Preparation of thermoresponsive cationic copolymer brush surfaces and application of the surface to separation of biomolecules

被引:110
作者
Nagase, Kenichi [1 ]
Kobayashi, Jun [1 ]
Kikuchi, Akihiko [2 ]
Akiyama, Yoshikatsu [1 ]
Kanazawa, Hideko [3 ]
Okano, Teruo [1 ]
机构
[1] Tokyo Womens Med Univ, Inst Adv Biomed Engn & Sci, Shinjuku Ku, Tokyo 1628666, Japan
[2] Tokyo Univ Sci, Dept Mat Sci & Technol, Chiba 2788510, Japan
[3] Kyoritsu Univ Pharm, Dept Phys Pharmaceut Chem, Minato Ku, Tokyo, Japan
关键词
D O I
10.1021/bm701427m
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have prepared poly(N-isopropylacrylamide (IPAAm)-co-2-(dimethylamino)ethylmethacrylate (DMAEMA)) brush-grafted silica bead surfaces through surface-initiated atom transfer radical polymerization (ATRP) using the CuCl/CuCl2/Me6TREN catalytic system in 2-propanol at 25 degrees C for 16 h. The prepared temperature-responsive surfaces were characterized by chromatographic analysis using the modified silica beads as stationary phases. Chromatographic retention times for adenosine nucleotides in aqueous mobile phases were significantly increased compared to that previously reported for other cationic hydrogel surfaces, indicating that strong electrostatic cationic copolymer brush interactions occur between the surfaces and nucleotide analytes. Retention times for adenosine nucleotides significantly decreased with increasing column temperature, explained by the decreasing basicity in the copolymer with increasing temperature. Step-temperature gradients from 10 to 50 degrees C shorten ATP retention times. These results indicate that cationic copolymer brush surfaces prepared by ATRP can rapidly alter their electrostatic properties by changing aqueous temperature.
引用
收藏
页码:1340 / 1347
页数:8
相关论文
共 36 条
[1]   Separation of nucleotides with an aqueous mobile phase using pH- and temperature-responsive polymer modified packing materials [J].
Ayano, E ;
Sakamoto, C ;
Kanazawa, H ;
Kikuchi, A ;
Okano, T .
ANALYTICAL SCIENCES, 2006, 22 (04) :539-543
[2]   Thermal response of poly(N-isopropylacrylamide) brushes probed by surface plasmon resonance [J].
Balamurugan, S ;
Mendez, S ;
Balamurugan, SS ;
O'Brien, MJ ;
López, GP .
LANGMUIR, 2003, 19 (07) :2545-2549
[3]   Thermo-responsive polymer nanoparticles with a core-shell micelle structure as site-specific drug carriers [J].
Cammas, S ;
Suzuki, K ;
Sone, C ;
Sakurai, Y ;
Kataoka, K ;
Okano, T .
JOURNAL OF CONTROLLED RELEASE, 1997, 48 (2-3) :157-164
[4]   SITE-SPECIFIC CONJUGATION OF A TEMPERATURE-SENSITIVE POLYMER TO A GENETICALLY-ENGINEERED PROTEIN [J].
CHILKOTI, A ;
CHEN, GH ;
STAYTON, PS ;
HOFFMAN, AS .
BIOCONJUGATE CHEMISTRY, 1994, 5 (06) :504-507
[5]   Thermo-responsive drug delivery from polymeric micelles constructed using block copolymers of poly(N-isopropylacrylamide) and poly(butylmethacrylate) [J].
Chung, JE ;
Yokoyama, M ;
Yamato, M ;
Aoyagi, T ;
Sakurai, Y ;
Okano, T .
JOURNAL OF CONTROLLED RELEASE, 1999, 62 (1-2) :115-127
[6]   5-COORDINATED HIGH-SPIN COMPLEXES OF BIVALENT COBALT NICKEL AND COPPER WITH TRIS(2-DIMETHYLAMINOETHYL)AMINE [J].
CIAMPOLINI, M ;
NARDI, N .
INORGANIC CHEMISTRY, 1966, 5 (01) :41-+
[7]   Temperature-responsive cell culture surfaces enable "on-off" affinity control between cell integrins and RGDS ligands [J].
Ebara, M ;
Yamato, M ;
Aoyagi, T ;
Kikuchi, A ;
Sakai, K ;
Okano, T .
BIOMACROMOLECULES, 2004, 5 (02) :505-510
[8]   MUTUAL INFLUENCE OF PH AND TEMPERATURE ON THE SWELLING OF IONIZABLE AND THERMOSENSITIVE HYDROGELS [J].
FEIL, H ;
BAE, YH ;
FEIJEN, J ;
KIM, SW .
MACROMOLECULES, 1992, 25 (20) :5528-5530
[9]  
Heskins M., 1968, J MACROMOL SCI CHEM, V2, P1441, DOI [10.1080/10601326808051910, DOI 10.1080/10601326808051910]
[10]   Thermal modulated interaction of aqueous steroids using polymer-grafted capillaries [J].
Idota, N ;
Kikuchi, A ;
Kobayashi, J ;
Akiyama, Y ;
Okano, T .
LANGMUIR, 2006, 22 (01) :425-430