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一种用于检测葡萄糖-6-磷酸脱氢酶缺乏症的新型基于纸的分析设备。

A new paper-based analytical device for detection of Glucose-6-phosphate dehydrogenase deficiency.

机构信息

Department of Clinical Microscopy, Faculty of Allied Health Sciences, Chulalongkorn University, Patumwan, Bangkok 10330, Thailand.

Department of Clinical Chemistry, Faculty of Allied Health Sciences, Chulalongkorn University, Patumwan, Bangkok 10330, Thailand.

出版信息

Talanta. 2017 Mar 1;164:534-539. doi: 10.1016/j.talanta.2016.12.026. Epub 2016 Dec 11.

Abstract

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a genetic haemolytic disorder. Most persons with G6PD deficiency are asymptomatic, but exposure to oxidant drugs, such as the anti-malarial drug primaquine, may induce haemolysis, which is commonly found in Asian countries. A reliable test is necessary for diagnosing the deficiency to prevent an acute haemolytic crisis. This study proposes a novel quantitative method to detect G6PD deficiency using paper-based analytical devices (G6PDD-PAD). Wax printing was utilized for fabricating circular reaction zone patterns in paper. The colorimetric assay is based on the formation of formazan via a reduction of tetra-nitro blue tetrazolium (TNBT) by the G6PD enzyme on G6PDD-PAD. Detection was achieved by capturing the colour using a desktop scanner and the colour intensity was analysed with Adobe Photoshop C56. The results showed that the G6PD activity analysed by G6PDD-PAD was highly correlated with the standard biochemical assay (SBA) (r=0.87, p<0.01). Moreover, good agreement by Bland-Altman bias plot was demonstrated between G6PDD-PAD and the SBA (mean bias 1.4 IU/gHb). The detection limit was 0 IU/gHb of G6PD activity. This study demonstrates the feasibility of using G6PDD-PAD. This simple, low-cost test ($0.1/test) should be useful for diagnosing G6PD deficiency in resource-limited settings.

摘要

葡萄糖-6-磷酸脱氢酶(G6PD)缺乏症是一种遗传性溶血性疾病。大多数 G6PD 缺乏症患者无症状,但接触氧化剂药物,如抗疟药物伯氨喹,可能会引发溶血性贫血,这种情况在亚洲国家很常见。为了预防急性溶血性危机,有必要进行可靠的检测来诊断该缺乏症。本研究提出了一种使用基于纸的分析装置(G6PDD-PAD)检测 G6PD 缺乏症的新定量方法。蜡印用于在纸上制造圆形反应区图案。比色测定法基于 G6PD 酶在 G6PDD-PAD 上将 G6P 还原为四硝基蓝四唑(TNBT)形成甲臜。通过台式扫描仪捕获颜色来进行检测,并使用 Adobe Photoshop C56 分析颜色强度。结果表明,G6PDD-PAD 分析的 G6PD 活性与标准生化测定法(SBA)高度相关(r=0.87,p<0.01)。此外,通过 Bland-Altman 偏差图显示,G6PDD-PAD 与 SBA 之间具有良好的一致性(平均偏差 1.4IU/gHb)。检测限为 0IU/gHb 的 G6PD 活性。本研究证明了使用 G6PDD-PAD 的可行性。这种简单、低成本的测试(每个测试$0.1)应该有助于在资源有限的环境中诊断 G6PD 缺乏症。

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