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Effect on in vitro cell response of the statistical insertion of N-(2-hydroxypropyl) methacrylamide on linear pro-dendronic polyamine’s gene carriers
[Display omitted] Statistical copolymers of N-(2-hydroxypropyl) methacrylamide (HPMA) and the dendronic methacrylic monomer 2-(3-(Bis(2-(diethylamino)ethyl)amino)propanamido)ethyl methacrylate (TEDETAMA, derived from N,N,N′,N′-tetraethyldiethylenetriamine, TEDETA), were synthesized through radical c...
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Published in: | European journal of pharmaceutics and biopharmaceutics 2015-06, Vol.93, p.303-310 |
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container_title | European journal of pharmaceutics and biopharmaceutics |
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creator | Redondo, Juan Alfonso Martínez-Campos, Enrique Navarro, Rodrigo Reinecke, Helmut Elvira, Carlos López-Lacomba, José Luis Gallardo, Alberto |
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Statistical copolymers of N-(2-hydroxypropyl) methacrylamide (HPMA) and the dendronic methacrylic monomer 2-(3-(Bis(2-(diethylamino)ethyl)amino)propanamido)ethyl methacrylate (TEDETAMA, derived from N,N,N′,N′-tetraethyldiethylenetriamine, TEDETA), were synthesized through radical copolymerization and evaluated in vitro as non-viral gene carriers. Three copolymers with nominal molar percentages of HPMA of 25%, 50% and 75% were prepared and studied comparatively to the positive controls poly-TEDETAMA and hyperbranched polyethyleneimine (PEI, 25kDa). Their ability to complex DNA at different N/P molar ratios, from 1/1 up to 8/1, was determined through agarose gel electrophoresis and Dynamic Light Scattering. The resulting complexes (polyplexes) were characterized and evaluated in vitro as possible non-viral gene carriers for Swiss-3T3 fibroblasts, using luciferase as reporter gene and a calcein cytocompatibility assay. All the copolymers, except the one with highest HPMA proportion (75 molar %) at the lowest N/P ratio, condensed DNA to a particle size between 100 and 300nm. The copolymers with 25 and 50 molar % of HPMA displayed higher transfection efficiency and cytocompatibility than the positive controls poly-TEDETAMA and PEI. A higher proportion of HPMA (75 molar %) led to copolymers that displayed very low transfection efficiency, despite their full cytocompatibility even at the highest N/P ratio. These results indicate that the statistical combination of TEDETAMA and HPMA and its fine compositional tuning in the copolymers may fulfill the fine balance of transfection efficiency and cytocompatibility in a superior way to the control poly-TEDETAMA and PEI. |
doi_str_mv | 10.1016/j.ejpb.2015.04.014 |
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Statistical copolymers of N-(2-hydroxypropyl) methacrylamide (HPMA) and the dendronic methacrylic monomer 2-(3-(Bis(2-(diethylamino)ethyl)amino)propanamido)ethyl methacrylate (TEDETAMA, derived from N,N,N′,N′-tetraethyldiethylenetriamine, TEDETA), were synthesized through radical copolymerization and evaluated in vitro as non-viral gene carriers. Three copolymers with nominal molar percentages of HPMA of 25%, 50% and 75% were prepared and studied comparatively to the positive controls poly-TEDETAMA and hyperbranched polyethyleneimine (PEI, 25kDa). Their ability to complex DNA at different N/P molar ratios, from 1/1 up to 8/1, was determined through agarose gel electrophoresis and Dynamic Light Scattering. The resulting complexes (polyplexes) were characterized and evaluated in vitro as possible non-viral gene carriers for Swiss-3T3 fibroblasts, using luciferase as reporter gene and a calcein cytocompatibility assay. All the copolymers, except the one with highest HPMA proportion (75 molar %) at the lowest N/P ratio, condensed DNA to a particle size between 100 and 300nm. The copolymers with 25 and 50 molar % of HPMA displayed higher transfection efficiency and cytocompatibility than the positive controls poly-TEDETAMA and PEI. A higher proportion of HPMA (75 molar %) led to copolymers that displayed very low transfection efficiency, despite their full cytocompatibility even at the highest N/P ratio. These results indicate that the statistical combination of TEDETAMA and HPMA and its fine compositional tuning in the copolymers may fulfill the fine balance of transfection efficiency and cytocompatibility in a superior way to the control poly-TEDETAMA and PEI.</description><identifier>ISSN: 0939-6411</identifier><identifier>EISSN: 1873-3441</identifier><identifier>DOI: 10.1016/j.ejpb.2015.04.014</identifier><identifier>PMID: 25937440</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Acrylamides - chemical synthesis ; Acrylamides - toxicity ; Animals ; Cationic polymers ; Cytocompatibility ; Dendrimers - chemical synthesis ; Dendrimers - toxicity ; Dendronic ; DNA - biosynthesis ; DNA - chemistry ; Electrophoresis, Agar Gel ; Fibroblasts - drug effects ; Fibroblasts - metabolism ; Gene Expression Regulation ; Genes, Reporter ; HPMA ; Light ; Luciferases - biosynthesis ; Luciferases - genetics ; Mice ; Models, Statistical ; Molecular Structure ; Nucleic Acid Conformation ; Particle Size ; Polyethyleneimine - analogs & derivatives ; Polyethyleneimine - chemical synthesis ; Polyethyleneimine - toxicity ; Scattering, Radiation ; Statistical copolymers ; Swiss 3T3 Cells ; Transfection ; Transfection - methods</subject><ispartof>European journal of pharmaceutics and biopharmaceutics, 2015-06, Vol.93, p.303-310</ispartof><rights>2015 Elsevier B.V.</rights><rights>Copyright © 2015 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-4fde155fa29ca9daefe8363a2df04a9881d013b343531f537945a0c63d75a2be3</citedby><cites>FETCH-LOGICAL-c356t-4fde155fa29ca9daefe8363a2df04a9881d013b343531f537945a0c63d75a2be3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27915,27916</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25937440$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Redondo, Juan Alfonso</creatorcontrib><creatorcontrib>Martínez-Campos, Enrique</creatorcontrib><creatorcontrib>Navarro, Rodrigo</creatorcontrib><creatorcontrib>Reinecke, Helmut</creatorcontrib><creatorcontrib>Elvira, Carlos</creatorcontrib><creatorcontrib>López-Lacomba, José Luis</creatorcontrib><creatorcontrib>Gallardo, Alberto</creatorcontrib><title>Effect on in vitro cell response of the statistical insertion of N-(2-hydroxypropyl) methacrylamide on linear pro-dendronic polyamine’s gene carriers</title><title>European journal of pharmaceutics and biopharmaceutics</title><addtitle>Eur J Pharm Biopharm</addtitle><description>[Display omitted]
Statistical copolymers of N-(2-hydroxypropyl) methacrylamide (HPMA) and the dendronic methacrylic monomer 2-(3-(Bis(2-(diethylamino)ethyl)amino)propanamido)ethyl methacrylate (TEDETAMA, derived from N,N,N′,N′-tetraethyldiethylenetriamine, TEDETA), were synthesized through radical copolymerization and evaluated in vitro as non-viral gene carriers. Three copolymers with nominal molar percentages of HPMA of 25%, 50% and 75% were prepared and studied comparatively to the positive controls poly-TEDETAMA and hyperbranched polyethyleneimine (PEI, 25kDa). Their ability to complex DNA at different N/P molar ratios, from 1/1 up to 8/1, was determined through agarose gel electrophoresis and Dynamic Light Scattering. The resulting complexes (polyplexes) were characterized and evaluated in vitro as possible non-viral gene carriers for Swiss-3T3 fibroblasts, using luciferase as reporter gene and a calcein cytocompatibility assay. All the copolymers, except the one with highest HPMA proportion (75 molar %) at the lowest N/P ratio, condensed DNA to a particle size between 100 and 300nm. The copolymers with 25 and 50 molar % of HPMA displayed higher transfection efficiency and cytocompatibility than the positive controls poly-TEDETAMA and PEI. A higher proportion of HPMA (75 molar %) led to copolymers that displayed very low transfection efficiency, despite their full cytocompatibility even at the highest N/P ratio. These results indicate that the statistical combination of TEDETAMA and HPMA and its fine compositional tuning in the copolymers may fulfill the fine balance of transfection efficiency and cytocompatibility in a superior way to the control poly-TEDETAMA and PEI.</description><subject>Acrylamides - chemical synthesis</subject><subject>Acrylamides - toxicity</subject><subject>Animals</subject><subject>Cationic polymers</subject><subject>Cytocompatibility</subject><subject>Dendrimers - chemical synthesis</subject><subject>Dendrimers - toxicity</subject><subject>Dendronic</subject><subject>DNA - biosynthesis</subject><subject>DNA - chemistry</subject><subject>Electrophoresis, Agar Gel</subject><subject>Fibroblasts - drug effects</subject><subject>Fibroblasts - metabolism</subject><subject>Gene Expression Regulation</subject><subject>Genes, Reporter</subject><subject>HPMA</subject><subject>Light</subject><subject>Luciferases - biosynthesis</subject><subject>Luciferases - genetics</subject><subject>Mice</subject><subject>Models, Statistical</subject><subject>Molecular Structure</subject><subject>Nucleic Acid Conformation</subject><subject>Particle Size</subject><subject>Polyethyleneimine - analogs & derivatives</subject><subject>Polyethyleneimine - chemical synthesis</subject><subject>Polyethyleneimine - toxicity</subject><subject>Scattering, Radiation</subject><subject>Statistical copolymers</subject><subject>Swiss 3T3 Cells</subject><subject>Transfection</subject><subject>Transfection - methods</subject><issn>0939-6411</issn><issn>1873-3441</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNp9kbtuFDEUhi1ERJYkL5ACuQzFDPbYnotEg6JwkSLSJLXltY-zXs3Yg-2NmI63QLweT4JHGyipTuHv_3WOP4QuKakpoe27fQ37eVs3hIqa8JpQ_gJtaN-xinFOX6INGdhQtZzSU_Q6pT0hhHeif4VOGzGwjnOyQT9vrAWdcfDYefzkcgxYwzjiCGkOPgEOFucd4JRVdik7rcZCJojZlUx5_FpdNdVuMTF8X-YY5mV8iyfIO6XjMqrJGVjLR-dBRVyAyoAvsHcaz2FcCuHh949fCT-CB6xVjA5iOkcnVo0JLp7nGXr4eHN__bm6vfv05frDbaWZaHPFrQEqhFXNoNVgFFjoWctUYyzhauh7aghlW8aZYNQK1g1cKKJbZjqhmi2wM3R17C2bfTtAynJyaf0A5SEckqRtz5joekoL2hxRHUNKEayco5tUXCQlchUi93IVIlchknBZhJTQm-f-w3YC8y_y10AB3h8BKFc-ldNl0g68BuNiESNNcP_r_wPXlKBr</recordid><startdate>20150601</startdate><enddate>20150601</enddate><creator>Redondo, Juan Alfonso</creator><creator>Martínez-Campos, Enrique</creator><creator>Navarro, Rodrigo</creator><creator>Reinecke, Helmut</creator><creator>Elvira, Carlos</creator><creator>López-Lacomba, José Luis</creator><creator>Gallardo, Alberto</creator><general>Elsevier B.V</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></search><sort><creationdate>20150601</creationdate><title>Effect on in vitro cell response of the statistical insertion of N-(2-hydroxypropyl) methacrylamide on linear pro-dendronic polyamine’s gene carriers</title><author>Redondo, Juan Alfonso ; Martínez-Campos, Enrique ; Navarro, Rodrigo ; Reinecke, Helmut ; Elvira, Carlos ; López-Lacomba, José Luis ; Gallardo, Alberto</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-4fde155fa29ca9daefe8363a2df04a9881d013b343531f537945a0c63d75a2be3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Acrylamides - chemical synthesis</topic><topic>Acrylamides - toxicity</topic><topic>Animals</topic><topic>Cationic polymers</topic><topic>Cytocompatibility</topic><topic>Dendrimers - chemical synthesis</topic><topic>Dendrimers - toxicity</topic><topic>Dendronic</topic><topic>DNA - biosynthesis</topic><topic>DNA - chemistry</topic><topic>Electrophoresis, Agar Gel</topic><topic>Fibroblasts - drug effects</topic><topic>Fibroblasts - metabolism</topic><topic>Gene Expression Regulation</topic><topic>Genes, Reporter</topic><topic>HPMA</topic><topic>Light</topic><topic>Luciferases - biosynthesis</topic><topic>Luciferases - genetics</topic><topic>Mice</topic><topic>Models, Statistical</topic><topic>Molecular Structure</topic><topic>Nucleic Acid Conformation</topic><topic>Particle Size</topic><topic>Polyethyleneimine - analogs & derivatives</topic><topic>Polyethyleneimine - chemical synthesis</topic><topic>Polyethyleneimine - toxicity</topic><topic>Scattering, Radiation</topic><topic>Statistical copolymers</topic><topic>Swiss 3T3 Cells</topic><topic>Transfection</topic><topic>Transfection - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Redondo, Juan Alfonso</creatorcontrib><creatorcontrib>Martínez-Campos, Enrique</creatorcontrib><creatorcontrib>Navarro, Rodrigo</creatorcontrib><creatorcontrib>Reinecke, Helmut</creatorcontrib><creatorcontrib>Elvira, Carlos</creatorcontrib><creatorcontrib>López-Lacomba, José Luis</creatorcontrib><creatorcontrib>Gallardo, Alberto</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>European journal of pharmaceutics and biopharmaceutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Redondo, Juan Alfonso</au><au>Martínez-Campos, Enrique</au><au>Navarro, Rodrigo</au><au>Reinecke, Helmut</au><au>Elvira, Carlos</au><au>López-Lacomba, José Luis</au><au>Gallardo, Alberto</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect on in vitro cell response of the statistical insertion of N-(2-hydroxypropyl) methacrylamide on linear pro-dendronic polyamine’s gene carriers</atitle><jtitle>European journal of pharmaceutics and biopharmaceutics</jtitle><addtitle>Eur J Pharm Biopharm</addtitle><date>2015-06-01</date><risdate>2015</risdate><volume>93</volume><spage>303</spage><epage>310</epage><pages>303-310</pages><issn>0939-6411</issn><eissn>1873-3441</eissn><abstract>[Display omitted]
Statistical copolymers of N-(2-hydroxypropyl) methacrylamide (HPMA) and the dendronic methacrylic monomer 2-(3-(Bis(2-(diethylamino)ethyl)amino)propanamido)ethyl methacrylate (TEDETAMA, derived from N,N,N′,N′-tetraethyldiethylenetriamine, TEDETA), were synthesized through radical copolymerization and evaluated in vitro as non-viral gene carriers. Three copolymers with nominal molar percentages of HPMA of 25%, 50% and 75% were prepared and studied comparatively to the positive controls poly-TEDETAMA and hyperbranched polyethyleneimine (PEI, 25kDa). Their ability to complex DNA at different N/P molar ratios, from 1/1 up to 8/1, was determined through agarose gel electrophoresis and Dynamic Light Scattering. The resulting complexes (polyplexes) were characterized and evaluated in vitro as possible non-viral gene carriers for Swiss-3T3 fibroblasts, using luciferase as reporter gene and a calcein cytocompatibility assay. All the copolymers, except the one with highest HPMA proportion (75 molar %) at the lowest N/P ratio, condensed DNA to a particle size between 100 and 300nm. The copolymers with 25 and 50 molar % of HPMA displayed higher transfection efficiency and cytocompatibility than the positive controls poly-TEDETAMA and PEI. A higher proportion of HPMA (75 molar %) led to copolymers that displayed very low transfection efficiency, despite their full cytocompatibility even at the highest N/P ratio. These results indicate that the statistical combination of TEDETAMA and HPMA and its fine compositional tuning in the copolymers may fulfill the fine balance of transfection efficiency and cytocompatibility in a superior way to the control poly-TEDETAMA and PEI.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>25937440</pmid><doi>10.1016/j.ejpb.2015.04.014</doi><tpages>8</tpages></addata></record> |
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subjects | Acrylamides - chemical synthesis Acrylamides - toxicity Animals Cationic polymers Cytocompatibility Dendrimers - chemical synthesis Dendrimers - toxicity Dendronic DNA - biosynthesis DNA - chemistry Electrophoresis, Agar Gel Fibroblasts - drug effects Fibroblasts - metabolism Gene Expression Regulation Genes, Reporter HPMA Light Luciferases - biosynthesis Luciferases - genetics Mice Models, Statistical Molecular Structure Nucleic Acid Conformation Particle Size Polyethyleneimine - analogs & derivatives Polyethyleneimine - chemical synthesis Polyethyleneimine - toxicity Scattering, Radiation Statistical copolymers Swiss 3T3 Cells Transfection Transfection - methods |
title | Effect on in vitro cell response of the statistical insertion of N-(2-hydroxypropyl) methacrylamide on linear pro-dendronic polyamine’s gene carriers |
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