Polymer-Aptamer Hybrid Emulsion Templating Yields Bioresponsive Nanocapsules
This article describes the synthesis of a DNA–polymer, being the nucleotide sequence an aptamer selected in vitro to target specifically the immunoglobulin E (IgE) protein, an allergy biomarker. Subsequent to coupling to poly(2‐alkyl‐2‐oxazoline) with N‐Boc protected amino acid side chains, the resu...
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Veröffentlicht in: | Advanced functional materials 2014-02, Vol.24 (8), p.1133-1139 |
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description | This article describes the synthesis of a DNA–polymer, being the nucleotide sequence an aptamer selected in vitro to target specifically the immunoglobulin E (IgE) protein, an allergy biomarker. Subsequent to coupling to poly(2‐alkyl‐2‐oxazoline) with N‐Boc protected amino acid side chains, the resulting amphiphilic DNA–polymer hybrid composed of the water‐soluble DNA fragment grafted to the hydrophobic polymer segment can be regarded as a high molecular weight analogue of a surfactant. It is demonstrated that the copolymer–aptamer stabilizes efficiently submicrometer size oil‐in‐water and water‐in‐oil emulsions, by dynamic light scattering, microscopy, and reflectometry. Particularly interesting is that the aptamer remains functional after coupling to a polymer backbone, stabilization of the emulsion droplets, and locking of the structure subsequent to cross‐linking polymerization. The resulting nanocapsules still target specifically the IgE protein. The biological‐stimulus responsiveness of the structures is of high potential for future developments of carriers for sustained and targeted delivery.
An IgE‐aptamer polymer hybrid efficiently stabilizes an emulsion. Since they specifically recognize immunoglobulin E, the resulting nanocapsules are biological‐stimulus responsive. |
doi_str_mv | 10.1002/adfm.201302475 |
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An IgE‐aptamer polymer hybrid efficiently stabilizes an emulsion. Since they specifically recognize immunoglobulin E, the resulting nanocapsules are biological‐stimulus responsive.</description><identifier>ISSN: 1616-301X</identifier><identifier>EISSN: 1616-3028</identifier><identifier>DOI: 10.1002/adfm.201302475</identifier><language>eng</language><publisher>Blackwell Publishing Ltd</publisher><subject>aptamers ; Biological effects ; Chemical Sciences ; Coupling (molecular) ; DNA copolymers ; Droplets ; Emulsions ; immunoglobulin E ; Immunoglobulins ; Nanostructure ; Physics ; poly(2-oxazoline) ; Polymerization ; Proteins</subject><ispartof>Advanced functional materials, 2014-02, Vol.24 (8), p.1133-1139</ispartof><rights>2013 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4315-553f1ba2d73dd45dd4ede5ccbb9542ae144513d89342ec2e2db2edf838b97003</citedby><cites>FETCH-LOGICAL-c4315-553f1ba2d73dd45dd4ede5ccbb9542ae144513d89342ec2e2db2edf838b97003</cites><orcidid>0000-0001-7840-1128</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.201302475$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fadfm.201302475$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,776,780,881,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://hal.science/hal-01564227$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Kedracki, Dawid</creatorcontrib><creatorcontrib>Maroni, Plinio</creatorcontrib><creatorcontrib>Schlaad, Helmut</creatorcontrib><creatorcontrib>Vebert-Nardin, Corinne</creatorcontrib><title>Polymer-Aptamer Hybrid Emulsion Templating Yields Bioresponsive Nanocapsules</title><title>Advanced functional materials</title><addtitle>Adv. Funct. Mater</addtitle><description>This article describes the synthesis of a DNA–polymer, being the nucleotide sequence an aptamer selected in vitro to target specifically the immunoglobulin E (IgE) protein, an allergy biomarker. Subsequent to coupling to poly(2‐alkyl‐2‐oxazoline) with N‐Boc protected amino acid side chains, the resulting amphiphilic DNA–polymer hybrid composed of the water‐soluble DNA fragment grafted to the hydrophobic polymer segment can be regarded as a high molecular weight analogue of a surfactant. It is demonstrated that the copolymer–aptamer stabilizes efficiently submicrometer size oil‐in‐water and water‐in‐oil emulsions, by dynamic light scattering, microscopy, and reflectometry. Particularly interesting is that the aptamer remains functional after coupling to a polymer backbone, stabilization of the emulsion droplets, and locking of the structure subsequent to cross‐linking polymerization. The resulting nanocapsules still target specifically the IgE protein. The biological‐stimulus responsiveness of the structures is of high potential for future developments of carriers for sustained and targeted delivery.
An IgE‐aptamer polymer hybrid efficiently stabilizes an emulsion. Since they specifically recognize immunoglobulin E, the resulting nanocapsules are biological‐stimulus responsive.</description><subject>aptamers</subject><subject>Biological effects</subject><subject>Chemical Sciences</subject><subject>Coupling (molecular)</subject><subject>DNA copolymers</subject><subject>Droplets</subject><subject>Emulsions</subject><subject>immunoglobulin E</subject><subject>Immunoglobulins</subject><subject>Nanostructure</subject><subject>Physics</subject><subject>poly(2-oxazoline)</subject><subject>Polymerization</subject><subject>Proteins</subject><issn>1616-301X</issn><issn>1616-3028</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqFkDtPwzAURi0EElBYmTPCkOJn04wt9IEoL6kSMFlOfAMGJw52CvTfkyqoYmO4ug-dc4cPoROC-wRjeq50UfYpJgxTnogddEAGZBC323B3O5OnfXQYwhvGJEkYP0CLe2fXJfh4VDeq7dF8nXmjo0m5ssG4KlpCWVvVmOolejZgdYjGxnkItauC-YToVlUuV3VYWQhHaK9QNsDxb--h5XSyvJjHi7vZ1cVoEeecERELwQqSKaoTpjUXbYEGkedZlgpOFRDOBWF6mDJOIadAdUZBF0M2zNIEY9ZDZ93bV2Vl7U2p_Fo6ZeR8tJCbGyZiwClNPknLnnZs7d3HCkIjSxNysFZV4FZBEkFxylLeptFD_Q7NvQvBQ7H9TbDcJCw3Ccttwq2QdsKXsbD-h5ajy-nNXzfuXBMa-N66yr_LQcJa_PF2JsfXD_yR8rFcsh8lno7w</recordid><startdate>20140201</startdate><enddate>20140201</enddate><creator>Kedracki, Dawid</creator><creator>Maroni, Plinio</creator><creator>Schlaad, Helmut</creator><creator>Vebert-Nardin, Corinne</creator><general>Blackwell Publishing Ltd</general><general>Wiley</general><scope>BSCLL</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><scope>1XC</scope><orcidid>https://orcid.org/0000-0001-7840-1128</orcidid></search><sort><creationdate>20140201</creationdate><title>Polymer-Aptamer Hybrid Emulsion Templating Yields Bioresponsive Nanocapsules</title><author>Kedracki, Dawid ; Maroni, Plinio ; Schlaad, Helmut ; Vebert-Nardin, Corinne</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4315-553f1ba2d73dd45dd4ede5ccbb9542ae144513d89342ec2e2db2edf838b97003</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>aptamers</topic><topic>Biological effects</topic><topic>Chemical Sciences</topic><topic>Coupling (molecular)</topic><topic>DNA copolymers</topic><topic>Droplets</topic><topic>Emulsions</topic><topic>immunoglobulin E</topic><topic>Immunoglobulins</topic><topic>Nanostructure</topic><topic>Physics</topic><topic>poly(2-oxazoline)</topic><topic>Polymerization</topic><topic>Proteins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kedracki, Dawid</creatorcontrib><creatorcontrib>Maroni, Plinio</creatorcontrib><creatorcontrib>Schlaad, Helmut</creatorcontrib><creatorcontrib>Vebert-Nardin, Corinne</creatorcontrib><collection>Istex</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><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Advanced functional materials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kedracki, Dawid</au><au>Maroni, Plinio</au><au>Schlaad, Helmut</au><au>Vebert-Nardin, Corinne</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Polymer-Aptamer Hybrid Emulsion Templating Yields Bioresponsive Nanocapsules</atitle><jtitle>Advanced functional materials</jtitle><addtitle>Adv. Funct. Mater</addtitle><date>2014-02-01</date><risdate>2014</risdate><volume>24</volume><issue>8</issue><spage>1133</spage><epage>1139</epage><pages>1133-1139</pages><issn>1616-301X</issn><eissn>1616-3028</eissn><abstract>This article describes the synthesis of a DNA–polymer, being the nucleotide sequence an aptamer selected in vitro to target specifically the immunoglobulin E (IgE) protein, an allergy biomarker. Subsequent to coupling to poly(2‐alkyl‐2‐oxazoline) with N‐Boc protected amino acid side chains, the resulting amphiphilic DNA–polymer hybrid composed of the water‐soluble DNA fragment grafted to the hydrophobic polymer segment can be regarded as a high molecular weight analogue of a surfactant. It is demonstrated that the copolymer–aptamer stabilizes efficiently submicrometer size oil‐in‐water and water‐in‐oil emulsions, by dynamic light scattering, microscopy, and reflectometry. Particularly interesting is that the aptamer remains functional after coupling to a polymer backbone, stabilization of the emulsion droplets, and locking of the structure subsequent to cross‐linking polymerization. The resulting nanocapsules still target specifically the IgE protein. The biological‐stimulus responsiveness of the structures is of high potential for future developments of carriers for sustained and targeted delivery.
An IgE‐aptamer polymer hybrid efficiently stabilizes an emulsion. Since they specifically recognize immunoglobulin E, the resulting nanocapsules are biological‐stimulus responsive.</abstract><pub>Blackwell Publishing Ltd</pub><doi>10.1002/adfm.201302475</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-7840-1128</orcidid></addata></record> |
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subjects | aptamers Biological effects Chemical Sciences Coupling (molecular) DNA copolymers Droplets Emulsions immunoglobulin E Immunoglobulins Nanostructure Physics poly(2-oxazoline) Polymerization Proteins |
title | Polymer-Aptamer Hybrid Emulsion Templating Yields Bioresponsive Nanocapsules |
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