致孔剂溶解度参数对大孔层析介质的结构影响研究
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摘要
分别以甲基丙烯酸缩水甘油醚酯和乙二醇二甲基丙烯酸酯为功能单体和交联剂,采用悬浮聚合方法制备了大孔聚合物微球。考察了致孔剂的组成及用量对微球的孔径、比表面积的影响,其中随着致孔剂中的良溶剂(二氯甲烷δ=9.7(cal/cm~3)~(1/2)和不良溶剂(正辛醇δ=10.3(cal/cm~3)~(1/2)的比例变化,致孔剂体系溶解度参数可调范围为9.89~10.09(cal/cm~3)~(1/2),随着致孔剂与聚合物之间溶解度差值的增加,微球的孔径随之增大而比表面积呈下降趋势。将此类微球偶联聚乙烯亚胺衍生为阴离子交换层析介质,以前沿分析法比较了不同孔径的微球的传质性能,其中孔径为257 nm的介质仍能保持较高的动态蛋白载量(45.1 mg/m L),表明此类大孔介质在高通量分离纯化应用方面具有很大潜力。
The macroporous microspheres were prepared through suspension polymerization and based on a copolymer of glycidyl methacrylate and ethylene glycol dimethacrylate. The effect of porogen on the microspheres structure was evaluated in terms of pore size and surface area. Porogen contained dichloromethane( δ = 9.7( cal/cm~3)~(1/2) and N-octanol( δ= 10.3( cal/cm~3)~(1/2) which corresponded to a good and poor solvent,respectively. The solubility parameter of porogen was controlled in the range of 9.89-10.09( cal/cm~3)~(1/2). The pore size of microspheres increased with the difference value of solubility parameter between the polymer and the porogen. On the contrary,the surface area of microspheres decreased in this study. The anion exchange media was prepared through coupling poly( ethylene imine) in the microspheres,and the proteins transport was determined by frontal analysis method. The macroporous microspheres with257 nm pore size could still afford a high proteins capacity( 45. 1 mg/m L). These macroporous supports showed a large potential in a rapid separation of proteins.
The macroporous microspheres were prepared through suspension polymerization and based on a copolymer of glycidyl methacrylate and ethylene glycol dimethacrylate. The effect of porogen on the microspheres structure was evaluated in terms of pore size and surface area. Porogen contained dichloromethane( δ = 9.7( cal/cm~3)~(1/2) and N-octanol( δ= 10.3( cal/cm~3)~(1/2) which corresponded to a good and poor solvent,respectively. The solubility parameter of porogen was controlled in the range of 9.89-10.09( cal/cm~3)~(1/2). The pore size of microspheres increased with the difference value of solubility parameter between the polymer and the porogen. On the contrary,the surface area of microspheres decreased in this study. The anion exchange media was prepared through coupling poly( ethylene imine) in the microspheres,and the proteins transport was determined by frontal analysis method. The macroporous microspheres with257 nm pore size could still afford a high proteins capacity( 45. 1 mg/m L). These macroporous supports showed a large potential in a rapid separation of proteins.
引文
1 Josic'D,Horn H,Schulz P,Schwinn H,Britsch L.J.Chromatogr.A,1998,796(2):289-298
2 Zhang R Y,Li Q,Li J,Zhou W Q,Ye P L,Gao Y,Ma G H,Su Z G.Mat.Sci.Eng.C,2012,32(8):2628-2633
3 Hahn R,Schlegel R,Jungbauer A.J.Chromatogr.B,2003,790(1):35-51
4 Noubar B A,Brookline M,Fred E R,West L I,Robert C D,Norwich J V.US Patent,5019270,1991
5 Wu L,Bai S,Sun Y.Biotechnol.Prog.,2003,19:1300-1306
6 Zhang M L,Sun Y.J.Chromatogr.A,2001,922(1-2):77-86
7 Zhou W Q,Gu T Y,Su Z G,Ma G H.Polymer,2007,48:1981-1988
8 Zhou W Q,Gu T Y,Su Z G,Ma G H.Eur.Polym.J.,2007,43(10):4493-4502
9 Svec F,Fréchet J M J.Chem.Mater.,1995,7:707-715
10 Zhou X,Xue B,Bai S,Sun Y.Biochem.Eng.J.,2002,11:13-17
11 ZHANG Rong-Yue,PAN Yi-Ting,JI De-Kun,LIU Cai.China Patent,20151046635465,2015张荣月,潘一廷,冀德坤,刘才.中国专利,2015104635465,2015
12 YU Tian,XU Cheng-Nan,YU Yuan,ZHAO Fei-Fei,PAN Yi-Ting,LIU Cai,HUANG Yong-Dong,ZHANG Rong-Yue.Chem.J.Chinese Universities,2016,37(9):1740-1743虞天,许成楠,于嫄,赵飞飞,潘一廷,刘才,黄永东,张荣月.高等学校化学学报,2016,37(9):1740-1743
13 Zhang R Y,Li Q,Gao Y,Li J,Huang Y D,Song C,Zhou W Q,Ma G H,Su Z G.J.Chromatogr.A,2014,1343:109-118
14 YU Yuan,WU Xing-Lan,LI Yin,HUANG Yi-Kang,JIANG Cheng-Wei,ZHAO Fei-Fei,WU Jie,ZHANG Rong-Yue.Chinese J.Anal.Chem.,2016,44(12):1874-1879于嫄,吴兴兰,李尹,黄逸康,姜成伟,赵飞飞,吴颉,张荣月.分析化学,2016,44(12):1874-1879
15 LIU Yu-Tang.Wuhan Huagong,1994,(3):1-21柳玉堂.武汉化工,1994,(3):1-21
16 Wu Y G,Dicky A,Giorgio C.J.Chromatogr.A,2015,1375:92-100
17 ZHENG Yu-Ying.Preparation and Characterization of Polymer Microspheres by Disperse Polymerization.Beijing:Science Press,2017:15郑玉婴.聚合物微球分散聚合法制备、结构及性能.北京:科学出版社,2017:15
2 Zhang R Y,Li Q,Li J,Zhou W Q,Ye P L,Gao Y,Ma G H,Su Z G.Mat.Sci.Eng.C,2012,32(8):2628-2633
3 Hahn R,Schlegel R,Jungbauer A.J.Chromatogr.B,2003,790(1):35-51
4 Noubar B A,Brookline M,Fred E R,West L I,Robert C D,Norwich J V.US Patent,5019270,1991
5 Wu L,Bai S,Sun Y.Biotechnol.Prog.,2003,19:1300-1306
6 Zhang M L,Sun Y.J.Chromatogr.A,2001,922(1-2):77-86
7 Zhou W Q,Gu T Y,Su Z G,Ma G H.Polymer,2007,48:1981-1988
8 Zhou W Q,Gu T Y,Su Z G,Ma G H.Eur.Polym.J.,2007,43(10):4493-4502
9 Svec F,Fréchet J M J.Chem.Mater.,1995,7:707-715
10 Zhou X,Xue B,Bai S,Sun Y.Biochem.Eng.J.,2002,11:13-17
11 ZHANG Rong-Yue,PAN Yi-Ting,JI De-Kun,LIU Cai.China Patent,20151046635465,2015张荣月,潘一廷,冀德坤,刘才.中国专利,2015104635465,2015
12 YU Tian,XU Cheng-Nan,YU Yuan,ZHAO Fei-Fei,PAN Yi-Ting,LIU Cai,HUANG Yong-Dong,ZHANG Rong-Yue.Chem.J.Chinese Universities,2016,37(9):1740-1743虞天,许成楠,于嫄,赵飞飞,潘一廷,刘才,黄永东,张荣月.高等学校化学学报,2016,37(9):1740-1743
13 Zhang R Y,Li Q,Gao Y,Li J,Huang Y D,Song C,Zhou W Q,Ma G H,Su Z G.J.Chromatogr.A,2014,1343:109-118
14 YU Yuan,WU Xing-Lan,LI Yin,HUANG Yi-Kang,JIANG Cheng-Wei,ZHAO Fei-Fei,WU Jie,ZHANG Rong-Yue.Chinese J.Anal.Chem.,2016,44(12):1874-1879于嫄,吴兴兰,李尹,黄逸康,姜成伟,赵飞飞,吴颉,张荣月.分析化学,2016,44(12):1874-1879
15 LIU Yu-Tang.Wuhan Huagong,1994,(3):1-21柳玉堂.武汉化工,1994,(3):1-21
16 Wu Y G,Dicky A,Giorgio C.J.Chromatogr.A,2015,1375:92-100
17 ZHENG Yu-Ying.Preparation and Characterization of Polymer Microspheres by Disperse Polymerization.Beijing:Science Press,2017:15郑玉婴.聚合物微球分散聚合法制备、结构及性能.北京:科学出版社,2017:15
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