Synthesis of 5-fluorouracil-imprinted polymers with multiple hydrogen bonding interactions

被引:37
作者
Kugimiya, A [1 ]
Mukawa, T [1 ]
Takeuchi, T [1 ]
机构
[1] Hiroshima City Univ, Fac Informat Sci, Lab Synth Biochem, Asaminami Ku, Hiroshima 7313194, Japan
关键词
D O I
10.1039/b010056k
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The antitumor active compound 5-fluorouracil (5-FU) was used as a target molecule and 5-FU-imprinted polymers were synthesized using 2,6-bis(acrylamido)pyridine and/or 2-(trifluoromethyl)acrylic acid as functional monomers. The 5-FU-imprinted polymers showed a higher affinity for 5-FU than that for 5-FU derivatives. By using both functional monomers simultaneously, the affinity and separation for 5-FU were improved.
引用
收藏
页码:772 / 774
页数:3
相关论文
共 13 条
[1]  
CABALLERO GA, 1985, CANCER TREAT REP, V69, P13
[2]   Molecularly imprinted polymers and their use in biomimetic sensors [J].
Haupt, K ;
Mosbach, K .
CHEMICAL REVIEWS, 2000, 100 (07) :2495-2504
[3]  
HUAN S, 1989, CANCER, V63, P419, DOI 10.1002/1097-0142(19890201)63:3<419::AID-CNCR2820630303>3.0.CO
[4]  
2-Z
[5]   SYNTHESIS AND PROPERTIES OF POLY(THIOETHER AMIDE)S FROM 2,6-BIS(ACRYLAMIDO)PYRIDINE AND DITHIOLS [J].
OIKAWA, E ;
MOTOMI, K ;
AOKI, T .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 1993, 31 (02) :457-465
[6]  
SHEA KJ, 1994, TRENDS POLYM SCI, V2, P166
[7]  
Sugamura K, 1997, CANCER, V79, P12, DOI 10.1002/(SICI)1097-0142(19970101)79:1<12::AID-CNCR3>3.3.CO
[8]  
2-T
[9]   Separation and sensing based on molecular recognition using molecularly imprinted polymers [J].
Takeuchi, T ;
Haginaka, J .
JOURNAL OF CHROMATOGRAPHY B, 1999, 728 (01) :1-20
[10]   Molecular imprinting: An approach to ''tailor-made'' synthetic polymers with biomimetic functions [J].
Takeuchi, T ;
Matsui, J .
ACTA POLYMERICA, 1996, 47 (11-12) :471-480