Single-Step Nanoplasmonic VEGF sub(165) Aptasensor for Early Cancer Diagnosis
Early cancer diagnosis is very important for the prevention or mitigation of metastasis. However, effective and efficient methods are needed to improve the diagnosis and assessment of cancer. Here, we report a single-step detection method using a nanoplasmonic aptamer sensor (aptasensor), targeting...
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Veröffentlicht in: | ACS nano 2012-09, Vol.6 (9), p.7607-7614-7607-7614 |
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description | Early cancer diagnosis is very important for the prevention or mitigation of metastasis. However, effective and efficient methods are needed to improve the diagnosis and assessment of cancer. Here, we report a single-step detection method using a nanoplasmonic aptamer sensor (aptasensor), targeting a vascular endothelial growth factor-165 (VEGF sub(165)), a predominant biomarker of cancer angiogenesis. Our single-step detection is accomplished by (1) specific target recognition by an aptamer-target molecule interaction and (2) direct readouts of the target recognition. The readout is achieved by inactivation of surface plasmon enhancement of fluorescent probes preattached to the aptamers. Our aptasensor provides the appropriate sensitivity for clinical diagnostics with a wide range of linear detection from 25 pg/mL to 25 mu g/mL (=from 1.25 pM to 1.25 mu M), high specificity for VEGF sub(165) against PDGF-BB, osteopontin (OPN), VEGF sub(121), NaCl, and temporal/thermal/biological stability. In experiments with 100% serum and saliva from clinical samples, readouts of the aptasensor and an ELISA for VEGF sub(165) show good agreement within the limit of the ELISA kit. We envision that our developed aptasensor holds utilities for point-of-care cancer prognostics by incorporating simplicity in detection, low-cost for test, and required small sample volumes. |
doi_str_mv | 10.1021/nn203833d |
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However, effective and efficient methods are needed to improve the diagnosis and assessment of cancer. Here, we report a single-step detection method using a nanoplasmonic aptamer sensor (aptasensor), targeting a vascular endothelial growth factor-165 (VEGF sub(165)), a predominant biomarker of cancer angiogenesis. Our single-step detection is accomplished by (1) specific target recognition by an aptamer-target molecule interaction and (2) direct readouts of the target recognition. The readout is achieved by inactivation of surface plasmon enhancement of fluorescent probes preattached to the aptamers. Our aptasensor provides the appropriate sensitivity for clinical diagnostics with a wide range of linear detection from 25 pg/mL to 25 mu g/mL (=from 1.25 pM to 1.25 mu M), high specificity for VEGF sub(165) against PDGF-BB, osteopontin (OPN), VEGF sub(121), NaCl, and temporal/thermal/biological stability. 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We envision that our developed aptasensor holds utilities for point-of-care cancer prognostics by incorporating simplicity in detection, low-cost for test, and required small sample volumes.</description><identifier>ISSN: 1936-0851</identifier><identifier>EISSN: 1936-086X</identifier><identifier>DOI: 10.1021/nn203833d</identifier><language>eng</language><subject>Assessments ; Cancer ; Diagnosis ; Diagnostic systems ; ELISA ; Fluorescence ; Nanostructure ; Saliva ; Target recognition</subject><ispartof>ACS nano, 2012-09, Vol.6 (9), p.7607-7614-7607-7614</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27911,27912</link.rule.ids></links><search><creatorcontrib>Cho, Hansang</creatorcontrib><creatorcontrib>Yeh, Erh-Chia</creatorcontrib><creatorcontrib>Sinha, Raghu</creatorcontrib><creatorcontrib>Laurence, Ted A</creatorcontrib><creatorcontrib>Bearinger, Jane P</creatorcontrib><creatorcontrib>Lee, Luke P</creatorcontrib><title>Single-Step Nanoplasmonic VEGF sub(165) Aptasensor for Early Cancer Diagnosis</title><title>ACS nano</title><description>Early cancer diagnosis is very important for the prevention or mitigation of metastasis. However, effective and efficient methods are needed to improve the diagnosis and assessment of cancer. Here, we report a single-step detection method using a nanoplasmonic aptamer sensor (aptasensor), targeting a vascular endothelial growth factor-165 (VEGF sub(165)), a predominant biomarker of cancer angiogenesis. Our single-step detection is accomplished by (1) specific target recognition by an aptamer-target molecule interaction and (2) direct readouts of the target recognition. The readout is achieved by inactivation of surface plasmon enhancement of fluorescent probes preattached to the aptamers. Our aptasensor provides the appropriate sensitivity for clinical diagnostics with a wide range of linear detection from 25 pg/mL to 25 mu g/mL (=from 1.25 pM to 1.25 mu M), high specificity for VEGF sub(165) against PDGF-BB, osteopontin (OPN), VEGF sub(121), NaCl, and temporal/thermal/biological stability. 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We envision that our developed aptasensor holds utilities for point-of-care cancer prognostics by incorporating simplicity in detection, low-cost for test, and required small sample volumes.</description><subject>Assessments</subject><subject>Cancer</subject><subject>Diagnosis</subject><subject>Diagnostic systems</subject><subject>ELISA</subject><subject>Fluorescence</subject><subject>Nanostructure</subject><subject>Saliva</subject><subject>Target recognition</subject><issn>1936-0851</issn><issn>1936-086X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNqVjq0OwjAURhsCCb-CN6gEMWjXtBuSwAADZoTgljI6UlJux-4meHsQBI_4co444iNkzNmMs5DPAUImYiGuLdLjC6ECFqtz--eSd0kf8c6YjOJI9cg-tXBzJkhrU9KDBl86jQ8PNqenZLuh2FwmXMkpXZa1RgPoK1p8lujKvehKQ24qurb6Bh4tDkmn0A7N6MsBmWyS42oXlJV_Ngbr7GExN85pML7BjEcqZPJzUYo_0jcv-kXm</recordid><startdate>20120905</startdate><enddate>20120905</enddate><creator>Cho, Hansang</creator><creator>Yeh, Erh-Chia</creator><creator>Sinha, Raghu</creator><creator>Laurence, Ted A</creator><creator>Bearinger, Jane P</creator><creator>Lee, Luke P</creator><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20120905</creationdate><title>Single-Step Nanoplasmonic VEGF sub(165) Aptasensor for Early Cancer Diagnosis</title><author>Cho, Hansang ; Yeh, Erh-Chia ; Sinha, Raghu ; Laurence, Ted A ; Bearinger, Jane P ; Lee, Luke P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_miscellaneous_17620508653</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Assessments</topic><topic>Cancer</topic><topic>Diagnosis</topic><topic>Diagnostic systems</topic><topic>ELISA</topic><topic>Fluorescence</topic><topic>Nanostructure</topic><topic>Saliva</topic><topic>Target recognition</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cho, Hansang</creatorcontrib><creatorcontrib>Yeh, Erh-Chia</creatorcontrib><creatorcontrib>Sinha, Raghu</creatorcontrib><creatorcontrib>Laurence, Ted A</creatorcontrib><creatorcontrib>Bearinger, Jane P</creatorcontrib><creatorcontrib>Lee, Luke P</creatorcontrib><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>ACS nano</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cho, Hansang</au><au>Yeh, Erh-Chia</au><au>Sinha, Raghu</au><au>Laurence, Ted A</au><au>Bearinger, Jane P</au><au>Lee, Luke P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Single-Step Nanoplasmonic VEGF sub(165) Aptasensor for Early Cancer Diagnosis</atitle><jtitle>ACS nano</jtitle><date>2012-09-05</date><risdate>2012</risdate><volume>6</volume><issue>9</issue><spage>7607</spage><epage>7614-7607-7614</epage><pages>7607-7614-7607-7614</pages><issn>1936-0851</issn><eissn>1936-086X</eissn><abstract>Early cancer diagnosis is very important for the prevention or mitigation of metastasis. However, effective and efficient methods are needed to improve the diagnosis and assessment of cancer. Here, we report a single-step detection method using a nanoplasmonic aptamer sensor (aptasensor), targeting a vascular endothelial growth factor-165 (VEGF sub(165)), a predominant biomarker of cancer angiogenesis. Our single-step detection is accomplished by (1) specific target recognition by an aptamer-target molecule interaction and (2) direct readouts of the target recognition. The readout is achieved by inactivation of surface plasmon enhancement of fluorescent probes preattached to the aptamers. Our aptasensor provides the appropriate sensitivity for clinical diagnostics with a wide range of linear detection from 25 pg/mL to 25 mu g/mL (=from 1.25 pM to 1.25 mu M), high specificity for VEGF sub(165) against PDGF-BB, osteopontin (OPN), VEGF sub(121), NaCl, and temporal/thermal/biological stability. In experiments with 100% serum and saliva from clinical samples, readouts of the aptasensor and an ELISA for VEGF sub(165) show good agreement within the limit of the ELISA kit. We envision that our developed aptasensor holds utilities for point-of-care cancer prognostics by incorporating simplicity in detection, low-cost for test, and required small sample volumes.</abstract><doi>10.1021/nn203833d</doi></addata></record> |
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subjects | Assessments Cancer Diagnosis Diagnostic systems ELISA Fluorescence Nanostructure Saliva Target recognition |
title | Single-Step Nanoplasmonic VEGF sub(165) Aptasensor for Early Cancer Diagnosis |
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