Synthesis of versatile chemical tools toward a structure/properties relationships study onto targeting colloids
As part of a drug delivery project, four aldehydes of the type Pam-Lys(Pam)-spacer-CO-CHO were synthesized to be included in targeting colloids. Though amphiphilic, they were obtained within reasonable yields (18–55%) and with high RP-HPLC purity (∼90%). Parallely, six complementary targeting peptid...
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Veröffentlicht in: | European journal of medicinal chemistry 2007, Vol.42 (1), p.114-124 |
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container_title | European journal of medicinal chemistry |
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creator | Jolimaitre, Pascale Poirier, Cécile Richard, Antoine Blanpain, Annick Delord, Brigitte Roux, Didier Bourel-Bonnet, Line |
description | As part of a drug delivery project, four aldehydes of the type Pam-Lys(Pam)-spacer-CO-CHO were synthesized to be included in targeting colloids. Though amphiphilic, they were obtained within reasonable yields (18–55%) and with high RP-HPLC purity (∼90%). Parallely, six complementary targeting peptides of the type H
2N-NH-CH
2-CO-spacer-YGRGDSP-NH
2 were prepared to be anchored onto colloids. Isolated yields are related to the spacer length and nature. To easily and rapidly modulate the distance between the peptide and the vesicle, every partners were elaborated on solid phase and the expected constructions were obtained by hydrazone ligation. One possible application is presented here with multilamellar vesicles targeting HUVEC cells. Preliminary results prove that the fine-tuning of the spacer length permits to optimize the recognition toward the target cells.
▪In a drug delivery project, four amphiphilic aldehydes and six hydrazinopeptides were synthesized to obtain targeting vesicles. The tuning of the spacer length influences the recognition toward the target cells. |
doi_str_mv | 10.1016/j.ejmech.2006.08.011 |
format | Article |
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2N-NH-CH
2-CO-spacer-YGRGDSP-NH
2 were prepared to be anchored onto colloids. Isolated yields are related to the spacer length and nature. To easily and rapidly modulate the distance between the peptide and the vesicle, every partners were elaborated on solid phase and the expected constructions were obtained by hydrazone ligation. One possible application is presented here with multilamellar vesicles targeting HUVEC cells. Preliminary results prove that the fine-tuning of the spacer length permits to optimize the recognition toward the target cells.
▪In a drug delivery project, four amphiphilic aldehydes and six hydrazinopeptides were synthesized to obtain targeting vesicles. The tuning of the spacer length influences the recognition toward the target cells.</description><identifier>ISSN: 0223-5234</identifier><identifier>EISSN: 1768-3254</identifier><identifier>DOI: 10.1016/j.ejmech.2006.08.011</identifier><identifier>PMID: 17011671</identifier><identifier>CODEN: EJMCA5</identifier><language>eng</language><publisher>Oxford: Elsevier Masson SAS</publisher><subject>Aldehydes - chemical synthesis ; Aldehydes - chemistry ; Amphiphilic ; Biological and medical sciences ; Cells, Cultured ; Chemical ligation ; Colloids ; Drug Carriers ; Drug Delivery Systems ; Endothelial Cells - metabolism ; Endothelium, Vascular - cytology ; Humans ; Hydrazones - chemical synthesis ; Hydrazones - chemistry ; Integrins - metabolism ; Ligands ; Medical sciences ; Miscellaneous ; Multilamellar vesicles ; Oligopeptides - chemical synthesis ; Oligopeptides - chemistry ; Oligopeptides - metabolism ; Pharmacology. Drug treatments ; Structure-Activity Relationship ; Structure/properties relationships ; Targeting colloids ; Umbilical Veins - cytology ; Vectorisation</subject><ispartof>European journal of medicinal chemistry, 2007, Vol.42 (1), p.114-124</ispartof><rights>2006 Elsevier Masson SAS</rights><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c390t-2a6be77722fafcd4514f28023095f4985a06198d7cc65689f1426d6a93a366063</citedby><cites>FETCH-LOGICAL-c390t-2a6be77722fafcd4514f28023095f4985a06198d7cc65689f1426d6a93a366063</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ejmech.2006.08.011$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,4010,27904,27905,27906,45976</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18529015$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17011671$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jolimaitre, Pascale</creatorcontrib><creatorcontrib>Poirier, Cécile</creatorcontrib><creatorcontrib>Richard, Antoine</creatorcontrib><creatorcontrib>Blanpain, Annick</creatorcontrib><creatorcontrib>Delord, Brigitte</creatorcontrib><creatorcontrib>Roux, Didier</creatorcontrib><creatorcontrib>Bourel-Bonnet, Line</creatorcontrib><title>Synthesis of versatile chemical tools toward a structure/properties relationships study onto targeting colloids</title><title>European journal of medicinal chemistry</title><addtitle>Eur J Med Chem</addtitle><description>As part of a drug delivery project, four aldehydes of the type Pam-Lys(Pam)-spacer-CO-CHO were synthesized to be included in targeting colloids. Though amphiphilic, they were obtained within reasonable yields (18–55%) and with high RP-HPLC purity (∼90%). Parallely, six complementary targeting peptides of the type H
2N-NH-CH
2-CO-spacer-YGRGDSP-NH
2 were prepared to be anchored onto colloids. Isolated yields are related to the spacer length and nature. To easily and rapidly modulate the distance between the peptide and the vesicle, every partners were elaborated on solid phase and the expected constructions were obtained by hydrazone ligation. One possible application is presented here with multilamellar vesicles targeting HUVEC cells. Preliminary results prove that the fine-tuning of the spacer length permits to optimize the recognition toward the target cells.
▪In a drug delivery project, four amphiphilic aldehydes and six hydrazinopeptides were synthesized to obtain targeting vesicles. The tuning of the spacer length influences the recognition toward the target cells.</description><subject>Aldehydes - chemical synthesis</subject><subject>Aldehydes - chemistry</subject><subject>Amphiphilic</subject><subject>Biological and medical sciences</subject><subject>Cells, Cultured</subject><subject>Chemical ligation</subject><subject>Colloids</subject><subject>Drug Carriers</subject><subject>Drug Delivery Systems</subject><subject>Endothelial Cells - metabolism</subject><subject>Endothelium, Vascular - cytology</subject><subject>Humans</subject><subject>Hydrazones - chemical synthesis</subject><subject>Hydrazones - chemistry</subject><subject>Integrins - metabolism</subject><subject>Ligands</subject><subject>Medical sciences</subject><subject>Miscellaneous</subject><subject>Multilamellar vesicles</subject><subject>Oligopeptides - chemical synthesis</subject><subject>Oligopeptides - chemistry</subject><subject>Oligopeptides - metabolism</subject><subject>Pharmacology. Drug treatments</subject><subject>Structure-Activity Relationship</subject><subject>Structure/properties relationships</subject><subject>Targeting colloids</subject><subject>Umbilical Veins - cytology</subject><subject>Vectorisation</subject><issn>0223-5234</issn><issn>1768-3254</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEFr3DAQhUVoSbZJ_kEpurQ3OyPJku1LoYS2CQR6aHsWijzOarGtrUZO2X9fhV3IrZeZy_cej4-x9wJqAcLc7Grczei3tQQwNXQ1CHHGNqI1XaWkbt6wDUipKi1Vc8HeEe0AQBuAc3Yh2gKbVmxY_HlY8hYpEI8jf8ZELocJud_iHLybeI5xonL_ujRwxymn1ec14c0-xT2mHJB4wqmk4kLbsKeCrMOBxyVHnl16whyWJ-7jNMUw0BV7O7qJ8Pr0L9nvb19_3d5VDz--399-eai86iFX0plHbNtWytGNfmi0aEbZgVTQ67HpO-3AiL4bWu-NNl0_ikaawbheOWUMGHXJPh17y8w_K1K2cyCP0-QWjCvZkum1blQBmyPoUyRKONp9CrNLByvAvoi2O3sUbV9EW-hscVdiH0796-OMw2voZLYAH0-Ao-JxTG7xgV65TssehC7c5yOHxcZzwGTJB1w8DiGhz3aI4f9L_gFIpZ-X</recordid><startdate>2007</startdate><enddate>2007</enddate><creator>Jolimaitre, Pascale</creator><creator>Poirier, Cécile</creator><creator>Richard, Antoine</creator><creator>Blanpain, Annick</creator><creator>Delord, Brigitte</creator><creator>Roux, Didier</creator><creator>Bourel-Bonnet, Line</creator><general>Elsevier Masson SAS</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>7X8</scope></search><sort><creationdate>2007</creationdate><title>Synthesis of versatile chemical tools toward a structure/properties relationships study onto targeting colloids</title><author>Jolimaitre, Pascale ; Poirier, Cécile ; Richard, Antoine ; Blanpain, Annick ; Delord, Brigitte ; Roux, Didier ; Bourel-Bonnet, Line</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-2a6be77722fafcd4514f28023095f4985a06198d7cc65689f1426d6a93a366063</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Aldehydes - chemical synthesis</topic><topic>Aldehydes - chemistry</topic><topic>Amphiphilic</topic><topic>Biological and medical sciences</topic><topic>Cells, Cultured</topic><topic>Chemical ligation</topic><topic>Colloids</topic><topic>Drug Carriers</topic><topic>Drug Delivery Systems</topic><topic>Endothelial Cells - metabolism</topic><topic>Endothelium, Vascular - cytology</topic><topic>Humans</topic><topic>Hydrazones - chemical synthesis</topic><topic>Hydrazones - chemistry</topic><topic>Integrins - metabolism</topic><topic>Ligands</topic><topic>Medical sciences</topic><topic>Miscellaneous</topic><topic>Multilamellar vesicles</topic><topic>Oligopeptides - chemical synthesis</topic><topic>Oligopeptides - chemistry</topic><topic>Oligopeptides - metabolism</topic><topic>Pharmacology. Drug treatments</topic><topic>Structure-Activity Relationship</topic><topic>Structure/properties relationships</topic><topic>Targeting colloids</topic><topic>Umbilical Veins - cytology</topic><topic>Vectorisation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jolimaitre, Pascale</creatorcontrib><creatorcontrib>Poirier, Cécile</creatorcontrib><creatorcontrib>Richard, Antoine</creatorcontrib><creatorcontrib>Blanpain, Annick</creatorcontrib><creatorcontrib>Delord, Brigitte</creatorcontrib><creatorcontrib>Roux, Didier</creatorcontrib><creatorcontrib>Bourel-Bonnet, Line</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>MEDLINE - Academic</collection><jtitle>European journal of medicinal chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jolimaitre, Pascale</au><au>Poirier, Cécile</au><au>Richard, Antoine</au><au>Blanpain, Annick</au><au>Delord, Brigitte</au><au>Roux, Didier</au><au>Bourel-Bonnet, Line</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of versatile chemical tools toward a structure/properties relationships study onto targeting colloids</atitle><jtitle>European journal of medicinal chemistry</jtitle><addtitle>Eur J Med Chem</addtitle><date>2007</date><risdate>2007</risdate><volume>42</volume><issue>1</issue><spage>114</spage><epage>124</epage><pages>114-124</pages><issn>0223-5234</issn><eissn>1768-3254</eissn><coden>EJMCA5</coden><abstract>As part of a drug delivery project, four aldehydes of the type Pam-Lys(Pam)-spacer-CO-CHO were synthesized to be included in targeting colloids. Though amphiphilic, they were obtained within reasonable yields (18–55%) and with high RP-HPLC purity (∼90%). Parallely, six complementary targeting peptides of the type H
2N-NH-CH
2-CO-spacer-YGRGDSP-NH
2 were prepared to be anchored onto colloids. Isolated yields are related to the spacer length and nature. To easily and rapidly modulate the distance between the peptide and the vesicle, every partners were elaborated on solid phase and the expected constructions were obtained by hydrazone ligation. One possible application is presented here with multilamellar vesicles targeting HUVEC cells. Preliminary results prove that the fine-tuning of the spacer length permits to optimize the recognition toward the target cells.
▪In a drug delivery project, four amphiphilic aldehydes and six hydrazinopeptides were synthesized to obtain targeting vesicles. The tuning of the spacer length influences the recognition toward the target cells.</abstract><cop>Oxford</cop><pub>Elsevier Masson SAS</pub><pmid>17011671</pmid><doi>10.1016/j.ejmech.2006.08.011</doi><tpages>11</tpages></addata></record> |
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subjects | Aldehydes - chemical synthesis Aldehydes - chemistry Amphiphilic Biological and medical sciences Cells, Cultured Chemical ligation Colloids Drug Carriers Drug Delivery Systems Endothelial Cells - metabolism Endothelium, Vascular - cytology Humans Hydrazones - chemical synthesis Hydrazones - chemistry Integrins - metabolism Ligands Medical sciences Miscellaneous Multilamellar vesicles Oligopeptides - chemical synthesis Oligopeptides - chemistry Oligopeptides - metabolism Pharmacology. Drug treatments Structure-Activity Relationship Structure/properties relationships Targeting colloids Umbilical Veins - cytology Vectorisation |
title | Synthesis of versatile chemical tools toward a structure/properties relationships study onto targeting colloids |
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