Reagent‐Free Covalent Immobilization of Biomolecules in a Microfluidic Organ‐On‐A‐Chip
Microfluidic systems have become integral for lab‐on‐a‐chip and organ‐on‐a‐chip applications across numerous disciplines. These systems, typically fabricated using polydimethylsiloxane (PDMS) chips on glass substrates, lack the bioactivity required for such applications. To overcome this, biomolecul...
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description | Microfluidic systems have become integral for lab‐on‐a‐chip and organ‐on‐a‐chip applications across numerous disciplines. These systems, typically fabricated using polydimethylsiloxane (PDMS) chips on glass substrates, lack the bioactivity required for such applications. To overcome this, biomolecules are immobilized using either oxygen (O2) plasma treatment or chemical reagents like amino silanes. However, O2 plasma treatments are unstable and cannot covalently immobilize biomolecules, while wet‐chemistry approaches are toxic, time‐consuming, and expensive. A novel microfluidic platform that combines two plasma surface treatments: Plasma‐activated coating (PAC) and atmospheric pressure plasma jet (APPJ), to enable reagent‐free covalent immobilization of biomolecules is described here. These surface treatments, unlike O2 plasma, covalently immobilized fibronectin on PDMS and glass, and significantly improved endothelial cell attachment and proliferation. By combining PAC and APPJ, a hybrid microfluidic platform with equivalent bond strength to standard O2 plasma devices, but with significantly enhanced endothelial cell growth in and artery‐on‐a‐chip model, is developed. This platform is also amenable to high‐shear applications such as coronary shear, with endothelial cells aligning with flow, as seen in human arteries. By providing reagent‐free covalent immobilization of biomolecules within a microfluidic system, this technology has the potential to radically improve organ‐on‐a‐chip development as well as lab‐on‐a‐chip systems, point‐of‐care diagnostics, and sensors.
By combining the novel plasma treatment techniques PAC and APPJ on PDMS and glass respectively, a microfluidic platform is developed, that for the first time enables reagent‐free covalent immobilization of biomolecules. Using this platform, improved endothelial cell growth is demonstrated relative to standard oxygen plasma treatments under both low and high‐shear conditions for multiple days. |
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By combining the novel plasma treatment techniques PAC and APPJ on PDMS and glass respectively, a microfluidic platform is developed, that for the first time enables reagent‐free covalent immobilization of biomolecules. Using this platform, improved endothelial cell growth is demonstrated relative to standard oxygen plasma treatments under both low and high‐shear conditions for multiple days.</description><identifier>ISSN: 1616-301X</identifier><identifier>EISSN: 1616-3028</identifier><identifier>DOI: 10.1002/adfm.202313664</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc</publisher><subject>Biocompatibility ; biofunctionalization ; Biomolecules ; Bonding strength ; Covalence ; covalent immobilization ; Endothelial cells ; Fibronectin ; Glass substrates ; Immobilization ; lab‐on‐a‐chip ; microfluidic device ; Microfluidics ; organ‐on‐a‐chip ; Oxygen plasma ; Plasma ; Plasma jets ; plasma surface treatment ; Polydimethylsiloxane ; Reagents ; surface modification ; Surface treatment</subject><ispartof>Advanced functional materials, 2024-07, Vol.34 (30), p.n/a</ispartof><rights>2024 The Authors. Advanced Functional Materials published by Wiley‐VCH GmbH</rights><rights>2024. This article is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3124-2cc08644681e4cb1da08915740adfbf68e43bc7676cf50b8f00c3631b83dd5223</cites><orcidid>0000-0003-3363-2664 ; 0000-0001-8294-7588 ; 0000-0001-6968-7283 ; 0000-0003-1498-9393</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fadfm.202313664$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fadfm.202313664$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids></links><search><creatorcontrib>Ashok, Deepu</creatorcontrib><creatorcontrib>Singh, Jasneil</creatorcontrib><creatorcontrib>Jiang, Shouyuan</creatorcontrib><creatorcontrib>Waterhouse, Anna</creatorcontrib><creatorcontrib>Bilek, Marcela</creatorcontrib><title>Reagent‐Free Covalent Immobilization of Biomolecules in a Microfluidic Organ‐On‐A‐Chip</title><title>Advanced functional materials</title><description>Microfluidic systems have become integral for lab‐on‐a‐chip and organ‐on‐a‐chip applications across numerous disciplines. These systems, typically fabricated using polydimethylsiloxane (PDMS) chips on glass substrates, lack the bioactivity required for such applications. To overcome this, biomolecules are immobilized using either oxygen (O2) plasma treatment or chemical reagents like amino silanes. However, O2 plasma treatments are unstable and cannot covalently immobilize biomolecules, while wet‐chemistry approaches are toxic, time‐consuming, and expensive. A novel microfluidic platform that combines two plasma surface treatments: Plasma‐activated coating (PAC) and atmospheric pressure plasma jet (APPJ), to enable reagent‐free covalent immobilization of biomolecules is described here. These surface treatments, unlike O2 plasma, covalently immobilized fibronectin on PDMS and glass, and significantly improved endothelial cell attachment and proliferation. By combining PAC and APPJ, a hybrid microfluidic platform with equivalent bond strength to standard O2 plasma devices, but with significantly enhanced endothelial cell growth in and artery‐on‐a‐chip model, is developed. This platform is also amenable to high‐shear applications such as coronary shear, with endothelial cells aligning with flow, as seen in human arteries. By providing reagent‐free covalent immobilization of biomolecules within a microfluidic system, this technology has the potential to radically improve organ‐on‐a‐chip development as well as lab‐on‐a‐chip systems, point‐of‐care diagnostics, and sensors.
By combining the novel plasma treatment techniques PAC and APPJ on PDMS and glass respectively, a microfluidic platform is developed, that for the first time enables reagent‐free covalent immobilization of biomolecules. Using this platform, improved endothelial cell growth is demonstrated relative to standard oxygen plasma treatments under both low and high‐shear conditions for multiple days.</description><subject>Biocompatibility</subject><subject>biofunctionalization</subject><subject>Biomolecules</subject><subject>Bonding strength</subject><subject>Covalence</subject><subject>covalent immobilization</subject><subject>Endothelial cells</subject><subject>Fibronectin</subject><subject>Glass substrates</subject><subject>Immobilization</subject><subject>lab‐on‐a‐chip</subject><subject>microfluidic device</subject><subject>Microfluidics</subject><subject>organ‐on‐a‐chip</subject><subject>Oxygen plasma</subject><subject>Plasma</subject><subject>Plasma jets</subject><subject>plasma surface treatment</subject><subject>Polydimethylsiloxane</subject><subject>Reagents</subject><subject>surface modification</subject><subject>Surface treatment</subject><issn>1616-301X</issn><issn>1616-3028</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><recordid>eNqFUMtKAzEUDaJgrW5dB1xPzauZdFlHRwstBVFwZchkkpoyM6mZjlJXfoLf6JeYUqlLF_cF55x77wHgHKMBRohcqtLWA4IIxZRzdgB6mGOeUETE4b7HT8fgpG2XCOE0pawHnu-NWphm_f35lQdjYObfVBVnOKlrX7jKfai18w30Fl45X_vK6K4yLXQNVHDmdPC26lzpNJyHhWqizHybxjGyF7c6BUdWVa05-6198JjfPGR3yXR-O8nG00RTTFhCtEaCM8YFNkwXuFRIjPAwZSg-VVguDKOFTnnKtR2iQliENOUUF4KW5ZAQ2gcXO91V8K-daddy6bvQxJWSIkEFia_jiBrsUPHstg3GylVwtQobiZHceii3Hsq9h5Ew2hHeXWU2_6Dl-Dqf_XF_AHMvePk</recordid><startdate>20240701</startdate><enddate>20240701</enddate><creator>Ashok, Deepu</creator><creator>Singh, Jasneil</creator><creator>Jiang, Shouyuan</creator><creator>Waterhouse, Anna</creator><creator>Bilek, Marcela</creator><general>Wiley Subscription Services, Inc</general><scope>24P</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SP</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><orcidid>https://orcid.org/0000-0003-3363-2664</orcidid><orcidid>https://orcid.org/0000-0001-8294-7588</orcidid><orcidid>https://orcid.org/0000-0001-6968-7283</orcidid><orcidid>https://orcid.org/0000-0003-1498-9393</orcidid></search><sort><creationdate>20240701</creationdate><title>Reagent‐Free Covalent Immobilization of Biomolecules in a Microfluidic Organ‐On‐A‐Chip</title><author>Ashok, Deepu ; Singh, Jasneil ; Jiang, Shouyuan ; Waterhouse, Anna ; Bilek, Marcela</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3124-2cc08644681e4cb1da08915740adfbf68e43bc7676cf50b8f00c3631b83dd5223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Biocompatibility</topic><topic>biofunctionalization</topic><topic>Biomolecules</topic><topic>Bonding strength</topic><topic>Covalence</topic><topic>covalent immobilization</topic><topic>Endothelial cells</topic><topic>Fibronectin</topic><topic>Glass substrates</topic><topic>Immobilization</topic><topic>lab‐on‐a‐chip</topic><topic>microfluidic device</topic><topic>Microfluidics</topic><topic>organ‐on‐a‐chip</topic><topic>Oxygen plasma</topic><topic>Plasma</topic><topic>Plasma jets</topic><topic>plasma surface treatment</topic><topic>Polydimethylsiloxane</topic><topic>Reagents</topic><topic>surface modification</topic><topic>Surface treatment</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ashok, Deepu</creatorcontrib><creatorcontrib>Singh, Jasneil</creatorcontrib><creatorcontrib>Jiang, Shouyuan</creatorcontrib><creatorcontrib>Waterhouse, Anna</creatorcontrib><creatorcontrib>Bilek, Marcela</creatorcontrib><collection>Wiley-Blackwell Open Access Titles</collection><collection>CrossRef</collection><collection>Electronics & Communications Abstracts</collection><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>Advanced functional materials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ashok, Deepu</au><au>Singh, Jasneil</au><au>Jiang, Shouyuan</au><au>Waterhouse, Anna</au><au>Bilek, Marcela</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reagent‐Free Covalent Immobilization of Biomolecules in a Microfluidic Organ‐On‐A‐Chip</atitle><jtitle>Advanced functional materials</jtitle><date>2024-07-01</date><risdate>2024</risdate><volume>34</volume><issue>30</issue><epage>n/a</epage><issn>1616-301X</issn><eissn>1616-3028</eissn><abstract>Microfluidic systems have become integral for lab‐on‐a‐chip and organ‐on‐a‐chip applications across numerous disciplines. These systems, typically fabricated using polydimethylsiloxane (PDMS) chips on glass substrates, lack the bioactivity required for such applications. To overcome this, biomolecules are immobilized using either oxygen (O2) plasma treatment or chemical reagents like amino silanes. However, O2 plasma treatments are unstable and cannot covalently immobilize biomolecules, while wet‐chemistry approaches are toxic, time‐consuming, and expensive. A novel microfluidic platform that combines two plasma surface treatments: Plasma‐activated coating (PAC) and atmospheric pressure plasma jet (APPJ), to enable reagent‐free covalent immobilization of biomolecules is described here. These surface treatments, unlike O2 plasma, covalently immobilized fibronectin on PDMS and glass, and significantly improved endothelial cell attachment and proliferation. By combining PAC and APPJ, a hybrid microfluidic platform with equivalent bond strength to standard O2 plasma devices, but with significantly enhanced endothelial cell growth in and artery‐on‐a‐chip model, is developed. This platform is also amenable to high‐shear applications such as coronary shear, with endothelial cells aligning with flow, as seen in human arteries. By providing reagent‐free covalent immobilization of biomolecules within a microfluidic system, this technology has the potential to radically improve organ‐on‐a‐chip development as well as lab‐on‐a‐chip systems, point‐of‐care diagnostics, and sensors.
By combining the novel plasma treatment techniques PAC and APPJ on PDMS and glass respectively, a microfluidic platform is developed, that for the first time enables reagent‐free covalent immobilization of biomolecules. Using this platform, improved endothelial cell growth is demonstrated relative to standard oxygen plasma treatments under both low and high‐shear conditions for multiple days.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/adfm.202313664</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0003-3363-2664</orcidid><orcidid>https://orcid.org/0000-0001-8294-7588</orcidid><orcidid>https://orcid.org/0000-0001-6968-7283</orcidid><orcidid>https://orcid.org/0000-0003-1498-9393</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Biocompatibility biofunctionalization Biomolecules Bonding strength Covalence covalent immobilization Endothelial cells Fibronectin Glass substrates Immobilization lab‐on‐a‐chip microfluidic device Microfluidics organ‐on‐a‐chip Oxygen plasma Plasma Plasma jets plasma surface treatment Polydimethylsiloxane Reagents surface modification Surface treatment |
title | Reagent‐Free Covalent Immobilization of Biomolecules in a Microfluidic Organ‐On‐A‐Chip |
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