CN106820161A - Aloe mineral crystalline substance and preparation method thereof - Google Patents
Aloe mineral crystalline substance and preparation method thereof Download PDFInfo
- Publication number
- CN106820161A CN106820161A CN201710087026.8A CN201710087026A CN106820161A CN 106820161 A CN106820161 A CN 106820161A CN 201710087026 A CN201710087026 A CN 201710087026A CN 106820161 A CN106820161 A CN 106820161A
- Authority
- CN
- China
- Prior art keywords
- parts
- aloe
- mineral
- brilliant
- salt
- 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
- 241001116389 Aloe Species 0.000 title claims abstract description 132
- 235000011399 aloe vera Nutrition 0.000 title claims abstract description 132
- 229910052500 inorganic mineral Inorganic materials 0.000 title claims abstract description 130
- 239000011707 mineral Substances 0.000 title claims abstract description 130
- 239000000126 substance Substances 0.000 title claims abstract description 44
- 238000002360 preparation method Methods 0.000 title abstract description 23
- 239000000843 powder Substances 0.000 claims abstract description 61
- 239000000203 mixture Substances 0.000 claims abstract description 52
- 239000002994 raw material Substances 0.000 claims abstract description 38
- 229940109850 royal jelly Drugs 0.000 claims abstract description 25
- 240000004808 Saccharomyces cerevisiae Species 0.000 claims abstract description 21
- 235000014680 Saccharomyces cerevisiae Nutrition 0.000 claims abstract description 21
- 235000021552 granulated sugar Nutrition 0.000 claims abstract description 17
- 235000011869 dried fruits Nutrition 0.000 claims abstract description 16
- 235000011389 fruit/vegetable juice Nutrition 0.000 claims abstract description 16
- 150000003839 salts Chemical class 0.000 claims abstract description 13
- 150000003751 zinc Chemical class 0.000 claims abstract description 13
- 159000000007 calcium salts Chemical class 0.000 claims abstract description 10
- 235000010755 mineral Nutrition 0.000 claims description 124
- 238000002156 mixing Methods 0.000 claims description 51
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 claims description 29
- 229940088594 vitamin Drugs 0.000 claims description 18
- 229930003231 vitamin Natural products 0.000 claims description 18
- 235000013343 vitamin Nutrition 0.000 claims description 18
- 239000011782 vitamin Substances 0.000 claims description 18
- 150000003722 vitamin derivatives Chemical class 0.000 claims description 17
- 229960003080 taurine Drugs 0.000 claims description 14
- 229940069521 aloe extract Drugs 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 12
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 claims description 11
- 244000131522 Citrus pyriformis Species 0.000 claims description 10
- 235000005976 Citrus sinensis Nutrition 0.000 claims description 10
- 240000002319 Citrus sinensis Species 0.000 claims description 10
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical group [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 9
- 229910052791 calcium Inorganic materials 0.000 claims description 9
- 235000011478 zinc gluconate Nutrition 0.000 claims description 9
- 235000005979 Citrus limon Nutrition 0.000 claims description 8
- 229960005069 calcium Drugs 0.000 claims description 8
- 239000011575 calcium Substances 0.000 claims description 8
- 235000013924 ferrous gluconate Nutrition 0.000 claims description 8
- 229920002678 cellulose Polymers 0.000 claims description 7
- 239000001913 cellulose Substances 0.000 claims description 7
- 235000005911 diet Nutrition 0.000 claims description 7
- 230000000378 dietary effect Effects 0.000 claims description 7
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 claims description 6
- CANRESZKMUPMAE-UHFFFAOYSA-L Zinc lactate Chemical compound [Zn+2].CC(O)C([O-])=O.CC(O)C([O-])=O CANRESZKMUPMAE-UHFFFAOYSA-L 0.000 claims description 6
- 235000013925 ferrous lactate Nutrition 0.000 claims description 6
- 235000000193 zinc lactate Nutrition 0.000 claims description 6
- WHMDKBIGKVEYHS-IYEMJOQQSA-L Zinc gluconate Chemical group [Zn+2].OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O WHMDKBIGKVEYHS-IYEMJOQQSA-L 0.000 claims description 4
- MKJXYGKVIBWPFZ-UHFFFAOYSA-L calcium lactate Chemical compound [Ca+2].CC(O)C([O-])=O.CC(O)C([O-])=O MKJXYGKVIBWPFZ-UHFFFAOYSA-L 0.000 claims description 4
- 239000001527 calcium lactate Substances 0.000 claims description 4
- 235000011086 calcium lactate Nutrition 0.000 claims description 4
- 229960002401 calcium lactate Drugs 0.000 claims description 4
- 239000004222 ferrous gluconate Substances 0.000 claims description 4
- 229960001645 ferrous gluconate Drugs 0.000 claims description 4
- VRIVJOXICYMTAG-IYEMJOQQSA-L iron(ii) gluconate Chemical group [Fe+2].OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O VRIVJOXICYMTAG-IYEMJOQQSA-L 0.000 claims description 4
- 239000011670 zinc gluconate Substances 0.000 claims description 4
- 229960000306 zinc gluconate Drugs 0.000 claims description 4
- 240000001548 Camellia japonica Species 0.000 claims description 3
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 claims description 3
- 240000002853 Nelumbo nucifera Species 0.000 claims description 3
- 235000006508 Nelumbo nucifera Nutrition 0.000 claims description 3
- 235000006510 Nelumbo pentapetala Nutrition 0.000 claims description 3
- 229930003316 Vitamin D Natural products 0.000 claims description 3
- QYSXJUFSXHHAJI-XFEUOLMDSA-N Vitamin D3 Natural products C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C/C=C1\C[C@@H](O)CCC1=C QYSXJUFSXHHAJI-XFEUOLMDSA-N 0.000 claims description 3
- 229930003427 Vitamin E Natural products 0.000 claims description 3
- 229930003448 Vitamin K Natural products 0.000 claims description 3
- 235000018597 common camellia Nutrition 0.000 claims description 3
- 239000004225 ferrous lactate Substances 0.000 claims description 3
- 229940037907 ferrous lactate Drugs 0.000 claims description 3
- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 claims description 3
- SHUZOJHMOBOZST-UHFFFAOYSA-N phylloquinone Natural products CC(C)CCCCC(C)CCC(C)CCCC(=CCC1=C(C)C(=O)c2ccccc2C1=O)C SHUZOJHMOBOZST-UHFFFAOYSA-N 0.000 claims description 3
- 235000019156 vitamin B Nutrition 0.000 claims description 3
- 239000011720 vitamin B Substances 0.000 claims description 3
- 235000019166 vitamin D Nutrition 0.000 claims description 3
- 239000011710 vitamin D Substances 0.000 claims description 3
- 150000003710 vitamin D derivatives Chemical class 0.000 claims description 3
- 235000019165 vitamin E Nutrition 0.000 claims description 3
- 229940046009 vitamin E Drugs 0.000 claims description 3
- 239000011709 vitamin E Substances 0.000 claims description 3
- 235000019168 vitamin K Nutrition 0.000 claims description 3
- 239000011712 vitamin K Substances 0.000 claims description 3
- 150000003721 vitamin K derivatives Chemical class 0.000 claims description 3
- 229940046008 vitamin d Drugs 0.000 claims description 3
- 229940046010 vitamin k Drugs 0.000 claims description 3
- 239000011576 zinc lactate Substances 0.000 claims description 3
- 229940050168 zinc lactate Drugs 0.000 claims description 3
- 229930091371 Fructose Natural products 0.000 claims description 2
- 229930003270 Vitamin B Natural products 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims description 2
- DKKCQDROTDCQOR-UHFFFAOYSA-L Ferrous lactate Chemical compound [Fe+2].CC(O)C([O-])=O.CC(O)C([O-])=O DKKCQDROTDCQOR-UHFFFAOYSA-L 0.000 claims 1
- 239000005715 Fructose Substances 0.000 claims 1
- 239000004576 sand Substances 0.000 claims 1
- 235000000346 sugar Nutrition 0.000 claims 1
- 230000000694 effects Effects 0.000 abstract description 34
- 239000000284 extract Substances 0.000 abstract description 10
- 230000036039 immunity Effects 0.000 abstract description 7
- 230000002124 endocrine Effects 0.000 abstract description 6
- 230000036541 health Effects 0.000 abstract description 6
- 230000004206 stomach function Effects 0.000 abstract description 4
- 239000013078 crystal Substances 0.000 abstract description 2
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical class [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 abstract 1
- 238000009472 formulation Methods 0.000 abstract 1
- 230000003014 reinforcing effect Effects 0.000 abstract 1
- 238000001035 drying Methods 0.000 description 24
- 238000010348 incorporation Methods 0.000 description 21
- AFHJQYHRLPMKHU-XXWVOBANSA-N Aloin Natural products O=C1c2c(O)cc(CO)cc2[C@H]([C@H]2[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O2)c2c1c(O)ccc2 AFHJQYHRLPMKHU-XXWVOBANSA-N 0.000 description 16
- AFHJQYHRLPMKHU-UHFFFAOYSA-N isobarbaloin Natural products OC1C(O)C(O)C(CO)OC1C1C2=CC(CO)=CC(O)=C2C(=O)C2=C(O)C=CC=C21 AFHJQYHRLPMKHU-UHFFFAOYSA-N 0.000 description 16
- AFHJQYHRLPMKHU-OSYMLPPYSA-N aloin A Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1[C@@H]1C2=CC(CO)=CC(O)=C2C(=O)C2=C(O)C=CC=C21 AFHJQYHRLPMKHU-OSYMLPPYSA-N 0.000 description 15
- 230000000052 comparative effect Effects 0.000 description 15
- 238000007873 sieving Methods 0.000 description 15
- 239000000463 material Substances 0.000 description 14
- 230000006870 function Effects 0.000 description 12
- 235000016709 nutrition Nutrition 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 238000010521 absorption reaction Methods 0.000 description 8
- 208000007882 Gastritis Diseases 0.000 description 7
- 230000009286 beneficial effect Effects 0.000 description 7
- 208000023652 chronic gastritis Diseases 0.000 description 7
- 230000002708 enhancing effect Effects 0.000 description 7
- 239000002245 particle Substances 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- 238000000227 grinding Methods 0.000 description 6
- 230000012010 growth Effects 0.000 description 5
- 239000004615 ingredient Substances 0.000 description 5
- 230000035764 nutrition Effects 0.000 description 5
- 239000000523 sample Substances 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- 238000007689 inspection Methods 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 230000004060 metabolic process Effects 0.000 description 4
- 235000018102 proteins Nutrition 0.000 description 4
- 102000004169 proteins and genes Human genes 0.000 description 4
- 108090000623 proteins and genes Proteins 0.000 description 4
- 102000004190 Enzymes Human genes 0.000 description 3
- 108090000790 Enzymes Proteins 0.000 description 3
- 206010067171 Regurgitation Diseases 0.000 description 3
- 210000001015 abdomen Anatomy 0.000 description 3
- 208000022531 anorexia Diseases 0.000 description 3
- 206010061428 decreased appetite Diseases 0.000 description 3
- 238000001514 detection method Methods 0.000 description 3
- 235000013305 food Nutrition 0.000 description 3
- 235000012208 gluconic acid Nutrition 0.000 description 3
- 210000000936 intestine Anatomy 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 244000005700 microbiome Species 0.000 description 3
- 230000008855 peristalsis Effects 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 208000024891 symptom Diseases 0.000 description 3
- DEQJBORXLQWRGV-UHFFFAOYSA-N 2-hydroxypropanoic acid;iron Chemical compound [Fe].CC(O)C(O)=O.CC(O)C(O)=O DEQJBORXLQWRGV-UHFFFAOYSA-N 0.000 description 2
- 208000019901 Anxiety disease Diseases 0.000 description 2
- 208000017667 Chronic Disease Diseases 0.000 description 2
- 101150076104 EAT2 gene Proteins 0.000 description 2
- 241000588724 Escherichia coli Species 0.000 description 2
- 206010061218 Inflammation Diseases 0.000 description 2
- 108091005804 Peptidases Proteins 0.000 description 2
- 235000014676 Phragmites communis Nutrition 0.000 description 2
- 239000004365 Protease Substances 0.000 description 2
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 235000001014 amino acid Nutrition 0.000 description 2
- 150000001413 amino acids Chemical class 0.000 description 2
- 230000033228 biological regulation Effects 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 230000000875 corresponding effect Effects 0.000 description 2
- 235000018417 cysteine Nutrition 0.000 description 2
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 235000013325 dietary fiber Nutrition 0.000 description 2
- 238000005538 encapsulation Methods 0.000 description 2
- 229930182470 glycoside Natural products 0.000 description 2
- 150000002338 glycosides Chemical class 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000004054 inflammatory process Effects 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 210000003205 muscle Anatomy 0.000 description 2
- 235000015097 nutrients Nutrition 0.000 description 2
- 230000000291 postprandial effect Effects 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 230000008929 regeneration Effects 0.000 description 2
- 238000011069 regeneration method Methods 0.000 description 2
- 210000002784 stomach Anatomy 0.000 description 2
- 208000002874 Acne Vulgaris Diseases 0.000 description 1
- 241000256844 Apis mellifera Species 0.000 description 1
- 206010010774 Constipation Diseases 0.000 description 1
- -1 Cysteine sulfurous acid carboxylic acid Chemical class 0.000 description 1
- 102000018832 Cytochromes Human genes 0.000 description 1
- 108010052832 Cytochromes Proteins 0.000 description 1
- LEVWYRKDKASIDU-QWWZWVQMSA-N D-cystine Chemical compound OC(=O)[C@H](N)CSSC[C@@H](N)C(O)=O LEVWYRKDKASIDU-QWWZWVQMSA-N 0.000 description 1
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 1
- 208000035240 Disease Resistance Diseases 0.000 description 1
- 241000588921 Enterobacteriaceae Species 0.000 description 1
- 102000006395 Globulins Human genes 0.000 description 1
- 108010044091 Globulins Proteins 0.000 description 1
- RGHNJXZEOKUKBD-SQOUGZDYSA-N Gluconic acid Natural products OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 1
- 208000005016 Intestinal Neoplasms Diseases 0.000 description 1
- XUJNEKJLAYXESH-REOHCLBHSA-N L-Cysteine Chemical compound SC[C@H](N)C(O)=O XUJNEKJLAYXESH-REOHCLBHSA-N 0.000 description 1
- 206010057249 Phagocytosis Diseases 0.000 description 1
- 108091000080 Phosphotransferase Proteins 0.000 description 1
- 241000255964 Pieridae Species 0.000 description 1
- 102000001253 Protein Kinase Human genes 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 210000001744 T-lymphocyte Anatomy 0.000 description 1
- 241000700605 Viruses Species 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 241000482268 Zea mays subsp. mays Species 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 206010000496 acne Diseases 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 125000000539 amino acid group Chemical group 0.000 description 1
- 208000007502 anemia Diseases 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- 230000036528 appetite Effects 0.000 description 1
- 235000019789 appetite Nutrition 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- 244000052616 bacterial pathogen Species 0.000 description 1
- 230000003796 beauty Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 238000009395 breeding Methods 0.000 description 1
- 230000001488 breeding effect Effects 0.000 description 1
- SMHNUIFHMAGAFL-UHFFFAOYSA-N calcium;2-hydroxypropanoic acid Chemical compound [Ca].CC(O)C(O)=O SMHNUIFHMAGAFL-UHFFFAOYSA-N 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 230000000711 cancerogenic effect Effects 0.000 description 1
- 231100000357 carcinogen Toxicity 0.000 description 1
- 239000003183 carcinogenic agent Substances 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 230000007969 cellular immunity Effects 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 235000008504 concentrate Nutrition 0.000 description 1
- 230000002153 concerted effect Effects 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 230000003138 coordinated effect Effects 0.000 description 1
- 229960003067 cystine Drugs 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 230000004069 differentiation Effects 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000000857 drug effect Effects 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 208000030172 endocrine system disease Diseases 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 238000010812 external standard method Methods 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- OVBPIULPVIDEAO-LBPRGKRZSA-N folic acid Chemical compound C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-LBPRGKRZSA-N 0.000 description 1
- 229960002737 fructose Drugs 0.000 description 1
- 239000000174 gluconic acid Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 208000006454 hepatitis Diseases 0.000 description 1
- 231100000283 hepatitis Toxicity 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 235000012907 honey Nutrition 0.000 description 1
- 230000036737 immune function Effects 0.000 description 1
- 210000000987 immune system Anatomy 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 201000002313 intestinal cancer Diseases 0.000 description 1
- 230000000968 intestinal effect Effects 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000008141 laxative Substances 0.000 description 1
- 230000002475 laxative effect Effects 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 210000005229 liver cell Anatomy 0.000 description 1
- 210000002540 macrophage Anatomy 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 235000012054 meals Nutrition 0.000 description 1
- 230000007721 medicinal effect Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000002906 microbiologic effect Effects 0.000 description 1
- 230000000116 mitigating effect Effects 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000000242 pagocytic effect Effects 0.000 description 1
- 230000008782 phagocytosis Effects 0.000 description 1
- 102000020233 phosphotransferase Human genes 0.000 description 1
- 230000035790 physiological processes and functions Effects 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 108060006633 protein kinase Proteins 0.000 description 1
- 238000001243 protein synthesis Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000012488 sample solution Substances 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 230000001502 supplementing effect Effects 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 230000005313 thymus development Effects 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 230000014616 translation Effects 0.000 description 1
- 238000002604 ultrasonography Methods 0.000 description 1
- 229940046001 vitamin b complex Drugs 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/88—Liliopsida (monocotyledons)
- A61K36/896—Liliaceae (Lily family), e.g. daylily, plantain lily, Hyacinth or narcissus
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/191—Carboxylic acids, e.g. valproic acid having two or more hydroxy groups, e.g. gluconic acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/702—Oligosaccharides, i.e. having three to five saccharide radicals attached to each other by glycosidic linkages
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K33/00—Medicinal preparations containing inorganic active ingredients
- A61K33/24—Heavy metals; Compounds thereof
- A61K33/26—Iron; Compounds thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K33/00—Medicinal preparations containing inorganic active ingredients
- A61K33/24—Heavy metals; Compounds thereof
- A61K33/30—Zinc; Compounds thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
- A61K35/56—Materials from animals other than mammals
- A61K35/63—Arthropods
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
- A61K35/56—Materials from animals other than mammals
- A61K35/63—Arthropods
- A61K35/64—Insects, e.g. bees, wasps or fleas
- A61K35/644—Beeswax; Propolis; Royal jelly; Honey
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/06—Fungi, e.g. yeasts
- A61K36/062—Ascomycota
- A61K36/064—Saccharomycetales, e.g. baker's yeast
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/88—Liliopsida (monocotyledons)
- A61K36/886—Aloeaceae (Aloe family), e.g. aloe vera
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Natural Medicines & Medicinal Plants (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Mycology (AREA)
- Botany (AREA)
- Microbiology (AREA)
- Alternative & Traditional Medicine (AREA)
- Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- Medical Informatics (AREA)
- Insects & Arthropods (AREA)
- Inorganic Chemistry (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Zoology (AREA)
- Molecular Biology (AREA)
- Medicines Containing Plant Substances (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Animal Husbandry (AREA)
Abstract
A kind of aloe mineral crystalline substance and preparation method thereof, wherein aloe mineral crystalline substance are made up of plurality of raw materials.In parts by weight, plurality of raw materials includes mineral salt, 0.06 0.1 parts of aloe extracts, 8 12 parts of taurines, 8 12 parts of Bee Pollens, 8 12 parts of FOSs, 45 55 parts of dried fruit juices, 8 12 parts of royal jelly freeze-dried powders, 80 120 portions of white granulated sugars and 8 12 parts of beer yeast powders.Mineral salt includes 0.08 0.15 parts of zinc salts, 0.1 0.25 parts of ferrous salts and 7.5 9.5 parts of calcium salts.Each component is the effect being mutually improved in aloe mineral crystal formulations, adjusts endocrine, removes internal harmful substance reinforcing stomach function, is built up health, and immunity of organisms is strengthened jointly.Meanwhile, the preparation method is simple to operate, and operating condition is easily achieved.
Description
Technical field
The present invention relates to field of food health care, and more particularly to a kind of aloe mineral crystalline substance and preparation method thereof.
Background technology
The effects such as aloe lets out under having sterilization, anti-inflammatory, moistening beauty, stomach invigorating, is immunized, regenerates, is widely used in skin care
On product, but in field of food health care using less, particularly aloe mineral are brilliant, the brilliant product category of aloe mineral on the market
And quantity is few, barbaloin and mineral matter equal size are low in the brilliant product of existing aloe mineral, and health-care effect is not good.
The content of the invention
Brilliant it is an object of the invention to provide a kind of aloe mineral, it can effectively remove internal harmful substance, improve and
Regulation endocrine, strengthens immunity of organisms.
Another object of the present invention is to provide a kind of aloe mineral brilliant preparation method, operated by the preparation method and walked
Rapid simple, operating condition is gentle, be easily achieved, with larger prospects for commercial application.
The present invention is solved its technical problem and is realized using following technical scheme：
The present invention proposes that a kind of aloe mineral are brilliant, and aloe mineral crystalline substance is made up of plurality of raw materials.In parts by weight, it is above-mentioned many
Planting raw material includes mineral salt, 0.06-0.1 parts of aloe extract, 8-12 parts of taurine, 8-12 parts of Bee Pollen, 8-12 parts of oligomeric fruit
Sugar, 45-55 parts of dried fruit juice, 8-12 parts of royal jelly freeze-dried powder, 80-120 portions of white granulated sugar and 8-12 parts of beer yeast powder.Mineral salt bag
Include 0.08-0.15 parts of zinc salt, 0.1-0.25 parts of ferrous salt and 7.5-9.5 parts of calcium salt.
The present invention proposes a kind of brilliant preparation method of aloe mineral, comprises the following steps and extracts 0.06-0.1 portions of aloe
Thing is mixed to get premix with 0.1-0.25 parts of ferrous salt again after mixing with 0.08-0.15 parts of zinc salt.By 7.5-9.5 parts of calcium
Salt, 8-12 part Bee Pollen, 8-12 parts of royal jelly freeze-dried powder, 8-12 parts of taurine, 8-12 parts of FOS, 8-12 parts of brewer's yeast
Mix with premix after powder mixing and continue to be mixed to get whole mixing with 45-55 parts of dried fruit juice, 80-120 portions of white granulated sugar successively
Thing.
The brilliant beneficial effect of aloe mineral of the present invention is：Each transgranular component of aloe mineral mutually acts synergistically, aloe
Stomach function can be strengthened, improve constitution, enhancing muscle power keeps full of vitality.Royal jelly can stablize immune system, there is provided dimension life
Element and mineral matter, so as to remove internal harmful substance.Bee Pollen can balance endotrophic, enhancing metabolism.FOS
Growth with brewer's yeast promotes enteric microorganism, further enhances function under the letting out of aloe.Mineral matter is then participated in and activated
The synthesis of enzyme, so as to strengthen immunity of organisms.Each material not only gives full play to its own in aloe mineral of the invention crystalline substance
Excellent or obvious effect, meanwhile, by with other matter interactions, itself excellent effect can be further enhanced, or
The function that itself is not manifested completely is embodied, and further improves and lifted the function of each material.
Specific embodiment
To make the purpose, technical scheme and advantage of the embodiment of the present invention clearer, below will be in the embodiment of the present invention
Technical scheme be clearly and completely described.Unreceipted actual conditions person, builds according to normal condition or manufacturer in embodiment
The condition of view is carried out.Agents useful for same or the unreceipted production firm person of instrument, are the conventional product that can be obtained by commercially available purchase
Product.
In the description of the invention, it is necessary to illustrate, term " first ", " second " etc. are only used for distinguishing description, without
It is understood that to indicate or implying relative importance.
The preparation method that aloe mineral are brilliant and aloe mineral are brilliant to the embodiment of the present invention is specifically described below.
A kind of aloe mineral provided in an embodiment of the present invention are brilliant, and aloe mineral crystalline substance is made up of plurality of raw materials.With weight portion
Meter, above-mentioned raw materials include mineral salt, 0.06-0.1 parts of aloe extract, 8-12 parts of taurine, 8-12 parts of Bee Pollen, 8-12 parts low
Fructooligosaccharides, 45-55 part dried fruit juice, 8-12 parts of royal jelly freeze-dried powder, 80-120 portions of white granulated sugar and 8-12 parts of beer yeast powder.Mineral
Salt includes 0.08-0.15 parts of zinc salt, 0.1-0.25 parts of ferrous salt and 7.5-9.5 parts of calcium salt.
When each transgranular raw material of aloe mineral uses aforementioned proportion, the synergy between each component can reach most
Good effect, and the ratio recorded above or below the embodiment of the present invention, the effect or function of each component will decrease, together
Synergy between Shi Zufen will also decrease and even disappear.Royal jelly provides the mineral that abundant mineral matter is provided with mineral salt
It is complementary to one another, to provide more rich mineral matter, while promoting the synthesis of protease, and then promotes body for the suction of albumen
Receive.FOS and beer yeast powder promote intestines peristalsis, promote effect of the aloe to enteron aisle, further enhance enteron aisle
Wriggle, promote absorption of the enteron aisle to various nutriments.And Bee Pollen enters with other materials such as royal jelly collective effect
One step section endocrine, removes internal harmful substance.
Although aloe is the brilliant basic substance for playing drug effect of aloe mineral, the embodiment of the present invention uses aloe and carries
Thing is taken, it contains the most active ingredient of aloe, and is high purity substance, therefore its usage amount should not be too high.It makes
The effect of other materials may be suppressed if consumption is too high, and then reduce the brilliant health-care effect of aloe mineral.
Aloe extract, the liquid of the slightly stickiness of water white transparency to brown is yellow fine powder after drying.There is no gas
Taste or slightly characteristic odor, its function of possessing aloe.Aloe has stomach invigorating, laxative, the function of enhancing immunity of organisms, because
Aloe mineral crystalline substance in this embodiment of the present invention possesses the function that aloe has.
Also known as beta-amino ethyl sulfonic acid, sterling is colourless or white ramp-like crystal, odorless to taurine.Taurine is a kind of sulfur-bearing
Non-protein amino acid, although it is not involved in protein synthesis, but it is closely related with the metabolism of cystine, cysteine.
Cysteine sulfurous acid carboxylic acid (CSAD) activity of human body synthesizing taurine is relatively low, relies primarily on the taurine in intake food
To meet body requirement.Therefore, aloe mineral are brilliant in the embodiment of the present invention has raising cellular immunity phagocytic function, promotes immune
The production function of globulin, while it can promote the absorption and consumption of internal lipid material.
The pollen load taken back when Bee Pollen is honeybee producting honey, the pollen in honeycomb by being formed after storage and fermentation.Its
Contain abundant amino acid, micro- and substantial amounts of active protease isoreactivity material.Therefore, in embodiments of the present invention
The brilliant phagocytosis activity for being capable of effective activating macrophage of aloe mineral, raising human disease resistance, and free radical can be effectively removed,
Prevent aging.Meanwhile, it is capable to kill Escherichia coli etc., and can prevent treating constipation.Preferably, Bee Pollen is rape pollen, popcorn
Any one in powder, camellia pollen, pollen pini and lotus powder.
Dried fruit juice is a kind of powder that fruit syrup concentrate drying is obtained, and it contains abundant vitamin and mineral matter.At this
In inventive embodiments, its vitamin for providing and mineral matter can promote the brilliant absorption and decomposition for protein of aloe mineral,
The brilliant nutritional ingredient of aloe mineral can be improved simultaneously, and can improve the brilliant eating mouth feel of aloe mineral.Preferably, dried fruit juice is
Sweet orange powder and lemon powder.
Royal jelly freeze-dried powder is material of the royal jelly by vacuum dehydrating at lower temperature out, and the content of its nutriment is general
3 times of royal jelly.In embodiments of the present invention royal jelly freeze-dried powder enable aloe mineral crystalline substance cell is repaired and
Regeneration, and then play oxidation resistant effect.And enable that aloe mineral crystalline substance kills hepatitis viruse, promotes liver cell regeneration,
Adjustment endocrine and metabolism, moreover it is possible to effectively improve a poor appetite, improve the health care of sleep and enhancing development, have extremely strong to human body
Healthcare function and medical effect.
Beer yeast powder contains abundant vitamin B complex, various vitamins, mineral matter, up to more than 50% protein,
It is the best source for supplementing good protein containing complete amino acid group.It can be enterobacteriaceae in embodiments of the present invention
Fall and nutriment is provided, promote the breeding of intestinal beneficial microbes.
Mineral salt is a kind of salt, for body provides mineral matter.The beneficial health of these mineral, it is easy to absorb.The present invention
Zinc salt provides Zn-ef ficiency for human body in embodiment, and Zn-ef ficiency ensure that thymus development, and normal differentiation T lymphocytes promote thin
Born of the same parents' immunologic function, while zinc can also promote the biosynthesis of protein.Preferably, zinc salt is zinc gluconate or zinc lactate.
Above two zinc salt can be absorbed by the body, but zinc lactate is applied to the crowd of more than 4 years old, and zinc gluconate is applied to institute
With crowd, therefore, the use zinc gluconate being more highly preferred to.
Ferrous salt participates in the synthesis of hemalbumin, cytochromes and various enzymes in embodiments of the present invention.Improve human body anaemia
Situation, lifts body immunity.Preferably, the ferrous salt for using is ferrous gluconate or ferrous lactate, more preferred with
Ferrous gluconate.Ferrous gluconate is compared ferrous lactate and is more easy to be absorbed by the body.
Calcium salt is primarily to calcium source can be supplemented in time in embodiments of the present invention.Preferably, calcium salt is gluconic acid
Calcium or calcium lactate, it is further preferred that being more easy to absorb using calcium gluconae.
It is further preferred that in plurality of raw materials also include vitamin, vitamin be vitamin B, vitamin K, vitamin D,
Any one in vitamin E.Setting up vitamin can further improve the transgranular nutriment of aloe mineral.
It is further preferred that also including cellulose in plurality of raw materials, cellulose is dietary cellulosic.Dietary fiber can enter
One step is effectively facilitated intestines peristalsis, promotes enteron aisle to each absorption of nutrient ingredients, accelerates the exclusion of harmful toxic matter.
The brilliant eating method of the aloe mineral is to use warm water Instant Drinks, but uses metal cup spoon.Avoid using gold
The transgranular nutriment of category cup spoon destruction aloe mineral.
The present invention provides a kind of aloe mineral brilliant preparation method：
S1,0.06-0.1 parts of aloe extract and 0.08-0.15 parts of zinc salt are mixed to get the first mixture；
Aloe extract and zinc salt ratio are close, and the two is mixed with beneficial to well mixed first, saves incorporation time, aloe
Mineral are brilliant to provide most basic nutriment.Aloe extract is well mixed beneficial to the association between follow-up each material first simultaneously
The generation of same-action.
Preferably, incorporation time is 2-5 minutes.In the range of this incorporation time, aloe extract can as far as possible with zinc
Salt is well mixed and does not waste the unnecessary time.It is further preferred that 0.06-0.09 parts of fibre can also be added in the first mixture
Dimension element.The corresponding enzyme of decomposition of cellulose is not contained in human body, therefore it can not be decomposed by human body and utilize, but it has absorption big
The excellent efficacies such as amount water, increase excrement amount, promotion intestines peristalsis, can make carcinogen shorter residence time in enteron aisle, right
The pessimal stimulation reduction effect of enteron aisle, so as to prevent the generation of intestinal cancer.Therefore, addition cellulose is conducive to enhancing aloe meeting mineral
Brilliant eating effect, using the teaching of the invention it is possible to provide more comprehensively nutrition.It is further preferred that cellulose is dietary fiber.
Further, 0.063-0.09 parts of vitamin can also be added in the first mixture, it is preferable that vitamin is vitamin
One kind in B, vitamin K, vitamin D, vitamin E.Vitamin is set up for aloe mineral crystalline substance provides more comprehensively nutrition, together
When, further increase the absorption of human body each nutriment transgranular to aloe mineral.
Further, while the first mixture is mixed to get, can by 7.5-9.5 parts of calcium salt, 8-12 parts of Bee Pollen,
8-12 parts of royal jelly freeze-dried powder, 8-12 parts of taurine, 8-12 parts of FOS, 8-12 parts of beer yeast powder are mixed to get second and mix
Compound.The close raw material of above-mentioned 6 kinds of ratios is mixed, is easy to 6 kinds of raw materials to be well mixed, saved incorporation time.Preferably,
Now incorporation time is 8-10 minutes.
S2, just the first mixture and 0.1-0.25 parts of ferrous salt are mixed to get the 3rd mixture；
The ratio of the first mixture being mixed to get and the ratio of ferrous salt are close, and the two mixing is uniformly mixed beneficial to ferrous salt
Close aloe mineral crystalline substance in, and then enable aloe extract it is various with mineral salt action, in follow-up edible Aloe mineral
When brilliant, aloe extract and different mineral salt actions can produce different physiological functions, improve aloe mineral it is brilliant each
Synergy between raw material, and then the brilliant edible range of aloe mineral is expanded, enhance the brilliant health-care effect of aloe mineral.
And the 3rd mixture as premix for obtaining.Preferably, the incorporation time for obtaining the 3rd mixture is 2-5 minutes.
S3, the second mixture and the 3rd mixture are mixed to get the 4th mixture, the 4th mixture and 45-55 parts of dried fruit juice
The 5th mixture is obtained, the 5th mixture is mixed to get the 6th mixture with 80-120 portions of white granulated sugar.
Using above-mentioned order by merging, equally allow for needing the ratio between the material of mixing, using above-mentioned mixing
Sequentially, it is more easy to be well mixed between each raw material, the mutually coordinated effect more conducively between nutriment can promote aloe ore deposit
The release of the transgranular nutritional ingredient of thing, while so that when each nutriment is had an effect, there are other enough corresponding nutrition
Material can occur concerted reaction, the brilliant health-care effect of lifting aloe mineral with it.
Preferably, the incorporation time of the second mixture and the 3rd mixture is 8-10 minutes.Due to the second mixture and
Three mixtures are blended abundant respectively, and incorporation time can be effectively saved herein.
Similarly, the 4th mixture has mixed the further perfect transgranular nutritional ingredients of aloe mineral with dried fruit juice, while entering
Promote to one step the absorption and utilization of each nutritional ingredient.Preferably, during the mixing that the 4th mixture mixes with dried fruit juice
Between be 5-8 minutes.It is further preferred that dried fruit juice is sweet orange powder and lemon powder.
5th mixture and 80-120 portions of white granulated sugar be also the ratio of now the 5th mixture and white granulated sugar quite, the two is mixed
During conjunction, incorporation time used is minimum, and most easily well mixed, and when being conducive to follow-up edible Aloe mineral brilliant, aloe mineral are transgranular
The dissolving of each material, and then the brilliant absorption efficiency of mineral can be lifted.Meanwhile, it is capable to for eater provides within the shortest time
Excellent mouthfeel.Preferably, the 5th mixture and the incorporation time of white granulated sugar are 5-8 minutes.And the 6th mixture for obtaining is i.e.
It is whole mixture.
In sum, each brilliant raw material of aloe mineral is mixed using above-mentioned 3 steps, can be maximum
Each raw material is well mixed, and it is time-consuming most short.And the nutrition that the aloe mineral crystalline substance being mixed to get according to the method described above contains
Material can effectively act synergistically, the brilliant health-care effect of enhancing aloe mineral.
S4, the 6th mixture is passed sequentially through crushing, sieving, drying, encapsulation, that inspection obtains aloe mineral is brilliant.
By after mixing, some large particulate matters being there may be in the 6th mixture, meanwhile, it is brilliant in order to lift aloe mineral
Aesthetic measure and be further well mixed and ensure follow-up edible Aloe mineral it is brilliant when with good mouthfeel, it is necessary to control
Make the particle diameter of the 6th mixture.To solve the problem, further crushed using the 6th mixture that will be obtained, crushing
Rotating speed is 2000-3000r/min, and the time of crushing is 3-7 minutes.
The brilliant particle diameter of aloe mineral after crushing can not be unified, in order to ensure the consistent of particle diameter, using sieving by particle diameter not
Qualified aloe mineral crystalline flour end or particle removal.The mesh number of sieving preferably is 70-90 mesh.The mesh number particle diameter phase of this scope
When, do not have too big obstruction sense when human body is swallowed, and this scope particle diameter nutriment dissolution rate faster and stripping quantity
It is bigger.
Each brilliant raw material of aloe mineral is contained within certain moisture, in order to extend the brilliant raw material of aloe mineral due to moisture
It is too high and content that reduce its nutriment or the interaction between them, or even raw material go mouldy, it is impossible to positive often to eat
With.In order to solve this problem, by sieving after the 6th mixture dry, the moisture of the 6th mixture is controlled 3%
Below.Further, dry drying temperature is 40-55 DEG C, and drying time is 30-45 minutes.Drying temperature energy in the range of this
Enough fully drying ensure that the transgranular nutriment of aloe mineral will not occur chemical change because of heating simultaneously, reduce it
Health-care effect.Meanwhile, the drying time in the range of this can be fully dried while ensure that the transgranular nutrients of aloe mineral
Matter will not occur chemical change because of heating, reduce its health-care effect.
The 6th mixture is packaged according to Production requirement after the completion of drying, it is 5g/ bags or 10g/ bags etc. to be encapsulated.
Every bag of aloe mineral crystalline substance is tested after the completion of encapsulation.Inspection project includes that the project of inspection includes moisture, ash content, lead, total
Arsenic and microbiological indicator (total plate count, Escherichia coli, mould, pathogenic bacteria).And normative reference uses national standard.
It is further preferred that in order to reduce influence of the environment to finished product during production aloe mineral crystalline substance, it is whole to prepare
The brilliant process of aloe mineral is produced in the environment purification that clean rank is 100,000 grades, while ensureing that temperature is in environment purification
18-26 DEG C, relative humidity is 45-65%.
Aloe mineral of the invention are brilliant, and stomach function can be effectively strengthened using material based on aloe, improve constitution,
Enhancing muscle power, keeps full of vitality.Then by aloe and royal jelly, Bee Pollen, FOS, brewer's yeast and mineral matter etc.
Plurality of raw materials interacts, and while lifting aloe acts on, further can farthest play effect of remaining raw material.Example
Promote the growth of enteric microorganism as FOS, brewer's yeast and aloe interact, further enhance under the letting out of aloe
Function.Mineral matter then participates in the synthesis with kinase, so as to strengthen immunity of organisms.Royal jelly and Bee Pollen etc. further increase
Strong body metabolism, nutriment in balanced body.
Feature of the invention and performance are described in further detail with reference to embodiments.
Embodiment 1
The aloe mineral crystalline substance that the present embodiment is provided is made up of plurality of raw materials.Plurality of raw materials includes 0.08g aloe extracts, 9g
Taurine, 10g rape pollens, 9g FOSs, 45g dried fruit juices, 10g royal jelly freeze-dried powders, 90g white granulated sugars, 9g brewer's yeasts
Powder, 0.15g zinc gluconates, 0.1g ferrous gluconates and 8g calcium gluconaes.Wherein 45g dried fruit juices include 20g sweet orange powder
With 25g lemon powders.
The preparation method of the aloe mineral crystalline substance that the present embodiment is provided：
0.08g aloe extracts and 0.15g zinc gluconates are carried out to be mixed to get the first mixture for the first time, for the first time
The incorporation time of mixing is 3 minutes.Meanwhile, by 8g calcium gluconaes, 10g rape pollens, 10g royal jelly freeze-dried powders, 9g ox sulphurs
Acid, 9g FOSs and 9g beer yeast powders are mixed to get the second mixture for the second time, second incorporation time of mixing
It is 9 minutes.First mixture carries out third time and is mixed to get the 3rd mixture with 0.1g ferrous gluconates, third time mixing
Incorporation time is 5 minutes.Second mixture mixes with the 3rd to carry out being mixed to get the 4th mixture for the 4th time, the 4th mixing
Incorporation time is 10 minutes.4th mixture carries out the 5th time and is mixed to get the 5th mixture, the 5th mixing with 45g dried fruit juices
The incorporation time of thing is 5 minutes.5th mixture carries out the 6th time and is mixed to get the 6th mixture, the 6th time with 90g white granulated sugars
The incorporation time of mixing is 7 minutes.
The 6th mixture is crushed after the completion of mixing, the rotating speed of crushing is 3000r/min, and the time of crushing is 4 points
Clock.Sieved after crushing, the mesh number of sieving is 80 mesh.Dried 40 minutes under the conditions of 45 DEG C after the completion of sieving.Then according to
5g/ bags are packaged, and finally carry out quality inspection.
Embodiment 2
The aloe mineral crystalline substance that the present embodiment is provided is made up of plurality of raw materials.Plurality of raw materials includes 0.06g aloe extracts, 8g
Taurine, 9g camellia pollens, 8g FOSs, 0.07g vitamin Bs, 0.06g dietary cellulosics, 20g sweet oranges powder, 30g lemon powders,
8g royal jelly freeze-dried powders, 100g white granulated sugars, 12g beer yeast powders, 0.08g zinc lactates, 0.15g ferrous lactates and 7.5g lactic acid
Calcium.
The preparation method of the aloe mineral crystalline substance that the present embodiment is provided is basically identical with the preparation method of embodiment 1, and difference exists
Changed in operating condition.0.07g vitamin Bs and 0.06g dietary cellulosics are included in first mixture, is mixed for the first time
Time be 4 minutes, the time of second mixing is 8 minutes, and the time of third time mixing is 4 minutes, the 4th mixing when
Between be 9 minutes, the 5th time mixing time be 6 minutes, the 6th time mixing time be 6 minutes.The rotating speed of crushing is 2500r/
Min, grinding time is 7 minutes, and the mesh number of sieving is 75 mesh, and drying temperature is 40 DEG C, and drying time is 35 minutes, clean rank
It is 100,000 grades.
Embodiment 3
The aloe mineral crystalline substance that the present embodiment is provided is made up of plurality of raw materials.Plurality of raw materials includes 0.1g aloe extracts, 11g
Taurine, 12g zasiokaurins, 11g FOSs, 0.09g vitamin Es, 0.08g dietary cellulosics, 35g sweet oranges powder, 20g lemons
Powder, 9g royal jelly freeze-dried powders, 80g white granulated sugars, 8g beer yeast powders, 0.1g zinc lactates, 0.2g ferrous lactates and 9g calcium lactates.
The method of the preparation aloe mineral crystalline substance that the present embodiment is provided is basically identical with the preparation method of embodiment 2, and difference exists
Changed in operating condition.The incorporation time of mixing is 2 minutes for the first time, and second time of mixing is 10 minutes, the 3rd
The time of secondary mixing is 2 minutes, and the 4th time of mixing is 8 minutes, and the 5th time of mixing is 7 minutes, and the 6th time mixed
The time of conjunction is 8 minutes.The rotating speed of crushing is 3000r/min, and grinding time is 4 minutes, and the mesh number of sieving is 70 mesh, dries temperature
It is 40 DEG C to spend, and drying time is 30 minutes.
Embodiment 4
The aloe mineral crystalline substance that the present embodiment is provided is made up of plurality of raw materials.Plurality of raw materials include 0.07g aloe extracts,
12g taurines, 8g zasiokaurins, 10g FOSs, 0.06g vitamin Es, 0.07g dietary cellulosics, 25g sweet oranges powder, 20g lemons
Lemon powder, 11g royal jelly freeze-dried powders, 110g white granulated sugars, 10g beer yeast powders, 0.12g zinc lactates, 0.25g ferrous lactates and 9.5g
Calcium lactate.
The method of the preparation aloe mineral crystalline substance that the present embodiment is provided is basically identical with the preparation method of embodiment 2, and difference exists
Changed in operating condition.The incorporation time of mixing is 5 minutes for the first time, and second time of mixing is 9 minutes, the 3rd
The time of secondary mixing is 3 minutes, and the 4th time of mixing is 10 minutes, and the 5th time of mixing is 8 minutes, and the 6th time mixed
The time of conjunction is 5 minutes.The rotating speed of crushing is 2000r/min, and grinding time is 5 minutes, and the mesh number of sieving is 90 mesh, dries temperature
It is 55 DEG C to spend, and drying time is 45 minutes.
Embodiment 5
The aloe mineral crystalline substance that the present embodiment is provided is made up of plurality of raw materials.Plurality of raw materials include 0.09g aloe extracts,
10g taurines, 11g pollen pinis, 12g FOSs, 0.08g vitamin Ks, 0.09g dietary cellulosics, 21g sweet oranges powder, 27g lemons
Lemon powder, 12g royal jelly freeze-dried powders, 120g white granulated sugars, 11g beer yeast powders, 0.09g zinc gluconates, 0.22g gluconic acids are sub-
Iron and 8.5g calcium gluconaes.
The method of the preparation aloe mineral crystalline substance that the present embodiment is provided is basically identical with the preparation method of embodiment 2, and difference exists
Changed in operating condition.The incorporation time of mixing is 4 minutes for the first time, and second time of mixing is 9 minutes, third time
The time of mixing is 5 minutes, and the 4th time of mixing is 9 minutes, and the 5th time of mixing is 7 minutes, the 6th mixing
Time be 6 minutes.The rotating speed of crushing is 2200r/min, and grinding time is 3 minutes, and the mesh number of sieving is 90 mesh, drying temperature
It it is 55 DEG C, drying time is 45 minutes.The mesh number of sieving is 85 mesh, and drying temperature is 47 DEG C, and drying time is 34 minutes.
Embodiment 6
The aloe mineral crystalline substance that the present embodiment is provided is made up of plurality of raw materials.Plurality of raw materials includes 0.08g aloe extracts, 8g
Taurine, 10g lotus powders, 9g FOSs, 0.07g vitamin Ds, 32g sweet oranges powder, 21g lemon powders, 9g royal jelly freeze-dried powders,
95g white granulated sugars, 10g beer yeast powders, 0.11g zinc gluconates, 0.18g ferrous gluconates and 7.8g calcium gluconaes.
The method of the preparation aloe mineral crystalline substance that the present embodiment is provided is basically identical with the preparation method of embodiment 2, and difference exists
Changed in operating condition.The incorporation time of mixing is 3 minutes for the first time, and second time of mixing is 8 minutes, third time
The time of mixing is 4 minutes, and the 4th time of mixing is 9 minutes, and the 5th time of mixing is 6 minutes, the 6th mixing
Time be 8 minutes.The rotating speed of crushing is 2800r/min, and grinding time is 6 minutes, and the mesh number of sieving is 90 mesh, drying temperature
It it is 55 DEG C, drying time is 45 minutes, the mesh number of sieving is 90 mesh, and drying temperature is 52 DEG C, and drying time is 42 minutes.
Embodiment 7
The aloe mineral crystalline substance that the present embodiment is provided is made up of plurality of raw materials.Plurality of raw materials include 0.07g aloe extracts,
10g taurines, 9g rape pollens, 10g FOSs, 0.08g vitamin Es, 30g sweet oranges powder, 21g lemon powders, 10g royal jelly freeze
Dry powder, 85g white granulated sugars, 9g beer yeast powders, 0.13g zinc gluconates, 0.23g ferrous gluconates and 8.3g gluconic acids
Calcium.
The method of the preparation aloe mineral crystalline substance that the present embodiment is provided is basically identical with the preparation method of embodiment 2, and difference exists
Changed in operating condition.The incorporation time of mixing is 5 minutes for the first time, and second time of mixing is 10 minutes, the 3rd
The time of secondary mixing is 3 minutes, and the 4th time of mixing is 8 minutes, and the 5th time of mixing is 7 minutes, and the 6th time mixed
The time of conjunction is 8 minutes.The rotating speed of crushing is 2600r/min, and grinding time is 7 minutes, and the mesh number of sieving is 90 mesh, dries temperature
It is 55 DEG C to spend, and drying time is 45 minutes, and the mesh number of sieving is 75 mesh, and drying temperature is 47 DEG C, and drying time is 34 minutes.
Experimental example
Comparative example 1 is free of other described in embodiment 1 only to contain the aloe extract consistent with the quantity of embodiment 1
The aloe mineral of component are brilliant.
Comparative example 2 is that the aloe mineral of the perfect product of market purchase are brilliant.
Experimental example 1
The detection of barbaloin
Barbaloin standard liquid is prepared using barbaloin standard items (barbaloin purity >=98%)：Accurately weigh barbaloin mark
Quasi- product 10mg, plus during mobile phase methanol+water (55+45) dissolves and moves into 100mL volumetric flasks, it is settled to scale.
The aloe mineral for weighing the embodiment 1-7, comparative example 1 and comparative example 2 of phase homogenous quantities are brilliant, in 50mL volumetric flasks,
Plus detection mobile phase (methyl alcohol+water (55+45)) 30mL dissolves, and is shaken through ultrasound and carries 5min plus mobile phase constant volume 50mL, centrifugation is heavy
Form sediment, supernatant is through (0.45 μm) filtering of filter membrane.It is inaccurate to draw standard liquid and the μ L of sample solution 10 injection high performance liquid chromatography
Instrument, it is qualitative with retention time according to above-mentioned chromatographic condition, the content of barbaloin in sample is calculated with external standard method.
Computing formula：
In formula：X --- barbaloin content in sample, (mg/mL)；
A1 --- the peak area of barbaloin in sample；
The mass concentration of C --- titer, mg/mL；
A2 --- the peak area of barbaloin in titer；
V --- sample constant volume, mL；
The quality of m --- sample, g (mL).
Result of calculation retains three significant digits.The results are shown in Table 1.
The content of the barbaloin of table 1
The content of the barbaloin surveyed by comparative example 1 and the result of comparative example 1, embodiment 1 is far above contrast
The barbaloin content of example 1, reason is probably that the material of other nutrition in embodiment 1 there are beneficial to the reed in aloe extract
The dissolving of luxuriant growth glycosides causes that the content of the barbaloin of detection in embodiment 1 increases.Can be with by contrasting comparative example 2 and embodiment 1-7
It was found that, the reed of the content higher than existing market perfection product of the barbaloin that the transgranular side of aloe mineral provided in an embodiment of the present invention obtains
Luxuriant growth glycosides content.And the transgranular barbaloin of aloe mineral has significant health-care effect, the guarantor of the result display embodiment 1-7 of the experimental example
Health-care effect of the strong effect better than comparative example 2.
Experimental example 2
35-45 Sui is selected, 450 Patients with Chronic Gastritis are divided into 9 groups of patients, wherein 7 groups of patients eat embodiment 1- respectively
7 aloe mineral are brilliant, and remaining 2 groups of patient eats identical quality versus' example 1 respectively and the aloe mineral of comparative example 2 are brilliant；It is daily early
8 points of morning and at 21 points in evening eat 2 times respectively, are taken after mixing it with water using 80 DEG C of hot water.Eating effect is filled in respectively at 28 days, 56 days.
Wherein, anorexia, post-prandial fullness, sour regurgitation, upper abdomen secret anguish symptom mitigation are judged to effectively；Anorexia, after the meal
It is effective that glutted, sour regurgitation, upper abdomen secret anguish symptom have at least one disappearance to be judged to；Anorexia, post-prandial fullness, sour regurgitation, upper abdomen are hidden
Pain symptom all disappears or finds that chronic gastritis disappears using gastrocopy, is judged to recovery from illness.Concrete outcome is shown in Table 2.
The chronic gastritis of table 2 improves situation survey graft
By table 2, comparative example 1 and comparative example 2 have certain health-care effect for chronic gastritis, but relative to this
The obvious poor and embodiment of the present invention of its effect for inventive embodiment.Take aloe mineral crystalline substance 56 provided in an embodiment of the present invention
The chronic gastritis for having 50% patient substantially after it is restored, and the chronic gastritis of 34% patient obtains significant effect, and contrasts
The chronic gastritis for only having 24% patient in example 2 is restored.
Experimental example 3
20-25 Sui is selected, 450 whelk patients are divided into 9 groups of patients, wherein 7 groups of patients eat embodiment 1-7 respectively
Aloe mineral are brilliant, and remaining 2 groups of patient eats identical quality versus' example 1 respectively and the aloe mineral of comparative example 2 are brilliant；Daily morning
8 points and at 21 points in evening eat 2 times respectively, are taken after mixing it with water using 80 DEG C of hot water.Eating effect is filled in respectively at 28 days, 56 days.
Wherein, rate reduction or whelk the inflammation reduction that will not have new whelk to grow or newly grow whelk judge
For effective, whelk inflammation is disappeared, a small amount of youth acne print disappears or a small amount of whelk dissipates and is judged to effective, whelk is disappeared
Mistake is judged to recovery from illness.Concrete outcome is shown in Table 3.
The whelk patient of table 3 improves situation
By table 3, contrast comparative example 1 finds that the embodiment of the present invention is adjusted for endocrine chronic disease with embodiment 1
Reason effect is much better than comparative example 1.The experimental data of contrast comparative example 2 and the embodiment of the present invention finds, the embodiment of the present invention for
It is brilliant that the conditioning effect of the chronic disease of whelk this class internal system imbalance is better than perfect aloe mineral.Should test result indicate that
The aloe mineral crystalline substance of this clearly demarcated embodiment has fabulous effect for the regulation of endocrinopathy.
In sum, each component of embodiment of the present invention 1-7 aloes mineral crystalline substance is the effect being mutually improved, and aloe can strengthen
Stomach function, builds up health；Royal jelly, adjusts endocrine, removes internal harmful substance；Bee Pollen, kidney-nourishing, consolidates, and improves and adjusts
Section incretory secretion；FOS and dusty yeast promote the growth of enteric microorganism, enhance function under the letting out of aloe, mineral
Matter：The synthesis with kinase is participated in, so as to strengthen immunity of organisms.
Embodiments described above is a part of embodiment of the invention, rather than whole embodiments.Reality of the invention
The detailed description for applying example is not intended to limit the scope of claimed invention, but is merely representative of selected implementation of the invention
Example.Based on the embodiment in the present invention, what those of ordinary skill in the art were obtained under the premise of creative work is not made
Every other embodiment, belongs to the scope of protection of the invention.
Claims (10)
1. a kind of aloe mineral are brilliant, it is characterised in that the aloe mineral crystalline substance is made up of plurality of raw materials, in parts by weight, described
Plurality of raw materials include mineral salt, 0.06-0.1 parts of aloe extract, 8-12 parts of taurine, 8-12 parts of Bee Pollen, 8-12 parts it is oligomeric
Fructose, 45-55 part dried fruit juice, 8-12 parts of royal jelly freeze-dried powder, 80-120 portions of white granulated sugar and 8-12 parts of beer yeast powder；The ore deposit
Thing salt includes 0.08-0.15 parts of zinc salt, 0.1-0.25 parts of ferrous salt and 7.5-9.5 parts of calcium salt.
2. aloe mineral according to claim 1 are brilliant, it is characterised in that the zinc salt is zinc gluconate or zinc lactate,
The ferrous salt is ferrous gluconate or ferrous lactate, and the calcium salt is calcium gluconae or calcium lactate.
3. aloe mineral according to claim 1 are brilliant, it is characterised in that the dried fruit juice is sweet orange powder and lemon powder.
4. aloe mineral according to claim 1 are brilliant, it is characterised in that the Bee Pollen be rape pollen, zasiokaurin,
Any one in camellia pollen, pollen pini and lotus powder.
5. aloe mineral according to claim 1 are brilliant, it is characterised in that the plurality of raw materials also includes vitamin, described
Vitamin is any one in vitamin B, vitamin K, vitamin D, vitamin E.
6. aloe mineral according to claim 1 are brilliant, it is characterised in that the plurality of raw materials also includes cellulose, described
Cellulose is dietary cellulosic.
7. it is a kind of to prepare the brilliant method of aloe mineral, it is characterised in that to comprise the following steps：In parts by weight, by 0.06-0.1
Part aloe extract is mixed to get premix with 0.1-0.25 parts of ferrous salt again after mixing with 0.08-0.15 parts of zinc salt；Will
7.5-9.5 parts of calcium salt, 8-12 parts of Bee Pollen, 8-12 parts of royal jelly freeze-dried powder, 8-12 parts of taurine, 8-12 parts of FOS, 8-
Mix with the premix after the mixing of 12 parts of beer yeast powders and continue successively with 45-55 parts of dried fruit juice, 80-120 parts of white sand
Sugar is mixed to get whole mixture.
8. it is according to claim 7 to prepare the brilliant method of aloe mineral, it is characterised in that to crush the whole mixture, powder
Broken rotating speed is 2000-3000r/min, and the time of crushing is 3-7 minutes.
9. it is according to claim 7 to prepare the brilliant method of aloe mineral, it is characterised in that to prepare the aloe mineral crystalline substance
Clean rank is 100,000 grades.
10. it is according to claim 7 to prepare the brilliant method of aloe mineral, it is characterised in that the end after to crushing mixes
Compound is dried, and dry temperature is 40-55 DEG C, and the dry time is 30-45 minutes.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201710087026.8A CN106820161A (en) | 2017-02-17 | 2017-02-17 | Aloe mineral crystalline substance and preparation method thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201710087026.8A CN106820161A (en) | 2017-02-17 | 2017-02-17 | Aloe mineral crystalline substance and preparation method thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN106820161A true CN106820161A (en) | 2017-06-13 |
Family
ID=59129122
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201710087026.8A Pending CN106820161A (en) | 2017-02-17 | 2017-02-17 | Aloe mineral crystalline substance and preparation method thereof |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN106820161A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN115363205A (en) * | 2022-08-08 | 2022-11-22 | 完美（广东）日用品有限公司 | Composition with immunity enhancing and anti-inflammatory functions and preparation method thereof |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101543293A (en) * | 2009-05-04 | 2009-09-30 | 完美（中国）日用品有限公司 | A health food with properties for intensifying human body immunity and supplementing mineral composition |
| CN101711858A (en) * | 2009-10-22 | 2010-05-26 | 岳德玺 | Medicine for treating cancer |
| CN105410568A (en) * | 2015-11-30 | 2016-03-23 | 蚌埠市福淋乳业有限公司 | Fruit flavored highland barley healthy drink and preparation method thereof |
| CN105831666A (en) * | 2016-03-25 | 2016-08-10 | 天津中天精科科技有限公司 | Probiotic honey composition and preparation method thereof |
-
2017
- 2017-02-17 CN CN201710087026.8A patent/CN106820161A/en active Pending
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101543293A (en) * | 2009-05-04 | 2009-09-30 | 完美（中国）日用品有限公司 | A health food with properties for intensifying human body immunity and supplementing mineral composition |
| CN101711858A (en) * | 2009-10-22 | 2010-05-26 | 岳德玺 | Medicine for treating cancer |
| CN105410568A (en) * | 2015-11-30 | 2016-03-23 | 蚌埠市福淋乳业有限公司 | Fruit flavored highland barley healthy drink and preparation method thereof |
| CN105831666A (en) * | 2016-03-25 | 2016-08-10 | 天津中天精科科技有限公司 | Probiotic honey composition and preparation method thereof |
Non-Patent Citations (2)
| Title |
|---|
| 中国特产大典编审委员会贵州卷编委会: "《中国特产大典•贵州卷》", 30 October 2010, 贵州人民出版社 * |
| 黄斌等: "《甘肃养蜂业"十二五"发展之路》", 30 June 2015, 甘肃科学技术出版社 * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN115363205A (en) * | 2022-08-08 | 2022-11-22 | 完美（广东）日用品有限公司 | Composition with immunity enhancing and anti-inflammatory functions and preparation method thereof |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN101756216B (en) | Yeast nutritious food and preparation method thereof | |
| CN108272073A (en) | A kind of weight losing meal-replacing powder and preparation method thereof | |
| CN103976110B (en) | A kind of coreopsis tinctoria flower tea is precious and preparation method thereof | |
| CN102511861A (en) | Thickened red jujube pulp added with oligosaccharide | |
| CN101361567A (en) | Multi-nutrilite composite yeast powder | |
| CN107853525A (en) | More nutritious food solid beverages that a kind of natural plants based on Konjak dietary fiber are made | |
| CN102511864B (en) | Jujube high-consistency stock | |
| CN103710237B (en) | A kind of bee wine and preparation method thereof | |
| CN106879902A (en) | Barley seedling powder solid beverage with and preparation method thereof | |
| CN105878397A (en) | Composition capable of regulating transportation stress of cattle and sheep | |
| CN106889389A (en) | A kind of wild white bur oral liquid and preparation method thereof | |
| CN106070813A (en) | Green tea powder nourishing medicinal granule | |
| CN103535576B (en) | Meal replacement powder containing pollen | |
| CN101496568A (en) | Mung bean or pea dietary fiber and method for producing the same | |
| CN106820161A (en) | Aloe mineral crystalline substance and preparation method thereof | |
| JP2007029020A (en) | Black vinegar health food and method for producing the same | |
| CN100479671C (en) | Method for preparing sour milk containing composite micron pollen pini and konjak for reducing-weight and lowering-blood sugar | |
| CN107712875A (en) | Black quinoa weight losing meal-replacing | |
| CN104432061B (en) | biological embryonic cell nutrient | |
| CN101396056B (en) | Pine-needle tuckahoe teat and preparation method thereof | |
| CN107502509A (en) | A kind of low alcohol content Raspberry health wine beverage and preparation method thereof | |
| CN106418498A (en) | Method for preparing enzyme by using lemons and galangal as main materials | |
| CN102511860B (en) | Thickened red jujube pulp added with phytosterin and being suitable for being taken by pregnant women | |
| CN100469253C (en) | Method for preparing tumor mutation-resisting yoghourt with micron ash tree pollen, pine pollen, bee pollen and ganoderma lucidum spore powder | |
| CN109090398A (en) | A kind of Chinese yam compound solid beverage and preparation method thereof |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PB01 | Publication | ||
| PB01 | Publication | ||
| SE01 | Entry into force of request for substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| RJ01 | Rejection of invention patent application after publication |
Application publication date: 20170613 |
|
| RJ01 | Rejection of invention patent application after publication |