately after standing still, pumping the primary solution into a sterilized primary solution storage tank with a vacuum extraction tank, wherein temperature of the solution is 50-60°C; pumping the primary solution into a sterilized hydrolysis tank, heating to 100°C for 15min for sterilization, cooling to 55-65°C and maintaining, adding alkali liquor to adjust pH value to neutral, adding enzyme preparation for hydrolysis for 7-9h, and then heating to 90°C for 15min for inactivation; adding diatomaceous earth and activated carbon, stirring, standing, and coarse filtering, circularly filtering for 0.5-1.5h by a plate-and-frame filter to obtain clear liquid; concentrating the clear solution to a concentration of 18-22 °Bonby a vacuum concentrator to obtain a concentrated solution; and
When the concentrate is clear, it is spray-dried to obtain the bovine thymosin.
Optionally, pickling the bovine thymus with acetic acid solution for 0.5-1.5h; then washing once with water, then pickling once with the acetic acid solution for 0.5-1.5h, and washing once with water to obtain the washed bovine thymus; cooking: adding water into a cooking tank, heating up while stirring, adding the washed bovine thymus and edible acetic acid at the same time, raising the temperature to 55°C in a lower part of the cooking pot and 65°C in an upper part thereof, keeping it warm for 60min, stopping stirring, letting stand for 0.5-1.5h, arld/504846 supernatant is primary solution; deslagging: immediately after standing still, pumping the primary solution into a sterilized primary solution storage tank with a vacuum extraction tank, wherein temperature of the solution is 55°C; hydrolysis: pumping the primary solution into a sterilized hydrolysis tank, heating to 100°C for 15min for sterilization, cooling to 55-65°C and maintaining, adding alkali liquor to adjust pH value to neutral, adding enzyme preparation for hydrolysis for 7-9h, and then heating to 90°C for 15min for inactivation; filtrating: adding diatomaceous earth and activated carbon with a mass ratio of 1:1 according to the mass ratio of 0.1%-0.2%, after stirring, standing, and coarse filtering, circularly filtering for 0.5-1.5h by a plate-and-frame filter to obtain clear liquid; concentration: concentrating the clear solution to a concentration of 18-22 °Bé by a vacuum concentrator to obtain a concentrated solution; and spray drying: when the concentrate is clear, it is spray-dried to obtain the bovine thymosin.
In another embodiment of the present application, the golden spherical membrane protein factor for regulating immune function of human body comprises raw material of the following parts by weight: 45-55 parts of the deep-sea cod peptide, 10-20 parts of the special whey spherical membrane, and 30-40 parts of the bovine thymosin.
More preferably, the golden spherical membrane protein factor for regulating immune function of human body comprises raw material of the following parts by weight: parts of the deep-sea cod peptide, 15 parts of the special whey spherical membrane, and 35 parts of the bovine thymosin.
It is worth noting that the embodiments of the present application supplement the special whey spherical membrane with the special deep-sea cod peptide and bovine thymosin in proportion. After a lot of innovative research, the formula obtained is scientific and reasonable.
Adjustment of any component or content ratio will directly affect its conditioning effect on the sub-health state. In addition, the present invention is a special dietary preparation, and the active ingredients of the preparation are all polypeptides and special whey spherical membranes. Through scientific and rational configuration, the preparation of the present invention is a special formula for restoring human breast milk, which has a function #504846 regulating immune function of human body and ensures that the human body can absorb immune factors and growth factors.
Further, a preparation method of the golden spherical membrane protein factor for regulating immune function of human body is that the obtained deep-sea cod peptide, special whey spherical membrane and bovine thymosin are evenly mixed to obtain loose powder, and the loose powder is prepared into tablets, hard capsules or soft capsules according to conventional preparation technology of traditional Chinese medicines.
The present invention is a health care product preparation, effective components of the preparation are all protein, and compatibility of the components is reasonable, and effects of each protein are as follows:
Deep-sea cod collagen peptide has small molecular weight and is easy to be absorbed.
Molecular weight of deep-sea cod collagen peptide is less than 1000Da, so it has good permeability, can be absorbed by the skin, fills in the skin matrix, stretches skin wrinkles, makes it elastic, moisturizes the skin, and delays aging. Moisturizing and moisturizing the skin Cod collagen peptides can effectively improve skin moisture. Deep-sea cod collagen peptides are rich in "macromolecular collagen” and "hydrophilic groups”, which can effectively promote the activity of collagen fiber cells, promote the synthesis of fresh collagen in the dermis of the skin, reduce the formation of melanin, remove freckles and whiten, and delay aging. Cod collagen peptide has obvious advantages both in molecular structure and physiological function, and it is the best choice for supplementing collagen and beauty.
The special whey spherical membrane is rich in a branched-chain amino acid called leucine.
Leucine is the most growth-promoting (anabolic amino acid). For this reason, special whey spherical membranes are effective in preventing age-related muscle loss and improving strength.
For muscle growth, special whey spherical membranes may be slightly better than other types of protein, such as casein or soy. Special whey spherical membranes might lower blood pressure in people with elevated blood pressure. It is due to a bioactive peptide called lactokinin. Much lower amounts of special whey spherical membranes (less than 3.25 g/day) mixed in milk drink$)504846 were not found to have a significant effect on blood pressure. Aids in the treatment of type 2 diabetes, these properties of special whey spherical membranes even rival diabetes medications such as sulfonylureas. Therefore, special whey spherical membranes can be effectively used as a complementary treatment for type 2 diabetes. Special whey spherical membranes are effective in regulating blood sugar levels, especially when taken before or with high carbohydrate meals. It may be especially useful for people with type 2 diabetes. Fights inflammation, which is part of the body's response to injury. Short-term inflammation can be beneficial, but in some cases it can become chronic. Chronic inflammation can be harmful and is a risk factor for many diseases. It may reflect an underlying medical condition or lifestyle habits that are damaging your health. High doses of special whey spherical membranes can reduce blood levels of C-reactive protein, suggesting that it can help reduce inflammation, such as in inflammatory bowel disease.
Bovine thymosin is a natural bioactive peptide with various physiological effects. An immunomodulatory effect: it can enhance the body's immunity, promote cellular immunity and humoral immunity, and inhibit inflammation. A function of growth and development: it can promote growth and development of children and increase their weight. An anti-fatigue effect: it can relieve fatigue, improve the body's endurance and disease resistance. A neuroprotective effect: it can protect nerve cells and improve the symptoms of nervous system diseases.
Hereinafter, examples of certain embodiments of the present application are given, which are not intended to limit the scope of the present application.
In addition, it should be noted that numerical values given in the following embodiments are as accurate as possible, but those skilled in the art understand that due to unavoidable measurement errors and experimental operation problems, each number should be understood as an approximation, rather than an absolutely accurate numerical value.
Embodiment 1
In the present embodiment, a golden spherical membrane protein factor for regulating immune function of human body comprises the following raw material in weight percentage: LU504846 53% of the deep sea cod peptide, 12% of the special whey spherical membrane, 35% of the bovine thymosin.
According to the formula of the above-mentioned a golden spherical membrane protein factor for regulating immune function of human body, the raw material is weighed for later use;
The deep sea cod peptide: selecting high-quality deep-sea cod in high-quality sea areas and cooperate with two sets of driving devices to place the deep-sea cod skin in an alkaline pool, a pool, an acid pool, and a pool in turn; grinding: washing the deep-sea cod skin from the pool with clean water into the colloid mill and grinding into a crude collagen solution; heating and enzymatic hydrolysis: transporting the crude collagen solution to the upper reaction furnace and mixing with the enzymatic solution at 90°C, and after stirring, the collagen peptide solution is obtained by static precipitation; filtrating: filtering the collagen peptide solution into the lower reaction furnace; high-temperature and high-pressure treatment: the temperature in the lower reaction furnace is 145°C, and the pressure is 0.4mpa for high-temperature and high-pressure treatment; freeze-drying: the collagen peptide solution after high-temperature and high-pressure treatment is frozen below -30°C for more than 6 hours; the soaking time in the alkaline pool, the soaking time in the acidic pool, the grinding time of the colloid mill, the reaction time of the upper reaction furnace and the lower reaction furnace is 50min.
The special whey spherical membrane: selecting fresh milk from pasture; adding 20% anhydrous ethanol into milk, stirring evenly, and then filtering after standing for 45min, adding the absolute ethanol to the obtained filtrate to make the absolute ethanol content reach 35%, continuously adding the absolute ethanol until the content gradually reaches 55%, stirring evenly, standing for 45min, centrifuging at 4000 rpm, and pouring out the supernatant, and vacuum drying or freeze drying the obtained precipitate, grinding it to 160 mesh with a universal pulverizer, and making into capsules or tablets; and removing residual products, packing and storing the qualified ones.
The bovine thymosin: pickling the bovine thymus with acetic acid solution for 1h; then washing once with water, then pickling once with the acetic acid solution for 1h, and washihg/504846 once with water to obtain the washed bovine thymus; cooking: adding water into a cooking tank, heating up while stirring, adding the washed bovine thymus and edible acetic acid at the same time, raising the temperature to 55°C in a lower part of the cooking pot and 65°C in an upper part thereof, keeping it warm for 60min, stopping stirring, letting stand for 1h, and supernatant is primary solution; deslagging: immediately after standing still, pumping the primary solution into a sterilized primary solution storage tank with a vacuum extraction tank, wherein temperature of the solution is 55°C; hydrolysis: pumping the primary solution into a sterilized hydrolysis tank, heating to 100°C for 15min for sterilization, cooling to 60°C and maintaining, adding alkali liquor to adjust pH value to neutral, adding enzyme preparation for hydrolysis for 8h, and then heating to 90°C for 15min for inactivation; filtrating: adding diatomaceous earth and activated carbon with a mass ratio of 1:1 according to the mass ratio of 0.2%, after stirring, standing, and coarse filtering, circularly filtering for 1h by a plate-and-frame filter to obtain clear liquid; concentration: concentrating the clear solution to a concentration of °Bé by a vacuum concentrator to obtain a concentrated solution; and spray drying: when the concentrate is clear, it is spray-dried to obtain the bovine thymosin.
The deep-sea cod peptide, the special whey spherical membrane, and the bovine thymosin peptide are evenly mixed to obtain loose powder, and the packaging is checked to obtain the golden spherical membrane protein factor product.
Embodiment 2
In the present embodiment, a golden spherical membrane protein factor for regulating immune function of human body comprises the following raw material in weight percentage: 50% of the deep sea cod peptide, 15% of the special whey spherical membrane, 35% of the bovine thymosin.
According to the formula of the above-mentioned a golden spherical membrane protein factor for regulating immune function of human body, the raw material is weighed for later use;
The deep sea cod peptide: selecting high-quality deep-sea cod in high-quality sea areas and cooperate with two sets of driving devices to place the deep-sea cod skin in an alkaline pool,l&/504846 pool, an acid pool, and a pool in turn; grinding: washing the deep-sea cod skin from the pool with clean water into the colloid mill and grinding into a crude collagen solution; heating and enzymatic hydrolysis: transporting the crude collagen solution to the upper reaction furnace and mixing with the enzymatic solution at 90°C, and after stirring, the collagen peptide solution is obtained by static precipitation; filtrating: filtering the collagen peptide solution into the lower reaction furnace; high-temperature and high-pressure treatment: the temperature in the lower reaction furnace is 145°C, and the pressure is 0.4mpa for high-temperature and high-pressure treatment; freeze-drying: the collagen peptide solution after high-temperature and high-pressure treatment is frozen below -30°C for more than 6 hours; the soaking time in the alkaline pool, the soaking time in the acidic pool, the grinding time of the colloid mill, the reaction time of the upper reaction furnace and the lower reaction furnace is 50min.
The special whey spherical membrane: selecting fresh milk from pasture; adding 20% anhydrous ethanol into milk, stirring evenly, and then filtering after standing for 45min, adding the absolute ethanol to the obtained filtrate to make the absolute ethanol content reach 35%, continuously adding the absolute ethanol until the content gradually reaches 55%, stirring evenly, standing for 45min, centrifuging at 4000 rpm, and pouring out the supernatant, and vacuum drying or freeze drying the obtained precipitate, grinding it to 160 mesh with a universal pulverizer, and making into capsules or tablets; and removing residual products, packing and storing the qualified ones.
The bovine thymosin: pickling the bovine thymus with acetic acid solution for 1h; then washing once with water, then pickling once with the acetic acid solution for 1h, and washing once with water to obtain the washed bovine thymus; cooking: adding water into a cooking tank, heating up while stirring, adding the washed bovine thymus and edible acetic acid at the same time, raising the temperature to 55°C in a lower part of the cooking pot and 65°C in an upper part thereof, keeping it warm for 60min, stopping stirring, letting stand for 1h, and supernatant is primary solution; deslagging: immediately after standing still, pumping the primary solution into a sterilized primary solution storage tank with a vacuum extraction tank,
wherein temperature of the solution is 55°C; hydrolysis: pumping the primary solution intoldJ504846 sterilized hydrolysis tank, heating to 100°C for 15min for sterilization, cooling to 60°C and maintaining, adding alkali liquor to adjust pH value to neutral, adding enzyme preparation for hydrolysis for 8h, and then heating to 90°C for 15min for inactivation; filtrating: adding diatomaceous earth and activated carbon with a mass ratio of 1:1 according to the mass ratio of 0.2%, after stirring, standing, and coarse filtering, circularly filtering for 1h by a plate-and-frame filter to obtain clear liquid; concentration: concentrating the clear solution to a concentration of °Bé by a vacuum concentrator to obtain a concentrated solution; and spray drying: when the concentrate is clear, it is spray-dried to obtain the bovine thymosin.
The deep-sea cod peptide, the special whey spherical membrane, and the bovine thymosin peptide are evenly mixed to obtain loose powder, and the packaging is checked to obtain the golden spherical membrane protein factor product.
Embodiment 3
In the present embodiment, a golden spherical membrane protein factor for regulating immune function of human body comprises the following raw material in weight percentage: 56% of the deep sea cod peptide, 11% of the special whey spherical membrane, 33% of the bovine thymosin.
According to the formula of the above-mentioned a golden spherical membrane protein factor for regulating immune function of human body, the raw material is weighed for later use;
The deep sea cod peptide: selecting high-quality deep-sea cod in high-quality sea areas and cooperating with two sets of driving devices to place the deep-sea cod skin in an alkaline pool, a pool, an acid pool, and a pool in turn; grinding: washing the deep-sea cod skin from the pool with clean water into the colloid mill and grinding into a crude collagen solution; heating and enzymatic hydrolysis: transporting the crude collagen solution to the upper reaction furnace and mixing with the enzymatic solution at 90°C, and after stirring, the collagen peptide solution is obtained by static precipitation; filtrating: filtering the collagen peptide solution into the lower reaction furnace; high-temperature and high-pressure treatment: the temperature in the lower reaction furnace is 145°C, and the pressure is 0.4mpa for high-temperature and high-pressure treatment; freeze-drying: the collagen peptide solution after high-temperatuté/504846 and high-pressure treatment is frozen below -30°C for more than 6 hours; the soaking time in the alkaline pool, the soaking time in the acidic pool, the grinding time of the colloid mill, the reaction time of the upper reaction furnace and the lower reaction furnace is 50min.
The special whey spherical membrane: selecting fresh milk from pasture; adding 20% anhydrous ethanol into milk, stirring evenly, and then filtering after standing for 45min, adding the absolute ethanol to the obtained filtrate to make the absolute ethanol content reach 35%, continuously adding the absolute ethanol until the content gradually reaches 55%, stirring evenly, standing for 45min, centrifuging at 4000 rpm, and pouring out the supernatant, and vacuum drying or freeze drying the obtained precipitate, grinding it to 160 mesh with a universal pulverizer, and making into capsules or tablets; and removing residual products, packing and storing the qualified ones.
The bovine thymosin: pickling the bovine thymus with acetic acid solution for 1h; then washing once with water, then pickling once with the acetic acid solution for 1h, and washing once with water to obtain the washed bovine thymus; cooking: adding water into a cooking tank, heating up while stirring, adding the washed bovine thymus and edible acetic acid at the same time, raising the temperature to 55°C in a lower part of the cooking pot and 65°C in an upper part thereof, keeping it warm for 60min, stopping stirring, letting stand for 1h, and supernatant is primary solution; deslagging: immediately after standing still, pumping the primary solution into a sterilized primary solution storage tank with a vacuum extraction tank, wherein temperature of the liquid is 55°C; hydrolysis: pumping the primary solution into a sterilized hydrolysis tank, heating to 100°C for 15min for sterilization, cooling to 60°C and maintaining, adding alkali liquor to adjust pH value to neutral, adding enzyme preparation for hydrolysis for 8h, and then heating to 90°C for 15min for inactivation; filtrating: adding diatomaceous earth and activated carbon with a mass ratio of 1:1 according to the mass ratio of 0.2%, after stirring, standing, and coarse filtering, circularly filtering for 1h by a plate-and-frame filter to obtain clear liquid; concentration: concentrating the clear solution to a concentration of °Bé by a vacuum concentrator to obtain a concentrated solution; and spray drying: when the concentrate is clear, it is spray-dried to obtain the bovine thymosin. LU504846
The deep-sea cod peptide, the special whey spherical membrane, and the bovine thymosin peptide are evenly mixed to obtain loose powder, and the packaging is checked to obtain the golden spherical membrane protein factor product.
Embodiment 4
In the present embodiment, a golden spherical membrane protein factor for regulating immune function of human body comprises the following raw material in weight percentage: 46% of the deep sea cod peptide, 10% of the special whey spherical membrane, 44% of the bovine thymosin.
According to the formula of the above-mentioned a golden spherical membrane protein factor for regulating immune function of human body, the raw material is weighed for later use;
The deep sea cod peptide: selecting high-quality deep-sea cod in high-quality sea areas and cooperate with two sets of driving devices to place the deep-sea cod skin in an alkaline pool, a pool, an acid pool, and a pool in turn; grinding: washing the deep-sea cod skin from the pool with clean water into the colloid mill and grinding into a crude collagen solution; heating and enzymatic hydrolysis: transporting the crude collagen solution to the upper reaction furnace and mixing with the enzymatic solution at 90°C, and after stirring, the collagen peptide solution is obtained by static precipitation; filtrating: filtering the collagen peptide solution into the lower reaction furnace; high-temperature and high-pressure treatment: the temperature in the lower reaction furnace is 145°C, and the pressure is 0.4mpa for high-temperature and high-pressure treatment; freeze-drying: the collagen peptide solution after high-temperature and high-pressure treatment is frozen below -30°C for more than 6 hours; the soaking time in the alkaline pool, the soaking time in the acidic pool, the grinding time of the colloid mill, the reaction time of the upper reaction furnace and the lower reaction furnace is 50min.
The special whey spherical membrane: selecting fresh milk from pasture; adding 20% anhydrous ethanol into milk, stirring evenly, and then filtering after standing for 45min, adding the absolute ethanol to the obtained filtrate to make the absolute ethanol content reach 35%/504846 continuously adding the absolute ethanol until the content gradually reaches 55%, stirring evenly, standing for 45min, centrifuging at 4000 rpm, and pouring out the supernatant, and vacuum drying or freeze drying the obtained precipitate, grinding it to 160 mesh with a universal pulverizer, and making into capsules or tablets; and removing residual products, packing and storing the qualified ones.
The bovine thymosin: pickling the bovine thymus with acetic acid solution for 1h; then washing once with water, then pickling once with the acetic acid solution for 1h, and washing once with water to obtain the washed bovine thymus; cooking: adding water into a cooking tank, heating up while stirring, adding the washed bovine thymus and edible acetic acid at the same time, raising the temperature to 55°C in a lower part of the cooking pot and 65°C in an upper part thereof, keeping it warm for 60min, stopping stirring, letting stand for 1h, and supernatant is primary solution; deslagging: immediately after standing still, pumping the primary solution into a sterilized primary solution storage tank with a vacuum extraction tank, wherein temperature of the solution is 55°C; hydrolysis: pumping the primary solution into a sterilized hydrolysis tank, heating to 100°C for 15min for sterilization, cooling to 60°C and maintaining, adding alkali liquor to adjust pH value to neutral, adding enzyme preparation for hydrolysis for 8h, and then heating to 90°C for 15min for inactivation; filtrating: adding diatomaceous earth and activated carbon with a mass ratio of 1:1 according to the mass ratio of 0.2%, after stirring, standing, and coarse filtering, circularly filtering for 1h by a plate-and-frame filter to obtain clear liquid; concentration: concentrating the clear solution to a concentration of °Bé by a vacuum concentrator to obtain a concentrated solution; and spray drying: when the concentrate is clear, it is spray-dried to obtain the bovine thymosin.
The deep-sea cod peptide, the special whey spherical membrane, and the bovine thymosin peptide are evenly mixed to obtain loose powder, and the packaging is checked to obtain the golden spherical membrane protein factor product.
The golden spherical membrane protein factor products prepared in Embodiments 1-4 are tested for quality, and test results are shown in Table 1 below: LU504846
Table 1
CN a
Weight difference (%) up to up to up to up to specification specification specification specification
Microbial Limit up to up to up to up to specification specification specification specification
The golden spherical membrane protein factor prepared in embodiment 2 is tested clinically, specifically as follows:
Clinical data: a randomized double-blind controlled trial for middle-aged and elderly people was carried out during the Japanese influenza epidemic. The study included 85 middle-aged and elderly people aged 48 to 80, and they were randomly divided into two groups as per the blinded experiment method. The intervention group took the golden spherical membrane immune protein factor every day, and the control group took ordinary peptide powder every day. The substances in the two groups were indistinguishable from the senses. After a period of time, the influence of factors such as the frequency of occurrence of symptoms of influenza infection in users after product intervention was evaluated. This application mainly evaluates the incidence of influenza symptoms among the participants during the trial period, and the relevant symptoms are obtained by recording daily body temperature and influenza-like symptoms in the volunteers' logbook. Table 2 shows the results of pairwise comparisons of the incidence of influenza symptoms between the intervention and control groups. According to the results, the incidence of influenza symptoms in the golden spherical membrane immune protein group was significantly lower than that in the thymus albumin group, and the difference was statistically significant (P<0.05).
Table 2 Percentage of influenza symptoms in each product group (stratified by age and LU504846 experimental products)
Experimental Golden spherical membrane Thymus albumin
Age P value place immune protein factor (n=39) (n=42) 48~55 1.32+3.01 4.724 6.97 <0.05 55-60 0.00+0.00 3.42+8.71 <0.05
Osaka 60~68 0.00+0.00 2.91+ 4.76 <0.05 68775 0.64+1.96 2.65+4.43 <0.05 75-80 1.00+0.82 3.86 + 5.21 <0.05
Total 0.59+1.16 3.516 + 6.02 <0.05
Meanwhile, the present application explores the impact of interventions on the duration of influenza symptoms. The duration of influenza symptoms was defined as the cumulative number of days from the onset of influenza symptoms (oral body temperature = 38°C, accompanied by at least one influenza-like symptom, such as cough, nasal congestion, sore throat, headache, muscle pain, weakness, dyspnea, retrosternal pain, or loss of appetite) to the disappearance of all symptoms during the trial period. According to the test results, among the volunteers with influenza symptoms, the duration of symptoms of the golden spherical membrane immune protein factor was about 3.322 days lower than that of the thymus albumin as a whole, and the difference was statistically significant (P<0.05). In addition, the duration of influenza symptoms in all age groups in the intervention group was significantly lower than that in the control group. The relevant results are shown in Table 3.
Table 3 Cumulative days of influenza symptoms in each experimental group during experimenktU504846 (all volunteers) mean + standard deviation
Experimental Golden spherical membrane Thymus albumin
Age P value place immune protein factor(n=39) (n=42) 48~55 1.32+3.01 4.724 6.97 <0.05 55-60 0.00+0.00 3.42+8.71 <0.05
Osaka 60~68 0.00+0.00 2.91+ 4.76 <0.05 68775 0.64+1.96 2.65+4.43 <0.05 75-80 1.00+0.82 3.86 + 5.21 <0.05
Total 0.59+1.16 3.516 + 6.02 <0.05
Finally, for test subjects, the present application further records the number of sick leave caused by influenza. During the whole experiment, five people took sick leave caused by influenza, wherein one person took the golden spherical membrane immune protein factor, and four people took thymus albumin. From the data in Table 4, it can be seen that the number of sick leave patients who took the golden spherical membrane immune protein factor was significantly lower than those who took thymus albumin, and the difference was statistically significant (P<0.05).
Table 4 Percentage of sick leave rate (stratified by product taken) caused by influenza in the experimental period group
Golden spherical membrane
Experimental
Age immune protein Thymus albumin P value place factor(n=39) 48755 0.00% 5.16% <0.05 55-60 2.67% 7.12% <0.05
Osaka 60~68 0.00% 5.13% <0.05 68~75 0.00% 6.71% <0.05 75~80 0.00% 2.01% <0.05
Total 2.67% 26.13% <0.05
In addition to the research experiments mentioned above, the present application further conducted a randomized double-blind crossover trial, specifically, 26 men and women who were overweight (BMI: 25-29.9kg/m2) or obese (BMI: 30-39.9kg/m2) were randomly divided into a group receiving the intervention of the golden spherical membrane immune protein factor and a control group not receiving the intervention of the golden spherical membrane immune protein factor. After 1-2 weeks of metabolism after equal caloric food intake, serum cytokines, adhesion factors, cortisol, and inflammatory markers were measured at 0, 1, 3, and 6 hours. Glucose, insulin, and lipid profiles in plasma were also analyzed. The results of the study showed that the area under the curve of total cholesterol, low-density lipoprotein, soluble intracellular adhesion molecules and insulin in the group receiving the intervention of the golden spherical membrane immune protein factor was lower than that in the control group not receiving the intervention, while the level of the anti-inflammatory factor IL-10 was increased.
This suggests that the addition of golden spherical membrane immune protein factor to a high-saturated-fat meal reduces postprandial insulinemia and inflammatory responses in overweight and obese adults. In addition, the trial also conducted related investigations, and the results showed that the intervention group had improvements in physical strength, sleep and skin, which may be attributed to the immune-enhancing and anti-oxidative effects of the golden spherical membrane immune protein factor.
In conclusion, the golden spherical membrane immune protein factor and related components thereof play a positive role in the immune prevention, gastrointestinal health and exercise ability improvement of the middle-aged and elderly. Taking the golden spherical membrane immune protein factor of the present application is a safe and effective dietary nutritional supplement for middle-aged and elderly people.
The above descriptions are only preferred embodiments of the present invention, and are not intended to limit the present invention. Any modifications, equivalent replacements and improvements made within spirit and principles of the present invention shall fall within the protection scope of the present invention.
Claims (8)
1. A golden spherical membrane protein factor for regulating immune function of human body, comprises raw materials of the following parts by weight: 30-56 parts of deep-sea cod peptide, 10-20 parts of special whey spherical membrane, and 10-44 parts of bovine thymosin; wherein, a preparation method of the special whey spherical membrane is as follows: adding 15-25% volume of absolute ethanol to milk, stirring evenly, and then filtering after standing for 30-60 min, adding the absolute ethanol to the obtained filtrate to make the absolute ethanol content reach 35% volume, continuously adding the absolute ethanol until the content gradually reaches 55% volume, stirring evenly, standing for 30-60 min, centrifuging at 3000-5000 rpm, and pouring out the supernatant, and obtaining the special whey spherical membrane.
2. The golden spherical membrane protein factor for regulating immune function of human body according to claim 1, comprises raw materials of the following parts by weight: 45-55 parts of the deep-sea cod peptide, 10-20 parts of the special whey spherical membrane, and 30-40 parts of the bovine thymosin.
3. The golden spherical membrane protein factor for regulating immune function of human body according to claim 1, comprises raw materials of the following parts by weight: parts of the deep-sea cod peptide, 15 parts of the special whey spherical membrane, and 35 parts of the bovine thymosin.
4. The golden spherical membrane protein factor for regulating immune function of human body according to claim 1, wherein the deep-sea cod peptide is obtained by soaking deep-sea cod skin in an alkaline solution, an aqueous solution, an acidic solution, and an aqueous solution, followed by colloid grinding, enzymatic hydrolysis by heating, high temperature and high pressure, and freeze-drying.
5. The golden spherical membrane protein factor for regulating immune function of human body according to claim 1 or claim 4, wherein a preparation method of the deep-sea cod peptide is: sequentially placing the deep-sea cod skin in alkaline solution, aqueous solution, acidic solution, and aqueous solution for soaking treatment; grinding the deep-sea cod skin soaked in the aqueous solution with a colloid mill to obtain a crude collagen solution; placing the crude collagen solution at a temperature of 85-95°C with the enzymolysis liquid for stirring, heating and enzymolysis treating, and then standing for precipitation after stirring to obtain a collagen peptide solution; placing the collagen peptide solution at a temperature of 140-150°C and a pressure of
0.4-0.5 mpa for high-temperature and high-pressure treatment; and freezing the collagen peptide solution after high-temperature and high-pressure treatment at -30°C for not less than 6 hours.
6. The golden spherical membrane protein factor for regulating immune function of human body according to claim 1, wherein the bovine thymosin is obtained by acid washing and aqueous treatment of bovine thymus, cooking, slag removal, hydrolysis, concentration and spray drying.
7. The golden spherical membrane protein factor for regulating immune function of human body according to claim 1 or claim 6, wherein a preparation method of the bovine thymosin is as follows: sequentially pickling the bovine thymus with acetic acid solution and washing the bovine thymus with the water solution; adding water into a cooking tank, heating up while stirring, adding the washed bovine thymus and edible acetic acid at the same time, raising the temperature to 55°C in a lower part of the cooking pot and 65°C in an upper part thereof, maintaining the temperature for 60 min, stopping stirring, letting stand for 0.5-1.5h, and supernatant is primary solution;
immediately after standing still, pumping the primary solution into a sterilized primak/W504846 solution storage tank with a vacuum extraction tank, wherein temperature of the solution is 50-60°C; pumping the primary solution into a sterilized hydrolysis tank, heating to 100°C for 15min for sterilization, cooling to 55-65°C and maintaining, adding alkali liquor to adjust pH value to neutral, adding enzyme preparation for hydrolysis for 7-9h, and then heating to 90°C for 15min for inactivation; adding diatomaceous earth and activated carbon, after stirring, standing, and coarse filtering, circularly filtering for 0.5-1.5h by a plate-and-frame filter to obtain clear liquid; concentrating the clear solution to a concentration of 18-22 °Bo by a vacuum concentrator to obtain a concentrated solution; and when the concentrate is clear, pray-drying the concentrate to obtain the bovine thymosin.
8. The golden spherical membrane protein factor for regulating immune function of human body according to claim 1, wherein the golden spherical membrane protein factor for regulating immune function of human body is in the form of tablets, hard capsules or soft capsules.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
LU504846A LU504846B1 (en) | 2023-08-01 | 2023-08-01 | Golden spherical membrane protein factor for regulating immune function of human body |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
LU504846A LU504846B1 (en) | 2023-08-01 | 2023-08-01 | Golden spherical membrane protein factor for regulating immune function of human body |
Publications (1)
Publication Number | Publication Date |
---|---|
LU504846B1 true LU504846B1 (en) | 2024-02-05 |
Family
ID=89808367
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
LU504846A LU504846B1 (en) | 2023-08-01 | 2023-08-01 | Golden spherical membrane protein factor for regulating immune function of human body |
Country Status (1)
Country | Link |
---|---|
LU (1) | LU504846B1 (en) |
-
2023
- 2023-08-01 LU LU504846A patent/LU504846B1/en active IP Right Grant
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP6828054B2 (en) | Walnut oligopeptide powder, its preparation method and use | |
CN111670997B (en) | Preparation method of immunity-enhancing compound protein peptide enzymatic hydrolysate, immunity-enhancing compound protein peptide beverage and preparation method thereof | |
CN102178314B (en) | Bitter buckwheat health care beverage with auxiliary function for lowering blood pressure and production process thereof | |
Shi et al. | The effects of supplementation with blueberry, cyanidin-3-O-β-glucoside, yoghurt and its peptides on obesity and related comorbidities in a diet-induced obese mouse model | |
EP3141255A1 (en) | Memory improving composition, preparation method and use thereof | |
CN108339112A (en) | A kind of alimentation composition for promoting wound healing, bedsore reparation, postoperative stress ulcer healing | |
CN113332354B (en) | Anti-saccharification anti-aging fermented composition and preparation method thereof | |
CN113519736A (en) | Intestinal health conditioning food and preparation method and application thereof | |
CA2871478C (en) | Pleuropterus multiflorus extract and dipsacus asperoides extract for stimulating the secretion of insulin-like growth factor and promoting bone structure growth, and method for preparing same | |
US20120100235A1 (en) | Papaya puree and uses thereof | |
LU504846B1 (en) | Golden spherical membrane protein factor for regulating immune function of human body | |
CN106822231A (en) | Biological bacterium solution with function of blood sugar reduction and preparation method thereof | |
CN103719864A (en) | Blood glucose-reducing natto combined capsule and preparation method thereof | |
CN102652561A (en) | Vegetable protein food for treating micro-disease or assisting medicament in rehabilitating sick body and production method thereof | |
CN115322859A (en) | Deer blood peptide wine and preparation method thereof | |
CN105995971A (en) | Nutritional liquid food for promoting diabetes recovery and preparation method thereof | |
CN109758568B (en) | A composition containing black-bone chicken egg white peptide, and its application in preparing medicines, antifatigue health food and food for treating dysmenorrhea | |
CN106805252A (en) | A kind of fish small peptide and its application in nutrition fortifier | |
CN110327373A (en) | Maggot infusing drugs in wine product is for treating the application in diabetes | |
CN110302213A (en) | Maggot is for treating the application in diabetes | |
WO2007118368A1 (en) | A pharmaceutical tea for reducing blood sugar and process thereof | |
CN108936689A (en) | Adjust the oral solution and preparation method thereof of immunity | |
CN111109490A (en) | Soybean lecithin solid beverage | |
CN104013853B (en) | A kind of composition of strong kidney kidney tonifying and preparation method thereof | |
CN113616771A (en) | Lyophilized powder of active protein extracted from placenta Cervi, placenta Cervi oral liquid and their preparation methods |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG | Patent granted |
Effective date: 20240205 |