2021
DOI: 10.1007/978-1-0716-1803-5_16
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Sample-to-Answer Microfluidic Nucleic Acid Testing (NAT) on Lab-on-a-Disc for Malaria Detection at Point of Need

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Cited by 5 publications
(3 citation statements)
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“…Therefore, the facility for the probe-based LAMP methods is more likely to be more costly than the traditional LAMP methods. It is worth noting that some portable fluorescence analyzers and isothermal fluorimeters with minimal laboratory resources are currently available or under development (Supplementary Table S1) [70][71][72][73][74][75]. Furthermore, end-point fluorescence detection requires much less instrumentation than real-time monitoring.…”
Section: Comparison Of the Probe-based Lamp Methods With The Traditio...mentioning
confidence: 99%
“…Therefore, the facility for the probe-based LAMP methods is more likely to be more costly than the traditional LAMP methods. It is worth noting that some portable fluorescence analyzers and isothermal fluorimeters with minimal laboratory resources are currently available or under development (Supplementary Table S1) [70][71][72][73][74][75]. Furthermore, end-point fluorescence detection requires much less instrumentation than real-time monitoring.…”
Section: Comparison Of the Probe-based Lamp Methods With The Traditio...mentioning
confidence: 99%
“…Additionally, its long detection time makes it unsuitable for point-of-care applications. Therefore, the principles of PCR are applied in microfluidic assays [104][105][106][107]. Thermal cycling can be achieved using two typical methods: spatially based and time-based thermal cycling.…”
Section: Thermal Cyclingmentioning
confidence: 99%
“…This innovation eliminates the need for thermal cycling and costly apparatus, marking substantial progress in the field. , Nevertheless, despite advances in developing these devices, significant limitations persist. At present, there exists no POC device capable of facilitating HIV viral load self-testing due to the following challenges: the inability to process whole blood samples, the absence of quantitative or semiquantitative capabilities within a single run, , and the requirement for reagents to be stored at room temperature for extended periods. These pressing issues highlight the critical need for the development of an advanced HIV viral load monitoring device, one that operates from sample to answer and is suited for point-of-need usage.…”
mentioning
confidence: 99%