CN101491596A - Method for separating berberine total alkaloid from extract liquid of traditional Chinese medicine - Google Patents
Method for separating berberine total alkaloid from extract liquid of traditional Chinese medicine Download PDFInfo
- Publication number
- CN101491596A CN101491596A CNA2007100984369A CN200710098436A CN101491596A CN 101491596 A CN101491596 A CN 101491596A CN A2007100984369 A CNA2007100984369 A CN A2007100984369A CN 200710098436 A CN200710098436 A CN 200710098436A CN 101491596 A CN101491596 A CN 101491596A
- Authority
- CN
- China
- Prior art keywords
- total alkaloids
- separating
- eluting
- berberine
- acid solution
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 229930013930 alkaloid Natural products 0.000 title claims abstract description 99
- 238000000034 method Methods 0.000 title claims abstract description 50
- 239000003814 drug Substances 0.000 title claims abstract description 23
- 239000007788 liquid Substances 0.000 title claims description 20
- 150000003797 alkaloid derivatives Chemical class 0.000 title abstract description 46
- YBHILYKTIRIUTE-UHFFFAOYSA-N berberine Chemical compound C1=C2CC[N+]3=CC4=C(OC)C(OC)=CC=C4C=C3C2=CC2=C1OCO2 YBHILYKTIRIUTE-UHFFFAOYSA-N 0.000 title description 14
- 229940093265 berberine Drugs 0.000 title description 14
- QISXPYZVZJBNDM-UHFFFAOYSA-N berberine Natural products COc1ccc2C=C3N(Cc2c1OC)C=Cc4cc5OCOc5cc34 QISXPYZVZJBNDM-UHFFFAOYSA-N 0.000 title description 14
- 239000000284 extract Substances 0.000 title description 13
- 239000003480 eluent Substances 0.000 claims abstract description 34
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 claims abstract description 28
- 239000002253 acid Substances 0.000 claims abstract description 25
- 239000003729 cation exchange resin Substances 0.000 claims abstract description 22
- 239000003513 alkali Substances 0.000 claims abstract description 15
- 239000012535 impurity Substances 0.000 claims abstract description 12
- 238000011033 desalting Methods 0.000 claims abstract description 4
- 238000006386 neutralization reaction Methods 0.000 claims abstract description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 35
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 33
- 239000011347 resin Substances 0.000 claims description 32
- 229920005989 resin Polymers 0.000 claims description 32
- 238000010828 elution Methods 0.000 claims description 28
- 238000000605 extraction Methods 0.000 claims description 20
- 239000002585 base Substances 0.000 claims description 16
- 150000003836 berberines Chemical class 0.000 claims description 15
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 10
- 239000003456 ion exchange resin Substances 0.000 claims description 6
- 229920003303 ion-exchange polymer Polymers 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 5
- 239000011780 sodium chloride Substances 0.000 claims description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 4
- 229940079593 drug Drugs 0.000 claims description 4
- 238000011068 loading method Methods 0.000 claims description 3
- 238000012545 processing Methods 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 230000002411 adverse Effects 0.000 claims description 2
- 239000000706 filtrate Substances 0.000 abstract description 22
- 239000003960 organic solvent Substances 0.000 abstract description 17
- 238000001914 filtration Methods 0.000 abstract description 2
- WITLAWYGGVAFLU-UHFFFAOYSA-N 3-(6-methoxy-1,3-benzodioxol-5-yl)-8,8-dimethylpyrano[2,3-f]chromen-4-one Chemical compound C1=CC(C)(C)OC2=CC=C(C(C(C3=CC=4OCOC=4C=C3OC)=CO3)=O)C3=C21 WITLAWYGGVAFLU-UHFFFAOYSA-N 0.000 abstract 6
- 239000000243 solution Substances 0.000 abstract 5
- 230000007547 defect Effects 0.000 abstract 1
- 238000011031 large-scale manufacturing process Methods 0.000 abstract 1
- 239000011259 mixed solution Substances 0.000 abstract 1
- 229940126680 traditional chinese medicines Drugs 0.000 abstract 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 41
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 40
- 239000006228 supernatant Substances 0.000 description 24
- 238000001556 precipitation Methods 0.000 description 22
- CGFYHILWFSGVJS-UHFFFAOYSA-N silicic acid;trioxotungsten Chemical compound O[Si](O)(O)O.O=[W]1(=O)O[W](=O)(=O)O[W](=O)(=O)O1.O=[W]1(=O)O[W](=O)(=O)O[W](=O)(=O)O1.O=[W]1(=O)O[W](=O)(=O)O[W](=O)(=O)O1.O=[W]1(=O)O[W](=O)(=O)O[W](=O)(=O)O1 CGFYHILWFSGVJS-UHFFFAOYSA-N 0.000 description 22
- 230000000694 effects Effects 0.000 description 19
- 238000010612 desalination reaction Methods 0.000 description 17
- 238000001035 drying Methods 0.000 description 17
- 238000007689 inspection Methods 0.000 description 17
- MXTLAHSTUOXGQF-UHFFFAOYSA-O Jatrorrhizine Chemical compound COC1=CC=C2C=C3C(C=C(C(=C4)O)OC)=C4CC[N+]3=CC2=C1OC MXTLAHSTUOXGQF-UHFFFAOYSA-O 0.000 description 13
- 229910052739 hydrogen Inorganic materials 0.000 description 13
- 239000001257 hydrogen Substances 0.000 description 13
- 239000012141 concentrate Substances 0.000 description 12
- 241000218176 Corydalis Species 0.000 description 11
- 238000005516 engineering process Methods 0.000 description 11
- 150000002431 hydrogen Chemical class 0.000 description 11
- PTPHDVKWAYIFRX-UHFFFAOYSA-N Palmatine Natural products C1C2=C(OC)C(OC)=CC=C2C=C2N1CCC1=C2C=C(OC)C(OC)=C1 PTPHDVKWAYIFRX-UHFFFAOYSA-N 0.000 description 10
- QUCQEUCGKKTEBI-UHFFFAOYSA-N palmatine Chemical compound COC1=CC=C2C=C(C3=C(C=C(C(=C3)OC)OC)CC3)[N+]3=CC2=C1OC QUCQEUCGKKTEBI-UHFFFAOYSA-N 0.000 description 10
- 241001407408 Berberis fortunei Species 0.000 description 8
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 8
- 150000002500 ions Chemical class 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 8
- 238000000926 separation method Methods 0.000 description 8
- 238000005325 percolation Methods 0.000 description 6
- 238000010992 reflux Methods 0.000 description 6
- 239000011734 sodium Substances 0.000 description 6
- 238000010521 absorption reaction Methods 0.000 description 5
- 239000003463 adsorbent Substances 0.000 description 5
- 238000007598 dipping method Methods 0.000 description 5
- 238000000746 purification Methods 0.000 description 5
- 230000001105 regulatory effect Effects 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- YZCKVEUIGOORGS-UHFFFAOYSA-N Hydrogen atom Chemical compound [H] YZCKVEUIGOORGS-UHFFFAOYSA-N 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 239000012567 medical material Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- YLRXAIKMLINXQY-ZDUSSCGKSA-O (S)-magnoflorine Chemical compound C1=C(OC)C(O)=C2C3=C(O)C(OC)=CC=C3C[C@@H]3[N+](C)(C)CCC1=C23 YLRXAIKMLINXQY-ZDUSSCGKSA-O 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- KYEAXNAYHSCLMT-CVVGWEDFSA-N Magnoflorine Natural products C[C@H]1OC=C2[C@@H]3[C@@H]1CN4CCc5c([nH]c6ccccc56)[C@@H]4[C@@H]3OC2=O KYEAXNAYHSCLMT-CVVGWEDFSA-N 0.000 description 3
- FDABVSXGAMFQQH-XZWHSSHBSA-N berbamunine Chemical compound CN1CCC2=CC(OC)=C(O)C=C2[C@H]1CC1=CC=C(O)C(OC2=CC=C(C=C2)C[C@@H]2N(C)CCC=3C=C(C(=CC=32)O)OC)=C1 FDABVSXGAMFQQH-XZWHSSHBSA-N 0.000 description 3
- 239000011575 calcium Substances 0.000 description 3
- JTZZGWPIBBTYNE-UHFFFAOYSA-N cavidine Natural products C1C2=C3OCOC3=CC=C2C(C)C2N1CCC1=C2C=C(OC)C(OC)=C1 JTZZGWPIBBTYNE-UHFFFAOYSA-N 0.000 description 3
- 229940126678 chinese medicines Drugs 0.000 description 3
- 230000007812 deficiency Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000007670 refining Methods 0.000 description 3
- KWGRBVOPPLSCSI-WPRPVWTQSA-N (-)-ephedrine Chemical compound CN[C@@H](C)[C@H](O)C1=CC=CC=C1 KWGRBVOPPLSCSI-WPRPVWTQSA-N 0.000 description 2
- RPAJSBKBKSSMLJ-DFWYDOINSA-N (2s)-2-aminopentanedioic acid;hydrochloride Chemical group Cl.OC(=O)[C@@H](N)CCC(O)=O RPAJSBKBKSSMLJ-DFWYDOINSA-N 0.000 description 2
- XQINTCORIZHGFD-AWEZNQCLSA-O (6as)-1,2,10-trimethoxy-6,6-dimethyl-5,6,6a,7-tetrahydro-4h-dibenzo[de,g]quinoline-6-ium-11-ol Chemical compound C1=C(OC)C(OC)=C2C3=C(O)C(OC)=CC=C3C[C@@H]3[N+](C)(C)CCC1=C23 XQINTCORIZHGFD-AWEZNQCLSA-O 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- DFOCUWZXJBAUSQ-URLMMPGGSA-N Berbamine Chemical compound C([C@@H]1N(C)CCC=2C=C(C(OC=3C(OC)=C(OC)C=C4CCN(C)[C@@H](C=34)CC=3C=C(C(=CC=3)O)O3)=CC=21)OC)C1=CC=C3C=C1 DFOCUWZXJBAUSQ-URLMMPGGSA-N 0.000 description 2
- DFOCUWZXJBAUSQ-UHFFFAOYSA-N Berbamine Natural products O1C(C(=CC=2)O)=CC=2CC(C=23)N(C)CCC3=CC(OC)=C(OC)C=2OC(=CC=23)C(OC)=CC=2CCN(C)C3CC2=CC=C1C=C2 DFOCUWZXJBAUSQ-UHFFFAOYSA-N 0.000 description 2
- 241000736253 Berberis bealei Species 0.000 description 2
- 240000008286 Berberis poiretii Species 0.000 description 2
- 241000037803 Coptis deltoidea Species 0.000 description 2
- 244000247747 Coptis groenlandica Species 0.000 description 2
- 235000002991 Coptis groenlandica Nutrition 0.000 description 2
- XDVZNDLANFJOQR-UHFFFAOYSA-N Coptisine Natural products O=Cc1c2OCOc2ccc1C=C3/NCCc4cc5OCOc5cc34 XDVZNDLANFJOQR-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-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
- RBBVPNQTBKHOEQ-KKSFZXQISA-O Phellodendrine Chemical compound C1CC2=CC(OC)=C(O)C=C2[C@H]2[N@+]1(C)CC(C=C(C(=C1)O)OC)=C1C2 RBBVPNQTBKHOEQ-KKSFZXQISA-O 0.000 description 2
- LOUPRKONTZGTKE-WZBLMQSHSA-N Quinine Chemical compound C([C@H]([C@H](C1)C=C)C2)C[N@@]1[C@@H]2[C@H](O)C1=CC=NC2=CC=C(OC)C=C21 LOUPRKONTZGTKE-WZBLMQSHSA-N 0.000 description 2
- 241000218201 Ranunculaceae Species 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 235000011114 ammonium hydroxide Nutrition 0.000 description 2
- 230000000202 analgesic effect Effects 0.000 description 2
- 230000003110 anti-inflammatory effect Effects 0.000 description 2
- PTOJXIKSKSASRB-UHFFFAOYSA-O candicine Chemical compound C[N+](C)(C)CCC1=CC=C(O)C=C1 PTOJXIKSKSASRB-UHFFFAOYSA-O 0.000 description 2
- YKPUWZUDDOIDPM-SOFGYWHQSA-N capsaicin Chemical compound COC1=CC(CNC(=O)CCCC\C=C\C(C)C)=CC=C1O YKPUWZUDDOIDPM-SOFGYWHQSA-N 0.000 description 2
- LUXPUVKJHVUJAV-UHFFFAOYSA-M coptisine, chloride Chemical compound [Cl-].C1=C2C=C(C3=C(C=C4OCOC4=C3)CC3)[N+]3=CC2=C2OCOC2=C1 LUXPUVKJHVUJAV-UHFFFAOYSA-M 0.000 description 2
- ASUTZQLVASHGKV-JDFRZJQESA-N galanthamine Chemical compound O1C(=C23)C(OC)=CC=C2CN(C)CC[C@]23[C@@H]1C[C@@H](O)C=C2 ASUTZQLVASHGKV-JDFRZJQESA-N 0.000 description 2
- GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical compound [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 238000005342 ion exchange Methods 0.000 description 2
- 238000002955 isolation Methods 0.000 description 2
- BQJCRHHNABKAKU-KBQPJGBKSA-N morphine Chemical compound O([C@H]1[C@H](C=C[C@H]23)O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4O BQJCRHHNABKAKU-KBQPJGBKSA-N 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 231100000614 poison Toxicity 0.000 description 2
- 230000001737 promoting effect Effects 0.000 description 2
- 210000000582 semen Anatomy 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 238000000638 solvent extraction Methods 0.000 description 2
- 239000003440 toxic substance Substances 0.000 description 2
- 238000002137 ultrasound extraction Methods 0.000 description 2
- DNXIKVLOVZVMQF-UHFFFAOYSA-N (3beta,16beta,17alpha,18beta,20alpha)-17-hydroxy-11-methoxy-18-[(3,4,5-trimethoxybenzoyl)oxy]-yohimban-16-carboxylic acid, methyl ester Natural products C1C2CN3CCC(C4=CC=C(OC)C=C4N4)=C4C3CC2C(C(=O)OC)C(O)C1OC(=O)C1=CC(OC)=C(OC)C(OC)=C1 DNXIKVLOVZVMQF-UHFFFAOYSA-N 0.000 description 1
- DKRYSHHGXFYAHR-UHFFFAOYSA-N 13beta-Hydroxy-Stylopine Natural products C1=C2C(O)C3C4=CC(OCO5)=C5C=C4CCN3CC2=C2OCOC2=C1 DKRYSHHGXFYAHR-UHFFFAOYSA-N 0.000 description 1
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 241000038207 Arcangelisia Species 0.000 description 1
- 241000133570 Berberidaceae Species 0.000 description 1
- 241001083847 Berberis Species 0.000 description 1
- 235000018554 Berberis poiretii Nutrition 0.000 description 1
- 241001408223 Berberis soulieana Species 0.000 description 1
- 241001408216 Berberis vernae Species 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 235000001258 Cinchona calisaya Nutrition 0.000 description 1
- 244000089795 Clausena lansium Species 0.000 description 1
- 241000037740 Coptis chinensis Species 0.000 description 1
- 241000040930 Corydalis tomentella Species 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241001481760 Erethizon dorsatum Species 0.000 description 1
- 235000011201 Ginkgo Nutrition 0.000 description 1
- 244000194101 Ginkgo biloba Species 0.000 description 1
- 235000008100 Ginkgo biloba Nutrition 0.000 description 1
- 241000218164 Menispermaceae Species 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- MAYJEFRPIKEYBL-OASIGRBWSA-N Obacunone Chemical compound C=1([C@@H]2OC(=O)[C@H]3O[C@@]43[C@]3(C)C(=O)C[C@H]5C(C)(C)OC(=O)C=C[C@]5(C)[C@H]3CC[C@]42C)C=COC=1 MAYJEFRPIKEYBL-OASIGRBWSA-N 0.000 description 1
- 240000002834 Paulownia tomentosa Species 0.000 description 1
- 241000972672 Phellodendron Species 0.000 description 1
- 241000972673 Phellodendron amurense Species 0.000 description 1
- 241001529246 Platymiscium Species 0.000 description 1
- 208000000474 Poliomyelitis Diseases 0.000 description 1
- 208000004880 Polyuria Diseases 0.000 description 1
- 240000000103 Potentilla erecta Species 0.000 description 1
- 235000016551 Potentilla erecta Nutrition 0.000 description 1
- LCQMZZCPPSWADO-UHFFFAOYSA-N Reserpilin Natural products COC(=O)C1COCC2CN3CCc4c([nH]c5cc(OC)c(OC)cc45)C3CC12 LCQMZZCPPSWADO-UHFFFAOYSA-N 0.000 description 1
- QEVHRUUCFGRFIF-SFWBKIHZSA-N Reserpine Natural products O=C(OC)[C@@H]1[C@H](OC)[C@H](OC(=O)c2cc(OC)c(OC)c(OC)c2)C[C@H]2[C@@H]1C[C@H]1N(C2)CCc2c3c([nH]c12)cc(OC)cc3 QEVHRUUCFGRFIF-SFWBKIHZSA-N 0.000 description 1
- 241001093501 Rutaceae Species 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 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 description 1
- 238000002479 acid--base titration Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 229940035676 analgesics Drugs 0.000 description 1
- 239000000730 antalgic agent Substances 0.000 description 1
- 230000001142 anti-diarrhea Effects 0.000 description 1
- 230000001754 anti-pyretic effect Effects 0.000 description 1
- 230000000259 anti-tumor effect Effects 0.000 description 1
- 230000000767 anti-ulcer Effects 0.000 description 1
- 239000002221 antipyretic Substances 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- 208000006673 asthma Diseases 0.000 description 1
- 230000036772 blood pressure Effects 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- VSJKWCGYPAHWDS-FQEVSTJZSA-N camptothecin Chemical compound C1=CC=C2C=C(CN3C4=CC5=C(C3=O)COC(=O)[C@]5(O)CC)C4=NC2=C1 VSJKWCGYPAHWDS-FQEVSTJZSA-N 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- 229960002504 capsaicin Drugs 0.000 description 1
- 235000017663 capsaicin Nutrition 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- JTZZGWPIBBTYNE-FKIZINRSSA-N cavidine Chemical compound C1C2=C3OCOC3=CC=C2[C@H](C)[C@H]2N1CCC1=C2C=C(OC)C(OC)=C1 JTZZGWPIBBTYNE-FKIZINRSSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- LOUPRKONTZGTKE-UHFFFAOYSA-N cinchonine Natural products C1C(C(C2)C=C)CCN2C1C(O)C1=CC=NC2=CC=C(OC)C=C21 LOUPRKONTZGTKE-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- KWGRBVOPPLSCSI-UHFFFAOYSA-N d-ephedrine Natural products CNC(C)C(O)C1=CC=CC=C1 KWGRBVOPPLSCSI-UHFFFAOYSA-N 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- YSJCIJQVDSPGTM-UHFFFAOYSA-M dehydrocavidine Chemical compound [Cl-].C1=C2C(C)=C(C3=C(C=C(C(=C3)OC)OC)CC3)[N+]3=CC2=C2OCOC2=C1 YSJCIJQVDSPGTM-UHFFFAOYSA-M 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 238000000502 dialysis Methods 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 230000035619 diuresis Effects 0.000 description 1
- 230000002526 effect on cardiovascular system Effects 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 229960002179 ephedrine Drugs 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 238000003810 ethyl acetate extraction Methods 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 229930003944 flavone Natural products 0.000 description 1
- 150000002212 flavone derivatives Chemical class 0.000 description 1
- 235000011949 flavones Nutrition 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 229960003980 galantamine Drugs 0.000 description 1
- ASUTZQLVASHGKV-UHFFFAOYSA-N galanthamine hydrochloride Natural products O1C(=C23)C(OC)=CC=C2CN(C)CCC23C1CC(O)C=C2 ASUTZQLVASHGKV-UHFFFAOYSA-N 0.000 description 1
- 210000000232 gallbladder Anatomy 0.000 description 1
- 229930182494 ginsenoside Natural products 0.000 description 1
- 229940089161 ginsenoside Drugs 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 241000411851 herbal medicine Species 0.000 description 1
- 208000019423 liver disease Diseases 0.000 description 1
- 238000005374 membrane filtration Methods 0.000 description 1
- 238000000874 microwave-assisted extraction Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229960005181 morphine Drugs 0.000 description 1
- 229920001206 natural gum Polymers 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- VSLDMVSILHVDSR-UHFFFAOYSA-N obacunone Natural products CC1(C)OC(=O)C=CC2(C)C1CC(=O)C3(C)C2CCC4(C)C(OC(=O)C5OC345)c6occc6 VSLDMVSILHVDSR-UHFFFAOYSA-N 0.000 description 1
- 239000001814 pectin Substances 0.000 description 1
- 229920001277 pectin Polymers 0.000 description 1
- 235000010987 pectin Nutrition 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000002085 persistent effect Effects 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000001397 quillaja saponaria molina bark Substances 0.000 description 1
- 229960000948 quinine Drugs 0.000 description 1
- 230000001172 regenerating effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- BJOIZNZVOZKDIG-MDEJGZGSSA-N reserpine Chemical compound O([C@H]1[C@@H]([C@H]([C@H]2C[C@@H]3C4=C([C]5C=CC(OC)=CC5=N4)CCN3C[C@H]2C1)C(=O)OC)OC)C(=O)C1=CC(OC)=C(OC)C(OC)=C1 BJOIZNZVOZKDIG-MDEJGZGSSA-N 0.000 description 1
- 229960003147 reserpine Drugs 0.000 description 1
- MDMGHDFNKNZPAU-UHFFFAOYSA-N roserpine Natural products C1C2CN3CCC(C4=CC=C(OC)C=C4N4)=C4C3CC2C(OC(C)=O)C(OC)C1OC(=O)C1=CC(OC)=C(OC)C(OC)=C1 MDMGHDFNKNZPAU-UHFFFAOYSA-N 0.000 description 1
- 229930182490 saponin Natural products 0.000 description 1
- 150000007949 saponins Chemical class 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- OGWKCGZFUXNPDA-XQKSVPLYSA-N vincristine Chemical compound C([N@]1C[C@@H](C[C@]2(C(=O)OC)C=3C(=CC4=C([C@]56[C@H]([C@@]([C@H](OC(C)=O)[C@]7(CC)C=CCN([C@H]67)CC5)(O)C(=O)OC)N4C=O)C=3)OC)C[C@@](C1)(O)CC)CC1=C2NC2=CC=CC=C12 OGWKCGZFUXNPDA-XQKSVPLYSA-N 0.000 description 1
- 229960004528 vincristine Drugs 0.000 description 1
- OGWKCGZFUXNPDA-UHFFFAOYSA-N vincristine Natural products C1C(CC)(O)CC(CC2(C(=O)OC)C=3C(=CC4=C(C56C(C(C(OC(C)=O)C7(CC)C=CCN(C67)CC5)(O)C(=O)OC)N4C=O)C=3)OC)CN1CCC1=C2NC2=CC=CC=C12 OGWKCGZFUXNPDA-UHFFFAOYSA-N 0.000 description 1
- VHBFFQKBGNRLFZ-UHFFFAOYSA-N vitamin p Natural products O1C2=CC=CC=C2C(=O)C=C1C1=CC=CC=C1 VHBFFQKBGNRLFZ-UHFFFAOYSA-N 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Landscapes
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines Containing Plant Substances (AREA)
Abstract
The invention discloses a method for separating total alkaloid from traditional Chinese medicine, in particular a method for separating jamaicin total alkaloid from an extracting solution of the traditional Chinese medicine, and belongs to the field of traditional Chinese medicines. The method comprises the following technical proposal: taking the extracting solution of the traditional Chinese medicine; adjusting the pH value of the extracting solution to between 1 and 7; filtering the extracting solution; taking and adding the filtrate to a cation exchange resin column; rinsing the filtrate and removing the impurities; eluting the filtrate with 0.5 to 15 percent acid liquor; collecting eluent; adding alkali to the eluent for neutralization; performing desalting treatment on the mixed solution; and obtaining the jamaicin total alkaloid. The method overcomes the defects of low extracting rate, large using level of organic solvent, complicated process, inability of large-scale production, and the like in the prior art, and can efficiently separate high purity of the jamaicin total alkaloid from the extracting solution of the traditional Chinese medicine.
Description
Technical field
The present invention relates to a kind of in the extraction separation method of pharmaceutically active ingredient, particularly relate to a kind of from Chinese medicine extraction liquid the method for extraction separation Radix Berberidis Amurensis bases total alkaloids, belong to the field of Chinese medicines.
Background technology
Chinese traditional medicine biology alkali is the class important substance that occurring in nature exists, be separated to kind more than 700 at present, they are maximum class determined curative effects in the Chinese medicine, broad-spectrum effective ingredient, especially cancer, hepatopathy and cardiovascular and cerebrovascular vessel, rheumatism major disease etc. are had unique curative effect, be used to relieving asthma as the ephedrine in the Herba Ephedrae, the reserpine in the Radix Rauvolfiae is used for blood pressure lowering, galantamine in the Bulbus Lycoridis Radiatae is effective in cure to poliomyelitis sequela, and contained morphine base is famous analgesics in the Semen Papaveris peel; Quinine alkali is valuable antipyretic; Capsaicin has many physiologically actives and strong and persistent anti-inflammatory analgesic action; Camptothecine in the Fructus seu radix camptothecae acuminatae (Fructus Camptothecae Acuminatae) and the vincristine in the Herba Catharanthi Rosei are used for antitumor etc.With berberine and berbamine is the Radix Berberidis Amurensis bases total alkaloids of representative, be present in Ranunculaceae, Rutaceae, Berberidaceae, the menispermaceous plants more, for example Rhizoma Coptidis, Corydalis thalictrifolia Franch. (Radix Corydalis Thalictrifoliae), Cortex Phellodendri, Cortex Phellodendri, Radix Berberidis, Mahonia fortunei (Lindl.) Fedde, Caulis Arcangelisiae etc., effects such as that this Alkaloid has is analgesic, antiinflammatory, antiulcer, function of gallbladder promoting are the very big alkaloids of a class clinical value.
At present, contain the extraction of Chinese traditional medicine biology bases medical material, how according to alkaloidal physicochemical property, adopt The suitable solvent such as water, sour water, acid alcohol and alkali alcohol etc., utilize dipping, percolation, decoction, backflow, technology such as ultrasonic that the alkaloids composition is extracted, extraction process is more perfect, and the alkaloid extraction ratio can reach more than 90%.But because the relative amount of alkaloid in Chinese medicine lower (most content are 0.01%-1%), certainly will introduce a large amount of impurity class compositions during extraction, as a large amount of starch, natural gum, pectin, phlegmatic temperament, pigment etc., giving further discards the dross and selects the essential has brought very big difficulty, thereby real technical bottleneck just is how to be further purified the alkaloid that enrichment extracts.At present, the purification process of extensive use mainly is alkalization back organic solvent extractionprocess and macroporous adsorbent resin method (" Chemistry for Chinese Traditional Medicine ", Xiao Chonghou chief editor,, Shanghai science tech publishing house in 1997 in the alkaloid purifying process; " in the Chinese herbal medicine alkaloid extraction with separate ", Cai Yanhua, Sichuan chemical industry, 2005. (1) 39).
Organic solvent extractionprocess is to utilize the lipotropy alkaloid to be dissolved in the lipotropy organic solvent, and the water-soluble character of its salt, the alkaloid soda acid is transformed, utilize organic solvent (commonly used as benzene, chloroform, ether etc.) extraction, remove a large amount of impurity, organic solvent extractionprocess is used comparatively extensive, but impurity such as a large amount of neutrality in alkalization back and nonpolar pigment easily are brought into, therefore separation efficiency and purity are lower, and use a large amount of organic solvents (generally extracting 5 times), and (extractor efficient is not high in operation inconvenience, and easily emulsifying) not good (organic solvent toxicity is big in safety, and inflammable and explosive), be laboratory process, be not suitable for the big production of industry.
The macroporous adsorbent resin isolation technics, effective ingredient in the selective absorption Chinese medicine extraction liquid is removed impurity.Compare with technology with traditional impurity-removing method, can dwindle medication dose, improved the quality of preparation, this method to water solublity preferably flavone, saponin etc. good separation and purification effect is arranged, as Semen Ginkgo class preparation at present commonly used and ginsenoside's preparation etc.But make with extra care for alkaloidal, the deficiency of this law maximum is: at first be the absorption difficulty, last sample medicinal liquid must be a weak solution, and basicity will suit, the low then alkaloid of basicity still is an ionization state, the adsorption rate of resin is low, the basicity height, and alkaloid is free type, macromole alkaloid poorly water-soluble and separating out, still can't upper prop, suitable alkaloid scope is very little, and kind is very little; Secondly, the nonpolar electrostatic absorption principle of macroporous adsorbent resin is too poor to the separation selectivity of alkaloid active ingredient and oil-soluble impurities, and in the solvent elution process owing to there is not a specific eluting solvent, alkaloid and a large amount of oil-soluble impurities often are washed down together, and the total alkaloids purity that final refining obtains is not high.
Also having emerging ion exchange resin isolation technics, is the purpose that reaches separation and purification by ion-exchange reactions.At present the technology that generally adopts in field of Chinese medicines institute is, after will containing alkaloidal solution and crossing post, with ammoniacal liquor or NaOH eluant solution, behind the collection eluent again with the organic solvent extraction alkaloid; The resin that perhaps will go up sample is with dipping by lye, and then with organic solvent reflux, extract, alkaloid.But this method step is loaded down with trivial details, organic solvent extraction, resin column is carried out steps such as organic solvent reflux, extract, in industrial very difficult realization, and very low with the efficient of alkali liquor eluting, only stays in the level of prepared in laboratory small sample, also can't realize big production.
More than these methods, ubiquity cost height, organic solvent consumption are big, poor selectivity, total alkaloids purity is low and can't realize deficiency such as big production, therefore, purification technique is still " bottleneck " problem of Chinese medicine separating bio alkali.
Summary of the invention
The method that the purpose of this invention is to provide a kind of safe, low-cost, high efficiency extraction separation Radix Berberidis Amurensis bases total alkaloids.
This goal of the invention realizes by following technology: get the Chinese medicine extraction liquid that contains Radix Berberidis Amurensis bases total alkaloids, adjust pH value 1 to 7, filter, get filtrate and be added on the cation exchange resin column, earlier with the water elution remove impurity, reuse 0.5%～15% acid solution eluting, collect eluent, add the alkali neutralization,, promptly get Radix Berberidis Amurensis bases total alkaloids through desalting processing.
In above-mentioned technical process, after the extracting solution that will contain total alkaloids transfers to proper acidity, alkaloid ionization becomes cation, nonbasic substances is not ionized, after extracting solution was crossed cation exchange resin column, the hydrion on ionized alkaloid organic ion and the resin column exchanged and is adsorbed on the resin column securely.Here the pH value of extracting solution is unsuitable too high or too low, if too high, it is neutral or alkaline that extracting solution is, and alkaloid can not ionization, also just can not finish the exchange process on the resin; If cross lowly, the hydrogen ion concentration in the extracting solution is too high, has hindered the hydrion on the resin column and has dissociated, and can not finish the resins exchange process well equally, thereby the pH value of finding to adjust extracting solution in the experiment is 1 to 7 to be proper.During with water elution, use be deionized water, to guarantee not introducing new ion interference, those just are not easy to be got off by water elution by the nonbasic substances of resin absorption during eluting, thus be attracted to resin column on the alkaloid organic ion separated.After this acid solution that adds higher concentration is again carried out eluting, because the hydrogen ion concentration in the acid solution is very high at this moment, will combine with resin competitively, thereby the alkaloid organic ion that will be adsorbed on the resin column exchanges, be dissolved in the sour eluent, flow out resin column, finish alkaloidal enrichment process.Afterwards, in eluent, add alkali and neutralize unnecessary acid,, can obtain Radix Berberidis Amurensis bases total alkaloids that purity is higher again through conventional desalting processing.
This technical process compared with prior art, technological process is not simple, not with an organic solvent, residual, the alkaloid rate of transform height of no resin monomer composition; Its important contribution also is, has broken ion-exchange capacity order rule, that is: Ca that traditional theory is thought
2+＞K
+≈ NH
4 +＞Na
+＞H
+Just under the influence of this traditional theory, in the ionic exchange resin of Radix Berberidis Amurensis bases total alkaloids all is that alkali liquor or ammoniacal liquor carry out eluting, perhaps earlier with in the alkali liquor and the free in theory alkaloid of resin column reuse organic solvent reflux, extract,, and the effect in the practical application is very undesirable and be unsuitable for big production.In technical scheme of the present invention, though hydrionic exchange capacity is the most weak, but by improving hydrionic concentration in the sour eluent, thereby offset the weak shortcoming of its exchange capacity, simultaneously under acid condition, the alkaloid that exchanges is dissolved in the acid solution rapidly, and is rushed out pillar, guarantee alkaloidal elute effect thus.And, carry out eluting with acid solution, in eluting, cation exchange resin column is regenerated, thereby can recycle, reduced the process of regenerating resin post behind the alkali liquor eluting, reduced cost.Technology of the present invention has broken through in the prior art traditional view and the technical process with the alkali liquor eluting fully, obtained beyond thought effect, improved the yield of Radix Berberidis Amurensis bases total alkaloids greatly, making cation exchange resin be used for refining separating berberine class total alkaloids in commercial production becomes possibility.
Based on above-mentioned technical process, the inventor has carried out further research again, and the parameter of each step of refinement filters out optimal case, and particular content is as follows:
1, the pH value scope of adjustment medicinal liquid is preferably 2 to 5 before the upper prop, and effect is more obvious.
2, used cation exchange resin can be macroporous type or gel-type strong acid ion exchange resin, can according to circumstances be processed in Hydrogen, sodium type or the ammonium type any when reality is used.
3, the post of used cation exchange resin column footpath there is no a fixed pattern with the ratio of post height, but considers to produce reality, post footpath: post height=1: 5～can obtain best effect at 1: 10 o'clock.
4, the liquor strength to sample on the resin column is that every ml is equivalent to crude drug 0.1～3g, and concrete condition can determine that if adopt modes such as dipping, percolation, the medicinal liquid that obtains will be rarer according to the pre-treatment mode of medicinal liquid; And if modes such as reflux, extract,, decoction are especially passed through concentration, the concentration of medicinal liquid will be bigger, but so long as in this scope, can both realize sample.Simultaneously, last sample speed is also adjusted according to the concentration of medicinal liquid in good time, satisfies substantially at 0.5～5 times of column volume/hour get final product.
5, go up sample loading mode and be typically chosen in from the post upper end upward sample, medicinal liquid flows through whole pillar by gravity flow power; The inventor finds, if sample on the adverse current, be about to medicinal liquid sample from the pillar bottom, by certain pressure, make medicinal liquid fill with whole pillar, thisly go up the maximum exchange efficient that sample loading mode can be brought into play pillar, when also having avoided from the upper end sample since the alkaloid exchange not exclusively take place shift to an earlier date penetration problem.This point also is the creationary discovery of inventor.
6, the used acid solution of eluting is preferably sulfuric acid solution or hydrochloric acid solution, and its concentration all is preferably 3%～6%.
7, the flow velocity of eluent is unsuitable too fast or slow excessively during eluting, if too fast, then the exchange of hydrion and alkaloid organic ion is insufficient, and acid solution is wasted more; If cross slowly, the alkaloid organic ion that then disintegrates down may adsorb back on the resin column again, influences elution efficiency.Experiment finds, elution speed remains on 2～6 times of column volumes/hour be advisable.Further preferred, elution speed remains on 4～6 times of column volumes/hour best.
8, the inventor also finds, improves elution efficiency if think more the highland, can not carry out the acid solution eluting immediately after the water elution remove impurity, but is full of acid solution earlier in resin column and leaves standstill more than 2 hours, generally need not surpass 12 hours, carry out eluting again.Through after leaving standstill, a large amount of alkaloid organic ions are exchanged by hydrion, perhaps are in half absorption, half dissociated state, and carry out eluting this moment, and the alkaloid concentration effect is obvious, and elution efficiency obviously improves.
9, in order further to improve elution efficiency, can also in the acid solution that eluting is used, add small amount of N H
4Cl, NaCl or CaCl
2, addition is unsuitable very few or too much, if very few, does not then have effect; If then easily saltouing because of salinity is too high influences the dissolubility of alkaloid organic ion too much.Experiment finds, in the eluent with NH
4 +, Na
+Or Ca
2+Be good when concentration is 0.1～1mol/L, further preferred, NH
4 +, Na
+Or Ca
2+Concentration best when being 0.1～0.3mol/L.
10, said desalination process can be the desalination method that dialysis desalination, membrane filtration are crossed desalination and other various medicine biological field routines in the technology, these methods comparative maturity all at present, and can channelization production.
11, in this method said Chinese medicine extraction liquid can be by dipping, percolation, ultrasonic, microwave or any mode in decocting extract and make, and the solvent that extracts can be in water, sour water, alcoholic solution, the acid ethanol solution any, but all belongs to the conventional extracting method of the present field of Chinese medicines.Distinctive points is, if make with dipping or percolation method, can directly go up sample; Obtain if extract, also will pass through steps such as precipitate with ethanol, filtration or centrifugal remove impurity, to guarantee the smooth of sample with additive method.
Need to prove that above-mentioned preferred technical parameter can carry out combination in any with basic technology according to the needs of practical situation, all can obtain good effect, the technical solution problem reaches purpose of the present invention.
Below by the contrast experiment advantage of the present invention is described.
One, experimental program:
Get Rhizoma Coptidis medical material 5000g, add 8 times of amounts of sour water of pH=3, soak a night, percolation is collected percolate to do not have a precipitation with the silico-tungstic acid inspection till, merges percolate, and is centrifugal, supernatant; Supernatant is five parts, carries out alkaloidal separation by following five kinds of methods respectively and purify:
(1) ion exchange resin+acid solution eluting: supernatant is regulated pH=3, on handled strong cation-exchanging resin 001 * 7 (Hydrogen well, blade diameter length ratio is 1: 8), last sample speed be 3 times of column volumes/hour, there is precipitation to stop to go up sample with the silico-tungstic acid inspection to effluent, it is colourless substantially that water is eluted to eluent, reuse 3% sulfuric acid solution eluting, elution speed be 4 times of column volumes/hour the speed eluting, eluent has precipitation the time to begin to receive with the silico-tungstic acid inspection, receiving eluent does not end to there is when precipitation with the silico-tungstic acid inspection, merge eluent, be neutralized to neutrality with sodium hydroxide, desalination (standby), drying gets Rhizoma Coptidis total alkaloids.
(2) the acid solution eluting of ion exchange resin+salt: supernatant is regulated pH=3, on handled strong cation-exchanging resin 001 * 7 (Hydrogen well, blade diameter length ratio is 1: 8), last sample speed be 3 times of column volumes/hour, there is precipitation to stop to go up sample with the silico-tungstic acid inspection to effluent, water is not eluted to when eluent has color substantially and stops, and 0.5% sulfuric acid solution of reuse 2% sodium chloride soaks resin.0.5% sulfuric acid solution eluting of reuse 2% sodium chloride, elution speed be 4 times of column volumes/hour, eluent begins to receive when with the silico-tungstic acid inspection precipitation being arranged, receive eluent to do not have with the silico-tungstic acid inspection precipitation up to, merge eluent, be neutralized to about pH=7 desalination (standby) with sodium hydroxide, concentrate drying gets Rhizoma Coptidis total alkaloids.
(3) ion exchange resin+reflux, extract: supernatant is regulated pH=3, on handled strong cation-exchanging resin 001 * 7 (Hydrogen, blade diameter length ratio are 1: 8) well, last sample speed be 3 times of column volumes/hour, there is precipitation to stop to go up sample with the silico-tungstic acid inspection to effluent, water is not eluted to when eluent has color substantially and stops eluting, and resin by pouring out in the post, is put in the porcelain dish and dried, it is an amount of to add 10% ammonia, stir, touched damp, be not advisable but do not touch with one's hand with hands.This resin is put in the apparatus,Soxhlet's,, chloroform solution is added anhydrous Na with chloroform reflux, extract, 2 hours
2SO
4After the dehydration, reclaim chloroform, the dry Rhizoma Coptidis total alkaloids that gets to the dried molassed pulpous state.
(4) macroporous adsorbent resin method: supernatant is regulated PH=10, on the DF01 type macroporous adsorbent resin handled well, last sample speed be 4 times of column volumes/hour, have precipitation to stop to go up sample with the silico-tungstic acid inspection to effluent, water is eluted to and stops eluting when eluent does not have color substantially.With alcohol-water (70: 30) is eluant, with 2.5 times of column volumes/hour speed carry out eluting, eluent has precipitation the time to begin to receive with the silico-tungstic acid inspection, receive eluent to do not have with the silico-tungstic acid inspection precipitation up to, merge eluent, reclaim ethanol, drying gets Rhizoma Coptidis total alkaloids.
(5) organic solvent extractionprocess: supernatant is regulated PH=10, divide three extractions with 10 times of amount chloroforms earlier, 10 times of amounts of reuse ethyl acetate extraction three times merges all extracts, and evaporate to dryness gets Rhizoma Coptidis total alkaloids.
Two, the result calculates: distinguish the weight of five kinds of technology gained of weighing total alkaloids, and be divided by with the medical material amount, get the yield of total alkaloids; Adopt the quantitative approach of acid base titration respectively, five kinds of method gained total alkaloidss are carried out assay, calculate the purity of total alkaloids.
Three, result's contrast, see the following form:
The effect assessment table of five kinds of technologies
By above comparing result as seen, technical scheme of the present invention can solve deficiency of the prior art, and improve significantly product quality, reduce cost, improve safety and producing feasibility, the present invention has reached goal of the invention.
Technical scheme of the present invention is suitable for the refining purification of Radix Berberidis Amurensis bases total alkaloids effective site.Rhizoma Coptidis is the dry rhizome of ranunculaceae plant Rhizoma Coptidis (Rhizoma Coptidis Coptis chinensis Franch.), Coptis deltoidea C.Y.Cheng et Hsiao (Coptis deltoidea C.Y.Cheng et Hsial) or Coptis Teeta Wall (Coptis teeta Wall.), record in 2005 editions one one 213 pages of Chinese Pharmacopoeia pharmacopeia, have effects such as eliminating fire and detoxication, heat clearing and damp drying.Corydalis thalictrifolia Franch. (Radix Corydalis Thalictrifoliae) is the herb of bloodroot hair Herba corydalis racemosae (Corydalis tomentella), has effects such as heat-clearing and toxic substances removing, antidiarrheal.Cortex Phellodendri is the dry bark of rutaceae wampee (Phellodendron Chinese Schneid) or Cortex Phellodendri (Phellodendron amurense Rupr.), record in 2005 editions one one 214 pages of Chinese Pharmacopoeia pharmacopeia, the former practises title " Cortex Phellodendri ", the latter practises title " Cortex Phellodendri ", has effects such as eliminating fire and detoxication, heat clearing and damp drying.Radix Berberidis is the root of Berberidaceae berberis porcupine quill (Berberis soulieana Schneid), little Radix Berberidis soulieanae (B.Wilson-aeHemsl.), berberis poiretii (B.Poiretii Schneid.) or spoonleaf barbarry herb (B.Vernae Schneid), effects such as tool heat clearing and damp drying, eliminating fire and detoxication.Mahonia fortunei (Lindl.) Fedde is root, stem, the leaf of Berberidaceae Mahonia fortunei (Lindl.) Fedde platymiscium Mahonia bealei (Fort.) Carr. Mahonia bealei (Fort.) Carr. and narrow leaf Mahonia fortunei (Lindl.) Fedde M.fortunei (Lindl) Fedde, has effects such as nourishing YIN and clearing away heat, heat-clearing and toxic substances removing.Caulis Arcangelisiae is Menispermaceae Caulis Arcangelisiae platymiscium Caulis Arcangelisiae Arcangelisia loureiri (Pierre) Diels ratan and root, has effects such as clearing away heat-damp and promoting diuresis, detoxifcation pain relieving.Above-mentioned six kinds of contained chemical constituents of medical material mostly are the berberine Alkaloid.Studies show that, their total alkaloidss separately are its main effective site, comprise berberine (berberine) in the Rhizoma Coptidis, coptisine (coptisine), palmatine (palmatine), jateorhizine (jatrorrhizine), magnoline (magnoflorine) etc.; Berberine in the Corydalis thalictrifolia Franch. (Radix Corydalis Thalictrifoliae) (berberine), Ka Weiding [(±) cavidine], thalictrifoline [(±) thalictrifoline], deydrokaividing (Corydalis Saxicolae, o.38% content be about, dehydrocavidine), dextrorotation 13-beta-hydroxy stylopine etc.; Berberine in the Cortex Phellodendri (berberine), and contain palmatine (palmatine), jateorhizine (jatrorrhizine), phellodendrine (phellodendrine), Caulis menispermi and appoint alkali (menisperine), white bridge alkali (candicine), Cortex Phellodendri paulownia (obacunone) etc.; Berberine in the Radix Berberidis (berberine), palmatine (palmatine), jateorhizine and berbamine (Shengbaian Pian) etc.; Berberine in the Mahonia fortunei (Lindl.) Fedde (berberine), palmatine (palmatine), jateorhizine (jatrorrhizine), magnoline (magnoflorine) etc.; Berberine in the Caulis Arcangelisiae (berberine), palmatine (palmatine), jateorhizine (jatrorrhizine), magnoline alkaloid components such as (magnoflorine).Confirm through a large amount of tests, the technology of cation exchange resin sour water eluting Radix Berberidis Amurensis bases total alkaloids, have that cost is low, organic solvent consumption less, the selectivity height, total alkaloids purity is high and help realizing advantage such as the big production of industry, for a brand-new platform has been created in the R﹠D and production of Chinese medicine Radix Berberidis Amurensis bases total alkaloids preparation.
The specific embodiment
Embodiment 1:
Get Rhizoma Coptidis decoction pieces 1000g, decoct with water 2 times, each 10 times of amounts decocted 2 hours, merged decoction liquor, centrifugal, regulate pH=3, centrifugal, supernatant is with 4 times of column volumes/hour by cation exchange resin (001 * 7, Hydrogen, blade diameter length ratio 1: 8), being washed to effluent does not have color, adds 3% sulphuric acid eluting, elution speed be 2 times of column volumes/hour, collect eluent, check negative (effluent drips 10% silico-tungstic acid does not have precipitation), be neutralized to neutrality with sodium hydroxide to alkaloid, desalination, the filtrate concentrate drying gets Rhizoma Coptidis total alkaloids.
Embodiment 2:
Get Rhizoma Coptidis decoction pieces 1000g, the sour water percolation that adds pH=5, merge the percolate thin up to 10000ml, centrifugal, regulate pH=1, centrifugal, supernatant is with 5 times of column volumes/hour by cation exchange resin (AmberliteIR--120, Hydrogen, blade diameter length ratio 1: 6), being washed to effluent does not have color, reuse 0.5% sulfuric acid solution eluting, elution speed be 4 times of column volumes/hour, soaked behind 2 times of column volumes of eluting 5 hours, be eluted to alkaloid again and check negative (effluent drips 10% silico-tungstic acid does not have precipitation), collect this part eluent, be neutralized to neutrality with calcium hydroxide, desalination, the filtrate concentrate drying gets Rhizoma Coptidis total alkaloids.
Embodiment 3:
Get Cortex Phellodendri decoction pieces 5kg, add 70% ethanol ultrasonic extraction twice, add 5 times of amounts at every turn, ultrasonic 0.5 hour, merge extractive liquid,, centrifugal, reclaim ethanol, add water to 5000ml, regulate pH=2, centrifugal, supernatant is with 2 times of column volumes/hour by last cation exchange resin (001 * 10, sodium type, blade diameter length ratio 1: 7), being washed to effluent does not have color, the sulfuric acid solution of the reuse 6% (CaCl that contains 1mol/L
2) eluting, elution speed be 5 times of column volumes/hour, collect eluent, check negative (effluent drips 10% silico-tungstic acid does not have precipitation) to alkaloid, be neutralized to neutrality with sodium hydroxide, desalination, the filtrate concentrate drying gets the Cortex Phellodendri total alkaloids.
Embodiment 4:
Get Radix Berberidis decoction pieces 10kg, decoct with water 2 times, each 10 times of amounts decocted 2 hours, merge decoction liquor, filter, it is 1.1 (60 ℃) that filtrate is concentrated into relative density, and adding ethanol to concentration is 70%, leave standstill, supernatant reclaims ethanol, adds water to 3000ml, regulates pH=4, centrifugal, supernatant is with 3 times of column volumes/hour by last cation exchange resin (AmberliteIR--120, Hydrogen, blade diameter length ratio 1: 6), be washed to effluent and do not have color, reuse 15% sulfuric acid solution eluting, elution speed be 6 times of column volumes/hour, collect eluent, to alkaloid inspection negative (effluent drips 10% silico-tungstic acid does not have precipitation), be neutralized to neutrality with sodium hydroxide, desalination, the filtrate concentrate drying gets the Radix Berberidis total alkaloids.
Embodiment 5:
Get Corydalis thalictrifolia Franch. (Radix Corydalis Thalictrifoliae) decoction pieces 10kg, decoct with water 2 times, each 10 times of amounts decocted 2 hours, merge decoction liquor, filter, it is 1.1 (60 ℃) that filtrate is concentrated into relative density, and adding ethanol to concentration is 70%, leave standstill, supernatant reclaims ethanol, adds water to 5000ml, regulates pH=5, centrifugal, supernatant is with 3 times of column volumes/hour by last cation exchange resin (D001 * 4, Hydrogen, blade diameter length ratio 1: 10), be washed to effluent and do not have color, reuse 3% sulfuric acid solution eluting, elution speed be 3 times of column volumes/hour, collect eluent, to alkaloid inspection negative (effluent drips 10% silico-tungstic acid does not have precipitation), be neutralized to neutrality with sodium hydroxide, desalination, the filtrate concentrate drying gets total alkaloids of meadowrueleaf corydalis root.
Embodiment 6:
Get Mahonia fortunei (Lindl.) Fedde decoction pieces 10kg, decoct with water 2 times, each 10 times of amounts decocted 2 hours, merge decoction liquor, filter, it is 1.1 (60 ℃) that filtrate is concentrated into relative density, and adding ethanol to concentration is 70%, leave standstill, supernatant reclaims ethanol, adds water to 4000ml, regulates pH=4, centrifugal, supernatant is with 0.5 times of column volume/hour by last cation exchange resin (Doulex 50, Hydrogen, blade diameter length ratio 1: 8), be washed to effluent and do not have color, reuse 0.5% sulfuric acid solution (sodium chloride that contains 0.1mol/L) eluting, elution speed be 5 times of column volumes/hour, collect eluent, to alkaloid inspection negative (effluent drips 10% silico-tungstic acid does not have precipitation), be neutralized to neutrality with sodium hydroxide, desalination, the filtrate concentrate drying gets the Mahonia fortunei (Lindl.) Fedde total alkaloids.
Embodiment 7:
Get Rhizoma Coptidis decoction pieces 10kg, decoct with water 2 times, each 10 times of amounts decocted 2 hours, merge decoction liquor, filter, it is 1.1 (60 ℃) that filtrate is concentrated into relative density, and adding ethanol to concentration is 70%, leave standstill, supernatant reclaims ethanol, adds water to 10000ml, regulates pH=3, centrifugal, supernatant is with 3 times of column volumes/hour by last cation exchange resin (001 * 5, Hydrogen, blade diameter length ratio 1: 8), be washed to effluent and do not have color, reuse 15% sulfuric acid solution (calcium chloride that contains 0.3mol/L) eluting, elution speed be 6 times of column volumes/hour, collect eluent, to alkaloid inspection negative (effluent drips 10% silico-tungstic acid does not have precipitation), be neutralized to neutrality with sodium hydroxide, desalination, the filtrate concentrate drying gets Rhizoma Coptidis total alkaloids.
Embodiment 8:
Get Radix Berberidis decoction pieces 1000g, decoct with water 2 times, each 10 times of amounts decocted 2 hours, merge decoction liquor, filter, it is 1.1 (60 ℃) that filtrate is concentrated into relative density, and adding ethanol to concentration is 70%, leave standstill, supernatant reclaims ethanol, adds water to 1000ml, regulates pH=3, centrifugal, supernatant is with 3 times of column volumes/hour by last cation exchange resin (001 * 5, Hydrogen, blade diameter length ratio 1: 8), be washed to effluent and do not have color, reuse 6% sulfuric acid solution eluting, elution speed be 4 times of column volumes/hour, collect eluent, to alkaloid inspection negative (effluent drips 10% silico-tungstic acid does not have precipitation), be neutralized to neutrality with sodium hydroxide, desalination, the filtrate concentrate drying gets the Radix Berberidis total alkaloids.
Embodiment 9:
Get Mahonia fortunei (Lindl.) Fedde decoction pieces 2000g, the sulfuric acid solution that adds pH=3, microwave extraction 2 times adds 5 times of volume microwave extractioies 0.5 hour at every turn, filters, the filtrate thin up is to 1600ml, regulate pH=6, centrifugal, supernatant is with 2 times of column volumes/hour by last cation exchange resin (001 * 15, Hydrogen, blade diameter length ratio 1: 6), being washed to effluent does not have color, reuse 5% sulfuric acid solution (ammonia chloride that contains 0.2mol/L) eluting, elution speed be 5 times of column volumes/hour, collect eluent, check negative (effluent drips 10% silico-tungstic acid does not have precipitation), be neutralized to neutrality with sodium hydroxide to alkaloid, desalination, the filtrate concentrate drying gets the Mahonia fortunei (Lindl.) Fedde total alkaloids.
Embodiment 10:
Get Cortex Phellodendri decoction pieces 5kg, add twice of 70% ethanol ultrasonic extraction, add 5 times of amounts at every turn, ultrasonic 0.5 hour, merge extractive liquid,, centrifugal, reclaim ethanol, add water to 5000ml, regulate pH=7, centrifugal, supernatant is so that 2 times of column volumes/hour by last large pores cation exchange resin, being washed to effluent does not have color, the sulfuric acid solution of reuse 4% (ammonia chloride of 0.6mol/L) eluting, elution speed be 5 times of column volumes/hour, collect eluent, check negative (effluent drips 10% silico-tungstic acid does not have precipitation), be neutralized to neutrality with sodium hydroxide to alkaloid, desalination, the filtrate concentrate drying gets the Cortex Phellodendri total alkaloids.
Embodiment 11:
Get Caulis Arcangelisiae decoction pieces 10kg, decoct with water 2 times, each 8 times of amounts decocted 2 hours, merge decoction liquor, filter, it is 1.05 (70 ℃) that filtrate is concentrated into relative density, and adding ethanol to concentration is 60%, leave standstill, supernatant reclaims ethanol, adds water to 4000ml, regulates pH=4, centrifugal, supernatant is with 3 times of column volumes/hour by last cation exchange resin (Doulex 50, Hydrogen, blade diameter length ratio 1: 8), be washed to effluent and do not have color, reuse 3% sulfuric acid solution eluting, elution speed be 3 times of column volumes/hour, collect eluent, to alkaloid inspection negative (effluent drips 10% silico-tungstic acid does not have precipitation), be neutralized to neutrality with sodium hydroxide, desalination, the filtrate concentrate drying gets the Caulis Arcangelisiae total alkaloids.
Claims (13)
1, a kind of from Chinese medicine extraction liquid the method for separating berberine class total alkaloids, it is characterized in that this method is: get the Chinese medicine extraction liquid that contains Radix Berberidis Amurensis bases total alkaloids, adjust pH value 1 to 7, be added on the cation exchange resin column, earlier with the water elution remove impurity, reuse 0.5%～15% acid solution eluting, collect eluent, add the alkali neutralization,, promptly get Radix Berberidis Amurensis bases total alkaloids through desalting processing.
2, the method for separating berberine class total alkaloids as claimed in claim 1 is characterized in that the preceding pH value scope of adjusting medicinal liquid of upper prop is 2 to 5.
3, the method for separating berberine class total alkaloids as claimed in claim 1 is characterized in that used cation exchange resin can be macroporous type or gel-type strong acid ion exchange resin.
4, the method for separating berberine class total alkaloids as claimed in claim 3 is characterized in that the post footpath of used cation exchange resin column: post height=1: 5～1: 10.
5, the method for separating berberine class total alkaloids as claimed in claim 1 is characterized in that in this method that the concentration of sample medicinal liquid is that every ml is equivalent to crude drug 0.1～3g, last sample speed be 0.5～5 times of column volume/hour.
6, the method for separating berberine class total alkaloids as claimed in claim 5 is characterized in that sample loading mode is preferably sample on the adverse current.
7, the method for separating berberine class total alkaloids as claimed in claim 1 is characterized in that eluting is used in this method acid solution is 3%～6% sulfuric acid solution or hydrochloric acid solution.
8, the method for separating berberine class total alkaloids as claimed in claim 7, it is characterized in that elution speed be 2～6 times of column volumes/hour.
9, the method for separating berberine class total alkaloids as claimed in claim 8, it is characterized in that elution speed be 4～6 times of column volumes/hour.
10, the method for separating berberine class total alkaloids as claimed in claim 1 is characterized in that after the water elution remove impurity, can be full of eluting earlier with acid solution and left standstill 2～12 hours in resin column, carries out eluting again.
11, the method for separating berberine class total alkaloids as claimed in claim 7 is characterized in that can also adding in the acid solution that eluting uses the NH of 0.1～1mol/L
4Cl, NaCl or CaCl
2
12, the method for separating berberine class total alkaloids as claimed in claim 11 is characterized in that the concentration of salt is preferably 0.1～0.3mol/L in the acid solution.
13, the Radix Berberidis Amurensis bases total alkaloids of any one described method preparation among the claim 1-12.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNA2007100984369A CN101491596A (en) | 2007-04-18 | 2007-04-18 | Method for separating berberine total alkaloid from extract liquid of traditional Chinese medicine |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNA2007100984369A CN101491596A (en) | 2007-04-18 | 2007-04-18 | Method for separating berberine total alkaloid from extract liquid of traditional Chinese medicine |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN101491596A true CN101491596A (en) | 2009-07-29 |
Family
ID=40922496
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNA2007100984369A Pending CN101491596A (en) | 2007-04-18 | 2007-04-18 | Method for separating berberine total alkaloid from extract liquid of traditional Chinese medicine |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN101491596A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102579710A (en) * | 2012-03-29 | 2012-07-18 | 黄荣 | Chinese medicine for treating ankylosing apondylitis and preparation method thereof |
| CN103933100A (en) * | 2013-01-17 | 2014-07-23 | 何欣 | Preparation method of total alkaloid of Chinese mahonia stem and applications of total alkaloid of Chinese mahonia stem in preparation of drugs for preventing and treating gastric ulcer |
| CN105055534A (en) * | 2015-08-07 | 2015-11-18 | 赵明东 | Production method of high purity Corydalis saxicola Bunting alkaloid |
| CN105535073A (en) * | 2015-12-30 | 2016-05-04 | 浙江省中医药研究院 | Apios fortunei maxim total alkaloid with anticancer effect as well as preparation method and application thereof |
| CN108014517A (en) * | 2017-12-20 | 2018-05-11 | 泰州医药城国科化物生物医药科技有限公司 | A kind of method using polysaccharide-based medium to Protoberberine Alkoloids enriching and purifying |
-
2007
- 2007-04-18 CN CNA2007100984369A patent/CN101491596A/en active Pending
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102579710A (en) * | 2012-03-29 | 2012-07-18 | 黄荣 | Chinese medicine for treating ankylosing apondylitis and preparation method thereof |
| CN102579710B (en) * | 2012-03-29 | 2013-09-25 | 黄荣 | Chinese medicine for treating ankylosing apondylitis and preparation method thereof |
| CN103933100A (en) * | 2013-01-17 | 2014-07-23 | 何欣 | Preparation method of total alkaloid of Chinese mahonia stem and applications of total alkaloid of Chinese mahonia stem in preparation of drugs for preventing and treating gastric ulcer |
| CN105055534A (en) * | 2015-08-07 | 2015-11-18 | 赵明东 | Production method of high purity Corydalis saxicola Bunting alkaloid |
| CN105055534B (en) * | 2015-08-07 | 2018-08-10 | 赵明东 | The production method of high-purity meadowrueleaf corydalis root alkaloid |
| CN105535073A (en) * | 2015-12-30 | 2016-05-04 | 浙江省中医药研究院 | Apios fortunei maxim total alkaloid with anticancer effect as well as preparation method and application thereof |
| CN105535073B (en) * | 2015-12-30 | 2021-01-19 | 浙江省中医药研究院 | A kind of total alkaloid with anticancer effect, preparation method and application |
| CN108014517A (en) * | 2017-12-20 | 2018-05-11 | 泰州医药城国科化物生物医药科技有限公司 | A kind of method using polysaccharide-based medium to Protoberberine Alkoloids enriching and purifying |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN101647828B (en) | Method for separating total alkaloid from sophora flavescens ait by using ion exchange resin | |
| CN101491619A (en) | Method for separating cytospaz total alkaloid from traditional Chinese medicine extract liquid | |
| CN101491596A (en) | Method for separating berberine total alkaloid from extract liquid of traditional Chinese medicine | |
| CN101698059A (en) | Method for separating dendrobium total alkaloids by ion exchange resin | |
| CN102172361A (en) | Method for separating traditional Chinese medicine total alkaloids by ion exchange resin | |
| CN101289472A (en) | Process for separating matrine-like total alkaloids form Chinese medicament extract | |
| CN101697983A (en) | Method for separating pegamun harmala total alkaloids by ion exchange resin | |
| CN101698057A (en) | Method for separating anoectochilus formosanus total alkaloids by ion exchange resin | |
| CN101491631A (en) | Method for separating verticine total alkaloids in traditional Chinese medicine extract | |
| CN102172366A (en) | Method for separating total alkaloids from motherwort by using ion exchange resin | |
| CN101491589A (en) | Method for separating greater celandine, eomecon chionantha hance or toddalia asiatica total alkaloids | |
| CN101697984A (en) | Method for separating incarvillea total alkaloids by ion exchange resin | |
| CN101698003B (en) | Method for separating rhizoma corydalis total alkaloids by ion exchange resin | |
| CN101697986B (en) | Method for separating catharanthus roseus total alkaloids by ion exchange resin | |
| CN101491554A (en) | Nicotiana tabacum total alkaloids separation method in Nicotiana tabacum extract | |
| CN101647854B (en) | Method for separating total alkaloid from sophora flavescens ait by using ion exchange resin | |
| CN101697982B (en) | Method for separating camptotheca total alkaloids by ion exchange resin | |
| CN101289471A (en) | Process for separating total alkaloids of corydalis rhizome form Chinese medicament extracting solution of corydalis rhizome | |
| CN101396434A (en) | Method for separating total alkaloids from dactylicapnos root | |
| CN101697992A (en) | Method for separating huperzia serrata total alkaloids by ion exchange resin | |
| CN101697999A (en) | Method for separating semen strychni total alkaloids by ion exchange resin | |
| CN101698022B (en) | Method for separating pepper total alkaloids by ion exchange resin | |
| CN102172365A (en) | Method for separating radix sophorae flavescentis total alkaloids by ion exchange resin | |
| CN102172362A (en) | Method for separating total alkaloids from Chinese medical extract by using ion exchange resin | |
| CN101491561A (en) | Amsonia sinensis total alkaloids separation method in Amsonia sinensis extract |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C02 | Deemed withdrawal of patent application after publication (patent law 2001) | ||
| WD01 | Invention patent application deemed withdrawn after publication |
Open date: 20090729 |