2016年第63回応用物理学会春季学術講演会

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一般セッション(ポスター講演)

12 有機分子・バイオエレクトロニクス » 12.7 医用工学・バイオチップ

[20p-P12-1~31] 12.7 医用工学・バイオチップ

2016年3月20日(日) 16:00 〜 18:00 P12 (屋内運動場)

16:00 〜 18:00

[20p-P12-15] Study on specific monitoring of histamine for allergy test

〇(M2)Yang Haoyue1、Saito Akiko Saito1、Kajisa Taira Kajisa2、Yanase Yuki3、Sakata Toshiya1 (1.School of Engineering, Univ. of Tokyo、2.PROVIGATE Inc.、3.Graduate School of Biomedical and Health Sciences, Hiroshima Univ.)

キーワード:Biosensor,MIP,histamine

Introduction
Allergy is a kind of closest disease in the worldwide and there is nearly half of Japanese population suffers from allergy. At present, the diagnosis of allergy takes long time and uses large amount of patient blood but less of accuracy. In order to develop a convenient and precise way for allergy diagnosis in clinical test, we consider histamine as the signal chemical secreted during type I allergy reaction to make a device to detect allergy. In this research, we made biosensor combine with field effect transistor (FET) and molecular imprinting polymer (MIP) for the selective device detecting histamine.

Experiment Methods and Results
Detection of Histamine by Extended Gate FET (EGFET) and MIP
From the previous research, we already sensed histamine secretion of allergy by Ion-sensitive FET (ISFET). We chose to use EGFET for modifying the gate surface by MIP to make selective device. MIP gel coated-gate FET with histamine template was fabricated by direct UV polymerization onto the Au gate electrode using monomers, which were consisting of acrylic acid as a main chain, ethylene glycol dimethacrylate as a cross linker, and mixing the target molecule, histamine, dissolved in dimethyl sulfoxide/water. After polymerization, histamine was removed from polymerized MIP film using organic solvent. The MIP gel we are using is composed by histamine 0.01g, acrylic acid 0.013g, EGDM 0.15g, DMSO up to 0.85g, PBS up to 1.0g. Up till now, we could sense histamine concentration at 0.1mM.
Confirm the selectivity of MIP for histamine
MIP works by the shape of target template and the function group link between MIP and target. In case when similar chemical of histamine affecting the result, we choose nicotine amide and histidine to check the selectivity of MIP for histamine. By the MIP device made for histamine, Nicotine amide and histidine solution at same concentration of histamine have been sensed. Regarding this results, we would like to talk about the details in the conference.