Department of Biosciences and Bioengineering , Indian Institute of Technology Guwahati , Guwahati , 781039 Assam , India.
Anal Chem. 2019 Mar 19;91(6):4213-4221. doi: 10.1021/acs.analchem.9b00670. Epub 2019 Mar 7.
Malaria diagnosis methods offering species-specific information on the causative parasites, along with their flexibility to use in different resource settings, have great demand for precise treatment and management of the disease. Herein, we report the detection of pan malaria and P. falciparum species using a dye-based reaction catalyzed by the biomarker enzymes Plasmodium lactate dehydrogenase ( PLDH) and Plasmodium falciparum glutamate dehydrogenase ( PfGDH), respectively, through instrument-based and instrument-free approaches. For the detection, two ssDNA aptamers specific to the corresponding PLDH and PfGDH were used. The aptamer-captured enzymes were detected through a substrate-dependent reaction coupled with the conversion of resazurin (blue, ∼λ) to resorufin (pink, ∼λ) dye. The reaction was monitored by measuring the fluorescence intensity at λ for resorufin, absorbance ratio (λ/λ), and change in color (blue to pink). The detection approach could be customized to a spectrophotometer-based method and an instrument-free device. For both the approaches, the biomarkers were captured from the serum samples with the help of aptamer-coated magnetic beads prior to the analysis to exclude potential interferences from the serum. In the instrument-free device, a medical syringe (5 mL) prefabricated with a magnet was used for in situ separation of the enzyme-captured beads from the reaction supernatant. The converted dye in the supernatant was then efficiently adsorbed over a DEAE cellulose-treated paper wick assembled in the syringe hose. The biomarkers could be detected by both qualitative and quantitative format following the color and pixel intensity, respectively, developed on the paper surface. The developed method and technique offered detection of the biomarkers within a clinically relevant dynamic range, with the limit of detection values in the picomolar level. Flexible detection capability, low cost, interference-free detections, and portable nature (for instrument-free devices) are the major advantages offered by the developed approaches.
疟疾诊断方法提供了有关致病寄生虫的种特异性信息,并且具有在不同资源环境中使用的灵活性,因此对于精确治疗和管理该疾病有很大的需求。在此,我们报告了使用基于染料的反应分别通过基于仪器和无仪器的方法来检测泛疟疾和恶性疟原虫物种,该反应由生物标志物酶乳酸脱氢酶(PLDH)和恶性疟原虫谷氨酸脱氢酶(PfGDH)催化。对于检测,使用了两种针对相应 PLDH 和 PfGDH 的 ssDNA 适体。通过与吖啶酯(蓝色,∼λ)转化为试卤灵(粉红色,∼λ)染料的底物依赖性反应来检测与适体结合的酶。通过测量λ处的荧光强度来监测反应,以获得用于检测的比值(λ/λ)和颜色变化(蓝色变为粉红色)。该检测方法可以定制为基于分光光度计的方法和无仪器设备。对于这两种方法,在分析之前,使用适体包被的磁性珠从血清样品中捕获生物标志物,以排除血清中可能存在的干扰。在无仪器设备中,使用预制有磁铁的 5 mL 医用注射器就地分离酶捕获的珠与反应上清液。然后,将上清液中转化的染料有效地吸附在组装在注射器软管中的 DEAE 纤维素处理过的纸芯上。可以通过定性和定量格式分别根据纸表面上开发的颜色和像素强度来检测生物标志物。开发的方法和技术提供了在临床相关的动态范围内检测生物标志物的能力,其检测限值为皮摩尔级。灵活的检测能力,低成本,无干扰检测以及便携性(对于无仪器设备)是开发方法的主要优势。