Preparation of a thermoresponsive polymer grafted polystyrene monolithic capillary for the separation of bioactive compounds

被引:10
作者
Koriyama, Takuya [1 ]
Asoh, Taka-Aki [1 ,2 ]
Kikuchi, Akihiko [1 ]
机构
[1] Tokyo Univ Sci, Dept Mat Sci & Technol, Katsushika Ku, 6-3-1 Niijuku, Tokyo 1258585, Japan
[2] Osaka City Univ, OCU Adv Res Inst Nat Sci & Technol, Sumiyoshi Ku, 3-3-138 Sugimotocho, Osaka 5588585, Japan
关键词
Poly(N-isopropylacrylamide); Polymer monolith; Capillary column; SI-ATRP; Thermoresponsive chromatography; LIQUID-CHROMATOGRAPHY; AQUEOUS CHROMATOGRAPHY; SURFACES; COLUMNS; SILICA; ADSORPTION; ATTACHMENT; PROTEINS; DELIVERY; BRUSHES;
D O I
10.1016/j.colsurfb.2016.08.021
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
To develop aqueous microseparation columns for bioactive compounds, a thermoresponsive polymer grafted polymer monolith was prepared inside silica capillaries having an I.D. of 100 pm by polymerization of styrene (St) with m/p-divinylbenzene (DVB) in the presence of polydimethylsiloxane as porogen, followed by surface-initiated atom transfer radical polymerization (SI-ATRP) of N-isopropylacrylamide (NIPAAm). SEM analysis indicated that the resulting poly(N-isopropylacrylamide) (PNIPAAm) grafted polystyrene monolith had a consecutive three-dimensionally interconnected structure and through pores, similar to the base polystyrene (PSt) monolith. The elution behavior of steroids with different hydrophobicity was evaluated using micro-high-performance liquid chromatography in sole aqueous mobile phase. Temperature dependent interaction changes were observed between steroids and the PNIPAAm modified surfaces. Furthermore, the interaction between bioactive compounds and the PNIPAAm grafted PSt surfaces was controlled and eventually separate these molecules with different hydrophobicities by simple temperature modulation in aqueous environment. The PNIPAAm grafted PSt monolithic capillary showed improved separation properties of bioactive compounds, compared with a PNIPAAm grafted hollow capillary in aqueous environment. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:408 / 415
页数:8
相关论文
共 33 条
[1]   Ultrathin poly(N-isopropylacrylamide) grafted layer on polystyrene surfaces for cell adhesion/detachment control [J].
Akiyama, Y ;
Kikuchi, A ;
Yamato, M ;
Okano, T .
LANGMUIR, 2004, 20 (13) :5506-5511
[2]   Protein Resistance of PNIPAAm Brushes: Application to Switchable Protein Adsorption [J].
Burkert, Sina ;
Bittrich, Eva ;
Kuntzsch, Marco ;
Mueller, Martin ;
Eichhorn, Klaus-Jochen ;
Bellmann, Cornelia ;
Uhlmann, Petra ;
Stamm, Manfred .
LANGMUIR, 2010, 26 (03) :1786-1795
[3]   Methacrylate monolithic columns of 320 μm ID for capillary liquid chromatography [J].
Coufal, P ;
Cihák, M ;
Suchánková, J ;
Tesarová, E ;
Bosáková, Z ;
Stulík, K .
JOURNAL OF CHROMATOGRAPHY A, 2002, 946 (1-2) :99-106
[4]   Thermoresponsive surface-grafted poly(N-isopropylacrylamide) copolymers:: Effect of phase transitions on protein and bacterial attachment [J].
Cunliffe, D ;
Alarcón, CD ;
Peters, V ;
Smith, JR ;
Alexander, C .
LANGMUIR, 2003, 19 (07) :2888-2899
[5]   Switchable surface traps for injectable bead-based chromatography in PDMS microfluidic channels [J].
Ebara, Mitsuhiro ;
Hoffman, John M. ;
Hoffman, Allan S. ;
Stayton, Patrick S. .
LAB ON A CHIP, 2006, 6 (07) :843-848
[6]   In situ control of cell adhesion using photoresponsive culture surface [J].
Edahiro, J ;
Sumaru, K ;
Tada, Y ;
Ohi, K ;
Takagi, T ;
Kameda, M ;
Shinbo, T ;
Kanamori, T ;
Yoshimi, Y .
BIOMACROMOLECULES, 2005, 6 (02) :970-974
[7]   Capillary columns with in situ formed porous monolithic packing for micro high-performance liquid chromatography and capillary electrochromatography [J].
Gusev, I ;
Huang, X ;
Horváth, C .
JOURNAL OF CHROMATOGRAPHY A, 1999, 855 (01) :273-290
[8]  
Hansch C., 1995, Exploring QSAR: Hydrophobic, Electronic, and Steric Constants
[9]   New Monolithic Capillary Columns with Well-Defined Macropores Based on Poly(styrene-co-divinylbenzene) [J].
Hasegawa, George ;
Kanamori, Kazuyoshi ;
Ishizuka, Norio ;
Nakanishi, Kazuki .
ACS APPLIED MATERIALS & INTERFACES, 2012, 4 (05) :2343-2347
[10]  
Heskins M., 1968, J Macromol Sci Chem A, V2, P1441, DOI [DOI 10.1080/10601326808051910, 10.1080/10601326808051910]