Synthesis and characterization of perfluoro- tert -butyl semifluorinated amphiphilic polymers and their potential application in hydrophobic drug delivery
Semifluorinated polymer surfactants, composed of a monomethyl poly(ethylene glycol) (mPEG) hydrophilic head group and either 1, 2, or 3 perfluoro- -butyl (PFtB) groups as the fluorophilic tail, were synthesized, and their aqueous self-assemblies were investigated as a potential design for theranosti...
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Veröffentlicht in: | Polymer chemistry 2014-11, Vol.5 (22), p.6461-6471 |
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creator | Decato, Sarah Bemis, Troy Madsen, Eric Mecozzi, Sandro |
description | Semifluorinated polymer surfactants, composed of a monomethyl poly(ethylene glycol) (mPEG) hydrophilic head group and either 1, 2, or 3 perfluoro-
-butyl (PFtB) groups as the fluorophilic tail, were synthesized, and their aqueous self-assemblies were investigated as a potential design for theranostic nanoparticles. Polymers with three PFtB groups (PFtB
) solely formed stable, spherical micelles, approximately 12 nm in size. These PFtB
surfactants demonstrate similar characteristics with those of polymers with linear perfluorocarbon tails, despite large differences in tail structure. For example, PFtB polymer solutions stably emulsified 20 v/v% sevoflurane with perfluorooctyl bromide (PFOB) as a stabilizer. However, these PFtB polymers have the additional potential to serve as F-MRI contrast agents. PFtB
micelles gave one narrow
F-NMR signal in D
O, with T
and T
parameters of approximately 500 and 100 ms, respectively.
F-MR images of PFtB polymer solutions at 1 mM gave intense signal at 4.7 T without sensitizers or selective excitation sequences. These preliminary data demonstrate the potential of PFtB polymers as a basic design, which can be further modified to serve as dual drug-delivery and imaging vehicles. |
doi_str_mv | 10.1039/c4py00882k |
format | Article |
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-butyl (PFtB) groups as the fluorophilic tail, were synthesized, and their aqueous self-assemblies were investigated as a potential design for theranostic nanoparticles. Polymers with three PFtB groups (PFtB
) solely formed stable, spherical micelles, approximately 12 nm in size. These PFtB
surfactants demonstrate similar characteristics with those of polymers with linear perfluorocarbon tails, despite large differences in tail structure. For example, PFtB polymer solutions stably emulsified 20 v/v% sevoflurane with perfluorooctyl bromide (PFOB) as a stabilizer. However, these PFtB polymers have the additional potential to serve as F-MRI contrast agents. PFtB
micelles gave one narrow
F-NMR signal in D
O, with T
and T
parameters of approximately 500 and 100 ms, respectively.
F-MR images of PFtB polymer solutions at 1 mM gave intense signal at 4.7 T without sensitizers or selective excitation sequences. These preliminary data demonstrate the potential of PFtB polymers as a basic design, which can be further modified to serve as dual drug-delivery and imaging vehicles.</description><identifier>ISSN: 1759-9954</identifier><identifier>EISSN: 1759-9962</identifier><identifier>DOI: 10.1039/c4py00882k</identifier><identifier>PMID: 25383100</identifier><language>eng</language><publisher>England</publisher><subject>Addition polymerization ; Contrast agents ; Drug delivery systems ; Micelles ; MPEG encoders ; Polymers ; Self assembly ; Surfactants</subject><ispartof>Polymer chemistry, 2014-11, Vol.5 (22), p.6461-6471</ispartof><rights>The Royal Society of Chemistry 2014 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c444t-b466a5b42287dd0bd530e121486a84f3700214fe673a3d897ab2cf34300c0c683</citedby><cites>FETCH-LOGICAL-c444t-b466a5b42287dd0bd530e121486a84f3700214fe673a3d897ab2cf34300c0c683</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,777,781,882,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25383100$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Decato, Sarah</creatorcontrib><creatorcontrib>Bemis, Troy</creatorcontrib><creatorcontrib>Madsen, Eric</creatorcontrib><creatorcontrib>Mecozzi, Sandro</creatorcontrib><title>Synthesis and characterization of perfluoro- tert -butyl semifluorinated amphiphilic polymers and their potential application in hydrophobic drug delivery</title><title>Polymer chemistry</title><addtitle>Polym Chem</addtitle><description>Semifluorinated polymer surfactants, composed of a monomethyl poly(ethylene glycol) (mPEG) hydrophilic head group and either 1, 2, or 3 perfluoro-
-butyl (PFtB) groups as the fluorophilic tail, were synthesized, and their aqueous self-assemblies were investigated as a potential design for theranostic nanoparticles. Polymers with three PFtB groups (PFtB
) solely formed stable, spherical micelles, approximately 12 nm in size. These PFtB
surfactants demonstrate similar characteristics with those of polymers with linear perfluorocarbon tails, despite large differences in tail structure. For example, PFtB polymer solutions stably emulsified 20 v/v% sevoflurane with perfluorooctyl bromide (PFOB) as a stabilizer. However, these PFtB polymers have the additional potential to serve as F-MRI contrast agents. PFtB
micelles gave one narrow
F-NMR signal in D
O, with T
and T
parameters of approximately 500 and 100 ms, respectively.
F-MR images of PFtB polymer solutions at 1 mM gave intense signal at 4.7 T without sensitizers or selective excitation sequences. These preliminary data demonstrate the potential of PFtB polymers as a basic design, which can be further modified to serve as dual drug-delivery and imaging vehicles.</description><subject>Addition polymerization</subject><subject>Contrast agents</subject><subject>Drug delivery systems</subject><subject>Micelles</subject><subject>MPEG encoders</subject><subject>Polymers</subject><subject>Self assembly</subject><subject>Surfactants</subject><issn>1759-9954</issn><issn>1759-9962</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqNks1qFTEUgAdRbKnd-ACSpQij-ZsksxHkUn-woKAuXIVMkulEM5OYZArTR-nTGnvbS11pCCQ55zsfJ3Ca5imCLxEk_StN4wahEPjng-YY8a5v-57hh4d7R4-a05x_wLoIopiwx80R7oggCMLj5vrLtpTJZpeBWgzQk0pKF5vclSouLCCMINo0-jWk0IKaKKAd1rJ5kO3sbuJuUcUaoOY4ubq90yAGv8027Z1V71INFbsUpzxQMVZmr3cLmDaTQpzCUOtMWi-Asd5d2rQ9aR6Nymd7enueNN_enn3dvW_PP737sHtz3mpKaWkHypjqBoqx4MbAwXQEWoQRFUwJOhIOYX2MlnGiiBE9VwPWI6EEQg01E-Skeb33xnWYrdG1zaS8jMnNKm0yKCf_zixukhfhUlKMOMa0Cp7fClL4tdpc5Oyytt6rxYY1SyQwY4gSLP6NcthzQRH8D5ThnnAMOa_oiz2qU8g52fHQPILyz5TIHf38_WZKPlb42f3vHtC7mSC_AZq-u-s</recordid><startdate>20141121</startdate><enddate>20141121</enddate><creator>Decato, Sarah</creator><creator>Bemis, Troy</creator><creator>Madsen, Eric</creator><creator>Mecozzi, Sandro</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7SR</scope><scope>JG9</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20141121</creationdate><title>Synthesis and characterization of perfluoro- tert -butyl semifluorinated amphiphilic polymers and their potential application in hydrophobic drug delivery</title><author>Decato, Sarah ; Bemis, Troy ; Madsen, Eric ; Mecozzi, Sandro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c444t-b466a5b42287dd0bd530e121486a84f3700214fe673a3d897ab2cf34300c0c683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Addition polymerization</topic><topic>Contrast agents</topic><topic>Drug delivery systems</topic><topic>Micelles</topic><topic>MPEG encoders</topic><topic>Polymers</topic><topic>Self assembly</topic><topic>Surfactants</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Decato, Sarah</creatorcontrib><creatorcontrib>Bemis, Troy</creatorcontrib><creatorcontrib>Madsen, Eric</creatorcontrib><creatorcontrib>Mecozzi, Sandro</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Materials Research Database</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Polymer chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Decato, Sarah</au><au>Bemis, Troy</au><au>Madsen, Eric</au><au>Mecozzi, Sandro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and characterization of perfluoro- tert -butyl semifluorinated amphiphilic polymers and their potential application in hydrophobic drug delivery</atitle><jtitle>Polymer chemistry</jtitle><addtitle>Polym Chem</addtitle><date>2014-11-21</date><risdate>2014</risdate><volume>5</volume><issue>22</issue><spage>6461</spage><epage>6471</epage><pages>6461-6471</pages><issn>1759-9954</issn><eissn>1759-9962</eissn><abstract>Semifluorinated polymer surfactants, composed of a monomethyl poly(ethylene glycol) (mPEG) hydrophilic head group and either 1, 2, or 3 perfluoro-
-butyl (PFtB) groups as the fluorophilic tail, were synthesized, and their aqueous self-assemblies were investigated as a potential design for theranostic nanoparticles. Polymers with three PFtB groups (PFtB
) solely formed stable, spherical micelles, approximately 12 nm in size. These PFtB
surfactants demonstrate similar characteristics with those of polymers with linear perfluorocarbon tails, despite large differences in tail structure. For example, PFtB polymer solutions stably emulsified 20 v/v% sevoflurane with perfluorooctyl bromide (PFOB) as a stabilizer. However, these PFtB polymers have the additional potential to serve as F-MRI contrast agents. PFtB
micelles gave one narrow
F-NMR signal in D
O, with T
and T
parameters of approximately 500 and 100 ms, respectively.
F-MR images of PFtB polymer solutions at 1 mM gave intense signal at 4.7 T without sensitizers or selective excitation sequences. These preliminary data demonstrate the potential of PFtB polymers as a basic design, which can be further modified to serve as dual drug-delivery and imaging vehicles.</abstract><cop>England</cop><pmid>25383100</pmid><doi>10.1039/c4py00882k</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Addition polymerization Contrast agents Drug delivery systems Micelles MPEG encoders Polymers Self assembly Surfactants |
title | Synthesis and characterization of perfluoro- tert -butyl semifluorinated amphiphilic polymers and their potential application in hydrophobic drug delivery |
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