TWI753292B - 耐鹽的多孔介質 - Google Patents
耐鹽的多孔介質 Download PDFInfo
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- TWI753292B TWI753292B TW108130814A TW108130814A TWI753292B TW I753292 B TWI753292 B TW I753292B TW 108130814 A TW108130814 A TW 108130814A TW 108130814 A TW108130814 A TW 108130814A TW I753292 B TWI753292 B TW I753292B
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- Prior art keywords
- porous medium
- porous
- polymerized monomer
- monomer
- glycol diglycidyl
- Prior art date
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- 150000003839 salts Chemical class 0.000 title description 4
- 239000012528 membrane Substances 0.000 claims abstract description 40
- 239000000178 monomer Substances 0.000 claims abstract description 40
- 239000012530 fluid Substances 0.000 claims abstract description 22
- 238000000034 method Methods 0.000 claims abstract description 18
- 238000000576 coating method Methods 0.000 claims abstract description 16
- 229920000642 polymer Polymers 0.000 claims abstract description 16
- 239000011248 coating agent Substances 0.000 claims abstract description 15
- 229910052751 metal Inorganic materials 0.000 claims abstract description 13
- 239000002184 metal Substances 0.000 claims abstract description 13
- 102000004169 proteins and genes Human genes 0.000 claims abstract description 10
- 108090000623 proteins and genes Proteins 0.000 claims abstract description 10
- 150000002739 metals Chemical class 0.000 claims abstract description 9
- 229920006037 cross link polymer Polymers 0.000 claims abstract description 7
- 239000011324 bead Substances 0.000 claims abstract description 4
- 239000000835 fiber Substances 0.000 claims abstract description 4
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- 239000000203 mixture Substances 0.000 claims description 12
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 11
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- 239000002202 Polyethylene glycol Substances 0.000 claims description 6
- 239000003431 cross linking reagent Substances 0.000 claims description 6
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims description 6
- 229920001223 polyethylene glycol Polymers 0.000 claims description 6
- 125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 6
- HDPLHDGYGLENEI-UHFFFAOYSA-N 2-[1-(oxiran-2-ylmethoxy)propan-2-yloxymethyl]oxirane Chemical compound C1OC1COC(C)COCC1CO1 HDPLHDGYGLENEI-UHFFFAOYSA-N 0.000 claims description 5
- AOBIOSPNXBMOAT-UHFFFAOYSA-N 2-[2-(oxiran-2-ylmethoxy)ethoxymethyl]oxirane Chemical compound C1OC1COCCOCC1CO1 AOBIOSPNXBMOAT-UHFFFAOYSA-N 0.000 claims description 5
- 229910006069 SO3H Inorganic materials 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 239000012535 impurity Substances 0.000 claims description 4
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
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- 238000004519 manufacturing process Methods 0.000 claims description 3
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- ZZXDRXVIRVJQBT-UHFFFAOYSA-M Xylenesulfonate Chemical compound CC1=CC=CC(S([O-])(=O)=O)=C1C ZZXDRXVIRVJQBT-UHFFFAOYSA-M 0.000 claims description 2
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- CQVKMVQRSNNAGO-UHFFFAOYSA-N 2-[4-formyl-3-methyl-n-(2-methylsulfonyloxyethyl)anilino]ethyl methanesulfonate Chemical compound CC1=CC(N(CCOS(C)(=O)=O)CCOS(C)(=O)=O)=CC=C1C=O CQVKMVQRSNNAGO-UHFFFAOYSA-N 0.000 claims 1
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- ZNZYKNKBJPZETN-WELNAUFTSA-N Dialdehyde 11678 Chemical compound N1C2=CC=CC=C2C2=C1[C@H](C[C@H](/C(=C/O)C(=O)OC)[C@@H](C=C)C=O)NCC2 ZNZYKNKBJPZETN-WELNAUFTSA-N 0.000 claims 1
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- VAZSKTXWXKYQJF-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)OOS([O-])=O VAZSKTXWXKYQJF-UHFFFAOYSA-N 0.000 description 5
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 5
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- XFTALRAZSCGSKN-UHFFFAOYSA-M sodium;4-ethenylbenzenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC=C(C=C)C=C1 XFTALRAZSCGSKN-UHFFFAOYSA-M 0.000 description 2
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- HQOVXPHOJANJBR-UHFFFAOYSA-N 2,2-bis(tert-butylperoxy)butane Chemical compound CC(C)(C)OOC(C)(CC)OOC(C)(C)C HQOVXPHOJANJBR-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
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Abstract
所揭示者為一種多孔介質,例如:珠粒、纖維或膜,其包括多孔撐體以及經交聯的聚合物塗層,其中該經交聯的聚合物塗層的聚合物包含至少一種經聚合的單體(A)、至少一種經聚合的單體(B)、至少一種經聚合的單體(C),其中單體(A)-(C)如本文中所定義。還揭示了製備所述多孔介質的方法,以及處理含有所欲蛋白質與一或多種帶負電荷的物質之流體的方法,或從用於微電子產業的有機溶劑中移除金屬的方法。
Description
本發明係關於多孔介質,以及製備所述多孔介質的方法,以及處理流體或從有機溶劑中移除金屬的方法。
單株抗體(mAb)的生產及其純化由於該過程的高成本持續造成問題。分離過程中生物分子必須經歷的數個純化步驟導致了高成本。舉例來說,純化步驟中的一個步驟是蛋白質A親和力層析,其中葡萄球菌的蛋白質A以高選擇性以及與Fab區域(藥物分子的活性區域)極小的交互作用與第1、2及4亞型的IgG分子結合。隨著生物科技市場的快速成長,這些純化步驟的改良對於將生物製劑及時地並以降低的成本引進市場變得更令人嚮往也更有價值。
在蛋白質純化期間,使用離子交換介質的精緻純化(polishing)步驟需要介質不僅對雜質要有選擇性,而且還要是具有高鹽導電率(例如:高達15mS/cm或更高)的耐受性原料。
前述內容顯示仍需要不僅對雜質有選擇性、而且還是具有高鹽導電率的耐受性原料的離子交換介質。
此外,對於用於微電子產業中可有效率地從微電子濕蝕刻化學物質(wet etching chemicals,WEC)及在微影術過程中移除痕量金屬離子的離子交換介質,仍存在有未滿足的需求。
本發明提供了多孔介質,例如:珠粒、纖維與膜,其包含帶有負電荷之經交聯的聚合物。所述介質具有耐鹽特性以及對於生物製劑、抗體及/或蛋白質(例如:IgG)在流速10CV/min時高達170mg/mL的高動態結合能力(dynamic binding capacity,DBC)。所述多孔介質亦有強力移除存在於有機溶劑(例如:用於微電子產業中的有機溶劑)中之金屬的能力。
圖1概要式地描繪根據本發明的一個具體實例之多孔介質(例如:膜)的製備。
圖2概要式地描繪根據本發明另一具體實例之多孔介質(例如:膜)的製備。
圖3描繪注射聚(磺酸丙烯醯胺基-2-甲基丙酯-共-(胺基丙基)甲基丙烯醯胺-共-N,N-二甲基丙烯醯胺)樣本之三合一偵測(triple detection)溶析特徵,其中1表示折射率(refractive index,RI),3表示黏度,2表示相對角雷射光散射(relative angle laser light scattering,RALS)數據,且4表示log MW。
圖4描繪根據本發明的一個具體實例注射聚(磺酸丙烯醯胺基-2-甲基丙酯-共-(胺基丙基)甲基丙烯醯胺-共-N,N-二甲基丙烯醯胺)樣本所獲得之MW分布圖的疊合,其中1表示標準化的重量分率(WF/dlog MW),2表示累積重量分率,且3表示馬克-霍溫克-櫻田(Mark-Houwink-Sakurada)圖(log([] vs log(M))。
圖5描繪根據實施例8之多孔膜在不同鹽濃度下之IgG 10%突破DBC。
圖6描繪圖5中所例示的多孔膜之IgG 10%突破DBC(實心黑柱)
比上市面上可購得的膜Natrix Sb-HD的突破表現(灰柱)。
圖7描繪實施例8之多孔膜的痕量金屬移除效率。
本發明提供耐鹽多孔介質,其包含多孔撐體以及經交聯的聚合物塗層,其中該經交聯的聚合物塗層包含至少一種經聚合的單體(A),至少一種經聚合的單體(B),以及至少一種經聚合的單體(C),其中單體(A)具有下式:CH2=C(R1)-C(=O)-NH-(CH2)n-NR2R3,其中n是1-6,單體(B)具有下式:CH2=C(R4)-C(=O)-NR5R6,且單體(C)具有下式:CH2=C(R8)-C(=O)-NH-C(R7)2-(CH2)m-X,其中m是1-3且X是SO3H或COOH;其中R1、R4及R8獨立地為H或C1-C6烷基,且R2、R3、R5、R6及R7獨立地為H、C1-C6烷基、C6-C10芳基、甲氧基甲基或三苯甲基。
在一個具體實例中,R1是C1-C6烷基且R4是H。在另一個具體實例中,R1是C1-C6烷基,R4是H,且R8是H。
本申請案通篇中,C1-C6烷基基團可具有1、2、3、4、5或6個碳原子;所述烷基基團可為線性或分支。烷基基團的實例包括甲基、乙基、正丙基、異丙基、正丁基、異丁基、三級丁基、正戊基、2-甲基丁基、正己基、2-甲基戊基及3-甲基戊基。
在本發明的一個具體實例中,R1是甲基。
在以上具體實例中的任一者中,R2及R3是H,且R5及R6獨立地是C1-C6烷基。
在以上具體實例中的任一者中,R2及R3是H,且R5及R6是甲基。
在以上具體實例中的任一者中,R2、R3、R5及R6獨立地是H、甲基、苯基、甲氧基甲基或三苯甲基。
在某些具體實例中,R2及R3是H,且R5及R6獨立地是甲基、苯基、甲氧基甲基或三苯甲基。
在以上具體實例中的任一者中,R7是烷基,較佳地為甲基。
在以上具體實例中的任一者中,所述共聚物包含一種經聚合的單體(A)、一種經聚合的單體(B)及一種經聚合的單體(C)。
在以上具體實例中的任一者中,所述共聚物包含一種經聚合的單體(A)、一種經聚合的單體(B)及兩種不同的經聚合的單體(C)。
在以上具體實例中的任一者中,經聚合的單體(C)的一種中的X是SO3H且在另一種經聚合的單體(C)中的X是COOH。
在一個具體實例中,所述介質是多孔膜。
在另一個具體實例中,所述介質是珠粒或纖維。
用於多孔介質中的離子交換聚合物可從任何合適的單體組合來製備,例如:- N,N-二甲基丙烯醯胺、N-(3-胺基丙基)甲基丙烯醯胺及磺酸2-丙烯醯胺基-2-甲基丙酯,- 磺酸2-丙烯醯胺基-2-甲基丙酯、N-(3-胺基丙基)甲基丙烯醯胺及N-異丙基丙烯醯胺,- 磺酸2-丙烯醯胺基-2-甲基丙酯、N-(3-胺基丙基)甲基丙烯醯胺及三級丁基丙烯醯胺,
- 磺酸2-丙烯醯胺基-2-甲基丙酯、N-(3-胺基丙基)甲基丙烯醯胺及乙基丙烯醯胺,- 磺酸2-丙烯醯胺基-2-甲基丙酯、N-(3-胺基丙基)甲基丙烯醯胺及苯基丙烯醯胺,- 磺酸2-丙烯醯胺基-2-甲基丙酯、N-(3-胺基丙基)甲基丙烯醯胺及二乙基丙烯醯胺,- 磺酸2-丙烯醯胺基-2-甲基丙酯、N-(3-胺基丙基)甲基丙烯醯胺及N-(異丁氧基甲基)丙烯醯胺,- 磺酸2-丙烯醯胺基-2-甲基丙酯、N-(3-胺基丙基)甲基丙烯醯胺及N-(三苯甲基)丙烯醯胺,- 磺酸2-丙烯醯胺基-2-甲基丙酯、N-(3-胺基丙基)甲基丙烯醯胺及N,N-二甲基丙烯醯胺,- 磺酸2-丙烯醯胺基-2-甲基丙酯、N-(2-胺基乙基)甲基丙烯醯胺及N-異丙基丙烯醯胺,- 磺酸2-丙烯醯胺基-2-甲基丙酯、N-(2-胺基乙基)甲基丙烯醯胺及三級丁基丙烯醯胺,- 磺酸2-丙烯醯胺基-2-甲基丙酯、N-(2-胺基乙基)甲基丙烯醯胺及苯基丙烯醯胺,- 磺酸2-丙烯醯胺基-2-甲基丙酯、N-(2-胺基乙基)甲基丙烯醯胺及二乙基丙烯醯胺,- 磺酸2-丙烯醯胺基-2-甲基丙酯、N-(2-胺基乙基)甲基丙烯醯胺及乙基丙烯醯胺,- 磺酸2-丙烯醯胺基-2-甲基丙酯、N-(2-胺基乙基)甲基丙烯醯胺及N-(異丁氧基甲基)甲基丙烯醯胺,
- 磺酸2-丙烯醯胺基-2-甲基丙酯、N-(2-胺基乙基)甲基丙烯醯胺及N-(三苯甲基)丙烯醯胺,及- 磺酸2-丙烯醯胺基-2-甲基丙酯、N-(2-胺基乙基)甲基丙烯醯胺及N,N-二甲基丙烯醯胺。
本發明在具體實例中提供以下者之一或多者:- 一種三元共聚物,其包含磺酸2-丙烯醯胺基-2-甲基丙酯、N-(3-胺基丙基)甲基丙烯醯胺及N-二甲基丙烯醯胺,- 一種三元共聚物,其包含丙烯酸、N-(3-胺基丙基)甲基丙烯醯胺及N-二甲基丙烯醯胺,- 一種三元共聚物,其包含磺酸2-丙烯醯胺基-2-甲基丙酯、N-(3-胺基丙基)甲基丙烯醯胺及N-二甲基丙烯醯胺並使用所述三元共聚物的一級胺部分在介質上交聯,- 一種三元共聚物,其包含磺酸2-丙烯醯胺基-2-甲基丙酯、胺基烷基甲基丙烯醯胺及N-二甲基丙烯醯胺,並使用所述三元共聚物的一級胺部分在介質上交聯,- 一種三元共聚物,其包含丙烯酸、N-(3-胺基丙基)甲基丙烯醯胺及N-二甲基丙烯醯胺,並使用一級的所述三元共聚物之胺部分在介質上交聯,- 一種三元共聚物,其包含磺酸2-丙烯醯胺基-2-甲基丙酯、N-(3-胺基丙基)甲基丙烯醯胺、N-二甲基丙烯醯胺或任何烷基丙烯醯胺,例如:N-三級丁基丙烯醯胺、N-苯基丙烯醯胺、N-二乙基丙烯醯胺、N-異丙基丙烯醯胺、N-乙基丙烯醯胺、N-二乙基甲基丙烯醯胺、N-(異丁氧基甲基)甲基丙烯醯胺、及N-(三苯基甲基)甲基丙烯醯胺,並使用所述三元共聚物的一級胺部分在介質上交聯,- 一種耐鹽離子交換多孔膜,其係衍生自一種三元共聚物,其包含磺酸2-丙烯醯胺基-2-甲基丙酯、N-(3-胺基丙基)甲基丙烯醯胺、N,N-二甲基丙烯醯胺或
任何烷基丙烯醯胺,例如:N-三級丁基丙烯醯胺、N-苯基丙烯醯胺、N,N-二乙基丙烯醯胺、N-異丙基丙烯醯胺、N-乙基丙烯醯胺、N,N-二乙基甲基丙烯醯胺、N-(異丁氧基甲基)甲基丙烯醯胺、及N-(三苯基甲基)甲基丙烯醯胺,並使用所述三元共聚物的一級胺部分在介質上交聯,其可有利地用於(例如)單株抗體捕獲、單株抗體精緻純化或病毒載體純化,- 一種耐鹽離子交換多孔膜,其中塗覆於多孔膜上的三元共聚物的耐鹽特性是有利地由所述聚合物的烷基丙烯醯胺部分所賦予,- 一種三元共聚物,其包含磺酸2-丙烯醯胺基-2-甲基丙酯、N-(3-胺基丙基)甲基丙烯醯胺、N-二甲基丙烯醯胺或任何烷基丙烯醯胺,例如:N-三級丁基丙烯醯胺、N-苯基丙烯醯胺、N,N-二乙基丙烯醯胺、N-異丙基丙烯醯胺、N-乙基丙烯醯胺、N,N-二乙基甲基丙烯醯胺、N-(異丁氧基甲基)甲基丙烯醯胺及N-(三苯基甲基)甲基丙烯醯胺,並使用一級胺部分在介質上交聯以形成陽離子交換多孔膜,其可有利地用於(例如)捕獲Micro E溶劑中的痕量金屬污染物,- 一種三元共聚物,其包含丙烯酸、N-(3-胺基丙基)甲基丙烯醯胺及N-二甲基丙烯醯胺,- 一種三元共聚物,其包含丙烯酸、N-(3-胺基丙基)甲基丙烯醯胺及N,N-二甲基丙烯醯胺,並使用所述三元共聚物的一級胺部分在介質上交聯,- 一種四元共聚物,其包含磺酸2-丙烯醯胺基-2-甲基丙酯、N-(3-胺基丙基)甲基丙烯醯胺、N,N-二甲基丙烯醯胺及N-三級丁基丙烯醯胺,- 一種四元共聚物,其包含磺酸2-丙烯醯胺基-2-甲基丙酯、N-(3-胺基丙基)甲基丙烯醯胺、N,N-二甲基丙烯醯胺及苯乙烯磺酸,- 一種四元共聚物,其包含磺酸2-丙烯醯胺基-2-甲基丙酯、N-(3-胺基丙基)甲基丙烯醯胺、N,N-二甲基丙烯醯胺及N-三級丁基丙烯醯胺,並使用所述四元共聚物的一級胺部分在介質上交聯,
- 一種四元共聚物,其包含磺酸2-丙烯醯胺基-2-甲基丙酯、N-(3-胺基丙基)甲基丙烯醯胺、N,N-二甲基丙烯醯胺及苯乙烯磺酸,並使用所述四元共聚物的一級胺部分在介質上交聯,- 一種四元共聚物,其包含磺酸2-丙烯醯胺基-2-甲基丙酯、N-(3-胺基丙基)甲基丙烯醯胺、N,N-二甲基丙烯醯胺及丙烯酸;及- 一種四元共聚物,其包含磺酸2-丙烯醯胺基-2-甲基丙酯、N-(3-胺基丙基)甲基丙烯醯胺、N,N-二甲基丙烯醯胺及丙烯酸,並使用所述四元共聚物的一級胺部分在介質上交聯。
所述共聚物的分子量範圍可以是任何合適的範圍,例如,從50到4000kD、100到3500kD、或200到1500kD、50到3126kD。最佳的分子量範圍是從207kD到1270kD,且在具體實例中,從50到3126kD,且較佳地從207kD到1270kD,其中所述分子量是以三合一偵測GPC分析來測定。
共聚單體可以任何合適的莫耳比存在於所述共聚物中,例如,提供在層析應用中高鹽耐受度的單體組合(特別是包含磺酸2-丙烯醯胺基-2-甲基丙酯、N-(3-胺基丙基)甲基丙烯醯胺及二甲基丙烯醯胺之三元共聚物)之範圍為從莫耳比例1:0.1:1到莫耳比例5:0.5:2。
在具體實例中,提供對於微電子溶劑應用中移除金屬離子之高離子交換能力之單體組合(特別是包含磺酸2-丙烯醯胺基-2-甲基丙酯、N-(3-胺基丙基)甲基丙烯醯胺與任何烷基丙烯醯胺(諸如N-三級丁基丙烯醯胺、N-苯基丙烯醯胺、N,N-二乙基丙烯醯胺、N-異丙基丙烯醯胺、N-乙基丙烯醯胺、N,N-二乙基甲基丙烯醯胺、N-(異丁氧基甲基)甲基丙烯醯胺、丙烯醯胺及N-(三苯甲基)甲基丙烯醯胺)的單體組合)的範圍是從莫耳比例1:0.1:1到莫耳比例5:0.5:2。
在具體實例中,對於膜的應用,影響層析應用中的鹽耐受度同時允許有效率地回收蛋白質之單體組合的範圍是從莫耳比例1:0.25:2到莫耳比例
2:0.5:1。此範圍特別可在使用包含以下者的三單體來形成在膜上交聯的聚合物的情況下應用:磺酸2-丙烯醯胺基-2-甲基丙酯、N-(3-胺基丙基)甲基丙烯醯胺與任何烷基丙烯醯胺(諸如N,N-二甲基丙烯醯胺、N-三級丁基丙烯醯胺、N-苯基丙烯醯胺、N,N-二乙基丙烯醯胺、N-異丙基丙烯醯胺、N-乙基丙烯醯胺、N,N-二乙基甲基丙烯醯胺、N-(異丁氧基甲基)甲基丙烯醯胺、丙烯醯胺及N-(三苯甲基)甲基丙烯醯胺)。
在具體實例中,當使用磺酸2-丙烯醯胺基-2-甲基丙酯、N-(3-胺基丙基)甲基丙烯醯胺及N,N-二甲基丙烯醯胺之三單體來形成在用於純化蛋白質的膜上交聯的聚合物時,提供高鹽耐受度並同時提供高達200mg/mL IgG之高動態結合能力的聚合物濃度範圍為以重量計從1%-10%。
本發明進一步提供產生多孔膜的方法,其包含:(i)使單體(A)、(B)及(C)之混合物聚合,以獲得三元共聚物,以及(ii)將(i)中所獲得的三元共聚物塗覆在多孔撐體上並原位交聯,以獲得配置於所述多孔撐體上的共聚物塗層。
單體的聚合可使用合適的起始劑進行-自由基、陽離子或陰離子起始劑,且特別是自由基起始劑,例如:熱活化自由基起始劑,諸如偶氮基化合物、過硫酸鹽、過氧化物、過酸、過乙酸鹽、及有機金屬化合物。自由基起始劑的例子包括AIBN、4,4-偶氮基雙(4-氰戊酸)、1,1'-偶氮基雙(環己烷碳腈)(1,1'-azobis(cyclohexanecarbonitrile))、過氧化苯甲醯、2,2-雙(三級丁基過氧)丁烷、1,1-雙(三級丁基過氧)環己烷、二異丙苯基過氧化物、過氧苯甲酸三級丁酯、過氧苯甲酸三級戊酯及過硫酸鉀。
根據所述方法,所述交聯包含二或多個基團,例如2、3、4或更多個交聯官能基,例如:選自二環氧化物、二醛、二鹵化物及二酯之交聯劑。例如,所述交聯劑是選自:乙二醇二環氧丙基醚、丙二醇二環氧丙基醚、甘油
基三環氧丙基醚、聚乙二醇二環氧丙基醚、二甲磺酸二醇酯與二甲苯磺酸酯及其任何組合。
本發明進一步提供一種處理含有痕量金屬之流體的方法,所述方法包含使所述流體與如上所述之介質或多孔膜接觸,並回收含有降低濃度的痕量金屬之流體。
根據本發明的一個具體實例,多孔膜可以是奈米多孔膜,例如:孔直徑為1nm至100nm之間的膜,或是微米多孔膜,例如:孔直徑為0.005μm至10μm之間的膜。
將塗層提供於其上的多孔撐體可以是任何合適的材料,例如:聚合物、金屬或陶瓷,且特別是聚合物,例如:聚碸(PSU)、聚醚碸(PES)、聚苯醚(PPE)、聚伸苯醚碸(PPES)、聚伸苯醚(PPO)、聚碳酸酯(PC)、聚(呔酮醚碸酮)(poly(phthalazinone ether sulfone ketone),PPESK)、聚醚醚酮(PEEK)、聚醚酮酮(PEKK)、聚醚醯亞胺(polyetherimide,PEI)及其摻合物。
在一個具體實例中,所述共聚物被塗覆且經交聯於以下者上以產生多孔介質或膜:多孔高密度聚乙烯膜、聚醚碸(polyether sulfone)膜、聚偏二氟乙烯膜、聚四氟乙烯膜、聚苯基碸(polyphenylsulfone)膜、聚伸苯硫(polyphenylene sulfide)膜、聚乙烯和聚丙烯膜、聚酯膜、熔噴(melt blown)聚酯膜、熔噴聚丙烯膜、纖維素膜、尼龍膜和聚氯乙烯/丙烯腈。
根據本發明之具體實例的多孔介質可以配置於容納裝置(housing)中,其包含至少一個入口及至少一個出口,並限定出至少一個入口及出口之間的流體流動路徑,其中至少一個本發明之膜或包含至少一個本發明之膜的濾器橫越所述流體流動路徑,以提供過濾裝置或過濾組件。在一個具體實例中,提供包含容納裝置的過濾裝置,所述容納裝置包含入口以及第一出口,並限定出所述入口及第一出口之間的第一流體流動路徑;以及至少一個本發明
的膜或包含至少一個本發明之膜的濾器,所述本發明的膜或包含至少一個本發明之膜的濾器被配置在容納裝置中而橫越所述第一流體流動路徑。
對於交錯流的應用,在一個具體實例中,至少一個本發明的多孔膜或包含至少一個本發明之膜的濾器被配置在容納裝置中,所述容納裝置包含至少一個入口以及至少兩個出口,並至少限定出所述入口及第一出口之間的第一流體流動路徑,以及所述入口及第二出口之間的第二流體流動路徑,其中本發明的膜或包含至少一個本發明之膜的濾器橫越所述第一流體流動路徑,以提供過濾裝置或過濾組件。在一個例示性的具體實例中,所述過濾裝置包含交錯流過濾組件、容納裝置,其包含入口、包含濃縮出口的第一出口以及包含可滲透出口的第二出口,並限定出所述入口及第一出口之間的第一流體流動路徑,以及所述入口及第二出口之間的第二流體流動路徑,其中至少一個本發明的膜或包含至少一個本發明之膜的濾器被設置於橫越所述第一流體流動路徑。
所述過濾裝置或組件可為可滅菌的。可採用任何具有合適形狀且提供入口及一或多個出口的容納裝置。
所述容納裝置可由任何合適的堅固的無法滲透的材料組裝,包含任何無法滲透的熱塑性材料,其與將處理的流體相容。舉例來說,所述容納裝置可以由金屬組裝,諸如不銹鋼,或由聚合物組裝,例如:透明或半透明的聚合物,諸如丙烯酸、聚丙烯、聚苯乙烯或聚碳酸酯樹脂。
以下實施例進一步例示本發明,但當然不應視為以任何方式限制其範圍。
實施例1
此實施例例示根據本發明的一個具體實例之三元共聚物溶液之製備方法。
製備聚(磺酸丙烯醯胺基-2-甲基丙酯-共-(胺基丙基)甲基丙烯醯胺-共-N,N-二甲基丙烯醯胺)的10%三元共聚物溶液:將磺酸2-丙烯醯胺基-2-甲基丙酯(15.6g,75mM)、N-(3-胺基丙基)甲基丙烯醯胺鹽酸鹽(4.5g,25mM)及N,N-二甲基丙烯醯胺(10g,100mM)與DI水(260g)以及8M NaOH(17.1g)混合,使混合物脫氣5分鐘,並添加過硫酸銨(0.690g,3mM)並混合。將反應混合物於60℃在氮氣下攪拌2小時,並使其冷卻至室溫以獲得三元共聚物溶液。
實施例2
此實施例例示根據本發明之另一具體實例的三元共聚物溶液之製備方法。
製備聚(苯乙烯磺酸-共-(胺基丙基)甲基丙烯醯胺-共-N,N-二甲基丙烯醯胺)的10%溶液:將4-乙烯基苯磺酸鈉(15.46g,75mM)、N-(3-胺基丙基)甲基丙烯醯胺鹽酸鹽(4.5g,25mM)及N,N-二甲基丙烯醯胺(10g,100mM)與DI水(260g)以及8M NaOH(17.1g)混合,使混合物脫氣5分鐘,且添加過硫酸銨(0.690g,3mM)。將反應混合物於60℃在氮氣下攪拌2小時,並使其冷卻至室溫以獲得三元共聚物溶液。
實施例3
此實施例例示根據本發明之另一具體實例的四元共聚物溶液之製備方法。
製備聚(磺酸丙烯醯胺基-2-甲基丙酯-共-(胺基丙基)甲基丙烯醯胺-共-N,N-二甲基丙烯醯胺-共-三級丁基丙烯醯胺),9.5%溶液:將磺酸2-丙烯醯胺基-2-甲基丙酯(10.45g,50mM)、N-(3-胺基丙基)甲基丙烯醯胺鹽酸鹽(2.24
g,12.5mM)、N,N-二甲基丙烯醯胺(5g,50mM)及三級丁基丙烯醯胺[1.6g,在IPA(9g)中12.6mM]與DI水(164.7g)及8M NaOH(10g)混合,使混合物脫氣5分鐘,並添加過硫酸銨(0.431g,1.9mM)。將反應混合物於60℃在氮氣下攪拌2小時,並使其冷卻至室溫以獲得上述四元共聚物溶液。
實施例4
此實施例例示根據本發明之另一具體實例的四元共聚物溶液之製備方法。
製備聚(磺酸丙烯醯胺基-2-甲基丙酯-共-(胺基丙基)甲基丙烯醯胺-共-N,N-二甲基丙烯醯胺-共-丙烯酸),10%溶液:將磺酸2-丙烯醯胺基-2-甲基丙酯(7.3g,35.3mM)、N-(3-胺基丙基)甲基丙烯醯胺鹽酸鹽(2.52g,14.1mM)、N,N-二甲基丙烯醯胺(7g,70.6mM)及丙烯酸[2.54g,在IPA(9g)中35.3mM]在DI水(155g)及8M NaOH(10g)中混合,使混合物脫氣5分鐘,並添加過硫酸銨(0.532g,2.3mM)。將反應混合物於60℃在氮氣下攪拌2小時,並使其冷卻至室溫以獲得上述四元共聚物溶液。
實施例5
此實施例例示根據本發明之進一步具體實例的四元共聚物溶液之製備方法。
製備聚(磺酸丙烯醯胺基-2-甲基丙酯-共-(胺基丙基)甲基丙烯醯胺-共-N,N-二甲基丙烯醯胺-共-苯乙烯磺酸),8%溶液:將4-乙烯基苯磺酸鈉(4.16g,20mM)、N-(3-胺基丙基)甲基丙烯醯胺鹽酸鹽(1.8g,10mM)、磺酸2-丙烯醯胺基-2-甲基丙酯(4.18g,20mM)及N,N-二甲基丙烯醯胺(4g,40mM)在含有8M NaOH(17.1g)的DI水(156.34g)中混合,脫氣5分鐘,接著添加過
硫酸銨(0.690g,3mM)。將反應混合物於60℃在氮氣下攪拌2小時,並使其冷卻至室溫以獲得上述共聚物溶液。
實施例6
此實施例例示根據本發明的一個具體實例之多孔膜的製備方法。
5%磺化聚合物塗層(100g混合):將10%來自實施例1的磺化聚合物(50g)與水(49g)、聚乙二醇二環氧丙基醚(150mg)及Triton X-100(850mg)混合,並攪拌至溶解。使用NaOH溶液將溶液的pH調整至10,以獲得塗層溶液。藉由浸泡塗覆以塗層溶液塗覆孔直徑3μm的HDPE膜。將經塗覆的膜夾在兩個移液管中間並從上往下刮過以提供HDPE膜上的薄塗層。使所述膜上的塗層在65℃下交聯一小時或在室溫下交聯隔夜。將得到的膜在冷水中淋溶(leach)24小時並使其乾燥。
實施例7
此實施例例示根據本發明的另一個具體實例之多孔膜的製備方法。
使磺酸2-丙烯醯胺基-2-甲基丙酯(104.5g,504mmol)與N,N-二甲基丙烯醯胺(50g,504mmol)、N-(3-胺基丙基)甲基丙烯醯胺HCl(22.4g,126mmol)與含有170g異丙醇的DI水(1.524kg)混合。以8M NaOH(100g)將混合物的pH值調整至9.6。使反應混合物以氮氣脫氣15分鐘,並添加過硫酸銨(3.88g 1.5mol%)。將混合物在60℃下攪拌2小時,並冷卻至室溫以獲得10%的聚合物溶液。
從上述10%聚合物溶液與0.85% Triton X100界面活性劑及0.45%二環氧化物交聯劑(聚乙二醇二環氧丙基醚)製備4%聚合物塗層溶液。調整所
述溶液的pH值至10,並以上述溶液浸泡塗覆孔直徑3μm的HDPE膜。將經塗覆的膜在65℃下熱交聯一小時,在DI水中淋溶隔夜,並在65℃下乾燥隔夜。
實施例8
此實施例例示根據本發明的一個具體實例的膜移除痕量金屬的能力。
基線:0.2μm膜樣本以100mL的IPA(10mL/min)、200mL的DIW、100mL的5% HCl、200mL DI水以及200mL的IPA沖洗。收集100mL的樣本,並以ICP-MS進行金屬分析。
金屬試驗(challenge):將得自實施例7的0.2μm膜樣本以加料的IPA(1ppb的金屬)在7mL/min的流出速度下進行試驗。將一開始的10mL流出物棄置,並將接下來的10mL流出物收集至PFA瓶中。使用ICP-MS進行金屬分析。以n=2重複此實驗。
所有本文中所引用的參考文獻,包括出版品、專利申請案及專利案皆以引用的方式併入,其程度等同於各參考文獻被各別且特定指出藉由引用的方式併入並且將其全部內容於本文中闡述。
除非於本文中以其他方式指明或是明確與前後文抵觸,術語「一(a)」和「一(an)」和「該/所述(the)」及「至少一個」以及類似的指示對象之使用在描述本發明的前後文中(特別是在以下申請專利範圍的前後文中)被認為是涵蓋單數及複數兩種情況。除非於本文中以其他方式指明或是明確與前後文抵觸,與一或多個項目之清單並用的術語「至少一」(例如:A及B中至少一者)之使用被認為是表示選自所列項目中的一項(A或B)或所列項目中二或多項的任意組合(A及B)。除非特別註明,術語「包含(comprising)」、「具有(having)」、「包括(including)」及「含有(containing)」被認為是開放適式用
語(即,意思是「包括,但不限於」)。除非於本文中特別指出,本文中數值的範圍之陳述僅用於作為引用落入該範圍中各個分別數值的簡略表達方式,且各個分別數值以如同已被各別詳列的方式併入說明書中。除非於本文中以其他方式指明或是明確與前後文抵觸,本文中所描述的所有方法可用任何合適的順序進行。除非以其他方式聲明,本文中所提供的任何以及所有實例的使用,或是示範性用語(例如:「諸如」),僅用於較佳地闡明本發明且並未對發明範圍作出限制。說明書中沒有用語應被視為指出任何非主張之要素對本發明的實施而言是必要的。
本文中描述了本發明的較佳具體實例,包括發明人所知實施本發明的最佳模式。在閱讀以上描述後,這些較佳具體實例的變異形式對於發明所屬技術領域中具有通常知識者而言可變得明顯。發明人預期發明所屬技術領域中具有通常知識者在適當時採用這些變異形式,且發明人意欲使本發明可以藉由本文中特定描述者以外的方式實施。因此,本發明如適當的法律所許可地包括本文所附的申請專利範圍中所陳述之標的的所有修改形式與等效形式。此外,除非於本文中以其他方式指明或是明確與前後文抵觸,本發明的範圍涵蓋任何前述要素以其所有可能的變異形式之組合。
Claims (20)
- 一種多孔介質,其包含多孔撐體以及經交聯的聚合物塗層,其中所述經交聯的聚合物塗層之聚合物包含至少一種經聚合的單體(A)、至少一種經聚合的單體(B)、至少一種經聚合的單體(C),以及交聯劑,所述交聯劑係選自丙二醇二環氧丙基醚、甘油基三環氧丙基醚、丙二醇二環氧丙基醚、聚乙二醇二環氧丙基醚、二醛、二鹵化物、二酯、二磺醯氯(disulfonyl chloride)及二醯鹵化物(diacyl halide),其中單體(A)具有下式:CH2=C(R1)-C(=O)-NH-(CH2)n-NR2R3,其中n是1-6,單體(B)具有下式:CH2=C(R4)-C(=O)-NR5R6,且單體(C)具有下式:CH2=C(R8)-C(=O)-NH-C(R7)2-(CH2)m-X,其中m是1-3且X是SO3H或COOH;其中R1、R4及R8獨立地為H或C1-C6烷基,且R2、R3、R5、R6及R7獨立地為H、C1-C6烷基、C6-C10芳基、甲氧基甲基或三苯甲基。
- 如請求項1之多孔介質,其中R1是C1-C6烷基且R4是H。
- 如請求項1或2之多孔介質,其中R1是甲基。
- 如請求項1或2之多孔介質,其中R2及R3是H,且R5及R6獨立地是C1-C6烷基。
- 如請求項1或2之多孔介質,其中R2及R3是H,且R5及R6是甲基。
- 如請求項1或2之多孔介質,其中R2、R3、R5及R6獨立地是H、甲基、苯基、甲氧基甲基或三苯甲基。
- 如請求項1或2之多孔介質,其中R2及R3是H,且R5及R6獨立地是甲基、苯基、甲氧基甲基或三苯甲基。
- 如請求項1或2之多孔介質,其中R7是烷基。
- 如請求項8之多孔介質,其中R7是甲基。
- 如請求項1或2之多孔介質,其中所述聚合物包含一種經聚合的單體(A)、一種經聚合的單體(B)及一種經聚合的單體(C)。
- 如請求項1或2之多孔介質,其中所述聚合物包含一種經聚合的單體(A)、一種經聚合的單體(B)及兩種不同的經聚合的單體(C)。
- 如請求項11之多孔介質,其中在一種經聚合的單體(C)中的X是SO3H且在另一種經聚合的單體(C)中的X是COOH。
- 如請求項1或2之多孔介質,其為多孔膜。
- 如請求項1或2之多孔介質,其為珠粒或纖維。
- 一種用於製造如請求項1-14中任一項之多孔介質的方法其包含:(i)使單體(A)、(B)及(C)之混合物聚合,以獲得三元共聚物,以及(ii)將(i)中所獲得的三元共聚物與交聯劑塗覆在多孔撐體上,並原位交聯以獲得配置於所述多孔撐體上經交聯的三元共聚物塗層,所述交聯劑係選自丙二醇二環氧丙基醚、甘油基三環氧丙基醚、丙二醇二環氧丙基醚、聚乙二醇二環氧丙基醚、二醛、二鹵化物、二酯、二磺醯氯及二醯鹵化物。
- 如請求項15之方法,其中該交聯劑是選自丙二醇二環氧丙基醚、甘油基三環氧丙基醚、聚乙二醇二環氧丙基醚、二甲磺酸二醇酯、及二醇二甲磺醯氯(glycol dimesoyl chloride)、二甲苯磺酸酯及其任何組合。
- 一種處理含有所欲蛋白質及一或多種雜質之流體的方法,該方 法包含使所述流體與如請求項1-14中任一項之多孔介質接觸,並以所述雜質濃度降低的情況回收所欲蛋白質。
- 如請求項17之方法,其中所欲蛋白質是抗體。
- 如請求項17之方法,其中所欲蛋白質是生物製劑。
- 一種處理含有痕量金屬之流體的方法,該方法包含使所述流體與如請求項1-12中任一項或請求項14之多孔介質或請求項13之多孔膜接觸,並回收含有降低濃度的痕量金屬之流體。
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JP6904510B2 (ja) | 2021-07-14 |
JP2020037099A (ja) | 2020-03-12 |
TW202019554A (zh) | 2020-06-01 |
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EP3617256A1 (en) | 2020-03-04 |
IL269013B1 (en) | 2023-12-01 |
EP3617256B1 (en) | 2022-01-19 |
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