CN105901646A - Pollen pini and sea salt containing plant salt and preparation method - Google Patents
Pollen pini and sea salt containing plant salt and preparation method Download PDFInfo
- Publication number
- CN105901646A CN105901646A CN201610282879.2A CN201610282879A CN105901646A CN 105901646 A CN105901646 A CN 105901646A CN 201610282879 A CN201610282879 A CN 201610282879A CN 105901646 A CN105901646 A CN 105901646A
- Authority
- CN
- China
- Prior art keywords
- salt
- pollen pini
- sea salt
- plant
- extract
- 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.)
- Withdrawn
Links
- 235000002639 sodium chloride Nutrition 0.000 title claims abstract description 175
- 150000003839 salts Chemical class 0.000 title claims abstract description 105
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 title claims abstract description 75
- 239000011780 sodium chloride Substances 0.000 title claims abstract description 69
- 238000002360 preparation method Methods 0.000 title claims abstract description 14
- 241000196324 Embryophyta Species 0.000 claims abstract description 70
- 239000000284 extract Substances 0.000 claims abstract description 44
- 238000005273 aeration Methods 0.000 claims abstract description 11
- 235000003935 Hippophae Nutrition 0.000 claims abstract description 10
- 241000229143 Hippophae Species 0.000 claims abstract description 10
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 claims abstract description 8
- ZMJBYMUCKBYSCP-UHFFFAOYSA-N Hydroxycitric acid Chemical compound OC(=O)C(O)C(O)(C(O)=O)CC(O)=O ZMJBYMUCKBYSCP-UHFFFAOYSA-N 0.000 claims abstract description 4
- 239000012267 brine Substances 0.000 claims abstract description 4
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 claims abstract description 4
- 239000000243 solution Substances 0.000 claims description 20
- 239000002994 raw material Substances 0.000 claims description 17
- 239000000843 powder Substances 0.000 claims description 13
- -1 by weight mark meter Substances 0.000 claims description 11
- 108090000790 Enzymes Proteins 0.000 claims description 9
- 102000004190 Enzymes Human genes 0.000 claims description 9
- 108010082495 Dietary Plant Proteins Proteins 0.000 claims description 7
- 239000004576 sand Substances 0.000 claims description 7
- MJKVTPMWOKAVMS-UHFFFAOYSA-N 3-hydroxy-1-benzopyran-2-one Chemical compound C1=CC=C2OC(=O)C(O)=CC2=C1 MJKVTPMWOKAVMS-UHFFFAOYSA-N 0.000 claims description 6
- 239000003153 chemical reaction reagent Substances 0.000 claims description 6
- 230000002255 enzymatic effect Effects 0.000 claims description 6
- 230000001681 protective effect Effects 0.000 claims description 6
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 5
- 229910001453 nickel ion Inorganic materials 0.000 claims description 5
- 229910052721 tungsten Inorganic materials 0.000 claims description 5
- 239000010937 tungsten Substances 0.000 claims description 5
- ILRCGYURZSFMEG-UHFFFAOYSA-N Salidroside Natural products OC1C(O)C(O)C(CO)OC1OCCC1=CC=C(O)C=C1 ILRCGYURZSFMEG-UHFFFAOYSA-N 0.000 claims description 4
- GAMYVSCDDLXAQW-AOIWZFSPSA-N Thermopsosid Natural products O(C)c1c(O)ccc(C=2Oc3c(c(O)cc(O[C@H]4[C@H](O)[C@@H](O)[C@H](O)[C@H](CO)O4)c3)C(=O)C=2)c1 GAMYVSCDDLXAQW-AOIWZFSPSA-N 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 4
- 229930003944 flavone Natural products 0.000 claims description 4
- 235000011949 flavones Nutrition 0.000 claims description 4
- ILRCGYURZSFMEG-RQICVUQASA-N salidroside Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)OC1OCCC1=CC=C(O)C=C1 ILRCGYURZSFMEG-RQICVUQASA-N 0.000 claims description 4
- VHBFFQKBGNRLFZ-UHFFFAOYSA-N vitamin p Natural products O1C2=CC=CC=C2C(=O)C=C1C1=CC=CC=C1 VHBFFQKBGNRLFZ-UHFFFAOYSA-N 0.000 claims description 4
- 241000894006 Bacteria Species 0.000 claims description 3
- OVSQVDMCBVZWGM-SJWGPRHPSA-N Hyperin Natural products O[C@H]1[C@H](O)[C@@H](O)[C@@H](CO)O[C@H]1OC1=C(C=2C=C(O)C(O)=CC=2)OC2=CC(O)=CC(O)=C2C1=O OVSQVDMCBVZWGM-SJWGPRHPSA-N 0.000 claims description 3
- FVQOMEDMFUMIMO-UHFFFAOYSA-N Hyperosid Natural products OC1C(O)C(O)C(CO)OC1OC1C(=O)C2=C(O)C=C(O)C=C2OC1C1=CC=C(O)C(O)=C1 FVQOMEDMFUMIMO-UHFFFAOYSA-N 0.000 claims description 3
- SNIXRMIHFOIVBB-UHFFFAOYSA-N N-Hydroxyl-tryptamine Chemical compound C1=CC=C2C(CCNO)=CNC2=C1 SNIXRMIHFOIVBB-UHFFFAOYSA-N 0.000 claims description 3
- 150000002212 flavone derivatives Chemical class 0.000 claims description 3
- 102000039446 nucleic acids Human genes 0.000 claims description 3
- 108020004707 nucleic acids Proteins 0.000 claims description 3
- 150000007523 nucleic acids Chemical class 0.000 claims description 3
- OVSQVDMCBVZWGM-DTGCRPNFSA-N quercetin 3-O-beta-D-galactopyranoside Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1OC1=C(C=2C=C(O)C(O)=CC=2)OC2=CC(O)=CC(O)=C2C1=O OVSQVDMCBVZWGM-DTGCRPNFSA-N 0.000 claims description 3
- BBFYUPYFXSSMNV-UHFFFAOYSA-N quercetin-7-o-galactoside Natural products OC1C(O)C(O)C(CO)OC1OC1=CC(O)=C2C(=O)C(O)=C(C=3C=C(O)C(O)=CC=3)OC2=C1 BBFYUPYFXSSMNV-UHFFFAOYSA-N 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 210000002966 serum Anatomy 0.000 abstract description 35
- 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 abstract description 6
- 241000700159 Rattus Species 0.000 abstract 1
- 235000012000 cholesterol Nutrition 0.000 abstract 1
- 230000000694 effects Effects 0.000 description 15
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 15
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 12
- 108010007622 LDL Lipoproteins Proteins 0.000 description 12
- 102000007330 LDL Lipoproteins Human genes 0.000 description 12
- 238000000034 method Methods 0.000 description 12
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- 108010023302 HDL Cholesterol Proteins 0.000 description 9
- FOIXSVOLVBLSDH-UHFFFAOYSA-N Silver ion Chemical compound [Ag+] FOIXSVOLVBLSDH-UHFFFAOYSA-N 0.000 description 9
- 239000003651 drinking water Substances 0.000 description 9
- 235000020188 drinking water Nutrition 0.000 description 9
- RVPVRDXYQKGNMQ-UHFFFAOYSA-N lead(2+) Chemical compound [Pb+2] RVPVRDXYQKGNMQ-UHFFFAOYSA-N 0.000 description 9
- 238000012360 testing method Methods 0.000 description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 8
- 108010028554 LDL Cholesterol Proteins 0.000 description 8
- HAYXDMNJJFVXCI-UHFFFAOYSA-N arsenic(5+) Chemical compound [As+5] HAYXDMNJJFVXCI-UHFFFAOYSA-N 0.000 description 8
- 238000002474 experimental method Methods 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 229910001385 heavy metal Inorganic materials 0.000 description 7
- 244000060011 Cocos nucifera Species 0.000 description 6
- 235000013162 Cocos nucifera Nutrition 0.000 description 6
- 235000013305 food Nutrition 0.000 description 6
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 6
- 102000004895 Lipoproteins Human genes 0.000 description 5
- 108090001030 Lipoproteins Proteins 0.000 description 5
- 230000008859 change Effects 0.000 description 5
- 229940088598 enzyme Drugs 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- 108010010234 HDL Lipoproteins Proteins 0.000 description 4
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- 239000008187 granular material Substances 0.000 description 4
- 229940046892 lead acetate Drugs 0.000 description 4
- 229910052748 manganese Inorganic materials 0.000 description 4
- 239000011572 manganese Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 230000009467 reduction Effects 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 3
- 210000004369 blood Anatomy 0.000 description 3
- 239000008280 blood Substances 0.000 description 3
- 230000037396 body weight Effects 0.000 description 3
- 238000002425 crystallisation Methods 0.000 description 3
- 230000008025 crystallization Effects 0.000 description 3
- 239000012153 distilled water Substances 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000001728 nano-filtration Methods 0.000 description 3
- 238000006385 ozonation reaction Methods 0.000 description 3
- 229910001961 silver nitrate Inorganic materials 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 206010002091 Anaesthesia Diseases 0.000 description 2
- GOLCXWYRSKYTSP-UHFFFAOYSA-N Arsenious Acid Chemical compound O1[As]2O[As]1O2 GOLCXWYRSKYTSP-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 102000004142 Trypsin Human genes 0.000 description 2
- 108090000631 Trypsin Proteins 0.000 description 2
- 230000037005 anaesthesia Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 239000003077 lignite Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 230000001629 suppression Effects 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 239000012588 trypsin Substances 0.000 description 2
- 239000006200 vaporizer Substances 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
- 241000628997 Flos Species 0.000 description 1
- 208000031226 Hyperlipidaemia Diseases 0.000 description 1
- 101001031591 Mus musculus Heart- and neural crest derivatives-expressed protein 2 Proteins 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- QGMRQYFBGABWDR-UHFFFAOYSA-M Pentobarbital sodium Chemical compound [Na+].CCCC(C)C1(CC)C(=O)NC(=O)[N-]C1=O QGMRQYFBGABWDR-UHFFFAOYSA-M 0.000 description 1
- 102000057297 Pepsin A Human genes 0.000 description 1
- 108090000284 Pepsin A Proteins 0.000 description 1
- 108091005804 Peptidases Proteins 0.000 description 1
- 239000004365 Protease Substances 0.000 description 1
- REFJWTPEDVJJIY-UHFFFAOYSA-N Quercetin Chemical compound C=1C(O)=CC(O)=C(C(C=2O)=O)C=1OC=2C1=CC=C(O)C(O)=C1 REFJWTPEDVJJIY-UHFFFAOYSA-N 0.000 description 1
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- 244000274883 Urtica dioica Species 0.000 description 1
- 235000009108 Urtica dioica Nutrition 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 235000001014 amino acid Nutrition 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 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
- 229950001002 cianidanol Drugs 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 230000000249 desinfective effect Effects 0.000 description 1
- 235000005911 diet Nutrition 0.000 description 1
- 230000037213 diet Effects 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 235000018927 edible plant Nutrition 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 235000021022 fresh fruits Nutrition 0.000 description 1
- 210000000232 gallbladder Anatomy 0.000 description 1
- 238000003304 gavage Methods 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 229930182470 glycoside Natural products 0.000 description 1
- 150000002338 glycosides Chemical class 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 238000001095 inductively coupled plasma mass spectrometry Methods 0.000 description 1
- 239000007928 intraperitoneal injection Substances 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 108010022197 lipoprotein cholesterol Proteins 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000001819 mass spectrum Methods 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 230000000474 nursing effect Effects 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 229960002275 pentobarbital sodium Drugs 0.000 description 1
- 229940111202 pepsin Drugs 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- IKGXIBQEEMLURG-BKUODXTLSA-N rutin Chemical compound O[C@H]1[C@H](O)[C@@H](O)[C@H](C)O[C@@H]1OC[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](OC=2C(C3=C(O)C=C(O)C=C3OC=2C=2C=C(O)C(O)=CC=2)=O)O1 IKGXIBQEEMLURG-BKUODXTLSA-N 0.000 description 1
- 229960004555 rutoside Drugs 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- PTLRDCMBXHILCL-UHFFFAOYSA-M sodium arsenite Chemical compound [Na+].[O-][As]=O PTLRDCMBXHILCL-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 229930193551 sterin Natural products 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 239000011573 trace mineral Substances 0.000 description 1
- 235000013619 trace mineral Nutrition 0.000 description 1
- 229960001322 trypsin Drugs 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
- 230000003442 weekly effect Effects 0.000 description 1
- 238000005303 weighing Methods 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
- A61K36/13—Coniferophyta (gymnosperms)
- A61K36/15—Pinaceae (Pine family), e.g. pine or cedar
-
- 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)
- A61K36/185—Magnoliopsida (dicotyledons)
-
- 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)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/24—Apocynaceae (Dogbane family), e.g. plumeria or periwinkle
-
- 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)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/73—Rosaceae (Rose family), e.g. strawberry, chokeberry, blackberry, pear or firethorn
- A61K36/734—Crataegus (hawthorn)
-
- 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)
- Natural Medicines & Medicinal Plants (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Alternative & Traditional Medicine (AREA)
- Biotechnology (AREA)
- Botany (AREA)
- Medical Informatics (AREA)
- Medicinal Chemistry (AREA)
- Microbiology (AREA)
- Mycology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
Abstract
The invention relates to pollen pini and sea salt containing plant salt and a preparation method thereof. The pollen pini and sea salt containing plant salt is characterized by being prepared from pollen pini, sea salt containing plant salt, natural Fructus Hippophae extract, Folium Crataegi extract, Garcinia Cambogia extract and Folium Apocyni Veneti extract. The preparation method is characterized by including an aeration step, and ozone is adopted for aeration at the aeration step, wherein the ozone concentration is 40-42mg/L, and the temperature of brine is 45-47DEG C. Under experimental conditions, the pollen pini and sea salt containing plant salt reduces TC (total cholesterol) concentration in serum of rats from 5.36+/-0.71mmol/L to 1.35+/-0.23mmol/L.
Description
Technical field
The present invention relates to plant salt of a kind of Pollen Pini and sea salt and preparation method thereof, belong to plant salt technical field.
Background technology
Pollen Pini contains multiple nutrients material, including 22 kinds of aminoacid, 14 kinds of vitamin and 30 various trace elements and
Substantial amounts of active protease, core, flavone compound and other active substance.Pollen Pini rich in protein many with free amine group
Presented in acid, content exceed milk, 5-7 times of egg；Ascorbic content is higher than fresh fruit and vegetable, is referred to as
' king of natural complex '.
In prior art, the most Pollen Pini not being joined in edible salt, preparation has the report of functional edible salt；Plant
Thing salt belongs to threpsology's category, and purely edible plant salt, to improve health, is not the most real, since it is desired that be eaten for a long time,
And the salt sea salt edible salt that to be us daily, therefore, invent a kind of can be eaten for a long time functional containing daily edible
The plant salt of salt is the problem that solution is presently required, and the present invention also needs to solve techniques below problem present in prior art:
1, in current edible salt, Pollen Pini is not contained；
2, current edible salt, does not possess T-CHOL (TC) in reduction rat blood serum, triglyceride (TG), low density lipoprotein, LDL
(LDL) content, improves the effect of the content of serum middle-high density lipoprotein (HDL)；
3, the edible salt of prior art, does not possess removal effect to the lead ion in serum, silver ion, arsenic ion, the most right
The selection removing effect of silver ion is bad；
4, current edible salt, salinity is the highest, long-term excess is edible be unfavorable for healthy.
Summary of the invention
For the deficiencies in the prior art, the present invention provides a kind of plant salt containing Pollen Pini and sea salt and preparation method thereof,
To realize following goal of the invention:
1, the present invention prepare containing Pollen Pini and the plant salt of sea salt, have reduction rat blood serum in T-CHOL (TC), glycerol
Three esters (TG), the content of low density lipoprotein, LDL (LDL), improves the effect of the content of serum middle-high density lipoprotein (HDL), especially
It is for reducing T-CHOL (TC), the effect highly significant of triglyceride (TG) content in serum；
2, the present invention prepare containing Pollen Pini and the plant salt of sea salt, lead ion, silver ion, arsenic ion in rat blood serum are had one
Fixed removal effect, particularly to the silver ion in serum, has removal effect the most significant, selective；
3, the present invention prepare containing Pollen Pini and the plant salt of sea salt, it is possible to suppression fat synthesis, promote fatty acid burning,
Reduce the absorption of food, in daily life, need not deliberately eat appetrol, i.e. can reach the effect of certain slimming.
In order to realize foregoing invention purpose, the technical solution used in the present invention is as follows:
It is a kind of containing Pollen Pini with the plant salt of sea salt, it is characterised in that: described containing Pollen Pini with the plant salt of sea salt, raw material includes
Pollen Pini and the plant salt containing sea salt.
The following is and the further of technique scheme is improved:
Described containing Pollen Pini with the plant salt of sea salt, raw material also includes: natural hippophae extract, Folium Crataegi extract, Fructus Resina garciniae
Extract, Herba Apocyni veneti extract.
Described containing Pollen Pini with the plant salt of sea salt, by weight mark meter, raw material includes: the plant salt 95-110 containing sea salt
Part, Pollen Pini 6-7 part, natural hippophae extract 4-6 part, Folium Crataegi extract 5-7 part, Fructus Resina garciniae extract 2-5 part, Herba Apocyni veneti
Extract 3-5 part.
Described Pollen Pini, fineness 150-170 mesh, Pollen pini thunbergii taken from by raw material, containing nucleic acid 4-5.5%, flavone 8-10%.
The described plant salt containing sea salt, NaCl content: 75-78%, total Lip river match dimension hplc: 1-1.5%, Determination of Salidroside:
0.8-1.1%, tungsten ion content 0.03-0.04mg/kg, nickel ion content 0.04-0.06mg/kg.
Described natural hippophae extract, composition includes: Hydroxycoumarin >=5%, hydroxytryptamine >=3%.
Described Folium Crataegi extract, composition includes: crataegutt content 70-75%, hyperin 5-15%.
Described Fructus Resina garciniae extract, hydroxycitrate acid content 35-40%, mesh number 210-240, total number of bacteria≤600/g.
It is a kind of containing Pollen Pini with the preparation method of the plant salt of sea salt, it is characterised in that: include aerating step, described aeration
Step uses ozone heap salt to carry out aeration, and described ozone concentration is 40-42mg/L, and brine temperature is 45-47 DEG C.
Described method also includes enzymolysis step；Described enzymolysis step need to add vegetable protein enzymatic protective reagent in extracting solution,
Described vegetable protein enzymatic protective reagent is 1.5-2% relative to the mass percent of Herba suadeae glaucae powder.
Owing to have employed technique scheme, the technique effect that the present invention reaches is as follows:
1, under conditions of this test, the present invention prepare containing Pollen Pini and the plant salt of sea salt, can be by TC concentration in rat blood serum
By 5.36 ± 0.71mmol/L, it is reduced to 1.35 ± 0.23mmol/L；
2, under conditions of this experiment, the present invention prepare containing Pollen Pini and the plant salt of sea salt, can be by TG concentration in rat blood serum
It is reduced to 0.42 ± 0.26mmol/L by 2.77 ± 0.42mmol/L；
3, under conditions of this experiment, the present invention prepare containing Pollen Pini and the plant salt of sea salt, can be by dense for LDL-C in rat blood serum
Degree is reduced to 2.33 ± 0.25mmol/L by 2.77 ± 0.34mmol/L；
4, under conditions of this experiment, the present invention prepare containing Pollen Pini and the plant salt of sea salt, can be by HDL-C in rat blood serum
Concentration is increased to 0.665 ± 0.06mmol/L by 0.53 ± 0.18mmol/L；
5, under conditions of this test, the present invention prepare containing Pollen Pini and the plant salt of sea salt, can be by lead ion in rat blood serum
Concentration, by 51.36 ± 2.65 micrograms/L, is reduced to 43.25 ± 0.25 micrograms/L；
6, under conditions of this test, the present invention prepare containing Pollen Pini and the plant salt of sea salt, can be by silver ion in rat blood serum
Concentration, by 52.14 ± 3.86 micrograms/L, is reduced to 2.15 ± 0.16 micrograms/L；
7, under conditions of this test, the present invention prepare containing Pollen Pini and the plant salt of sea salt, can be by arsenic ion in rat blood serum
Concentration, by 51.63 ± 4.32 micrograms/L, is reduced to 42.65 ± 3.54 micrograms/L；
8, the present invention prepare containing Pollen Pini and the plant salt of sea salt, it is possible to suppression fat synthesis, promote fatty acid burning,
Reduce the absorption of food, in daily life, need not deliberately eat appetrol, i.e. can reach the effect of certain slimming.
Detailed description of the invention
Embodiment 1 is containing Pollen Pini and the plant salt of sea salt
In parts by weight, including following raw material components:
Plant salt containing sea salt 95 parts, Pollen Pini 6 parts, natural hippophae extract 4 parts, Folium Crataegi extract 5 parts, Fructus Resina garciniae extract
Thing 2 parts, Herba Apocyni veneti extract 3 parts；
The described plant salt containing sea salt, NaCl content: 75-78%, the match of total Lip river dimension hplc: 1-1.5%, Determination of Salidroside: 0.8-
1.1%, tungsten ion content 0.03-0.04mg/kg, lead ion content 0mg/kg, nickel ion content 0.04-0.06mg/kg；
Described Pollen Pini, fineness 150-170 mesh, Pollen pini thunbergii taken from by raw material, containing nucleic acid 4-5.5%, flavone 8-10%；
Described natural hippophae extract, Hydroxycoumarin >=5%, hydroxytryptamine >=3%；
Described Folium Crataegi extract, crataegutt content 70-75%, hyperin 5-15%；
Described Fructus Resina garciniae extract, hydroxycitrate acid content 35-40%, mesh number 210-240, total number of bacteria≤600/g, mycete
Number and yeast sum≤30/g；
Described Herba Apocyni veneti extract, globulariacitrin content 9-11%, catechin content 5-8%, quercetin content 1.5-2.5%, mesh number≤
80 mesh.
Embodiment 2 is containing Pollen Pini and the plant salt of sea salt
Use each raw material described in embodiment 1, only change the proportioning of each raw material, change into:
In parts by weight, including following raw material components:
Plant salt containing sea salt 100 parts, Pollen Pini 7 parts, natural hippophae extract 5 parts, Folium Crataegi extract 6 parts, Fructus Resina garciniae carry
Take thing 3 parts, Herba Apocyni veneti extract 4 parts；
Embodiment 3 is containing Pollen Pini and the plant salt of sea salt
Use each raw material described in embodiment 1, only change the proportioning of each raw material, change into:
In parts by weight, including following raw material components:
Plant salt containing sea salt 110 parts, Pollen Pini 6 parts, natural hippophae extract 6 parts, Folium Crataegi extract 7 parts, Fructus Resina garciniae carry
Take thing 5 parts, Herba Apocyni veneti extract 5 parts；
Embodiment 4 one kinds, containing Pollen Pini and the preparation method of the plant salt of sea salt, comprises the following steps:
One, the preparation of the plant salt containing sea salt
Step 1, aeration removing heavy metals
(1) precipitation filters
Filter: taking coastal salt, tungsten ion content is at 15-20mg/L, lead ion content 26-30mg/L after testing, and nickel ion contains
Amount 8-12mg/L, squeezes into salt in sedimentation tank, precipitates 2-2.5h.
Mechanical filter: by remove heavy metal ion salt through mechanical filter remove bulky grain solid impurity therein and
Mechanicalness impurity；
Nanofiltration: the salt after mechanical filter carries out nanofiltration process, nanofiltration temperature to control at 35-38 DEG C, and Stress control exists
0.2-0.3MPa。
(2) aeration removing heavy metals
Aeration: the salt after filtering carries out ozonation aerated process 120-150min in being passed through ozone treatment apparatus；Described salt
In ozone concentration be 40-42mg/L, brine temperature is 45-47 DEG C.
Absorption: the salt after ozonation aerated process pass through adsorbing material adsorption filtration, adsorbing material be manganese sand, Cortex cocois radicis (Cocos nucifera L.) powder and
Activated carbon granule, the sea water after ozonation aerated process filters from top to bottom.Manganese sand, Exocarpium cocois (Cocos nucifera L) powder and activated carbon in adsorbing material
Granule, the order being gradually increased according to particle diameter from top to bottom is filled.
The particle diameter of the upper strata manganese sand grains of sand is 1.5-2 mm, and the particle diameter of intermediate layer Cortex cocois radicis (Cocos nucifera L.) powder is 1-1.2mm, described lower floor
The particle diameter of activated carbon granule is 2-3mm.
Through the salt that manganese sand, Exocarpium cocois (Cocos nucifera L) powder and activated carbon granule filter, enter in brown coal filtering layer and filter, its
The height of middle brown coal filtering layer is 100-130 millimeter.
Described Exocarpium cocois (Cocos nucifera L) powder is through modified, and described Exocarpium cocois (Cocos nucifera L) powder is modified by acetic acid, described acetic acid
Concentration is 15-17%.
After aeration removes heavy metal ion, the salt of heavy metal ion must be removed.
Prepared by step 2, Herba suadeae glaucae salt extracting solution
Extraction:
Take dry Herba suadeae glaucae powder, with solid-liquid ratio 1:7-9, extraction time 60-80min hour.Described leach step: be in frequency
1850-2100MHz, power is to carry out hot dipping under the microwave of 18-20KW and water ring pump effect that power is 1.5-1.6KW to carry, leaching
Temperature raising degree is 65-68 DEG C, and vacuum is 0.5-0.6MPa, and extraction time 50-70min obtains lixiviating solution.
Enzymolysis:
(1) by the lixiviating solution of preparation, adding vegetable protein enzymatic protective reagent, vegetable protein enzymatic protective reagent is relative to the matter of Herba suadeae glaucae powder
Amount percent is 1.5-2%；Described vegetable protein enzymatic protective reagent is pulullan polysaccharide；
(2) in feed liquid, add food commercially available protein enzyme, obtain reactant liquor, be in terms of 100% by Herba suadeae glaucae dry powder oeverall quality, food
It is 3-5% by the addition of commercially available protein enzyme；
Food commercially available protein enzyme is trypsin, pepsic compound enzyme, in described compound enzyme, trypsin and pepsin
The mass ratio of enzyme is 1:2-5；
(3) stirring reactant liquor is to being sufficiently mixed, and enzymolysis time is 180-220min；
(4) heating enzyme denaturing is lived, and 15-17min enzyme denaturing can be maintained to live at 135-155 DEG C.
Decolouring:
Take the supernatant after enzymolysis, add commercially available Radix Rhodiolae extract, and described Radix Rhodiolae extract (total Luo Saiwei: 5-10%, red
Herba hylotelephii erythrosticti glycosides: 3-7%) the 35-45% that addition is Herba suadeae glaucae total mass fraction；Extracting solution is heated to 40-42 DEG C, and dropping acetic acid is adjusted
Joint pH is 5-6, adds flocculant, and flocculant addition is the 2-3% of extracting solution quality；Opening stirring, stir speed (S.S.) is 100-
120rpm, continuously stirred 30-45min；
Decoloured to obtain Herba suadeae glaucae salt extracting solution.
Step 3, evaporative crystallization:
The salt removing heavy metal is evaporated crystallizing according to the following steps:
A (), in the salt removing heavy metal, adds distilled water and Herba suadeae glaucae salt extracting solution, (Herba suadeae glaucae salt extracting solution
Addition is: in terms of Herba suadeae glaucae powder, for the 28-31% of sodium chloride in salt) prepare the salt that concentration is 20-22%, by preheating
Temperature after device preheating is 72-75 DEG C；
B the salt after () preheating enters vaporizer, in controlling vaporizer, temperature is 95-98 DEG C, obtains the concentrated solution of 26-28%；
C () concentrated solution enters crystallizer, in control crystallizer, temperature is 102 DEG C, when the crystal salt height in crystallizer to 15cm
Time, carrying out salt discharge, the salt slurry after crystallization enters dehydration, drying steps.
Step 4, be dried
Salt slurry after crystallization is sent into drying bed be dried, the plant salt of sea salt must be contained.
The plant salt containing sea salt prepared by above method, component content is: NaCl content: 75-78%, total Luo Saiwei
Content: 1-1.5%, Determination of Salidroside: 0.8-1.1%, tungsten ion content 0.03-0.04mg/kg, lead ion content 0mg/kg,
Nickel ion content 0.04-0.06mg/kg.
Two: containing Pollen Pini and the preparation of the plant salt of sea salt
Weigh each raw material according to formula, by Pollen Pini, natural hippophae extract, Folium Crataegi extract, Fructus Resina garciniae extract, spread out
Plant salt containing sea salt prepared by nettle extract, the present invention, mixing, after pulverizing, after disinfecting, obtain the present invention containing Flos pini
Powder and the plant salt of sea salt.
The present invention prepare containing Pollen Pini and the plant salt of sea salt, have the effect that
(1) present invention prepare containing Pollen Pini and the plant salt of sea salt, it is possible to decrease T-CHOL (TC) in rat blood serum, glycerol three
Ester (TG), the content of low density lipoprotein, LDL (LDL), improves the content of serum middle-high density lipoprotein (HDL).
The Adult SD strain male rat 60 provided by Guangdong Medical Lab Animal Center, body weight 160～220g, dynamic
Thing list cage is fed, and based on feedstuff, feedstuff (calcium content is 1.33%, phosphorus content 0.95%), sets up rat by high lipoprotein emulsion gavage
Hyperlipidemia model, after having tested, utilizes 3% pentobarbital sodium (30mg kg-1) intraperitoneal injection of anesthesia, and retroorbital venous is adopted by clump
Blood (0.5ml), with 4 DEG C, 3000rpm, centrifugal 15min, measures detection serum total cholesterol (TC), triglyceride (TG), low close
Degree lipoprotein cholesterol (LDL-C) and HDL-C (HDL-C) content.
Experiment sets blank group (A group), model control group (B group) embodiment 1 matched group (C group), embodiment 2 matched group
(D group) and embodiment 3 matched group (E group) totally 5 groups, often 12 white mouse of group.
A group is normal rat, only feeds normal feedstuff and distilled water；
B group, after modeling success, only feeds normal feedstuff and distilled water.Model criteria: TC(mmol/L) >=5.00；TG(mmol/
L) >=2.5；LDL-C(mmol/L) >=2.5；HDL-C(mmol/L)≤0.6.
C group, D group, E group, after modeling success, the solution that plant salt prepared by nursing normal feedstuff and the present invention is made into.
It is 3g by human body solar eclipse recommended amounts, sets animal given low as 3-5 times of human body solar eclipse dosage, by system of the present invention
Standby plant salt is configured to the plant salt solution of 2mg/ml, after slack tank stomach processes 60d, and detection serum total cholesterol (TC), glycerol
Three esters (TG), low-density lipoprotein cholesterol (LDL-C) and HDL-C (HDL-C) content.
Table 2 present invention prepare containing Pollen Pini and the plant salt of sea salt, to T-CHOL in rat blood serum (TC), glycerol
Three esters (TG), low-density lipoprotein cholesterol (LDL-C) and the impact of HDL-C (HDL-C) content are relevant
Value is arithmetic mean of instantaneous value ± standard deviation, is shown in Table 1:
Table 1
As can be seen from the above table, the present invention prepare containing Pollen Pini and the plant salt of sea salt, there is total gallbladder in reduction rat blood serum
Sterin (TC), triglyceride (TG), the content of low density lipoprotein, LDL (LDL), improves containing of serum middle-high density lipoprotein (HDL)
The effect of amount.
Under conditions of this test, 1.35 can be reduced to by TC concentration in rat blood serum by 5.36 ± 0.71mmol/L ±
0.23mmol/L；
Under conditions of this experiment, can by TG concentration in rat blood serum by 2.77 ± 0.42mmol/L be reduced to 0.42 ±
0.26mmol/L；
Under conditions of this experiment, can by LDL-C concentration in rat blood serum by 2.77 ± 0.34mmol/L be reduced to 2.33 ±
0.25mmol/L；
Under conditions of this experiment, can by HDL-C concentration in rat blood serum by 0.53 ± 0.18mmol/L be increased to 0.665 ±
0.06mmol/L。
(2) present invention prepare containing Pollen Pini and the plant salt of sea salt, to the lead ion in rat blood serum, silver ion, arsenic
Ion has preferable removal effect.
The Adult SD strain male rat 60 provided by Guangdong Medical Lab Animal Center, body weight 160～220g, dynamic
Thing list cage is fed, feedstuff (calcium content is 1.33%, phosphorus content 0.95%) based on feedstuff.
Experiment sets blank group (A group), (C group, is divided into C1, C2, C3 to model control group (B group) embodiment 1 matched group
Group), embodiment 2 matched group (D group is divided into D1, D2, D3 group) and embodiment 3 matched group (component E becomes E1, E2, E3) totally 11
Group, often 12 white mouse of group.
A group is normal rat, only feeds normal feedstuff and deionized water；
B group, drinking-water changes 0.15% lead acetate drinking-water into and normal feedstuff is fed；
Component C becomes C1, C2, C3 group, and it is molten that drinking-water changes 0.15% lead acetate, 0.15% silver nitrate solution, 0.15% sodium arsenite respectively into
The good normal feedstuff that plant salt prepared by liquid drinking-water and the present invention is in harmonious proportion is fed.
D group is divided into D1, D2, D3 group, and drinking-water changes 0.15% lead acetate, 0.15% silver nitrate solution, 0.15% arsenious acid respectively into
The good normal feedstuff that plant salt prepared by sodium solution drinking-water and the present invention is in harmonious proportion is fed.
Component E becomes E1, E2, E3 group, drinking-water to change 0.15% lead acetate, 0.15% silver nitrate solution, 0.15% arsenious acid respectively into
The good normal feedstuff that plant salt prepared by sodium solution drinking-water and the present invention is in harmonious proportion is fed.
It is 3g by human body solar eclipse recommended amounts, sets animal given low as 5 times of human body solar eclipse dosage, claim one every five to eight days
Secondary body weight and record weekly diet, amount of drinking water, fasting 12 hours before weighing.Feed to 50d.Period notes changing cage, changes water, changes
Food, it is ensured that water, provand are abundant.
Blood lead content measures: feed after terminating, rat anesthesia, and Hearts takes blood, and room temperature stands 1 hour, 7000 turns, from
Heart 5min, collects serum.Taking 400 HL serum and be dissolved in 1.6 milliliters of nitric acid, 85 DEG C of Water bath 4-6 hour, by inductive etc.
Gas ions mass spectrum (ICP-MS) measures lead ion therein, silver ion, arsenic ion content.
The present invention prepare containing Pollen Pini and the plant salt of sea salt, lead ion, silver ion, arsenic ion in rat blood serum are contained
The impact of amount, correlation is arithmetic mean of instantaneous value ± standard deviation, is shown in Table 2:
Table 2
As can be seen from the above table, the present invention prepare containing Pollen Pini and the plant salt of sea salt, have reduction rat blood serum in lead from
Son, silver ion, the effect of arsenic ion content.
Under conditions of this test, can be reduced to by plumbum ion concentration in rat blood serum by 51.36 ± 2.65 micrograms/L
43.25 ± 0.25 micrograms/L；
Under conditions of this test, 2.15 can be reduced to by concentration of silver ions in rat blood serum by 52.14 ± 3.86 micrograms/L ±
0.16 microgram/L；
Under conditions of this test, 42.65 can be reduced to by arsenic ion concentration in rat blood serum by 51.63 ± 4.32 micrograms/L ±
3.54 micrograms/L.
Except as otherwise noted with art technology conventional unit, the percent employed in the present invention is weight percent
Number, ratio of the present invention, it is mass ratio.
Finally it is noted that the foregoing is only the preferred embodiments of the present invention, it is not limited to the present invention,
Although being described in detail the present invention with reference to previous embodiment, for a person skilled in the art, it still may be used
So that the technical scheme described in foregoing embodiments to be modified, or wherein portion of techniques feature is carried out equivalent.
All within the spirit and principles in the present invention, any modification, equivalent substitution and improvement etc. made, should be included in the present invention's
Within protection domain.
Claims (10)
1. one kind contains Pollen Pini and the plant salt of sea salt, it is characterised in that: described containing Pollen Pini with the plant salt of sea salt, raw material bag
Include Pollen Pini and the plant salt containing sea salt.
The most according to claim 1 a kind of containing Pollen Pini with the plant salt of sea salt, it is characterised in that: described containing Pollen Pini and
The plant salt of sea salt, raw material also includes: natural hippophae extract, Folium Crataegi extract, Fructus Resina garciniae extract, Herba Apocyni veneti are extracted
Thing.
The most according to claim 1 a kind of containing Pollen Pini with the plant salt of sea salt, it is characterised in that: described containing Pollen Pini and
The plant salt of sea salt, by weight mark meter, raw material includes: the plant salt 95-110 part containing sea salt, Pollen Pini 6-7 part, natural sand
Spine extract 4-6 part, Folium Crataegi extract 5-7 part, Fructus Resina garciniae extract 2-5 part, Herba Apocyni veneti extract 3-5 part.
It is the most according to claim 1 a kind of containing Pollen Pini with the plant salt of sea salt, it is characterised in that: described Pollen Pini, carefully
Degree 150-170 mesh, Pollen pini thunbergii taken from by raw material, containing nucleic acid 4-5.5%, containing flavone 8-10%.
It is the most according to claim 1 a kind of containing Pollen Pini with the plant salt of sea salt, it is characterised in that: described planting containing sea salt
Thing salt, NaCl content: 75-78%, total Lip river match dimension hplc: 1-1.5%, Determination of Salidroside: 0.8-1.1%, tungsten ion content
0.03-0.04mg/kg, nickel ion content 0.04-0.06mg/kg.
It is the most according to claim 2 a kind of containing Pollen Pini with the plant salt of sea salt, it is characterised in that: described natural sand
In spine extract, Hydroxycoumarin >=5%, hydroxytryptamine >=3%.
It is the most according to claim 2 a kind of containing Pollen Pini with the plant salt of sea salt, it is characterised in that:
Described Folium Crataegi extract, crataegutt content 70-75%, hyperin 5-15%.
It is the most according to claim 2 a kind of containing Pollen Pini with the plant salt of sea salt, it is characterised in that: described Fructus Resina garciniae extracts
Thing, hydroxycitrate acid content 35-40%, mesh number 210-240, total number of bacteria≤600/g.
9. the preparation method of the plant salt containing Pollen Pini and sea salt, it is characterised in that: including aerating step, described aeration walks
Rapid employing ozone heap salt carries out aeration, and described ozone concentration is 40-42mg/L, and brine temperature is 45-47 DEG C.
It is the most according to claim 9 a kind of containing Pollen Pini with the preparation method of the plant salt of sea salt, it is characterised in that: also
Including enzymolysis step；Described enzymolysis step need to add vegetable protein enzymatic protective reagent, described vegetable protein enzyme protection in extracting solution
The addition of agent is 1.5-2% relative to the mass percent of Herba suadeae glaucae powder.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201610282879.2A CN105901646A (en) | 2016-05-03 | 2016-05-03 | Pollen pini and sea salt containing plant salt and preparation method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201610282879.2A CN105901646A (en) | 2016-05-03 | 2016-05-03 | Pollen pini and sea salt containing plant salt and preparation method |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN105901646A true CN105901646A (en) | 2016-08-31 |
Family
ID=56753288
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201610282879.2A Withdrawn CN105901646A (en) | 2016-05-03 | 2016-05-03 | Pollen pini and sea salt containing plant salt and preparation method |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN105901646A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108283306A (en) * | 2017-12-27 | 2018-07-17 | 天津佰亿达企业管理股份有限公司 | A kind of health-care hippophae rhamnoide edible salt and preparation method thereof |
| CN112654259A (en) * | 2018-07-23 | 2021-04-13 | 杭州尤美特科技有限公司 | Functional plant salt and preparation method and application thereof |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101040711A (en) * | 2006-03-24 | 2007-09-26 | 孙贻超 | The application of Suaeda plant extraction in the food having health-care and weight-losing functions |
| CN103570163A (en) * | 2013-11-21 | 2014-02-12 | 潍坊滨海开发区华海水产养殖有限公司 | Removing method of exceeding iron-manganese heavy metal in underground seawater |
-
2016
- 2016-05-03 CN CN201610282879.2A patent/CN105901646A/en not_active Withdrawn
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101040711A (en) * | 2006-03-24 | 2007-09-26 | 孙贻超 | The application of Suaeda plant extraction in the food having health-care and weight-losing functions |
| CN103570163A (en) * | 2013-11-21 | 2014-02-12 | 潍坊滨海开发区华海水产养殖有限公司 | Removing method of exceeding iron-manganese heavy metal in underground seawater |
Non-Patent Citations (6)
| Title |
|---|
| 《健康大讲堂》编委会: "《高血脂吃什么？禁什么？》", 28 February 2015 * |
| 刘素华等: "植物盐及其研究进展", 《中国食品添加剂》 * |
| 刘绍贵等: "《临床常用中草药鉴别与应用》", 31 July 2015 * |
| 周秋丽等: "《现代中药基础研究与临床》", 30 June 2012 * |
| 艾尔•敏德尔: "《新维生素圣经》", 30 September 2015 * |
| 谢宇: "《健康小博士-医药百科》", 31 January 2010 * |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108283306A (en) * | 2017-12-27 | 2018-07-17 | 天津佰亿达企业管理股份有限公司 | A kind of health-care hippophae rhamnoide edible salt and preparation method thereof |
| CN112654259A (en) * | 2018-07-23 | 2021-04-13 | 杭州尤美特科技有限公司 | Functional plant salt and preparation method and application thereof |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN101991165B (en) | Sweet potato leaf-perilla leaf composite beverage and preparation method thereof | |
| CN107996932B (en) | Turmeric beverage and preparation method thereof | |
| CN111437297A (en) | Composition for preventing and treating cancer-induced fatigue and application thereof | |
| CN105901646A (en) | Pollen pini and sea salt containing plant salt and preparation method | |
| CN108552369A (en) | A kind of tea-drinking preparation method for material of the active material containing golden camellia tea | |
| CN105231227B (en) | A kind of numb corn milk production method of fire | |
| CN112189758A (en) | Chinese herbal medicine feed additive containing pithecellobium clypearia and preparation method and application thereof | |
| CN107375652A (en) | A kind of CHUANBEI PIPA GAO and preparation method thereof | |
| KR101197605B1 (en) | manufacturing method of feed containing sulphur and method of breeding a livestock with feed containing sulphur | |
| CN108567070A (en) | A kind of meat goose cultivation feed rich in various trace elements | |
| CN108157545A (en) | A kind of guava leaf liquid beverage and preparation method thereof | |
| WO2018129897A1 (en) | Black tea extract and preparation method therefor | |
| CN107320576A (en) | A kind of extracting method of black tea golden flower nutritional ingredients | |
| CN105962286A (en) | Plant salt containing lavandulaangustifoliamill extract and preparation method of plant salt | |
| CN105919021A (en) | Vegetable salt containing sea salt and nori extract as well as preparation method thereof | |
| CN105901648A (en) | Astaxanthin and sea salt containing plant salt and preparation method thereof | |
| CN107568524A (en) | A kind of preparation technology of selenium-rich Passion Fruit Juice | |
| CN103536670A (en) | Composition for improving alimentary anemia as well as preparation method thereof | |
| CN1345587A (en) | Trace element equilibrium agent obtained from sea water and use thereof | |
| CN108719536A (en) | A kind of teenager disappears fat kelp oolong tea and preparation method thereof | |
| CN106578671A (en) | Feed additive for therapy of ascites of cynoglossus semilaevis and preparation method of same | |
| CN105962280A (en) | Vegetable salt containing grifola frondosa polysaccharide and sea salt as well as preparation method thereof | |
| CN105942433A (en) | Plant salt containing pine pollen extracts and preparation method thereof | |
| CN106668560A (en) | Pollen pini cordyceps composition with functions of cancer-prevention and cancer-resistance and preparation method thereof | |
| KR20100003068A (en) | A functional salt and a method of preparing the same |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| WW01 | Invention patent application withdrawn after publication |
Application publication date: 20160831 |
|
| WW01 | Invention patent application withdrawn after publication |