Kenichiro Todoroki

Prof. Dr. Kenichiro Todoroki

Laboratory of Analytical and Bio-Analytical Chemistry, School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka 422-8526, Japan
orcid

Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 February 2020 in Journal of Pharmaceutical and Biomedical Analysis
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Journal Article
Closed access
Kenichiro TodorokiKenichiro Todoroki
Kenichiro Todoroki
HMHajime Mizuno
Hajime Mizuno
ESEiji Sugiyama
Eiji Sugiyama
TTToshimasa Toyo’oKa
Toshimasa Toyo’oKa

4 March 2019 in Analytical Chemistry
Verified
Journal Article
Closed access
TTTakahiro Takayama
Takahiro Takayama
HMHajime Mizuno
Hajime Mizuno
TTToshimasa Toyo’oKa
Toshimasa Toyo’oKa
HAHiroyasu Akatsu
Hiroyasu Akatsu
KIKoichi Inoue
Koichi Inoue
Kenichiro TodorokiKenichiro Todoroki
Kenichiro Todoroki

22 January 2022 in Biosensors and Bioelectronics
Verified
Journal Article
Closed access
TSTaro Saito
Taro Saito
YSYutaka Shimizu
Yutaka Shimizu
KTKaori Tsukakoshi
Kaori Tsukakoshi
KAKoichi Abe
Koichi Abe
JLJinhee Lee
Jinhee Lee
KIKazunori Ikebukuro
Kazunori Ikebukuro

22 January 2019 in Analytical Chemistry
Verified
Journal Article
Closed access
TYTomohiro Yamada
Tomohiro Yamada
TSTaro Saito
Taro Saito
YHYoshia Hill
Yoshia Hill
YSYutaka Shimizu
Yutaka Shimizu
KTKaori Tsukakoshi
Kaori Tsukakoshi
Kenichiro TodorokiKenichiro Todoroki
Kenichiro Todoroki

17 February 2020 in Organic & Biomolecular Chemistry
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Journal Article
Closed access
PDF file
HEHiromichi Egami
Hiromichi Egami
SNSatoshi Nakagawa
Satoshi Nakagawa
YKYuki Katsura
Yuki Katsura
MKMasakatsu Kanazawa
Masakatsu Kanazawa
SNShingo Nishiyama
Shingo Nishiyama
YHYoshitaka Hamashima
Yoshitaka Hamashima
Dihydromethidine (DHM) labeled with 18 F at the para position of the benzene ring has been developed as a positron emission tomography (PET) radiotracer for non-invasive imaging of reactive oxygen species (ROS).

12 February 2021 in The Analyst
Verified
Journal Article
Closed access
PDF file
DADaiki Asakawa
Daiki Asakawa
HMHajime Mizuno
Hajime Mizuno
ESEiji Sugiyama
Eiji Sugiyama
Kenichiro TodorokiKenichiro Todoroki
Kenichiro Todoroki
Liquid chromatography–tandem mass spectrometry (LC–MS/MS) is interfaced with electrospray ionization (ESI), which generally produces intact gas-phase ions of biomolecules. However, ESI induces the fragmentation of tryptophan-derived metabolites, which are known to act as neurotransmitters and psychoactive drugs. Tryptophan-derived metabolites undergo N–Cα bond dissociation during ESI, producing a fragment ion with a spiro[cyclopropane-indolium] backbone. Fragmentation is suppressed by the presence of an α-carboxyl group and the modification of amino groups. In particular, tryptamine and serotonin, which lack such functional groups, produce more intense fragment-ion signals than protonated molecules. The multiple reaction monitoring (MRM)-based quantitative analysis of tryptamine and serotonin used the fragment ions produced from in-source collision-induced dissociation as the precursor ions, which improved the signal-to-noise ratio of the resulting spectra. The present method allows for the quantitative analysis of tryptamine and serotonin with high sensitivity.