CN1545896A - Anoxia resistant anti-fatigued tea effervescence decoction piece and preparation method thereof - Google Patents
Anoxia resistant anti-fatigued tea effervescence decoction piece and preparation method thereof Download PDFInfo
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- CN1545896A CN1545896A CNA2003101111200A CN200310111120A CN1545896A CN 1545896 A CN1545896 A CN 1545896A CN A2003101111200 A CNA2003101111200 A CN A2003101111200A CN 200310111120 A CN200310111120 A CN 200310111120A CN 1545896 A CN1545896 A CN 1545896A
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- 206010021143 Hypoxia Diseases 0.000 title claims abstract description 32
- 238000002360 preparation method Methods 0.000 title claims abstract description 8
- 206010002660 Anoxia Diseases 0.000 title claims description 25
- 241000976983 Anoxia Species 0.000 title claims description 25
- 230000007953 anoxia Effects 0.000 title claims description 25
- 241001122767 Theaceae Species 0.000 title 1
- 244000269722 Thea sinensis Species 0.000 claims abstract description 38
- 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 30
- 235000013616 tea Nutrition 0.000 claims abstract description 30
- 230000002929 anti-fatigue Effects 0.000 claims abstract description 23
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims abstract description 14
- 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 12
- 235000009569 green tea Nutrition 0.000 claims abstract description 9
- 239000000843 powder Substances 0.000 claims abstract description 9
- 235000017557 sodium bicarbonate Nutrition 0.000 claims abstract description 7
- 229910000030 sodium bicarbonate Inorganic materials 0.000 claims abstract description 7
- 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 claims abstract description 6
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 claims abstract description 6
- 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 claims abstract description 6
- 229930003471 Vitamin B2 Natural products 0.000 claims abstract description 6
- 229930003268 Vitamin C Natural products 0.000 claims abstract description 6
- 238000000034 method Methods 0.000 claims abstract description 6
- 229960002477 riboflavin Drugs 0.000 claims abstract description 6
- 235000019164 vitamin B2 Nutrition 0.000 claims abstract description 6
- 239000011716 vitamin B2 Substances 0.000 claims abstract description 6
- 235000019154 vitamin C Nutrition 0.000 claims abstract description 6
- 239000011718 vitamin C Substances 0.000 claims abstract description 6
- 229930003451 Vitamin B1 Natural products 0.000 claims abstract description 4
- 229960003495 thiamine Drugs 0.000 claims abstract description 4
- 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 claims abstract description 4
- 235000010374 vitamin B1 Nutrition 0.000 claims abstract description 4
- 239000011691 vitamin B1 Substances 0.000 claims abstract description 4
- 239000002994 raw material Substances 0.000 claims description 34
- 239000000463 material Substances 0.000 claims description 24
- 239000002245 particle Substances 0.000 claims description 16
- 239000008187 granular material Substances 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 13
- 239000007779 soft material Substances 0.000 claims description 10
- 239000007921 spray Substances 0.000 claims description 8
- 239000000080 wetting agent Substances 0.000 claims description 8
- 238000001816 cooling Methods 0.000 claims description 6
- 238000002156 mixing Methods 0.000 claims description 6
- 238000010298 pulverizing process Methods 0.000 claims description 6
- 108010011485 Aspartame Proteins 0.000 claims description 5
- 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 description 5
- 239000000605 aspartame Substances 0.000 claims description 5
- 229960003438 aspartame Drugs 0.000 claims description 5
- 235000010357 aspartame Nutrition 0.000 claims description 5
- 239000000049 pigment Substances 0.000 claims description 5
- 239000011230 binding agent Substances 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 238000005469 granulation Methods 0.000 claims description 4
- 230000003179 granulation Effects 0.000 claims description 4
- 238000007873 sieving Methods 0.000 claims description 4
- 238000004080 punching Methods 0.000 claims 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 claims 1
- 229930006000 Sucrose Natural products 0.000 claims 1
- 235000019628 coolness Nutrition 0.000 claims 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 abstract description 8
- 230000007954 hypoxia Effects 0.000 abstract description 5
- 239000011780 sodium chloride Substances 0.000 abstract description 4
- 235000003599 food sweetener Nutrition 0.000 abstract 1
- 239000003765 sweetening agent Substances 0.000 abstract 1
- 241000699670 Mus sp. Species 0.000 description 10
- 239000008280 blood Substances 0.000 description 10
- 210000004369 blood Anatomy 0.000 description 10
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 6
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 6
- 230000009182 swimming Effects 0.000 description 5
- 229930003270 Vitamin B Natural products 0.000 description 4
- 235000013361 beverage Nutrition 0.000 description 4
- 235000019156 vitamin B Nutrition 0.000 description 4
- 239000011720 vitamin B Substances 0.000 description 4
- 229920002527 Glycogen Polymers 0.000 description 3
- PNNCWTXUWKENPE-UHFFFAOYSA-N [N].NC(N)=O Chemical compound [N].NC(N)=O PNNCWTXUWKENPE-UHFFFAOYSA-N 0.000 description 3
- 239000012467 final product Substances 0.000 description 3
- 230000006870 function Effects 0.000 description 3
- 229940096919 glycogen Drugs 0.000 description 3
- 230000002440 hepatic effect Effects 0.000 description 3
- 239000004310 lactic acid Substances 0.000 description 3
- 235000014655 lactic acid Nutrition 0.000 description 3
- 238000012856 packing Methods 0.000 description 3
- 235000011164 potassium chloride Nutrition 0.000 description 3
- 239000001103 potassium chloride Substances 0.000 description 3
- 238000007789 sealing Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 208000004880 Polyuria Diseases 0.000 description 2
- RYYVLZVUVIJVGH-UHFFFAOYSA-N caffeine Chemical compound CN1C(=O)N(C)C(=O)C2=C1N=CN2C RYYVLZVUVIJVGH-UHFFFAOYSA-N 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
- 230000035619 diuresis Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003792 electrolyte Substances 0.000 description 2
- 235000013402 health food Nutrition 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 description 2
- 229930003231 vitamin Natural products 0.000 description 2
- 235000013343 vitamin Nutrition 0.000 description 2
- 239000011782 vitamin Substances 0.000 description 2
- 229940088594 vitamin Drugs 0.000 description 2
- 150000003722 vitamin derivatives Chemical class 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 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 description 1
- 102000005862 Angiotensin II Human genes 0.000 description 1
- 101800000733 Angiotensin-2 Proteins 0.000 description 1
- 208000012639 Balance disease Diseases 0.000 description 1
- 206010008418 Cheilosis Diseases 0.000 description 1
- 206010019233 Headaches Diseases 0.000 description 1
- 206010020772 Hypertension Diseases 0.000 description 1
- CZGUSIXMZVURDU-JZXHSEFVSA-N Ile(5)-angiotensin II Chemical compound C([C@@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC=1NC=NC=1)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CC=1C=CC=CC=1)C([O-])=O)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(N)=[NH2+])NC(=O)[C@@H]([NH3+])CC([O-])=O)C(C)C)C1=CC=C(O)C=C1 CZGUSIXMZVURDU-JZXHSEFVSA-N 0.000 description 1
- 206010022998 Irritability Diseases 0.000 description 1
- LPHGQDQBBGAPDZ-UHFFFAOYSA-N Isocaffeine Natural products CN1C(=O)N(C)C(=O)C2=C1N(C)C=N2 LPHGQDQBBGAPDZ-UHFFFAOYSA-N 0.000 description 1
- 206010028372 Muscular weakness Diseases 0.000 description 1
- 206010029216 Nervousness Diseases 0.000 description 1
- 206010030113 Oedema Diseases 0.000 description 1
- NPYPAHLBTDXSSS-UHFFFAOYSA-N Potassium ion Chemical compound [K+] NPYPAHLBTDXSSS-UHFFFAOYSA-N 0.000 description 1
- 208000034189 Sclerosis Diseases 0.000 description 1
- 208000013738 Sleep Initiation and Maintenance disease Diseases 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical compound [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 description 1
- 206010047700 Vomiting Diseases 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 230000001154 acute effect Effects 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 208000008445 altitude sickness Diseases 0.000 description 1
- 229950006323 angiotensin ii Drugs 0.000 description 1
- 230000001093 anti-cancer Effects 0.000 description 1
- 230000004596 appetite loss Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 210000001124 body fluid Anatomy 0.000 description 1
- 239000010839 body fluid Substances 0.000 description 1
- 229960001948 caffeine Drugs 0.000 description 1
- VJEONQKOZGKCAK-UHFFFAOYSA-N caffeine Natural products CN1C(=O)N(C)C(=O)C2=C1C=CN2C VJEONQKOZGKCAK-UHFFFAOYSA-N 0.000 description 1
- 210000000748 cardiovascular system Anatomy 0.000 description 1
- ADRVNXBAWSRFAJ-UHFFFAOYSA-N catechin Natural products OC1Cc2cc(O)cc(O)c2OC1c3ccc(O)c(O)c3 ADRVNXBAWSRFAJ-UHFFFAOYSA-N 0.000 description 1
- 235000005487 catechin Nutrition 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 229950001002 cianidanol Drugs 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000035622 drinking Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 201000006549 dyspepsia Diseases 0.000 description 1
- 230000037149 energy metabolism Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 208000001780 epistaxis Diseases 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000009661 fatigue test Methods 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 231100000869 headache Toxicity 0.000 description 1
- 230000001631 hypertensive effect Effects 0.000 description 1
- 230000001146 hypoxic effect Effects 0.000 description 1
- 230000036039 immunity Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 206010022437 insomnia Diseases 0.000 description 1
- 235000021266 loss of appetite Nutrition 0.000 description 1
- 208000019017 loss of appetite Diseases 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 210000004877 mucosa Anatomy 0.000 description 1
- 210000003205 muscle Anatomy 0.000 description 1
- 210000000663 muscle cell Anatomy 0.000 description 1
- 230000036473 myasthenia Effects 0.000 description 1
- 210000005036 nerve Anatomy 0.000 description 1
- 210000000653 nervous system Anatomy 0.000 description 1
- 231100000957 no side effect Toxicity 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 230000035790 physiological processes and functions Effects 0.000 description 1
- 150000008442 polyphenolic compounds Chemical class 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 235000021395 porridge Nutrition 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 229910001414 potassium ion Inorganic materials 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
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- 229910001415 sodium ion Inorganic materials 0.000 description 1
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- 210000002700 urine Anatomy 0.000 description 1
- 230000008673 vomiting Effects 0.000 description 1
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- Tea And Coffee (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
Abstract
The invention relates to a tea effervescent medicinal herbal pieces for antifatigue and hypoxia resistance and its preparing process, wherein the tea effervescent herbal pieces comprises 30%-40% weight portion of green tea powder, 1.0%-1.35% weight portion of KCl, 1.0%-1.35% weight portion of NaCl, 5%-10% weight portion of vitamin C, 15%-17% weight portion of sodium hydrogen carbonate, 29%-31% weight portion of citric acid, 6%-7% weight portion of sweetener, 0.01%-0.05% weight portion of vitamin B1, and 0.05%-0.1% weight portion of vitamin B2. The invention also discloses its preparation process.
Description
Technical field
The present invention relates to health food and preparation method thereof, be specifically related to a kind of anoxia enduring, antifatigue tea effervescence decoction piece and preparation method thereof.
Background technology
After the people who lives in the Plain enters the plateau, because anoxia is very big to the influence of function of human body, cause work capacity to descend, above sea level higher, work capacity descends more obviously.On the one hand, because plateau wind is big, air drying makes human body forfeiture washiness, and susceptible is thirsty, and skin, mucosa drying often are dewatered, phenomenons such as cheilosis and epistaxis, so need keep the skin wet in time.Discover that high altitude anoxia can influence people's the sense of taste, the people likes eating the beverage of food, particularly sour-sweet flavor of sour-sweet taste on the plateau rather well received.On the other hand, body fluid running imbalance during human body anoxia, the electrolyte balance disorder, with diuresis and water retention, so common AMS patient has face, hands or foot periphery edema phenomenon, severe AMS patient's urine amount obviously is less than patients with mild.Take the diuresis measure, reduce water retention, positive effect is arranged alleviating acute high altitude reaction.But there is certain toxic and side effects in present measure.Therefore, how to strengthen the ability that the people enters body anti-hypoxia behind the plateau and to improve the labour force be the problem that presses for solution.But, also do not occur with tea beverage at present as anoxia enduring and antifatigue health food.
Summary of the invention
The purpose of this invention is to provide a kind of anoxia enduring, antifatigue tea effervescence decoction piece and preparation method thereof, it can significantly improve the hypoxia-bearing capability and the highly anti-fatigue ability of body, have no side effect, it is little, in light weight to have volume, sanitation and hygiene, long shelf-life, convenient carrying are particularly suitable for the people and drink under altitude environment.
A kind of anoxia enduring of the present invention, antifatigue tea effervescence decoction piece contain the vitamin C, the sodium bicarbonate of 15%--17% (weight), the citric acid of 29%--31% (weight), the aspartame of 6%--7% (weight), the vitamin B1 of 0.01%-0.05% (weight), the vitamin B2 of vitamin B2 0.05%-0.1% (weight) of NaCI, 5%--10% (weight) of KCI, 3.0%-3.5% (weight) of green tea powder, the 1.0%-1.35% (weight) of 30%--40% (weight).Green tea powder is a Main Ingredients and Appearance of the present invention, because the alloxuric bodies in the green tea powder (caffeine, theophylline etc.), tea polyphenols, polysaccharide, tea pigment, vitamin, and inorganic elements etc. with health role, can suppress accumulation, blood fat reducing, the prevention of arterial medicated porridge sclerosis of cholesterol in blood; Effective ingredient γ-An Jidingsuan in the green tea powder has the Angiotensin II of inhibition to produce, and treats hypertensive effect; Aldehydes matter in the green tea powder particularly catechin has the function that strengthens blood capillary toughness and bring high blood pressure down.Adding vitamin, is because vitamin C has physiological function widely, and anticancer, blood fat reducing, raising body immunity and resisting oxygen lack are arranged; Vitamin B1 has the function of improving nervous system and cardiovascular system, can alleviate symptoms such as headache that high altitude anoxia causes, nervous, vomiting, insomnia, tired, loss of appetite, dyspepsia and myasthenia of limbs; Vitamin B2 can be improved the energy metabolism of high altitude anoxia, alleviates altitude sickness and keeps muscle power.Adding sodium chloride and potassium chloride, is because sodium ion and potassium ion participate in the multiple physiological and biochemical procedure of body, can improve nerve, muscle cell irritability, keep the cylinder electrolyte balance.Adding sodium bicarbonate, is to solve CO because sodium bicarbonate is met moisture
2, help the disintegrate of tablet to dissolve, discharge effective ingredient, simultaneously sodium bicarbonate also the scalable pH value in suitable scope.The effect that adds citric acid and aspartame is that the present invention has sour-sweet taste, to be adapted at plateau staff's taste.
A kind of anoxia enduring of the present invention, antifatigue tea effervescence decoction piece its preparation method the steps include: raw material pulverizing → batching → mixing → system soft material → pelletize → oven dry → cooling → granulate → tabletting;
Raw material pulverizing: raw material that granularity is bigger before batching, pulverize on pulverizer as citric acid etc. in advance, and cross 100 mesh sieves; Its role is to guarantee tablet aesthetic in appearance, color and luster is even, also can make raw material mix homogeneously in the course of processing in addition, thereby guarantee that tablet quality is stable;
Batching: weigh raw material by above-mentioned weight proportion;
Mix: the raw material that content is more is poured in the mixer earlier, starts agitator with the raw material mix homogeneously, and the more raw material of poor raw material and content mixes employing equivalent and increases progressively mixing method step by step;
The system soft material: spray wetting agent pigment solution is painted on mixed material, thereafter the organic solution of the binding agent of spray about 3% on mixed material;
Pelletize: the soft material that makes is caused 14 purpose granules on granulation machine, the granule of making places pallet;
Oven dry: the wet granular in the pallet is placed 70 ℃ of baking taking-ups after 1 hour down, in dry environment cooling down;
Granulate: through sieving, make the material particles degree even, and remove the material particles that is unsuitable for the tabletting requirement;
Tabletting: in dried material particles, add 1% disintegrating agent, 0.5% wetting agent, drop into behind the mix homogeneously in the tablet machine, with conglobate tea effervescence decoction piece of material particles punching press or oval-shaped tea effervescence decoction piece; To get final product in packer monolithic sealing packing through the tea effervescence decoction piece that is up to the standards.
Zoopery is the result prove: a kind of anoxia enduring of the present invention, antifatigue tea effervescence decoction piece can significantly improve the hypoxia-bearing capability and the highly anti-fatigue ability of body.
30 white mice are divided into two groups, and 15 every group, the C group is matched group, and the T group is the hypoxia endurance test group; Make beverage with a kind of anoxia enduring of the present invention, antifatigue tea effervescence decoction piece, drink 7 days to the white mice of T group after, together carry out the airtight anoxia test with the white mice of C group; The life span of C group is that 26.49 ± 2.86 (min), standard tolerance time are 10.62 ± 0.97 (min100mL
-1), the life span of T group is that 29.75 ± 4.53 (min), standard tolerance time are 12.03 ± 1.92 (min100mL
-1); Experimental result shows: a kind of anoxia enduring of the present invention, antifatigue tea effervescence decoction piece can improve the ability of white mice anoxia enduring.
60 white mice are divided into two groups, and 30 every group, the C group is matched group, and the T group is the anti-fatigue test group; Make beverage with a kind of anoxia enduring of the present invention, antifatigue tea effervescence decoction piece, drink 7 days to the white mice of T group after, carry out the swimming with a load attached to the body experiment with the white mice one of the C group swimming case (100cm * 80cm * 70cm, depth of water 50cm, 25 ℃ of water temperatures) that coexists; C group swimming time is 12.07 ± 6.50 (min), and T group swimming time is 22.49 ± 18.63 (min); Experimental result shows: a kind of anoxia enduring of the present invention, antifatigue tea effervescence decoction piece can improve the anti-fatigue ability of white mice.
From above two groups, respectively get 10 white mice, measure relevant biochemical indicator; The blood urea nitrogen of C group is 8.70 ± 0.35 (mmol.L
-1), blood lactic acid is 7.31 ± 0.49 (mmol.L
-1), hepatic glycogen is 92.87 ± 4.13 (mg.100g
-1), the blood urea nitrogen of T group is 7.23 ± 0.50 (mmol.L
-1), blood lactic acid is 4.73 ± 0.30 (mmol.L
-1), hepatic glycogen is 128.63 ± 4.14 (mg.100g
-1); Experimental result shows: a kind of anoxia enduring of the present invention, antifatigue tea effervescence decoction piece can make the blood urea nitrogen and the decline of blood lactic acid, the hepatic glycogen that carry out the white mice after swimming with a load attached to the body is tested raise.
With the beverage that a kind of anoxia enduring of the present invention, antifatigue tea effervescence decoction piece are made, taste is sour-sweet, is adapted at the taste of staff under the hypoxic plateau environment, can significantly improve the hypoxia-bearing capability and the highly anti-fatigue ability of body after drinking; It is little, in light weight, easy to carry to have volume, the advantage of sanitation and hygiene, long shelf-life.
The specific embodiment
Must test by the related request of stipulating in the national standard to the raw material that uses.
Embodiment 1, gets green tea powder 35kg, potassium chloride 1.2kg, sodium chloride 3.3kg, vitamin C 8kg, sodium bicarbonate 16.4kg, citric acid 29kg, aspartame 7kg, vitamin B
10.05kg, vitamin B
20.05kg be raw material, prepare a kind of anoxia enduring of the present invention, antifatigue tea effervescence decoction piece according to the following steps:
Raw material pulverizing: raw material that granularity is bigger before batching, pulverize on pulverizer as citric acid etc. in advance, and cross 100 mesh sieves;
Batching: weigh raw material by above-mentioned weight proportion;
Mix: the raw material that content is more is poured in the mixer earlier, starts agitator with the raw material mix homogeneously, and the more raw material of poor raw material and content mixes employing equivalent and increases progressively mixing method step by step;
The system soft material: spray wetting agent pigment solution is painted on mixed material, thereafter the organic solution of the binding agent of spray about 3% on mixed material;
Pelletize: the soft material that makes is caused 14 purpose granules on granulation machine, the granule of making places pallet;
Oven dry: the wet granular in the pallet is placed 70 ℃ of baking taking-ups after 1 hour down, in dry environment cooling down;
Granulate: through sieving, make the material particles degree even, and remove the material particles that is unsuitable for the tabletting requirement;
Tabletting: in dried material particles, add 1% disintegrating agent, 0.5% wetting agent, drop into behind the mix homogeneously in the tablet machine, with the conglobate tea effervescence decoction piece of material particles punching press; To get final product in packer monolithic sealing packing through the tea effervescence decoction piece that is up to the standards.
Embodiment 2, get green tea powder 39kg, potassium chloride 1kg, sodium chloride 3.5kg, vitamin C 5kg, sodium bicarbonate 15.4kg, citric acid 30kg, aspartame 6kg, vitamin B
10.03kg, vitamin B
20.07kg be raw material, prepare a kind of anoxia enduring of the present invention, antifatigue tea effervescence decoction piece according to the following steps:
Raw material pulverizing: raw material that granularity is bigger before batching, pulverize on pulverizer as citric acid etc. in advance, and cross 100 mesh sieves;
Batching: weigh raw material by above-mentioned weight proportion;
Mix: the raw material that content is more is poured in the mixer earlier, starts agitator with the raw material mix homogeneously, and the more raw material of poor raw material and content mixes employing equivalent and increases progressively mixing method step by step;
The system soft material: spray wetting agent pigment solution is painted on mixed material, thereafter the organic solution of the binding agent of spray about 3% on mixed material;
Pelletize: the soft material that makes is caused 14 purpose granules on granulation machine, the granule of making places pallet;
Oven dry: the wet granular in the pallet is placed 70 ℃ of baking taking-ups after 1 hour down, in dry environment cooling down;
Granulate: through sieving, make the material particles degree even, and remove the material particles that is unsuitable for the tabletting requirement;
Tabletting: in dried material particles, add 1% disintegrating agent, 0.5% wetting agent, drop in the tablet machine behind the mix homogeneously, material particles is struck out oval-shaped tea effervescence decoction piece; To get final product in packer monolithic sealing packing through the tea effervescence decoction piece that is up to the standards.
Claims (2)
1, a kind of anoxia enduring, antifatigue tea effervescence decoction piece contain the vitamin C, the sodium bicarbonate of 15%-17% (weight), the citric acid of 29%-31% (weight), the aspartame of 6%-7% (weight), the vitamin B1 of 0.01%-0.05% (weight), the vitamin B2 of vitamin B2 0.05%-0.1% (weight) of NaCI, 5%-10% (weight) of KCI, 3.0%-3.5% (weight) of green tea powder, the 1.0%-1.35% (weight) of 30%-40% (weight).
2, as the preparation method of claim 1 anoxia enduring, antifatigue tea effervescence decoction piece, the steps include: raw material pulverizing → batching → mixing → system soft material → pelletize → oven dry → cooling → granulate → tabletting;
Raw material pulverizing: raw material that granularity is bigger before batching, pulverize on pulverizer as citric acid, white sugar etc. in advance, and cross 100 mesh sieves; Batching: weigh raw material by above-mentioned weight proportion;
Mix: the raw material that content is more is poured in the mixer earlier, starts agitator with the raw material mix homogeneously, and the more raw material of poor raw material and content mixes employing equivalent and increases progressively mixing method step by step;
The system soft material: spray wetting agent pigment solution is painted on mixed material, thereafter the organic solution of the binding agent of spray about 3% on mixed material;
Pelletize: the soft material that makes is caused 14 purpose granules on granulation machine, the granule of making places pallet;
Oven dry: the wet granular in the pallet is placed 70 ℃ of baking taking-up coolings after 1 hour down;
Granulate: through sieving, make the material particles degree even, and remove the material particles that is unsuitable for the tabletting requirement;
Tabletting: in dried material particles, add 1% disintegrating agent, 0.5% wetting agent, drop in the tablet machine, behind the mix homogeneously with conglobate tea effervescence decoction piece of material particles punching press or oval-shaped tea effervescence decoction piece.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 200310111120 CN1269416C (en) | 2003-12-04 | 2003-12-04 | Anoxia resistant anti-fatigued tea effervescence decoction piece and preparation method thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 200310111120 CN1269416C (en) | 2003-12-04 | 2003-12-04 | Anoxia resistant anti-fatigued tea effervescence decoction piece and preparation method thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1545896A true CN1545896A (en) | 2004-11-17 |
| CN1269416C CN1269416C (en) | 2006-08-16 |
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| CN 200310111120 Expired - Lifetime CN1269416C (en) | 2003-12-04 | 2003-12-04 | Anoxia resistant anti-fatigued tea effervescence decoction piece and preparation method thereof |
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Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1313012C (en) * | 2005-04-14 | 2007-05-02 | 王伦全 | Catechin effervescence tablet |
| CN101069534B (en) * | 2006-05-12 | 2011-07-27 | 上海科宝生物技术有限公司 | Theaflavin tablet and drink |
| CN101214014B (en) * | 2008-01-02 | 2011-08-10 | 南京农业大学 | Production technology of barley seedling powder and product thereof |
| CN102349892A (en) * | 2011-08-17 | 2012-02-15 | 江门市新会区光华生物科技有限公司 | High-content vitamin C tablets and preparation method thereof |
| US8367127B2 (en) * | 2006-05-19 | 2013-02-05 | Suntory Holdings Limited | Tea beverages containing proanthocyanidins |
| CN103931984A (en) * | 2014-01-21 | 2014-07-23 | 中国人民解放军第三军医大学 | Effervescent tablet used for in-time physical power replenishment in exercise, and applications thereof |
| CN106107404A (en) * | 2016-06-16 | 2016-11-16 | 李卫平 | A kind of effervescent tablet of effective alleviation labor pains |
| CN107927245A (en) * | 2017-11-30 | 2018-04-20 | 重庆藏天露生物科技有限公司 | A kind of functional solid beverage and its preparation process for improving anoxia endurance |
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2003
- 2003-12-04 CN CN 200310111120 patent/CN1269416C/en not_active Expired - Lifetime
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1313012C (en) * | 2005-04-14 | 2007-05-02 | 王伦全 | Catechin effervescence tablet |
| CN101069534B (en) * | 2006-05-12 | 2011-07-27 | 上海科宝生物技术有限公司 | Theaflavin tablet and drink |
| US8367127B2 (en) * | 2006-05-19 | 2013-02-05 | Suntory Holdings Limited | Tea beverages containing proanthocyanidins |
| CN101214014B (en) * | 2008-01-02 | 2011-08-10 | 南京农业大学 | Production technology of barley seedling powder and product thereof |
| CN102349892A (en) * | 2011-08-17 | 2012-02-15 | 江门市新会区光华生物科技有限公司 | High-content vitamin C tablets and preparation method thereof |
| CN103931984A (en) * | 2014-01-21 | 2014-07-23 | 中国人民解放军第三军医大学 | Effervescent tablet used for in-time physical power replenishment in exercise, and applications thereof |
| CN106107404A (en) * | 2016-06-16 | 2016-11-16 | 李卫平 | A kind of effervescent tablet of effective alleviation labor pains |
| CN107927245A (en) * | 2017-11-30 | 2018-04-20 | 重庆藏天露生物科技有限公司 | A kind of functional solid beverage and its preparation process for improving anoxia endurance |
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| CN1269416C (en) | 2006-08-16 |
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