QT PRODACT : Inter- and Intra-facility Variability of the Action Potential Assay Using Isolated Guinea-Pig Papillary Muscles
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概要
- 論文の詳細を見る
Sixteen pharmaceutical companies and 6 contract research organizations in QT PRODACT acquired data on the action potentials in isolated guinea-pig papillary muscles using a standard protocol established by the QT PRODACT. Inter- and intra-facility variability for each of the parameters in the pre-application values and Δ% change after vehicle (0.1% DMSO) or dl-sotalol (30 μmol/L) treatment were examined using a nested model. Inter-facility variability of each of the parameters in the pre-application values were Vmax > APDs = APD30–90 > APA = RMP (descending order). The inter-facility variability of all of the parameters was almost the same or was less as compared with the intra-facility variability. Inter-facility variability for the Δ% change for each parameter after dl-sotalol treatment showed a tendency similar to the results for the pre-application values. Comparing the inter- and the intra-facility variability, the inter-facility variation did not exceed the intra-facility variation. All facilities found that dl-sotalol prolonged APD. Therefore, it is suggested that the test system using this standard protocol is useful as a non-clinical evaluation system for QT prolongation. Moreover, the results are considered to be directly comparable between multiple facilities. Supplementary material (Appendix): available only at http://dx.doi.org/10.1254/jphs.QT-B5.
- 社団法人 日本薬理学会の論文
- 2005-12-31
著者
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Yamamoto Keiji
日本製薬工業協会
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Yamamoto Keiji
Development Research Center Takeda Pharmaceutical Co. Ltd.
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Shimosato Takashi
Research Department Nissei Bilis Co. Ltd.
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TABO Mitsuyasu
Safety Assessment Department, Chugai Pharmaceutical Co., Ltd.
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Tabo Mitsuyasu
中外製薬
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Yamamoto Keiji
Non-clinical Evaluation Subcommittee Drug Evaluation Committee Japan Pharmaceutical Manufactures Ass
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Yamada Masayuki
Clinical Data & Development Management Planning & Management Department Kissei Pharmaceutica
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MORI Tatsuya
Toxicological Research Laboratories, Kyowa Hakko Kogyo Co., Ltd.
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SHIMADA Chiaki
Research and Development Center, Fuso Pharmaceutical Industries, Ltd.
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KOBAYASHI Kazuo
Pharmacodynamics Research Laboratories, Sankyo Co., Ltd.
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YAMAZAKI Ryuzaburo
Non-Clinical Quality Assurance Section, Taisho Pharmaceutical Co., Ltd.
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KITANI Shin-ichi
Research Administration Department, Ina Research, Inc.
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SUGANAMI Hideki
Biostatistics and Data Management Department, Kowa Co., Ltd.
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Kitani Shin-ichi
Pharmacology & Toxicology Department Ina Research Inc.
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Yamamoto Keiji
Development Research Center Takeda Pharmaceutical Co.
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Yamamoto Keiji
Drug Safety Research Laboratories Tanabe Seiyaku Co. Ltd.
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Yano Koji
Drug Safety Research Laboratories Tanabe Seiyaku Co. Ltd.
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Mori Tatsuya
Toxicological Research Laboratories Kyowa Hakko Kogyo Co. Ltd.
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Kii Yoshihide
Safety Research Laboratories Dainippon Sumitomo Pharma Co. Ltd.
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Suganami Hideki
Biostatistics And Data Management Department Kowa Co. Ltd.
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Shimada Chiaki
Research And Development Center Fuso Pharmaceutical Industries Ltd.
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Yamada Kiyoshi
Pharmaceutical Research Laboratories Toray Industries Inc.
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Kuriyama Kazuya
Toxicology Research Laboratories Kissei Pharmaceutical Co. Ltd.
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Suganami Hideki
Research Department Saitama Daiichi Pharmaceutical Co. Ltd.
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Kiitani Shinichi
Pharmacology & Toxicology Department Ina Research Inc.
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Shimosato Takashi
Department Of Pharmacology Shiga University Of Medical Sciences
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Yamazaki Ryuzaburo
Non-clinical Quality Assurance Section Taisho Pharmaceutical Co. Ltd.
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Kobayashi Kazuo
Pharmacodynamics Research Laboratories Sankyo Co. Ltd.
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Yamamoto Keiji
Non-clinical Evaluation Subcommittee Drug Evaluation Committee Japan Pharmaceutical Manufactures Ass
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Yamada Masayuki
Clinical Biometrics Planning And Managing Department Kissei Pharmaceutical Co. Ltd.
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