CN1269416C - 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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- CN1269416C CN1269416C CN 200310111120 CN200310111120A CN1269416C CN 1269416 C CN1269416 C CN 1269416C CN 200310111120 CN200310111120 CN 200310111120 CN 200310111120 A CN200310111120 A CN 200310111120A CN 1269416 C CN1269416 C CN 1269416C
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- 238000002360 preparation method Methods 0.000 title claims abstract description 9
- 206010021143 Hypoxia Diseases 0.000 title abstract description 13
- 206010002660 Anoxia Diseases 0.000 title description 6
- 241000976983 Anoxia Species 0.000 title description 6
- 230000007953 anoxia Effects 0.000 title description 6
- 241001122767 Theaceae Species 0.000 title 1
- 244000269722 Thea sinensis Species 0.000 claims abstract description 36
- 239000002994 raw material Substances 0.000 claims abstract description 35
- 235000013616 tea Nutrition 0.000 claims abstract description 32
- 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
- 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
- 238000001816 cooling Methods 0.000 claims abstract description 7
- 238000002156 mixing Methods 0.000 claims abstract description 7
- 238000010298 pulverizing process Methods 0.000 claims abstract description 7
- 108010011485 Aspartame Proteins 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
- 229930003268 Vitamin C Natural products 0.000 claims abstract description 6
- 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 6
- 239000000605 aspartame Substances 0.000 claims abstract description 6
- 229960003438 aspartame Drugs 0.000 claims abstract description 6
- 235000010357 aspartame Nutrition 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
- 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 5
- 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 5
- 229930003471 Vitamin B2 Natural products 0.000 claims abstract description 5
- 229960002477 riboflavin Drugs 0.000 claims abstract description 5
- 235000019164 vitamin B2 Nutrition 0.000 claims abstract description 5
- 239000011716 vitamin B2 Substances 0.000 claims abstract description 5
- 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
- 239000000463 material Substances 0.000 claims description 24
- 239000002245 particle Substances 0.000 claims description 24
- 230000002929 anti-fatigue Effects 0.000 claims description 22
- 230000000496 anti-anoxic effect Effects 0.000 claims description 19
- 239000011122 softwood Substances 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 8
- 239000007921 spray Substances 0.000 claims description 8
- 239000000080 wetting agent Substances 0.000 claims description 8
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims description 7
- 238000005469 granulation Methods 0.000 claims description 6
- 230000003179 granulation Effects 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 235000020985 whole grains Nutrition 0.000 claims description 6
- 239000000049 pigment Substances 0.000 claims description 5
- 239000000853 adhesive Substances 0.000 claims description 4
- 230000001070 adhesive effect Effects 0.000 claims description 4
- 239000007884 disintegrant Substances 0.000 claims description 4
- 238000007873 sieving Methods 0.000 claims description 4
- 238000004080 punching Methods 0.000 claims description 3
- 235000019628 coolness Nutrition 0.000 claims 1
- 235000021552 granulated sugar Nutrition 0.000 claims 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 abstract description 8
- 230000006870 function Effects 0.000 abstract description 4
- 239000011780 sodium chloride Substances 0.000 abstract description 4
- 230000000694 effects Effects 0.000 abstract description 3
- 230000001105 regulatory effect Effects 0.000 abstract description 2
- 231100000331 toxic Toxicity 0.000 abstract description 2
- 230000002588 toxic effect Effects 0.000 abstract description 2
- 238000002791 soaking Methods 0.000 abstract 4
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 abstract 1
- 238000013329 compounding Methods 0.000 abstract 1
- 239000008187 granular material Substances 0.000 abstract 1
- 238000004806 packaging method and process Methods 0.000 abstract 1
- 239000007779 soft material Substances 0.000 abstract 1
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 6
- 239000008280 blood Substances 0.000 description 6
- 210000004369 blood Anatomy 0.000 description 6
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 6
- 238000012856 packing Methods 0.000 description 6
- 230000009182 swimming Effects 0.000 description 5
- 235000013361 beverage Nutrition 0.000 description 4
- 230000007954 hypoxia Effects 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
- 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
- 239000001103 potassium chloride Substances 0.000 description 3
- 235000011164 potassium chloride Nutrition 0.000 description 3
- 238000007789 sealing Methods 0.000 description 3
- 239000004480 active ingredient Substances 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
- 239000003792 electrolyte Substances 0.000 description 2
- 208000001780 epistaxis Diseases 0.000 description 2
- 235000013402 health food Nutrition 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
- 239000011782 vitamin Substances 0.000 description 2
- 235000013343 vitamin Nutrition 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
- 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
- 206010030302 Oliguria Diseases 0.000 description 1
- 208000004880 Polyuria 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
- 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
- 208000022531 anorexia Diseases 0.000 description 1
- 230000001093 anti-cancer Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000008901 benefit Effects 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
- 206010061428 decreased appetite Diseases 0.000 description 1
- 230000035619 diuresis 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
- 238000005516 engineering process Methods 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
- 229960003692 gamma aminobutyric acid Drugs 0.000 description 1
- BTCSSZJGUNDROE-UHFFFAOYSA-N gamma-aminobutyric acid Chemical compound NCCCC(O)=O BTCSSZJGUNDROE-UHFFFAOYSA-N 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 231100000869 headache Toxicity 0.000 description 1
- 230000036541 health Effects 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
- 150000002632 lipids Chemical class 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 210000004400 mucous membrane Anatomy 0.000 description 1
- 210000003205 muscle Anatomy 0.000 description 1
- 210000000663 muscle cell Anatomy 0.000 description 1
- 230000011224 negative regulation of urine volume 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
- 230000008092 positive effect Effects 0.000 description 1
- 229910001414 potassium ion Inorganic materials 0.000 description 1
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- 229910001415 sodium ion Inorganic materials 0.000 description 1
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- Coloring Foods And Improving Nutritive Qualities (AREA)
- Tea And Coffee (AREA)
Abstract
The present invention relates to an effervescent soaking tea tablet with the functions of resisting oxygen deficiency and resisting fatigue and a preparation method thereof. The effervescent soaking tea tablet contains the following components by the weight percentage: 30 to 40% of green tea powder, 1.0 to 1.35% of KCl, 3.0 to 3.5% of NaCl, 5 to 10% of vitamin C, 15 to 17% of sodium bicarbonate, 29 to 31% of citric acid, 6 to 7% of aspartame, 0.01 to 0.05% of vitamin B1 and 0.05 to 0.1% of vitamin B2. The preparation method comprises the steps of checking raw materials, pulverizing, compounding, mixing, preparing soft materials, granulating, baking, cooling, regulating granules, tabletting and packaging. The effervescent soaking tea tablet can obviously enhance the oxygen deficiency resistance and the fatigue resistance of human bodies, and has the characteristics of no toxic or side effect, small volume, small weight, good sanitation, long shelf life and good portability; the effervescent soaking tea tablet is especially suitable for people in altitude environment to drink.
Description
Technical field
The present invention relates to health food and preparation method thereof, be specifically related to tea effervescence decoction piece of a kind of anti-anoxic, antifatigue and preparation method thereof.
Background technology
After the people who lives in the Plain enters the plateau, because anoxic is very big to the influence of function of human body, cause labour capacity to descend, above sea level higher, labour capacity descends more obviously.On the one hand, because plateau wind is big, the air drying makes human body forfeiture washiness, and susceptible is thirsty, and skin, mucous membrane drying often are dewatered, lip is dry and cracked and phenomenon such as nosebleed 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 antidiuresis and water retention, so common AMS patient has face, hand or pin periphery oedema 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 effect in present measure.Therefore, how to strengthen the ability that the people enters the anti-anoxic of body behind the plateau and to improve the labour be the problem that presses for solution.But, also do not have at present to occur with the health food of tea beverage as anti-anoxic and antifatigue.
Summary of the invention
The purpose of this invention is to provide tea effervescence decoction piece of a kind of anti-anoxic, antifatigue 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.
The tea effervescence decoction piece of a kind of anti-anoxic of the present invention, antifatigue contains the vitamin C, the sodium acid carbonate 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).The 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 the accumulation of cholesterol in blood, reduce blood fat, the sclerosis of prevention of arterial congee; Active ingredient GABA 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 capillary toughness and bring high blood pressure down.Adding vitamin, is because vitamin C has physiological function widely, and anticancer, reducing blood lipid, 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, anorexia, indigestion and weakness of limbs; Vitamin B2 can improve the energetic supersession 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 acid carbonate, is to solve CO because sodium acid carbonate is met moisture
2, help the disintegration of tablet to dissolve, discharge active ingredient, sodium acid carbonate also can be regulated the pH value in suitable scope simultaneously.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.
The tea effervescence decoction piece its preparation method of a kind of anti-anoxic of the present invention, antifatigue the steps include: raw material pulverizing → batching → mixing → system softwood → granulation → oven dry → cooling → whole grain → compressing tablet;
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, and raw material is mixed in process, 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 raw material is mixed, and the more raw material of poor raw material and content mixes employing equivalent and increases progressively mixing method step by step;
The system softwood: spray wetting agent pigment solution is painted on mixed material, thereafter the organic solution of the adhesive of spray about 3% on mixed material;
Granulation: the softwood that makes is caused 14 purpose particles on granulator, the particle 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;
Whole grain: through sieving, make the material particles degree even, and remove the material particles that is unsuitable for the compressing tablet requirement;
Compressing tablet: in dried material particles, add 1% disintegrant, 0.5% wetting agent, mix the back and drop in the tablet press machine, with conglobate tea effervescence decoction piece of material particles punching press or oval-shaped tea effervescence decoction piece; To get final product in packing machine monolithic sealing packing through the tea effervescence decoction piece that is up to the standards.
Zoopery is the result prove: the tea effervescence decoction piece of a kind of anti-anoxic of the present invention, antifatigue can significantly improve the hypoxia-bearing capability and the highly anti-fatigue ability of body.
30 small white mouses are divided into two groups, and 15 every group, the C group is control group, and the T group is the hypoxia endurance test group; Tea effervescence decoction piece with a kind of anti-anoxic of the present invention, antifatigue is made beverage, drink 7 days to the small white mouse of T group after, together carry out the airtight anoxia test with the small white mouse 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: the tea effervescence decoction piece of a kind of anti-anoxic of the present invention, antifatigue can improve the ability of the anti-anoxic of small white mouse.
60 small white mouses are divided into two groups, and 30 every group, the C group is control group, and the T group is the anti-fatigue test group; Tea effervescence decoction piece with a kind of anti-anoxic of the present invention, antifatigue is made beverage, drink 7 days to the small white mouse of T group after, carry out the swimming with a load attached to the body experiment with the small white mouse 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: the tea effervescence decoction piece of a kind of anti-anoxic of the present invention, antifatigue can improve the anti-fatigue ability of small white mouse.
From above two groups, respectively get 10 small white mouses, measure relevant biochemical indicator; The 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 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: the tea effervescence decoction piece of a kind of anti-anoxic of the present invention, antifatigue can make the urea nitrogen and the decline of blood lactic acid, the hepatic glycogen that carry out the small white mouse after swimming with a load attached to the body is tested raise.
With the beverage that the tea effervescence decoction piece of a kind of anti-anoxic of the present invention, antifatigue is 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 acid carbonate 16.4kg, citric acid 29kg, Aspartame 7kg, Cobastab
10.05kg, Cobastab
20.05kg be raw material, prepare the tea effervescence decoction piece of a kind of anti-anoxic of the present invention, antifatigue 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 raw material is mixed, and the more raw material of poor raw material and content mixes employing equivalent and increases progressively mixing method step by step;
The system softwood: spray wetting agent pigment solution is painted on mixed material, thereafter the organic solution of the adhesive of spray about 3% on mixed material;
Granulation: the softwood that makes is caused 14 purpose particles on granulator, the particle 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;
Whole grain: through sieving, make the material particles degree even, and remove the material particles that is unsuitable for the compressing tablet requirement;
Compressing tablet: in dried material particles, add 1% disintegrant, 0.5% wetting agent, mix the back and drop in the tablet press machine, with the conglobate tea effervescence decoction piece of material particles punching press; To get final product in packing machine 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 acid carbonate 15.4kg, citric acid 30kg, Aspartame 6kg, Cobastab
10.03kg, Cobastab
20.07kg be raw material, prepare the tea effervescence decoction piece of a kind of anti-anoxic of the present invention, antifatigue 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 raw material is mixed, and the more raw material of poor raw material and content mixes employing equivalent and increases progressively mixing method step by step;
The system softwood: spray wetting agent pigment solution is painted on mixed material, thereafter the organic solution of the adhesive of spray about 3% on mixed material;
Granulation: the softwood that makes is caused 14 purpose particles on granulator, the particle 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;
Whole grain: through sieving, make the material particles degree even, and remove the material particles that is unsuitable for the compressing tablet requirement;
Compressing tablet: in dried material particles, add 1% disintegrant, 0.5% wetting agent, mix the back and drop in the tablet press machine, material particles is struck out oval-shaped tea effervescence decoction piece; To get final product in packing machine monolithic sealing packing through the tea effervescence decoction piece that is up to the standards.
Claims (2)
1, the tea effervescence decoction piece of a kind of anti-anoxic, antifatigue contains the green tea powder, the KCI of 1.0%-1.35% weight, the NaCI of 3.0%-3.5% weight, the vitamin C of 5%-10% weight, the sodium acid carbonate 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 0.05%-0.1% weight of 30%-40% weight.
2, the preparation method of the tea effervescence decoction piece of a kind of anti-anoxic according to claim 1, antifatigue the steps include: raw material pulverizing → batching → mixing → system softwood → granulation → oven dry → cooling → whole grain → compressing tablet;
Raw material pulverizing: raw material that granularity is bigger before batching comprises that citric acid, white granulated sugar pulverize in advance, and crosses 100 mesh sieves on pulverizer; 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 raw material is mixed, and the more raw material of poor raw material and content mixes employing equivalent and increases progressively mixing method step by step;
The system softwood: spray wetting agent pigment solution is painted on mixed material, thereafter the organic solution of the adhesive of spray 3% on mixed material;
Granulation: the softwood that makes is caused 14 purpose particles on granulator, the particle of making places pallet;
Oven dry: the wet granular in the pallet is placed 70 ℃ of baking taking-up coolings after 1 hour down;
Whole grain: through sieving, make the material particles degree even, and remove the material particles that is unsuitable for the compressing tablet requirement;
Compressing tablet: in dried material particles, add 1% disintegrant, 0.5% wetting agent, mix the back and drop in the tablet press machine, with conglobate tea effervescence decoction piece of material particles punching press or oval-shaped tea effervescence decoction piece.
Priority Applications (1)
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CN 200310111120 CN1269416C (en) | 2003-12-04 | 2003-12-04 | Anoxia resistant anti-fatigued tea effervescence decoction piece and preparation method thereof |
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CN 200310111120 CN1269416C (en) | 2003-12-04 | 2003-12-04 | Anoxia resistant anti-fatigued tea effervescence decoction piece and preparation method thereof |
Publications (2)
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CN1545896A CN1545896A (en) | 2004-11-17 |
CN1269416C true 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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Families Citing this family (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 |
JP2007306872A (en) * | 2006-05-19 | 2007-11-29 | Suntory Ltd | Proanthocyanidin-containing tea beverage |
CN101214014B (en) * | 2008-01-02 | 2011-08-10 | 南京农业大学 | Production technology of barley seedling powder and product thereof |
CN102349892B (en) * | 2011-08-17 | 2013-01-16 | 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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2003
- 2003-12-04 CN CN 200310111120 patent/CN1269416C/en not_active Expired - Lifetime
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