Evaluation and EUA validation of a production ready portable, Point-of-Need Platform for detection of COVID-19 direct from nasal swabs in 30 minutes.
Evaluation and EUA validation of a production ready portable, Point-of-Need Platform for detection of COVID-19 direct from nasal swabs in 30 minutes.
批准号:
72668
负责人:
金额:
$92.76万
依托单位:
依托单位国家:
英国
项目类别:
Collaborative R&D
财政年份:
2020
资助国家:
英国
项目状态:
已结题
起止时间:
2020 至 --
中文摘要
BG Research有一种简化的方法来测试患者是否有病毒引起的感染,QuRapID-XF技术。它是为应对埃博拉疫情而开发的,可以直接从患者样本进行便携式检测。这消除了对实验室或专家用户的需求--这一点很重要,因为它是为非洲农村资源匮乏的环境而设计的。该项目将产生一种直接来自鼻拭子的新冠肺炎感染测试,可以在任何地方使用,例如在入境口岸或通过急救人员。点对点测试(APT)将是有效应对英国新冠肺炎的关键。这种方法是一个高度敏感的便携平台,确保可以快速识别和隔离受感染的患者和那些没有症状但受感染的(早期)患者。。便携式分子检测系统可以在任何地方使用,并在患者等待的30分钟内给出结果。这项新冠肺炎检测将直接从鼻拭子中检测,但该技术直接从唾液、血液、尿液或其他原始样本中检测。QuRapID-XF检测很简单,因此可以由士兵和护士等非专家人员进行,并且可以进行大量的等待测试。基于分子诊断学的抗原测试比横向流动测试、免疫学测试敏感许多倍,可用于区分引起呼吸道症状(如流感)的不同病毒疾病。该项目将见证这一平台技术的大规模发布。PHE将能够将自己的检测部署到平台上,以快速应对未来血液传播和呼吸道病毒疾病的爆发。QuRapID-XF还可以为较贫穷的发展中国家带来低成本的检测。由于这种方法不需要提取核酸,并使用我们自己的试剂和仪器,因此不会出现与检测有关的供应链问题,因此将有可能快速提供大量检测,以应对未来的任何疫情。该检测将在多个地点和国家进行性能评估,确保检测将高度敏感。这项技术使英国能够应对生物安全威胁,并在全球范围内应对人类或兽医病毒疾病的爆发,减少疾病造成的死亡率和经济损失。
英文摘要
BG Research have a simplified method for testing patients for infections caused by viruses, the QuRapID-XF technology. Developed in response to the Ebola outbreak, it enables portable testing directly from patient samples. This removes the need for a lab or expert users -- important as it was designed to be used in resource poor environments in rural Africa.This project will generate a direct from nasal swab test for COVID-19 infections that could be used anywhere, for example at ports of entry or via first responder. At-Point-Testing (APT) will be vital to effectively deal with COVID-19 in the UK. This approach is a highly sensitive, portable platform that ensures infected and those with no symptoms but infected(early stage) patients can be rapidly identified and isolated . . The portable molecular testing system can be used anywhere and gives results within 30 minutes while the patient waits . Hence facilitating immediate isolation and contact tracing.This COVID-19 test will work directly from nasal swabs, but the technology detects directly from saliva, blood, urine or other crude samples. QuRapID-XF assays are simple, so can be performed by non-expert personnel such as soldiers and nurses and large numbers of while-you-wait tests could be performed. Antigen tests based on molecular diagnostics are many times more sensitive than lateral flow tests, immunological tests, and can be used to differentiate between different viral diseases causing e.g. respiratory symptoms, such as the flu.This project will see the scaled release of this platform technology.PHE will be able to deploy their own assays onto the platform to rapidly respond to future outbreaks of blood borne and respiratory viral diseases. QuRapID-XF can also bring low cost testing to poorer developing nations.As the approach doesn't require nucleic acid extraction and uses our own reagent and instrument, there will be none of the supply chain issues seen relating to testing and so it will be possible to deliver large numbers of tests rapidly in response to any future outbreaks.The assay will go through a performance evaluation at multiple sites and countries, ensuring that the test will be highly sensitive. This technology allows the UK to respond to biosecurity threats, and outbreaks of human or veterinary viral diseases globally, reducing mortality and economic losses caused by disease.
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