Detection of urinary microRNA biomarkers using diazo sulfonamide-modified screen printed carbon electrodes
This paper describes a straightforward electrochemical method for rapid and robust urinary microRNA (miRNA) quantification using disposable biosensors that can discriminate between urine from diabetic kidney disease (DKD) patients and control subjects. Aberrant miRNA expression has been observed in...
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Veröffentlicht in: | RSC advances 2021-05, Vol.11 (31), p.18832-18839 |
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creator | Smith, Daniel A Simpson, Kate Lo Cicero, Matteo Newbury, Lucy J Nicholas, Philip Fraser, Donald J Caiger, Nigel Redman, James E Bowen, Timothy |
description | This paper describes a straightforward electrochemical method for rapid and robust urinary microRNA (miRNA) quantification using disposable biosensors that can discriminate between urine from diabetic kidney disease (DKD) patients and control subjects. Aberrant miRNA expression has been observed in several major human disorders, and we have identified a urinary miRNA signature for DKD. MiRNAs therefore have considerable promise as disease biomarkers, and techniques to quantify these transcripts from clinical samples have significant clinical and commercial potential. Current RT-qPCR-based methods require technical expertise, and more straightforward methods such as electrochemical detection offer attractive alternatives. We describe a method to detect urinary miRNAs using diazo sulfonamide-modified screen printed carbon electrode-based biosensors that is amenable to parallel analysis. These sensors showed a linear response to buffered miR-21, with a 17 fM limit of detection, and successfully discriminated between urine samples (
n
= 6) from DKD patients and unaffected control subjects (
n
= 6) by differential miR-192 detection. Our technique for quantitative miRNA detection in liquid biopsies has potential for development as a platform for non-invasive high-throughput screening and/or to complement existing diagnostic procedures in disorders such as DKD.
In this study we have developed an electrochemical microRNA biosensor sensitive to 17 fM and capable of detecting an established downregulation of urinary miR-192 in diabetic kidney disease patients. |
doi_str_mv | 10.1039/d0ra09874d |
format | Article |
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n
= 6) from DKD patients and unaffected control subjects (
n
= 6) by differential miR-192 detection. Our technique for quantitative miRNA detection in liquid biopsies has potential for development as a platform for non-invasive high-throughput screening and/or to complement existing diagnostic procedures in disorders such as DKD.
In this study we have developed an electrochemical microRNA biosensor sensitive to 17 fM and capable of detecting an established downregulation of urinary miR-192 in diabetic kidney disease patients.</description><identifier>ISSN: 2046-2069</identifier><identifier>EISSN: 2046-2069</identifier><identifier>DOI: 10.1039/d0ra09874d</identifier><identifier>PMID: 34123373</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Biomarkers ; Biosensors ; Carbon ; Chemistry ; Disease control ; Disorders ; Electrochemical analysis ; Kidney diseases ; MicroRNAs ; Ribonucleic acid ; RNA ; Sulfonamides</subject><ispartof>RSC advances, 2021-05, Vol.11 (31), p.18832-18839</ispartof><rights>This journal is © The Royal Society of Chemistry.</rights><rights>Copyright Royal Society of Chemistry 2021</rights><rights>This journal is © The Royal Society of Chemistry 2021 The Royal Society of Chemistry</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c469t-ac65c7c411d8e34d77d73a0dfcd2084d497a097057e080cf37c9b6601efcd6933</citedby><cites>FETCH-LOGICAL-c469t-ac65c7c411d8e34d77d73a0dfcd2084d497a097057e080cf37c9b6601efcd6933</cites><orcidid>0000-0003-3145-3160 ; 0000-0001-6050-0435 ; 0000-0001-5492-2869</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8144888/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8144888/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34123373$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Smith, Daniel A</creatorcontrib><creatorcontrib>Simpson, Kate</creatorcontrib><creatorcontrib>Lo Cicero, Matteo</creatorcontrib><creatorcontrib>Newbury, Lucy J</creatorcontrib><creatorcontrib>Nicholas, Philip</creatorcontrib><creatorcontrib>Fraser, Donald J</creatorcontrib><creatorcontrib>Caiger, Nigel</creatorcontrib><creatorcontrib>Redman, James E</creatorcontrib><creatorcontrib>Bowen, Timothy</creatorcontrib><title>Detection of urinary microRNA biomarkers using diazo sulfonamide-modified screen printed carbon electrodes</title><title>RSC advances</title><addtitle>RSC Adv</addtitle><description>This paper describes a straightforward electrochemical method for rapid and robust urinary microRNA (miRNA) quantification using disposable biosensors that can discriminate between urine from diabetic kidney disease (DKD) patients and control subjects. Aberrant miRNA expression has been observed in several major human disorders, and we have identified a urinary miRNA signature for DKD. MiRNAs therefore have considerable promise as disease biomarkers, and techniques to quantify these transcripts from clinical samples have significant clinical and commercial potential. Current RT-qPCR-based methods require technical expertise, and more straightforward methods such as electrochemical detection offer attractive alternatives. We describe a method to detect urinary miRNAs using diazo sulfonamide-modified screen printed carbon electrode-based biosensors that is amenable to parallel analysis. These sensors showed a linear response to buffered miR-21, with a 17 fM limit of detection, and successfully discriminated between urine samples (
n
= 6) from DKD patients and unaffected control subjects (
n
= 6) by differential miR-192 detection. Our technique for quantitative miRNA detection in liquid biopsies has potential for development as a platform for non-invasive high-throughput screening and/or to complement existing diagnostic procedures in disorders such as DKD.
In this study we have developed an electrochemical microRNA biosensor sensitive to 17 fM and capable of detecting an established downregulation of urinary miR-192 in diabetic kidney disease patients.</description><subject>Biomarkers</subject><subject>Biosensors</subject><subject>Carbon</subject><subject>Chemistry</subject><subject>Disease control</subject><subject>Disorders</subject><subject>Electrochemical analysis</subject><subject>Kidney diseases</subject><subject>MicroRNAs</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>Sulfonamides</subject><issn>2046-2069</issn><issn>2046-2069</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNpdksFLHDEYxUOpuIt68d4S6KUIU5NJJpm5FBZXa0EURM8hm3yzzTqTrMlMQf96s1271eaShO_H4728IHRMyTdKWHNqSdSkqSW3H9C0JFwUJRHNxzfnCTpKaUXyEhUtBd1HE8ZpyZhkU7SawwBmcMHj0OIxOq_jE-6dieH2eoYXLvQ6PkBMeEzOL7F1-jngNHZt8Lp3Foo-WNc6sDiZCODxOmsM-Wp0XGRV6LJ8DBbSIdprdZfg6HU_QPcX53dnl8XVzY-fZ7OrwnDRDIU2ojLScEptDYxbKa1kmtjW2JLU3PJG5sCSVBJITUzLpGkWQhAKmRANYwfo-1Z3PS56sAb8EHWnsq8c5UkF7dT7iXe_1DL8VjXlvK7rLPD1VSCGxxHSoHqXDHSd9hDGpMqKE0mbim7QL_-hqzBGn-NlijFWlSXdODrZUvlVU4rQ7sxQojYtqjm5nf1pcZ7hz2_t79C_nWXg0xaIyeym_74BewHhB6N6</recordid><startdate>20210525</startdate><enddate>20210525</enddate><creator>Smith, Daniel A</creator><creator>Simpson, Kate</creator><creator>Lo Cicero, Matteo</creator><creator>Newbury, Lucy J</creator><creator>Nicholas, Philip</creator><creator>Fraser, Donald J</creator><creator>Caiger, Nigel</creator><creator>Redman, James E</creator><creator>Bowen, Timothy</creator><general>Royal Society of Chemistry</general><general>The Royal Society of Chemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-3145-3160</orcidid><orcidid>https://orcid.org/0000-0001-6050-0435</orcidid><orcidid>https://orcid.org/0000-0001-5492-2869</orcidid></search><sort><creationdate>20210525</creationdate><title>Detection of urinary microRNA biomarkers using diazo sulfonamide-modified screen printed carbon electrodes</title><author>Smith, Daniel A ; Simpson, Kate ; Lo Cicero, Matteo ; Newbury, Lucy J ; Nicholas, Philip ; Fraser, Donald J ; Caiger, Nigel ; Redman, James E ; Bowen, Timothy</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c469t-ac65c7c411d8e34d77d73a0dfcd2084d497a097057e080cf37c9b6601efcd6933</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Biomarkers</topic><topic>Biosensors</topic><topic>Carbon</topic><topic>Chemistry</topic><topic>Disease control</topic><topic>Disorders</topic><topic>Electrochemical analysis</topic><topic>Kidney diseases</topic><topic>MicroRNAs</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>Sulfonamides</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Smith, Daniel A</creatorcontrib><creatorcontrib>Simpson, Kate</creatorcontrib><creatorcontrib>Lo Cicero, Matteo</creatorcontrib><creatorcontrib>Newbury, Lucy J</creatorcontrib><creatorcontrib>Nicholas, Philip</creatorcontrib><creatorcontrib>Fraser, Donald J</creatorcontrib><creatorcontrib>Caiger, Nigel</creatorcontrib><creatorcontrib>Redman, James E</creatorcontrib><creatorcontrib>Bowen, Timothy</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>RSC advances</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Smith, Daniel A</au><au>Simpson, Kate</au><au>Lo Cicero, Matteo</au><au>Newbury, Lucy J</au><au>Nicholas, Philip</au><au>Fraser, Donald J</au><au>Caiger, Nigel</au><au>Redman, James E</au><au>Bowen, Timothy</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Detection of urinary microRNA biomarkers using diazo sulfonamide-modified screen printed carbon electrodes</atitle><jtitle>RSC advances</jtitle><addtitle>RSC Adv</addtitle><date>2021-05-25</date><risdate>2021</risdate><volume>11</volume><issue>31</issue><spage>18832</spage><epage>18839</epage><pages>18832-18839</pages><issn>2046-2069</issn><eissn>2046-2069</eissn><abstract>This paper describes a straightforward electrochemical method for rapid and robust urinary microRNA (miRNA) quantification using disposable biosensors that can discriminate between urine from diabetic kidney disease (DKD) patients and control subjects. Aberrant miRNA expression has been observed in several major human disorders, and we have identified a urinary miRNA signature for DKD. MiRNAs therefore have considerable promise as disease biomarkers, and techniques to quantify these transcripts from clinical samples have significant clinical and commercial potential. Current RT-qPCR-based methods require technical expertise, and more straightforward methods such as electrochemical detection offer attractive alternatives. We describe a method to detect urinary miRNAs using diazo sulfonamide-modified screen printed carbon electrode-based biosensors that is amenable to parallel analysis. These sensors showed a linear response to buffered miR-21, with a 17 fM limit of detection, and successfully discriminated between urine samples (
n
= 6) from DKD patients and unaffected control subjects (
n
= 6) by differential miR-192 detection. Our technique for quantitative miRNA detection in liquid biopsies has potential for development as a platform for non-invasive high-throughput screening and/or to complement existing diagnostic procedures in disorders such as DKD.
In this study we have developed an electrochemical microRNA biosensor sensitive to 17 fM and capable of detecting an established downregulation of urinary miR-192 in diabetic kidney disease patients.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>34123373</pmid><doi>10.1039/d0ra09874d</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-3145-3160</orcidid><orcidid>https://orcid.org/0000-0001-6050-0435</orcidid><orcidid>https://orcid.org/0000-0001-5492-2869</orcidid><oa>free_for_read</oa></addata></record> |
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source | DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; PubMed Central Open Access |
subjects | Biomarkers Biosensors Carbon Chemistry Disease control Disorders Electrochemical analysis Kidney diseases MicroRNAs Ribonucleic acid RNA Sulfonamides |
title | Detection of urinary microRNA biomarkers using diazo sulfonamide-modified screen printed carbon electrodes |
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