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公开(公告)号：JP2016061772A
公开(公告)日：2016-04-25
申请号：JP2014228341
申请日：2014-11-10
申请人： アイセンス,インコーポレーテッド
IPC分类号： C12Q1/00 , C12Q1/26 , C12Q1/54 , C12Q1/60 , C12Q1/61 , C12M1/40 , G01N27/327 , G01N27/416
CPC分类号： G01N27/3274 , G01N27/3272 , G01N33/48707 , G01N33/49
摘要： 【課題】血液の濃度を測定する電気化学的バイオセンサにおいて、赤血球容積率による測定誤差を減少させることのできる生体試料内の分析対象物質の濃度測定方法および測定装置を提供する。 【解決手段】電気化学的バイオセンサに全血試料を注入した後、一定時間直流電圧を印加して得られた感応電流から分析対象物質の濃度を求める対時間電流法に対して、直流電圧を印加して得られる感応電流値と前記一定時間の直流電圧に続いて、短時間に数個の階段化されたはしご形摂動電圧をさらに印加して得られる全体感応電流から予め定められたフィーチャーを得る。得られたフィーチャーを関数で結合して検定式を作り、この検定式を用いて測定対象物質の濃度を計算する。 【選択図】図3
摘要翻译： 要解决的问题：提供一种用于测量生物样品中分析物浓度的方法和装置，其能够减少由测量血液浓度的电化学生物传感器中的红细胞体积引起的测量误差。解决方案： 关于计时电流法，其中在将全血样品注入电化学生物传感器之后，从通过施加DC电压获得的敏感电流获得分析物的浓度一定时间，从灵敏度获得预定特征 通过施加DC电压和通过在特定时间之后的DC电压之后的短时间内进一步施加几个梯级扰动电位而获得的所有敏感电流获得的电流。 通过将获得的特征与功能组合而产生校准表达式，并使用校准表达式计算用于测量的物质的浓度。选择图：图3
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公开(公告)号：JP2008306942A
公开(公告)日：2008-12-25
申请号：JP2007155194
申请日：2007-06-12
申请人： Fujifilm Corp , 富士フイルム株式会社
发明人： KAGEYAMA SHIGEKI , TANAKA HIDEAKI
CPC分类号： G01N33/526 , C12Q1/44 , G01N2333/92
摘要： PROBLEM TO BE SOLVED: To provide a dry analysis element for measuring pancreatic lipase which is high in selectivity with respect to pancreatic lipase and improves correlation of many specimens.
SOLUTION: This dry analysis element for measuring the pancreatic lipase in a body fluid, having at least one developed layer and/or reagent layer which contains a diglyceride or a triglyceride of a 12C to 22C-long chain alkyl fatty acid, a monoglyceride lipase, and a glycerol-measuring reagent is such that the developed layer and/or reagent layer contain two or more anionic surfactants, and at least one of the anionic surfactants is an alkylphenylsulfonate.
COPYRIGHT: (C)2009,JPO&INPIT摘要翻译： 要解决的问题：提供一种用于测量相对于胰脂肪酶的选择性高的胰脂肪酶的干燥分析元件并改善许多标本的相关性。 解决方案：用于测量体液中的胰脂肪酶的干燥分析元件，其具有至少一个显影层和/或试剂层，其含有12℃至22℃长链烷基脂肪酸的甘油二酯或甘油三酯， 单甘油脂肪酶和甘油测定试剂使得显影层和/或试剂层含有两种或更多种阴离子表面活性剂，并且至少一种阴离子表面活性剂是烷基苯基磺酸盐。 版权所有（C）2009，JPO＆INPIT
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5.发明专利
公开(公告)号：JP2002369680A
公开(公告)日：2002-12-24
申请号：JP2001180548
申请日：2001-06-14
申请人： Toyobo Co Ltd , 東洋紡績株式会社
摘要： PROBLEM TO BE SOLVED: To provide a method for stabilizing glycerophosphate oxidase and to obtain its composition.
SOLUTION: The method for stabilizing the glycerophosphate oxidase is characterized by making the glycerophosphate oxidase coexist with piperazine-1,4-bis(2-ethanesulfonic acid) or its salt.
COPYRIGHT: (C)2003,JPO摘要翻译： 要解决的问题：提供稳定甘油磷酸酯氧化酶并获得其组成的方法。 解决方案：稳定甘油磷酸氧化酶的方法的特征在于使甘油磷酸酯氧化酶与哌嗪-1,4-双（2-乙磺酸）或其盐共存。
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公开(公告)号：JP2002262864A
公开(公告)日：2002-09-17
申请号：JP2001071695
申请日：2001-03-14
摘要： PROBLEM TO BE SOLVED: To provide a new catalase stabilizer, to provide an ingredient-assaying reagent containing the stabilizer, and to provide a method for stabilizing catalase using the reagent. SOLUTION: This catalase stabilizer comprises a compound of the general formula [1] (wherein, nR are each independently H, a lower alkyl, lower alkoxy or halogen atom; R is H, a lower alkyl or lower alkoxy; R is an alkylene; M is H, an alkali metal, alkaline earth metal or ammonium ion; and n is an integer of 1-5).
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公开(公告)号：JP2002159299A
公开(公告)日：2002-06-04
申请号：JP2001266872
申请日：2001-09-04
申请人： KYOWA MEDEX CO LTD
发明人： MIYAUCHI KAZUTO , MIIKE AKIRA
IPC分类号： G01N33/50 , C12Q1/25 , C12Q1/26 , C12Q1/28 , C12Q1/34 , C12Q1/48 , C12Q1/58 , C12Q1/60 , C12Q1/61 , G01N33/62 , G01N33/70 , G01N33/92
摘要： PROBLEM TO BE SOLVED: To provide a method for assaying a substance designed to mitigate the influence of the other components coexisting therewith in a specimen, thus useful in clinical diagnoses, and to provide a reagent for the above method. SOLUTION: This method for assaying a substance is characterized by comprising the following practice: the substance in a specimen is brought into a stoichiometric quantity of hydrogen peroxide by making use of an enzymatic reaction, the hydrogen peroxide is then reacted with a chromogen in the presence of a peroxidase and also a compound of the general formula (I) [R1 and R2 are each H or a (substituted) lower alkyl; R3 is H or joined with R1 to form NH-(CH2)n as R3-R1 (wherein, n is an integer of 2-4); R4 is a single bond or alkylene; R5 is O- or R6-X-(R6 is an optionally substituted alkylene; X is COO, SO2O or OPO2O); Y is R7-NH (R7 is an optionally 1-3 hydroxy-substituted cholanoyl group)], and a colorimetric determination is made by measuring the absorption in the visible region of the resulting colored reaction liquid by the use of an automatic analyzer.
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公开(公告)号：JPH10262697A
公开(公告)日：1998-10-06
申请号：JP7482997
申请日：1997-03-27
申请人： ASAHI CHEMICAL IND
发明人： KOGA SHINJI
摘要： PROBLEM TO BE SOLVED: To accurately measure ADP by previously deleting the ADP present in a test solution or the ADP present in a reaction liquid or formed by the reaction, allowing ADP-depending hexokinase to act on the deleted test solution, and measuring the product amount. SOLUTION: This method for measuring one of an enzyme forming ADP in a test solution or a substrate thereof by using an enzymatic reaction comprises a step for previously deleting the ADP present in a test solution or the ADP present in the first reaction liquid or formed by the first reaction by using pyruvic acid kinase or creatine kinase in the presence of magnesium ion and substrate for the ADP, a step for allowing ADP-depending hexokinase catalyzing a reaction of the formula to act on the ADP formed by the second reaction, and a step for measuring the amount of the produced glucose-6- phosphate or AMP to readily measure the objective ADP in high accuracy.
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