首页> 外文期刊>Tropical Medicine and International Health: TM and IH >An improved, simple screening method for detection of glucose-6-phosphate dehydrogenase deficiency.
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An improved, simple screening method for detection of glucose-6-phosphate dehydrogenase deficiency.

机译:一种改进的简单筛选方法,用于检测6-磷酸葡萄糖脱氢酶缺乏症。

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摘要

We established a new, simple and rapid screening method for detection of glucose-6-phosphate dehydrogenase (G6PD)-deficiency by using a new formazan substrate, 2-(2-methoxy-4-nitrophenyl)-3-(4-nitrophenyl)-5-(2,4-disulfophenyl)-2H tetrazolium monosodium salt (WST-8) with a hydrogen carrier of 1-methoxyphenazine methosulfate (1-methoxy PMS), instead of a combination of 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H tetrazolium bromide (MTT) and phenazine methosulfate (PMS), as used in many previous formazan methods. WST-8 does not react with haemoglobin, and the formed formazan is highly water-soluble, differing from MTT. Thus, the whole procedure can be performed in aqueous solution in a tube or well without any special equipment other than micropipettes. Within 1 h at room temperature, the strong orange colour of the WST-8 formazan formed in normal blood samples could be distinguished, by naked eye, from G6PD-deficient blood samples with less than 50% residual activity. We also found that reagents in the WST-8/1-methoxy PMS method were more resistant against exposure to sunlight than those in an MTT/PMS method. As the new method is both qualitative and quantitative, it is possible to express G6PD activity as increase of NADPH concentration by reading absorbance at 460 nm after incubation for 30 or 60 min.
机译:我们建立了一种新的,简单,快速的筛选方法,通过使用新的甲for底物2-(2-甲氧基-4-硝基苯基)-3-(4-硝基苯基)检测葡萄糖6-磷酸脱氢酶(G6PD)缺陷。 -5-(2,4-二磺基苯基)-2H四唑一钠盐(WST-8),其氢载体为1-甲氧基吩嗪硫酸甲酯(1-甲氧基PMS),而不是3-(4,5-二甲基- 2-噻唑基)-2,5-二苯基-2H溴化四氮唑(MTT)和吩嗪硫酸甲酯(PMS),在许多以前的甲for方法中都使用过。 WST-8不与血红蛋白反应,形成的甲an具有高度水溶性,与MTT不同。因此,整个过程可以在试管或孔中的水溶液中进行,无需使用除微量移液器外的任何专用设备。在室温下1小时之内,用肉眼可将正常血液样本中形成的WST-8甲the的深橙色与残留活性低于50%的G6PD不足的血液样本区分开。我们还发现,WST-8 / 1-甲氧基PMS方法中的试剂比MTT / PMS方法中的试剂更耐日光照射。由于该新方法既定性又定量,因此通过孵育30分钟或60分钟后在460 nm处读取吸光度,可以将G6PD活性表达为NADPH浓度的增加。

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