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Takayama, Takahiro, Mochizuki, Toshiki, Todoroki, Kenichiro, Min, Jun Zhe, Mizuno, Hajime, Inoue, Koichi, Akatsu, Hiroyasu, Noge, Ichiro, Toyo'oka, Toshimasa (2015) A novel approach for LC-MS/MS-based chiral metabolomics fingerprinting and chiral metabolomics extraction using a pair of enantiomers of chiral derivatization reagents. Analytica Chimica Acta, 898. 73-84 doi:10.1016/j.aca.2015.10.010

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Reference TypeJournal (article/letter/editorial)
TitleA novel approach for LC-MS/MS-based chiral metabolomics fingerprinting and chiral metabolomics extraction using a pair of enantiomers of chiral derivatization reagents
JournalAnalytica Chimica Acta
AuthorsTakayama, TakahiroAuthor
Mochizuki, ToshikiAuthor
Todoroki, KenichiroAuthor
Min, Jun ZheAuthor
Mizuno, HajimeAuthor
Inoue, KoichiAuthor
Akatsu, HiroyasuAuthor
Noge, IchiroAuthor
Toyo'oka, ToshimasaAuthor
Year2015 (October)Volume898
PublisherElsevier BV
DOIdoi:10.1016/j.aca.2015.10.010Search in ResearchGate
Generate Citation Formats
Mindat Ref. ID3255334Long-form Identifiermindat:1:5:3255334:9
GUID0
Full ReferenceTakayama, Takahiro, Mochizuki, Toshiki, Todoroki, Kenichiro, Min, Jun Zhe, Mizuno, Hajime, Inoue, Koichi, Akatsu, Hiroyasu, Noge, Ichiro, Toyo'oka, Toshimasa (2015) A novel approach for LC-MS/MS-based chiral metabolomics fingerprinting and chiral metabolomics extraction using a pair of enantiomers of chiral derivatization reagents. Analytica Chimica Acta, 898. 73-84 doi:10.1016/j.aca.2015.10.010
Plain TextTakayama, Takahiro, Mochizuki, Toshiki, Todoroki, Kenichiro, Min, Jun Zhe, Mizuno, Hajime, Inoue, Koichi, Akatsu, Hiroyasu, Noge, Ichiro, Toyo'oka, Toshimasa (2015) A novel approach for LC-MS/MS-based chiral metabolomics fingerprinting and chiral metabolomics extraction using a pair of enantiomers of chiral derivatization reagents. Analytica Chimica Acta, 898. 73-84 doi:10.1016/j.aca.2015.10.010
In(2015) Analytica Chimica Acta Vol. 898. Elsevier BV

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Mochizuki, Toshiki, Taniguchi, Sayuri, Tsutsui, Haruhito, Min, Jun Zhe, Inoue, Koichi, Todoroki, Kenichiro, Toyo’oka, Toshimasa (2013) Relative quantification of enantiomers of chiral amines by high-throughput LC–ESI-MS/MS using isotopic variants of light and heavy l-pyroglutamic acids as the derivatization reagents. Analytica Chimica Acta, 773. 76-82 doi:10.1016/j.aca.2013.02.026
Takayama, Takahiro, Kuwabara, Tomohiro, Maeda, Toshio, Noge, Ichiro, Kitagawa, Yutaka, Inoue, Koichi, Todoroki, Kenichiro, Min, Jun Zhe, Toyo’oka, Toshimasa (2015) Profiling of chiral and achiral carboxylic acid metabolomics: synthesis and evaluation of triazine-type chiral derivatization reagents for carboxylic acids by LC-ESI-MS/MS and the application to saliva of healthy volunteers and diabetic patients. Analytical and Bioanalytical Chemistry, 407 (3) 1003-1014 doi:10.1007/s00216-014-8275-9
Takayama, Takahiro, Mizuno, Hajime, Toyo’oka, Toshimasa, Akatsu, Hiroyasu, Inoue, Koichi, Todoroki, Kenichiro (2019) Isotope Corrected Chiral and Achiral Nontargeted Metabolomics: An Approach for High Accuracy and Precision Metabolomics Based on Derivatization and Its Application to Cerebrospinal Fluid of Patients with Alzheimer’s Disease. Analytical Chemistry, 91 (7). 4396-4404 doi:10.1021/acs.analchem.8b04852
Mochizuki, Toshiki, Takayama, Takahiro, Todoroki, Kenichiro, Inoue, Koichi, Min, Jun Zhe, Toyo’oka, Toshimasa (2015) Towards the chiral metabolomics: Liquid chromatography–mass spectrometry based dl-amino acid analysis after labeling with a new chiral reagent, (S)-2,5-dioxopyrrolidin-1-yl-1-(4,6-dimethoxy-1,3,5-triazin-2-yl)pyrrolidine-2-carboxylate, and the application to saliva of healthy volunteers. Analytica Chimica Acta, 875. 73-82 doi:10.1016/j.aca.2015.02.054
Mochizuki, Toshiki, Todoroki, Kenichiro, Inoue, Koichi, Min, Jun Zhe, Toyo’oka, Toshimasa (2014) Isotopic variants of light and heavy l-pyroglutamic acid succinimidyl esters as the derivatization reagents for dl-amino acid chiral metabolomics identification by liquid chromatography and electrospray ionization mass spectrometry. Analytica Chimica Acta, 811. 51-59 doi:10.1016/j.aca.2013.12.016
Kuwabara, Tomohiro, Takayama, Takahiro, Todoroki, Kenichiro, Inoue, Koichi, Min, Jun Zhe, Toyo’oka, Toshimasa (2014) Evaluation of a series of prolylamidepyridines as the chiral derivatization reagents for enantioseparation of carboxylic acids by LC–ESI–MS/MS and the application to human saliva. Analytical and Bioanalytical Chemistry, 406 (11) 2641-2649 doi:10.1007/s00216-014-7637-7
Tsutsui, Haruhito, Mochizuki, Toshiki, Maeda, Toshio, Noge, Ichiro, Kitagawa, Yutaka, Min, Jun Zhe, Todoroki, Kenichiro, Inoue, Koichi, Toyo’oka, Toshimasa (2012) Simultaneous determination of dl-lactic acid and dl-3-hydroxybutyric acid enantiomers in saliva of diabetes mellitus patients by high-throughput LC–ESI-MS/MS. Analytical and Bioanalytical Chemistry, 404 (6) 1925-1934 doi:10.1007/s00216-012-6320-0
Todoroki, Kenichiro, Ishii, Yasuhiro, Ide, Takafumi, Min, Jun Zhe, Inoue, Koichi, Huang, Xin, Zhang, Wei, Hamashima, Yoshitaka, Toyo’oka, Toshimasa (2015) Advanced dress-up chiral columns: New removable chiral stationary phases for enantioseparation of chiral carboxylic acids. Analytica Chimica Acta, 882. 101-111 doi:10.1016/j.aca.2015.03.037
TAKAYAMA, Takahiro, MIZUNO, Hajime, TOYO’OKA, Toshimasa, TODOROKI, Kenichiro (2019) Introducing an Experimental Design Approach for Efficient Optimization of Chiral Derivatization Conditions for D- and L-Glyceric Acids. Analytical Sciences, 35 (9). 1053-1056 doi:10.2116/analsci.19n013
TODOROKI, Kenichiro, KUDOH, Yuto, NAKAMURA, Misuzu, SHIMIZU, Yuki, SASAKI, Takamitsu, OTSUKI, Hideyuki, WADA, Keisuke, MIN, Jun Zhe, MIZUNO, Hajime, YOSHINARI, Kouichi, TOYO’OKA, Toshimasa (2018) Sensitive and Comprehensive LC-MS/MS Analyses of Chiral Pharmaceuticals and Their Hepatic Metabolites Using Ovomucoid Column. Analytical Sciences, 34 (9). 1011-1015 doi:10.2116/analsci.18scp05
Fukui, Serina, Takayama, Takahiro, Toyo’oka, Toshimasa, Mizuno, Hajime, Todoroki, Kenichiro (2019) An accurate differential analysis of carboxylic acids in beer using ultra high-performance liquid chromatography–quadrupole time-of-flight mass spectrometry based on chiral derivatization combining three isotopic reagents. Talanta, 205. 120146pp. doi:10.1016/j.talanta.2019.120146
 
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