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Direct TLC/MALDI–MS coupling for modified polyamidoamine dendrimers analyses
•TLC separates the species present in polyamidoamine samples according to their polarity.•TLC/MALDI allows us to attribute more easily the fragment ions as they are aligned with their precursor ions with the same Rf.•TLC/MALDI is easy, fast and requires small quantities of material. Polyamidoamine (...
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Published in: | Analytica chimica acta 2014-01, Vol.808, p.144-150 |
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container_title | Analytica chimica acta |
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creator | Leriche, Emma-Dune Hubert-Roux, Marie Grossel, Martin C. Lange, Catherine M. Afonso, Carlos Loutelier-Bourhis, Corinne |
description | •TLC separates the species present in polyamidoamine samples according to their polarity.•TLC/MALDI allows us to attribute more easily the fragment ions as they are aligned with their precursor ions with the same Rf.•TLC/MALDI is easy, fast and requires small quantities of material.
Polyamidoamine (PAMAM) are synthetic dendrimers which present attractive properties for the biological and biomedical fields, as they proved to be efficient drug and gene carriers. In order to increase their transfection efficiency, chemical modifications of the amino end-groups had been reported. In this work, the synthesis of the ammonia-cored G1(N) PAMAM and the consecutive chemical modification with glycine or phenylalanine amino-acids were monitored using the coupling of thin layer chromatography (TLC) with matrix–assisted laser desorption ionization–mass spectrometry (MALDI–MS). Thus, the monitoring of the PAMAM synthesis included the identification of the by-products such as defective structures of PAMAM dendrimers as well as the study of phenylalanine-grafted PAMAM oligomer distribution. |
doi_str_mv | 10.1016/j.aca.2013.09.037 |
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Polyamidoamine (PAMAM) are synthetic dendrimers which present attractive properties for the biological and biomedical fields, as they proved to be efficient drug and gene carriers. In order to increase their transfection efficiency, chemical modifications of the amino end-groups had been reported. In this work, the synthesis of the ammonia-cored G1(N) PAMAM and the consecutive chemical modification with glycine or phenylalanine amino-acids were monitored using the coupling of thin layer chromatography (TLC) with matrix–assisted laser desorption ionization–mass spectrometry (MALDI–MS). Thus, the monitoring of the PAMAM synthesis included the identification of the by-products such as defective structures of PAMAM dendrimers as well as the study of phenylalanine-grafted PAMAM oligomer distribution.</description><identifier>ISSN: 0003-2670</identifier><identifier>EISSN: 1873-4324</identifier><identifier>DOI: 10.1016/j.aca.2013.09.037</identifier><identifier>PMID: 24370100</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Ammonia - chemistry ; Analytical chemistry ; Byproducts ; Chemical Sciences ; Chemistry Techniques, Analytical - methods ; Chromatography, Thin Layer ; Dendrimers ; Dendrimers - chemistry ; Drugs ; Glycine - chemistry ; Joining ; MALDI ; Oligomers ; Pharmaceutical Preparations - analysis ; Phenylalanine ; Phenylalanine - chemistry ; Polyamidoamine dendrimers ; Polyamines - chemistry ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization ; Synthesis ; Tandem mass spectrometry ; Thin layer chromatography ; TLC</subject><ispartof>Analytica chimica acta, 2014-01, Vol.808, p.144-150</ispartof><rights>2013 Elsevier B.V.</rights><rights>Copyright © 2013 Elsevier B.V. All rights reserved.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c486t-645d29b3a616c9ab7c5390074b1e578ffbf6c000e1530a709fb500d1fa01a9043</citedby><cites>FETCH-LOGICAL-c486t-645d29b3a616c9ab7c5390074b1e578ffbf6c000e1530a709fb500d1fa01a9043</cites><orcidid>0000-0002-2406-5664 ; 0000-0003-4986-4590 ; 0000-0002-3361-1532</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24370100$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-01107942$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Leriche, Emma-Dune</creatorcontrib><creatorcontrib>Hubert-Roux, Marie</creatorcontrib><creatorcontrib>Grossel, Martin C.</creatorcontrib><creatorcontrib>Lange, Catherine M.</creatorcontrib><creatorcontrib>Afonso, Carlos</creatorcontrib><creatorcontrib>Loutelier-Bourhis, Corinne</creatorcontrib><title>Direct TLC/MALDI–MS coupling for modified polyamidoamine dendrimers analyses</title><title>Analytica chimica acta</title><addtitle>Anal Chim Acta</addtitle><description>•TLC separates the species present in polyamidoamine samples according to their polarity.•TLC/MALDI allows us to attribute more easily the fragment ions as they are aligned with their precursor ions with the same Rf.•TLC/MALDI is easy, fast and requires small quantities of material.
Polyamidoamine (PAMAM) are synthetic dendrimers which present attractive properties for the biological and biomedical fields, as they proved to be efficient drug and gene carriers. In order to increase their transfection efficiency, chemical modifications of the amino end-groups had been reported. In this work, the synthesis of the ammonia-cored G1(N) PAMAM and the consecutive chemical modification with glycine or phenylalanine amino-acids were monitored using the coupling of thin layer chromatography (TLC) with matrix–assisted laser desorption ionization–mass spectrometry (MALDI–MS). Thus, the monitoring of the PAMAM synthesis included the identification of the by-products such as defective structures of PAMAM dendrimers as well as the study of phenylalanine-grafted PAMAM oligomer distribution.</description><subject>Ammonia - chemistry</subject><subject>Analytical chemistry</subject><subject>Byproducts</subject><subject>Chemical Sciences</subject><subject>Chemistry Techniques, Analytical - methods</subject><subject>Chromatography, Thin Layer</subject><subject>Dendrimers</subject><subject>Dendrimers - chemistry</subject><subject>Drugs</subject><subject>Glycine - chemistry</subject><subject>Joining</subject><subject>MALDI</subject><subject>Oligomers</subject><subject>Pharmaceutical Preparations - analysis</subject><subject>Phenylalanine</subject><subject>Phenylalanine - chemistry</subject><subject>Polyamidoamine dendrimers</subject><subject>Polyamines - chemistry</subject><subject>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</subject><subject>Synthesis</subject><subject>Tandem mass spectrometry</subject><subject>Thin layer chromatography</subject><subject>TLC</subject><issn>0003-2670</issn><issn>1873-4324</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqNkc9u1DAQhy0EokvhAbigHOGQdCa247U4rbYtrZTCgXK2HP8Br5J4iXcr7Y136Bv2SfCypce2F1u2vvlpZj5C3iNUCNicrCptdFUD0gpkBVS8IDOcC1oyWrOXZAYAtKwbAUfkTUqr_KwR2GtyVDMqAAFm5OtpmJzZFNft8uRq0Z5e3v25vfpemLhd92H8Wfg4FUO0wQdni3Xsd3oINuZjdIV1o53C4KZU6FH3u-TSW_LK6z65d_f3Mflxfna9vCjbb18ul4u2NGzebMqGcVvLjuoGGyN1JwynEkCwDh0Xc-8735jcrkNOQQuQvuMAFr0G1BIYPSafDrm_dK_WuQk97VTUQV0sWrX_A0QQktU3mNmPB3Y9xd9blzZqCMm4vteji9uksBHzvEIpnoUir5mk9dMo53nXgkvxNMokCGBc7OfCA2qmmNLk_MNwCGrvXK1Udq72zhVIlZ3nmg_38dtucPah4r_kDHw-AC4buQluUskENxpn_7lXNoZH4v8CENO42w</recordid><startdate>20140115</startdate><enddate>20140115</enddate><creator>Leriche, Emma-Dune</creator><creator>Hubert-Roux, Marie</creator><creator>Grossel, Martin C.</creator><creator>Lange, Catherine M.</creator><creator>Afonso, Carlos</creator><creator>Loutelier-Bourhis, Corinne</creator><general>Elsevier B.V</general><general>Elsevier Masson</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><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0002-2406-5664</orcidid><orcidid>https://orcid.org/0000-0003-4986-4590</orcidid><orcidid>https://orcid.org/0000-0002-3361-1532</orcidid></search><sort><creationdate>20140115</creationdate><title>Direct TLC/MALDI–MS coupling for modified polyamidoamine dendrimers analyses</title><author>Leriche, Emma-Dune ; Hubert-Roux, Marie ; Grossel, Martin C. ; Lange, Catherine M. ; Afonso, Carlos ; Loutelier-Bourhis, Corinne</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c486t-645d29b3a616c9ab7c5390074b1e578ffbf6c000e1530a709fb500d1fa01a9043</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Ammonia - chemistry</topic><topic>Analytical chemistry</topic><topic>Byproducts</topic><topic>Chemical Sciences</topic><topic>Chemistry Techniques, Analytical - methods</topic><topic>Chromatography, Thin Layer</topic><topic>Dendrimers</topic><topic>Dendrimers - chemistry</topic><topic>Drugs</topic><topic>Glycine - chemistry</topic><topic>Joining</topic><topic>MALDI</topic><topic>Oligomers</topic><topic>Pharmaceutical Preparations - analysis</topic><topic>Phenylalanine</topic><topic>Phenylalanine - chemistry</topic><topic>Polyamidoamine dendrimers</topic><topic>Polyamines - chemistry</topic><topic>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</topic><topic>Synthesis</topic><topic>Tandem mass spectrometry</topic><topic>Thin layer chromatography</topic><topic>TLC</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Leriche, Emma-Dune</creatorcontrib><creatorcontrib>Hubert-Roux, Marie</creatorcontrib><creatorcontrib>Grossel, Martin C.</creatorcontrib><creatorcontrib>Lange, Catherine M.</creatorcontrib><creatorcontrib>Afonso, Carlos</creatorcontrib><creatorcontrib>Loutelier-Bourhis, Corinne</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><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Analytica chimica acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Leriche, Emma-Dune</au><au>Hubert-Roux, Marie</au><au>Grossel, Martin C.</au><au>Lange, Catherine M.</au><au>Afonso, Carlos</au><au>Loutelier-Bourhis, Corinne</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Direct TLC/MALDI–MS coupling for modified polyamidoamine dendrimers analyses</atitle><jtitle>Analytica chimica acta</jtitle><addtitle>Anal Chim Acta</addtitle><date>2014-01-15</date><risdate>2014</risdate><volume>808</volume><spage>144</spage><epage>150</epage><pages>144-150</pages><issn>0003-2670</issn><eissn>1873-4324</eissn><abstract>•TLC separates the species present in polyamidoamine samples according to their polarity.•TLC/MALDI allows us to attribute more easily the fragment ions as they are aligned with their precursor ions with the same Rf.•TLC/MALDI is easy, fast and requires small quantities of material.
Polyamidoamine (PAMAM) are synthetic dendrimers which present attractive properties for the biological and biomedical fields, as they proved to be efficient drug and gene carriers. In order to increase their transfection efficiency, chemical modifications of the amino end-groups had been reported. In this work, the synthesis of the ammonia-cored G1(N) PAMAM and the consecutive chemical modification with glycine or phenylalanine amino-acids were monitored using the coupling of thin layer chromatography (TLC) with matrix–assisted laser desorption ionization–mass spectrometry (MALDI–MS). Thus, the monitoring of the PAMAM synthesis included the identification of the by-products such as defective structures of PAMAM dendrimers as well as the study of phenylalanine-grafted PAMAM oligomer distribution.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>24370100</pmid><doi>10.1016/j.aca.2013.09.037</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-2406-5664</orcidid><orcidid>https://orcid.org/0000-0003-4986-4590</orcidid><orcidid>https://orcid.org/0000-0002-3361-1532</orcidid></addata></record> |
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subjects | Ammonia - chemistry Analytical chemistry Byproducts Chemical Sciences Chemistry Techniques, Analytical - methods Chromatography, Thin Layer Dendrimers Dendrimers - chemistry Drugs Glycine - chemistry Joining MALDI Oligomers Pharmaceutical Preparations - analysis Phenylalanine Phenylalanine - chemistry Polyamidoamine dendrimers Polyamines - chemistry Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization Synthesis Tandem mass spectrometry Thin layer chromatography TLC |
title | Direct TLC/MALDI–MS coupling for modified polyamidoamine dendrimers analyses |
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