CN1699396A - Process for preparing notoginseng diol saponin - Google Patents
Process for preparing notoginseng diol saponin Download PDFInfo
- Publication number
- CN1699396A CN1699396A CN 200510075039 CN200510075039A CN1699396A CN 1699396 A CN1699396 A CN 1699396A CN 200510075039 CN200510075039 CN 200510075039 CN 200510075039 A CN200510075039 A CN 200510075039A CN 1699396 A CN1699396 A CN 1699396A
- Authority
- CN
- China
- Prior art keywords
- notoginseng
- saponin
- notoginseng glycol
- preparation
- glycol saponin
- 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.)
- Granted
Links
- 229930182490 saponin Natural products 0.000 title claims abstract description 90
- 239000001397 quillaja saponaria molina bark Substances 0.000 title claims abstract description 89
- -1 diol saponin Chemical class 0.000 title claims abstract description 87
- 241000180649 Panax notoginseng Species 0.000 title claims abstract description 84
- 235000003143 Panax notoginseng Nutrition 0.000 title claims abstract description 83
- 238000004519 manufacturing process Methods 0.000 title abstract description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 61
- 239000011347 resin Substances 0.000 claims abstract description 22
- 229920005989 resin Polymers 0.000 claims abstract description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 20
- 239000012153 distilled water Substances 0.000 claims abstract description 18
- 239000007788 liquid Substances 0.000 claims abstract description 11
- 239000000843 powder Substances 0.000 claims abstract description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 70
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 70
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 34
- 244000131316 Panax pseudoginseng Species 0.000 claims description 26
- 235000003181 Panax pseudoginseng Nutrition 0.000 claims description 25
- 239000000741 silica gel Substances 0.000 claims description 24
- 229910002027 silica gel Inorganic materials 0.000 claims description 24
- 229960001866 silicon dioxide Drugs 0.000 claims description 24
- 238000002360 preparation method Methods 0.000 claims description 22
- 239000000284 extract Substances 0.000 claims description 21
- 239000003463 adsorbent Substances 0.000 claims description 19
- 238000001035 drying Methods 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 9
- 239000012043 crude product Substances 0.000 claims description 8
- 239000012530 fluid Substances 0.000 claims description 8
- 229930182494 ginsenoside Natural products 0.000 claims description 7
- 229940089161 ginsenoside Drugs 0.000 claims description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 6
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 claims description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 4
- 238000001816 cooling Methods 0.000 claims description 4
- 238000010828 elution Methods 0.000 claims description 4
- 239000000706 filtrate Substances 0.000 claims description 4
- 238000011010 flushing procedure Methods 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 4
- 238000007654 immersion Methods 0.000 claims description 4
- 239000012046 mixed solvent Substances 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- 239000000178 monomer Substances 0.000 claims description 4
- 230000007935 neutral effect Effects 0.000 claims description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 4
- 229920002554 vinyl polymer Polymers 0.000 claims description 4
- 239000003960 organic solvent Substances 0.000 claims description 3
- 239000002994 raw material Substances 0.000 claims description 3
- 230000006837 decompression Effects 0.000 claims description 2
- DZGCGKFAPXFTNM-UHFFFAOYSA-N ethanol;hydron;chloride Chemical compound Cl.CCO DZGCGKFAPXFTNM-UHFFFAOYSA-N 0.000 claims description 2
- 238000000034 method Methods 0.000 abstract description 11
- 239000000243 solution Substances 0.000 abstract description 11
- 230000008569 process Effects 0.000 abstract description 3
- SYFJYASKXNAXKC-UHFFFAOYSA-N Panaxadiol Natural products CC1(C)CCCC(O1)C2CCC3(C)C2C(O)CC4C5(C)CCC(O)C(C)(C)C5CCC34C SYFJYASKXNAXKC-UHFFFAOYSA-N 0.000 abstract 4
- 238000010521 absorption reaction Methods 0.000 abstract 1
- 239000012141 concentrate Substances 0.000 abstract 1
- 239000012045 crude solution Substances 0.000 abstract 1
- 238000000605 extraction Methods 0.000 abstract 1
- 231100000053 low toxicity Toxicity 0.000 abstract 1
- 238000007670 refining Methods 0.000 abstract 1
- 235000017709 saponins Nutrition 0.000 description 67
- 241000700159 Rattus Species 0.000 description 33
- 241000699666 Mus <mouse, genus> Species 0.000 description 30
- CGIGDMFJXJATDK-UHFFFAOYSA-N indomethacin Chemical compound CC1=C(CC(O)=O)C2=CC(OC)=CC=C2N1C(=O)C1=CC=C(Cl)C=C1 CGIGDMFJXJATDK-UHFFFAOYSA-N 0.000 description 20
- 238000012360 testing method Methods 0.000 description 16
- 230000000202 analgesic effect Effects 0.000 description 15
- 239000003814 drug Substances 0.000 description 15
- 230000007170 pathology Effects 0.000 description 14
- 230000008961 swelling Effects 0.000 description 14
- 239000008280 blood Substances 0.000 description 13
- 230000000694 effects Effects 0.000 description 13
- 208000002193 Pain Diseases 0.000 description 12
- 230000003110 anti-inflammatory effect Effects 0.000 description 12
- 210000004369 blood Anatomy 0.000 description 12
- 230000002496 gastric effect Effects 0.000 description 12
- 238000001802 infusion Methods 0.000 description 12
- 229960000905 indomethacin Drugs 0.000 description 10
- 238000000528 statistical test Methods 0.000 description 10
- 239000002671 adjuvant Substances 0.000 description 9
- 230000003203 everyday effect Effects 0.000 description 9
- 206010003246 arthritis Diseases 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 8
- 230000006870 function Effects 0.000 description 8
- 231100000862 numbness Toxicity 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 7
- 238000002347 injection Methods 0.000 description 7
- 239000007924 injection Substances 0.000 description 7
- 230000004089 microcirculation Effects 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 206010018691 Granuloma Diseases 0.000 description 6
- 206010061218 Inflammation Diseases 0.000 description 6
- 206010030113 Oedema Diseases 0.000 description 6
- 230000004054 inflammatory process Effects 0.000 description 6
- 239000002504 physiological saline solution Substances 0.000 description 6
- 230000008929 regeneration Effects 0.000 description 6
- 238000011069 regeneration method Methods 0.000 description 6
- 230000000452 restraining effect Effects 0.000 description 6
- 241001465754 Metazoa Species 0.000 description 5
- 241000699670 Mus sp. Species 0.000 description 5
- 230000009471 action Effects 0.000 description 5
- 230000017531 blood circulation Effects 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 201000003068 rheumatic fever Diseases 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 238000010171 animal model Methods 0.000 description 4
- 201000010099 disease Diseases 0.000 description 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 4
- 210000002683 foot Anatomy 0.000 description 4
- 230000023597 hemostasis Effects 0.000 description 4
- 230000000144 pharmacologic effect Effects 0.000 description 4
- 206010039073 rheumatoid arthritis Diseases 0.000 description 4
- 206010012442 Dermatitis contact Diseases 0.000 description 3
- VYZAHLCBVHPDDF-UHFFFAOYSA-N Dinitrochlorobenzene Chemical compound [O-][N+](=O)C1=CC=C(Cl)C([N+]([O-])=O)=C1 VYZAHLCBVHPDDF-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 208000010247 contact dermatitis Diseases 0.000 description 3
- 230000007812 deficiency Effects 0.000 description 3
- 210000003205 muscle Anatomy 0.000 description 3
- 230000001737 promoting effect Effects 0.000 description 3
- 238000011160 research Methods 0.000 description 3
- 150000007949 saponins Chemical class 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 208000011580 syndromic disease Diseases 0.000 description 3
- 238000002560 therapeutic procedure Methods 0.000 description 3
- FUFLCEKSBBHCMO-UHFFFAOYSA-N 11-dehydrocorticosterone Natural products O=C1CCC2(C)C3C(=O)CC(C)(C(CC4)C(=O)CO)C4C3CCC2=C1 FUFLCEKSBBHCMO-UHFFFAOYSA-N 0.000 description 2
- 240000006409 Acacia auriculiformis Species 0.000 description 2
- MFYSYFVPBJMHGN-ZPOLXVRWSA-N Cortisone Chemical compound O=C1CC[C@]2(C)[C@H]3C(=O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 MFYSYFVPBJMHGN-ZPOLXVRWSA-N 0.000 description 2
- MFYSYFVPBJMHGN-UHFFFAOYSA-N Cortisone Natural products O=C1CCC2(C)C3C(=O)CC(C)(C(CC4)(O)C(=O)CO)C4C3CCC2=C1 MFYSYFVPBJMHGN-UHFFFAOYSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- 240000001624 Espostoa lanata Species 0.000 description 2
- 235000009161 Espostoa lanata Nutrition 0.000 description 2
- 229920000715 Mucilage Polymers 0.000 description 2
- 235000002789 Panax ginseng Nutrition 0.000 description 2
- 210000001744 T-lymphocyte Anatomy 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 210000000544 articulatio talocruralis Anatomy 0.000 description 2
- 239000010839 body fluid Substances 0.000 description 2
- 230000037396 body weight Effects 0.000 description 2
- 235000010418 carrageenan Nutrition 0.000 description 2
- 239000000679 carrageenan Substances 0.000 description 2
- 229940113118 carrageenan Drugs 0.000 description 2
- 229920001525 carrageenan Polymers 0.000 description 2
- 208000037976 chronic inflammation Diseases 0.000 description 2
- 208000037893 chronic inflammatory disorder Diseases 0.000 description 2
- 230000004087 circulation Effects 0.000 description 2
- 229960004544 cortisone Drugs 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 210000005069 ears Anatomy 0.000 description 2
- ROAYSRAUMPWBQX-UHFFFAOYSA-N ethanol;sulfuric acid Chemical compound CCO.OS(O)(=O)=O ROAYSRAUMPWBQX-UHFFFAOYSA-N 0.000 description 2
- 239000008899 fufang danshen Substances 0.000 description 2
- JYGXADMDTFJGBT-VWUMJDOOSA-N hydrocortisone Chemical compound O=C1CC[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 JYGXADMDTFJGBT-VWUMJDOOSA-N 0.000 description 2
- 230000002757 inflammatory effect Effects 0.000 description 2
- 231100000915 pathological change Toxicity 0.000 description 2
- 230000036285 pathological change Effects 0.000 description 2
- 230000003285 pharmacodynamic effect Effects 0.000 description 2
- 230000003449 preventive effect Effects 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 230000004044 response Effects 0.000 description 2
- 238000010254 subcutaneous injection Methods 0.000 description 2
- 239000007929 subcutaneous injection Substances 0.000 description 2
- 230000001225 therapeutic effect Effects 0.000 description 2
- 210000001835 viscera Anatomy 0.000 description 2
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 2
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- 241001419719 Anisodus carniolicoides Species 0.000 description 1
- 208000006820 Arthralgia Diseases 0.000 description 1
- 241000416162 Astragalus gummifer Species 0.000 description 1
- 108700031361 Brachyury Proteins 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 206010014080 Ecchymosis Diseases 0.000 description 1
- 208000009386 Experimental Arthritis Diseases 0.000 description 1
- 206010020751 Hypersensitivity Diseases 0.000 description 1
- 206010062717 Increased upper airway secretion Diseases 0.000 description 1
- 238000012449 Kunming mouse Methods 0.000 description 1
- 240000001307 Myosotis scorpioides Species 0.000 description 1
- 235000005035 Panax pseudoginseng ssp. pseudoginseng Nutrition 0.000 description 1
- 235000003140 Panax quinquefolius Nutrition 0.000 description 1
- 206010036030 Polyarthritis Diseases 0.000 description 1
- 240000007164 Salvia officinalis Species 0.000 description 1
- 206010070834 Sensitisation Diseases 0.000 description 1
- 208000007536 Thrombosis Diseases 0.000 description 1
- 229920001615 Tragacanth Polymers 0.000 description 1
- 230000003187 abdominal effect Effects 0.000 description 1
- 238000004378 air conditioning Methods 0.000 description 1
- 208000030961 allergic reaction Diseases 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000003042 antagnostic effect Effects 0.000 description 1
- 230000001760 anti-analgesic effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000002917 arthritic effect Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 210000004204 blood vessel Anatomy 0.000 description 1
- 210000001124 body fluid Anatomy 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000006757 chemical reactions by type Methods 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000009849 deactivation Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 230000004069 differentiation Effects 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 210000003414 extremity Anatomy 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 210000003194 forelimb Anatomy 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 235000008434 ginseng Nutrition 0.000 description 1
- 210000000548 hind-foot Anatomy 0.000 description 1
- 108010084652 homeobox protein PITX1 Proteins 0.000 description 1
- 229960000890 hydrocortisone Drugs 0.000 description 1
- 230000036039 immunity Effects 0.000 description 1
- 238000002513 implantation Methods 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 238000011081 inoculation Methods 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 230000009545 invasion Effects 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 239000002398 materia medica Substances 0.000 description 1
- 230000002107 myocardial effect Effects 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 230000035764 nutrition Effects 0.000 description 1
- 230000000414 obstructive effect Effects 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 244000052769 pathogen Species 0.000 description 1
- 230000001717 pathogenic effect Effects 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 208000026435 phlegm Diseases 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 208000030428 polyarticular arthritis Diseases 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000000770 proinflammatory effect Effects 0.000 description 1
- 235000005412 red sage Nutrition 0.000 description 1
- 230000002040 relaxant effect Effects 0.000 description 1
- 206010039083 rhinitis Diseases 0.000 description 1
- 230000008313 sensitization Effects 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 208000010110 spontaneous platelet aggregation Diseases 0.000 description 1
- 239000007858 starting material 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
- 239000000126 substance Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 235000010487 tragacanth Nutrition 0.000 description 1
- 239000000196 tragacanth Substances 0.000 description 1
- 229940116362 tragacanth Drugs 0.000 description 1
- 229960005486 vaccine Drugs 0.000 description 1
- 230000024883 vasodilation Effects 0.000 description 1
- 210000003462 vein Anatomy 0.000 description 1
- 239000011800 void material Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 239000009306 yunnan baiyao Substances 0.000 description 1
Landscapes
- Steroid Compounds (AREA)
Abstract
The invention discloses a process for preparing notoginseng diol saponin, which includes following steps: crushing the notoginseng, and adding ethanol solution whose concentration is 60% to immerse and percoalte the notoginseng, and then collecting the percoalted liquid and reducing pressure to concentrate the same, and then using distilled water to dilute the concentrated liquid, and then slowly filling the liquid into the large-hole absorption resin separating column, and using 60% ethanol to elute, and then collecting the 60% ethanol elutriant and then concentrating the same by reducing pressure to obtain panaxadiol saponin crude solution whose relative density is 1.10, and refining the same to obtain notoginseng panaxadiol saponin in light claybank powder form. The notoginseng panaxadiol saponin extracted by the provided process contains all glycols saponin in the notoginseng, and the extraction rate can reach 82 to 88%. The notoginseng panaxadiol saponin prepared by the provided process is the active component in notoginseng which can detumescence and analgecize, and has low toxicity, low cost, stable quality and high safety.
Description
Invention field
The invention relates to a kind of extracting method of medicinal plant, more particularly about a kind of preparation method who from pseudo-ginseng, extracts notoginseng glycol saponin.
Background technology
Pseudo-ginseng always is that a kind of famous and precious traditional Chinese medicine has diffusing stasis of blood hemostasia and detumescence analgesic therapy effect, and in the traditional Chinese medicine compound, the compound of particularly treating wound all be unable to do without it, as Yunnan baiyao, ginseng seven kinds of impairments medicine, Anisodus carniolicoides C.Y.Wu et C.Chen etc.In the less compound of flavour of a drug in modern age also commonly used it, as famous FUFANG DANSHEN PIAN (pseudo-ginseng, the red sage root) dripping pill.
The private power of single medicinal material is special, is Chinese medicine preparation " seven sides' " " odd-numbered prescription ", and pseudo-ginseng also has single method with Herba indigoferae Pseudotinctoriae when the clinical use of tradition.
Notoginseng glycol saponin is the single medicinal material pseudo-ginseng saponin extract of (having another name called pseudo-ginseng, Panax pseudoginseng), is the efficient part of pseudo-ginseng subduing swelling and relieving pain, the main effective constituent ginsenoside Rb that contains the subduing swelling and relieving pain work
1And Rd.
Pseudo-ginseng another name pseudo-ginseng, Panax pseudoginseng are Araliaceae Panax Panaxnotoginseng (Burk) F.H.Chen rhizome, main product in Yunnan, Guangxi.Pseudo-ginseng is one of conventional Chinese medicine, and the main component of its biological activity and pharmacological action is a saponins.The pharmacological results shows that Radix Notoginseng total arasaponins can increase blood flow volume, vasodilation, reduction arteriotony and myocardial consumption of oxygen, improves the human body function and reaches the anoxybiotic tolerance, and effects such as the platelet aggregation of supression, reduction blood viscosity are arranged.
" Chinese pharmacopoeia claims: pseudo-ginseng effect " stasis of blood of loosing hemostasis, subduing swelling and relieving pain ".Compendium of Material Medica claims: Radix Notoginseng " sweet, little hardship, temperature is nontoxic " cures mainly " hemostasis, loose blood, analgesic therapy ".
The sick system of numbness is by plain body deficiency, and healthy tendency is empty partially, interspaces of skin and muscles being loose, and perverse trend invasion and attack such as weakened defensive QI and sense chill the are damp and hot and channels and collaterals resistance is closed, QI-blood circulation is not smooth, so that muscle arthralgia, numbness, is weighing, joint stuffiness and form bi Zheng.Just say " slightly managing and interior not hard person kind sick numbness " as far back as " Ling Shu Miraculous Pivot or Divine Axis five becomes "." all numbness doors of Prescriptions for Succouring the Sick " said: " all because of body void, space between skin and muscles is empty, and the air humidity gas of having a cold forms numbness also ".
Bi Zheng is just sick true, then for a long time vital QI being weakened and pathogen being violent, the time of simulataneous insufficiency and excessive of being more.Three kinds of pathological changes appear in bi Zheng easily: the one, and with the passing of time the damp and hot numbness of chill do not heal, and qi-blood-body fluid is moved not smooth pathology day very, blood-vessel obstructive, the skin ecchymosis appears in body fluid cohesion, so that the turbid resistance numbness of hemostasis phlegm channels and collaterals, tubercle around the joint, arthroncus, diseases such as joint stuffiness.The 2nd, disease makes the qi and blood damage for a long time, presents in various degree deficiency of qi and blood or syndrome such as caused by liver and kidney deficiency.The 3rd, bi Zheng does not heal, and the syndrome of internal organs numbness appears in disease and internal organs by channels and collaterals.Many the imposing respectively according to the damp and hot inclined to one side victory of chill of medical circles dispeled the wind at all times, and it is cold to loose, and dehumidifying is relaxed through the Coryza Treated by Syndrome Differentiation of vein relaxing, is aided with benefit and fills blood, and strengthens the body resistance to consolidate the constitution and reaches the purpose of normal circulation of qi and blood.
Up to now, do not see relevant specialty report with notoginseng glycol saponin treatment bi Zheng.
The inventor after years of research and found that, many compositions in the Radix Notoginseng total arasaponins are invalid to the human body therapy bi Zheng, real effective is notoginseng glycol saponin etc., the character of relevant notoginseng glycol saponin, pharmacological action, preparation method and the effect of human body be there is no report.
Summary of the invention
The objective of the invention is to overcome the defective that prior art exists, a kind of method of extracting notoginseng glycol saponin from pseudo-ginseng is provided.
Second purpose of the present invention provides a kind of preparation method that can treat the notoginseng glycol saponin of bi Zheng.
These and other objects of the present invention will further embody by detailed description below and illustrate.
The preparation method of notoginseng glycol saponin of the present invention comprises the following steps:
1, gets pseudo-ginseng and pulverized sieve No. one, add concentration and be 60% alcohol immersion, diacolation, collect percolate;
2, percolate concentrating under reduced pressure reclaims ethanol;
3, concentrated solution dilutes with distilled water, slowly is added in the macroporous adsorbent resin separator column, uses distilled water, 40% ethanol and 60% ethanol elution successively, collects 60% ethanol eluate;
4,60% ethanol eluate is 1.10 diol saponin crude product solution through being evaporated to relative density;
5, the diol saponin crude product solution is admixed silica gel, abundant mixing, and drying under reduced pressure must be mixed sample silica gel;
6, will mix sample silica gel and pack in the chromatography column of 23 times of silica gel,, check, and collect and contain ginsenoside R with the silica gel G plate with the mixed solvent wash-out that contains vinyl acetic monomer, second alcohol and water
B1, R
dStream part Deng composition;
7, elutriant filters, and filtrate decompression is concentrated into relative density 1.33 fluid extracts;
8, fluid extract drying under reduced pressure gets dry extract, and dry extract is pulverized, and promptly gets the notoginseng glycol saponin of light yellowish brown powder.
Further, in notoginseng glycol saponin preparation method of the present invention, its raw material is 8: 10 with the ratio of macroporous adsorbent resin, the post footpath of macroporous adsorbent resin with the ratio of post height is: 30: 160, macroporous adsorbent resin is the styrene type interpolymer, model is D-101, the macroporous adsorbent resin separator column is good for handling balance, and Determination of Residual Organic Solvents meets the pharmaceutical grade standard-required on inspection: benzene is less than 2ppm, toluene, dimethylbenzene, divinylbenzene are less than 20ppm, and described concentrating under reduced pressure or drying under reduced pressure temperature are for being lower than 50 ℃.
In the preparation method of notoginseng glycol saponin of the present invention, also comprise the macroporous adsorbent resin regeneration step, be about to used macroporous adsorbent resin separator column with 1% hydrochloric acid or sulfuric acid ethanol liquid soaked overnight, continue, can reuse with ethanol, Diluted Alcohol washing and extremely neutral with distilled water flushing.
In the preparation method of notoginseng glycol saponin of the present invention, also comprise post layer silica regeneration step, be about to used silica gel, it is colourless to be eluted to effluent liquid with distilled water, takes out the silica gel baking, when oven temperature rises to 120 ± 2 ℃, stop heating, naturally cooling can use.
The notoginseng glycol saponin that extracts with method of the present invention has comprised whole glycols saponin(es of pseudo-ginseng, wherein ginsenoside Rg
1Content is not less than 56%, and Rd is not less than 15%, and the two adds up to 82-88%.Content height, steady quality, color and luster is good, will can satisfy the requirement of modernized Chinese medicine fully with its Chinese medicine preparation that is raw material is made, and cost is low, the notoginseng glycol saponin loss is few.Compare with traditional solvent extration, do not use toxicity and volatile organic solvent in the technical process, safe and reliable, the production technique of Jian Huaing greatly.
The notoginseng glycol saponin that extracts with method of the present invention has significant anti-inflammatory, detumescence, analgesic activity, and the immune inflammation of adjuvant arthritis model is also had tangible anti-inflammatory action; Can treat rheumatisms such as rheumatoid arthritis and rheumatic arthritis.
Below in conjunction with embodiment in detail the present invention is described in detail, can not limits this but embodiment only is used for explanation
Scope of invention.
In the present invention, if not refer in particular to, all part, per-cents are weight unit, and all equipment and starting material etc. all can be buied from market or the industry is commonly used.
Embodiment
Example 1: be prepared according to the following steps:
1, gets 100 gram pseudo-ginseng and pulverized sieve No. one, add concentration and be 60% alcohol immersion, diacolation, the collection percolate;
2, percolate concentrating under reduced pressure, temperature are 50 ℃, reclaim ethanol;
3, concentrated solution is diluted to the 500-600 milliliter with distilled water, (the post footpath with the ratio of post height is: 30: 160 slowly to be added to the macroporous adsorbent resin separator column, in 100 milliliters of D101 resins are housed) in, use 500 ml distilled waters, 1000 milliliter of 40% ethanol and 1000 milliliter of 60% ethanol elution successively, flow velocity be 0.5 times of bed volume/hour, collect 60% ethanol eluate;
4,60% ethanol eluate is 1.10 diol saponin crude product solution through being evaporated to relative density when temperature is 50 ℃;
5, the diol saponin crude product solution is admixed in the silica gel (ordinary method and ratio), abundant mixing, drying under reduced pressure must be mixed sample silica gel;
6, will mix sample silica gel and pack in 23 times of silicagel columns, contain mixed solvent (three's ratio is: 1: 1: the 10) wash-out of vinyl acetic monomer, second alcohol and water, check, and collect and contain ginsenoside R with the silica gel G plate with the 600-800 milliliter
B1, R
dStream part Deng composition;
7, elutriant filters, and to get relative density be 1.33 fluid extract to concentrating under reduced pressure when filtrate was 50 ℃ in temperature;
8, with the fluid extract drying under reduced pressure, get dry extract, dry extract is pulverized, promptly get about 2.15 grams of notoginseng glycol saponin of light yellowish brown powder;
9, macroporous adsorbent resin regeneration: used macroporous adsorbent resin separator column was soaked 12-24 hour with 1% hydrochloride ethanol liquid, reduce the alcohol concn wash-out gradually, extremely neutral with distilled water flushing at last;
10, post layer silica regeneration step: with used silica gel, it is colourless to be eluted to effluent liquid with distilled water, takes out the silica gel baking, when oven temperature rises to 120 ± 2 ℃, stops heating, and naturally cooling can use.
Example 2: be prepared according to the following steps:
1, gets 50 gram pseudo-ginseng and pulverized sieve No. one, add concentration and be 60% alcohol immersion, diacolation, the collection percolate;
2, percolate concentrating under reduced pressure, temperature are 50 ℃, reclaim ethanol;
3, concentrated solution is diluted to the 250-300 milliliter with distilled water, centrifugal, filtration, the aqueous solution slowly is added to the macroporous adsorbent resin separator column, and (the post footpath with the ratio of post height is: 30: 160, in 40 milliliters of D101 resins are housed) in, use 200 ml distilled waters, 300 milliliter of 40% ethanol and 400 milliliter of 60% ethanol elution successively, flow velocity be 0.6 times of bed volume/hour, collect 60% ethanol eluate;
4,60% ethanol eluate is 1.10 diol saponin crude product solution through being evaporated to relative density when temperature is 50 ℃;
5, the diol saponin crude product solution is admixed in the silica gel (ordinary method and ratio), abundant mixing, drying under reduced pressure must be mixed sample silica gel;
6, will mix sample silica gel and pack in 23 times of silicagel columns, contain mixed solvent (three's ratio is: 1: 0.8: the 10) wash-out of vinyl acetic monomer, second alcohol and water, check, and collect and contain ginsenoside R with the silica gel G plate with the 100-300 milliliter
B1, R
dStream part Deng composition;
7, elutriant filters, and to get relative density be 1.33 fluid extract to concentrating under reduced pressure when filtrate was 50 ℃ in temperature;
8, with the fluid extract drying under reduced pressure, get dry extract, dry extract is pulverized, promptly get about 0.98 gram of notoginseng glycol saponin of light yellowish brown powder;
9, macroporous adsorbent resin regeneration: used macroporous adsorbent resin separator column is soaked with 1% hydrochloric acid or sulfuric acid ethanol liquid, reduce the alcohol concn wash-out gradually, continue with distilled water flushing to neutral;
10, post layer silica regeneration step: with used silica gel, it is colourless to be eluted to effluent liquid with distilled water, takes out the silica gel baking, when oven temperature rises to 120 ± 2 ℃, stops heating, and naturally cooling can use.
Example 3: the anti-inflammatory of notoginseng glycol saponin and the effect of suppression pain
The fallow medicinal powder lot number 940201 that provided by Tianjin Inst. of Materia Medica plant chamber by reagent thing notoginseng glycol saponin, content R
B1=59.15 Rd=15.10% are mixed with the solution of desired concn with distilled water before the test, for the laboratory animal gastric infusion.
The Kunming mouse that laboratory animal provides with the court's Animal House production (body weight 19-23g) removes immunity and is male with invigorate blood circulation test and Wistar kind rat (body weight 120-150g)) raise in the observation ward of central air-conditioning is arranged, feed is the full nutrition piece material that central medicine inspecting institute produces, the drink tap water, conformity certification Tianjin moving 001.
INDOMETHACIN is the pulvis that Tianjin pharmacy two factories of central authorities give, and the tragacanth mucilage with 1.0% is mixed with the suspension of 1.0 mg/ml concentration, for the laboratory animal gastric infusion.
Test method and result
One, the resist inflammation on repercussive function of notoginseng glycol saponin
1,50 male mices is used in this test that influences of mouse dropsy of ear, be divided into 5 groups at random, 10 every group.Every day, gastric infusion was 1 time, successive administration 5 days, and control group administered physiological saline, after the last administration 30 minutes, drip 0.05 milliliter of Oleum Tiglii proinflammatory agent to every mouse left side auricular concha, put to death after 2 hours.Cut left and right sides ear, lay with the position auricle, weigh with 9 millimeters punch tool of diameter, with the difference of two ear weight as mouse dropsy of ear degree.Take the mean and the control group comparison, advance statistical test result (seeing Table 1) and find the notoginseng glycol saponin oral administration, to the restraining effect highly significant of mouse dropsy of ear, and have certain dose-effect relationship, its magnitude relation equation y=0.097
X+ 5.629 (r=0.8834)
Table 1 notoginseng glycol saponin is to the anti-inflammatory action of mouse dropsy of ear
*p＜0.05 **P＜0.01 ***P＜0.001
2,50 male rats, random packet, 10 every group are used in swollen this test that influences to the rat foot.1 successive administration of gastric infusion every day 4 days, control group administered physiological saline.After the last administration 30 minutes, cause inflammation for 0.05 milliliter at left hind foot pad subcutaneous injection 1.0% lrish moss mucilage.Respectively cause scorching before and cause scorching afterwards 30,60,120 and 180 minutes, measure rat with projector (amplifying 6 times) and cause scorching limb (right hind) ankle joint below 0.5 centimeters diameter, with causing difference before and after scorching as swollen account degree, take the mean and control group relatively, carry out statistical test.Result's (seeing Table 2) finds notoginseng glycol saponin to the swollen restraining effect highly significant of rat foot, and on this experimental inflammatory model, the anti-inflammatory action of notoginseng glycol saponin is not less than the INDOMETHACIN of 5 milligrams of/kilogram dosage.
Table 2 notoginseng glycol saponin is to the swollen influence of rat carrageenan foot
*p＜0.05
**p＜0.01
***p＜0.001
3,50 male rats are used in this test that influences of rat assist agent arthritis, be divided into 5 groups at random, 10 every group.The preparation system of adjuvant adds the bacille Calmette-Guerin vaccine of deactivation in advance in the incomplete freund adjuvant of sterilization in advance, grinds the adjuvant that is mixed with 10 mg/ml concentration.The model preparation is adopted at 0.1 milliliter of adjuvant of every right back sufficient pad portion's intradermal injection of rat, induces arthritic generation.(1) influence to the primary pathology is 200 milligrams/kilogram in causing scorching preceding 4 days beginning dosages, 100 milligrams/kilogram and 50 milligrams/kilogram, and control group physiological saline.Every day, gastric infusion was 1 time, caused inflammation in 30 minutes after the last administration, observed to cause scorching back 18 hours and the 8th day swollen degree of adjuvant injection parapodum.Measure the diameter (amplifying 6 times) of 0.5 centimeters under every rat right hind leg ankle joint with projector, so that the difference before and after scorching is made the swelling degree, take the mean and the control group comparison, carry out statistical test, result's (seeing Table 3) shows the anti-inflammatory action highly significant of notoginseng glycol saponin to rat assist agent arthritis primary pathology, and the effect of three dosage all is not less than the INDOMETHACIN of 2.5 milligrams of/kilogram dosage.
(2), to the influence of Secondary cases pathology in adjuvant injection back beginning in the 8th day gastric infusion, dosage is the same, every day 1 time, successive administration to the 30 days, observe the preventive and therapeutic effect of notoginseng glycol saponin, from the self administration of medication, every 4-5 days to the Secondary cases pathology, with the left back vola thickness of miking rat (adjuvant injection offside, represent with millimeter), as the index of Secondary cases pathology swelling degree, take the mean and the control group comparison, carry out statistical test, the results are shown among the table.The visible notoginseng glycol saponin of result from table to the swollen preventive and therapeutic effect highly significant of parapodum, points out this medicine can stop and alleviate the generation of rat assist agent arthritis Secondary cases pathology to the adjuvant injection.
Table 3 notoginseng glycol saponin is to the influence of rat assist agent arthritis primary pathology
*p＜0.05
**p＜0.01
***p＜0.001
(3), the influence to the general pathology removes the swelling degree of observing left back foot (adjuvant injection offside), outside the index as polyarthritis, also observe forelimb, ear and general pathologies such as afterbody pathology incidence and severity, press 0-4 level point system record, the into statistical test of taking the mean, result's (seeing Table 5) finds that notoginseng glycol saponin can stop the generation of general pathology equally.
Table 4 notoginseng glycol saponin is to the influence of rat assist agent arthritis Secondary cases pathology
*p＜0.05
**p＜0.01
***p＜0.001
Table 5 notoginseng glycol saponin is to the influence of rat assist agent arthritis general pathology
*p＜0.05
**p＜0.01
***p＜0.001
4,50 male rats, random packet, 10 every group are used in swollen this test that influences to rat granuloma.Administration in advance 4 days, every day 1 time, dosage is 200 milligrams/kilogram, 100 milligrams/kilogram and 50 milligrams/kilogram, control rats is given physiological saline.Behind the 4th day gastric infusion 30 minutes, use the etherization rat, at oxter inoculation cotton balls, continued administration then 7 days.Put to death rat in 24 hours after the last administration, peel off granuloma induced by implantation of cotton pellets, claim weight in wet base earlier, the back is dry in 80 degree baking ovens, claims dry weight again, and it is heavy to deduct cotton balls, and it is heavy promptly to get granuloma.Take the mean and the control group comparison, carry out statistical test, result's (seeing Table 6) finds that notoginseng glycol saponin is remarkable to the swollen restraining effect of rat granuloma, points out this medicine that chronic inflammatory diseases is also had tangible anti-inflammatory action, the cortisone of the not little 10mg/kg of its action intensity.
Table 6 notoginseng glycol saponin is to the swollen influence of rat granuloma
*p＜0.05
**p＜0.01
***p＜0.001
Two, the analgesic activity of notoginseng glycol saponin
1,50 male mices, random packet, 10 every group are used in this test that influences of mouse acetic acid twisting reaction.Every day, gastric infusion was 1 time, successive administration 4 days, and after the last administration 30 minutes, 02 milliliter/mouse of abdominal injection 0.6% acetum was turned round the body number of times with every mouse in second of the register record 10 minutes after 10 minutes.Do physiological saline and INDOMETHACIN control group simultaneously, that calculates every group of mouse on average turns round the body number, relatively carries out statistical test with control group, and result's (seeing Table 7) finds the analgesic activity highly significant of notoginseng glycol saponin on this model.
Table 7 notoginseng glycol saponin is to the analgesic activity of mouse acetic acid twisting reaction
*p＜0.05
**p＜0.01
***p＜0.001
2, to mouse water-bath whipping reaction to influence laboratory animal and grouping and administration situation thereof the same, after administration in the 4th day 30,90,120 minutes, respectively 55 ± 0.Measure the mouse whipping response latency in the 5 degree water-baths, as threshold of pain index, take the mean and the control group comparison, carry out statistical test, the threshold of pain of the visible pseudo-ginseng alcohol of result's (seeing Table 8) saponin oral liquor administration can the raising very significantly mouse water-bath whipping, its analgesic activity does not have to surpass the INDOMETHACIN of 5 milligrams of/kilogram dosage.
3,50 male rats are used in this test that influences of rat water-bath whipping reaction, be divided into 5 groups at random, 10 every group.Every day, gastric infusion was 1 time, successive administration 3 days, after the last administration 30,90 and 120 minutes, measure the rat whipping response latency in 55 ± 0.5 degree waters bath with thermostatic control, as threshold of pain index, do physiological saline and INDOMETHACIN control group simultaneously, that calculates every group of rat on average turns round number, relatively carries out statistical test with control group.Result's (seeing Table 9) finds that notoginseng glycol saponin also has certain analgesic activity on this model.
Table 8 notoginseng glycol saponin is to the analgesic activity of mouse water-bath whipping reaction
*p＜0.05
**p＜0.01
***p＜0.001
Table 9 notoginseng glycol saponin is to the analgesic activity of rat water-bath whipping reaction
*p＜0.05
**p＜0.01
***p＜0.001
Three, to the influence of the tardy property of mouse contact dermatitis
50 mouse are used in this test, are divided into 5 groups at random, 10 every group.Male and female half and half.Every day, gastric infusion was 1 time, and successive administration 10 days after administration in the 3rd day 30 minutes, is given 20 milliliters of sensitization of every mouse back subcutaneous injection 7%DNCB acetone soln.After the last administration 30 minutes, after attacking 16 hours, 15 milliliters of the DNCB acetone solns of coating same concentrations on every mouse left side auricular concha put to death mouse, take off auricle with the punch tool of 9 mm dias, weigh, make the swelling degree with left and right sides auricle weight difference.Result's (seeing Table 10) finds that notoginseng glycol saponin can suppress the tardy property of DNCB inductive mouse contact dermatitis significantly, but effect is not as good as the cortisone of 10 milligrams of/kilogram dosage.Notoginseng glycol saponin has significant antagonistic action to the caused VI allergic reaction type of haptens, points out this medicine that the T lymphocyte function is had certain influence.
Table 10 notoginseng glycol saponin is to the influence of the tardy property of mouse contact dermatitis
*p＜0.05
**p＜0.01
***p＜0.001
Three, microcirculation of mouse auricle is influenced
40 mouse are used in this test, are divided into 4 groups at random, 10 every group.Male and female half and half.Take out 2 mouse for every group before the administration, (4 * 22) observe the wide capillary vessel number of hits of auris dextra under dissecting microscope, as the microcirculation of mouse auricle normal value, and general 3-4 milligram/kilogram mouse ear.Gastric infusion then, every day 1 time, successive administration 3 days, after the last administration 30 minutes, in the mouse auris dextra capillary vessel number of hits of observing every group.Take the mean and the control group comparison, carry out statistical test, result's (seeing Table 11) finds that notoginseng glycol saponin truly has effect promoting blood circulation and removing blood stasis, blood is scarlet, it increases Mice Auricle microcirculation highly significant, but effect is not as good as the FUFANG DANSHEN DIWAN of 5 milligrams of/kilogram dosage, and the function of pseudo-ginseng is a promoting blood circulation and hemostasis, subduing swelling and relieving pain.The test materials that has reported has fully proved the subduing swelling and relieving pain effect of notoginseng glycol saponin, also provide experimental basis for treating swelling and ache of bi Zheng clinically in the future, this test is according to " herbal pharmacology experimental technique " the 104th page, select the Mice Auricle microcirculation to observe as the live body microcirculation, found that notoginseng glycol saponin also has significant function of promoting blood circulation to disperse blood clots, have the major function of pseudo-ginseng thereby disclosed notoginseng glycol saponin.
Table 11 notoginseng glycol saponin influences microcirculation of mouse auricle
*p＜0.05
**p＜0.01
***p＜0.001
Conclusion (of pressure testing)
4 kinds of experimental inflammatory models and 2 kinds of analgesic test models are used in this test, carry out main pharmacodynamics research, the anti-inflammatory and analgesic effect that the result proves the notoginseng glycol saponin gastric infusion is highly significant all, have disclosed the effect that pseudo-ginseng truly has subduing swelling and relieving pain.Though the pathogeny of rheumatic arthritis and rheumatoid arthritis is still not fully aware of,, our test-results shows that notoginseng glycol saponin can treat the scorching disease of rheumatism such as scorching rheumatic arthritis.
The effect highly significant of notoginseng glycol saponin anti-experimental character oedema inflammation shows as the restraining effect of the caused mouse dropsy of ear of Oleum Tiglii byer force, and has tangible dose-dependence.In addition, also highly significant of the restraining effect of the swollen or arthroncus of rat foot due to the on Carrageenan, the anti-inflammatory action on these two kinds of models all is not less than INDOMETHACIN.
As everyone knows, rat assist agent arthritis is an immune inflammation model, and its pathogeny is similar to people's rheumatoid arthritis with pathological change.In the different onset stage of this model, the anti-inflammatory action of highly significant all can appear in notoginseng glycol saponin, and its action intensity also is not less than INDOMETHACIN.
In addition, notoginseng glycol saponin also has tangible anti-inflammatory action to chronic inflammatory diseases, and it shows as rat granuloma swollen restraining effect and hydrocortisone suitable.
The anti-inflammatory action of The above results proof notoginseng glycol saponin is strong and scope is wide.
The notoginseng glycol saponin oral administration to the analgesic activity of rat and mouse also highly significant, can improve the threshold of pain of warm stimulation, can reduce the caused body number of times of turning round of chemical algogen again.On these 2 kinds of analgesic test models, the notoginseng diol soap to poh mouse analgesic activity not second to INDOMETHACIN, but to the analgesic activity of rat whipping reaction not as INDOMETHACIN, may be through the few reason of medicine number of times according to one's analysis.
Function with reference to pseudo-ginseng cures mainly, and has carried out main pharmacodynamics research around subduing swelling and relieving pain, found that above-mentioned pharmacological action characteristics, provides experimental basis for treating swelling and ache of bi Zheng such as rheumatoid arthritis and rheumatic arthritis clinically.
This test-results is also found the notoginseng glycol saponin oral administration, and the mouse T lymphocyte function is had very significantly influence, and microcirculation has to Mice Auricle very significantly increases microcirculatory effect, and the blood inner blood is scarlet in the capillary vessel.The above results further provides foundation for swelling and ache of bi Zheng such as this medicine treatment rheumatic arthritis and rheumatoid Guan Yan.
Claims (10)
1, a kind of preparation method of notoginseng glycol saponin is characterized in that comprising the following steps:
A, get pseudo-ginseng and pulverized sieve No. one, add concentration and be 60% alcohol immersion, diacolation, collect percolate;
B, percolate concentrating under reduced pressure reclaim ethanol;
C, concentrated solution dilute with distilled water, slowly are added in the macroporous adsorbent resin separator column, use distilled water, 40% ethanol and 60% ethanol elution successively, collect 60% ethanol eluate;
D, 60% ethanol eluate are 1.10 diol saponin crude product solution through being evaporated to relative density;
E, diol saponin crude product solution are admixed silica gel, abundant mixing, and drying under reduced pressure must be mixed sample silica gel;
F, will mix sample silica gel and pack in 23 times of silicagel columns,, check, and collect and contain ginsenoside R with the silica gel G plate with the mixed solvent wash-out that contains vinyl acetic monomer, second alcohol and water
B1, R
dStream part Deng composition;
G, elutriant filter, and filtrate decompression is concentrated into phase density 1.33 fluid extracts;
H, fluid extract drying under reduced pressure get dry extract, and dry extract is pulverized, and promptly get the notoginseng glycol saponin of light yellowish brown powder.
2, the preparation method of notoginseng glycol saponin according to claim 1 is characterized in that the raw material and the ratio of macroporous adsorbent resin are 10: 1.
3, the preparation method of notoginseng glycol saponin according to claim 1, the post footpath that it is characterized in that macroporous adsorbent resin with the ratio of post height is: 30: 160.
4, the preparation method of notoginseng glycol saponin according to claim 1 is characterized in that described macroporous adsorbent resin is the styrene type interpolymer, and model is D-101.
5, the preparation method of notoginseng glycol saponin according to claim 1 is characterized in that described macroporous adsorbent resin separator column is good for handling balance.
6, the preparation method of notoginseng glycol saponin according to claim 1, it is characterized in that also comprising used macroporous adsorbent resin separator column is washed with 1% hydrochloride ethanol liquid, reduce the alcohol concn wash-out gradually,, can reuse until extremely neutral with distilled water flushing.
7, the preparation method of notoginseng glycol saponin according to claim 1 is characterized in that also comprising that it is colourless to be eluted to effluent liquid with distilled water with used silica gel, the baking of taking-up silica gel, when oven temperature rises to 120 ± 2 ℃, stop heating, naturally cooling can use.
8, the preparation method of notoginseng glycol saponin according to claim 1 is characterized in that described concentrating under reduced pressure or drying under reduced pressure temperature are 50 ± 5 ℃.
9, the preparation method of notoginseng glycol saponin according to claim 1 is characterized in that the notoginseng glycol saponin that extracts has comprised the whole glycols saponin(es in the pseudo-ginseng, wherein ginsenoside Rg
1Content is not less than 56%, and Rd content is not less than 12%, and the two adds up to 82-88%.
10, the preparation method of notoginseng glycol saponin according to claim 1 is characterized in that organic solvent residual thing content benzene is less than 2ppm in the notoginseng glycol saponin, and toluene, dimethylbenzene and divinylbenzene are all less than 20ppm.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2005100750390A CN100471865C (en) | 2004-08-04 | 2005-06-08 | Process for preparing notoginseng diol saponin |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 200410070156 CN1603334A (en) | 2004-08-04 | 2004-08-04 | Process for preparing notoginseng diol saponin |
| CN200410070156.3 | 2004-08-04 | ||
| CNB2005100750390A CN100471865C (en) | 2004-08-04 | 2005-06-08 | Process for preparing notoginseng diol saponin |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1699396A true CN1699396A (en) | 2005-11-23 |
| CN100471865C CN100471865C (en) | 2009-03-25 |
Family
ID=35475660
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB2005100750390A Active CN100471865C (en) | 2004-08-04 | 2005-06-08 | Process for preparing notoginseng diol saponin |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN100471865C (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101007035B (en) * | 2007-01-25 | 2010-12-01 | 上海中药创新研究中心 | Application of notoginseng glycol saponins for treating memory deterioration |
| CN105131070A (en) * | 2015-09-21 | 2015-12-09 | 成都艾比科生物科技有限公司 | Method for directly extracting panasadiol saponins from pseudo-ginseng |
| CN106173149A (en) * | 2016-07-13 | 2016-12-07 | 文山学院 | The detection method of extractive content in a kind of Radix Notoginseng hard sugar, preparation method and Radix Notoginseng hard sugar |
| CN114736262A (en) * | 2022-04-11 | 2022-07-12 | 云南现代民族药工程技术研究中心 | Extraction and separation method of pseudo-ginseng medicinal material |
-
2005
- 2005-06-08 CN CNB2005100750390A patent/CN100471865C/en active Active
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101007035B (en) * | 2007-01-25 | 2010-12-01 | 上海中药创新研究中心 | Application of notoginseng glycol saponins for treating memory deterioration |
| CN105131070A (en) * | 2015-09-21 | 2015-12-09 | 成都艾比科生物科技有限公司 | Method for directly extracting panasadiol saponins from pseudo-ginseng |
| CN106173149A (en) * | 2016-07-13 | 2016-12-07 | 文山学院 | The detection method of extractive content in a kind of Radix Notoginseng hard sugar, preparation method and Radix Notoginseng hard sugar |
| CN114736262A (en) * | 2022-04-11 | 2022-07-12 | 云南现代民族药工程技术研究中心 | Extraction and separation method of pseudo-ginseng medicinal material |
Also Published As
| Publication number | Publication date |
|---|---|
| CN100471865C (en) | 2009-03-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN102824497B (en) | Bone rheumatism pain relieving liquid and preparation method thereof | |
| CN1836720A (en) | Chinese medicine composition for treating arthritis or gout and preparing method thereof | |
| CN103386022A (en) | Chinese medicine composition for treating tuberculous pleurisy | |
| CN1699396A (en) | Process for preparing notoginseng diol saponin | |
| CN1927878A (en) | Clematis chinensis total saponin and treatment action thereof for rheumatoild disease | |
| CN100344299C (en) | Medicine for treating woman's dysmenorrhea and preparing process thereof | |
| CN1197614C (en) | Chinese medicine cap sule for treating prostatic disorders | |
| CN1772257A (en) | Fatty liver treating notoginseng prepn and its prepn process | |
| CN1687092A (en) | General glycoside extractive of xanthium and preparation method | |
| CN103705578A (en) | Traditional Chinese medicine preparation with functions of reducing blood fat and inhibiting blood glucose increase and preparation method thereof | |
| CN1712055A (en) | Chinese medicinal preparation (litholytic capsule) for treating urinific calculus | |
| CN1739678A (en) | Medicine for treating pain caused by wind, cold and wetness evils and its prepn | |
| CN1603334A (en) | Process for preparing notoginseng diol saponin | |
| CN1186067C (en) | Medicine for curing acute injury of muscle and tendon and its preparation method | |
| CN105326872A (en) | Preparation method for herba patriniae extract with therapeutical effect on ulcerative colitis | |
| CN1248709C (en) | Chinese medicine prepn for stopping drug addiction | |
| CN101028451A (en) | Chinese medicine for treating tic douloureux | |
| CN104095912A (en) | Traditional Chinese medicine formula for treating rheumatism bone disease and preparation method of Chinese patent medicine of traditional Chinese medicine formula | |
| CN103623109A (en) | Traditional Chinese medicine composition for treating ischemic cerebrovascular disease and preparation method thereof | |
| CN1150918C (en) | Medicine containing active components of Panax japonicum root and preparing process thereof | |
| CN1907315A (en) | Orthopaedics disease treating and preventing medicinal composition | |
| CN112089783B (en) | Application of traditional Chinese medicine composition in preparation of medicine for preventing or/and treating obesity | |
| CN105998758A (en) | Preparation methods of traditional Chinese medicinal composition for treating hypertension and preparation of traditional Chinese medicinal composition | |
| CN101053624A (en) | Traditional Chinese medicinal for treating prostatic hyperplasia and chronic prostatitis and its preparation process | |
| CN105816548A (en) | Traditional Chinese medicinal composition for treating wind-heat type common colds, and preparation method thereof |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| ASS | Succession or assignment of patent right |
Owner name: CHENGDU SHENHE PHARMACEUTICAL CO., LTD. Free format text: FORMER OWNER: LI MINGJIN Effective date: 20101208 |
|
| C41 | Transfer of patent application or patent right or utility model | ||
| COR | Change of bibliographic data |
Free format text: CORRECT: ADDRESS; FROM: 610041 10/F, TOWER A, HUOJU BUILDING, NO.16, CHUANGYE ROAD, GAOXIN AVENUE, HIGH-TECH ZONE, CHENGDU CITY, SICHUAN PROVINCE TO: 611630 YUHONG ROAD, HESHAN TOWN, PUJIANG COUNTY, CHENGDU CITY, SICHUAN PROVINCE |
|
| TR01 | Transfer of patent right |
Effective date of registration: 20101208 Address after: Yu Hong Lu, Heshan Pujiang County town of Chengdu City, Sichuan province 611630 Patentee after: Chengdu Shenhe Pharmaceutical Co., Ltd. Address before: 10, building 16, building A, Torch Hotel, No. 610041, Gaoxin Road, hi tech Zone, Chengdu, Sichuan Patentee before: Li Mingjin |
|
| PE01 | Entry into force of the registration of the contract for pledge of patent right |
Denomination of invention: Process for preparing notoginseng diol saponin Effective date of registration: 20120106 Granted publication date: 20090325 Pledgee: Bank of East Asia (China) Co., Ltd. Chengdu branch Pledgor: Chengdu Shenhe Pharmaceutical Co., Ltd. Registration number: 2012990000015 |
|
| PC01 | Cancellation of the registration of the contract for pledge of patent right | ||
| PC01 | Cancellation of the registration of the contract for pledge of patent right |
Date of cancellation: 20181022 Granted publication date: 20090325 Pledgee: Bank of East Asia (China) Co., Ltd. Chengdu branch Pledgor: Chengdu Shenhe Pharmaceutical Co., Ltd. Registration number: 2012990000015 |
|
| TR01 | Transfer of patent right |
Effective date of registration: 20190429 Address after: 610000 No. 4 Chunjiang Lane, Heshan Town, Pujiang County, Chengdu City, Sichuan Province Patentee after: Li Mingjin Address before: 611630 Yuhong Road, Heshan Town, Pujiang County, Chengdu City, Sichuan Province Patentee before: Chengdu Shenhe Pharmaceutical Co., Ltd. |
|
| TR01 | Transfer of patent right |