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首页> 外文期刊>Malaria Journal >Development of a colloidal gold-based lateral flow dipstick immunoassay for rapid qualitative and semi-quantitative analysis of artesunate and dihydroartemisinin
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Development of a colloidal gold-based lateral flow dipstick immunoassay for rapid qualitative and semi-quantitative analysis of artesunate and dihydroartemisinin

机译:胶体金基侧向量油尺免疫分析技术的开发,用于对青蒿琥酯和双氢青蒿素进行快速定性和半定量分析

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Background Artemisinin-based combination therapy (ACT) plays an indispensable role in malaria control and elimination. However, the circulation of counterfeit, substandard drugs has greatly threatened malaria elimination campaigns. Most methods for the analysis of artemisinin and its derivatives require expensive equipment and sophisticated instrumentation. A convenient, easy-to-use diagnostic device for rapid evaluation of the quality of artemisinin drugs at the point-of-care is still lacking. In this study a lateral flow dipstick immunoassay was developed for qualitative and semi-quantitative analysis of artesunate (ATS) and dihydroartemisinin (DHA) in anti-malarial drugs. Methods This assay was based on a monoclonal antibody (mAb) raised against ATS. ATS-bovine serum albumin and goat anti-mouse IgG, used as the test capture reagent and the control capture reagent, were coated on the nitrocellulose membrane to form the test line and control line, respectively. The conjugate pad was saturated with the gold-labelled anti-ATS mAb. Results The indicator range of the dipsticks, defined as lowest concentration of the target analytes between which the test line was not visible, were 100-200 and 200-500 ng mL-1 for ATS and DHA, respectively. No competitive inhibition was observed up to 5,000 ng mL-1 of quinine, chloroquine diphosphate salt, primaquine phosphate, pyrimethamine, lumefantrine, amodiaquine, piperaquine tetraphosphate tetrahydrate or pyronaridine tetraphosphate. Semi-quantitative analysis of ATS and DHA in commercial drugs and raw drug materials with the dipsticks produced result agreeable with those determined by high performance liquid chromatography (HPLC). Storage test showed that the indicator range for artemisinins remained unchanged after a week at 37°C and increased four-folds after six months of storage at 4°C or ambient temperature. Conclusions The new selected mAb 3D82G7 with high avidity and broad cross reactivity for artemisinins was used to develop and optimize a dipstick immunoassay for qualitative and semi-quantitative analysis of ATS and DHA in anti-malarial drugs. The semi-quantitative analysis of ATS and DHA in commercial drugs and raw drug materials, and the specificity test of the artemisinin-related drugs both proved the accurate performance of the developed dipsticks for semi-quantitation of ACT samples. The dipstick may be used as a point-of-care device for identifying substandard and counterfeit ATS- and DHA-containing anti-malarial drugs.
机译:背景基于青蒿素的联合治疗(ACT)在控制和消除疟疾中起着不可或缺的作用。但是,假冒伪劣药品的流通极大地威胁了消除疟疾的运动。分析青蒿素及其衍生物的大多数方法都需要昂贵的设备和复杂的仪器。仍然缺乏一种方便,易于使用的诊断设备,可以在现场即时评估青蒿素药物的质量。在这项研究中,开发了一种侧向量油尺免疫测定法,用于抗疟药中青蒿琥酯(ATS)和双氢青蒿素(DHA)的定性和半定量分析。方法该测定基于针对ATS的单克隆抗体(mAb)。将用作测试捕获试剂和对照捕获试剂的ATS牛血清白蛋白和山羊抗小鼠IgG分别涂在硝酸纤维素膜上以形成测试线和对照线。共轭垫被金标记的抗ATS mAb饱和。结果试纸的指示剂范围定义为ATS和DHA的目标分析物的最低浓度,在该浓度之间看不到测试线,分别为100-200和200-500 ng mL-1。直至5,000 ng mL-1的奎宁,氯喹二磷酸盐,伯氨喹磷酸酯,乙胺嘧啶,lumefantrine,氨二醌,哌喹四磷酸四水合物或吡喃四氢呋喃,未观察到竞争性抑制作用。使用量油尺对商品药品和原料药中的ATS和DHA进行半定量分析,结果与高效液相色谱(HPLC)测定的结果相吻合。储存测试表明,青蒿素的指标范围在37°C一周后保持不变,在4°C或环境温度下六个月储存后增加了四倍。结论新选择的对青蒿素具有高亲和力和广泛交叉反应性的mAb 3D82G7用于开发和优化试纸免疫分析法,用于抗疟疾药物中ATS和DHA的定性和半定量分析。商业药品和原料药中ATS和DHA的半定量分析以及青蒿素相关药物的特异性测试均证明了所开发的量油尺可用于ACT样品的半定量。量油计可用作识别不合格和伪造的含ATS和DHA的抗疟疾药物的护理台设备。

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