Loading…

PEGylated Dendrimers with Core Functionality for Biological Applications

The synthesis of a variety of core functionalized PEGylated polyester dendrimers and their in vitro and in vivo properties are described in this report. These water-soluble dendrimers have been designed to carry eight functional groups on their dendritic core for a variety of biological applications...

Full description

Saved in:
Bibliographic Details
Published in:Bioconjugate chemistry 2008-02, Vol.19 (2), p.461-469
Main Authors: Guillaudeu, Steven J, Fox, Megan E, Haidar, Yarah M, Dy, Edward E, Szoka, Francis C, Fréchet, Jean M. J
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-a441t-8d3194b219ef8f0022cf9e1e22d262c0b847138e260d0fff521a8d2de7400e683
cites cdi_FETCH-LOGICAL-a441t-8d3194b219ef8f0022cf9e1e22d262c0b847138e260d0fff521a8d2de7400e683
container_end_page 469
container_issue 2
container_start_page 461
container_title Bioconjugate chemistry
container_volume 19
creator Guillaudeu, Steven J
Fox, Megan E
Haidar, Yarah M
Dy, Edward E
Szoka, Francis C
Fréchet, Jean M. J
description The synthesis of a variety of core functionalized PEGylated polyester dendrimers and their in vitro and in vivo properties are described in this report. These water-soluble dendrimers have been designed to carry eight functional groups on their dendritic core for a variety of biological applications such as drug delivery and in vivo imaging as well as eight solubilizing groups. Using a common symmetrical aliphatic ester dendritic core and trifunctional amino acid moieties, a library of dendrimers with phenols, alkyl alcohols, alkynes, ketones, and carboxylic acid functionalities has been synthesized without the need for column chromatography. The amines were PEGylated, leaving the other functionality of the amino acid available for further manipulation such as the attachment of drugs and/or labels. Radiolabeling experiments with the PEGylated dendrimers showed that they had a long circulation half-life in mice, confirming the potential of this class of dendrimers for therapeutic and/or diagnostic applications. A carboxylic acid functionalized dendrimer was elaborated to carry doxorubicin bound via a hydrazone bond. The drug-loaded carrier accumulated more in tumors and less in healthy organs than the clinically used PEGylated liposomal formulation Doxil. The efficient synthesis, high versatility, and favorable biological properties make these PEGylated polyester dendrimers promising structures for therapeutic and/or imaging applications.
doi_str_mv 10.1021/bc700264g
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_754548585</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>70315799</sourcerecordid><originalsourceid>FETCH-LOGICAL-a441t-8d3194b219ef8f0022cf9e1e22d262c0b847138e260d0fff521a8d2de7400e683</originalsourceid><addsrcrecordid>eNqF0VFrFDEQB_Agiq3VB7-ALIKKD6szs8km-1jPticcWPB8DrndSd26dzmTXfS-vTnuaEFBnzIwP_4ZZoR4jvAOgfD9qtUAVMubB-IUFUEpDdLDXIOsSjRAJ-JJSrcA0KChx-IEDeqKSJ-K-fXF1W5wI3fFR950sV9zTMXPfvxWzELk4nLatGMfNm7ox13hQyw-9GEIN33rhuJ8ux1yse-np-KRd0PiZ8f3THy9vFjO5uXi89Wn2fmidFLiWJquwkauCBv2xuepqfUNIxN1VFMLKyM1Voaphg6894rQmY461hKAa1OdiTeH3G0MPyZOo133qeVhcBsOU7JaSSWNMirL1_-WUKHSTfNfSKA1adwnvvwD3oYp5t1kgzU2VDdVRm8PqI0hpcjebvNWXdxZBLs_l707V7YvjoHTas3dvTzeJ4PyAPo08q-7vovfba0rrezy-otdLFGBnCu7n_DVwbs23Q_398e_AY1IqA8</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>216192693</pqid></control><display><type>article</type><title>PEGylated Dendrimers with Core Functionality for Biological Applications</title><source>American Chemical Society:Jisc Collections:American Chemical Society Read &amp; Publish Agreement 2022-2024 (Reading list)</source><creator>Guillaudeu, Steven J ; Fox, Megan E ; Haidar, Yarah M ; Dy, Edward E ; Szoka, Francis C ; Fréchet, Jean M. J</creator><creatorcontrib>Guillaudeu, Steven J ; Fox, Megan E ; Haidar, Yarah M ; Dy, Edward E ; Szoka, Francis C ; Fréchet, Jean M. J</creatorcontrib><description>The synthesis of a variety of core functionalized PEGylated polyester dendrimers and their in vitro and in vivo properties are described in this report. These water-soluble dendrimers have been designed to carry eight functional groups on their dendritic core for a variety of biological applications such as drug delivery and in vivo imaging as well as eight solubilizing groups. Using a common symmetrical aliphatic ester dendritic core and trifunctional amino acid moieties, a library of dendrimers with phenols, alkyl alcohols, alkynes, ketones, and carboxylic acid functionalities has been synthesized without the need for column chromatography. The amines were PEGylated, leaving the other functionality of the amino acid available for further manipulation such as the attachment of drugs and/or labels. Radiolabeling experiments with the PEGylated dendrimers showed that they had a long circulation half-life in mice, confirming the potential of this class of dendrimers for therapeutic and/or diagnostic applications. A carboxylic acid functionalized dendrimer was elaborated to carry doxorubicin bound via a hydrazone bond. The drug-loaded carrier accumulated more in tumors and less in healthy organs than the clinically used PEGylated liposomal formulation Doxil. The efficient synthesis, high versatility, and favorable biological properties make these PEGylated polyester dendrimers promising structures for therapeutic and/or imaging applications.</description><identifier>ISSN: 1043-1802</identifier><identifier>EISSN: 1520-4812</identifier><identifier>DOI: 10.1021/bc700264g</identifier><identifier>PMID: 18173227</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Amino acids ; Animals ; Cell Line, Tumor ; Chemical synthesis ; Dendrimers - chemistry ; Dendrimers - pharmacokinetics ; Magnetic Resonance Spectroscopy ; Mice ; Organic chemicals ; Polyethylene Glycols - chemistry ; Polyethylene Glycols - pharmacokinetics ; Rodents ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization ; Tissue Distribution ; Tumors</subject><ispartof>Bioconjugate chemistry, 2008-02, Vol.19 (2), p.461-469</ispartof><rights>Copyright © 2008 American Chemical Society</rights><rights>Copyright American Chemical Society Feb 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a441t-8d3194b219ef8f0022cf9e1e22d262c0b847138e260d0fff521a8d2de7400e683</citedby><cites>FETCH-LOGICAL-a441t-8d3194b219ef8f0022cf9e1e22d262c0b847138e260d0fff521a8d2de7400e683</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18173227$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Guillaudeu, Steven J</creatorcontrib><creatorcontrib>Fox, Megan E</creatorcontrib><creatorcontrib>Haidar, Yarah M</creatorcontrib><creatorcontrib>Dy, Edward E</creatorcontrib><creatorcontrib>Szoka, Francis C</creatorcontrib><creatorcontrib>Fréchet, Jean M. J</creatorcontrib><title>PEGylated Dendrimers with Core Functionality for Biological Applications</title><title>Bioconjugate chemistry</title><addtitle>Bioconjugate Chem</addtitle><description>The synthesis of a variety of core functionalized PEGylated polyester dendrimers and their in vitro and in vivo properties are described in this report. These water-soluble dendrimers have been designed to carry eight functional groups on their dendritic core for a variety of biological applications such as drug delivery and in vivo imaging as well as eight solubilizing groups. Using a common symmetrical aliphatic ester dendritic core and trifunctional amino acid moieties, a library of dendrimers with phenols, alkyl alcohols, alkynes, ketones, and carboxylic acid functionalities has been synthesized without the need for column chromatography. The amines were PEGylated, leaving the other functionality of the amino acid available for further manipulation such as the attachment of drugs and/or labels. Radiolabeling experiments with the PEGylated dendrimers showed that they had a long circulation half-life in mice, confirming the potential of this class of dendrimers for therapeutic and/or diagnostic applications. A carboxylic acid functionalized dendrimer was elaborated to carry doxorubicin bound via a hydrazone bond. The drug-loaded carrier accumulated more in tumors and less in healthy organs than the clinically used PEGylated liposomal formulation Doxil. The efficient synthesis, high versatility, and favorable biological properties make these PEGylated polyester dendrimers promising structures for therapeutic and/or imaging applications.</description><subject>Amino acids</subject><subject>Animals</subject><subject>Cell Line, Tumor</subject><subject>Chemical synthesis</subject><subject>Dendrimers - chemistry</subject><subject>Dendrimers - pharmacokinetics</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Mice</subject><subject>Organic chemicals</subject><subject>Polyethylene Glycols - chemistry</subject><subject>Polyethylene Glycols - pharmacokinetics</subject><subject>Rodents</subject><subject>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</subject><subject>Tissue Distribution</subject><subject>Tumors</subject><issn>1043-1802</issn><issn>1520-4812</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqF0VFrFDEQB_Agiq3VB7-ALIKKD6szs8km-1jPticcWPB8DrndSd26dzmTXfS-vTnuaEFBnzIwP_4ZZoR4jvAOgfD9qtUAVMubB-IUFUEpDdLDXIOsSjRAJ-JJSrcA0KChx-IEDeqKSJ-K-fXF1W5wI3fFR950sV9zTMXPfvxWzELk4nLatGMfNm7ox13hQyw-9GEIN33rhuJ8ux1yse-np-KRd0PiZ8f3THy9vFjO5uXi89Wn2fmidFLiWJquwkauCBv2xuepqfUNIxN1VFMLKyM1Voaphg6894rQmY461hKAa1OdiTeH3G0MPyZOo133qeVhcBsOU7JaSSWNMirL1_-WUKHSTfNfSKA1adwnvvwD3oYp5t1kgzU2VDdVRm8PqI0hpcjebvNWXdxZBLs_l707V7YvjoHTas3dvTzeJ4PyAPo08q-7vovfba0rrezy-otdLFGBnCu7n_DVwbs23Q_398e_AY1IqA8</recordid><startdate>20080201</startdate><enddate>20080201</enddate><creator>Guillaudeu, Steven J</creator><creator>Fox, Megan E</creator><creator>Haidar, Yarah M</creator><creator>Dy, Edward E</creator><creator>Szoka, Francis C</creator><creator>Fréchet, Jean M. J</creator><general>American Chemical Society</general><scope>BSCLL</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>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20080201</creationdate><title>PEGylated Dendrimers with Core Functionality for Biological Applications</title><author>Guillaudeu, Steven J ; Fox, Megan E ; Haidar, Yarah M ; Dy, Edward E ; Szoka, Francis C ; Fréchet, Jean M. J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a441t-8d3194b219ef8f0022cf9e1e22d262c0b847138e260d0fff521a8d2de7400e683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Amino acids</topic><topic>Animals</topic><topic>Cell Line, Tumor</topic><topic>Chemical synthesis</topic><topic>Dendrimers - chemistry</topic><topic>Dendrimers - pharmacokinetics</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Mice</topic><topic>Organic chemicals</topic><topic>Polyethylene Glycols - chemistry</topic><topic>Polyethylene Glycols - pharmacokinetics</topic><topic>Rodents</topic><topic>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</topic><topic>Tissue Distribution</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Guillaudeu, Steven J</creatorcontrib><creatorcontrib>Fox, Megan E</creatorcontrib><creatorcontrib>Haidar, Yarah M</creatorcontrib><creatorcontrib>Dy, Edward E</creatorcontrib><creatorcontrib>Szoka, Francis C</creatorcontrib><creatorcontrib>Fréchet, Jean M. J</creatorcontrib><collection>Istex</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>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Bioconjugate chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Guillaudeu, Steven J</au><au>Fox, Megan E</au><au>Haidar, Yarah M</au><au>Dy, Edward E</au><au>Szoka, Francis C</au><au>Fréchet, Jean M. J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>PEGylated Dendrimers with Core Functionality for Biological Applications</atitle><jtitle>Bioconjugate chemistry</jtitle><addtitle>Bioconjugate Chem</addtitle><date>2008-02-01</date><risdate>2008</risdate><volume>19</volume><issue>2</issue><spage>461</spage><epage>469</epage><pages>461-469</pages><issn>1043-1802</issn><eissn>1520-4812</eissn><abstract>The synthesis of a variety of core functionalized PEGylated polyester dendrimers and their in vitro and in vivo properties are described in this report. These water-soluble dendrimers have been designed to carry eight functional groups on their dendritic core for a variety of biological applications such as drug delivery and in vivo imaging as well as eight solubilizing groups. Using a common symmetrical aliphatic ester dendritic core and trifunctional amino acid moieties, a library of dendrimers with phenols, alkyl alcohols, alkynes, ketones, and carboxylic acid functionalities has been synthesized without the need for column chromatography. The amines were PEGylated, leaving the other functionality of the amino acid available for further manipulation such as the attachment of drugs and/or labels. Radiolabeling experiments with the PEGylated dendrimers showed that they had a long circulation half-life in mice, confirming the potential of this class of dendrimers for therapeutic and/or diagnostic applications. A carboxylic acid functionalized dendrimer was elaborated to carry doxorubicin bound via a hydrazone bond. The drug-loaded carrier accumulated more in tumors and less in healthy organs than the clinically used PEGylated liposomal formulation Doxil. The efficient synthesis, high versatility, and favorable biological properties make these PEGylated polyester dendrimers promising structures for therapeutic and/or imaging applications.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>18173227</pmid><doi>10.1021/bc700264g</doi><tpages>9</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1043-1802
ispartof Bioconjugate chemistry, 2008-02, Vol.19 (2), p.461-469
issn 1043-1802
1520-4812
language eng
recordid cdi_proquest_miscellaneous_754548585
source American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)
subjects Amino acids
Animals
Cell Line, Tumor
Chemical synthesis
Dendrimers - chemistry
Dendrimers - pharmacokinetics
Magnetic Resonance Spectroscopy
Mice
Organic chemicals
Polyethylene Glycols - chemistry
Polyethylene Glycols - pharmacokinetics
Rodents
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
Tissue Distribution
Tumors
title PEGylated Dendrimers with Core Functionality for Biological Applications
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T14%3A37%3A05IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=PEGylated%20Dendrimers%20with%20Core%20Functionality%20for%20Biological%20Applications&rft.jtitle=Bioconjugate%20chemistry&rft.au=Guillaudeu,%20Steven%20J&rft.date=2008-02-01&rft.volume=19&rft.issue=2&rft.spage=461&rft.epage=469&rft.pages=461-469&rft.issn=1043-1802&rft.eissn=1520-4812&rft_id=info:doi/10.1021/bc700264g&rft_dat=%3Cproquest_cross%3E70315799%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-a441t-8d3194b219ef8f0022cf9e1e22d262c0b847138e260d0fff521a8d2de7400e683%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=216192693&rft_id=info:pmid/18173227&rfr_iscdi=true