A sample-to-answer, quantitative real-time PCR system with low-cost, gravity-driven microfluidic cartridge for rapid detection of SARS-CoV-2, influenza A/B, and human papillomavirus 16/18
The pandemic of coronavirus disease 2019 (COVID-19), due to the novel coronavirus (SARS-CoV-2), has created an unprecedented threat to the global health system, especially in resource-limited areas. This challenge shines a spotlight on the urgent need for a point-of-care (POC) quantitative real-time...
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description | The pandemic of coronavirus disease 2019 (COVID-19), due to the novel coronavirus (SARS-CoV-2), has created an unprecedented threat to the global health system, especially in resource-limited areas. This challenge shines a spotlight on the urgent need for a point-of-care (POC) quantitative real-time PCR (qPCR) test for sensitive and rapid diagnosis of viral infections. In a POC system, a closed, single-use, microfluidic cartridge is commonly utilized for integration of nucleic acid preparation, PCR amplification and florescence detection. But, most current cartridge systems often involve complicated nucleic acid extraction
via
active pumping that relies on cumbersome external hardware, causing increases in system complexity and cost. In this work, we demonstrate a gravity-driven cartridge design for an integrated viral RNA/DNA diagnostic test that does not require auxiliary hardware for fluid pumping due to adopted extraction-free amplification. This microfluidic cartridge only contains two reaction chambers for nucleic acid lysis and amplification respectively, enabling a fast qPCR test in less than 30 min. This gravity-driven pumping strategy can help simplify and minimize the microfluidic cartridge, thus enabling high-throughput (up to 12 test cartridges per test) molecular detection
via
a small cartridge readout system. Thus, this work addresses the scalability limitation of POC molecular testing and can be run in any settings. We verified the analytical sensitivity and specificity of the cartridge testing for respiratory pathogens and sexually transmitted diseases using SARS-CoV-2, influenza A/B RNA samples, and human papillomavirus 16/18 DNA samples. Our cartridge system exhibited a comparable detection performance to the current gold standard qPCR instrument ABI 7500. Moreover, our system showed very high diagnostic accuracy for viral RNA/DNA detection that was well validated by ROC curve analysis. The sample-to-answer molecular testing system reported in this work has the advantages of simplicity, rapidity, and low cost, making it highly promising for prevention and control of infectious diseases in poor-resource areas.
We present a low-cost microfluidic cartridge design scheme that combines gravity-driven passive microfluidic pumping with extraction-free amplification to achieve "sample-in, answer-out" point-of-care nucleic acid detection within 30 minutes. |
doi_str_mv | 10.1039/d2lc00434h |
format | Article |
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via
active pumping that relies on cumbersome external hardware, causing increases in system complexity and cost. In this work, we demonstrate a gravity-driven cartridge design for an integrated viral RNA/DNA diagnostic test that does not require auxiliary hardware for fluid pumping due to adopted extraction-free amplification. This microfluidic cartridge only contains two reaction chambers for nucleic acid lysis and amplification respectively, enabling a fast qPCR test in less than 30 min. This gravity-driven pumping strategy can help simplify and minimize the microfluidic cartridge, thus enabling high-throughput (up to 12 test cartridges per test) molecular detection
via
a small cartridge readout system. Thus, this work addresses the scalability limitation of POC molecular testing and can be run in any settings. We verified the analytical sensitivity and specificity of the cartridge testing for respiratory pathogens and sexually transmitted diseases using SARS-CoV-2, influenza A/B RNA samples, and human papillomavirus 16/18 DNA samples. Our cartridge system exhibited a comparable detection performance to the current gold standard qPCR instrument ABI 7500. Moreover, our system showed very high diagnostic accuracy for viral RNA/DNA detection that was well validated by ROC curve analysis. The sample-to-answer molecular testing system reported in this work has the advantages of simplicity, rapidity, and low cost, making it highly promising for prevention and control of infectious diseases in poor-resource areas.
We present a low-cost microfluidic cartridge design scheme that combines gravity-driven passive microfluidic pumping with extraction-free amplification to achieve "sample-in, answer-out" point-of-care nucleic acid detection within 30 minutes.</description><identifier>ISSN: 1473-0197</identifier><identifier>EISSN: 1473-0189</identifier><identifier>DOI: 10.1039/d2lc00434h</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Amplification ; Cartridges ; Coronaviruses ; COVID-19 ; Deoxyribonucleic acid ; Diagnostic systems ; Disease transmission ; DNA ; Genetic testing ; Hardware ; Human papillomavirus ; Infectious diseases ; Influenza ; Low cost ; Microfluidics ; Nucleic acids ; Public health ; Pumping ; Real time ; Ribonucleic acid ; RNA ; Sensitivity analysis ; Severe acute respiratory syndrome coronavirus 2 ; Viral diseases ; Viral infections</subject><ispartof>Lab on a chip, 2022-09, Vol.22 (18), p.3436-3452</ispartof><rights>Copyright Royal Society of Chemistry 2022</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c314t-1722ed22d868cf017ec3a3f7d727c0c8efc3eb5065b304a6a51dd2436e8c557d3</citedby><cites>FETCH-LOGICAL-c314t-1722ed22d868cf017ec3a3f7d727c0c8efc3eb5065b304a6a51dd2436e8c557d3</cites><orcidid>0000-0003-4449-309X ; 0000-0002-5826-5752</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Zai, Yunfeng</creatorcontrib><creatorcontrib>Min, Chao</creatorcontrib><creatorcontrib>Wang, Zunliang</creatorcontrib><creatorcontrib>Ding, Yongjun</creatorcontrib><creatorcontrib>Zhao, Huan</creatorcontrib><creatorcontrib>Su, Enben</creatorcontrib><creatorcontrib>He, Nongyue</creatorcontrib><title>A sample-to-answer, quantitative real-time PCR system with low-cost, gravity-driven microfluidic cartridge for rapid detection of SARS-CoV-2, influenza A/B, and human papillomavirus 16/18</title><title>Lab on a chip</title><description>The pandemic of coronavirus disease 2019 (COVID-19), due to the novel coronavirus (SARS-CoV-2), has created an unprecedented threat to the global health system, especially in resource-limited areas. This challenge shines a spotlight on the urgent need for a point-of-care (POC) quantitative real-time PCR (qPCR) test for sensitive and rapid diagnosis of viral infections. In a POC system, a closed, single-use, microfluidic cartridge is commonly utilized for integration of nucleic acid preparation, PCR amplification and florescence detection. But, most current cartridge systems often involve complicated nucleic acid extraction
via
active pumping that relies on cumbersome external hardware, causing increases in system complexity and cost. In this work, we demonstrate a gravity-driven cartridge design for an integrated viral RNA/DNA diagnostic test that does not require auxiliary hardware for fluid pumping due to adopted extraction-free amplification. This microfluidic cartridge only contains two reaction chambers for nucleic acid lysis and amplification respectively, enabling a fast qPCR test in less than 30 min. This gravity-driven pumping strategy can help simplify and minimize the microfluidic cartridge, thus enabling high-throughput (up to 12 test cartridges per test) molecular detection
via
a small cartridge readout system. Thus, this work addresses the scalability limitation of POC molecular testing and can be run in any settings. We verified the analytical sensitivity and specificity of the cartridge testing for respiratory pathogens and sexually transmitted diseases using SARS-CoV-2, influenza A/B RNA samples, and human papillomavirus 16/18 DNA samples. Our cartridge system exhibited a comparable detection performance to the current gold standard qPCR instrument ABI 7500. Moreover, our system showed very high diagnostic accuracy for viral RNA/DNA detection that was well validated by ROC curve analysis. The sample-to-answer molecular testing system reported in this work has the advantages of simplicity, rapidity, and low cost, making it highly promising for prevention and control of infectious diseases in poor-resource areas.
We present a low-cost microfluidic cartridge design scheme that combines gravity-driven passive microfluidic pumping with extraction-free amplification to achieve "sample-in, answer-out" point-of-care nucleic acid detection within 30 minutes.</description><subject>Amplification</subject><subject>Cartridges</subject><subject>Coronaviruses</subject><subject>COVID-19</subject><subject>Deoxyribonucleic acid</subject><subject>Diagnostic systems</subject><subject>Disease transmission</subject><subject>DNA</subject><subject>Genetic testing</subject><subject>Hardware</subject><subject>Human papillomavirus</subject><subject>Infectious diseases</subject><subject>Influenza</subject><subject>Low cost</subject><subject>Microfluidics</subject><subject>Nucleic acids</subject><subject>Public health</subject><subject>Pumping</subject><subject>Real time</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>Sensitivity analysis</subject><subject>Severe acute respiratory syndrome coronavirus 2</subject><subject>Viral diseases</subject><subject>Viral infections</subject><issn>1473-0197</issn><issn>1473-0189</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNpd0ctu1DAUBuAIgUQpbNgjHYkNQmPGlyROltNwKdJIoBbYRq590nHl2KntdDS8Gi9HyqAisfJZfL-P5b8oXjL6jlHRrg13mtJSlLtHxQkrpSCUNe3jh7mVT4tnKd1Qyqqybk6KXxtIapwckhyI8mmPcQW3s_LZZpXtHUJE5Ui2I8LX7gLSIWUcYW_zDlzYEx1SXsF1VHc2H4iJS8LDaHUMg5utsRq0ijlac40whAhRTdaAwYw62-AhDHC5ubgkXfhB-AqsX2LofyrYrM9WoLyB3TwqD9OScy6My544J2D1mjXPiyeDcglf_D1Pi-8fP3zrzsn2y6fP3WZLtGBlJkxyjoZz09SNHiiTqIUSgzSSS011g4MWeFXRuroStFS1qpgxvBQ1NrqqpBGnxZvjvVMMtzOm3I82aXROeQxz6rmkvJU1K-lCX_9Hb8Ic_fK6RTFRtm1V3au3R7V8U0oRh36KdlTx0DPa3_fYv-fb7k-P5wt-dcQx6Qf3r2fxG2oxmuc</recordid><startdate>20220913</startdate><enddate>20220913</enddate><creator>Zai, Yunfeng</creator><creator>Min, Chao</creator><creator>Wang, Zunliang</creator><creator>Ding, Yongjun</creator><creator>Zhao, Huan</creator><creator>Su, Enben</creator><creator>He, Nongyue</creator><general>Royal Society of Chemistry</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SP</scope><scope>7TB</scope><scope>7U5</scope><scope>8FD</scope><scope>FR3</scope><scope>L7M</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-4449-309X</orcidid><orcidid>https://orcid.org/0000-0002-5826-5752</orcidid></search><sort><creationdate>20220913</creationdate><title>A sample-to-answer, quantitative real-time PCR system with low-cost, gravity-driven microfluidic cartridge for rapid detection of SARS-CoV-2, influenza A/B, and human papillomavirus 16/18</title><author>Zai, Yunfeng ; Min, Chao ; Wang, Zunliang ; Ding, Yongjun ; Zhao, Huan ; Su, Enben ; He, Nongyue</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c314t-1722ed22d868cf017ec3a3f7d727c0c8efc3eb5065b304a6a51dd2436e8c557d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Amplification</topic><topic>Cartridges</topic><topic>Coronaviruses</topic><topic>COVID-19</topic><topic>Deoxyribonucleic acid</topic><topic>Diagnostic systems</topic><topic>Disease transmission</topic><topic>DNA</topic><topic>Genetic testing</topic><topic>Hardware</topic><topic>Human papillomavirus</topic><topic>Infectious diseases</topic><topic>Influenza</topic><topic>Low cost</topic><topic>Microfluidics</topic><topic>Nucleic acids</topic><topic>Public health</topic><topic>Pumping</topic><topic>Real time</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>Sensitivity analysis</topic><topic>Severe acute respiratory syndrome coronavirus 2</topic><topic>Viral diseases</topic><topic>Viral infections</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zai, Yunfeng</creatorcontrib><creatorcontrib>Min, Chao</creatorcontrib><creatorcontrib>Wang, Zunliang</creatorcontrib><creatorcontrib>Ding, Yongjun</creatorcontrib><creatorcontrib>Zhao, Huan</creatorcontrib><creatorcontrib>Su, Enben</creatorcontrib><creatorcontrib>He, Nongyue</creatorcontrib><collection>CrossRef</collection><collection>Electronics & Communications Abstracts</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Lab on a chip</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zai, Yunfeng</au><au>Min, Chao</au><au>Wang, Zunliang</au><au>Ding, Yongjun</au><au>Zhao, Huan</au><au>Su, Enben</au><au>He, Nongyue</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A sample-to-answer, quantitative real-time PCR system with low-cost, gravity-driven microfluidic cartridge for rapid detection of SARS-CoV-2, influenza A/B, and human papillomavirus 16/18</atitle><jtitle>Lab on a chip</jtitle><date>2022-09-13</date><risdate>2022</risdate><volume>22</volume><issue>18</issue><spage>3436</spage><epage>3452</epage><pages>3436-3452</pages><issn>1473-0197</issn><eissn>1473-0189</eissn><abstract>The pandemic of coronavirus disease 2019 (COVID-19), due to the novel coronavirus (SARS-CoV-2), has created an unprecedented threat to the global health system, especially in resource-limited areas. This challenge shines a spotlight on the urgent need for a point-of-care (POC) quantitative real-time PCR (qPCR) test for sensitive and rapid diagnosis of viral infections. In a POC system, a closed, single-use, microfluidic cartridge is commonly utilized for integration of nucleic acid preparation, PCR amplification and florescence detection. But, most current cartridge systems often involve complicated nucleic acid extraction
via
active pumping that relies on cumbersome external hardware, causing increases in system complexity and cost. In this work, we demonstrate a gravity-driven cartridge design for an integrated viral RNA/DNA diagnostic test that does not require auxiliary hardware for fluid pumping due to adopted extraction-free amplification. This microfluidic cartridge only contains two reaction chambers for nucleic acid lysis and amplification respectively, enabling a fast qPCR test in less than 30 min. This gravity-driven pumping strategy can help simplify and minimize the microfluidic cartridge, thus enabling high-throughput (up to 12 test cartridges per test) molecular detection
via
a small cartridge readout system. Thus, this work addresses the scalability limitation of POC molecular testing and can be run in any settings. We verified the analytical sensitivity and specificity of the cartridge testing for respiratory pathogens and sexually transmitted diseases using SARS-CoV-2, influenza A/B RNA samples, and human papillomavirus 16/18 DNA samples. Our cartridge system exhibited a comparable detection performance to the current gold standard qPCR instrument ABI 7500. Moreover, our system showed very high diagnostic accuracy for viral RNA/DNA detection that was well validated by ROC curve analysis. The sample-to-answer molecular testing system reported in this work has the advantages of simplicity, rapidity, and low cost, making it highly promising for prevention and control of infectious diseases in poor-resource areas.
We present a low-cost microfluidic cartridge design scheme that combines gravity-driven passive microfluidic pumping with extraction-free amplification to achieve "sample-in, answer-out" point-of-care nucleic acid detection within 30 minutes.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/d2lc00434h</doi><tpages>17</tpages><orcidid>https://orcid.org/0000-0003-4449-309X</orcidid><orcidid>https://orcid.org/0000-0002-5826-5752</orcidid></addata></record> |
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subjects | Amplification Cartridges Coronaviruses COVID-19 Deoxyribonucleic acid Diagnostic systems Disease transmission DNA Genetic testing Hardware Human papillomavirus Infectious diseases Influenza Low cost Microfluidics Nucleic acids Public health Pumping Real time Ribonucleic acid RNA Sensitivity analysis Severe acute respiratory syndrome coronavirus 2 Viral diseases Viral infections |
title | A sample-to-answer, quantitative real-time PCR system with low-cost, gravity-driven microfluidic cartridge for rapid detection of SARS-CoV-2, influenza A/B, and human papillomavirus 16/18 |
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