| Project/Area Number |
11640609
|
|---|
| Research Category |
Grant-in-Aid for Scientific Research (C)
|
| Allocation Type | Single-year Grants |
|---|
| Section | 一般 |
|---|
| Research Field |
分離・精製・検出法
|
|---|
| Research Institution | Yamaguchi University |
|---|
Principal Investigator |
NAGAOKA Tsutomu Yamaguchi University, Faculty of Engineering, Professor, 工学部, 教授 (00172510)
|
|---|
| Co-Investigator(Kenkyū-buntansha) |
NAKAYAMA Masaharu Yamaguchi University, Faculty of Engineering, Research Associate, 工学部, 助手 (70274181)
OGURA Kotaro Yamaguchi University, Faculty of Engineering, Professor, 工学部, 教授 (40035077)
|
|---|
| Project Period (FY) |
1999 – 2000
|
| Project Status |
Completed (Fiscal Year 2000)
|
| Budget Amount *help |
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2000: ¥1,200,000 (Direct Cost: ¥1,200,000)
Fiscal Year 1999: ¥2,300,000 (Direct Cost: ¥2,300,000)
|
|---|
| Keywords | Conducting Potymer / Overoxidation / Molecular Recognition / Enantiomer / Amino Acid / Sensor / Templated Potymer / Polypyrrole |
|---|
| Research Abstract |
Overoxidized polypyrrole films templated with L-glutamate have been utilized for enantiomeric separation of L-and D-glutamic acid. Various important fabrication factors controlling the performance of the overoxidized polypyrrole films have been investigated using fluorescence spectrometry in conjugation with the electrochemical quartz crystal microbalance technique. The measured fluorescence intensity was related to the concentration of glutamate taken up into the films. It was found that L-glutamate was inserted about 30 times as much into the film as D-glutamate. Several key parameters such as applied potential, and pH of amino acid solution were varied so as to achieve the optimum sensor response. The sensor templated with L-glutamic acid also exhibited excellent selectivity over several other L-and D-amino acids. Higher enantioselectivity of overoxidized polypyrrole film than that for previously reported imprinted polymers can be attributed to the potential-induced uptake/release of targeted molecules.
|
