JPH0124795B2 - - Google Patents
Info
- Publication number
- JPH0124795B2 JPH0124795B2 JP54139878A JP13987879A JPH0124795B2 JP H0124795 B2 JPH0124795 B2 JP H0124795B2 JP 54139878 A JP54139878 A JP 54139878A JP 13987879 A JP13987879 A JP 13987879A JP H0124795 B2 JPH0124795 B2 JP H0124795B2
- Authority
- JP
- Japan
- Prior art keywords
- compound
- concentration
- adsorption
- elution
- resin
- 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.)
- Expired
Links
- 238000001179 sorption measurement Methods 0.000 claims description 51
- 229920005989 resin Polymers 0.000 claims description 35
- 239000011347 resin Substances 0.000 claims description 35
- 238000000034 method Methods 0.000 claims description 23
- 239000011148 porous material Substances 0.000 claims description 22
- 239000007864 aqueous solution Substances 0.000 claims description 13
- HSHGZXNAXBPPDL-HZGVNTEJSA-N 7beta-aminocephalosporanic acid Chemical class S1CC(COC(=O)C)=C(C([O-])=O)N2C(=O)[C@@H]([NH3+])[C@@H]12 HSHGZXNAXBPPDL-HZGVNTEJSA-N 0.000 claims description 8
- 239000003480 eluent Substances 0.000 claims description 8
- 229920001187 thermosetting polymer Polymers 0.000 claims description 5
- 239000007853 buffer solution Substances 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 description 40
- 238000010828 elution Methods 0.000 description 26
- 229940126062 Compound A Drugs 0.000 description 24
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 24
- 239000000243 solution Substances 0.000 description 21
- 238000006243 chemical reaction Methods 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- HOKIDJSKDBPKTQ-GLXFQSAKSA-N cephalosporin C Chemical compound S1CC(COC(=O)C)=C(C(O)=O)N2C(=O)[C@@H](NC(=O)CCC[C@@H](N)C(O)=O)[C@@H]12 HOKIDJSKDBPKTQ-GLXFQSAKSA-N 0.000 description 12
- 239000007788 liquid Substances 0.000 description 11
- 230000002378 acidificating effect Effects 0.000 description 10
- 239000012535 impurity Substances 0.000 description 10
- 239000000126 substance Substances 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 238000011084 recovery Methods 0.000 description 8
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 229920001429 chelating resin Polymers 0.000 description 6
- 238000000746 purification Methods 0.000 description 6
- 239000011550 stock solution Substances 0.000 description 6
- -1 cephalosporin compound Chemical class 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000008363 phosphate buffer Substances 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 229930186147 Cephalosporin Natural products 0.000 description 4
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- 239000006227 byproduct Substances 0.000 description 4
- 229940124587 cephalosporin Drugs 0.000 description 4
- 229920006037 cross link polymer Polymers 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 238000000926 separation method Methods 0.000 description 4
- 238000000638 solvent extraction Methods 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 239000003463 adsorbent Substances 0.000 description 3
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 3
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 3
- 239000000356 contaminant Substances 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- CHRJZRDFSQHIFI-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;styrene Chemical compound C=CC1=CC=CC=C1.C=CC1=CC=CC=C1C=C CHRJZRDFSQHIFI-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 241000228417 Sarocladium strictum Species 0.000 description 2
- 239000000872 buffer Substances 0.000 description 2
- 230000003139 buffering effect Effects 0.000 description 2
- 150000001780 cephalosporins Chemical class 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000000855 fermentation Methods 0.000 description 2
- 230000004151 fermentation Effects 0.000 description 2
- HHLFWLYXYJOTON-UHFFFAOYSA-N glyoxylic acid Chemical compound OC(=O)C=O HHLFWLYXYJOTON-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 239000012266 salt solution Substances 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- 241000589519 Comamonas Species 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 102100021102 Hyaluronidase PH-20 Human genes 0.000 description 1
- 102000004316 Oxidoreductases Human genes 0.000 description 1
- 108090000854 Oxidoreductases Proteins 0.000 description 1
- 241000589516 Pseudomonas Species 0.000 description 1
- 101150055528 SPAM1 gene Proteins 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000007805 chemical reaction reactant Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910000365 copper sulfate Inorganic materials 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- 230000009849 deactivation Effects 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
- 235000019800 disodium phosphate Nutrition 0.000 description 1
- 229910000397 disodium phosphate Inorganic materials 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- GTFMAONWNTUZEW-UHFFFAOYSA-N glutaramic acid Chemical compound NC(=O)CCCC(O)=O GTFMAONWNTUZEW-UHFFFAOYSA-N 0.000 description 1
- VANNPISTIUFMLH-UHFFFAOYSA-N glutaric anhydride Chemical compound O=C1CCCC(=O)O1 VANNPISTIUFMLH-UHFFFAOYSA-N 0.000 description 1
- 239000000383 hazardous chemical Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229920006113 non-polar polymer Polymers 0.000 description 1
- 239000008055 phosphate buffer solution Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 238000002336 sorption--desorption measurement Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000013076 target substance Substances 0.000 description 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 150000003952 β-lactams Chemical class 0.000 description 1
Landscapes
- Cephalosporin Compounds (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13987879A JPS5665894A (en) | 1979-10-31 | 1979-10-31 | Purification of 7-aminocephalosporanic acid derivative |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13987879A JPS5665894A (en) | 1979-10-31 | 1979-10-31 | Purification of 7-aminocephalosporanic acid derivative |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5665894A JPS5665894A (en) | 1981-06-03 |
JPH0124795B2 true JPH0124795B2 (de) | 1989-05-15 |
Family
ID=15255665
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP13987879A Granted JPS5665894A (en) | 1979-10-31 | 1979-10-31 | Purification of 7-aminocephalosporanic acid derivative |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5665894A (de) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2014157091A (ja) * | 2013-02-15 | 2014-08-28 | Central Research Institute Of Electric Power Industry | 地下水の年代測定装置及び地下水の年代測定方法 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS50106996A (de) * | 1974-01-23 | 1975-08-22 | ||
JPS5276486A (en) * | 1975-12-18 | 1977-06-27 | Meiji Seika Kaisha Ltd | Purification of cephalosporin c |
JPS52128294A (en) * | 1976-04-20 | 1977-10-27 | Fujisawa Pharmaceut Co Ltd | Separation and purification of cephalosporins |
-
1979
- 1979-10-31 JP JP13987879A patent/JPS5665894A/ja active Granted
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS50106996A (de) * | 1974-01-23 | 1975-08-22 | ||
JPS5276486A (en) * | 1975-12-18 | 1977-06-27 | Meiji Seika Kaisha Ltd | Purification of cephalosporin c |
JPS52128294A (en) * | 1976-04-20 | 1977-10-27 | Fujisawa Pharmaceut Co Ltd | Separation and purification of cephalosporins |
Also Published As
Publication number | Publication date |
---|---|
JPS5665894A (en) | 1981-06-03 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4615806A (en) | Removal of iodide compounds from non-aqueous organic media | |
US2541420A (en) | Purification of streptomycin by carboxylic acid type ion exchange resins | |
KR890001245B1 (ko) | 트립토판의 정제방법 | |
JPH07116230B2 (ja) | 糖ペプチド抗生物質の回収方法 | |
PL81295B1 (de) | ||
US6730497B2 (en) | Process for preparing cephalosporanic acid derivatives using β-ketoacid derivatives | |
KR890001010B1 (ko) | 세프트아지딤의 회수방법 | |
JPH0124795B2 (de) | ||
US4028355A (en) | Cephalosporin purification process | |
US4145539A (en) | Process for isolation and purification of cephalosporin compound | |
USH328H (en) | Purification of cephalosporins | |
JP2002509933A (ja) | セファロスポリンの発酵製造の新規な方法 | |
US3941657A (en) | Purification of d-aminoacid oxidase | |
JPH06345683A (ja) | ピルビン酸の精製方法 | |
JPH04112866A (ja) | プロスタグランジンの精製法 | |
US2643210A (en) | Vitamin b12-active substance elution from montmorillonite absorbent | |
JPH0564627B2 (de) | ||
KR910003112A (ko) | 에피데르민의 수득, 분리 및 정제방법 | |
JPH02178288A (ja) | 3―ヒドロキシメチル―7―アミノセフエムカルボン酸の精製法 | |
JPS6210511B2 (de) | ||
KR800001596B1 (ko) | 복상식 수지 칼럼을 이용한 세파로스포린 c의 선별 회수법 | |
JPH0559917B2 (de) | ||
US4128546A (en) | Process for the purification of FR-1923 substance | |
JPH04112797A (ja) | イソマルトオリゴ糖の製造方法 | |
JPS6052753B2 (ja) | 7−アミノセフエム化合物の精製法 |