JP2010533758A5 - - Google Patents
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- JP2010533758A5 JP2010533758A5 JP2010516501A JP2010516501A JP2010533758A5 JP 2010533758 A5 JP2010533758 A5 JP 2010533758A5 JP 2010516501 A JP2010516501 A JP 2010516501A JP 2010516501 A JP2010516501 A JP 2010516501A JP 2010533758 A5 JP2010533758 A5 JP 2010533758A5
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- Prior art keywords
- acid
- salt
- formula
- crosslinked polymer
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- Prior art date
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- 150000003839 salts Chemical class 0.000 claims 12
- 239000011780 sodium chloride Substances 0.000 claims 12
- 229920000642 polymer Polymers 0.000 claims 11
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims 5
- VVJKKWFAADXIJK-UHFFFAOYSA-N Allylamine Chemical compound NCC=C VVJKKWFAADXIJK-UHFFFAOYSA-N 0.000 claims 4
- MUBZPKHOEPUJKR-UHFFFAOYSA-N oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-K [O-]P([O-])([O-])=O Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 3
- 150000001875 compounds Chemical class 0.000 claims 3
- 239000010452 phosphate Substances 0.000 claims 3
- 239000002904 solvent Substances 0.000 claims 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-M 3-carboxy-2-(carboxymethyl)-2-hydroxypropanoate Chemical compound OC(=O)CC(O)(C(O)=O)CC([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-M 0.000 claims 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N Benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 claims 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate dianion Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims 2
- RFDAIACWWDREDC-FRVQLJSFSA-N Glycocholic acid Chemical compound C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(=O)NCC(O)=O)C)[C@@]2(C)[C@@H](O)C1 RFDAIACWWDREDC-FRVQLJSFSA-N 0.000 claims 2
- FEWJPZIEWOKRBE-XIXRPRMCSA-N Mesotartaric acid Chemical compound OC(=O)[C@@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-XIXRPRMCSA-N 0.000 claims 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims 2
- WBWWGRHZICKQGZ-HZAMXZRMSA-N Taurocholic acid Chemical compound C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(=O)NCCS(O)(=O)=O)C)[C@@]2(C)[C@@H](O)C1 WBWWGRHZICKQGZ-HZAMXZRMSA-N 0.000 claims 2
- WEVYAHXRMPXWCK-UHFFFAOYSA-N acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims 2
- 235000010323 ascorbic acid Nutrition 0.000 claims 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims 2
- -1 cholic acid anion Chemical class 0.000 claims 2
- 239000003431 cross linking reagent Substances 0.000 claims 2
- 150000004820 halides Chemical class 0.000 claims 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxyl anion Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims 2
- 239000003999 initiator Substances 0.000 claims 2
- 239000002245 particle Substances 0.000 claims 2
- KWYUFKZDYYNOTN-UHFFFAOYSA-M potassium hydroxide Inorganic materials [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims 2
- 150000003568 thioethers Chemical class 0.000 claims 2
- NXOLVMFMAFCDSR-UHFFFAOYSA-M 2-(chloromethyl)oxirane;prop-2-en-1-amine;N-prop-2-enyldecan-1-amine;trimethyl-[6-(prop-2-enylamino)hexyl]azanium;chloride Chemical compound [Cl-].NCC=C.ClCC1CO1.CCCCCCCCCCNCC=C.C[N+](C)(C)CCCCCCNCC=C NXOLVMFMAFCDSR-UHFFFAOYSA-M 0.000 claims 1
- BHQCQFFYRZLCQQ-UMZBRFQRSA-N 4-[(3R,5S,7R,12S)-3,7,12-trihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoic acid Chemical class C([C@H]1C[C@H]2O)[C@H](O)CCC1(C)C1C2C2CCC(C(CCC(O)=O)C)C2(C)[C@@H](O)C1 BHQCQFFYRZLCQQ-UMZBRFQRSA-N 0.000 claims 1
- 239000005711 Benzoic acid Substances 0.000 claims 1
- 229940093761 Bile Salts Drugs 0.000 claims 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N Carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims 1
- BHQCQFFYRZLCQQ-OELDTZBJSA-N Cholic acid Chemical compound C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(O)=O)C)[C@@]2(C)[C@@H](O)C1 BHQCQFFYRZLCQQ-OELDTZBJSA-N 0.000 claims 1
- 239000004380 Cholic acid Substances 0.000 claims 1
- 229920002905 Colesevelam Polymers 0.000 claims 1
- 229940099347 Glycocholic Acid Drugs 0.000 claims 1
- 108010007979 Glycocholic Acid Proteins 0.000 claims 1
- 150000000994 L-ascorbates Chemical class 0.000 claims 1
- 206010027417 Metabolic acidosis Diseases 0.000 claims 1
- UIIMBOGNXHQVGW-UHFFFAOYSA-M NaHCO3 Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims 1
- JRKICGRDRMAZLK-UHFFFAOYSA-N Peroxydisulfuric acid Chemical compound OS(=O)(=O)OOS(O)(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-N 0.000 claims 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N Phosphite Chemical compound [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 claims 1
- ZNSIZMQNQCNRBW-UHFFFAOYSA-N Sevelamer Chemical group NCC=C.ClCC1CO1 ZNSIZMQNQCNRBW-UHFFFAOYSA-N 0.000 claims 1
- 229960003693 Sevelamer Drugs 0.000 claims 1
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Vitamin C Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims 1
- 235000011054 acetic acid Nutrition 0.000 claims 1
- 150000001242 acetic acid derivatives Chemical class 0.000 claims 1
- 150000001450 anions Chemical class 0.000 claims 1
- 239000011668 ascorbic acid Substances 0.000 claims 1
- 229960005070 ascorbic acid Drugs 0.000 claims 1
- 235000010233 benzoic acid Nutrition 0.000 claims 1
- 150000001558 benzoic acid derivatives Chemical class 0.000 claims 1
- 239000003833 bile salt Substances 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 229940099352 cholate Drugs 0.000 claims 1
- 229960002471 cholic acid Drugs 0.000 claims 1
- 235000019416 cholic acid Nutrition 0.000 claims 1
- 235000015165 citric acid Nutrition 0.000 claims 1
- 150000001860 citric acid derivatives Chemical class 0.000 claims 1
- 229960001152 colesevelam Drugs 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- QAOWNCQODCNURD-UHFFFAOYSA-M hydrogensulfate Chemical compound OS([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 claims 1
- 239000011630 iodine Chemical group 0.000 claims 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical group II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims 1
- 229910052740 iodine Chemical group 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 125000001624 naphthyl group Chemical group 0.000 claims 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims 1
- 150000001451 organic peroxides Chemical class 0.000 claims 1
- 229940039748 oxalate Drugs 0.000 claims 1
- 235000006408 oxalic acid Nutrition 0.000 claims 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 claims 1
- 239000000546 pharmaceutic aid Substances 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims 1
- 229920000083 poly(allylamine) Polymers 0.000 claims 1
- 239000011541 reaction mixture Substances 0.000 claims 1
- 239000012453 solvate Substances 0.000 claims 1
- 229940086735 succinate Drugs 0.000 claims 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 claims 1
- 239000001384 succinic acid Substances 0.000 claims 1
- 235000011044 succinic acid Nutrition 0.000 claims 1
- QAOWNCQODCNURD-UHFFFAOYSA-L sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 238000003786 synthesis reaction Methods 0.000 claims 1
- 230000002194 synthesizing Effects 0.000 claims 1
- 239000011975 tartaric acid Substances 0.000 claims 1
- 235000002906 tartaric acid Nutrition 0.000 claims 1
- 229960001367 tartaric acid Drugs 0.000 claims 1
- 229940095064 tartrate Drugs 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
Claims (20)
- 式(IV)の架橋剤/アリルアミン比が、約5%から約50%wt%、好ましくは約10%から約30%wt%、より好ましくは約20%から約30%wt%である請求項1に記載の方法。
- 式(IV)の化合物の塩が、ハロゲン化物、リン酸塩、亜リン酸塩、炭酸塩、重炭酸塩、硫酸塩、重硫酸塩、水酸化物、硝酸塩、過硫酸塩、亜硫酸塩、硫化物、酢酸塩、アスコルビン酸塩、安息香酸塩、クエン酸塩、クエン酸二水素、クエン酸水素、シュウ酸塩、コハク酸塩、酒石酸塩、タウロコール酸塩、グリココール酸塩、及びコール酸塩からなる群から選択される無機又は有機塩である請求項1に記載の方法。
- 上記塩は二塩酸塩である請求項2に記載の方法。
- ラジカル開始剤がアゾ化合物又は無機又は有機過酸化物である請求項1から4の何れか一項に記載の方法。
- 溶媒が水/アセトニトリルの混合物である請求項1から5の何れか一項に記載の方法。
- 反応混合物に少なくとも適切な界面活性剤を添加することを更に含む請求項1から5の何れか一項に記載の方法。
- 最終の架橋ポリ(アリルアミン)ポリマーを塩基、例えばNaOH、Na2CO3、NaHCO3、KOH、K2CO3、KHCO3、好ましくはNaOH又はNa2CO3で処理することを更に含む請求項1から7の何れか一に記載の方法。
- 架橋ポリマーがセベラマーである請求項1から8の何れか一項に記載の方法。
- 得られた粒子の少なくとも90重量%が、350μmより小さく、好ましくは300μmより小さく、より好ましくは260μmより小さく、より好ましくは200μmより小さいサイズを有する請求項9に記載の方法。
- 請求項1から10の何れか一項の方法によって製造される架橋ポリマー又はその塩。
- 塩化物イオンの含有量が0.1%より低い請求項1から10の何れか一項の方法で製造される架橋ポリマー。
- 16から18mEq/gの間からなるリン酸結合能を持つ請求項1から10の何れか一項の方法で製造される架橋ポリマー。
- 患者からリン酸を除去するための請求項1から10の何れか一項に記載の方法で製造される架橋ポリマー又はその塩。
- 患者からのリン酸を除去し、及び/又は代謝性アシドーシスを治療するための請求項1から10の方法で製造される架橋ポリマーの炭酸塩。
- コレセベラムの合成における中間体としての、請求項1から10の何れか一項の方法に従って製造した架橋ポリマー又はその塩の使用。
- 患者から胆汁酸塩を除去するための医薬の製造のための中間体としての、請求項1から10の何れか一項に記載の方法によって製造された架橋ポリマー又はその塩の使用。
- 350μmより小さく、好ましくは300μmより小さく、より好ましくは260μmより小さく、より好ましくは200μmより小さいサイズを有する少なくとも90重量%の粒子を有する請求項1から10の何れか一項に記載の方法によって製造された架橋ポリマー又はその塩を、場合によっては少なくとも一の薬学的に許容可能な賦形剤と共に含有する薬学的製剤。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP07112604A EP2016947A1 (en) | 2007-07-17 | 2007-07-17 | Novel one step process for preparing cross-linked poly(allylamine) polymers |
PCT/EP2008/059303 WO2009010531A1 (en) | 2007-07-17 | 2008-07-16 | Novel one step process for preparing cross-linked poly(allylamine) polymers |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2010533758A JP2010533758A (ja) | 2010-10-28 |
JP2010533758A5 true JP2010533758A5 (ja) | 2011-07-14 |
Family
ID=38921775
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2010516501A Pending JP2010533758A (ja) | 2007-07-17 | 2008-07-16 | 架橋ポリ(アリルアミン)ポリマーを調製するための新規な一工程方法 |
Country Status (17)
Country | Link |
---|---|
US (1) | US8394416B2 (ja) |
EP (2) | EP2016947A1 (ja) |
JP (1) | JP2010533758A (ja) |
KR (1) | KR20100051616A (ja) |
CN (1) | CN101743012B (ja) |
AT (1) | ATE493136T1 (ja) |
BR (1) | BRPI0813829A2 (ja) |
CA (1) | CA2697130A1 (ja) |
DE (1) | DE602008004259D1 (ja) |
DK (1) | DK2175866T3 (ja) |
ES (1) | ES2358381T3 (ja) |
HK (1) | HK1140945A1 (ja) |
HR (1) | HRP20110181T1 (ja) |
PL (1) | PL2175866T3 (ja) |
PT (1) | PT2175866E (ja) |
SI (1) | SI2175866T1 (ja) |
WO (1) | WO2009010531A1 (ja) |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8404784B2 (en) | 2008-12-03 | 2013-03-26 | Navinta Llc | Manufacturing process of making polymeric amine salts |
US20120088886A1 (en) * | 2009-06-16 | 2012-04-12 | Watson Pharma Private Limited | Processes for the preparation of sevelamer carbonate |
IT1404163B1 (it) | 2011-02-01 | 2013-11-15 | Chemi Spa | Processo per la preparazione di poliallilamine reticolate o loro sali farmaceuticamente accettabili |
CN102796262B (zh) * | 2011-05-24 | 2014-11-12 | 北大方正集团有限公司 | 一种碳酸司维拉姆的制备方法 |
CN102796259B (zh) * | 2011-05-24 | 2014-11-12 | 北大方正集团有限公司 | 碳酸司维拉姆的制备方法 |
CN103012789B (zh) * | 2011-09-23 | 2015-02-25 | 北大方正集团有限公司 | 烟酸司维拉姆的制备方法 |
CN102675510B (zh) * | 2012-05-28 | 2014-04-02 | 诚达药业股份有限公司 | 司维拉姆的合成工艺 |
CN102942646B (zh) * | 2012-10-26 | 2016-06-29 | 青岛正大海尔制药有限公司 | 一种高分子聚合物的合成与分离纯化方法 |
EP3578185B1 (en) | 2013-06-05 | 2020-08-05 | Tricida Inc. | Proton-binding polymers for oral administration |
CN104448139B (zh) * | 2014-11-21 | 2016-08-17 | 新发药业有限公司 | 一种盐酸考来维仑的制备方法 |
BR122021001914B1 (pt) | 2014-12-10 | 2024-02-27 | Tricida, Inc | Processo para preparação de um polímero de amina reticulada |
MA41202A (fr) * | 2014-12-18 | 2017-10-24 | Genzyme Corp | Copolymères polydiallymine réticulé pour le traitement du diabète de type 2 |
US11406661B2 (en) * | 2016-05-06 | 2022-08-09 | Tricida, Inc. | HCl-binding compositions for and methods of treating acid-base disorders |
CN106008813B (zh) * | 2016-06-15 | 2017-11-14 | 新发药业有限公司 | 溶液聚合制备盐酸考来维仑的方法 |
KR101853260B1 (ko) * | 2016-11-29 | 2018-06-14 | 주식회사 퍼슨 | 세벨라머 카보네이트의 제조방법 |
AU2017388956A1 (en) | 2016-12-28 | 2019-07-11 | Fujifilm Corporation | Emulsion of nitrogen atom-containing polymer or salt thereof, production method therefor, and production method for particles |
CN110831984B (zh) * | 2017-07-05 | 2023-06-06 | 日东纺绩株式会社 | 高纯度烯丙胺(共)聚合物及其制造方法 |
US10934380B1 (en) | 2017-09-25 | 2021-03-02 | Tricida, Inc. | Crosslinked poly(allylamine) polymer pharmaceutical compositions |
WO2019078197A1 (ja) | 2017-10-16 | 2019-04-25 | 富士フイルム株式会社 | 高リン血症治療剤 |
EP3703706A4 (en) | 2017-11-03 | 2022-04-27 | Tricida Inc. | COMPOSITIONS AND METHOD FOR TREATING ACID-BASE DISORDERS |
CN108751208B (zh) * | 2018-06-05 | 2020-06-30 | 山东师范大学 | 一种无表面活性剂微乳液制备的单分散二氧化硅纳米球及其制备方法 |
Family Cites Families (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE757856A (fr) * | 1969-10-27 | 1971-04-22 | Michelin & Cie | Perfectionnements aux polyurethanes vulcanisables au soufre |
JPS6090243A (ja) | 1983-10-25 | 1985-05-21 | Nitto Boseki Co Ltd | 小球状モノアリルアミン橋かけ重合体の製造方法 |
JP2862933B2 (ja) * | 1990-02-06 | 1999-03-03 | 東芝シリコーン株式会社 | N―アルケニル―n―グリシジル(メタ)アクリルアミド化合物の製造方法 |
JP2967952B2 (ja) * | 1991-07-23 | 1999-10-25 | 日本化薬株式会社 | 多孔性ポリマーの製造方法 |
US5496545A (en) * | 1993-08-11 | 1996-03-05 | Geltex Pharmaceuticals, Inc. | Phosphate-binding polymers for oral administration |
US5667775A (en) * | 1993-08-11 | 1997-09-16 | Geltex Pharmaceuticals, Inc. | Phosphate-binding polymers for oral administration |
US5414068A (en) * | 1994-01-24 | 1995-05-09 | Rohm And Haas Company | Crosslinked anion exchange particles and method for producing the particles |
TW474813B (en) * | 1994-06-10 | 2002-02-01 | Geltex Pharma Inc | Alkylated composition for removing bile salts from a patient |
JP3952223B2 (ja) * | 1997-05-28 | 2007-08-01 | 日東紡績株式会社 | アリルアミン重合体 |
TW568788B (en) * | 1998-10-12 | 2004-01-01 | Chugai Pharmaceutical Co Ltd | Polymer combining with phosphoric acid and preparation containing the same |
JP3363143B2 (ja) * | 1998-10-12 | 2003-01-08 | 中外製薬株式会社 | リン酸結合性ポリマー粒子 |
US6362266B1 (en) | 1999-09-03 | 2002-03-26 | The Dow Chemical Company | Process for reducing cohesiveness of polyallylamine polymer gels during drying |
US6733780B1 (en) | 1999-10-19 | 2004-05-11 | Genzyme Corporation | Direct compression polymer tablet core |
GB2374072B (en) * | 2000-06-16 | 2004-09-22 | Nippon Catalytic Chem Ind | Crosslinked polymer method for manufacturing it and use thereof |
AU2002252632B2 (en) | 2001-04-18 | 2004-09-23 | Genzyme Corporation | Low salt forms of polyallylamine |
US7459502B2 (en) * | 2003-11-03 | 2008-12-02 | Ilypsa, Inc. | Pharmaceutical compositions comprising crosslinked polyamine polymers |
US7985418B2 (en) | 2004-11-01 | 2011-07-26 | Genzyme Corporation | Aliphatic amine polymer salts for tableting |
PT1924246E (pt) * | 2005-09-15 | 2016-02-10 | Genzyme Corp | Formulação sachê para polímeros com funcionalidade amina |
-
2007
- 2007-07-17 EP EP07112604A patent/EP2016947A1/en not_active Withdrawn
-
2008
- 2008-07-16 DE DE602008004259T patent/DE602008004259D1/de active Active
- 2008-07-16 WO PCT/EP2008/059303 patent/WO2009010531A1/en active Application Filing
- 2008-07-16 CN CN2008800248423A patent/CN101743012B/zh not_active Expired - Fee Related
- 2008-07-16 DK DK08775124.4T patent/DK2175866T3/da active
- 2008-07-16 SI SI200830184T patent/SI2175866T1/sl unknown
- 2008-07-16 BR BRPI0813829-0A2A patent/BRPI0813829A2/pt not_active IP Right Cessation
- 2008-07-16 KR KR1020107001256A patent/KR20100051616A/ko not_active Application Discontinuation
- 2008-07-16 ES ES08775124T patent/ES2358381T3/es active Active
- 2008-07-16 CA CA2697130A patent/CA2697130A1/en not_active Abandoned
- 2008-07-16 US US12/668,758 patent/US8394416B2/en not_active Expired - Fee Related
- 2008-07-16 PT PT08775124T patent/PT2175866E/pt unknown
- 2008-07-16 EP EP08775124A patent/EP2175866B1/en not_active Not-in-force
- 2008-07-16 JP JP2010516501A patent/JP2010533758A/ja active Pending
- 2008-07-16 AT AT08775124T patent/ATE493136T1/de active
- 2008-07-16 PL PL08775124T patent/PL2175866T3/pl unknown
-
2010
- 2010-08-03 HK HK10107371.2A patent/HK1140945A1/xx not_active IP Right Cessation
-
2011
- 2011-03-11 HR HR20110181T patent/HRP20110181T1/hr unknown
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