scholarly journals Hardware Integration and Software Design of Automated Nucleic acid extraction System based on Magnetic Bead Separation Method

Author(s):  
Yang Yu ◽  
Yongjie Dou ◽  
Qian Li ◽  
Xiaoli Zhao ◽  
Jiansheng Xu ◽  
...  
2021 ◽  
Author(s):  
Simon Haile ◽  
Aidan M. Nikiforuk ◽  
Pawan K. Pandoh ◽  
David D. W. Twa ◽  
Duane E. Smailus ◽  
...  

AbstractThe COVID-19 pandemic has highlighted the need for generic reagents and flexible systems in diagnostic testing. Magnetic bead-based nucleic acid extraction protocols using 96-well plates on open liquid handlers are readily amenable to meet this need. Here, one such approach is rigorously optimized to minimize cross-well contamination while maintaining sensitivity.Article SummaryA scalable, non-proprietary, magnetic bead-based automated nucleic acid extraction protocol optimised for minimum cross-well contamination


2012 ◽  
Vol 84 (6) ◽  
pp. 906-911 ◽  
Author(s):  
C. Mengelle ◽  
J.-M. Mansuy ◽  
K. Sandres-Sauné ◽  
C. Barthe ◽  
J. Boineau ◽  
...  

2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Nan Li ◽  
Minjie Shen ◽  
Jiajia Liu ◽  
Li Zhang ◽  
Huili Wang ◽  
...  

AbstractCoronavirus disease 2019 (COVID-19) has emerged, rapidly spread and caused significant morbidity and mortality worldwide. There is an urgent public health need for rapid, sensitive, specific, and on-site diagnostic tests for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. In this study, a fully integrated and portable analyzer was developed to detect SARS-CoV-2 from swab samples based on solid-phase nucleic acid extraction and reverse transcription loop-mediated isothermal amplification (RT-LAMP). The swab can be directly inserted into a cassette for multiplexed detection of respiratory pathogens without pre-preparation. The overall detection process, including swab rinsing, magnetic bead-based nucleic acid extraction, and 8-plex real-time RT-LAMP, can be automatically performed in the cassette within 80 min. The functionality of the cassette was validated by detecting the presence of a SARS-CoV-2 pseudovirus and three other respiratory pathogens, i.e., Klebsiella pneumoniae, Pseudomonas aeruginosa, and Stenotrophomonas maltophilia. The limit of detection (LoD) for the SARS-CoV-2 pseudovirus was 2.5 copies/μL with both primer sets (N gene and ORF1ab gene), and the three bacterial species were successfully detected with an LoD of 2.5 colony-forming units (CFU)/μL in 800 μL of swab rinse. Thus, the analyzer developed in this study has the potential to rapidly detect SARS-CoV-2 and other respiratory pathogens on site in a “raw-sample-in and answer-out” manner.


Viruses ◽  
2020 ◽  
Vol 12 (11) ◽  
pp. 1227
Author(s):  
Sabrina Halecker ◽  
Thomas C. Mettenleiter ◽  
Martin Beer ◽  
Bernd Hoffmann

To assist the global eradication of peste des petits ruminants virus (PPRV), a molecular test for the rapid and reliable detection of PPRV was developed which additionally enables the detection of pathogens relevant for differential diagnostics. For this purpose, the necessary time frame of a magnetic bead-based nucleic acid extraction protocol was markedly shortened to 7 min and 13 s. The optimized extraction was run on a BioSprint 15 platform. Furthermore, a high-speed multi-well RT-qPCR for the genome detection of PPRV and additional important pathogens such as Foot-and-mouth disease virus, Parapoxvirus ovis, Goatpox virus, and Mycoplasma capricolum subsp. capripneumoniae was established and combined with suitable internal control assays. The here-described qPCR is based on a lyophilized master mix and takes only around 30 to 40 min. Several qPCR cyclers were evaluated regarding their suitability for fast-cycling approaches and for their diagnostic performance in a high-speed RT-qPCR. The final evaluation was conducted on the BioRad CFX96 and also on a portable Liberty16 qPCR cycler. The new molecular test designated as “FastCheckFLI PPR-like”, which is based on rapid nucleic acid extraction and high-speed RT-qPCR, delivered reliable results in less than one hour, allowing its use also in a pen-side scenario.


Lab on a Chip ◽  
2016 ◽  
Vol 16 (1) ◽  
pp. 132-141 ◽  
Author(s):  
Kyungsup Han ◽  
Yong-Jin Yoon ◽  
Yong Shin ◽  
Mi Kyoung Park

We have developed a Self-powered Switch-controlled Nucleic acid Extraction System (SSNES) to overcome the limitation of LOC technology in POC applications. The SSNES have a potential to be widely used as powerless, fully-disposable and user-friendly system for DNA extraction.


The Analyst ◽  
2019 ◽  
Vol 144 (23) ◽  
pp. 7032-7040 ◽  
Author(s):  
Juxin Yin ◽  
Jiumei Hu ◽  
Jingjing Sun ◽  
Ben Wang ◽  
Ying Mu

This work showcases a PTFE-based nucleic acid extraction system for point-of-care and integration of digital PCR.


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