Functionalization of Polyethylene Terephthalate (PETE) Membranes for the Enhancement of Cellular Adhesion in Organ-on-a-Chip Devices
Experimental reproducibility in organ-on-chip (OOC) devices is a challenging issue, mainly caused by cell adhesion problems, as OOC devices are made of bioinert materials not suitable for natural cellularization of their surfaces. To improve cell adhesion, several surface functionalization technique...
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creator | Sobejano de la Merced, Carlos Doveri, Lavinia Muñoz Santoro, Tomás García, Javier Garmendia, Junkal Cortés Domínguez, Iván Díaz Fernández, Yuri Antonio Ortiz de Solórzano, Carlos |
description | Experimental reproducibility in organ-on-chip (OOC) devices is a challenging issue, mainly caused by cell adhesion problems, as OOC devices are made of bioinert materials not suitable for natural cellularization of their surfaces. To improve cell adhesion, several surface functionalization techniques have been proposed, among which the simple use of an intermediate layer of adsorbed proteins has become the preferred one by OOC users. This way, the cells use surface receptors to adhere to the adsorbed proteins, which are in turn attached to the surface. However, as protein adsorption is based on weak electrostatic bonding between the coating proteins and the substrate, this method produces suboptimal results: as the weak electrostatic bonds break, cells detach, leading to poor, heterogeneous cellularization. To solve this problem, we present a surface functionalization method for polyethylene terephthalate (PETE) membranes, commonly used in multilayer organ-on-chip devices to support cellular layers. This protocol involves hydrolyzation of the membrane, followed by (3-dimethylaminopropyl) carbodiimide (EDC) and N-hydroxysuccinimide (NHS) activation, resulting in covalent bonding between the membrane and coating proteins, much stronger than the weak electrostatic bonding provided by simple adsorption. As evaluation, we first measured the effect of the functionalization protocol in the morphological and mechanical integrity of the membranes. Next, we confirmed protein coating efficiency using the ζ potential and surface tension of the functionalized membranes coated with collagen type I, polylysine, gelatin, albumin, fetal bovine serum (FBS), and Matrigel. Finally, we showed that our method significantly improves the attachment of epithelial (A549) and endothelial (EA.hy926) cell lines under static conditions, especially in collagen-coated membranes, which were further tested under dynamic conditions, showing statistically significant improvement in cell attachment compared to uncoated or collagen-adsorbed only membranes. |
doi_str_mv | 10.1021/acsami.4c17706 |
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To improve cell adhesion, several surface functionalization techniques have been proposed, among which the simple use of an intermediate layer of adsorbed proteins has become the preferred one by OOC users. This way, the cells use surface receptors to adhere to the adsorbed proteins, which are in turn attached to the surface. However, as protein adsorption is based on weak electrostatic bonding between the coating proteins and the substrate, this method produces suboptimal results: as the weak electrostatic bonds break, cells detach, leading to poor, heterogeneous cellularization. To solve this problem, we present a surface functionalization method for polyethylene terephthalate (PETE) membranes, commonly used in multilayer organ-on-chip devices to support cellular layers. This protocol involves hydrolyzation of the membrane, followed by (3-dimethylaminopropyl) carbodiimide (EDC) and N-hydroxysuccinimide (NHS) activation, resulting in covalent bonding between the membrane and coating proteins, much stronger than the weak electrostatic bonding provided by simple adsorption. As evaluation, we first measured the effect of the functionalization protocol in the morphological and mechanical integrity of the membranes. Next, we confirmed protein coating efficiency using the ζ potential and surface tension of the functionalized membranes coated with collagen type I, polylysine, gelatin, albumin, fetal bovine serum (FBS), and Matrigel. Finally, we showed that our method significantly improves the attachment of epithelial (A549) and endothelial (EA.hy926) cell lines under static conditions, especially in collagen-coated membranes, which were further tested under dynamic conditions, showing statistically significant improvement in cell attachment compared to uncoated or collagen-adsorbed only membranes.</description><identifier>ISSN: 1944-8244</identifier><identifier>ISSN: 1944-8252</identifier><identifier>EISSN: 1944-8252</identifier><identifier>DOI: 10.1021/acsami.4c17706</identifier><identifier>PMID: 39772398</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Adsorption ; Animals ; Biological and Medical Applications of Materials and Interfaces ; Cell Adhesion - drug effects ; Humans ; Lab-On-A-Chip Devices ; Membranes, Artificial ; Microphysiological Systems ; Polyethylene Terephthalates - chemistry ; Surface Properties</subject><ispartof>ACS applied materials & interfaces, 2025-01, Vol.17 (3), p.4529-4542</ispartof><rights>2025 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-a215t-d347ac62bca0ac8845db5db6a367d3d676dee952a2fd4f8bb762269bfef69ff33</cites><orcidid>0000-0001-5660-7694 ; 0009-0002-4858-9523 ; 0009-0009-8065-3194 ; 0000-0002-7440-2737 ; 0000-0003-3422-8663 ; 0009-0000-2452-1458 ; 0000-0001-8720-0205 ; 0000-0003-2553-6779</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acsami.4c17706$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acsami.4c17706$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39772398$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sobejano de la Merced, Carlos</creatorcontrib><creatorcontrib>Doveri, Lavinia</creatorcontrib><creatorcontrib>Muñoz Santoro, Tomás</creatorcontrib><creatorcontrib>García, Javier</creatorcontrib><creatorcontrib>Garmendia, Junkal</creatorcontrib><creatorcontrib>Cortés Domínguez, Iván</creatorcontrib><creatorcontrib>Díaz Fernández, Yuri Antonio</creatorcontrib><creatorcontrib>Ortiz de Solórzano, Carlos</creatorcontrib><title>Functionalization of Polyethylene Terephthalate (PETE) Membranes for the Enhancement of Cellular Adhesion in Organ-on-a-Chip Devices</title><title>ACS applied materials & interfaces</title><addtitle>ACS Appl. Mater. Interfaces</addtitle><description>Experimental reproducibility in organ-on-chip (OOC) devices is a challenging issue, mainly caused by cell adhesion problems, as OOC devices are made of bioinert materials not suitable for natural cellularization of their surfaces. To improve cell adhesion, several surface functionalization techniques have been proposed, among which the simple use of an intermediate layer of adsorbed proteins has become the preferred one by OOC users. This way, the cells use surface receptors to adhere to the adsorbed proteins, which are in turn attached to the surface. However, as protein adsorption is based on weak electrostatic bonding between the coating proteins and the substrate, this method produces suboptimal results: as the weak electrostatic bonds break, cells detach, leading to poor, heterogeneous cellularization. To solve this problem, we present a surface functionalization method for polyethylene terephthalate (PETE) membranes, commonly used in multilayer organ-on-chip devices to support cellular layers. This protocol involves hydrolyzation of the membrane, followed by (3-dimethylaminopropyl) carbodiimide (EDC) and N-hydroxysuccinimide (NHS) activation, resulting in covalent bonding between the membrane and coating proteins, much stronger than the weak electrostatic bonding provided by simple adsorption. As evaluation, we first measured the effect of the functionalization protocol in the morphological and mechanical integrity of the membranes. Next, we confirmed protein coating efficiency using the ζ potential and surface tension of the functionalized membranes coated with collagen type I, polylysine, gelatin, albumin, fetal bovine serum (FBS), and Matrigel. Finally, we showed that our method significantly improves the attachment of epithelial (A549) and endothelial (EA.hy926) cell lines under static conditions, especially in collagen-coated membranes, which were further tested under dynamic conditions, showing statistically significant improvement in cell attachment compared to uncoated or collagen-adsorbed only membranes.</description><subject>Adsorption</subject><subject>Animals</subject><subject>Biological and Medical Applications of Materials and Interfaces</subject><subject>Cell Adhesion - drug effects</subject><subject>Humans</subject><subject>Lab-On-A-Chip Devices</subject><subject>Membranes, Artificial</subject><subject>Microphysiological Systems</subject><subject>Polyethylene Terephthalates - chemistry</subject><subject>Surface Properties</subject><issn>1944-8244</issn><issn>1944-8252</issn><issn>1944-8252</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2025</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kE1LxDAQQIMofqxePUqOKnRtkzRpj7KuH6DoYT2XaTqxlTZZk1ZYz_5wu-zqTQhkDm8eySPkNImnScySK9ABumYqdKJULHfIYZILEWUsZbt_sxAH5CiE9ziWnMXpPjnguVKM59kh-b4drO4bZ6FtvmA9UGfoi2tX2NerFi3SBXpc1n0NLfRIz1_mi_kFfcKu9GAxUOM87Wukc1uD1dih7deKGbbt0IKn11WNYe1tLH32b2AjZyOIZnWzpDf42WgMx2TPQBvwZHtPyOvtfDG7jx6f7x5m148RsCTto4oLBVqyUkMMOstEWpXjkcClqngllawQ85QBM5UwWVkqyZjMS4NG5sZwPiHnG-_Su48BQ190TdDjQ8ePuCEUPEl5pgQT2YhON6j2LgSPplj6pgO_KpK4WJcvNuWLbflx4WzrHsoOqz_8N_UIXG6AcbF4d4Mfk4f_bD9KNpBF</recordid><startdate>20250122</startdate><enddate>20250122</enddate><creator>Sobejano de la Merced, Carlos</creator><creator>Doveri, Lavinia</creator><creator>Muñoz Santoro, Tomás</creator><creator>García, Javier</creator><creator>Garmendia, Junkal</creator><creator>Cortés Domínguez, Iván</creator><creator>Díaz Fernández, Yuri Antonio</creator><creator>Ortiz de Solórzano, Carlos</creator><general>American Chemical Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-5660-7694</orcidid><orcidid>https://orcid.org/0009-0002-4858-9523</orcidid><orcidid>https://orcid.org/0009-0009-8065-3194</orcidid><orcidid>https://orcid.org/0000-0002-7440-2737</orcidid><orcidid>https://orcid.org/0000-0003-3422-8663</orcidid><orcidid>https://orcid.org/0009-0000-2452-1458</orcidid><orcidid>https://orcid.org/0000-0001-8720-0205</orcidid><orcidid>https://orcid.org/0000-0003-2553-6779</orcidid></search><sort><creationdate>20250122</creationdate><title>Functionalization of Polyethylene Terephthalate (PETE) Membranes for the Enhancement of Cellular Adhesion in Organ-on-a-Chip Devices</title><author>Sobejano de la Merced, Carlos ; Doveri, Lavinia ; Muñoz Santoro, Tomás ; García, Javier ; Garmendia, Junkal ; Cortés Domínguez, Iván ; Díaz Fernández, Yuri Antonio ; Ortiz de Solórzano, Carlos</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a215t-d347ac62bca0ac8845db5db6a367d3d676dee952a2fd4f8bb762269bfef69ff33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2025</creationdate><topic>Adsorption</topic><topic>Animals</topic><topic>Biological and Medical Applications of Materials and Interfaces</topic><topic>Cell Adhesion - drug effects</topic><topic>Humans</topic><topic>Lab-On-A-Chip Devices</topic><topic>Membranes, Artificial</topic><topic>Microphysiological Systems</topic><topic>Polyethylene Terephthalates - chemistry</topic><topic>Surface Properties</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sobejano de la Merced, Carlos</creatorcontrib><creatorcontrib>Doveri, Lavinia</creatorcontrib><creatorcontrib>Muñoz Santoro, Tomás</creatorcontrib><creatorcontrib>García, Javier</creatorcontrib><creatorcontrib>Garmendia, Junkal</creatorcontrib><creatorcontrib>Cortés Domínguez, Iván</creatorcontrib><creatorcontrib>Díaz Fernández, Yuri Antonio</creatorcontrib><creatorcontrib>Ortiz de Solórzano, Carlos</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>ACS applied materials & interfaces</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sobejano de la Merced, Carlos</au><au>Doveri, Lavinia</au><au>Muñoz Santoro, Tomás</au><au>García, Javier</au><au>Garmendia, Junkal</au><au>Cortés Domínguez, Iván</au><au>Díaz Fernández, Yuri Antonio</au><au>Ortiz de Solórzano, Carlos</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Functionalization of Polyethylene Terephthalate (PETE) Membranes for the Enhancement of Cellular Adhesion in Organ-on-a-Chip Devices</atitle><jtitle>ACS applied materials & interfaces</jtitle><addtitle>ACS Appl. Mater. Interfaces</addtitle><date>2025-01-22</date><risdate>2025</risdate><volume>17</volume><issue>3</issue><spage>4529</spage><epage>4542</epage><pages>4529-4542</pages><issn>1944-8244</issn><issn>1944-8252</issn><eissn>1944-8252</eissn><abstract>Experimental reproducibility in organ-on-chip (OOC) devices is a challenging issue, mainly caused by cell adhesion problems, as OOC devices are made of bioinert materials not suitable for natural cellularization of their surfaces. To improve cell adhesion, several surface functionalization techniques have been proposed, among which the simple use of an intermediate layer of adsorbed proteins has become the preferred one by OOC users. This way, the cells use surface receptors to adhere to the adsorbed proteins, which are in turn attached to the surface. However, as protein adsorption is based on weak electrostatic bonding between the coating proteins and the substrate, this method produces suboptimal results: as the weak electrostatic bonds break, cells detach, leading to poor, heterogeneous cellularization. To solve this problem, we present a surface functionalization method for polyethylene terephthalate (PETE) membranes, commonly used in multilayer organ-on-chip devices to support cellular layers. This protocol involves hydrolyzation of the membrane, followed by (3-dimethylaminopropyl) carbodiimide (EDC) and N-hydroxysuccinimide (NHS) activation, resulting in covalent bonding between the membrane and coating proteins, much stronger than the weak electrostatic bonding provided by simple adsorption. As evaluation, we first measured the effect of the functionalization protocol in the morphological and mechanical integrity of the membranes. Next, we confirmed protein coating efficiency using the ζ potential and surface tension of the functionalized membranes coated with collagen type I, polylysine, gelatin, albumin, fetal bovine serum (FBS), and Matrigel. Finally, we showed that our method significantly improves the attachment of epithelial (A549) and endothelial (EA.hy926) cell lines under static conditions, especially in collagen-coated membranes, which were further tested under dynamic conditions, showing statistically significant improvement in cell attachment compared to uncoated or collagen-adsorbed only membranes.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>39772398</pmid><doi>10.1021/acsami.4c17706</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0001-5660-7694</orcidid><orcidid>https://orcid.org/0009-0002-4858-9523</orcidid><orcidid>https://orcid.org/0009-0009-8065-3194</orcidid><orcidid>https://orcid.org/0000-0002-7440-2737</orcidid><orcidid>https://orcid.org/0000-0003-3422-8663</orcidid><orcidid>https://orcid.org/0009-0000-2452-1458</orcidid><orcidid>https://orcid.org/0000-0001-8720-0205</orcidid><orcidid>https://orcid.org/0000-0003-2553-6779</orcidid></addata></record> |
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subjects | Adsorption Animals Biological and Medical Applications of Materials and Interfaces Cell Adhesion - drug effects Humans Lab-On-A-Chip Devices Membranes, Artificial Microphysiological Systems Polyethylene Terephthalates - chemistry Surface Properties |
title | Functionalization of Polyethylene Terephthalate (PETE) Membranes for the Enhancement of Cellular Adhesion in Organ-on-a-Chip Devices |
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