Tokushima University / Educator and Researcher Directory --- Kitaike, Syuji

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Tokushima University ⟩ Graduate School of Biomedical Sciences ⟩ 医学域 ⟩ Support Center for Advanced Medical Sciences ⟩

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Research

Field of Study

○	Informatics
○	機械工作学

Subject of Study

○	学習システムの研究
○	分析システムの開発と応用

Book / Paper

Academic Paper (Judged Full Paper):

1.	Michiyasu Nakao, Akihito Nakamura, Shoki Yamada, Syuji Kitaike and Shigeki Sano : Concentration-dependence of specific rotation of optically active glycerol analogues and structurally related compounds: The significance of intermolecular hydrogen bonding, Results in Chemistry, Vol.7, 101415--, 2024. (Summary) Specific rotation of optically active glycerol analogues, (S)-3-(benzyloxy)propane-1,2-diol [(S)-1], (S)-3-methoxypropane-1,2-diol [(S)-6] and (S)-3-phenoxypropane-1,2-diol [(S)-13], changed its sign from (+) to () with increasing concentration in CHCl3, whereas no significant concentration-dependent change was observed in MeOH. The 1H NMR spectrum of (S)-1 showed concentration-dependent changes of the chemical shift in CDCl3. Intermolecular interaction by OHOH hydrogen bonds was suggested by single crystal X-ray crystallography of (S)-13. The concentration-dependent changes of specific rotation of (S)-1, (S)-6, and (S)-13 in CHCl3 can therefore be presumed to be due to self-assembly of these compounds via intermolecular hydrogen bonding at high concentration. The remarkable concentration-dependent changes in specific rotation were also observed to occur in the compounds with related chemical structures, such as (S)-3-hydroxy-4-methoxy-4-oxobutanoic acid [(S)-10], (S)-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acid [Boc-L-Pro-OH, (S)-14], (R)-3-hydroxy-4,4-dimethylhydrofran-2(3H)-one [(R)-15], (R)-tetrahydrofuran-2-carboxylic acid [(R)-16], (S)-3-methyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]butanoic acid [Boc-L-Val-OH, (S)-17], (R)-oxiran-2-ylmethanol [(R)-18], and (4S)-4-isopropyloxazolidin-2-one [(S)-19]. The existence of intermolecular interaction by C=OHO hydrogen bonds was suggested by single crystal X-ray crystallography of (S)-10, (S)-13, and (S)-14. Thus, this series of chiral compounds have multiple functional groups in appropriate positions that serve as hydrogen-bond donors and/or acceptors, resulting in significant concentration-dependent changes of specific rotation. (Keyword) glycerol / intermolecular hydrogen bonding / concentration dependence / specific rotation / 1H NMR spectroscopy / X-ray crystallography (Tokushima University Institutional Repository) ● Metadata: 119086 (Link to Publication Site) ● Publication site (DOI): 10.1016/j.rechem.2024.101415 (Link to Search Site for Scientific Articles) ● CiNii @ National Institute of Informatics (CRID): 1050299595812169728 ● Summary page in Scopus @ Elsevier: 2-s2.0-85187313350 (Tokushima University Institutional Repository: 119086, DOI: 10.1016/j.rechem.2024.101415, CiNii: 1050299595812169728, Elsevier: Scopus)
2.	Michiyasu Nakao, Akihito Nakamura, Tomoyuki Takesue, Syuji Kitaike, Hiro-O Ito and Shigeki Sano : Synthesis of Novel Phosphorus-Substituted Stable Isoindoles by a Three-Component Coupling Reaction of ortho-Phthalaldehyde, 9,10-Dihydro-9-oxa-10-phosphaphenanthrene 10-Oxide, and Primary Amines, SynOpen, Vol.7, No.3, 394-400, 2023. (Summary) A three-component coupling reaction of ortho-phthalaldehyde, 9,10-dihydro-9-oxa-10-phosphaphenanthrene 10-oxide, and various primary amines readily afforded novel phosphorus-substituted stable isoindoles in good to excellent yields. The importance of the reversible ring-opening of 9,10-dihydro-9-oxa-10-phosphaphenanthrene 10-oxide by methanolysis in the three-component coupling reaction became apparent. (Keyword) OPA method / isoindoles / ortho-phthalaldehyde / 9,10-dihydro-9- oxa-10-phosphaphenanthrene 10-oxide / primary amines / isoindolin-1-ones / ring-opening / methanolysis (Tokushima University Institutional Repository) ● Metadata: 118534 (Link to Publication Site) ● Publication site (DOI): 10.1055/a-2148-9433 (Link to Search Site for Scientific Articles) ● Summary page in Scopus @ Elsevier: 2-s2.0-85170846368 (Tokushima University Institutional Repository: 118534, DOI: 10.1055/a-2148-9433, Elsevier: Scopus)
3.	Michiyasu Nakao, Ken Horikoshi, Syuji Kitaike and Shigeki Sano : Efficient One-Pot, Three-Step Synthesis of 1,2,3,5-Tetrasubstituted Pyrroles via Aza-Michael Addition of Methyl 3-Iminoacrylates, Heterocycles, Vol.106, No.8, 1397-1406, 2023. (Summary) An efficient one-pot, three-step procedure for the aza-Michael addition of methyl 3-iminoacrylates with secondary amines followed by intramolecular cyclization and silylation successfully afforded novel 1,2,3,5-tetrasubstituted pyrroles in high yields. (Keyword) aza-Michael addition / 1,4,5-trisubstituted 1,3-dihydro-2H-pyrrol-2-one / 1,2,3,5-tetrasubstituted pyrrole / methyl 3-iminoacrylate / one-pot reaction (Tokushima University Institutional Repository) ● Metadata: 118458 (Link to Publication Site) ● Publication site (DOI): 10.3987/COM-23-14876 (Link to Search Site for Scientific Articles) ● Search Scopus @ Elsevier (DOI): 10.3987/COM-23-14876 (Tokushima University Institutional Repository: 118458, DOI: 10.3987/COM-23-14876)
4.	Michiyasu Nakao, Munehisa Toguchi, Ken Horikoshi, Syuji Kitaike and Shigeki Sano : Synthesis of Novel 2,3-Disubstituted Thiophenes via Tandem Thia-Michael/Aldol Reaction of Allenyl Esters, Heterocycles, Vol.104, No.2, 379-388, 2022. (Summary) A tandem thia-Michael/aldol reaction of allenyl esters and mercaptoacetaldehyde in the presence of triethylamine provided 2,3,4-trisubstituted tetrahydrothiophenes. Novel 2,3-disubstituted thiophenes were obtained in high yield by the subsequent dehydration of the 2,3,4-trisubstituted tetrahydrothiophenes using p-toluenesulfonic acid monohydrate as an effective catalyst. (Keyword) thia-Michael/aldol reaction / 2,3,4-trisubstituted tetrahydrothiophene / 2,3-disubstituted thiophene / allenyl ester / 1,4-dithiane-2,5-diol (Tokushima University Institutional Repository) ● Metadata: 117165 (Link to Publication Site) ● Publication site (DOI): 10.3987/COM-21-14575 (Link to Search Site for Scientific Articles) ● Search Scopus @ Elsevier (DOI): 10.3987/COM-21-14575 (Tokushima University Institutional Repository: 117165, DOI: 10.3987/COM-21-14575)
5.	Michiyasu Nakao, Tomomi Shozui, Daisuke Inoue, Takahito Ihara, Syuji Kitaike and Shigeki Sano : Catalytic Asymmetric Ring-Opening of σ-Symmetric Cyclic Carbonates with Chiral Sulfonamide-Amine Catalysts, Heterocycles, Vol.103, No.2, 1011-1022, 2021. (Summary) Enantioselective ring-opening of σ-symmetric six-membered cyclic carbonates with benzyl alcohol catalyzed by 20 mol% of chiral amino sulfonamide catalysts afforded chiral acyclic carbonates in up to 79% ee. (Keyword) Ring opening / Cyclic carbonate / Chiral amino sulfonamide / asymmetric synthesis / organocatalysts (Tokushima University Institutional Repository) ● Metadata: 116119 (Link to Publication Site) ● Publication site (DOI): 10.3987/COM-20-S(K)42 (Link to Search Site for Scientific Articles) ● Search Scopus @ Elsevier (DOI): 10.3987/COM-20-S(K)42 (Tokushima University Institutional Repository: 116119, DOI: 10.3987/COM-20-S(K)42)
6.	Michiyasu Nakao, Ayumu Adachi, Syuji Kitaike and Shigeki Sano : Synthesis of Three Stereoisomers of Erythrochelin, a Hydroxamate-Type Tetrapeptide Siderophore from Saccharopolyspora erythraea, Heterocycles, Vol.101, No.1, 347-356, 2020. (Summary) Details of the synthesis of three stereoisomers of erythrochelin, a hydroxamate-type tetrapeptide siderophore produced by Saccharopolyspora erythraea, were described. Both enantiomers of protected δ-N-hydroxyornithine were used as key intermediates in the synthesis of stereoisomers of erythrochelin containing a (3S,6S)-3,6-disubstituted-2,5-diketopiperazine ring. From comparisons of 1H and 13C NMR spectra, neither of stereoisomers provided a match for the erythrochelin spectral data, and the absolute configuration of erythrochelin was unambiguously reconfirmed to be (R,R,S,S). (Keyword) erythrochelin / siderophore / absolute configuration / 2,5-diketopiperazine / δ-N-hydroxyornithine (Tokushima University Institutional Repository) ● Metadata: 114107 (Link to Publication Site) ● Publication site (DOI): 10.3987/COM-19-S(F)27 (Link to Search Site for Scientific Articles) ● Search Scopus @ Elsevier (DOI): 10.3987/COM-19-S(F)27 (Tokushima University Institutional Repository: 114107, DOI: 10.3987/COM-19-S(F)27)
7.	Michiyasu Nakao, Nanako Nishikiori, Akihito Nakamura, Murasaki Miyagi, Nao Shibata, Syuji Kitaike, Makoto Fukui, Hiro-O Ito and Shigeki Sano : Synthesis of Sterically Protected Isoindoles from ortho-Phthalaldehyde, SynOpen, Vol.2, No.1, 50-57, 2018. (Summary) o-Phthalaldehyde (OPA) reacts with O-protected tris(hydroxyalkyl)aminomethanes in the presence of 1-propanethiol to afford a novel class of stable isoindoles. Steric protection provided by the bulkiness of C 3-symmetric primary amines derived from tris(hydroxymethyl)aminomethane could be significant for the stabilization of 1-alkylthio-2-alkyl-substituted isoindoles derived from OPA. A plausible reaction mechanism is proposed to explain the formation of the isoindole and an isoindolin-1-one by-product. (Keyword) o-phthalaldehyde / isoindole / steric protection / isoindolin-1-one (Tokushima University Institutional Repository) ● Metadata: 113941 (Link to Publication Site) ● Publication site (DOI): 10.1055/s-0036-1591932 (Link to Search Site for Scientific Articles) ● Search Scopus @ Elsevier (DOI): 10.1055/s-0036-1591932 (Tokushima University Institutional Repository: 113941, DOI: 10.1055/s-0036-1591932)
8.	Michiyasu Nakao, Kazue Tanaka, Syuji Kitaike and Shigeki Sano : Synthesis of Fluorine-Containing Analogues of 1-Lysoglycerophospholipids via HornerWadsworthEmmons Reaction, Synthesis, Vol.49, No.16, 3654-3661, 2017. (Summary) An efficient method of synthesizing fluorine-containing analogues of 1-lysoglycerophospholipids (1-LPLs) by introducing a palmitoyl moiety starting from bis(2,2,2-trifluoroethyl)phosphonoacetate (StillGennari reagent) is described. The method effectively employs HornerWadsworthEmmons reagents as masked 1-LPL derivatives to prepare a series of analogues of 1-lysophosphatidic acid (1-LPA), 1-lysophosphatidylethanolamine (1-LPE), and 1-lysophosphatidylcholine (1-LPC). (Keyword) lysoglycerophospholipid / HornerWadsworthEmmons reaction / fluorine / lysophosphatidic acid / lysophosphatidylethanolamine / lysophosphatidylcholine (Tokushima University Institutional Repository) ● Metadata: 113940 (Link to Publication Site) ● Publication site (DOI): 10.1055/s-0036-1588826 (Link to Search Site for Scientific Articles) ● Search Scopus @ Elsevier (DOI): 10.1055/s-0036-1588826 (Tokushima University Institutional Repository: 113940, DOI: 10.1055/s-0036-1588826)
9.	Shigeki Sano, Eiko Kujime, Hiroko Tanaka, Syuji Kitaike and Michiyasu Nakao : Enzymatic Synthesis of Chiral P-Stereogenic Phosphonoacetates, Chemical Data Collections, Vol.5/6, 12-20, 2016. (Summary) In this data article, we describe the enzymatic kinetic resolution of a series of racemic mixed phosphonoacetates, which were successfully prepared from methyl bis(2,2,2-trifluoroethyl)phosphonoacetate (Still-Gennari reagent) by alcoholysis with -symmetrical secondary alcohols in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU). Porcine liver esterase (PLE)-catalyzed kinetic resolution of some of these racemic mixed phosphonoacetates proceeded in a highly stereoselective manner to furnish the chiral P-stereogenic phosphonoacetates (up to > 99% ee). (Keyword) stereogenic phosphorus atom / methyl bis(2,2,2-trifluoroethyl)phosphonoacetate / Horner-Wadsworth-Emmons reagent / kinetic resolution / enzymatic hydrolysis / X-ray crystal structure (Tokushima University Institutional Repository) ● Metadata: 113939 (Link to Publication Site) ● Publication site (DOI): 10.1016/j.cdc.2016.09.001 (Link to Search Site for Scientific Articles) ● Search Scopus @ Elsevier (DOI): 10.1016/j.cdc.2016.09.001 (Tokushima University Institutional Repository: 113939, DOI: 10.1016/j.cdc.2016.09.001)
10.	Michiyasu Nakao, Shunsuke Tsuji, Syuji Kitaike and Shigeki Sano : Synthesis of Erythrochelin: A Hydroxamate-Type Siderophore from Saccharopolyspora erythraea, Synthesis, Vol.48, No.23, 4149-4154, 2016. (Summary) Erythrochelin, a hydroxamate-type siderophore produced by Saccharopolyspora erythraea, is synthesized for the first time. A key building block of erythrochelin containing the 2,5-diketopiperazine ring is prepared by intramolecular cyclization of the corresponding dipep- tide precursor derived from two kinds of protected -N-hydroxy-L-orni- thines. Consecutive condensation of the building block with protected D-serine and protected -N-hydroxy-D-ornithine, followed by deprotec- tion, furnishes erythrochelin. (Keyword) erythrochelin / rhodotorulic acid / siderophore / 2,5-diketo- piperazine / electrospray ionization mass spectrometry (Tokushima University Institutional Repository) ● Metadata: 113938 (Link to Publication Site) ● Publication site (DOI): 10.1055/s-0035-1560564 (Link to Search Site for Scientific Articles) ● Search Scopus @ Elsevier (DOI): 10.1055/s-0035-1560564 (Tokushima University Institutional Repository: 113938, DOI: 10.1055/s-0035-1560564)
11.	Shigeki Sano, Masanori Kamura, Akihito Nakamura, Syuji Kitaike and Michiyasu Nakao : Asymmetric Synthesis of cis-4a,5,8,8a-Tetrahydrophthalazin-1(2H)-one Derivatives Based on Organocatalytic Alcoholysis of Cyclic Dicarboxylic Anhydride, Heterocycles, Vol.93, No.1, 391-398, 2016. (Summary) Asymmetric synthesis of optically active cis-4-phenyl-4a,5,8,8a- tetrahydrophthalazin-1(2H)-one and its N-alkylated derivatives based on an organocatalytic enantioselective alcoholysis of cyclic dicarboxylic anhydride was described. (Keyword) cis-4a,5,8,8a-tetrahydrophthalazin-1(2H)-one / organocatalysts / enantioselective alcoholysis / chiral sulfonamide / phosphodiesterase type 4 (Tokushima University Institutional Repository) ● Metadata: 113936 (Link to Publication Site) ● Publication site (DOI): 10.3987/COM-15-S(T)17 (Link to Search Site for Scientific Articles) ● Search Scopus @ Elsevier (DOI): 10.3987/COM-15-S(T)17 (Tokushima University Institutional Repository: 113936, DOI: 10.3987/COM-15-S(T)17)
12.	Shuhei Horio, Syuji Kitaike, Ryoji Fukabori, Takashi Ueyama and Kazuto Kobayashi : Close relationship between histamine H1 receptor-expressing neurons and CRH neurons in the mouse hypothalamic paraventricular nucleus., The Journal of Physiological Sciences, Vol.65, S293, 2015.
13.	Michiyasu Nakao, Shintaro Fukayama, Syuji Kitaike and Shigeki Sano : Synthesis of Rhodotorulic Acid and Its 1,4-Dimethylated Derivative, Heterocycles, Vol.90, No.2, 1309-1316, 2015. (Keyword) rhodotorulic acid / diketopiperazine / siderophore / microwave irradiation / N-hydroxyacetamide (Link to Publication Site) ● Publication site (DOI): 10.3987/COM-14-S(K)67 (Link to Search Site for Scientific Articles) ● CiNii @ National Institute of Informatics (CRID): 1520854805248223232 ● Summary page in Scopus @ Elsevier: 2-s2.0-84923241589 (DOI: 10.3987/COM-14-S(K)67, CiNii: 1520854805248223232, Elsevier: Scopus)
14.	Shigeki Sano, Keisuke Matsuura, Hayato Sumiyoshi, Akira Miki, Syuji Kitaike and Michiyasu Nakao : Reinvestigation of 1,3,4-Thiadiazol-2(3H)-Iminium Bromide in the Two-Step Synthesis of Imdazo[2,1-b][1,3,4]-Thiadiazoles, Heterocycles, Vol.89, No.4, 1041-1053, 2014. (Keyword) 1,3,4-thiadiazol-2(3H)-iminium bromide / imidazo[2,1-b][1,3,4]thiadiazole / thiadiazole / imidazole / microwave irradiation (Link to Publication Site) ● Publication site (DOI): 10.3987/COM-14-12938 (Link to Search Site for Scientific Articles) ● Summary page in Scopus @ Elsevier: 2-s2.0-84897532461 (DOI: 10.3987/COM-14-12938, Elsevier: Scopus)
15.	Syuji Kitaike : 実験動物解析装置の設計と試作 -高架式十字迷路, Journal of Medical Technology, Vol.57, No.7, 819-820, 2013. (Keyword) 行動実験 / 十字迷路 / トラッキングシステム
16.	S Horio, Syuji Kitaike, Y Minokoshi, N Kai, K Kobayashi, T Ueyama and H Fukui : Selective ablation of histamine H1 receptor-expressing neurons in the hypothalamic paraventricular nucleus increased food intake and body weight gain., The Journal of Physiological Sciences, Vol.62, S209, 2012.
17.	Shigeki Sano, Yoshinori Okubo, Atsushi Handa, Michiyasu Nakao, Syuji Kitaike, Yoshimitsu Nagao and Hisao Kakegawa : Reinvestigation of the Synthesis of Isoliquiritigenin (ILG): Application of Horner-Wadsworth-Emmons Reaction and Claisen-Schmidt Condensation, Chemical & Pharmaceutical Bulletin, Vol.59, No.7, 885-888, 2011. (Summary) Isoliquiritigenin [ILG, (E)-1] was readily prepared via the Horner-Wadsworth-Emmons reactions using β-ketophosphonates 5a, b. An improved protocol for the synthesis of (E)-1 via the Claisen-Schmidt condensation was also presented. (Keyword) isoliquiritigenin / chalcone / Horner-Wadsworth-Emmons reaction / Claisen-Schmidt condensation / cis-trans isomerization (Link to Publication Site) ● Publication site (DOI): 10.1248/cpb.59.885 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 21720042 ● Search Scopus @ Elsevier (PMID): 21720042 ● Search Scopus @ Elsevier (DOI): 10.1248/cpb.59.885 (DOI: 10.1248/cpb.59.885, PubMed: 21720042)
18.	Shigeki Sano, Michiyasu Nakao, Masanori Takeyasu, Syuji Kitaike, Yasuko Yoshioka and Yoshimitsu Nagao : Use of Diketopiperazines for Determining Absolute Configurations of α-Substituted Serines by ¹H-NMR Spectroscopy, Heterocycles, Vol.79, No.1, 781-789, 2009. (Keyword) Diketopiperazine / Absolute Configuration / α-SubstitutedSerine / 1H-NMR Analysis / DKP Method (Link to Publication Site) ● Publication site (DOI): 10.3987/COM-08-S(D)47 (Link to Search Site for Scientific Articles) ● CiNii @ National Institute of Informatics (CRID): 1520010379846386176 ● Search Scopus @ Elsevier (DOI): 10.3987/COM-08-S(D)47 (DOI: 10.3987/COM-08-S(D)47, CiNii: 1520010379846386176)
19.	Shigeki Sano, Michiyasu Nakao, Masanori Takeyasu, Chiyo Yamamoto, Syuji Kitaike, Yasuko Yoshioka and Yoshimitsu Nagao : Chemoenzymatic Synthesis of α-Substituted Serines via Enantiodivergent Transformation, The Open Organic Chemistry Journal, Vol.3, 22-34, 2009. (Link to Publication Site) ● Publication site (DOI): 10.2174/1874095200903010022 (Link to Search Site for Scientific Articles) ● Search Scopus @ Elsevier (DOI): 10.2174/1874095200903010022 (DOI: 10.2174/1874095200903010022)

Academic Paper (Unrefereed Paper):

1.	Syuji Kitaike : 有機微量元素分析における流路系の対策と検討, 技術支援部技術報告, Vol.1, 2018. (Tokushima University Institutional Repository) ● Metadata: 113403 (Tokushima University Institutional Repository: 113403)

Proceeding of Domestic Conference:

1.	Syuji Kitaike and Eiji Yoshida : アカデミックプラットフォームを目指した研究支援ネットワークシステムの開発と評価, 第16回情報科学技術フォーラム講演論文集, Sep. 2017. (Keyword) 共用システム / プラットフォーム
2.	Syuji Kitaike and 葉田善章 : 薬用植物園における支援アプリを用いた観察方法の改善, FIT2015 第14回情報科学技術フォーラム講演論文集, Sep. 2015.
3.	Shuhei Horio, Syuji Kitaike, Fukabori Ryoji, Ueyama Takashi and Kobayashi Kazuto : マウス視床下部室傍核のヒスタミンH1受容体発現ニューロンとCRHニューロンの関係, 第92回日本生理学会大会, Mar. 2015.
4.	Shuhei Horio, Syuji Kitaike, 箕越靖彦, Kobayashi Kazuto, Ueyama Takashi and Hiroyuki Fukui : マウス視床下部室傍核のヒスタミンH1受容体発現ニューロンの選択的死滅による摂食亢進と体重増加, 第89回日本生理学会大会, Mar. 2012.
5.	Shuhei Horio, Syuji Kitaike, Tetsuya Shiuchi, 箕越靖彦, 三宝誠, 平林敬浩, 八木健, 甲斐信行, 上山敬司 and Hiroyuki Fukui : Selective ablation of histamine H1 receptor-expressing neurons in the hypothalamus to study their role in the regulation of food intake, 第88回日本生理学会大会第116回日本解剖学会総会・全国学術集会合同大会, Mar. 2011.

Et cetera, Workshop:

1.	Syuji Kitaike : 酵素反応におけるセンサを用いたガス産生判定の試み, 生理学技術研究会, No.46, 100-101, Aug. 2024.
2.	Syuji Kitaike : スピルリナの抗酸化能と酵母αグルコシダーゼに及ぼす影響, 生理学技術研究会, No.45, 80-81, Aug. 2023.
3.	Syuji Kitaike : オオムラサキ成虫抽出液の抗酸化作用の検討, 生理学技術研究会, No.44, 44-45, Aug. 2022.
4.	Syuji Kitaike : 白金ナノ粒子液の抗酸化能評価, 生理学技術研究会, No.43, 42-43, Jul. 2021.
5.	Syuji Kitaike : 蛍光顕微鏡を用いた簡易抗酸化力評価の検討, 生理学技術研究会, No.42, 88-89, Aug. 2020.
6.	Syuji Kitaike : 共同利用機器HPLC/MSにおけるTLC法の活用, 生理学技術研究会, No.41, 104-105, Jul. 2019.
7.	Syuji Kitaike and Masayuki Shono : 顕微鏡下における培養液自動交換システムの検討, 生理学技術研究会, No.40, 102-103, Jul. 2018.
8.	Syuji Kitaike and Masayuki Shono : 培養液pH簡易測定自動制御システムの開発, 生理学技術研究会, No.39, 94-95, Jun. 2017.
9.	Syuji Kitaike : オープンフィールド試験装置の製作, 生理学技術研究会, No.38, 86-87, Jun. 2016.
10.	Syuji Kitaike : 創薬における化合物ライブラリーシステムの構築, 生理学技術研究会, No.37, 106-107, Jul. 2015.
11.	Syuji Kitaike : 自発運動量測定装置の製作, 生理学技術研究会, No.36, 150-151, Jul. 2014.
12.	Syuji Kitaike : The manufacturing of the elevated plus-maze test device, 生理学技術研究会, No.35, 108-109, Jun. 2013.
13.	Syuji Kitaike : 明暗往来試験装置の製作, 生理学技術研究会, No.30, 158-159, May 2008.
14.	Syuji Kitaike : 共同利用における分析機器について -原因と対応策-, 生理学技術研究会, No.29, 166-167, May 2007.
15.	Syuji Kitaike : 有機微量元素分析におけるデータベース活用事例, 生理学技術研究会, No.28, 166-167, May 2006.
16.	Syuji Kitaike : 地域IP網を利用したセキュリティネットワークの構築, 生理学技術研究会, No.27, 160-161, May 2005.
17.	Syuji Kitaike : RASを用いたデータ取得, 生理学技術研究会, No.26, 184-185, Jul. 2004.
18.	Syuji Kitaike : セキュリティサーバーにおけるiptablesスクリプトの作成, 生理学技術研究会, No.25, 90-91, Jul. 2003.

Report:

1.	Syuji Kitaike : 徳島大学薬学部附属薬用植物園におけるフィールドサービスの構築, 徳島大学大学院HBS研究部教育・研究技術支援部報告書, 45-47, Mar. 2014. (Keyword) Wi-fiアクセスポイント導入に向けて
2.	Syuji Kitaike : 新潟大学工学部技術部状況調査報告, 徳島大学大学院HBS研究部教育・研究技術支援部報告書, 62-65, Mar. 2014.
3.	Syuji Kitaike : 浜松医科大学技術部状況調査, 徳島大学大学院HBS研究部教育・研究技術支援部報告書, 12-15, Mar. 2014.
4.	Syuji Kitaike : タブレット端末を利用した薬用植物情報提供への試み, 薬学部だより, No.10, 3, Jul. 2012.
5.	Syuji Kitaike : iPadとネットワーク, 薬学部だより, No.8, 6, Jul. 2011.

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