Shion Imoto
Gulf Coast Regional Blood Center
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Publication
Featured researches published by Shion Imoto.
American Journal of Clinical Pathology | 2004
Katsuyasu Saigo; Shion Imoto; Makoto Hashimoto; Hisashi Mito; Junko Moriya; Tadanobu Chinzei; Yoshitsugu Kubota; Shigehiro Numada; Toshiyuki Ozawa; Shunichi Kumagai
The efficacy of a noninvasive hemoglobin monitoring device (Astrin, Sysmex, Kobe, Japan) was evaluated for healthy volunteers and for patients with hematologic disorders. At the same time, the effects of WBC counts on noninvasive monitoring were studied by clinical evaluation and in ex vivo experiments. The hemoglobin levels determined by the device (Ast-Hb) and a conventional analyzer (T-Hb) were compared. The coefficient of correlation between findings with the Ast-Hb and the T-Hb for healthy volunteers was r = 0.626, whereas that for patients with hematologic disorders was r = 0.762. A comparison of the ratios of measurement errors in hemoglobin levels by Ast-Hb and T-Hb indicated that the number of WBCs had no effect on hemoglobin monitoring. Moreover, ex vivo studies using isolated WBCs and an optical model that imitates blood vessels and tissue in human fingers confirmed these results. Therefore, this new hemoglobin monitoring device can be expected to be useful for continuous hemoglobin monitoring.
American Journal of Clinical Pathology | 2004
Katsuyasu Saigo; Shion Imoto; Makoto Hashimoto; Hisashi Mito; Junko Moriya; Tadanobu Chinzei; Yoshitsugu Kubota; Shigehiro Numada; Toshiyuki Ozawa; Shunichi Kumagai
The efficacy of a noninvasive hemoglobin monitoring device (Astrim, Sysmex, Kobe, Japan) was evaluated for healthy volunteers and for patients with hematologic disorders. At the same time, the effects of WBC counts on noninvasive monitoring were studied by clinical evaluation and in ex vivo experiments. The hemoglobin levels determined by the device (Ast-Hb) and a conventional analyzer (T-Hb) were compared. The coefficient of correlation between findings with the Ast-Hb and the T-Hb for healthy volunteers was r = 0.626, whereas that for patients with hematologic disorders was r = 0.762. A comparison of the ratios of measurement errors in hemoglobin levels by Ast-Hb and T-Hb indicated that the number of WBCs had no effect on hemoglobin monitoring. Moreover, ex vivo studies using isolated WBCs and an optical model that imitates blood vessels and tissue in human fingers confirmed these results. Therefore, this new hemoglobin monitoring device can be expected to be useful for continuous hemoglobin monitoring.
Journal of the Japan Society of Blood Transfusion | 2003
Mariko Yamashita; Hirofumi Minami; Yoshihiro Bouike; Osamu Ikeda; Chie Nishimura; Masako Ishitani; Yoshisuke Nose; Shion Imoto; Hisashi Mito; Kaoru Nishiyama
Homogenate of matured roe of the female loach (Misgurnus anguillicaudatus) was absorbed with the stromas of A and O red cells. A lectin could be obtained after centrifugation to remove the stromas. This crude lectin was further purified by column chromatography on DEAF-cellulose (DE-52). Agglutination was carried out by centrifugation after reaction with 5% washed RBC and 22% polymerized bovine albumin.This crude or partially purified lectin reacted with B and AB red cells but not A, O or acquired B red cells. The subgroups (B3, Bm, A1B3, A2B3, A1Bm A1Bx) of red cells could not react. This lectin was therefore defined as B-specific lectin.Agglutinating activity was inhibited by monosaccharides such as L-rhamnose and L-mannose more effective than by D-galactose, D-fucose, L-arabinose and L-lyxose. Other monosaccharides failed to inhibit agglutination. Oligosaccharides possessing a galactose residue as a terminus such as trisaccharide (raffinose) and tetrasaccharide (stachyose) also inhibited agglutinatin.This B-specific lectin may be suitable for application to ABO blood typing by a manual or automatic mechanical procedure like A1 or H lectin.
Clinical and Laboratory Haematology | 2002
Katsuyasu Saigo; Meiyi Jiang; C. Tanaka; Keiji Fujimoto; A. Kobayashi; K. Nozu; K. Iijima; Ryukichi Ryo; T. Sugimoto; Shion Imoto; Shunichi Kumagai
Clinical and Laboratory Haematology | 2001
Meiyi Jiang; Katsuyasu Saigo; Shunichi Kumagai; Shion Imoto; Yoshiyuki Kosaka; Hideaki Matsumoto; Keiji Fujimoto
Internal Medicine | 2002
Noritatsu Yamaike; Katsuyasu Saigo; Shion Imoto; Hideyuki Miyachi; Shiho Morita; Yuichiro Maeda; Yoshinobu Tomofuji; Tadanobu Chinzei
International Journal of Hematology | 2010
Yasuyoshi Morita; Akihisa Kanamaru; Yasushi Miyazaki; Daisuke Imanishi; Fumiharu Yagasaki; Mitsune Tanimoto; Kazutaka Kuriyama; Kobayashi T; Shion Imoto; Kazunori Ohnishi; Tomoki Naoe; Ryuzo Ohno
Transfusion Medicine | 2010
Shion Imoto; K. Kawamura; Y. Tokumine; N. Araki; S. Akita; C. Nishimura; Hiroyuki Inaba; K. Saigo; O. Mabuchi; H. Okazaki
Transfusion and Apheresis Science | 2005
Makoto Hashimoto; Katsuyasu Saigo; Yukie Jyokei; Manami Kishimoto; Mariko Takenokuchi; Nobuo Araki; Shion Imoto; Kikuyo Taniguchi; Shunichi Kumagai
Cancer Genetics and Cytogenetics | 2003
Katsuyasu Saigo; Shunichi Kumagai; Mieko Kogi; Shion Imoto; Ken-ichi Hamano; Shiho Morita; Tadanobu Chinzei; Tamio Koizumi; Eiji Tatsumi