CN106387585A - Taurine electrolyte sports solid beverage and production technology thereof - Google Patents
Taurine electrolyte sports solid beverage and production technology thereof Download PDFInfo
- Publication number
- CN106387585A CN106387585A CN201610775054.4A CN201610775054A CN106387585A CN 106387585 A CN106387585 A CN 106387585A CN 201610775054 A CN201610775054 A CN 201610775054A CN 106387585 A CN106387585 A CN 106387585A
- Authority
- CN
- China
- Prior art keywords
- taurine
- powder
- fine powder
- mixing
- cobastab
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 title claims abstract description 100
- 229960003080 taurine Drugs 0.000 title claims abstract description 50
- 239000007787 solid Substances 0.000 title claims abstract description 32
- 235000013361 beverage Nutrition 0.000 title claims abstract description 30
- 239000003792 electrolyte Substances 0.000 title claims abstract description 30
- 238000005516 engineering process Methods 0.000 title claims description 18
- 238000004519 manufacturing process Methods 0.000 title claims description 17
- 239000000843 powder Substances 0.000 claims abstract description 91
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims abstract description 51
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims abstract description 36
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims abstract description 33
- 235000005979 Citrus limon Nutrition 0.000 claims abstract description 21
- 239000001103 potassium chloride Substances 0.000 claims abstract description 18
- 235000011164 potassium chloride Nutrition 0.000 claims abstract description 18
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 claims abstract description 16
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 claims abstract description 16
- 229930003268 Vitamin C Natural products 0.000 claims abstract description 16
- 239000008101 lactose Substances 0.000 claims abstract description 16
- 239000002994 raw material Substances 0.000 claims abstract description 16
- 235000019154 vitamin C Nutrition 0.000 claims abstract description 16
- 239000011718 vitamin C Substances 0.000 claims abstract description 16
- WBZFUFAFFUEMEI-UHFFFAOYSA-M Acesulfame k Chemical compound [K+].CC1=CC(=O)[N-]S(=O)(=O)O1 WBZFUFAFFUEMEI-UHFFFAOYSA-M 0.000 claims abstract description 14
- 229960004998 acesulfame potassium Drugs 0.000 claims abstract description 14
- 235000010358 acesulfame potassium Nutrition 0.000 claims abstract description 14
- 239000000619 acesulfame-K Substances 0.000 claims abstract description 14
- ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 claims abstract description 13
- ROHFNLRQFUQHCH-UHFFFAOYSA-N Leucine Natural products CC(C)CC(N)C(O)=O ROHFNLRQFUQHCH-UHFFFAOYSA-N 0.000 claims abstract description 13
- 239000000463 material Substances 0.000 claims abstract description 12
- 108010011485 Aspartame Proteins 0.000 claims abstract description 10
- IAOZJIPTCAWIRG-QWRGUYRKSA-N aspartame Chemical compound OC(=O)C[C@H](N)C(=O)N[C@H](C(=O)OC)CC1=CC=CC=C1 IAOZJIPTCAWIRG-QWRGUYRKSA-N 0.000 claims abstract description 10
- 239000000605 aspartame Substances 0.000 claims abstract description 10
- 235000010357 aspartame Nutrition 0.000 claims abstract description 10
- 229960003438 aspartame Drugs 0.000 claims abstract description 10
- 244000248349 Citrus limon Species 0.000 claims abstract 7
- 238000002156 mixing Methods 0.000 claims description 80
- 239000011812 mixed powder Substances 0.000 claims description 39
- 238000003756 stirring Methods 0.000 claims description 30
- 239000000203 mixture Substances 0.000 claims description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 21
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 claims description 16
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 15
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 15
- 239000011122 softwood Substances 0.000 claims description 15
- 238000012856 packing Methods 0.000 claims description 12
- 239000002245 particle Substances 0.000 claims description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 11
- 230000000694 effects Effects 0.000 claims description 11
- 230000008569 process Effects 0.000 claims description 11
- 239000002253 acid Substances 0.000 claims description 9
- 235000013399 edible fruits Nutrition 0.000 claims description 9
- 229960003511 macrogol Drugs 0.000 claims description 9
- 239000007938 effervescent tablet Substances 0.000 claims description 8
- 239000003513 alkali Substances 0.000 claims description 7
- 239000003826 tablet Substances 0.000 claims description 7
- 235000020985 whole grains Nutrition 0.000 claims description 6
- 230000005540 biological transmission Effects 0.000 claims description 5
- 239000011734 sodium Substances 0.000 claims description 5
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 4
- 238000007689 inspection Methods 0.000 claims description 4
- 239000011591 potassium Substances 0.000 claims description 4
- 229910052700 potassium Inorganic materials 0.000 claims description 4
- 229910052708 sodium Inorganic materials 0.000 claims description 4
- 239000007909 solid dosage form Substances 0.000 claims description 4
- 229910001220 stainless steel Inorganic materials 0.000 claims description 4
- 239000010935 stainless steel Substances 0.000 claims description 4
- PFTAWBLQPZVEMU-DZGCQCFKSA-N (+)-catechin Chemical compound C1([C@H]2OC3=CC(O)=CC(O)=C3C[C@@H]2O)=CC=C(O)C(O)=C1 PFTAWBLQPZVEMU-DZGCQCFKSA-N 0.000 claims description 3
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 claims description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims description 3
- 235000013339 cereals Nutrition 0.000 claims description 3
- 230000008859 change Effects 0.000 claims description 3
- 230000003749 cleanliness Effects 0.000 claims description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 3
- 229960003136 leucine Drugs 0.000 claims description 3
- 235000005772 leucine Nutrition 0.000 claims description 3
- 238000012946 outsourcing Methods 0.000 claims description 3
- 238000005453 pelletization Methods 0.000 claims description 3
- 239000008213 purified water Substances 0.000 claims description 3
- 235000017557 sodium bicarbonate Nutrition 0.000 claims description 3
- 229910000030 sodium bicarbonate Inorganic materials 0.000 claims description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- LXNHXLLTXMVWPM-UHFFFAOYSA-N pyridoxine Chemical compound CC1=NC=C(CO)C(CO)=C1O LXNHXLLTXMVWPM-UHFFFAOYSA-N 0.000 abstract description 7
- AUNGANRZJHBGPY-SCRDCRAPSA-N Riboflavin Chemical compound OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-SCRDCRAPSA-N 0.000 abstract description 5
- RADKZDMFGJYCBB-UHFFFAOYSA-N pyridoxal hydrochloride Natural products CC1=NC=C(CO)C(C=O)=C1O RADKZDMFGJYCBB-UHFFFAOYSA-N 0.000 abstract description 5
- AUNGANRZJHBGPY-UHFFFAOYSA-N D-Lyxoflavin Natural products OCC(O)C(O)C(O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-UHFFFAOYSA-N 0.000 abstract description 4
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 abstract description 4
- 229960002477 riboflavin Drugs 0.000 abstract description 4
- 229960003495 thiamine Drugs 0.000 abstract description 4
- 239000011691 vitamin B1 Substances 0.000 abstract description 4
- 229930003451 Vitamin B1 Natural products 0.000 abstract description 3
- 229930003471 Vitamin B2 Natural products 0.000 abstract description 3
- 229960002816 potassium chloride Drugs 0.000 abstract description 3
- 235000010374 vitamin B1 Nutrition 0.000 abstract description 3
- 235000019164 vitamin B2 Nutrition 0.000 abstract description 3
- 239000011716 vitamin B2 Substances 0.000 abstract description 3
- 235000019158 vitamin B6 Nutrition 0.000 abstract description 3
- 239000011726 vitamin B6 Substances 0.000 abstract description 3
- 229940011671 vitamin b6 Drugs 0.000 abstract description 3
- 230000035622 drinking Effects 0.000 abstract description 2
- 235000001968 nicotinic acid Nutrition 0.000 abstract description 2
- 239000011664 nicotinic acid Substances 0.000 abstract description 2
- 229960003512 nicotinic acid Drugs 0.000 abstract description 2
- DPJRMOMPQZCRJU-UHFFFAOYSA-M thiamine hydrochloride Chemical compound Cl.[Cl-].CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N DPJRMOMPQZCRJU-UHFFFAOYSA-M 0.000 abstract 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 abstract 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 abstract 1
- 229940093429 polyethylene glycol 6000 Drugs 0.000 abstract 1
- 239000000600 sorbitol Substances 0.000 abstract 1
- 239000000047 product Substances 0.000 description 26
- 244000131522 Citrus pyriformis Species 0.000 description 14
- CVSVTCORWBXHQV-UHFFFAOYSA-N creatine Chemical compound NC(=[NH2+])N(C)CC([O-])=O CVSVTCORWBXHQV-UHFFFAOYSA-N 0.000 description 12
- 230000033001 locomotion Effects 0.000 description 12
- 235000013305 food Nutrition 0.000 description 10
- 230000006870 function Effects 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- 229960003624 creatine Drugs 0.000 description 6
- 239000006046 creatine Substances 0.000 description 6
- 235000003599 food sweetener Nutrition 0.000 description 6
- 210000003205 muscle Anatomy 0.000 description 6
- 239000013589 supplement Substances 0.000 description 6
- 239000003765 sweetening agent Substances 0.000 description 6
- 229930003231 vitamin Natural products 0.000 description 6
- 235000013343 vitamin Nutrition 0.000 description 6
- 239000011782 vitamin Substances 0.000 description 6
- 229940088594 vitamin Drugs 0.000 description 6
- 150000003722 vitamin derivatives Chemical class 0.000 description 6
- 238000013341 scale-up Methods 0.000 description 5
- 235000011496 sports drink Nutrition 0.000 description 5
- 239000013078 crystal Substances 0.000 description 4
- 230000029087 digestion Effects 0.000 description 4
- 230000012010 growth Effects 0.000 description 4
- 230000036541 health Effects 0.000 description 4
- JZRWCGZRTZMZEH-UHFFFAOYSA-N thiamine Chemical compound CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N JZRWCGZRTZMZEH-UHFFFAOYSA-N 0.000 description 4
- 102000004407 Lactalbumin Human genes 0.000 description 3
- 108090000942 Lactalbumin Proteins 0.000 description 3
- 229930006000 Sucrose Natural products 0.000 description 3
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 3
- 230000033228 biological regulation Effects 0.000 description 3
- 238000007599 discharging Methods 0.000 description 3
- 235000019162 flavin adenine dinucleotide Nutrition 0.000 description 3
- 239000011714 flavin adenine dinucleotide Substances 0.000 description 3
- VWWQXMAJTJZDQX-UYBVJOGSSA-N flavin adenine dinucleotide Chemical compound C1=NC2=C(N)N=CN=C2N1[C@@H]([C@H](O)[C@@H]1O)O[C@@H]1CO[P@](O)(=O)O[P@@](O)(=O)OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C2=NC(=O)NC(=O)C2=NC2=C1C=C(C)C(C)=C2 VWWQXMAJTJZDQX-UYBVJOGSSA-N 0.000 description 3
- 229940093632 flavin-adenine dinucleotide Drugs 0.000 description 3
- 239000000796 flavoring agent Substances 0.000 description 3
- 235000019634 flavors Nutrition 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 230000004060 metabolic process Effects 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 235000018102 proteins Nutrition 0.000 description 3
- 102000004169 proteins and genes Human genes 0.000 description 3
- 108090000623 proteins and genes Proteins 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000005720 sucrose Substances 0.000 description 3
- 101000693916 Gallus gallus Albumin Proteins 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- DRBBFCLWYRJSJZ-UHFFFAOYSA-N N-phosphocreatine Chemical compound OC(=O)CN(C)C(=N)NP(O)(O)=O DRBBFCLWYRJSJZ-UHFFFAOYSA-N 0.000 description 2
- 150000001413 amino acids Chemical class 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 210000001124 body fluid Anatomy 0.000 description 2
- 239000010839 body fluid Substances 0.000 description 2
- 150000001720 carbohydrates Chemical class 0.000 description 2
- 235000014633 carbohydrates Nutrition 0.000 description 2
- 210000002318 cardia Anatomy 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 239000007884 disintegrant Substances 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 235000011194 food seasoning agent Nutrition 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 235000013402 health food Nutrition 0.000 description 2
- 210000002216 heart Anatomy 0.000 description 2
- 230000036737 immune function Effects 0.000 description 2
- 238000001727 in vivo Methods 0.000 description 2
- 210000003734 kidney Anatomy 0.000 description 2
- 239000002417 nutraceutical Substances 0.000 description 2
- 235000021436 nutraceutical agent Nutrition 0.000 description 2
- 235000016709 nutrition Nutrition 0.000 description 2
- 230000035764 nutrition Effects 0.000 description 2
- 230000009965 odorless effect Effects 0.000 description 2
- 230000035790 physiological processes and functions Effects 0.000 description 2
- NHZMQXZHNVQTQA-UHFFFAOYSA-N pyridoxamine Chemical compound CC1=NC=C(CO)C(CN)=C1O NHZMQXZHNVQTQA-UHFFFAOYSA-N 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 235000019605 sweet taste sensations Nutrition 0.000 description 2
- 235000019157 thiamine Nutrition 0.000 description 2
- 239000011721 thiamine Substances 0.000 description 2
- 230000035922 thirst Effects 0.000 description 2
- 238000012549 training Methods 0.000 description 2
- -1 vitamin C Compound Chemical class 0.000 description 2
- DQJCDTNMLBYVAY-ZXXIYAEKSA-N (2S,5R,10R,13R)-16-{[(2R,3S,4R,5R)-3-{[(2S,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5-(ethylamino)-6-hydroxy-2-(hydroxymethyl)oxan-4-yl]oxy}-5-(4-aminobutyl)-10-carbamoyl-2,13-dimethyl-4,7,12,15-tetraoxo-3,6,11,14-tetraazaheptadecan-1-oic acid Chemical compound NCCCC[C@H](C(=O)N[C@@H](C)C(O)=O)NC(=O)CC[C@H](C(N)=O)NC(=O)[C@@H](C)NC(=O)C(C)O[C@@H]1[C@@H](NCC)C(O)O[C@H](CO)[C@H]1O[C@H]1[C@H](NC(C)=O)[C@@H](O)[C@H](O)[C@@H](CO)O1 DQJCDTNMLBYVAY-ZXXIYAEKSA-N 0.000 description 1
- QCVGEOXPDFCNHA-UHFFFAOYSA-N 5,5-dimethyl-2,4-dioxo-1,3-oxazolidine-3-carboxamide Chemical compound CC1(C)OC(=O)N(C(N)=O)C1=O QCVGEOXPDFCNHA-UHFFFAOYSA-N 0.000 description 1
- 206010000060 Abdominal distension Diseases 0.000 description 1
- 102000002322 Egg Proteins Human genes 0.000 description 1
- 108010000912 Egg Proteins Proteins 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 229930091371 Fructose Natural products 0.000 description 1
- 239000005715 Fructose Substances 0.000 description 1
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 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
- 229920002527 Glycogen Polymers 0.000 description 1
- 102000002068 Glycopeptides Human genes 0.000 description 1
- 108010015899 Glycopeptides Proteins 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 102000008934 Muscle Proteins Human genes 0.000 description 1
- 108010074084 Muscle Proteins Proteins 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229910006069 SO3H Inorganic materials 0.000 description 1
- 108010073771 Soybean Proteins Proteins 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 238000012271 agricultural production Methods 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 208000007502 anemia Diseases 0.000 description 1
- 230000003064 anti-oxidating effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 235000019568 aromas Nutrition 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 210000004556 brain Anatomy 0.000 description 1
- 210000003169 central nervous system Anatomy 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- 239000005515 coenzyme Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000013256 coordination polymer Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 206010012601 diabetes mellitus Diseases 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 235000014103 egg white Nutrition 0.000 description 1
- 210000000969 egg white Anatomy 0.000 description 1
- 235000013601 eggs Nutrition 0.000 description 1
- 230000002124 endocrine Effects 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 235000020776 essential amino acid Nutrition 0.000 description 1
- 239000003797 essential amino acid Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 210000004051 gastric juice Anatomy 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 229940096919 glycogen Drugs 0.000 description 1
- 230000009931 harmful effect Effects 0.000 description 1
- 230000012447 hatching Effects 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 229910001410 inorganic ion Inorganic materials 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000002427 irreversible effect Effects 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- 244000144972 livestock Species 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 235000012054 meals Nutrition 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 230000007102 metabolic function Effects 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000003020 moisturizing effect Effects 0.000 description 1
- 230000003387 muscular Effects 0.000 description 1
- 210000005036 nerve Anatomy 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 229950007002 phosphocreatine Drugs 0.000 description 1
- 229920001184 polypeptide Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 230000022558 protein metabolic process Effects 0.000 description 1
- 235000005974 protein supplement Nutrition 0.000 description 1
- 229940116540 protein supplement Drugs 0.000 description 1
- 229960003581 pyridoxal Drugs 0.000 description 1
- 235000008164 pyridoxal Nutrition 0.000 description 1
- 239000011674 pyridoxal Substances 0.000 description 1
- 235000008151 pyridoxamine Nutrition 0.000 description 1
- 239000011699 pyridoxamine Substances 0.000 description 1
- 235000008160 pyridoxine Nutrition 0.000 description 1
- 239000011677 pyridoxine Substances 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 238000006479 redox reaction Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000003507 refrigerant Substances 0.000 description 1
- 210000001525 retina Anatomy 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 235000019192 riboflavin Nutrition 0.000 description 1
- 239000002151 riboflavin Substances 0.000 description 1
- 230000035807 sensation Effects 0.000 description 1
- 235000019615 sensations Nutrition 0.000 description 1
- 210000002027 skeletal muscle Anatomy 0.000 description 1
- 235000013555 soy sauce Nutrition 0.000 description 1
- 235000019710 soybean protein Nutrition 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 230000009469 supplementation Effects 0.000 description 1
- 230000035900 sweating Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- WBWWGRHZICKQGZ-HZAMXZRMSA-N taurocholic acid Chemical compound C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(=O)NCCS(O)(=O)=O)C)[C@@]2(C)[C@@H](O)C1 WBWWGRHZICKQGZ-HZAMXZRMSA-N 0.000 description 1
- 239000002699 waste material Substances 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
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
- A23L2/385—Concentrates of non-alcoholic beverages
- A23L2/39—Dry compositions
-
- 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
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
- A23L2/40—Effervescence-generating compositions
-
- 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
Abstract
The invention discloses a taurine electrolyte sports solid beverage, which comprises the following raw materials by weight: 0.015 gram of vitamin B1, 0.015 gram of vitamin B2, 0.015 gram of vitamin B6, 2.3 grams of vitamin C, 1.3 grams of taurine, and 1.5 grams of potassium chloride, and comprises the following auxiliary materials by weight: 360 grams of citric acid, 230 grams of sodium bicarbonate, 5 grams of polyethylene glycol 6000, 170 grams of lactose, 192.855 grams of sorbitol, 10 grams of aspartame, 3 grams of acesulfame potassium, 9 grams of leucine, 5 grams of lemon essence, and 10 grams of lemon powder. Vitamin B1, vitamin B2, vitamin B6, nicotinic acid, taurine, and potassium chloride are the main raw material of the solid beverage. The solid beverage is suitable for drinking after/before exercise and is capable of relieving fatigue.
Description
Technical field
The present invention relates to field of health care food, more particularly, to taurine electrolyte flow solid beverage and its production technology.
Background technology
Sports food one class can targetedly meet movement human metabolism and physiological function demand, has high nutrition close
Degree and the food of high bioactivity, its reasonable supplement can promote the health of movement human and the raising of locomitivity.
In 27 food functions that health food administrative department of China sets, only enhancing immunologic function, anti-oxidation function,
Improve the health care of sleep function, function of physical fatigue alleviation, improve iron-resistant oxygen tolerance and improve alimentary anemia function etc. 6 be with
Motion correlation.
The nutraceutical relevant with sports food comprises:
(1) energy supplement class
The representative of this based food is its main component of various sports drinks is carbohydrate, can quickly mend after use
Fill energy.Its main component is sugar, has the polysaccharide such as glucose (absorbing rapid), compound sugar, sucrose, fructose.In sports drink also
Several mineral materials, vitamin and taurine should be contained.
Effect:Supplement before, during and after motion, prevent the decomposition with muscle protein in reduction of income training process, delayed motion
The generation of fatigue, promotes Fatique after Sports to recover.More importantly after energy abundance, locomitivity and muscle do all can be big
Big raising.
(2) increase flesh class
1. albumen powder:The species of albumen powder is more, has lactalbumin, Chicken Albumin, soybean protein and junket egg albumen etc..Each hatching egg
White different qualities:Lactalbumin absorbs the fastest, absorptivity highest, and it is very short to can reach for 157. its half-life, so once not
Cross 30 grams, taken after mixing it with water with milk and can delay its digestion time, it is optimal protein supplement after training.Chicken Albumin absorbs
Utilization rate and biochemistry are worth and are below lactalbumin, but its digestion time relatively medium (1.5-3 hour).Therefore it can
To be continually provided the needs to protein for the body.Caseic digestion time slowly, can reach 2.5-4 hour with
On, take before being suitable near water.
2. creatine
Creatine is primarily present in meat food.Human body daily creatine requirement be about 2 grams, by meals obtain 1 gram, another 1 gram
Internal synthesis.The forceful action of creatine supplementation:ADP+CP→ATP+C(1) muscular strength amount and lean body mass are increased, oral creatine makes
Phosphocreatine content in muscle improves 20. and (2) increase muscle degree of enclosing:Creatine brings muscle into water, so that muscle volume is increased
Greatly, cell is conducive to absorb amino acid, synthetic protein.
3. glycopeptide beverage
DOMS is difficult to recover, and supplements sugar, the bland of polypeptide contributes to tired fast quick-recovery, muscle glycogen after motion
Fast quick-recovery is the key that organism fatigue recovers.
For a long time, most people all thinks that drinking substantial amounts of frozen water quenches one's thirst most, and in fact, this is merely capable of temporarily suppressing
Thirsty sensation, but can increase and urinate and perspire, or even so that internal inorganic ion is further lost, and increase the heart, kidney burden,
Dilution gastric juice, extends the recovery time of body fluid.Because water is low pressure it is impossible to directly permeate body fluid, rapidly for absorption of human body, institute
During with mouth parched and tongue scorched, suddenly fill frozen water, still can not quench the thirst at once, on the contrary because having drunk too much water and abdominal distension is felt bad.After sweating, simple moisturizing
It is inadequate it is necessary to mend " liquid ", " liquid " refers to the balance solution of water and electrolyte simultaneously.
Existing energy supplement nutraceutical, with aqua in commercial type, its maximum shortcoming is exactly to be difficult to major part
In carrying, relatively heavier, and the sports drink based on pulvis, when brewed, the easy conglomeration of solid, it is not easy to dissolve, it is effective
Composition can not discharge completely, and its waste is larger, its dissolving ratio large percentage.
Content of the invention
For above-mentioned problem, the present invention is intended to provide taurine electrolyte flow solid beverage and its production work
Skill, with vitamin B1, vitamin B2, vitamin B6, nicotinic acid, taurine, potassium chloride, potassium chloride is as primary raw material system for the present invention
Become taurine electrolyte flow solid beverage, taken before suitable players motion and after motion, there is alleviation physical fatigue
Effect.
To achieve these goals, the technical solution adopted in the present invention is as follows:
Taurine electrolyte flow solid beverage, described taurine electrolyte flow solid beverage dispensing includes raw material:Vitamin
B10.015g, Cobastab20.015g, Cobastab60.015g, Catergen .3g, taurine 1.3g, potassium chloride 1.5g;Auxiliary material:
Citric acid 360g, sodium acid carbonate 230g, Macrogol 6000 5g, lactose 170g, D-sorbite 192.855g, Aspartame
10g, acesulfame potassium 3g, leucine 9g, lemon extract 5g, lemon fruit powder 10g.
Preferably, described six kinds of raw materials are all pressed powder, and described taurine electrolyte flow solid beverage is made
Solid dosage forms.
Product of the present invention is for players, before motion, alleviates physical fatigue afterwards, mainly to supplement multivitamin,
Taurine, based on electrolyte, each raw material concrete function is as follows:
Cobastab1:Cobastab1Also known as thiamine, or claim aneurine, be a kind of B race dimension life that scientist finds earliest
Element.Cobastab1It is a kind of water soluble vitamin, will not save in human body it is therefore desirable to be supplemented daily.
Cobastab2:Cobastab2Also known as riboflavin, it is a kind of water soluble vitamin.It is soluble in alkaline solution, molten in strong acid
Stable in liquid.Heat-resisting, resistance to oxidation, illumination and ultraviolet irradiation cause irreversible decomposition.With FMN in body
(FMN) and two kinds of form coenzyme of flavin adenine dinucleotide (FAD) (FAD) participate in redox reactions, play the effect passing hydrogen, with
The energetic supersession of body is closely related, plays an important role in carbohydrate, lipid, protein metabolism[
Cobastab6:Cobastab6Also known as pyridoxol, take in and can be transformed into pyridoxal and pyridoxamine in vivo, be a kind of water soluble vitamin
Raw element.It participates in the activity of internal more than 50 kinds of enzyme systems, safeguards the function of central nervous system, is energy production, fat, albumen
Matter metabolism, vitamin necessary to hemochrome generation, belong to vitamin needed by human.
Vitamin C:Also known as ascorbic acid, vitamin C is micro necessary to human nutrition, growth organising to vitamin C
Compound, has epochmaking effect to the metabolism of body, growth, growth, health.
Taurine:Taurine(taurine)The entitled Tau of chemistry, its structural formula is NH2CH2CH2SO3H.Ox
Sulfonic acid also known as Taurine, cholaic acid, taurine, Taurine, gain the name because separating from fel bovis first within 1827.Ox sulphur
Acid rich content in the histoorgans such as the brain of mammal, the heart, liver, kidney, retina, skeletal muscle and leucocyte, is to contain in vivo
Amount highest free amino acid.Taurine is not the constituent of protein, is but a kind of conditionally essential amino acid, it is not only
Participate in the growth metabolism of body as a kind of nutriment, and participate in maintaining the immunologic function of body, to nerve, digestion, life
Grow, angiocarpy, the normal performance of the physiological function such as endocrine have important adjustment effect.
Potassium chloride:Potassium chloride in food service industry, can be used as salt substitute be applied to agricultural production, aquatic products, livestock products, fermentation,
Seasoning, can, instant food etc., make low Na prod, to reduce the too high harmful effect to body of sodium content;It is also used for strengthening
Potassium(For human electrolyte), prepare sports drink etc.;The maximum usage amount that China's regulation can be used for Cardia Salt is 350g/
Kg, maximum usage amount 60g/kg in Cardia Salt soy sauce, maximum usage amount 0.2g/kg in sports drink.
Citric acid:Gas-producing disintegrant.Citric acid also known as citric acid are colourless or white crystalline particle or powder, odorless,
Taste is extremely sour, soluble in water, and the aqueous solution is in acidity, is conventional acid source in effervescent tablet.Citric acid specifies by life in GB 2760
Produce requirement to add, the addition in product of the present invention is 36%, this addition meets process requirements and is safety using amount.
Sodium acid carbonate:Gas-producing disintegrant.Sodium acid carbonate is white crystalline powder, is conventional alkali source in effervescent tablet,
Sodium acid carbonate specifies that in GB 2760 addition is 23% in product of the present invention, and this addition is full by producing requirement interpolation
Sufficient process requirements and be safety using amount.
Macrogol 6000:Lubricant.Macrogol 6000 is white waxy solid thin slice or particulate powder, is soluble in
Water, is a kind of conventional soluble oil in effervescent tablet.Macrogol 6000 specifies by production requirement in GB 2760
Add, in product of the present invention, addition is 0.5%, this addition meets process requirements and is safety using amount.
Lactose:Filler.Lactose be white to pale yellow crystals or mealy crystal, micro- sweet, free from extraneous odour, mouthfeel soluble in water
Well, and there is certain viscosity, it is usually used in tablet as filler.In product of the present invention, the addition of lactose is 17%, and this adds
Dosage meets process requirements and the taking dose for safety.
D-sorbite:Sweetener.D-sorbite also known as sorbierite, are white crystalline powder, thin slice or particle, have suction
Moist.D-sorbite has refrigerant sweet taste, and its sugariness is about the half of sucrose, as sweetener, good mouthfeel.D-sorbite is in GB
In 2760, regulation is added by producing requirement, and in product of the present invention, addition is 657.6mg/ piece, and this dosage meets technique need
Ask and be safe taking dose.
Aspartame:Sweetener.Aspartame is white crystals particle or powder, is slightly soluble in water and ethanol.Aspartame
There is sweet taste height, the low feature of heat, diabetic or fat personage also can take, and be a kind of conventional sweetener.A Si
Ba Tian specifies to add according to producing requirement in GB 2760, and the addition in product of the present invention is 1.0%, makes effervesce
Piece good mouthfeel.
Acesulfame potassium:Sweetener.Acesulfame potassium also known as acesulfame potassium, are colourless crystallization or white crystalline powder
End, soluble in water, sugariness is higher than sucrose, and in good taste, empty calory, is also a kind of conventional synthetic sweetener.Acesulfame potassium
In GB 2760, regulation maximum usage amount is 0.4%, and in product of the present invention, addition is 0.3%, and consumption safety and sugariness meet
Product demand.
Leucine:Seasoning fumet.Leucine is white crystals or crystalline powder, odorless, in GB 2760《Allow
The food synthetic perfume list using》Interior, product aroma of pure of the present invention can be made after interpolation.Leucine is in product of the present invention
Addition be 0.9%.
Lemon extract:Flavor enhancement.Product of the present invention has citris aromas, can lift product odour of the present invention and mouth after interpolation
Sense, makes product easy passive movement personage accept, and the addition in product of the present invention is 0.5%.
Lemon fruit powder:Flavor enhancement.Lemon fruit powder is soluble in water, stable in properties, is conventional flavor enhancement, is conducive to improving and produces
The taste smell of product and mouthfeel.The addition of product lemon fruit powder of the present invention is 40mg/ piece.
The production technology of taurine electrolyte flow solid beverage, comprises the following steps:
Step(One)Sieve:Cobastab1, Cobastab2, Cobastab6, vitamin C, taurine, potassium chloride, citric acid, carbonic acid
Hydrogen sodium, lactose, D-sorbite cross 80 mesh sieves respectively, obtain each fine powder, standby;
Step(Two)Weigh:Weigh Cobastab by formula rate1Fine powder, Cobastab2Fine powder, Cobastab6Fine powder, vitamin C
Fine powder, taurine fine powder, potassium chloride fine powder, citric acid fine powder, sodium bicarbonate fine powder, lactose fine powder, D-sorbite fine powder, poly- second
Glycol 6000, Aspartame, acesulfame potassium, leucine lemon extract, lemon fruit powder, standby;
Step(Three)Mixing:Use level mixing apparatus, by Cobastab1Fine powder, Cobastab2Fine powder, Cobastab6Fine powder, ox
Sulfonic acid fine powder mixes, and time 5min obtains mixed powder 1;Potassium chloride fine powder is mixed with mixed powder 1, time 10min, obtain mixed powder
2;Vitamin C fine powder is mixed with mixed powder 2 equal increments, obtains mixed powder 3;Lactose fine powder is mixed with mixed powder 3 equal increments
Close, obtain mixed powder 4;Citric acid fine powder is mixed with mixed powder 4, time 30min, obtain mixed powder 5, standby;Sodium acid carbonate is thin
Powder is mixed with D-sorbite fine powder, time 30min, obtains mixed powder 6, standby;By acesulfame potassium, lemon extract, A Siba
Sweet, leucine, Macrogol 6000 mixing, time 10min, obtain mixed powder 7, standby;
Step(Four)Softwood processed:95% ethanol is added in mixed powder 5, stir to obtain softwood 1;Purified water is added to mixed
Close in powder 6, stir to obtain softwood 2;
Step(Five)Pelletize:Respectively softwood 1, softwood 2 are crossed 16 mesh sieves and pelletized, obtain wet granular 1, wet granular 2, adopt in pelletization
Pelletized with acid source and alkali source;
Step(Six)Dry, whole grain:Respectively by wet granular 1, wet granular 2 at a temperature of 40-50 DEG C, it is dried to moisture≤5%, mistake
16 mesh sieve whole grains, obtain particle 1, particle 2;
Step(Seven)Always mix:Use level mixing apparatus, mixed powder 7 is mixed with particle 2 equal increments, obtains mixture;General
Grain 1, mixture mixing 15min, obtain total mixture;
Step(Eight)Compressing tablet:By total mixture compressing tablet, obtain effervescent tablet, 4g/ piece, temperature 18-25 DEG C, relative humidity≤65%;
Step(Nine)Select;
Step(Ten)Inner packing, external packing;
Step(11)Quality inspection;
Step(12)Warehouse-in.
Preferably, step(Five)Middle acid source, alkali source are separately pelletized, it is to avoid react in technical process, reduce effervesce effect
Really.
Preferably, step(Two)And step(Seven)Described in horizontal mixing apparatus include mix inner core, mixing outer tube,
Bearing group, inside are provided with shaft, motor one and the motor two of cavity, pass through between described mixing inner core and described mixing outer tube
One circle ball rotates and connects, and described mixing outer tube is arranged on operating desk.
Preferably, fixation is welded to connect cylinder in described bearing group, described connecting cylinder mixes wherein the one of inner core with described
End is fixedly connected, and described shaft is horizontally through the axis hole of described bearing group and extends to the inside of described mixing inner core.
Preferably, the outer end of described shaft is in transmission connection with described motor one by belt one, described connecting cylinder leads to
Cross belt two to be in transmission connection with described motor two.
Preferably, the position on described shaft, outside located at described mixing inner core connects breather pipe, described shaft
The upper, position within located at described mixing inner core arranges some agitating rollers, all located at stirring hook on each described agitating roller,
The end of each described stirring hook is provided with perforate.
Preferably, being additionally provided with feed cap in described mixing outer tube, mixing on inner core relevant position, described feed cap and institute
State mixing outer tube to be detachably connected, described feed cap is set to magnetic feed cap, described mixing outer tube adopts irony material, described mixed
Close inner core and adopt stainless steel.
Preferably, from supplementary material remove outsourcing feed into clean area to inner packing operation workshop cleanliness factor be 30
Ten thousand grades.
The invention has the beneficial effects as follows:Compared with prior art, it is an advantage of the current invention that
First, this product is with Cobastab1, Cobastab2, Cobastab6, vitamin C, taurine, potassium chloride be primary raw material, six
Plant raw material and be all pressed powder, suitably make solid dosage forms.Effervescent tablet technique is simpler, is easily mastered, and is conducive to industrializing
Produce, and smooth appearance, attractive in appearance, beneficial to absorb, good stability, easy to carry, additionally, this product contain fruity, good mouthfeel, take after mixing it with water
Conveniently, the suitable population children of this product preferably and teenager take, and therefore the formulation of this product are set to effervescent tablet;And chlorine
Change potassium and be made for taurine electrolyte flow solid beverage as primary raw material, take before suitable players motion and after motion
With having the effect alleviating physical fatigue;
Secondly, the raw material of the present invention and partial supplementary material are substantially powder, and the health food of this kind of powder is in the mistake processed
In journey, the uniformity of mixing is its most important index, and the efficiency mixing is also the efficiency of whole preparation technology, mixes
The efficiency high of conjunction, then the efficiency of entirety preparation is just high, and the present invention abandons the mode of existing vertical stirring, equal because vertically stir
Evenness is poor, and stirring efficiency is low, can there is stirring dead angle, therefore the present invention adopts a kind of new horizontal mixing apparatus, and this level mixes
Equipment is rotated using mixing inner core and shaft simultaneously, and one rotates counterclockwise, and one rotates clockwise, and this level mixes
Equipment assists the mixing of preparation technology and always mixes step, can not only improve the efficiency of mixing, and mixture homogeneity is high.
Brief description
Fig. 1 position present invention process flow chart.
Fig. 2 is the schematic front view of the horizontal mixing apparatus of the present invention.
Fig. 3 position present invention mixing inner core and the schematic diagram mixing outer tube.
Wherein:1- mixing outer tube, 2- mixing inner core, 3- ball, 4- bearing group, 5- shaft, 6- motor one, 7- belt
One, 8- motor two, 9- belt two, 10- connecting cylinder, 11- agitating roller, 12- stirs hook, 13- breather pipe, 14- feed cap, 15-
Operating desk, 16- discharging lid.
Specific embodiment
In order that those of ordinary skill in the art is better understood on technical scheme, below in conjunction with the accompanying drawings and
Embodiment is further described to technical scheme.
Embodiment:Taurine electrolyte flow solid beverage, described taurine electrolyte flow solid beverage dispensing includes
Raw material:Cobastab10.015g, Cobastab20.015g, Cobastab60.015g, Catergen .3g, taurine 1.3g, chlorination
Potassium 1.5g;Auxiliary material:Citric acid 360g, sodium acid carbonate 230g, Macrogol 6000 5g, lactose 170g, D-sorbite
192.855g, Aspartame 10g, acesulfame potassium 3g, leucine 9g, lemon extract 5g, lemon fruit powder 10g;Described six kinds
Raw material is all pressed powder, and described taurine electrolyte flow solid beverage makes solid dosage forms.
Referring to the drawings shown in 1, the production technology of taurine electrolyte flow solid beverage, comprise the following steps:
Step(One)Sieve:Cobastab1, Cobastab2, Cobastab6, vitamin C, taurine, potassium chloride, citric acid, carbonic acid
Hydrogen sodium, lactose, D-sorbite cross 80 mesh sieves respectively, obtain each fine powder, standby;
Step(Two)Weigh:Weigh Cobastab by formula rate1Fine powder, Cobastab2Fine powder, Cobastab6Fine powder, vitamin C
Fine powder, taurine fine powder, potassium chloride fine powder, citric acid fine powder, sodium bicarbonate fine powder, lactose fine powder, D-sorbite fine powder, poly- second
Glycol 6000, Aspartame, acesulfame potassium, leucine lemon extract, lemon fruit powder, standby;
Step(Three)Mixing:Use level mixing apparatus, by Cobastab1Fine powder, Cobastab2Fine powder, Cobastab6Fine powder, ox
Sulfonic acid fine powder mixes, and time 5min obtains mixed powder 1;Potassium chloride fine powder is mixed with mixed powder 1, time 10min, obtain mixed powder
2;Vitamin C fine powder is mixed with mixed powder 2 equal increments, obtains mixed powder 3;Lactose fine powder is mixed with mixed powder 3 equal increments
Close, obtain mixed powder 4;Citric acid fine powder is mixed with mixed powder 4, time 30min, obtain mixed powder 5, standby;Sodium acid carbonate is thin
Powder is mixed with D-sorbite fine powder, time 30min, obtains mixed powder 6, standby;By acesulfame potassium, lemon extract, A Siba
Sweet, leucine, Macrogol 6000 mixing, time 10min, obtain mixed powder 7, standby;
For making each distributed components of this product, first Cobastab1, Cobastab2, Cobastab6, several consumption of taurine less mixed
Close uniformly, then add the slightly larger potassium chloride of consumption and mix;Again because vitamin C consumption is that remaining several raw material dosage is total and about 10
Times, therefore using equal increments method, vitamin C is mixed with other raw materials;
Referring to the drawings shown in 2-3:Horizontal mixing apparatus includes mixing inner core 2, mixing outer tube 1, bearing group 4, inside are provided with cavity
Shaft 5, motor 1 and motor 28, rotated by a circle ball 3 between described mixing inner core 2 and described mixing outer tube 1
Connect, medial surface setting one circle ball 3 half groove of mixing outer tube 1, the lateral surface setting one circle ball 3 half of described mixing inner core 2
Groove, ball 3 half groove on mixing outer tube 1 is arranged on ball 3 with the corresponding setting of ball 3 half groove on mixing inner core 2, ball 3
In half groove, and described mixing outer tube 1 is arranged on operating desk 15, on described mixing outer tube 1, mixing inner core 2 relevant position also
It is provided with feed cap 14, described feed cap 14 is detachably connected with the described outer tube 1 that mixes, and described feed cap 14 is set to magnetic feed cap
14, described mixing outer tube 1 adopts irony material, and described mixing inner core 2 adopts stainless steel, in described feed cap 14 opposite face
It is additionally provided with discharging lid 16, described discharging lid 16 is identical with described feed cap 14 structure, and feed cap 14 can also lead in whipping process
Cross magnetic to be more tightly connected with the described outer tube 1 that mixes, prevent material leakage;In described bearing group 4, fixation is welded to connect cylinder 10, described
Connecting cylinder 10 is fixedly connected with described wherein one end mixing inner core 2, and bearing group 4 is provided with two bearings, and two bearings pass through even
Connect cylinder 10 integrally connected, and described shaft 5 is horizontally through the axis hole of described bearing group 4 and extends to described mixing inner core 2
Internal;The outer end of described shaft 5 is in transmission connection with described motor 1 by belt 1, and described connecting cylinder 10 passes through belt two
9 are in transmission connection with described motor 28, and motor 1 and motor 28 are arranged on the same side, and it is inverse that shaft 5 passes through belt 1 drive
Hour hands rotate, and mixing inner core 2 passes through belt 29 drive and rotates clockwise;On described shaft 5, outside described mixing inner core 2
The position in portion connects breather pipe 13, and the position on described shaft 5, within located at described mixing inner core 2 arranges some agitating rollers
11, all located at stirring hook 12 on each described agitating roller 11, the end of each described stirring hook 12 is provided with perforate;
Specifically:During mixing, motor 1 drives shaft 5 to stir counterclockwise by belt 1, and motor 28 passes through belt 29
Drive mixing inner core 2 to rotate clockwise, during mixing, mixing inner core 2 also rotates, and turn to contrary, increase material with shaft 5
Between friction, clash into dynamics, mix great efforts, secondly, setting stirring hook 12 on shaft 5, stirring hook 12 is stainless
Steel material, stirring hook 12 setting be avoid exist stirring dead angle, that is, shaft 5 stir less than position, shaft 5
It is passed through compressed air, the perforate from stirring hook 12 end for the compressed air is outwards sprayed, further during inherent stirring
The dynamics improving stirring, by reverse mixing, stirring hook 12 and air agitation, more preferably, the uniformity is more for the effect of stirring
Height, the efficiency of stirring doubles, and mixing time shortens about half;
Step(Four)Softwood processed:95% ethanol is added in mixed powder 5, stir to obtain softwood 1;Purified water is added to mixed
Close in powder 6, stir to obtain softwood 2;
Step(Five)Pelletize:Respectively softwood 1, softwood 2 are crossed 16 mesh sieves and pelletized, obtain wet granular 1, wet granular 2, adopt in pelletization
Pelletized with acid source and alkali source;Acid source, alkali source are separately pelletized, it is to avoid react in technical process, reduce effervesce effect;
Step(Six)Dry, whole grain:Respectively by wet granular 1, wet granular 2 at a temperature of 40-50 DEG C, it is dried to moisture≤5%, mistake
16 mesh sieve whole grains, obtain particle 1, particle 2;
Step(Seven)Always mix:Use level mixing apparatus, as the horizontal mixing apparatus in step 3, by mixed powder 7 with
Grain 2 equal increments mixing, obtains mixture;By particle 1, mixture mixing 15min, obtain total mixture;
Step(Eight)Compressing tablet:By total mixture compressing tablet, obtain effervescent tablet, 4g/ piece, temperature 18-25 DEG C, relative humidity≤65%;
Step(Nine)Select;
Step(Ten)Inner packing, external packing;Inner packing, meets the medicinal polypropylene vial of YBB00112002 oral administration solid by 10/pipe
Standard;External packing, meets GB/T 6543 transportation and packing list corrugated case and the standard of double corrugation case;
Step(11)Quality inspection:Product inspection is carried out by Quality Inspector;
Step(12)Warehouse-in.
It feed into clean area from supplementary material removing outsourcing and be 300,000 grades to inner packing operation workshop cleanliness factor;
Scale up test is verified
Inventory expands 10 times respectively according to formula ratio respectively, carries out three batches of enlarged experiment tests, and result is as follows:
First scale up test survey report
Second batch scale up test survey report
3rd batch of scale up test survey report
Through three batches of scale up test and correlation test checking, the product that process above is obtained, indices all meet company standard
Related request, so technique is reasonable.
General principle, principal character and the advantages of the present invention of the present invention have been shown and described above.The technology of the industry
, it should be appreciated that the present invention is not restricted to the described embodiments, the simply explanation described in above-described embodiment and specification is originally for personnel
The principle of invention, without departing from the spirit and scope of the present invention, the present invention also has various changes and modifications, these changes
Change and improvement both falls within scope of the claimed invention.Claimed scope by appending claims and its
Equivalent thereof.
Claims (10)
1. taurine electrolyte flow solid beverage is it is characterised in that described taurine electrolyte flow solid beverage dispensing bag
Include raw material:Cobastab10.015g, Cobastab20.015g, Cobastab60.015g, Catergen .3g, taurine 1.3g, chlorine
Change potassium 1.5g;Auxiliary material:Citric acid 360g, sodium acid carbonate 230g, Macrogol 6000 5g, lactose 170g, D-sorbite
192.855g, Aspartame 10g, acesulfame potassium 3g, leucine 9g, lemon extract 5g, lemon fruit powder 10g.
2. taurine electrolyte flow solid beverage according to claim 1 and its production technology it is characterised in that:Described
Six kinds of raw materials are all pressed powder, and described taurine electrolyte flow solid beverage makes solid dosage forms.
3. the production technology of taurine electrolyte flow solid beverage is it is characterised in that comprise the following steps:
Step(One)Sieve:Cobastab1, Cobastab2, Cobastab6, vitamin C, taurine, potassium chloride, citric acid, carbonic acid
Hydrogen sodium, lactose, D-sorbite cross 80 mesh sieves respectively, obtain each fine powder, standby;
Step(Two)Weigh:Weigh Cobastab by formula rate1Fine powder, Cobastab2Fine powder, Cobastab6Fine powder, vitamin C
Fine powder, taurine fine powder, potassium chloride fine powder, citric acid fine powder, sodium bicarbonate fine powder, lactose fine powder, D-sorbite fine powder, poly- second
Glycol 6000, Aspartame, acesulfame potassium, leucine lemon extract, lemon fruit powder, standby;
Step(Three)Mixing:Use level mixing apparatus, by Cobastab1Fine powder, Cobastab2Fine powder, Cobastab6Fine powder, ox
Sulfonic acid fine powder mixes, and time 5min obtains mixed powder 1;Potassium chloride fine powder is mixed with mixed powder 1, time 10min, obtain mixed powder
2;Vitamin C fine powder is mixed with mixed powder 2 equal increments, obtains mixed powder 3;Lactose fine powder is mixed with mixed powder 3 equal increments
Close, obtain mixed powder 4;Citric acid fine powder is mixed with mixed powder 4, time 30min, obtain mixed powder 5, standby;Sodium acid carbonate is thin
Powder is mixed with D-sorbite fine powder, time 30min, obtains mixed powder 6, standby;By acesulfame potassium, lemon extract, A Siba
Sweet, leucine, Macrogol 6000 mixing, time 10min, obtain mixed powder 7, standby;
Step(Four)Softwood processed:95% ethanol is added in mixed powder 5, stir to obtain softwood 1;Purified water is added to mixed
Close in powder 6, stir to obtain softwood 2;
Step(Five)Pelletize:Respectively softwood 1, softwood 2 are crossed 16 mesh sieves and pelletized, obtain wet granular 1, wet granular 2, adopt in pelletization
Pelletized with acid source and alkali source;
Step(Six)Dry, whole grain:Respectively by wet granular 1, wet granular 2 at a temperature of 40-50 DEG C, it is dried to moisture≤5%, mistake
16 mesh sieve whole grains, obtain particle 1, particle 2;
Step(Seven)Always mix:Use level mixing apparatus, mixed powder 7 is mixed with particle 2 equal increments, obtains mixture;General
Grain 1, mixture mixing 15min, obtain total mixture;
Step(Eight)Compressing tablet:By total mixture compressing tablet, obtain effervescent tablet, 4g/ piece, temperature 18-25 DEG C, relative humidity≤65%;
Step(Nine)Select;
Step(Ten)Inner packing, external packing;
Step(11)Quality inspection;
Step(12)Warehouse-in.
4. the production technology of taurine electrolyte flow solid beverage according to claim 3 is it is characterised in that step
(Five)Middle acid source, alkali source are separately pelletized, it is to avoid react in technical process, reduce effervesce effect.
5. the production technology of taurine electrolyte flow solid beverage according to claim 3 is it is characterised in that step
(Two)And step(Seven)Described in horizontal mixing apparatus include mix inner core, mixing outer tube, bearing group, inside be provided with cavity
Shaft, motor one and motor two, are rotated by a circle ball between described mixing inner core and described mixing outer tube and connect, and institute
State mixing outer tube to be arranged on operating desk.
6. the production technology of taurine electrolyte flow solid beverage according to claim 5 is it is characterised in that described axle
Hold fixation in group and be welded to connect cylinder, described connecting cylinder is fixedly connected with described wherein one end mixing inner core, and described shaft
It is horizontally through the axis hole of described bearing group and extend to the inside of described mixing inner core.
7. the production technology of taurine electrolyte flow solid beverage according to claim 6 is it is characterised in that described stir
The outer end mixing axle is in transmission connection with described motor one by belt one, and described connecting cylinder is driven with described motor two by belt two
Connect.
8. the production technology of the taurine electrolyte flow solid beverage according to any one of claim 5-7, its feature exists
In the position on described shaft, outside located at described mixing inner core connects breather pipe, on described shaft, located at described mixed
Close the position within inner core and some agitating rollers are set, all located at stirring hook, each described stirring on each described agitating roller
The end of hook is provided with perforate.
9. the production technology of taurine electrolyte flow solid beverage according to claim 8 is it is characterised in that described
Mixing outer tube, mixing are additionally provided with feed cap on inner core relevant position, and described feed cap is detachably connected with the described outer tube that mixes, institute
State feed cap and be set to magnetic feed cap, described mixing outer tube adopts irony material, described mixing inner core adopts stainless steel.
10. the production technology of taurine electrolyte flow solid beverage according to claim 9 is it is characterised in that from former
Auxiliary material removing outsourcing feed into clean area and is 300,000 grades to inner packing operation workshop cleanliness factor.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610775054.4A CN106387585A (en) | 2016-08-31 | 2016-08-31 | Taurine electrolyte sports solid beverage and production technology thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610775054.4A CN106387585A (en) | 2016-08-31 | 2016-08-31 | Taurine electrolyte sports solid beverage and production technology thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
CN106387585A true CN106387585A (en) | 2017-02-15 |
Family
ID=58002371
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201610775054.4A Pending CN106387585A (en) | 2016-08-31 | 2016-08-31 | Taurine electrolyte sports solid beverage and production technology thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN106387585A (en) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107997181A (en) * | 2017-12-29 | 2018-05-08 | 宣城柏维力生物工程有限公司 | A kind of collagen effervescent tablet and preparation method thereof |
CN108095124A (en) * | 2017-12-29 | 2018-06-01 | 宣城柏维力生物工程有限公司 | A kind of zinc gluconate effervescent tablet and its preparation process |
CN108419962A (en) * | 2018-02-27 | 2018-08-21 | 广州彤博士健康科技有限公司 | Adjust the drink with function formula and preparation method of electrolyte |
CN108684999A (en) * | 2018-04-12 | 2018-10-23 | 华大精准营养(深圳)科技有限公司 | A kind of motor function beverage |
CN108967806A (en) * | 2017-05-31 | 2018-12-11 | 江苏汉典生物科技股份有限公司 | Vitamin c effervescent tablet and preparation method thereof |
CN109527325A (en) * | 2018-11-20 | 2019-03-29 | 江苏汉典生物科技股份有限公司 | A kind of sports type effervescent tablet and preparation method thereof |
CN109662320A (en) * | 2017-10-13 | 2019-04-23 | 广州每日膳道生物科技有限公司 | A kind of composite electrolyte sports nutrient replenisher and preparation method thereof |
CN111194849A (en) * | 2018-11-16 | 2020-05-26 | 广州每日膳道生物科技有限公司 | 0-degree sports solid beverage and preparation process thereof |
CN112471378A (en) * | 2020-11-20 | 2021-03-12 | 宣城柏维力生物工程有限公司 | Electrolyte effervescent tablet and production method thereof |
CN112544847A (en) * | 2020-12-04 | 2021-03-26 | 北京大学第三医院(北京大学第三临床医学院) | Sports solid beverage for enhancing endurance and preparation method thereof |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1148351A (en) * | 1994-05-16 | 1997-04-23 | 尼罗有限公司 | Compacting granulator |
CN102150724A (en) * | 2011-03-30 | 2011-08-17 | 姜天安 | Functional mixture for refreshing and remitting physical fatigue and visual fatigue and application thereof |
CN202427419U (en) * | 2011-12-23 | 2012-09-12 | 自贡华启正光生态农林有限公司 | Mixing granulator |
CN203778028U (en) * | 2013-08-21 | 2014-08-20 | 涡阳县金宝农化科技有限公司 | Roller-central shaft stirring type fertilizer granulating device |
CN104397800A (en) * | 2014-11-28 | 2015-03-11 | 哈尔滨墨医生物技术有限公司 | Blueberry effervescent instant beverage and preparation method thereof |
CN104489850A (en) * | 2014-12-05 | 2015-04-08 | 黑龙江众生生物工程有限公司 | Solid compound bacteria beverage and preparation method thereof |
CN104621671A (en) * | 2013-11-12 | 2015-05-20 | 江苏艾兰得营养品有限公司 | Solid sports drink |
CN205216725U (en) * | 2015-12-24 | 2016-05-11 | 石雅娟 | Novel food mixing machine |
-
2016
- 2016-08-31 CN CN201610775054.4A patent/CN106387585A/en active Pending
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1148351A (en) * | 1994-05-16 | 1997-04-23 | 尼罗有限公司 | Compacting granulator |
CN102150724A (en) * | 2011-03-30 | 2011-08-17 | 姜天安 | Functional mixture for refreshing and remitting physical fatigue and visual fatigue and application thereof |
CN202427419U (en) * | 2011-12-23 | 2012-09-12 | 自贡华启正光生态农林有限公司 | Mixing granulator |
CN203778028U (en) * | 2013-08-21 | 2014-08-20 | 涡阳县金宝农化科技有限公司 | Roller-central shaft stirring type fertilizer granulating device |
CN104621671A (en) * | 2013-11-12 | 2015-05-20 | 江苏艾兰得营养品有限公司 | Solid sports drink |
CN104397800A (en) * | 2014-11-28 | 2015-03-11 | 哈尔滨墨医生物技术有限公司 | Blueberry effervescent instant beverage and preparation method thereof |
CN104489850A (en) * | 2014-12-05 | 2015-04-08 | 黑龙江众生生物工程有限公司 | Solid compound bacteria beverage and preparation method thereof |
CN205216725U (en) * | 2015-12-24 | 2016-05-11 | 石雅娟 | Novel food mixing machine |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108967806A (en) * | 2017-05-31 | 2018-12-11 | 江苏汉典生物科技股份有限公司 | Vitamin c effervescent tablet and preparation method thereof |
CN109662320A (en) * | 2017-10-13 | 2019-04-23 | 广州每日膳道生物科技有限公司 | A kind of composite electrolyte sports nutrient replenisher and preparation method thereof |
CN107997181A (en) * | 2017-12-29 | 2018-05-08 | 宣城柏维力生物工程有限公司 | A kind of collagen effervescent tablet and preparation method thereof |
CN108095124A (en) * | 2017-12-29 | 2018-06-01 | 宣城柏维力生物工程有限公司 | A kind of zinc gluconate effervescent tablet and its preparation process |
CN108419962A (en) * | 2018-02-27 | 2018-08-21 | 广州彤博士健康科技有限公司 | Adjust the drink with function formula and preparation method of electrolyte |
CN108684999A (en) * | 2018-04-12 | 2018-10-23 | 华大精准营养(深圳)科技有限公司 | A kind of motor function beverage |
CN111194849A (en) * | 2018-11-16 | 2020-05-26 | 广州每日膳道生物科技有限公司 | 0-degree sports solid beverage and preparation process thereof |
CN109527325A (en) * | 2018-11-20 | 2019-03-29 | 江苏汉典生物科技股份有限公司 | A kind of sports type effervescent tablet and preparation method thereof |
CN112471378A (en) * | 2020-11-20 | 2021-03-12 | 宣城柏维力生物工程有限公司 | Electrolyte effervescent tablet and production method thereof |
CN112544847A (en) * | 2020-12-04 | 2021-03-26 | 北京大学第三医院(北京大学第三临床医学院) | Sports solid beverage for enhancing endurance and preparation method thereof |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN106387585A (en) | Taurine electrolyte sports solid beverage and production technology thereof | |
CN106360179A (en) | Electrolyte sports beverage and preparation process thereof | |
CN102389116B (en) | Effervescent tablet for alleviating physical fatigue and preparation technology thereof | |
CN101049150B (en) | Edible nourishment health care potassium salt with extensive use | |
CN102067935B (en) | Red date and tremella jam for frozen beverage and preparation method thereof | |
US6037375A (en) | Nutrient composition | |
CN104026699B (en) | A kind of sports drink and preparation method | |
CN103918965A (en) | Physical fatigue alleviating beverage | |
CN106889412A (en) | One kind is refreshed oneself anti-fatigue solid beverage | |
CN103432161A (en) | Multivitamin mineral effervescent tablet and preparation method thereof | |
CN104522675B (en) | Composition of anti-endurance type fatigue and preparation method thereof | |
CN105707263A (en) | Low-fat and high-protein milk drunk after exercise and preparation method thereof | |
CN102823874A (en) | Pomegranate effervescent tablets and preparation method thereof | |
CN109619249A (en) | A kind of algae oil DHA zincification gel candy and preparation method thereof | |
CN106937743A (en) | A kind of antisecosis agent and preparation method thereof | |
CN108606269B (en) | Sports nutritional supplement and preparation method thereof | |
CN106491840A (en) | A kind of composition for relieving asthenopia and preparation method thereof | |
CN106418067B (en) | health beverage for supplementing physical strength and relieving fatigue | |
CN106387586A (en) | Whey protein and beta-hydroxy-methyl butyrate sport drink and production technology thereof | |
CN102228087A (en) | Loquat milk beverage and preparation method thereof | |
CN107375322A (en) | Children and juvenile multivitamin mineral effervescent tablet and preparation method thereof | |
JPH06327435A (en) | Nutrition-supplying composition | |
CN102613645A (en) | Sugar-free l-carnitine beverage | |
CN104664534A (en) | Electrolyte beverage and production process thereof | |
CN102132920B (en) | Potassium enriched rhodomyrtus tomentosa hassk beverage and preparation method thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20170215 |
|
RJ01 | Rejection of invention patent application after publication |