Loading…
Nanosponge Tunability in Size and Crosslinking Density
We describe a protocol for the synthesis of linear polyesters containing pendant epoxide functionality and their incorporation into a nanosponge with controlled dimensions. This approach begins with synthesis of a functionalized lactone which is key to the pendant functionalization of the resulting...
Saved in:
Published in: | Journal of visualized experiments 2017-08 (126) |
---|---|
Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | 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-c382t-bf5388969e07540c83a33839fb7737a420a96691c410cd28e567074d28c733003 |
---|---|
cites | |
container_end_page | |
container_issue | 126 |
container_start_page | |
container_title | Journal of visualized experiments |
container_volume | |
creator | Kendrick-Williams, Laken L Harth, Eva |
description | We describe a protocol for the synthesis of linear polyesters containing pendant epoxide functionality and their incorporation into a nanosponge with controlled dimensions. This approach begins with synthesis of a functionalized lactone which is key to the pendant functionalization of the resulting polymer. Valerolactone (VL) and allyl-valerolactone (AVL) are then copolymerized using ring-opening polymerization. Post-polymerization modification is then used to install an epoxide moiety on some or all of the pendant allyl groups. Epoxy-amine chemistry is employed to form nanoparticles in a dilute solution of both polymer and small molecule diamine crosslinker based on the desired nanosponge size and crosslinking density. Nanosponge sizes can be characterized by transmission electron microscopy (TEM) imaging to determine the dimension and distribution. This method provides a pathway by which highly tunable polyesters can create tunable nanoparticles, which can be used for small molecule drug encapsulation. Due to the nature of the backbone, these particles are hydrolytically and enzymatically degradable for a controlled release of a wide range of hydrophobic small molecules. |
doi_str_mv | 10.3791/56073 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5614001</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1929887761</sourcerecordid><originalsourceid>FETCH-LOGICAL-c382t-bf5388969e07540c83a33839fb7737a420a96691c410cd28e567074d28c733003</originalsourceid><addsrcrecordid>eNpVkM1Lw0AQxRdRbK39FyQXwUt0NpPsx0WQ-glFD1bwtmy2m7qabmo2Eepfb2prqad5MD_ezHuEDCmcI5f0ImPAcY_0qUwhBsFf93d0jxyF8A7AEsjEIeklQoAUyPqEPWpfhUXlZzaatF7nrnTNMnI-enbfNtJ-Go3qKoTS-Q_nZ9G19aEDjslBoctgh5s5IC-3N5PRfTx-unsYXY1jgyJp4rzIUAjJpAWepWAEakSBssg5R67TBLRkTFKTUjDTRNiMceBppwxHBMABuVz7Ltp8bqfG-qbWpVrUbq7rpaq0U_833r2pWfWlMkZTANoZnG0M6uqztaFRcxeMLUvtbdUGRWUiheCcrdDTNWpWgWtbbM9QUKuO1W_HHXey-9OW-isVfwA14HTz</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1929887761</pqid></control><display><type>article</type><title>Nanosponge Tunability in Size and Crosslinking Density</title><source>PubMed Central</source><creator>Kendrick-Williams, Laken L ; Harth, Eva</creator><creatorcontrib>Kendrick-Williams, Laken L ; Harth, Eva</creatorcontrib><description>We describe a protocol for the synthesis of linear polyesters containing pendant epoxide functionality and their incorporation into a nanosponge with controlled dimensions. This approach begins with synthesis of a functionalized lactone which is key to the pendant functionalization of the resulting polymer. Valerolactone (VL) and allyl-valerolactone (AVL) are then copolymerized using ring-opening polymerization. Post-polymerization modification is then used to install an epoxide moiety on some or all of the pendant allyl groups. Epoxy-amine chemistry is employed to form nanoparticles in a dilute solution of both polymer and small molecule diamine crosslinker based on the desired nanosponge size and crosslinking density. Nanosponge sizes can be characterized by transmission electron microscopy (TEM) imaging to determine the dimension and distribution. This method provides a pathway by which highly tunable polyesters can create tunable nanoparticles, which can be used for small molecule drug encapsulation. Due to the nature of the backbone, these particles are hydrolytically and enzymatically degradable for a controlled release of a wide range of hydrophobic small molecules.</description><identifier>ISSN: 1940-087X</identifier><identifier>EISSN: 1940-087X</identifier><identifier>DOI: 10.3791/56073</identifier><identifier>PMID: 28809836</identifier><language>eng</language><publisher>United States: MyJove Corporation</publisher><subject>Amines - chemistry ; Chemistry ; Chemistry Techniques, Synthetic - methods ; Cross-Linking Reagents - chemistry ; Epoxy Compounds - chemistry ; Hydrophobic and Hydrophilic Interactions ; Lactones - chemistry ; Microscopy, Electron, Transmission - methods ; Nanoparticles - chemistry ; Nanostructures - chemistry ; Polyesters - chemical synthesis ; Polyesters - chemistry ; Polymerization</subject><ispartof>Journal of visualized experiments, 2017-08 (126)</ispartof><rights>Copyright © 2017, Journal of Visualized Experiments 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c382t-bf5388969e07540c83a33839fb7737a420a96691c410cd28e567074d28c733003</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5614001/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5614001/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28809836$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kendrick-Williams, Laken L</creatorcontrib><creatorcontrib>Harth, Eva</creatorcontrib><title>Nanosponge Tunability in Size and Crosslinking Density</title><title>Journal of visualized experiments</title><addtitle>J Vis Exp</addtitle><description>We describe a protocol for the synthesis of linear polyesters containing pendant epoxide functionality and their incorporation into a nanosponge with controlled dimensions. This approach begins with synthesis of a functionalized lactone which is key to the pendant functionalization of the resulting polymer. Valerolactone (VL) and allyl-valerolactone (AVL) are then copolymerized using ring-opening polymerization. Post-polymerization modification is then used to install an epoxide moiety on some or all of the pendant allyl groups. Epoxy-amine chemistry is employed to form nanoparticles in a dilute solution of both polymer and small molecule diamine crosslinker based on the desired nanosponge size and crosslinking density. Nanosponge sizes can be characterized by transmission electron microscopy (TEM) imaging to determine the dimension and distribution. This method provides a pathway by which highly tunable polyesters can create tunable nanoparticles, which can be used for small molecule drug encapsulation. Due to the nature of the backbone, these particles are hydrolytically and enzymatically degradable for a controlled release of a wide range of hydrophobic small molecules.</description><subject>Amines - chemistry</subject><subject>Chemistry</subject><subject>Chemistry Techniques, Synthetic - methods</subject><subject>Cross-Linking Reagents - chemistry</subject><subject>Epoxy Compounds - chemistry</subject><subject>Hydrophobic and Hydrophilic Interactions</subject><subject>Lactones - chemistry</subject><subject>Microscopy, Electron, Transmission - methods</subject><subject>Nanoparticles - chemistry</subject><subject>Nanostructures - chemistry</subject><subject>Polyesters - chemical synthesis</subject><subject>Polyesters - chemistry</subject><subject>Polymerization</subject><issn>1940-087X</issn><issn>1940-087X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNpVkM1Lw0AQxRdRbK39FyQXwUt0NpPsx0WQ-glFD1bwtmy2m7qabmo2Eepfb2prqad5MD_ezHuEDCmcI5f0ImPAcY_0qUwhBsFf93d0jxyF8A7AEsjEIeklQoAUyPqEPWpfhUXlZzaatF7nrnTNMnI-enbfNtJ-Go3qKoTS-Q_nZ9G19aEDjslBoctgh5s5IC-3N5PRfTx-unsYXY1jgyJp4rzIUAjJpAWepWAEakSBssg5R67TBLRkTFKTUjDTRNiMceBppwxHBMABuVz7Ltp8bqfG-qbWpVrUbq7rpaq0U_833r2pWfWlMkZTANoZnG0M6uqztaFRcxeMLUvtbdUGRWUiheCcrdDTNWpWgWtbbM9QUKuO1W_HHXey-9OW-isVfwA14HTz</recordid><startdate>20170804</startdate><enddate>20170804</enddate><creator>Kendrick-Williams, Laken L</creator><creator>Harth, Eva</creator><general>MyJove Corporation</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>5PM</scope></search><sort><creationdate>20170804</creationdate><title>Nanosponge Tunability in Size and Crosslinking Density</title><author>Kendrick-Williams, Laken L ; Harth, Eva</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c382t-bf5388969e07540c83a33839fb7737a420a96691c410cd28e567074d28c733003</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Amines - chemistry</topic><topic>Chemistry</topic><topic>Chemistry Techniques, Synthetic - methods</topic><topic>Cross-Linking Reagents - chemistry</topic><topic>Epoxy Compounds - chemistry</topic><topic>Hydrophobic and Hydrophilic Interactions</topic><topic>Lactones - chemistry</topic><topic>Microscopy, Electron, Transmission - methods</topic><topic>Nanoparticles - chemistry</topic><topic>Nanostructures - chemistry</topic><topic>Polyesters - chemical synthesis</topic><topic>Polyesters - chemistry</topic><topic>Polymerization</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kendrick-Williams, Laken L</creatorcontrib><creatorcontrib>Harth, Eva</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>PubMed Central (Full Participant titles)</collection><jtitle>Journal of visualized experiments</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kendrick-Williams, Laken L</au><au>Harth, Eva</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nanosponge Tunability in Size and Crosslinking Density</atitle><jtitle>Journal of visualized experiments</jtitle><addtitle>J Vis Exp</addtitle><date>2017-08-04</date><risdate>2017</risdate><issue>126</issue><issn>1940-087X</issn><eissn>1940-087X</eissn><abstract>We describe a protocol for the synthesis of linear polyesters containing pendant epoxide functionality and their incorporation into a nanosponge with controlled dimensions. This approach begins with synthesis of a functionalized lactone which is key to the pendant functionalization of the resulting polymer. Valerolactone (VL) and allyl-valerolactone (AVL) are then copolymerized using ring-opening polymerization. Post-polymerization modification is then used to install an epoxide moiety on some or all of the pendant allyl groups. Epoxy-amine chemistry is employed to form nanoparticles in a dilute solution of both polymer and small molecule diamine crosslinker based on the desired nanosponge size and crosslinking density. Nanosponge sizes can be characterized by transmission electron microscopy (TEM) imaging to determine the dimension and distribution. This method provides a pathway by which highly tunable polyesters can create tunable nanoparticles, which can be used for small molecule drug encapsulation. Due to the nature of the backbone, these particles are hydrolytically and enzymatically degradable for a controlled release of a wide range of hydrophobic small molecules.</abstract><cop>United States</cop><pub>MyJove Corporation</pub><pmid>28809836</pmid><doi>10.3791/56073</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1940-087X |
ispartof | Journal of visualized experiments, 2017-08 (126) |
issn | 1940-087X 1940-087X |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5614001 |
source | PubMed Central |
subjects | Amines - chemistry Chemistry Chemistry Techniques, Synthetic - methods Cross-Linking Reagents - chemistry Epoxy Compounds - chemistry Hydrophobic and Hydrophilic Interactions Lactones - chemistry Microscopy, Electron, Transmission - methods Nanoparticles - chemistry Nanostructures - chemistry Polyesters - chemical synthesis Polyesters - chemistry Polymerization |
title | Nanosponge Tunability in Size and Crosslinking Density |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-25T23%3A31%3A51IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Nanosponge%20Tunability%20in%20Size%20and%20Crosslinking%20Density&rft.jtitle=Journal%20of%20visualized%20experiments&rft.au=Kendrick-Williams,%20Laken%20L&rft.date=2017-08-04&rft.issue=126&rft.issn=1940-087X&rft.eissn=1940-087X&rft_id=info:doi/10.3791/56073&rft_dat=%3Cproquest_pubme%3E1929887761%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c382t-bf5388969e07540c83a33839fb7737a420a96691c410cd28e567074d28c733003%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1929887761&rft_id=info:pmid/28809836&rfr_iscdi=true |