Redox‐responsive polyethyleneimine‐coated magnetic iron oxide nanoparticles for controllable gene delivery and magnetic resonance imaging
Recently, theranostic candidates that provide a combination of gene delivery and image diagnosis have attracted much interest in medical research. However, there are still many challenges for their clinical applications, such as uncontrollable gene delivery, high cytotoxicity, low transfection effic...
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Veröffentlicht in: | Polymer international 2020-02, Vol.69 (2), p.206-214 |
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description | Recently, theranostic candidates that provide a combination of gene delivery and image diagnosis have attracted much interest in medical research. However, there are still many challenges for their clinical applications, such as uncontrollable gene delivery, high cytotoxicity, low transfection efficiency and reduced image contrast. Herein, redox‐responsive polyethyleneimine‐coated magnetic iron oxide nanoparticles (IONs@rPEI) were prepared for both efficient gene delivery and magnetic resonance (MR) imaging. Firstly, crosslinked rPEI was synthesized by Michael addition reaction with N,N‐bis(acryloyl)cystamine, dopamine and low‐molecular‐weight branched PEI. The rPEI was then coated onto IONs by ligand exchange reaction forming IONs@rPEI. The physicochemical properties of the IONs@rPEI, such as chemical structure, size, zeta potential and DNA condensation ability, were investigated. In addition, a rapid degradation of the as‐prepared nanoparticles was observed, which was triggered by reducing glutathione via destruction of disulfide linkages suggesting a potential controllable DNA release in tumor cells. In MR imaging detection, the IONs@rPEI had a high T2 relaxivity of 81 L mmol−1 s−1 indicating a potential usage as MR imaging contrast reagent. In cell assay, the IONs@rPEI exhibited low cytotoxicity and good transfection efficiency. In conclusion, the as‐prepared crosslinked IONs@rPEI can be used as a promising technology platform for gene therapy and MR imaging in theranostics. © 2019 Society of Chemical Industry
Schematic illustration of the preparation and gene delivery process of IONs@rPEI/DNA complexes. |
doi_str_mv | 10.1002/pi.5943 |
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Schematic illustration of the preparation and gene delivery process of IONs@rPEI/DNA complexes.</description><identifier>ISSN: 0959-8103</identifier><identifier>EISSN: 1097-0126</identifier><identifier>DOI: 10.1002/pi.5943</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>Coatings ; Crosslinking ; Cytotoxicity ; Deoxyribonucleic acid ; Disulfide bonds ; DNA ; Dopamine ; Gene therapy ; gene transfection ; Gene transfer ; Glutathione ; Image contrast ; Ions ; Iron oxides ; Magnetic resonance imaging ; Medical imaging ; Medical research ; Michael reaction ; MR imaging ; Nanoparticles ; Organic chemistry ; Physicochemical properties ; Polyethyleneimine ; Precision medicine ; Reagents ; redox‐responsive ; theranostics ; Therapeutic applications ; Toxicity ; Transfection ; Tumor cells ; Zeta potential</subject><ispartof>Polymer international, 2020-02, Vol.69 (2), p.206-214</ispartof><rights>2019 Society of Chemical Industry</rights><rights>Copyright © 2020 Society of Chemical Industry</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3263-17aca495376d57e9d584dfa84de226a72e552b016f9fe0080a419840983f1ffa3</citedby><cites>FETCH-LOGICAL-c3263-17aca495376d57e9d584dfa84de226a72e552b016f9fe0080a419840983f1ffa3</cites><orcidid>0000-0001-5637-4173</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%2Fpi.5943$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fpi.5943$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids></links><search><creatorcontrib>Peng, Si</creatorcontrib><creatorcontrib>Wang, Qiu‐yue</creatorcontrib><creatorcontrib>Xiao, Xue</creatorcontrib><creatorcontrib>Wang, Rui</creatorcontrib><creatorcontrib>Lin, Juan</creatorcontrib><creatorcontrib>Zhou, Qing‐han</creatorcontrib><creatorcontrib>Wu, Li‐na</creatorcontrib><title>Redox‐responsive polyethyleneimine‐coated magnetic iron oxide nanoparticles for controllable gene delivery and magnetic resonance imaging</title><title>Polymer international</title><description>Recently, theranostic candidates that provide a combination of gene delivery and image diagnosis have attracted much interest in medical research. However, there are still many challenges for their clinical applications, such as uncontrollable gene delivery, high cytotoxicity, low transfection efficiency and reduced image contrast. Herein, redox‐responsive polyethyleneimine‐coated magnetic iron oxide nanoparticles (IONs@rPEI) were prepared for both efficient gene delivery and magnetic resonance (MR) imaging. Firstly, crosslinked rPEI was synthesized by Michael addition reaction with N,N‐bis(acryloyl)cystamine, dopamine and low‐molecular‐weight branched PEI. The rPEI was then coated onto IONs by ligand exchange reaction forming IONs@rPEI. The physicochemical properties of the IONs@rPEI, such as chemical structure, size, zeta potential and DNA condensation ability, were investigated. In addition, a rapid degradation of the as‐prepared nanoparticles was observed, which was triggered by reducing glutathione via destruction of disulfide linkages suggesting a potential controllable DNA release in tumor cells. In MR imaging detection, the IONs@rPEI had a high T2 relaxivity of 81 L mmol−1 s−1 indicating a potential usage as MR imaging contrast reagent. In cell assay, the IONs@rPEI exhibited low cytotoxicity and good transfection efficiency. In conclusion, the as‐prepared crosslinked IONs@rPEI can be used as a promising technology platform for gene therapy and MR imaging in theranostics. © 2019 Society of Chemical Industry
Schematic illustration of the preparation and gene delivery process of IONs@rPEI/DNA complexes.</description><subject>Coatings</subject><subject>Crosslinking</subject><subject>Cytotoxicity</subject><subject>Deoxyribonucleic acid</subject><subject>Disulfide bonds</subject><subject>DNA</subject><subject>Dopamine</subject><subject>Gene therapy</subject><subject>gene transfection</subject><subject>Gene transfer</subject><subject>Glutathione</subject><subject>Image contrast</subject><subject>Ions</subject><subject>Iron oxides</subject><subject>Magnetic resonance imaging</subject><subject>Medical imaging</subject><subject>Medical research</subject><subject>Michael reaction</subject><subject>MR imaging</subject><subject>Nanoparticles</subject><subject>Organic chemistry</subject><subject>Physicochemical properties</subject><subject>Polyethyleneimine</subject><subject>Precision medicine</subject><subject>Reagents</subject><subject>redox‐responsive</subject><subject>theranostics</subject><subject>Therapeutic applications</subject><subject>Toxicity</subject><subject>Transfection</subject><subject>Tumor cells</subject><subject>Zeta potential</subject><issn>0959-8103</issn><issn>1097-0126</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp1kMlKBDEQhoMoOC74CgEPHqTHLL0kRxlcBgYU0XOT6a6MGTJJm7RL33wBwWf0Scw4Hrx4qYKqr_6_qhA6omRMCWFnnRkXMudbaESJrDJCWbmNRkQWMhOU8F20F-OSECKklCP0cQetf_t6_wwQO--ieQHceTtA_zhYcGBWxkFqN1710OKVWjjoTYNN8A77N9MCdsr5ToVUtRCx9gE33vXBW6vmFvAiqeAWbFIOA1buj0jy9Gm6AWxSzbjFAdrRykY4_M376OHy4n5ync1urqaT81nWcFbyjFaqUbkseFW2RQWyLUTeapUCMFaqikFRsDmhpZYa0qVE5VSKnEjBNdVa8X10vNHtgn96htjXS_8cXLKsGee5kIIInqiTDdUEH2MAXXchLRqGmpJ6_eu6M_X614k83ZCvxsLwH1bfTn_ob7W3hHw</recordid><startdate>202002</startdate><enddate>202002</enddate><creator>Peng, Si</creator><creator>Wang, Qiu‐yue</creator><creator>Xiao, Xue</creator><creator>Wang, Rui</creator><creator>Lin, Juan</creator><creator>Zhou, Qing‐han</creator><creator>Wu, Li‐na</creator><general>John Wiley & Sons, Ltd</general><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>JG9</scope><orcidid>https://orcid.org/0000-0001-5637-4173</orcidid></search><sort><creationdate>202002</creationdate><title>Redox‐responsive polyethyleneimine‐coated magnetic iron oxide nanoparticles for controllable gene delivery and magnetic resonance imaging</title><author>Peng, Si ; Wang, Qiu‐yue ; Xiao, Xue ; Wang, Rui ; Lin, Juan ; Zhou, Qing‐han ; Wu, Li‐na</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3263-17aca495376d57e9d584dfa84de226a72e552b016f9fe0080a419840983f1ffa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Coatings</topic><topic>Crosslinking</topic><topic>Cytotoxicity</topic><topic>Deoxyribonucleic acid</topic><topic>Disulfide bonds</topic><topic>DNA</topic><topic>Dopamine</topic><topic>Gene therapy</topic><topic>gene transfection</topic><topic>Gene transfer</topic><topic>Glutathione</topic><topic>Image contrast</topic><topic>Ions</topic><topic>Iron oxides</topic><topic>Magnetic resonance imaging</topic><topic>Medical imaging</topic><topic>Medical research</topic><topic>Michael reaction</topic><topic>MR imaging</topic><topic>Nanoparticles</topic><topic>Organic chemistry</topic><topic>Physicochemical properties</topic><topic>Polyethyleneimine</topic><topic>Precision medicine</topic><topic>Reagents</topic><topic>redox‐responsive</topic><topic>theranostics</topic><topic>Therapeutic applications</topic><topic>Toxicity</topic><topic>Transfection</topic><topic>Tumor cells</topic><topic>Zeta potential</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Peng, Si</creatorcontrib><creatorcontrib>Wang, Qiu‐yue</creatorcontrib><creatorcontrib>Xiao, Xue</creatorcontrib><creatorcontrib>Wang, Rui</creatorcontrib><creatorcontrib>Lin, Juan</creatorcontrib><creatorcontrib>Zhou, Qing‐han</creatorcontrib><creatorcontrib>Wu, Li‐na</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Materials Research Database</collection><jtitle>Polymer international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Peng, Si</au><au>Wang, Qiu‐yue</au><au>Xiao, Xue</au><au>Wang, Rui</au><au>Lin, Juan</au><au>Zhou, Qing‐han</au><au>Wu, Li‐na</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Redox‐responsive polyethyleneimine‐coated magnetic iron oxide nanoparticles for controllable gene delivery and magnetic resonance imaging</atitle><jtitle>Polymer international</jtitle><date>2020-02</date><risdate>2020</risdate><volume>69</volume><issue>2</issue><spage>206</spage><epage>214</epage><pages>206-214</pages><issn>0959-8103</issn><eissn>1097-0126</eissn><abstract>Recently, theranostic candidates that provide a combination of gene delivery and image diagnosis have attracted much interest in medical research. However, there are still many challenges for their clinical applications, such as uncontrollable gene delivery, high cytotoxicity, low transfection efficiency and reduced image contrast. Herein, redox‐responsive polyethyleneimine‐coated magnetic iron oxide nanoparticles (IONs@rPEI) were prepared for both efficient gene delivery and magnetic resonance (MR) imaging. Firstly, crosslinked rPEI was synthesized by Michael addition reaction with N,N‐bis(acryloyl)cystamine, dopamine and low‐molecular‐weight branched PEI. The rPEI was then coated onto IONs by ligand exchange reaction forming IONs@rPEI. The physicochemical properties of the IONs@rPEI, such as chemical structure, size, zeta potential and DNA condensation ability, were investigated. In addition, a rapid degradation of the as‐prepared nanoparticles was observed, which was triggered by reducing glutathione via destruction of disulfide linkages suggesting a potential controllable DNA release in tumor cells. In MR imaging detection, the IONs@rPEI had a high T2 relaxivity of 81 L mmol−1 s−1 indicating a potential usage as MR imaging contrast reagent. In cell assay, the IONs@rPEI exhibited low cytotoxicity and good transfection efficiency. In conclusion, the as‐prepared crosslinked IONs@rPEI can be used as a promising technology platform for gene therapy and MR imaging in theranostics. © 2019 Society of Chemical Industry
Schematic illustration of the preparation and gene delivery process of IONs@rPEI/DNA complexes.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><doi>10.1002/pi.5943</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-5637-4173</orcidid></addata></record> |
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subjects | Coatings Crosslinking Cytotoxicity Deoxyribonucleic acid Disulfide bonds DNA Dopamine Gene therapy gene transfection Gene transfer Glutathione Image contrast Ions Iron oxides Magnetic resonance imaging Medical imaging Medical research Michael reaction MR imaging Nanoparticles Organic chemistry Physicochemical properties Polyethyleneimine Precision medicine Reagents redox‐responsive theranostics Therapeutic applications Toxicity Transfection Tumor cells Zeta potential |
title | Redox‐responsive polyethyleneimine‐coated magnetic iron oxide nanoparticles for controllable gene delivery and magnetic resonance imaging |
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