Deposition transfection technology using a DNA complex with a thermoresponsive cationic star polymer
A novel non-viral gene transfection method in which DNA complexes were kept in contact with a deposition surface (deposition transfection) was developed. We designed a novel aqueous thermoresponsive adsorbent material for DNA deposition, which was a star-shaped copolymer with 4-branched chains. Each...
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creator | Zhou, Yue-Min Ishikawa, Ayaka Okahashi, Ryohei Uchida, Kingo Nemoto, Yasushi Nakayama, Mitsuko Nakayama, Yasuhide |
description | A novel non-viral gene transfection method in which DNA complexes were kept in contact with a deposition surface (deposition transfection) was developed. We designed a novel aqueous thermoresponsive adsorbent material for DNA deposition, which was a star-shaped copolymer with 4-branched chains. Each chain is comprised of a cationic poly(
N,N-dimethylaminopropyl acrylamide) (PDMAPAAm) block (Mn: ca. 3000 g·mol
−
1
), which formed an inner domain for DNA binding and a thermoresponsive poly(
N-isopropylacrylamide) (PNIPAM) block (Mn: ca. 6000 g·mol
−
1
), which formed an outer domain for surface adsorption. Complex formation between the copolymer and the luciferase-encoding plasmid DNA occurred immediately upon simple mixing in an aqueous medium; polyplexes approximately 100 nm in size were formed. Because the lower critical solution temperature of the polyplexes was approximately 35 °C, they could deposit on the substrate by precipitation from an aqueous solution upon warming, which was confirmed by quartz crystal microbalance (QCM) method and water contact angle measurement. When COS-1 cells were cultured on the polyplex-deposited substrate in a culture medium, the luciferase activity observed was higher than that observed on a DNA-coated substrate with or without the cationic polymer before and after complete adhesion and by conventional solution transfection using the polyplexes. The activity was enhanced with an increase in the charge ratio (surfactant/pDNA) with permissible cellular cytotoxicity. |
doi_str_mv | 10.1016/j.jconrel.2007.08.026 |
format | Article |
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N,N-dimethylaminopropyl acrylamide) (PDMAPAAm) block (Mn: ca. 3000 g·mol
−
1
), which formed an inner domain for DNA binding and a thermoresponsive poly(
N-isopropylacrylamide) (PNIPAM) block (Mn: ca. 6000 g·mol
−
1
), which formed an outer domain for surface adsorption. Complex formation between the copolymer and the luciferase-encoding plasmid DNA occurred immediately upon simple mixing in an aqueous medium; polyplexes approximately 100 nm in size were formed. Because the lower critical solution temperature of the polyplexes was approximately 35 °C, they could deposit on the substrate by precipitation from an aqueous solution upon warming, which was confirmed by quartz crystal microbalance (QCM) method and water contact angle measurement. When COS-1 cells were cultured on the polyplex-deposited substrate in a culture medium, the luciferase activity observed was higher than that observed on a DNA-coated substrate with or without the cationic polymer before and after complete adhesion and by conventional solution transfection using the polyplexes. The activity was enhanced with an increase in the charge ratio (surfactant/pDNA) with permissible cellular cytotoxicity.</description><identifier>ISSN: 0168-3659</identifier><identifier>EISSN: 1873-4995</identifier><identifier>DOI: 10.1016/j.jconrel.2007.08.026</identifier><identifier>PMID: 17881077</identifier><identifier>CODEN: JCREEC</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Acrylamides - chemical synthesis ; Acrylamides - toxicity ; Acrylic Resins - chemical synthesis ; Acrylic Resins - toxicity ; Animals ; Biological and medical sciences ; Cationic polymer ; Cations ; Cell Survival - drug effects ; Cercopithecus aethiops ; Chemical Precipitation ; COS Cells ; Deposition transfection ; DNA - chemistry ; DNA - metabolism ; DNA delivery ; General pharmacology ; Genes, Reporter ; Luciferases - metabolism ; Medical sciences ; Molecular Structure ; Particle Size ; Pharmaceutical technology. Pharmaceutical industry ; Pharmacology. Drug treatments ; Reverse transfection ; Temperature ; Thermoresponsive polymer ; Transfection - methods</subject><ispartof>Journal of controlled release, 2007-11, Vol.123 (3), p.239-246</ispartof><rights>2007 Elsevier B.V.</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c515t-8ba0213c5735990fedef97459ec3e450a06f3fa9add081eca9e76481bbab3d0a3</citedby><cites>FETCH-LOGICAL-c515t-8ba0213c5735990fedef97459ec3e450a06f3fa9add081eca9e76481bbab3d0a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0168365907004300$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19220011$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17881077$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhou, Yue-Min</creatorcontrib><creatorcontrib>Ishikawa, Ayaka</creatorcontrib><creatorcontrib>Okahashi, Ryohei</creatorcontrib><creatorcontrib>Uchida, Kingo</creatorcontrib><creatorcontrib>Nemoto, Yasushi</creatorcontrib><creatorcontrib>Nakayama, Mitsuko</creatorcontrib><creatorcontrib>Nakayama, Yasuhide</creatorcontrib><title>Deposition transfection technology using a DNA complex with a thermoresponsive cationic star polymer</title><title>Journal of controlled release</title><addtitle>J Control Release</addtitle><description>A novel non-viral gene transfection method in which DNA complexes were kept in contact with a deposition surface (deposition transfection) was developed. We designed a novel aqueous thermoresponsive adsorbent material for DNA deposition, which was a star-shaped copolymer with 4-branched chains. Each chain is comprised of a cationic poly(
N,N-dimethylaminopropyl acrylamide) (PDMAPAAm) block (Mn: ca. 3000 g·mol
−
1
), which formed an inner domain for DNA binding and a thermoresponsive poly(
N-isopropylacrylamide) (PNIPAM) block (Mn: ca. 6000 g·mol
−
1
), which formed an outer domain for surface adsorption. Complex formation between the copolymer and the luciferase-encoding plasmid DNA occurred immediately upon simple mixing in an aqueous medium; polyplexes approximately 100 nm in size were formed. Because the lower critical solution temperature of the polyplexes was approximately 35 °C, they could deposit on the substrate by precipitation from an aqueous solution upon warming, which was confirmed by quartz crystal microbalance (QCM) method and water contact angle measurement. When COS-1 cells were cultured on the polyplex-deposited substrate in a culture medium, the luciferase activity observed was higher than that observed on a DNA-coated substrate with or without the cationic polymer before and after complete adhesion and by conventional solution transfection using the polyplexes. The activity was enhanced with an increase in the charge ratio (surfactant/pDNA) with permissible cellular cytotoxicity.</description><subject>Acrylamides - chemical synthesis</subject><subject>Acrylamides - toxicity</subject><subject>Acrylic Resins - chemical synthesis</subject><subject>Acrylic Resins - toxicity</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cationic polymer</subject><subject>Cations</subject><subject>Cell Survival - drug effects</subject><subject>Cercopithecus aethiops</subject><subject>Chemical Precipitation</subject><subject>COS Cells</subject><subject>Deposition transfection</subject><subject>DNA - chemistry</subject><subject>DNA - metabolism</subject><subject>DNA delivery</subject><subject>General pharmacology</subject><subject>Genes, Reporter</subject><subject>Luciferases - metabolism</subject><subject>Medical sciences</subject><subject>Molecular Structure</subject><subject>Particle Size</subject><subject>Pharmaceutical technology. Pharmaceutical industry</subject><subject>Pharmacology. Drug treatments</subject><subject>Reverse transfection</subject><subject>Temperature</subject><subject>Thermoresponsive polymer</subject><subject>Transfection - methods</subject><issn>0168-3659</issn><issn>1873-4995</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcFO3DAURa2KqkxpPwHkDd0lfR7Hsb1CCFpaCbUbWFuO88J4lMTBzlDm7-vRRGLJyrJ17vXTeYScMygZsPr7tty6MEbsyzWALEGVsK4_kBVTkheV1uKErDKnCl4LfUo-p7QFAMEr-YmcMqkUAylXpL3FKSQ_-zDSOdoxdeiOF3SbMfThaU93yY9P1NLbP9fUhWHq8ZX-8_MmP80bjEOImKYwJv-C1NlD2juaZhvpFPr9gPEL-djZPuHX5Twjjz9_PNz8Ku7_3v2-ub4vnGBiLlRjYc24E5ILraHDFjstK6HRcawEWKg73llt2xYUQ2c1yrpSrGlsw1uw_Ix8O_ZOMTzvMM1m8Mlh39sRwy4ZpmvFuYYMiiPoYkgpYmem6Acb94aBOeg1W7PoNQe9BpTJenPuYvlg1wzYvqUWnxm4XACbnO27bNT59Mbpda5jLHNXRw6zjheP0STncXTY-pgXYNrg3xnlP4Alngc</recordid><startdate>20071120</startdate><enddate>20071120</enddate><creator>Zhou, Yue-Min</creator><creator>Ishikawa, Ayaka</creator><creator>Okahashi, Ryohei</creator><creator>Uchida, Kingo</creator><creator>Nemoto, Yasushi</creator><creator>Nakayama, Mitsuko</creator><creator>Nakayama, Yasuhide</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><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>7QO</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope></search><sort><creationdate>20071120</creationdate><title>Deposition transfection technology using a DNA complex with a thermoresponsive cationic star polymer</title><author>Zhou, Yue-Min ; Ishikawa, Ayaka ; Okahashi, Ryohei ; Uchida, Kingo ; Nemoto, Yasushi ; Nakayama, Mitsuko ; Nakayama, Yasuhide</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c515t-8ba0213c5735990fedef97459ec3e450a06f3fa9add081eca9e76481bbab3d0a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Acrylamides - chemical synthesis</topic><topic>Acrylamides - toxicity</topic><topic>Acrylic Resins - chemical synthesis</topic><topic>Acrylic Resins - toxicity</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cationic polymer</topic><topic>Cations</topic><topic>Cell Survival - drug effects</topic><topic>Cercopithecus aethiops</topic><topic>Chemical Precipitation</topic><topic>COS Cells</topic><topic>Deposition transfection</topic><topic>DNA - chemistry</topic><topic>DNA - metabolism</topic><topic>DNA delivery</topic><topic>General pharmacology</topic><topic>Genes, Reporter</topic><topic>Luciferases - metabolism</topic><topic>Medical sciences</topic><topic>Molecular Structure</topic><topic>Particle Size</topic><topic>Pharmaceutical technology. Pharmaceutical industry</topic><topic>Pharmacology. Drug treatments</topic><topic>Reverse transfection</topic><topic>Temperature</topic><topic>Thermoresponsive polymer</topic><topic>Transfection - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhou, Yue-Min</creatorcontrib><creatorcontrib>Ishikawa, Ayaka</creatorcontrib><creatorcontrib>Okahashi, Ryohei</creatorcontrib><creatorcontrib>Uchida, Kingo</creatorcontrib><creatorcontrib>Nemoto, Yasushi</creatorcontrib><creatorcontrib>Nakayama, Mitsuko</creatorcontrib><creatorcontrib>Nakayama, Yasuhide</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Journal of controlled release</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhou, Yue-Min</au><au>Ishikawa, Ayaka</au><au>Okahashi, Ryohei</au><au>Uchida, Kingo</au><au>Nemoto, Yasushi</au><au>Nakayama, Mitsuko</au><au>Nakayama, Yasuhide</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Deposition transfection technology using a DNA complex with a thermoresponsive cationic star polymer</atitle><jtitle>Journal of controlled release</jtitle><addtitle>J Control Release</addtitle><date>2007-11-20</date><risdate>2007</risdate><volume>123</volume><issue>3</issue><spage>239</spage><epage>246</epage><pages>239-246</pages><issn>0168-3659</issn><eissn>1873-4995</eissn><coden>JCREEC</coden><abstract>A novel non-viral gene transfection method in which DNA complexes were kept in contact with a deposition surface (deposition transfection) was developed. We designed a novel aqueous thermoresponsive adsorbent material for DNA deposition, which was a star-shaped copolymer with 4-branched chains. Each chain is comprised of a cationic poly(
N,N-dimethylaminopropyl acrylamide) (PDMAPAAm) block (Mn: ca. 3000 g·mol
−
1
), which formed an inner domain for DNA binding and a thermoresponsive poly(
N-isopropylacrylamide) (PNIPAM) block (Mn: ca. 6000 g·mol
−
1
), which formed an outer domain for surface adsorption. Complex formation between the copolymer and the luciferase-encoding plasmid DNA occurred immediately upon simple mixing in an aqueous medium; polyplexes approximately 100 nm in size were formed. Because the lower critical solution temperature of the polyplexes was approximately 35 °C, they could deposit on the substrate by precipitation from an aqueous solution upon warming, which was confirmed by quartz crystal microbalance (QCM) method and water contact angle measurement. When COS-1 cells were cultured on the polyplex-deposited substrate in a culture medium, the luciferase activity observed was higher than that observed on a DNA-coated substrate with or without the cationic polymer before and after complete adhesion and by conventional solution transfection using the polyplexes. The activity was enhanced with an increase in the charge ratio (surfactant/pDNA) with permissible cellular cytotoxicity.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>17881077</pmid><doi>10.1016/j.jconrel.2007.08.026</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acrylamides - chemical synthesis Acrylamides - toxicity Acrylic Resins - chemical synthesis Acrylic Resins - toxicity Animals Biological and medical sciences Cationic polymer Cations Cell Survival - drug effects Cercopithecus aethiops Chemical Precipitation COS Cells Deposition transfection DNA - chemistry DNA - metabolism DNA delivery General pharmacology Genes, Reporter Luciferases - metabolism Medical sciences Molecular Structure Particle Size Pharmaceutical technology. Pharmaceutical industry Pharmacology. Drug treatments Reverse transfection Temperature Thermoresponsive polymer Transfection - methods |
title | Deposition transfection technology using a DNA complex with a thermoresponsive cationic star polymer |
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