원문정보
Binding Characteristics of Molecularly Imprinted Polymers for Ibuprofen Enantiomers
초록
영어
The molecularly imprinted polymers(MIPs) synthesized at various polymerization conditions were examined as ibuprofen receptors in terms of binding characteristics. The 4-vinylpyridine polymers had 1.2 times higher adsorption capability for (S)-(+)-ibuprofen than the methacrylic acid polymers. The methacrylic acid polymers synthesized by UV radiation had 1.9 times higher selectivity for (S)-(+)-ibuprofen compared to those by thermal initiation. Effects of various solvents for binding were also examined in this research. According to the Scatchard analysis, the (S)-(+)-ibuprofen artificial receptors had two different kinds of binding sites for (S)-(+)-ibuprofen while having only single kind of binding site for ketoprofen. The binding sites of (S)-(+)-ibuprofen, n were calculated as 4.3~4.9 mol/g and the dissociation constants, K? were 0.68 mM for the specific binding.
목차
재료 및 방법
시약 및 재료
인공 Receptor의 제조
Batch Binding
Scatchard 분석
결과 및 토의
혼합용매의 영향
결합 kinetics 연구
중합조건 및 단체량종류의 영향
MIPs의 receptor 특성
요약
감사
참고문헌
