首页> 美国卫生研究院文献>The American Journal of Tropical Medicine and Hygiene >Rapid and Specific Drug Quality Testing Assay for Artemisinin and Its Derivatives Using a Luminescent Reaction and Novel Microfluidic Technology
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Rapid and Specific Drug Quality Testing Assay for Artemisinin and Its Derivatives Using a Luminescent Reaction and Novel Microfluidic Technology

机译:利用发光反应和新型微流技术对青蒿素及其衍生物进行快速而专一的药物质量检测

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摘要

Globally, it is estimated that about 10–30% of pharmaceuticals are of poor quality. Poor-quality drugs lead to long-term drug resistance, create morbidity, and strain the financial structure of the health system. The current technologies for substandard drug detection either are too expensive for low-resource regions or only provide qualitative results. To address the current limitations with point-of-care technologies, we have developed an affordable and robust assay to quantify the amount of active pharmaceutical ingredients (APIs) to test product quality. Our novel assay consists of two parts: detection reagent (probe) and a microfluidic testing platform. As antimalarials are of high importance in the global fight against malaria and are often substandard, they are chosen as the model to validate our assay. As a proof-of-concept, we have tested the assay with artesunate pure and substandard samples (Arsuamoon tablets) from Africa and compared with the conventional 96-well plate with spectrophotometer to demonstrate the quantitative efficacy and performance of our system.
机译:在全球范围内,估计约有10%至30%的药品质量较差。劣质药物会导致长期耐药性,造成发病,并使卫生系统的财务结构紧张。对于资源不足的地区,当前用于次标准药物检测的技术要么太昂贵,要么只能提供定性结果。为了解决即时医疗技术的当前局限性,我们开发了一种价格合理且功能强大的测定法,用于量化活性药物成分(API)的数量以测试产品质量。我们的新型检测方法包括两部分:检测试剂(探针)和微流体检测平台。由于抗疟药在全球抗击疟疾中非常重要,而且通常不合格,因此选择抗疟药作为验证我们分析的模型。作为概念验证,我们已经使用来自非洲的青蒿琥酯纯净和不合格样品(Arsuamoon片剂)测试了该测定方法,并与带有分光光度计的常规96孔板进行了比较,以证明我们系统的定量功效和性能。

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