Loading…

Synthesis and Characterization of Dendrimer-Based Polysarcosine Star Polymers: Well-Defined, Versatile Platforms Designed for Drug-Delivery Applications

This paper describes the synthesis of star polymers designed for future drug-delivery applications. A generation-5 lysine dendrimer was used as a macroinitiator for the ring-opening polymerization of the sarcosine N-carboxyanhydride monomer to produce 32-arm star polymers with narrow molar mass dist...

Full description

Saved in:
Bibliographic Details
Published in:Biomacromolecules 2020-08, Vol.21 (8), p.3332-3341
Main Authors: England, Richard M, Moss, Jennifer I, Gunnarsson, Anders, Parker, Jeremy S, Ashford, Marianne B
Format: Article
Language:English
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-a319t-3c0ca44dd6b14ed39e718cfbfb63039c7d19e33f166e3cbedd66b7b133d943663
cites cdi_FETCH-LOGICAL-a319t-3c0ca44dd6b14ed39e718cfbfb63039c7d19e33f166e3cbedd66b7b133d943663
container_end_page 3341
container_issue 8
container_start_page 3332
container_title Biomacromolecules
container_volume 21
creator England, Richard M
Moss, Jennifer I
Gunnarsson, Anders
Parker, Jeremy S
Ashford, Marianne B
description This paper describes the synthesis of star polymers designed for future drug-delivery applications. A generation-5 lysine dendrimer was used as a macroinitiator for the ring-opening polymerization of the sarcosine N-carboxyanhydride monomer to produce 32-arm star polymers with narrow molar mass distributions and desirable hydrodynamic size control. Fluorescent dye-labeled polymers were dosed in mice to measure plasma pharmacokinetics. Long circulation times were observed, representing ideal properties for biophysical targeting of tumors. In vivo efficacy of one of these star polymers conjugated to the therapeutic molecule SN-38 was evaluated in mice bearing SW620 xenografted tumors to demonstrate high antitumor activity and low body weight loss compared to the SN-38 prodrug irinotecan and this shows the potential of these delivery systems. As a further build, we demonstrated that these star polymers can be easily chain-end-functionalized with useful chemical moieties, giving opportunities for future receptor-targeting strategies. Finally, we describe the synthetic advantages of these star polymers that make them attractive from a pharmaceutical manufacturing perspective and report characterization of the polymers with a variety of techniques.
doi_str_mv 10.1021/acs.biomac.0c00768
format article
fullrecord <record><control><sourceid>acs_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1021_acs_biomac_0c00768</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>e38033770</sourcerecordid><originalsourceid>FETCH-LOGICAL-a319t-3c0ca44dd6b14ed39e718cfbfb63039c7d19e33f166e3cbedd66b7b133d943663</originalsourceid><addsrcrecordid>eNp9UElOwzAUtRBIlMIFWPkAJNhx6jTsSlsGqRKVyrCMHPu7deXGlZ0ihZNwXNxhzeoPb7D_Q-iWkpSSjN4LGdLauI2QKZGEFHx4hnp0kPEk5yQ7P_SDpCjK4hJdhbAmhJQsH_TQ76Jr2hUEE7BoFB6vhBeyBW9-RGtcg53GE2iUNxvwyaMIoPDc2S4IL10wDeBFK_xhFQnhAX-BtckEdITUHf6Mu-hjAc-taLXzmxDtgllGFMcRT_xuGenWfIPv8Gi7tUYeHg7X6EILG-DmVPvo42n6Pn5JZm_Pr-PRLBGMlm3CJJEiz5XiNc1BsRIKOpS61jVnhJWyULQExjTlHJisIRJ5XdSUMVXmjHPWR9nRV3oXggddbeOxwncVJdU-2ypmWx2zrU7ZRlF6FO2xtdv5Jn7xP8EfIEuDkw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Synthesis and Characterization of Dendrimer-Based Polysarcosine Star Polymers: Well-Defined, Versatile Platforms Designed for Drug-Delivery Applications</title><source>American Chemical Society:Jisc Collections:American Chemical Society Read &amp; Publish Agreement 2022-2024 (Reading list)</source><creator>England, Richard M ; Moss, Jennifer I ; Gunnarsson, Anders ; Parker, Jeremy S ; Ashford, Marianne B</creator><creatorcontrib>England, Richard M ; Moss, Jennifer I ; Gunnarsson, Anders ; Parker, Jeremy S ; Ashford, Marianne B</creatorcontrib><description>This paper describes the synthesis of star polymers designed for future drug-delivery applications. A generation-5 lysine dendrimer was used as a macroinitiator for the ring-opening polymerization of the sarcosine N-carboxyanhydride monomer to produce 32-arm star polymers with narrow molar mass distributions and desirable hydrodynamic size control. Fluorescent dye-labeled polymers were dosed in mice to measure plasma pharmacokinetics. Long circulation times were observed, representing ideal properties for biophysical targeting of tumors. In vivo efficacy of one of these star polymers conjugated to the therapeutic molecule SN-38 was evaluated in mice bearing SW620 xenografted tumors to demonstrate high antitumor activity and low body weight loss compared to the SN-38 prodrug irinotecan and this shows the potential of these delivery systems. As a further build, we demonstrated that these star polymers can be easily chain-end-functionalized with useful chemical moieties, giving opportunities for future receptor-targeting strategies. Finally, we describe the synthetic advantages of these star polymers that make them attractive from a pharmaceutical manufacturing perspective and report characterization of the polymers with a variety of techniques.</description><identifier>ISSN: 1525-7797</identifier><identifier>EISSN: 1526-4602</identifier><identifier>DOI: 10.1021/acs.biomac.0c00768</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>Biomacromolecules, 2020-08, Vol.21 (8), p.3332-3341</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a319t-3c0ca44dd6b14ed39e718cfbfb63039c7d19e33f166e3cbedd66b7b133d943663</citedby><cites>FETCH-LOGICAL-a319t-3c0ca44dd6b14ed39e718cfbfb63039c7d19e33f166e3cbedd66b7b133d943663</cites><orcidid>0000-0002-0199-6159 ; 0000-0002-4758-3181</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids></links><search><creatorcontrib>England, Richard M</creatorcontrib><creatorcontrib>Moss, Jennifer I</creatorcontrib><creatorcontrib>Gunnarsson, Anders</creatorcontrib><creatorcontrib>Parker, Jeremy S</creatorcontrib><creatorcontrib>Ashford, Marianne B</creatorcontrib><title>Synthesis and Characterization of Dendrimer-Based Polysarcosine Star Polymers: Well-Defined, Versatile Platforms Designed for Drug-Delivery Applications</title><title>Biomacromolecules</title><addtitle>Biomacromolecules</addtitle><description>This paper describes the synthesis of star polymers designed for future drug-delivery applications. A generation-5 lysine dendrimer was used as a macroinitiator for the ring-opening polymerization of the sarcosine N-carboxyanhydride monomer to produce 32-arm star polymers with narrow molar mass distributions and desirable hydrodynamic size control. Fluorescent dye-labeled polymers were dosed in mice to measure plasma pharmacokinetics. Long circulation times were observed, representing ideal properties for biophysical targeting of tumors. In vivo efficacy of one of these star polymers conjugated to the therapeutic molecule SN-38 was evaluated in mice bearing SW620 xenografted tumors to demonstrate high antitumor activity and low body weight loss compared to the SN-38 prodrug irinotecan and this shows the potential of these delivery systems. As a further build, we demonstrated that these star polymers can be easily chain-end-functionalized with useful chemical moieties, giving opportunities for future receptor-targeting strategies. Finally, we describe the synthetic advantages of these star polymers that make them attractive from a pharmaceutical manufacturing perspective and report characterization of the polymers with a variety of techniques.</description><issn>1525-7797</issn><issn>1526-4602</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9UElOwzAUtRBIlMIFWPkAJNhx6jTsSlsGqRKVyrCMHPu7deXGlZ0ihZNwXNxhzeoPb7D_Q-iWkpSSjN4LGdLauI2QKZGEFHx4hnp0kPEk5yQ7P_SDpCjK4hJdhbAmhJQsH_TQ76Jr2hUEE7BoFB6vhBeyBW9-RGtcg53GE2iUNxvwyaMIoPDc2S4IL10wDeBFK_xhFQnhAX-BtckEdITUHf6Mu-hjAc-taLXzmxDtgllGFMcRT_xuGenWfIPv8Gi7tUYeHg7X6EILG-DmVPvo42n6Pn5JZm_Pr-PRLBGMlm3CJJEiz5XiNc1BsRIKOpS61jVnhJWyULQExjTlHJisIRJ5XdSUMVXmjHPWR9nRV3oXggddbeOxwncVJdU-2ypmWx2zrU7ZRlF6FO2xtdv5Jn7xP8EfIEuDkw</recordid><startdate>20200810</startdate><enddate>20200810</enddate><creator>England, Richard M</creator><creator>Moss, Jennifer I</creator><creator>Gunnarsson, Anders</creator><creator>Parker, Jeremy S</creator><creator>Ashford, Marianne B</creator><general>American Chemical Society</general><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-0199-6159</orcidid><orcidid>https://orcid.org/0000-0002-4758-3181</orcidid></search><sort><creationdate>20200810</creationdate><title>Synthesis and Characterization of Dendrimer-Based Polysarcosine Star Polymers: Well-Defined, Versatile Platforms Designed for Drug-Delivery Applications</title><author>England, Richard M ; Moss, Jennifer I ; Gunnarsson, Anders ; Parker, Jeremy S ; Ashford, Marianne B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a319t-3c0ca44dd6b14ed39e718cfbfb63039c7d19e33f166e3cbedd66b7b133d943663</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>England, Richard M</creatorcontrib><creatorcontrib>Moss, Jennifer I</creatorcontrib><creatorcontrib>Gunnarsson, Anders</creatorcontrib><creatorcontrib>Parker, Jeremy S</creatorcontrib><creatorcontrib>Ashford, Marianne B</creatorcontrib><collection>CrossRef</collection><jtitle>Biomacromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>England, Richard M</au><au>Moss, Jennifer I</au><au>Gunnarsson, Anders</au><au>Parker, Jeremy S</au><au>Ashford, Marianne B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and Characterization of Dendrimer-Based Polysarcosine Star Polymers: Well-Defined, Versatile Platforms Designed for Drug-Delivery Applications</atitle><jtitle>Biomacromolecules</jtitle><addtitle>Biomacromolecules</addtitle><date>2020-08-10</date><risdate>2020</risdate><volume>21</volume><issue>8</issue><spage>3332</spage><epage>3341</epage><pages>3332-3341</pages><issn>1525-7797</issn><eissn>1526-4602</eissn><abstract>This paper describes the synthesis of star polymers designed for future drug-delivery applications. A generation-5 lysine dendrimer was used as a macroinitiator for the ring-opening polymerization of the sarcosine N-carboxyanhydride monomer to produce 32-arm star polymers with narrow molar mass distributions and desirable hydrodynamic size control. Fluorescent dye-labeled polymers were dosed in mice to measure plasma pharmacokinetics. Long circulation times were observed, representing ideal properties for biophysical targeting of tumors. In vivo efficacy of one of these star polymers conjugated to the therapeutic molecule SN-38 was evaluated in mice bearing SW620 xenografted tumors to demonstrate high antitumor activity and low body weight loss compared to the SN-38 prodrug irinotecan and this shows the potential of these delivery systems. As a further build, we demonstrated that these star polymers can be easily chain-end-functionalized with useful chemical moieties, giving opportunities for future receptor-targeting strategies. Finally, we describe the synthetic advantages of these star polymers that make them attractive from a pharmaceutical manufacturing perspective and report characterization of the polymers with a variety of techniques.</abstract><pub>American Chemical Society</pub><doi>10.1021/acs.biomac.0c00768</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-0199-6159</orcidid><orcidid>https://orcid.org/0000-0002-4758-3181</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 1525-7797
ispartof Biomacromolecules, 2020-08, Vol.21 (8), p.3332-3341
issn 1525-7797
1526-4602
language eng
recordid cdi_crossref_primary_10_1021_acs_biomac_0c00768
source American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)
title Synthesis and Characterization of Dendrimer-Based Polysarcosine Star Polymers: Well-Defined, Versatile Platforms Designed for Drug-Delivery Applications
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-23T11%3A20%3A24IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-acs_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthesis%20and%20Characterization%20of%20Dendrimer-Based%20Polysarcosine%20Star%20Polymers:%20Well-Defined,%20Versatile%20Platforms%20Designed%20for%20Drug-Delivery%20Applications&rft.jtitle=Biomacromolecules&rft.au=England,%20Richard%20M&rft.date=2020-08-10&rft.volume=21&rft.issue=8&rft.spage=3332&rft.epage=3341&rft.pages=3332-3341&rft.issn=1525-7797&rft.eissn=1526-4602&rft_id=info:doi/10.1021/acs.biomac.0c00768&rft_dat=%3Cacs_cross%3Ee38033770%3C/acs_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-a319t-3c0ca44dd6b14ed39e718cfbfb63039c7d19e33f166e3cbedd66b7b133d943663%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true