CN1060533A - 诊断和识别胸痛早期发作的诊断盒 - Google Patents

诊断和识别胸痛早期发作的诊断盒 Download PDF

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CN1060533A
CN1060533A CN91109633A CN91109633A CN1060533A CN 1060533 A CN1060533 A CN 1060533A CN 91109633 A CN91109633 A CN 91109633A CN 91109633 A CN91109633 A CN 91109633A CN 1060533 A CN1060533 A CN 1060533A
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Abstract

本发明公布的诊断用诊验盒是为了评价在患者 胸痛发作初期究竟胸痛是否源于心脏,以及将变异性 心绞痛和心脏梗塞区别开。该试验盒是由一个为接 受和保留患者血液和血清样品的接受器和悬浮于载 体上的至少三个单克隆和多克隆抗体。每个抗体与 一不同的蛋白相互补,该蛋白是在心肌梗塞早期从心 肌中释放的,每个抗体有相应的试剂,后者对每个抗 体与相应蛋白反应时作出独立的应答。对试剂作出 应答的综合揭示了患者诊断时的状况。

Description

本发明涉及新的药板形式的一步诊断试验法,用来作为一种精确、简便、迅速和便携的诊断方法,以判断患者的胸痛是否源于心脏,并在患者胸痛的早期发作时区别出是易变性心绞痛还是心肌梗塞(“MI”)。特别是本药板用酶免疫试验夹层干化学形式同时测定了心脏受损伤时或损伤后血清或血浆中出现的三种不同的物质或标示物的水平。在本发明的优选的实施例中,这三个标示物是肌酸激酶(CK),肌红蛋白和肌浆球蛋白轻链(MLC)。
心肌梗塞的紧急诊断取决于内科长征的敏锐性和对患者症状的评估,例如胸痛或胸压迫感,显可能放射到下到臂部,上到颈部,疲劳,要死的感觉,呼吸短促,苍白,皮肤冷湿,外周发绀或数丝状脉。
大多数北美的胸痛患者在发作6小时内报告给医生或急诊室。因此,在MI早期阶段进行有效的诊断试验是至关重要的。
有数种心脏检查方法用于诊察MI。这些检查方法包括ECG,SGOT/AST,LDH,CK-MB免疫试验和NA乳液肌红蛋白颗粒增强试验。然而还没有用单一酶心脏检查法能使急诊室医生确定胸痛是来自心脏或不是来自心脏的原因。而且只有在确证了是心肌梗塞后,才开始溶解血栓的治疗。这种治疗开始得越早,患者完全康复的可能性就越大或至少使心脏损伤只在最低程度。因此,内科先生确定这种疼痛是心脏性的还是非心脏性的,是至关重要的。
心电图(ECG)可用来诊察MI。然而只有心脏受到严重损伤时心电图才能诊断出。ECG的诊断特异性对开始阶段的胸痛只有51%。因此,ECG不适宜用于MI的早期诊察。
血清谷氨酸草酰乙酸转氨酶/天门冬氨酸转氨酶(SGOT/AST)在心肌中有高浓度,是占优势的酶。血清试验测定SGOT水平可用来诊断心肌梗塞。然而,SGOT只在胸痛发作后的大约8-10小时后才开始升高,在24-36小时内达到峰值,5-7天后恢复正常。患者在胸痛早期和紧急处置时SGOT在诊断心肌梗塞上是没有特殊帮助的。SGOT对心肌也不是特异的。已发现许多包含骨骼肌的组织,如肝和肾脏,由于肌肉注射,休克,肝脏病和肝充血时,SGOT被释放,因此这在诊察特异的心脏组织损害上价值不大。
乳酸脱氢酶(LDH)在许多组织中浓度很高,这些组织包括心脏,骨骼肌和肝脏,检查血清中LDH的存在的试验被用来诊断心肌梗塞。在五种普通的同型中心脏主要含有LDH1和LDH2。胸痛发作24-36小时后LDH水平开始增高,48-72小时后达峰值,4-8天后回复正常。因此,患者在胸痛早期不能用LDH作为MI的指标。此外对心脏损伤LDH不是特异的,在肺栓塞、溶血,肝充血,肾脏病和骨骼肌损伤时LDH会出现。这种特异性的缺乏降低了LDH作为诊断手段的应用。
肌酸激酶(CK)是肌肉组织中的一种酶。CK催化肌酸和三磷酸腺苷(ATP)转变为磷酸肌酸和二磷酸腺苷(ADP)的反应。CK的数个同功酶中的CK-MB在心脏组织中。CK-MB对诊查心肌梗塞是个灵敏的标示物,因为它在心肌组织受损伤时释放出。故而CK-MB存在于受损伤患者的血清之中,图1说明了患者血清中CK浓度与时间的关系(文献Lee  T.H.等(1986)Ann.Intern.Med.105,221-233)。
CK-MB免疫试验是诊断心肌梗塞的标准检查法。美国专利No.4900662公布了CK-MB的应用方法,题目是“CK-MM心肌梗塞免疫试验”。
Shah在USP4900662中公布了在患者心肌梗塞后测定血清中初始增高的CK-MM-a(CK-MM的异型)浓度和同时测定CK-MM-a和CK-MM-b的方法。用这个方法可提供一种对梗塞的时间的精确估计。该方法包括测定血清中CK-MM-a和CK-MM-b的总浓度和CK-MM-a的浓度,以确定心肌梗塞急性期的时间。公布的试剂包括有CK-MM-a的多克隆抗体和单克隆抗体,这类抗体并不明显地与CK-MB,CK-MM-b或CK-MM-c结合,有抗CK-MM-b抗体,它不会明显地与CK-MB,CK-MM-a或CK-MM-c结合,有抗CK-MM-a+b抗体,它可与CK-MM-a和CK-MM-b结合,但不能明显地与CK-MB或CK-MM-c结合,还包括这些抗体的标记的衍生物,固着这些抗体的不溶性的支持物,以及含有一种或多种这些试剂的药盒。酶标记的和放射性标记的CK试剂特别有用。
单独使用CK-MB作为诊断标示物是有些困难的。首先,心肌梗塞发作后只有在6-8小时后CK-MB的血清浓度才增高,而且12小时后才达峰,造成早期紧急诊断和治疗的困难。
第二,CK-MB试验必须在实验室中由训练有素的技术员进行。在非城区不易进行这样的试验,结果也不能迅速得的解析,致使延误了诊断,因此,就患者等候诊断的住院费而言,增加了保证机构的负担。
第三,CK-MB处于正常骨骼肌组织中,因此,使该试验结果对心脏不够特异,诊断不够肯定。
肌红蛋白是位于骨骼肌或心肌细胞膜的邻近的另一种蛋白质。细胞膜的通透性一旦变得异常,例如心脏缺血时的一个可逆状态,肌红蛋白立即被细胞排出。在胸痛发作1.5小时内,在血清中即可检查出肌红蛋白。医学研究团体认为,心肌坏死释放肌红蛋白,因此它是心肌损伤的一个有用的早期标示物。图2说明了血清中肌红蛋白浓度与时间的关系(文献:Grenadier  E.等(1981)Am.Heart  J.105,408-416;Seguin  J.等(1988)J.Thorac  Car-diovasc  Surg.95,294-297)。
胸痛发作后2-3小时内若未检查出血清肌红蛋白水平增高,则在确定疼痛原因时可排除急性心肌梗塞。
“NA乳液肌红蛋白颗粒增强测定”是检查肌红蛋白的市场有售的药盒。这种检查试验是基于人体体液中存在的抗原与共价链偶联于聚苯乙烯颗粒上的抗肌红蛋白抗体间的反应。把样品、N肌红蛋白试剂、一种除掉非特异性反应的溶液和N反应缓冲液自动地移液到比包池内,温孵12分钟后用浊度法测定光散射,同标准曲线计算肌红蛋白的浓度。
放射免疫试验也可测定肌红蛋白,但还有一种无酶联结的免疫吸附剂检验(ELISA)装置也能采用。
单用肌红蛋白指标诊断心肌梗塞具有困难性。肌红蛋白不能指出心肌操作的特殊类型,例如心肌梗塞,在像休克、肾脏病,横纹肌溶解和肌病等各样不同的情况下,也可有肌红蛋白存在。此外,血清和血浆中肌红蛋白的浓度通常随年令与性别而变,健康的正常人浓度变化范围很宽,血清浓度高达90ug/l时通常认为是健康人群的高限。因此,对此人可能是正常水平的浓度,对其它人就可能是严重问题的指征,做诊断时要比预料的准确度略差。
肌浆球蛋白轻链(MLC)是肌浆球蛋白肌原纤维的整体部分,但其功能尚不清楚,MLC存在于快、慢、心房和心室肌肉之中,已知MLC对心脏缺血非常敏感。心肌坏死后血清中迅速出现MLC,提高的浓度可维持长达10天,图3说明了患者血清中MLC浓度与时间的关系(文献:Wang  J.等(1989)Clin.Chimica  Acta  181,325-336;Jackowski  G.,Symmes  J.等(1989)Circulation  Suppl  11,80,355)。
MLC确定溶血栓治疗是否成功也有预后的价值。MLC的浓度越高,预后越差,也表明梗塞越严重。在数天内浓度下降表示患者趋于康复,而高高低低或平台样曲线表明有梗塞趋势需做手术。
MLC主要有两种,称作MLC1和MLC2,存在于心肌细胞胞浆的可溶性库中,也可完整的存在于肌浆球蛋白肌原纤维中,心室肌细胞中的MLC2,或许还有MLC1与慢骨骼肌细胞中的同型是一样的。心脏疼痛患者的MLC1水平提高80-85%。MLC1对易变性心绞痛和冠心病是非常灵敏的指征。
其它类的心脏标示物,如低分子量的心肌蛋白(LMWCP)可作为心脏的标示物。这类标示物的实例包括收缩器官的成分,即肌钙蛋白,肌钙蛋白-T,肌钙蛋白-I和肌钙蛋白C,线粒体酶,如三糖P异构酶,易自心脏释放出的低分子量多肽,以及局部缺血发作后早期就释放的肌纤维膜蛋白或蛋白片数,特别是分子量为15kd的肌纤维膜蛋白和100kd的复合糖蛋白对心脏是特异的。
该心脏肌钙蛋白-I同型可抑制心肌收缩间静止期的肌纤蛋白和肌浆球蛋白分子间的相互作用。在MI后4-6小时内患者血清内出现肌钙蛋白I,并且这种增高的水平持续7-8天。图4说明了肌钙蛋白-I浓度与时间的关系。(文献:Cummins  B.,Auckland  M.L.和Cummins  P.(1987)Am.Heart  J.113,1333-1344)。肌钙蛋白-I对心脏是特异的标示物,在诊查是心肌损伤还是骨骼肌损伤时,比其它标示物更灵敏。
肌钙蛋白-T是薄丝状的肌钙蛋白-原肌球蛋白的复合物的构成成份,联结原肌球蛋白骨架和肌钙蛋白-I肌钙蛋白C复合物,肌钙蛋白-T是个碱性蛋白质,在心脏和快、慢骨骼肌中具有同型。MI发作后3小时内血清中即出现并且增高的水平至少持续10天。图5说明了肌钙蛋白-T的浓度与时间的关系(文献:Katus  H.A.等(1989)J.Mol.Cell  Cardiol.21,1349-1453)。肌钙蛋白-T的释放按双相的样式,对心脏是特异的,并且对MI非常灵敏。
肌浆球蛋白重链(MHC)和原肌球蛋白是分子量较大的蛋白质,也可作为心脏的标示物。MHC是肌肉主要收缩蛋白的构成部分。在心肌细胞坏死和随后的膜的不可逆损伤后,MHC的片断就会由心室中释放到血清中。虽然在心肌细胞坏死后,MHC片断不会迅速出现于血清中,但在MI后MHC增高的浓度至少持续10天,并且在MI后第4天可观测到MHC的峰值。图6说明了MHC浓度与时间的关系(文献:Leger  J.O.C.等(1985)Eur.J.of  Clin.Invet.15,422-429;Sequin  J.R.等(1989)J.Thorac.Cardiovase  Surga,397-401)。MHC释放曲线下面积与心肌细胞损伤程度有非常好的相关性。然而在MI的急性期MHC水平对临床价值不大。
原肌球蛋白是由两个多肽形成的二聚体,是肌肉收缩的调节系统的构成部分。在心肌梗塞发作后大约7-8小时,可检测出血清中的原肌球蛋白。如同CK-MB一样,它对心肌梗塞非常敏感。图7说明了MLC浓度与时间的关系(文献:CumminsP.等(1981)Clin.Sci.60,251-259)然而,骨骼肌损伤时,原肌球蛋白的浓度也会增高,因此它不是心脏特异性的。
现用的心肌梗塞的标准诊断方法都有局限性。在胸痛发作后,没有一种方法能立即提供非常灵敏、特异迅速和简便的诊断检查,例如在急救车或医生办公室中。
本发明是在胸痛发作的早期测定患者血液或血清中因心脏损伤存在的至少三种不同的标示物,并将它们综合在一起,以提供一种心肌梗塞诊断的改良方法,用于易变性心绞痛或MI的早期诊断。
以前的诊断方法的缺陷可用一种准确、快速和便携的一步式诊断板加以克服,以用于急诊处置中检测心脏受损伤的患者血清中存在的至少三种标示物。试验结果将确定患者是患了易变性心绞痛还是心肌梗塞。MI的早期诊断仍能在早期开始进行溶血栓治疗。因而心脏损伤会降到最低水平,从而增加了患者的生存机会。即使在疼痛发作数天之后,本诊断板的试验结果也可以区分易变性心绞痛和心肌梗塞。该诊断板是利用酶免疫试验夹层干化学型板。用这种板进行系列的短暂的测定,可为内科医生提供关于心脏损伤的程度和溶血栓处置的预后的信息。本发明的优越实施例中,这三个标示物是肌酸激酶(CK),肌红蛋白和肌原纤维轻链(MLC)。
本发明的一个内容是提供了一种诊断用试验盒,用以在患者胸痛的早期发作时检查出心肌梗塞。该试验盒包括一个可容纳和保留患者血液或血清样品的贮存部和一个与血样进行反应的检测装置。该检测装置的组成是,至少有三种悬浮于载体上的单克隆或多克隆抗体,每一种抗体与早期心肌梗塞时自心肌释放的不同的蛋白质相互补,以及独立地与应答互补的蛋白进行反应的各个抗体的相应的试剂。与试剂反应的效果的综合,应提示诊断时患者心脏的状况。
本发明的实施例用图加以说明。
图1是血清中CK浓度与时间的关系作图;
图2是血清中肌红蛋白浓度与时间的作图;
图3是血清中MLC浓度与时间的作图;
图4是血清中肌钙蛋白-I浓度与时间的作图;
图5是血清中肌钙蛋白-T浓度与时间的作图;
图6是血清中MHC浓度与时间的作图;
图7是血清中原肌球蛋白浓度与时间的作图;
图8是优选的实施例的平面观;
图9是图8实例的分解透视图;
图10是图18的实例中膜的偏斜图;
图11是膜的第二个实例的偏斜图。
本发总的用图8加以说明。本发明的优选实例是一块如1所示的板。
所用板的样式是已知的,可以买到,该板的形状与现用的综合妊娠试验板相似,可以买到,商品名为BIOSIGN。
板是由聚丙烯片构成,分前板10和后板12。前板10有一显示窗口14,每一个心脏标示物对应一个口,还有一个样品口16,如图9所示。在前板10下面有一块暴露的干化学膜18,后者用适当的方法粘连在前板10的背面。后板12有个绕其一周的边20,以与前板10严格扣合。这样,把膜18封在前后板之间。
前板和后板的扣合如所述的那样,但还有许多其它的适宜的联结方法,对熟悉此类技艺的人来说这是明显的。
前板10也能提供一块区域13,上面可写上患者的姓名和身份,也可用来书写测定结果。
关于图10,膜18是单克隆和多克隆抗体的载体。在优选的实例中,将血液或血清按箭头方向由一端流向另一端。端点22与样品窗口16对在一起。固定不动的抗体24层压在或连到抗体一酶结合物26上,后者针对抗原的不同的表位,而不会被抗体24识别。抗体24与肌浆球蛋白互补。同样,抗体28层压在相应的试剂30上。抗体28互补于CK-MB。同样,抗体32层压在试剂34上。抗体32与肌浆球蛋白轻链互补。抗体36与正常血液或血清中存在的任何蛋白互补。抗体36层压在试剂38上。
单克隆和多克隆抗体可用常规方法,由制备多克隆抗体的哺乳动物中制取。
在优选实例中用标记的试剂,该抗体试剂标记到或用化学方法键合于可被观测或测定的特定的部位,以便对血清或血液中存在的抗体或干化学膜上抗体的存在加以验证或定量。可以与本发明的用作诊断工具的抗体相结合的配基和基团,包括有元素、化合物或生物物质,它们所具有的物理或化学特性可用来区别与它们链合的抗体与其它的抗体。
每个心脏标示物至少需要两种类型为单/多或兔/多,山羊/多的抗体。这些抗体对它们的心脏免疫原进行亲合性纯化,再用交叉吸附法对非相关种属的免疫原进一步纯化,以除去非特异性免疫球蛋白。
使用时诊断师例如内科医生、急救车护理或护士将三滴或低于100ul的患者血清或血液加到样品窗口16中。样品会由于毛细作用沿膜18移动并相继与抗体和试剂对(24和26,28和30,32和34以及36和38)相接触。
若血样中有特异的心脏标示物,则与固定在膜上的抗体相结合。相应的试剂也会与之反应并可由试剂颜色的改变而看出。这种颜色的变化与血样中标示物的浓度成比例。这样,若在一定时间间隔用此试验盒检查,可以确定标示物的浓度增高或降低,作为诊断工具。在3-5分钟内就能完成检查结果。
在优选的实例中,测定的样品中的各个心脏标示物均会出现一个蓝色色带。色带的深浅强度可用反射计定量,颜色的强度与特定的标示物的浓度相关。反射计可包括有微处理机,在板上被检测的每个心脏标示物的定量结果以浓度大小和患者的姓名或身份一起打印出来。
用三滴或低于100ul的血清或血浆测定时,标示物的浓度为0.5ng/ml-25ng/ml最为敏感,每次测定和数次测定之间的精确度,变异系数低于15%。
在测定中所用的心脏标示物将取决于那些标示物的性质。优选实例用的板有肌红蛋白、MLC和CK-MB,如图8所示。
肌红蛋白从心肌细胞中释放非常早,它不是心脏所特异的,对心肌梗塞和坏死有非常高的灵敏性,在无坏死情况下的缺氧损伤是不会释放出的。MLC是心脏特异性的,用以区别心脏性的和非心脏性的疼痛,它的释放也快但不像肌红蛋白那样快。CK-MB可将心绞痛和心肌梗塞区分开,但只有在胸痛发作6小时后才能检测出,因此不能单独用于急诊诊断。
如果所用的心脏的三个标示物是CK-MB,肌红蛋白和MLC,参考图1,2,和3,其结果对诊断可用如下的解析。
若诊断板显示阳性的MLC和阴性的肌红蛋白和CK-MB,则提示患者的胸痛是心脏性的,原因是易变性心绞痛。
若肌红蛋白和MLC是阳性结果,CK-MB是阴性的,提示为早期心肌梗塞,可开始干预治疗。
若三种都是阳性结果,提示为心肌梗塞。
若MLC和CK-MB是阳性,肌红蛋白为阴性,则提示为心肌梗塞。
若肌红蛋白和CK-MB为阳性而MLC为阴性,则患者可能有骨骼肌损伤(假阳性)或是心肌梗塞中期。
在这种情况下该试验不能区分假阳性和“小”的心肌梗塞,因为MLC释放曲线在数个间隔中稍许下沉,病人可能有轻度心内膜下梗塞,并且在“下沉”时刻测定。当梗塞很小时,这种“下沉”几乎达到正常水平,因而测定的患者MLC为阴性。阳性诊断要依赖于CK-MB的存在。
心肌梗塞大的患者,MLC的“下沉”并不大到与正常水平一样,因此MLC仍可检测出。
其它实例的试验板是用同样的格式,抗体有不同的组合,这样来评估心脏的不同的标出物。
为了保证在患者胸痛的早期能用这种试验板检测出心肌组织的损伤,必须用至少一种相应于在心脏损伤的初期有大量的存在的标示物的抗体,即例如CK,肌浆球蛋白轻链或肌球蛋白。具有CK、肌浆球蛋白轻链或肌球蛋白特征和性质的低分子量心脏蛋白也可用在药盒中,
适宜的蛋白和酶可选自:肌钙蛋白,肌钙蛋白-I,肌钙蛋白C,肌钙蛋白-T和肌纤维膜蛋白,三糖磷酸异构酶或者具有肌酸激酶、肌浆蛋白轻链或肌球蛋白特性和性质的各种重分子量心脏蛋白。
其它蛋白质例如原肌球蛋白和肌浆球蛋白重链也可加到诊断盒中。如果患者前来求诊是在胸痛发作许多小时后而且患者的MI处于较晚阶段,则该试验盒可检测MI。
第二个实例是膜18上可有一层被捕获的抗体124及相应的试剂126。同样为了检测其它各个标示物,要有成对的相应的抗体和试剂,即128和130,132和134以及对照组对136和138。使用时,把血样滴到每对试药上,用上述相同的方式读出结果。
干化学膜118可用吸收性物质120支持。吸收性物质120可增加血清向膜内的透入力。
另一个试验盒的实例是用血样品管,这种管通常用来从患者身上抽取血样,管的内壁作为单克隆和多克隆抗体及试剂的载体。从患者身上抽取血样后,使用者只要振摇样品管,抗体就会与血液反应。如果血液中存在心脏蛋白,就会发生如前所述的颜色变化。
本发明书虽然对优选实例作了阐述和说明,但不要认为本发明只局限于这些持定的实例。对本技术熟悉的会作许多变换和改进。本发明的界定可参见权利要求。

Claims (18)

1、在患者胸痛发作早期诊察心肌梗塞的一种诊断试验盒,它包括有一个可容纳和保留患者血液或血清样品的贮存部和一个与血样进行反应的检测装置。该检测装置的组成是,至少有三种悬浮于载体上的单克隆或多克隆抗体,每一种抗体与心肌梗塞早期自心肌释放的各种蛋白之一相互补,以及独自地应与互补的蛋白进行反应的各个抗体的相应的试剂,并把试剂反应的结果综合起来以提示作诊断时患者的心脏状况。
2、按照权利要求1的一种诊断试验盒,其特征是,该单克隆和多克隆抗体与下列蛋白质或酶的至少三种相互补:肌酸激酶,肌红蛋白,肌浆蛋白轻链,肌钙蛋白,肌钙蛋白-Ⅰ,肌钙蛋白C,肌钙蛋白-T和肌纤维膜蛋白,三糖磷酸异构酶或者具有肌酸激酶、肌红蛋白或肌浆球蛋白轻链、特征和性质的各种低分子量心脏蛋白,肌球蛋白或者具有肌酸激酶、肌红蛋白或肌浆球层白轻链特征和性质的各种高分子量心脏蛋白,其中至少有两种要选自肌酸激酶、肌红蛋白、肌浆球蛋白轻链和肌钙蛋白-T。
3、按照权利要求2的一种诊断用试验盒,其特征是,该单克隆和多克隆抗体是一种固定不动的抗体,层压在其相应的试剂上,该试剂是抗体-酶结合物,针对不同的表位而不会被抗体识别。
4、按照权利要求3的一种诊断用试验盒,其特征是,当每一种抗体与其相应的蛋白反应时的应答,是该试剂改变颜色。
5、按照权利要求4的一种诊断用试验盒,其特征是,该颜色的改变与样品中互补的蛋白质浓度成比例。
6、按照权利要求5的一种诊断用试验盒,其特征是,该接受器是有一个用来接受样品的样品窗口和一个用来展现试剂的展示窗口的前板,一个后板和封闭装置,用以确保前板和后板把载体封在当中,从而形成整体。
7、按照权利要求6的一种诊断用试验盒,其特征是,该载体是个干化学膜。
8、按照权利要求7的一种诊断用试验盒,其特征是,所说的膜是被吸收性物质所支持,以增强样品向检验部位的渗入。
9、按照权利要求8的一种诊断用试验盒,其特征是,该膜延伸到加样窗口和显示窗口处,抗体及其相应的试剂在空间上的关系是从加样窗口进到显示窗口。
10、按照权利要求9的一种诊断用试验盒,其特征是,该前板用来显示鉴定蛋白抗体反应的定位。
11、按照权利要求10的一种诊断用试验盒,其特征是,前板还连接一反射计,以定量样品中蛋白的浓度。
12、按照权利要求11的一种诊断用试验盒,其特征是,该检测手段包括一个对照抗体,它与血清中正常存在的蛋白质相互补,和一个相应的试剂,该试剂对于相互补的蛋白进行反应的对照抗体可作出应答,这样的应答结果提示该试验是有效的。
13、按照权利要求12的一种诊断用试验盒,其特征是,该对照抗体和相应的蛋白在载体上的位置要远离加样窗口以指示该试验真实地完成了。
14、按照权利要求5的一种诊断用试验盒,其特征是,该接受器是一种封闭式的清洁的容器,该载体是容器的边。
15、按照权利要求13或14的一种诊断用试验盒,其特征是,单克隆和多克隆抗体与肌酸激酶和肌红蛋白互补。
16、抗照权利要求15的一种诊断用试验盒,其特征是,这些抗体与肌酸激酶,肌红蛋白和肌钙蛋白-T互补。
17、按照权利要求15和一种诊断用试验,其特征是,这些抗体与肌酸激酶、肌红蛋白和肌钙蛋白-T互补。
18、按照权利要求15和一种诊断用试验,其特征是,在用少于100nl样品时,该试验对标示物浓度为0.5ng/ml-25ng/ml是灵敏的。每次测定和数次测定的准确度,变异系数低于15%。
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Families Citing this family (88)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5710008B1 (en) * 1990-10-12 1999-09-07 Spectral Diagnostics Inc Method and device for diagnosing and distinguishing chest pain in early onset thereof
US5604105B1 (en) * 1990-10-12 1999-08-24 Spectral Diagnostics Inc Method and device for diagnosingand distinguishing chest pain in early onset thereof
DE69332454T2 (de) * 1992-08-03 2003-03-20 Marconi Optical Components Ltd Trennverfahren
US5807752A (en) * 1992-09-11 1998-09-15 Boehringer Mannheim Corporation Assay using an unblocked solid phase with immobilized analyte binding partner
DE4243648A1 (de) * 1992-12-23 1994-07-07 Boehringer Mannheim Gmbh Verfahren zur Bestimmung von Herzmuskelnekrosen mittels Antikörper gegen das N-terminale Troponin I-Peptid
FR2701954B1 (fr) * 1993-02-23 1995-07-07 Pasteur Sanofi Diagnostics Composition stabilisée de troponine pour immunoessais et procédé de stabilisation de troponine pour immunoessais.
JPH09503050A (ja) * 1993-05-17 1997-03-25 フォートロン バイオサイエンス インク. 心臓トロポニン▲i▼のアッセイ
CA2130280C (en) * 1993-08-24 1999-08-31 Lilian Lee Method for purification of cardiac troponin i
US5658801A (en) * 1994-05-03 1997-08-19 Spectral Diagnostics Inc. Medical test kit
US5573957A (en) * 1994-09-28 1996-11-12 Spectral Diagnostics, Inc. Monoclonal antibody to human cardiac myoglobin
US5702905A (en) * 1994-09-28 1997-12-30 Spectral Diagnostics Monoclonal antibody to human ventricular myosin light chains
WO1996010076A1 (en) * 1994-09-28 1996-04-04 Spectral Diagnostics Inc. A monoclonal antibody to human cardiac troponin i
US6991907B1 (en) 1995-04-18 2006-01-31 Biosite, Inc. Methods for the assay of troponin I and T and complexes of troponin I and T and selection of antibodies for use in immunoassays
US6627404B1 (en) 1995-04-18 2003-09-30 Biosite, Inc. Methods for improving the recovery of troponin I and T in membranes, filters and vessels
US6174686B1 (en) 1995-04-18 2001-01-16 Biosite Diagnostics, Inc. Methods for the assay of troponin I and T and complexes of troponin I and T and selection of antibodies for use in immunoassays
US5795725A (en) * 1995-04-18 1998-08-18 Biosite Diagnostics Incorporated Methods for the assay of troponin I and T and selection of antibodies for use in immunoassays
FR2734267B1 (fr) * 1995-05-16 1997-08-01 Pasteur Sanofi Diagnostics Composition stabilisee de troponine pour immunoessais et procede de preparation d'une telle composition stabilisee
WO1997006725A1 (en) * 1995-08-17 1997-02-27 Duke University Method of assessing reperfusion after thrombolytic therapy
AU6764196A (en) * 1995-08-31 1997-03-19 First Medical, Inc. Methods and antibodies for detecting creatine kinase
US6611634B2 (en) 1996-03-19 2003-08-26 University Of Utah Research Foundation Lens and associatable flow cell
JPH09304393A (ja) * 1996-05-15 1997-11-28 Ind Technol Res Inst 急性心筋梗塞診断キット
US5690103A (en) * 1996-06-20 1997-11-25 Groth; Torgny Lars Detection/exclusion of acute myocardial infarction using neural network analysis of measurements of biochemical markers
US6156521A (en) * 1997-12-19 2000-12-05 Biosite Diagnostics, Inc. Methods for the recovery and measurement of troponin complexes
US5834210A (en) * 1997-05-23 1998-11-10 Spectral Diagnostics, Inc. Stable troponin subunits and complexes
US6248869B1 (en) 1997-05-29 2001-06-19 Medical Analysis Systems, Inc. Troponin I forms and use of the same
ATE489633T1 (de) 1997-06-10 2010-12-15 Lpath Inc Verfahren zum frühzeitigen nachweis herzerkrankungen
US5961470A (en) * 1997-07-09 1999-10-05 Wagner; David A. Breath test for assessing hepatic function
US7384751B1 (en) * 1997-07-16 2008-06-10 Queen's University At Kingston Methods of diagnosing muscle damage
US6222619B1 (en) 1997-09-18 2001-04-24 University Of Utah Research Foundation Diagnostic device and method
US6475785B1 (en) 1997-12-18 2002-11-05 Spectral Diagnostics, Inc. Single-chain polypeptides comprising troponin I N-terminal fragments and troponin C
US6077676A (en) * 1997-12-18 2000-06-20 Spectral Diagnostics, Inc. Single-chain polypeptides comprising troponin I and troponin C
US6214629B1 (en) 1998-08-06 2001-04-10 Spectral Diagnostics, Inc. Analytical test device and method for use in medical diagnoses
US6410341B1 (en) 1998-08-06 2002-06-25 Spectral Diagnostics, Inc. Analytical test device and method for use in medical diagnoses
US6171870B1 (en) 1998-08-06 2001-01-09 Spectral Diagnostics, Inc. Analytical test device and method for use in medical diagnoses
US6432126B1 (en) * 1998-09-30 2002-08-13 C.R. Bard, Inc. Flexible vascular inducing implants
US20030215359A1 (en) * 1998-10-02 2003-11-20 Ischemia Technologies, Inc. Tests for the rapid evaluation of ischemic states and kits
US7449338B2 (en) * 1998-10-02 2008-11-11 Ischemia Technologies, Inc. Tests for the rapid evaluation of ischemic states and kits
US7070937B1 (en) 1998-10-02 2006-07-04 Ischemia Technologies, Inc. Marker useful for detection and measurement of free radical damage and method
US20050142613A1 (en) * 1998-10-02 2005-06-30 David Bar-Or Test for the rapid evaluation of ischemic states and kits
US6475743B1 (en) 1998-10-02 2002-11-05 Ischemia Technologies, Inc. Marker useful for detection and measurement of free radical damage and method
US7282369B2 (en) * 1998-10-02 2007-10-16 Ischemia Technologies, Inc. Tests for the rapid evaluation of ischemic states and kits
GB9827411D0 (en) 1998-12-11 1999-02-03 Axis Biochemicals Asa Dipstick assay
CA2263063C (en) * 1999-02-26 2004-08-10 Skye Pharmatech Incorporated Method for diagnosing and distinguishing stroke and diagnostic devices for use therein
US6780606B1 (en) * 1999-02-26 2004-08-24 Synx Pharma, Inc. Method for diagnosing and distinguishing stroke and diagnostic devices for use therein
US7618782B1 (en) 1999-10-18 2009-11-17 Queen's University At Kingston Methods of diagnosing muscle damage
US7078486B2 (en) * 1999-12-10 2006-07-18 Spectral Diagnostics, Inc. Single-chain polypeptides comprising troponin I and troponin C
GB9929140D0 (en) * 1999-12-10 2000-02-02 Univ Geneve Diagnostic assay for stroke
AU5828201A (en) * 2000-03-10 2001-09-17 Univ Geneve Diagnostic assay for transmissible spongiform encephalopathies
US7204847B1 (en) 2000-07-28 2007-04-17 C. R. Bard, Inc. Implant anchor systems
RU2286172C2 (ru) * 2000-08-17 2006-10-27 Трипеп Аб Вакцины, содержащие рибавирин, и способы их использования
AU2001292151B2 (en) 2000-08-17 2006-05-04 Tripep Ab Vaccines containing ribavirin and methods of use thereof
US6680059B2 (en) * 2000-08-29 2004-01-20 Tripep Ab Vaccines containing ribavirin and methods of use thereof
US7022830B2 (en) * 2000-08-17 2006-04-04 Tripep Ab Hepatitis C virus codon optimized non-structural NS3/4A fusion gene
CA2419295A1 (en) * 2000-08-21 2002-02-28 Queen's University At Kingston Methods and kits for separation and detection of proteins in biological samples
US6673562B2 (en) * 2000-08-24 2004-01-06 Spectral Diagnostics, Inc. Differential immunoassay
US20030199000A1 (en) * 2001-08-20 2003-10-23 Valkirs Gunars E. Diagnostic markers of stroke and cerebral injury and methods of use thereof
US7524635B2 (en) 2003-04-17 2009-04-28 Biosite Incorporated Methods and compositions for measuring natriuretic peptides and uses thereof
US20040176914A1 (en) * 2001-04-13 2004-09-09 Biosite Incorporated Methods and compositions for measuring biologically active natriuretic peptides and for improving their therapeutic potential
US20030219734A1 (en) * 2001-04-13 2003-11-27 Biosite Incorporated Polypeptides related to natriuretic peptides and methods of their identification and use
US7713705B2 (en) 2002-12-24 2010-05-11 Biosite, Inc. Markers for differential diagnosis and methods of use thereof
US7632647B2 (en) * 2001-04-13 2009-12-15 Biosite Incorporated Use of B-type natriuretic peptide as a prognostic indicator in acute coronary syndromes
ATE458199T1 (de) * 2001-05-04 2010-03-15 Biosite Inc Diagnostische marker der akuten koronaren syndrome und ihre verwendungen
US20040209307A1 (en) * 2001-08-20 2004-10-21 Biosite Incorporated Diagnostic markers of stroke and cerebral injury and methods of use thereof
CA2457775A1 (en) * 2001-08-20 2003-02-27 Biosite Incorporated Diagnostic markers of stroke and cerebral injury and methods of use thereof
US7608406B2 (en) * 2001-08-20 2009-10-27 Biosite, Inc. Diagnostic markers of stroke and cerebral injury and methods of use thereof
US20040219509A1 (en) * 2001-08-20 2004-11-04 Biosite, Inc. Diagnostic markers of stroke and cerebral injury and methods of use thereof
US6461828B1 (en) 2001-09-04 2002-10-08 Syn X Pharma Conjunctive analysis of biological marker expression for diagnosing organ failure
US20050130245A1 (en) * 2001-09-17 2005-06-16 Syn X Pharma, Inc. Diagnosis and treatment of early pre-type-1 diabetes utilizing neuronal proteins
US20030054414A1 (en) * 2001-09-17 2003-03-20 George Jackowski Diagnosis and treatment of early pre-type-1 diabetes utilizing glial fibrillary acidic protein
US20040067512A1 (en) * 2001-11-09 2004-04-08 Neurogenetics, Inc. Single nucleotide polymorphisms and mutations on Alpha-2-Macroglobulin
WO2003051174A2 (en) * 2001-11-09 2003-06-26 Neurogenetics, Inc. Single nucleotide polymorphisms and mutations on alpha-2-macroglobulin
US20050014198A1 (en) * 2002-07-11 2005-01-20 Leong Ng Assays and kits for detecting and monitoring heart disease
GB0216191D0 (en) * 2002-07-11 2002-08-21 Univ Leicester Plasma urotensin in human heart failure
GB0224425D0 (en) * 2002-10-21 2002-11-27 Univ Leicester Method for prediction of cardiac disease
JP4727997B2 (ja) * 2005-01-12 2011-07-20 シスメックス株式会社 イムノクロマトグラフィー用キット
WO2007031867A2 (en) 2005-05-25 2007-03-22 Tripep Ab A hepatitis c virus non-stru tural ns3/4a fusion gene
EP1896851B1 (en) * 2005-06-28 2013-08-21 ZBx Corporation Membrane array and analytical device
AU2007284651B2 (en) * 2006-08-09 2014-03-20 Institute For Systems Biology Organ-specific proteins and methods of their use
US20090214593A1 (en) * 2007-08-16 2009-08-27 Tripep Ab Immunogen platform
US8071561B2 (en) * 2007-08-16 2011-12-06 Chrontech Pharma Ab Immunogen platform
EP2425247A4 (en) * 2009-04-28 2013-01-23 Innovative Lab Technologies Inc IMMUNOCHROMATOGRAPHIC LATERAL FLOW TEST DEVICES
CA2761156C (en) * 2009-05-07 2017-03-14 University Of Cincinnati Methods of preventing ischemic injury using peripheral nociceptive stimulation
US20110306148A1 (en) 2010-06-14 2011-12-15 Siemens Healthcare Diagnostics Inc. Composition for use as an assay reagent
EP2596347B1 (en) 2010-07-22 2017-09-06 Hach Company Alkalinity analysis using a lab-on-a-chip
WO2012060845A1 (en) * 2010-11-05 2012-05-10 University Of Cincinnati Methods of preventing ischemic injury using peripheral nociceptive stimulation
US20140370502A1 (en) 2011-09-08 2014-12-18 Nexus Dx, Inc. Multilevel analyte assay
US9180449B2 (en) 2012-06-12 2015-11-10 Hach Company Mobile water analysis
USD768872S1 (en) 2012-12-12 2016-10-11 Hach Company Cuvette for a water analysis instrument

Family Cites Families (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5411231A (en) * 1977-06-27 1979-01-27 Daiichi Radioisotope Lab Production of purified antiimyoglobin antibody and quantitative analysis of myoglobin
US4353982A (en) * 1980-04-10 1982-10-12 Hoffmann-La Roche Inc. Immunochemical assay for creatine kinase-MB isoenzyme
US4624916A (en) * 1984-04-06 1986-11-25 International Immunoassay Laboratories, Inc. Process and composition for the rapid quantitation of small levels of creative kinase-MB isoenzyme
US4999285A (en) * 1984-11-15 1991-03-12 Syntex (U.S.A.) Inc. Chromatographic cassette
IE59210B1 (en) * 1985-11-14 1994-01-26 Univ Washington Creatine kinase mb determination method
JPS62151192A (ja) * 1985-12-24 1987-07-06 Denka Seiken Co Ltd ヒト心筋ミオシン軽鎖に対する単一クロ−ン抗体
DE3640318A1 (de) * 1986-11-26 1988-06-09 Boehringer Mannheim Gmbh Verfahren und testtraeger zur bestimmung eines analyten
DE3707746A1 (de) * 1987-03-11 1988-09-22 Boehringer Mannheim Gmbh Spezifische antikoerper gegen herzmuskelmyosin-leichtketten, ihre herstellung und verwendung in einem reagenz zur bestimmung von herzmuskelmyosin-leichtketten
CA1303983C (en) * 1987-03-27 1992-06-23 Robert W. Rosenstein Solid phase assay
US4857453A (en) * 1987-04-07 1989-08-15 Syntex (U.S.A.) Inc. Immunoassay device
CA1340557C (en) * 1987-04-09 1999-05-25 Christine A. Vitkauskas Ckmb assay and monoclonal antibodies for use in same
CA1313616C (en) * 1987-06-01 1993-02-16 Robert B. Sargeant Lateral flow, non-bibulous membrane protocols
US4900662A (en) * 1987-07-21 1990-02-13 International Immunoassay Laboratories, Inc. CK-MM myocardial infarction immunoassay
JPS6461664A (en) * 1987-08-18 1989-03-08 Maikurobaiorojikaru Res Corp Solid phase enzyme immunological inspection system and processing therefor
JPH01233298A (ja) * 1988-03-11 1989-09-19 Boehringer Mannheim Gmbh 抗体、その製造法、hmlcを測定するための試薬、ならびにモノクローナル抗体
DE3814370A1 (de) * 1988-04-28 1989-11-09 Boehringer Mannheim Gmbh Testtraeger fuer die analyse einer probenfluessigkeit, verfahren zur durchfuehrung einer solchen analyse und herstellungsverfahren
JPH01302162A (ja) * 1988-05-31 1989-12-06 Tosoh Corp ヒトミオグロビンの測定方法
US5087556A (en) * 1989-05-17 1992-02-11 Actimed Laboratories, Inc. Method for quantitative analysis of body fluid constituents
GB8916718D0 (en) * 1989-07-21 1989-09-06 Vioclone Biolog Inc Use of creatine kinase and its isozyme ck-mb and human ventricular myosin light chain 1 in the diagnosis of heart failure

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GB9111965D0 (en) 1991-07-24
BR9104431A (pt) 1992-06-09
CN1036155C (zh) 1997-10-15
JP2628421B2 (ja) 1997-07-09
CA2027434A1 (en) 1992-04-13
NZ239938A (en) 1994-03-25
GB2248688A (en) 1992-04-15
KR920008491A (ko) 1992-05-28
DE4122886C2 (de) 2000-03-02
MX9101550A (es) 1992-07-08
US5290678A (en) 1994-03-01
AR247634A1 (es) 1995-01-31
BE1004994A5 (fr) 1993-03-16
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DE4122886A1 (de) 1992-04-16
ITMI912687A1 (it) 1993-04-10
AU8475791A (en) 1992-04-16
JPH04258765A (ja) 1992-09-14
ES2070658B1 (es) 1995-12-16
ITMI912687A0 (it) 1991-10-10
FR2667944B1 (fr) 1993-07-30
IT1251682B (it) 1995-05-19
AU654672B2 (en) 1994-11-17
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FR2667944A1 (fr) 1992-04-17
ES2070658A1 (es) 1995-06-01

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