CN103698505A - 一种高效稳定的tmb显色液及其制备方法 - Google Patents

一种高效稳定的tmb显色液及其制备方法 Download PDF

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CN103698505A
CN103698505A CN201310682191.XA CN201310682191A CN103698505A CN 103698505 A CN103698505 A CN 103698505A CN 201310682191 A CN201310682191 A CN 201310682191A CN 103698505 A CN103698505 A CN 103698505A
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谭柏清
李志明
甘宜梧
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Biobase Biodustry Shandong Co Ltd
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Abstract

市场上TMB显色液存在稳定性差,保存时间短,显色背景高,灵敏度低等的缺点,本发明提供了一种高效稳定的TMB显色液。其特征在于,各组分的摩尔浓度或质量分数为:TMB的摩尔浓度为1.2mmol/L,H2O2的摩尔浓度为3.1mmol/L,曲拉通X-405的质量分数为0.3%,过氧化脲的质量分数为0.5%,醋酸钠的摩尔浓度为0.2mol/L,L(+)-酒石酸的摩尔浓度为0.027mol/L。本发明为TMB单相显色液,使用前无需混合,可以减少人为操作过程中的误差,通过引入非离子表面活性剂,使单相TMB显色液可以长期稳定保存。

Description

一种高效稳定的TMB显色液及其制备方法
技术领域
本发明涉及临床体外检测技术,特别涉及一种高效稳定的TMB显色液及其制备方法。
背景技术
自从Engvall和Perlman(1971)首次报道建立酶联免疫吸附试验(Enzyme-Linked Immunosorbent Assays,ELISA)以来,由于ELISA具有快速、敏感、简便、易于标准化等优点,使其得到迅速的发展和广泛应用。目前酶免疫分析(EIA)技术,已被广泛应用于抗原,半抗原或抗体的定量或定性检测分析。酶联免疫吸附 (ELISA) 检测方法虽然有很多种,但各种方法都离不开酶结合物和显色剂。在 ELISA 试剂中应用最广泛的酶是辣根过氧化物酶 (HRP),而该系统的显色剂有多种,目前市场最常用的是TMB (3,3’,5,5’- 四甲基联苯胺)。辣根过氧化物酶(HRP)及其藕联物是酶联免疫分析技术中常用的一种酶,由于3,3',5,5'-四甲基联苯胺(TMB)在HRP的显色反应体系中,比其它色原具有更高的灵敏度且无至癌性而被广泛应用。
TMB(3,3’,5,5’-四甲基联苯胺)是一种新型HRP(辣根过氧化物酶)色原底物。相对其他显色底物,TMB 以显色高效、无毒、不致癌、稳定性好等特点成为 ELISA 检测的主流显色剂。在ELISA检测时,HRP催化过氧化物释放出氧使 TMB 被氧化成蓝色的产物,加入酸性的终止液终止反应后,蓝色溶液变成橙黄色,在 450nm 波长有最大吸收峰。通过测量吸光度,便可定性或定量判断出被检测物的含量。
常见的 TMB 显色试剂多由几个组分共同组成,并且常需要现配现用,使用不便,且容易导致检测结果不太稳定。一般市场常见 TMB 显色试剂通常分为 A、B 两种贮存液,使用需将两者按比例混合,操作繁琐且容易错配,常导致实验失败。此外,市场上也有少见的单相的TMB 显色液,但常常存在稳定性差,保存时间短,显色背景高,灵敏度低等的缺点。
发明内容
针对上述技术背景,本发明提供了一种高效稳定的TMB显色液及其制备方法。
本发明的一种高效稳定的TMB显色液,其特征在于,各组分的摩尔浓度或质量分数为:TMB的摩尔浓度为1.2mmol/L,H2O2的摩尔浓度为3.1mmol/L,曲拉通X-405的质量分数为0.3%,过氧化脲的质量分数为0.5%,醋酸钠的摩尔浓度为0.2mol/L,L(+)-酒石酸的摩尔浓度为0.027 mol/L。
所述的一种高效稳定的TMB显色液的制备方法,其特征在于包括以下步骤:
a.制备A液:以10mL二甲亚砜为溶剂,缓慢加入TMB,搅拌均匀使其充分溶解。
b.制备B液:取1L蒸馏水,加入醋酸钠16.406g使之终摩尔浓度为0.2mol/L;然后加入L(+)-酒石酸4.1g使之终摩尔浓度为0.027 mol/L,溶液最终pH值约为5.0。
c.在B液中加入适量A液、曲拉通X-405(Triton X-405)、H2O2和过氧化脲,使TMB终摩尔浓度为1.2 mmol/L,H2O2终摩尔浓度为3.1mmol/L,曲拉通X-405(Triton X-405)的终质量分数为0.3%,过氧化脲的终质量分数为0.5%。
本发明的使用方法:
用适当的干净容器(用纯净水反复冲洗),倒出适量的单组分TMB显色液,待达到室温后即可进行如下步骤:
a)    加液:加完HRP结合物并温育一定时间后,洗板3-5次,每孔加TMB显色液100uL。 根据实验需要,在室温(15-25°C)或37°C下温育10-30分钟。 
b)    终止:加等体积的1mol/L盐酸或硫酸溶液可终止反应,孔中反应液由蓝色变为黄色。
c)    读数:终止反应后30分钟内在450nm处读数。
相比市场常见TMB显色液而言,本发明为TMB单相显色液,使用前无需混合,简化操作流程,方便快捷,可以减少人为操作过程中的误差。通过引入非离子表面活性剂,促进TMB的溶解和稳定,使单相TMB显色液可以长期稳定保存,在2~8℃条件下保存有效期可达3年,并且显色终止后读数稳定。
附图说明
下面结合附图对本发明的具体实施方式作进一步详细的说明。
图1 实施例1方法制备的TMB显色液用酸溶液终止反应后TMB黄色产物的稳定性。
图2 实施例1方法制备的TMB显色液存放时间段后的稳定性。
具体实施方式
实施例1
本发明所述的一种高效稳定的TMB 显色液的制备方法包括如下步骤:
a.制备A液:以10mL二甲亚砜为溶剂,缓慢加入TMB,搅拌均匀使其充分溶解。
b.制备B液:取1L蒸馏水,加入醋酸钠16.406g充分溶解,使之终摩尔浓度为0.2mol/L;然后加入L(+)-酒石酸(L(+)-2,3-二羟基丁二酸)4.1g充分溶解,使之终摩尔浓度为0.027 mol/L, 溶液最终pH值约为5.0。
c.在B液中加入适量A液、曲拉通X-405(Triton X-405)、H2O2和过氧化脲,使TMB终摩尔浓度为1.2 mmol/L,H2O2终摩尔浓度为3.1mmol/L,曲拉通X-405(Triton X-405)的终质量分数为0.3%,过氧化脲的终质量分数为0.5%,醋酸钠的摩尔浓度为0.2mol/L,L(+)-酒石酸的摩尔浓度为0.027 mol/L。
实施例2
将实施例1的TMB显色液与国家食品药品监督管理局认可的某公司商品化的TMB显色液(简称为:对比显色液1)进行对比。
该对比显色液配方,其中各组分的摩尔浓度或质量分数为:
TMB的摩尔浓度为2.0mmol/L,
H2O2的摩尔浓度为4.0mmol/L,
过氧化脲的质量分数为0.1%,
磷酸氢二钠的摩尔浓度为0.1mol/L,
柠檬酸的摩尔浓度为0.013 mol/L。
以丙型肝炎病毒核心抗原试剂盒(双抗体夹心法ELISA)为例,显色15min后终止反应,在终止反应后的0,15,30,45,60min时测得OD值(λ=450nm)。用酸溶液终止反应后,计算TMB黄色产物的稳定性。
对比结果见说明书附图图1。由图1可以看出,实施例1方法得到的TMB显色液在终止反应后,TMB黄色产物的稳定性明显优于对比组TMB显色液。实施例1方法得到的TMB显色液在终止反应30分钟后,TMB换色产物几乎没有衰减;在终止反应60min时,仅有轻微衰减,稳定性明显提高。
实施例3
将用实施例1的方法制备的TMB显色液与国家食品药品监督管理局认可的某公司商品化的TMB显色液进行比较(简称为:对比显色液1)。
以丙型肝炎病毒核心抗原试剂盒(双抗体夹心法ELISA)为例,分别用实施例1的方法制备的TMB显色液和国家食品药品监督管理局认可的某公司商品化的TMB显色液(简称为:对比显色液1)做显色剂,测试丙肝核心抗原(HCV-cAg)标准品(浓度:80pg/mL),测试完成后试剂盒等均放置在2-8℃保存,每隔2个月测试一次,记录OD值。
对比结果见说明书附图图2。由图2可知,实施例1的方法制备的TMB显色液可以长期稳定存放,至少可以放置3年。
由此可见,相比市场常见TMB显色液而言,本发明为TMB单相显色液,使用时无需混合,简化操作流程,方便快捷,极大的减少人为操作误差。此外,通过加入非离子表面活性剂曲拉通X-405(Triton X-405),促进TMB的溶解和稳定,使单相TMB显色液可以长期稳定保存,在2~8℃条件下有效期3年,并且显色终止后读数稳定。可证明,本发明所涉及的TMB显色液具有高效稳定的特点,使用方便,可以满足酶联免疫试剂盒对显色底物液的各项要求。

Claims (2)

1.一种高效稳定的TMB显色液,其特征在于,各组分的摩尔浓度或质量分数为:TMB的摩尔浓度为1.2mmol/L,H2O2的摩尔浓度为3.1mmol/L,曲拉通X-405的质量分数为0.3%,过氧化脲的质量分数为0.5%,醋酸钠的摩尔浓度为0.2mol/L,L(+)-酒石酸的摩尔浓度为0.027 mol/L。
2.根据权利要求1中的一种高效稳定的TMB显色液的制备方法,其特征在于包括以下步骤:
a.制备A液:以10mL二甲亚砜为溶剂,缓慢加入TMB,搅拌均匀使其充分溶解,TMB最终摩尔浓度为0.12mol/L;
b.制备B液:取1L蒸馏水,加入醋酸钠16.406g充分溶解,使之终摩尔浓度为0.2mol/L;然后加入L(+)-酒石酸4.1g充分溶解,使之终摩尔浓度为0.027 mol/L, 溶液最终pH值约为5.0;
c.在B液中加入适量A液、曲拉通X-405、H2O2和过氧化脲,使TMB终摩尔浓度为1.2 mmol/L,H2O2终摩尔浓度为3.1mmol/L,曲拉通X-405的终质量分数为0.3%,过氧化脲的终质量分数为0.5%。
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CN104459109A (zh) * 2014-11-25 2015-03-25 成都威尔诺生物科技有限公司 一种用于酶联免疫反应的单组份tmb显色液
CN105116141A (zh) * 2015-07-02 2015-12-02 深圳市卫光生物制品股份有限公司 一种单组份tmb显色液及其制备方法
CN105974107A (zh) * 2016-07-13 2016-09-28 广州捷倍斯生物科技有限公司 单组份tmb显色液及其配制方法
CN106153907A (zh) * 2015-03-25 2016-11-23 霍普金斯(北京)医学诊断科技有限公司 一种基于胶体金的酶联免疫显色试剂
CN107190050A (zh) * 2016-03-14 2017-09-22 华东理工大学 一种hrp活性测定及h2o2浓度检测的试剂盒及其应用

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CN104459109A (zh) * 2014-11-25 2015-03-25 成都威尔诺生物科技有限公司 一种用于酶联免疫反应的单组份tmb显色液
CN104459109B (zh) * 2014-11-25 2016-03-23 成都威尔诺生物科技有限公司 一种用于酶联免疫反应的单组份tmb显色液
CN106153907A (zh) * 2015-03-25 2016-11-23 霍普金斯(北京)医学诊断科技有限公司 一种基于胶体金的酶联免疫显色试剂
CN105116141A (zh) * 2015-07-02 2015-12-02 深圳市卫光生物制品股份有限公司 一种单组份tmb显色液及其制备方法
CN107190050A (zh) * 2016-03-14 2017-09-22 华东理工大学 一种hrp活性测定及h2o2浓度检测的试剂盒及其应用
CN107190050B (zh) * 2016-03-14 2020-10-27 华东理工大学 一种hrp活性测定及h2o2浓度检测的试剂盒及其应用
CN105974107A (zh) * 2016-07-13 2016-09-28 广州捷倍斯生物科技有限公司 单组份tmb显色液及其配制方法

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