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Polymer Chemistry Influences Monocytic Uptake of Polyanhydride Nanospheres
Purpose To demonstrate that polyanhydride copolymer chemistry affects the uptake and intracellular compartmentalization of nanospheres by THP-1 human monocytic cells. Methods Polyanhydride nanospheres were prepared by an anti-solvent nanoprecipitation technique. Morphology and particle diameter were...
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Published in: | Pharmaceutical research 2009-03, Vol.26 (3), p.683-690 |
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description | Purpose To demonstrate that polyanhydride copolymer chemistry affects the uptake and intracellular compartmentalization of nanospheres by THP-1 human monocytic cells. Methods Polyanhydride nanospheres were prepared by an anti-solvent nanoprecipitation technique. Morphology and particle diameter were confirmed via scanning election microscopy and quasi-elastic light scattering, respectively. The effects of varying polymer chemistry on nanosphere and fluorescently labeled protein uptake by THP-1 cells were monitored by laser scanning confocal microscopy. Results Polyanhydride nanoparticles composed of poly(sebacic anhydride) (SA), and 20:80 and 50:50 copolymers of 1,6-bis-(p-carboxyphenoxy)hexane (CPH) anhydride and SA were fabricated with similar spherical morphology and particle diameter (200 to 800 nm). Exposure of the nanospheres to THP-1 monocytes showed that poly(SA) and 20:80 CPH:SA nanospheres were readily internalized whereas 50:50 CPH:SA nanospheres had limited uptake. The chemistries also differentially enhanced the uptake of a red fluorescent protein-labeled antigen. Conclusions Nanosphere and antigen uptake by monocytes can be directly correlated to the chemistry of the nanosphere. These results demonstrate the importance of choosing polyanhydride chemistries that facilitate enhanced interactions with antigen presenting cells that are necessary in the initiation of efficacious immune responses. |
doi_str_mv | 10.1007/s11095-008-9760-7 |
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Methods Polyanhydride nanospheres were prepared by an anti-solvent nanoprecipitation technique. Morphology and particle diameter were confirmed via scanning election microscopy and quasi-elastic light scattering, respectively. The effects of varying polymer chemistry on nanosphere and fluorescently labeled protein uptake by THP-1 cells were monitored by laser scanning confocal microscopy. Results Polyanhydride nanoparticles composed of poly(sebacic anhydride) (SA), and 20:80 and 50:50 copolymers of 1,6-bis-(p-carboxyphenoxy)hexane (CPH) anhydride and SA were fabricated with similar spherical morphology and particle diameter (200 to 800 nm). Exposure of the nanospheres to THP-1 monocytes showed that poly(SA) and 20:80 CPH:SA nanospheres were readily internalized whereas 50:50 CPH:SA nanospheres had limited uptake. The chemistries also differentially enhanced the uptake of a red fluorescent protein-labeled antigen. Conclusions Nanosphere and antigen uptake by monocytes can be directly correlated to the chemistry of the nanosphere. These results demonstrate the importance of choosing polyanhydride chemistries that facilitate enhanced interactions with antigen presenting cells that are necessary in the initiation of efficacious immune responses.</description><identifier>ISSN: 0724-8741</identifier><identifier>EISSN: 1573-904X</identifier><identifier>DOI: 10.1007/s11095-008-9760-7</identifier><identifier>PMID: 18987960</identifier><identifier>CODEN: PHREEB</identifier><language>eng</language><publisher>Boston: Boston : Springer US</publisher><subject>adjuvants ; Antigen-Presenting Cells ; Antigens, Surface - administration & dosage ; Biochemistry ; Biological and medical sciences ; Biomedical and Life Sciences ; Biomedical Engineering and Bioengineering ; Biomedicine ; Cell Line ; Cellular biology ; Chemical Precipitation ; chemistry ; Decanoic Acids - chemical synthesis ; Decanoic Acids - chemistry ; Decanoic Acids - pharmacokinetics ; Dicarboxylic Acids - chemistry ; Drug Carriers - chemical synthesis ; Drug Carriers - chemistry ; Drug Carriers - pharmacokinetics ; General pharmacology ; Hexanes - chemistry ; Humans ; immune response ; Immunology ; Leukocytes ; Medical Law ; Medical sciences ; Microscopy, Confocal ; Microscopy, Electron, Scanning ; Monocytes - metabolism ; Nanoparticles ; Nanospheres - chemistry ; Particle Size ; Pharmaceutical sciences ; Pharmaceutical technology. Pharmaceutical industry ; Pharmacology. Drug treatments ; Pharmacology/Toxicology ; Pharmacy ; polyanhydride ; Polyanhydrides - chemical synthesis ; Polyanhydrides - chemistry ; Polyanhydrides - pharmacokinetics ; Polyesters - chemical synthesis ; Polyesters - chemistry ; Polyesters - pharmacokinetics ; Polymers ; Research Paper ; Surface Properties ; Vaccines - administration & dosage</subject><ispartof>Pharmaceutical research, 2009-03, Vol.26 (3), p.683-690</ispartof><rights>Springer Science+Business Media, LLC 2008</rights><rights>2009 INIST-CNRS</rights><rights>Springer Science+Business Media, LLC 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c454t-d393958202d6bf8da1113b189ab411141dd3b30be53c6e7753d63ce66da202513</citedby><cites>FETCH-LOGICAL-c454t-d393958202d6bf8da1113b189ab411141dd3b30be53c6e7753d63ce66da202513</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21200749$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18987960$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ulery, Bret D</creatorcontrib><creatorcontrib>Phanse, Yashdeep</creatorcontrib><creatorcontrib>Sinha, Avanti</creatorcontrib><creatorcontrib>Wannemuehler, Michael J</creatorcontrib><creatorcontrib>Narasimhan, Balaji</creatorcontrib><creatorcontrib>Bellaire, Bryan H</creatorcontrib><title>Polymer Chemistry Influences Monocytic Uptake of Polyanhydride Nanospheres</title><title>Pharmaceutical research</title><addtitle>Pharm Res</addtitle><addtitle>Pharm Res</addtitle><description>Purpose To demonstrate that polyanhydride copolymer chemistry affects the uptake and intracellular compartmentalization of nanospheres by THP-1 human monocytic cells. Methods Polyanhydride nanospheres were prepared by an anti-solvent nanoprecipitation technique. Morphology and particle diameter were confirmed via scanning election microscopy and quasi-elastic light scattering, respectively. The effects of varying polymer chemistry on nanosphere and fluorescently labeled protein uptake by THP-1 cells were monitored by laser scanning confocal microscopy. Results Polyanhydride nanoparticles composed of poly(sebacic anhydride) (SA), and 20:80 and 50:50 copolymers of 1,6-bis-(p-carboxyphenoxy)hexane (CPH) anhydride and SA were fabricated with similar spherical morphology and particle diameter (200 to 800 nm). Exposure of the nanospheres to THP-1 monocytes showed that poly(SA) and 20:80 CPH:SA nanospheres were readily internalized whereas 50:50 CPH:SA nanospheres had limited uptake. The chemistries also differentially enhanced the uptake of a red fluorescent protein-labeled antigen. Conclusions Nanosphere and antigen uptake by monocytes can be directly correlated to the chemistry of the nanosphere. These results demonstrate the importance of choosing polyanhydride chemistries that facilitate enhanced interactions with antigen presenting cells that are necessary in the initiation of efficacious immune responses.</description><subject>adjuvants</subject><subject>Antigen-Presenting Cells</subject><subject>Antigens, Surface - administration & dosage</subject><subject>Biochemistry</subject><subject>Biological and medical sciences</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedical Engineering and Bioengineering</subject><subject>Biomedicine</subject><subject>Cell Line</subject><subject>Cellular biology</subject><subject>Chemical Precipitation</subject><subject>chemistry</subject><subject>Decanoic Acids - chemical synthesis</subject><subject>Decanoic Acids - chemistry</subject><subject>Decanoic Acids - pharmacokinetics</subject><subject>Dicarboxylic Acids - chemistry</subject><subject>Drug Carriers - chemical synthesis</subject><subject>Drug Carriers - chemistry</subject><subject>Drug Carriers - pharmacokinetics</subject><subject>General pharmacology</subject><subject>Hexanes - chemistry</subject><subject>Humans</subject><subject>immune response</subject><subject>Immunology</subject><subject>Leukocytes</subject><subject>Medical Law</subject><subject>Medical sciences</subject><subject>Microscopy, Confocal</subject><subject>Microscopy, Electron, Scanning</subject><subject>Monocytes - metabolism</subject><subject>Nanoparticles</subject><subject>Nanospheres - chemistry</subject><subject>Particle Size</subject><subject>Pharmaceutical sciences</subject><subject>Pharmaceutical technology. Pharmaceutical industry</subject><subject>Pharmacology. Drug treatments</subject><subject>Pharmacology/Toxicology</subject><subject>Pharmacy</subject><subject>polyanhydride</subject><subject>Polyanhydrides - chemical synthesis</subject><subject>Polyanhydrides - chemistry</subject><subject>Polyanhydrides - pharmacokinetics</subject><subject>Polyesters - chemical synthesis</subject><subject>Polyesters - chemistry</subject><subject>Polyesters - pharmacokinetics</subject><subject>Polymers</subject><subject>Research Paper</subject><subject>Surface Properties</subject><subject>Vaccines - administration & dosage</subject><issn>0724-8741</issn><issn>1573-904X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqFkU9v1DAQxS1ERbeFD8AFIqRyC8zYjh0fq1ULReWPBCtxsxzb6aZk48VODvn2eJUVlTjQg2VL_r03M28IeYnwDgHk-4QIqioB6lJJAaV8QlZYSVYq4D-fkhVIystacjwlZyndQwZR8WfkFGtVSyVgRT59C_2887FYb_2uS2Oci5uh7Sc_WJ-Kz2EIdh47W2z2o_nli9AWB4EZtrOLnfPFFzOEtN_66NNzctKaPvkXx_ucbK6vfqw_lrdfP9ysL29Lyys-lo4ppqqaAnWiaWtnEJE1uSPT8Pzk6BxrGDS-YlZ4KSvmBLNeCGeypkJ2Tt4uvvsYfk8-jTo3bn3fm8GHKWkhasV4Po-BFDjWDFgG3_wD3ocpDnkITSmVOWrkGcIFsjGkFH2r97HbmThrBH1Yh17WoXPK-rAOLbPm1dF4anbePSiO-Wfg4giYZE3fRjPYLv3lKNJszA-j0IVL-Wu48_Ghw_9Vf72IWhO0uYvZePOdAjLASoHIUf4By4SqDA</recordid><startdate>20090301</startdate><enddate>20090301</enddate><creator>Ulery, Bret D</creator><creator>Phanse, Yashdeep</creator><creator>Sinha, Avanti</creator><creator>Wannemuehler, Michael J</creator><creator>Narasimhan, Balaji</creator><creator>Bellaire, Bryan H</creator><general>Boston : Springer US</general><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</general><scope>FBQ</scope><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>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20090301</creationdate><title>Polymer Chemistry Influences Monocytic Uptake of Polyanhydride Nanospheres</title><author>Ulery, Bret D ; Phanse, Yashdeep ; Sinha, Avanti ; Wannemuehler, Michael J ; Narasimhan, Balaji ; Bellaire, Bryan H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c454t-d393958202d6bf8da1113b189ab411141dd3b30be53c6e7753d63ce66da202513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>adjuvants</topic><topic>Antigen-Presenting Cells</topic><topic>Antigens, Surface - administration & dosage</topic><topic>Biochemistry</topic><topic>Biological and medical sciences</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedical Engineering and Bioengineering</topic><topic>Biomedicine</topic><topic>Cell Line</topic><topic>Cellular biology</topic><topic>Chemical Precipitation</topic><topic>chemistry</topic><topic>Decanoic Acids - chemical synthesis</topic><topic>Decanoic Acids - chemistry</topic><topic>Decanoic Acids - pharmacokinetics</topic><topic>Dicarboxylic Acids - chemistry</topic><topic>Drug Carriers - chemical synthesis</topic><topic>Drug Carriers - chemistry</topic><topic>Drug Carriers - pharmacokinetics</topic><topic>General pharmacology</topic><topic>Hexanes - chemistry</topic><topic>Humans</topic><topic>immune response</topic><topic>Immunology</topic><topic>Leukocytes</topic><topic>Medical Law</topic><topic>Medical sciences</topic><topic>Microscopy, Confocal</topic><topic>Microscopy, Electron, Scanning</topic><topic>Monocytes - metabolism</topic><topic>Nanoparticles</topic><topic>Nanospheres - chemistry</topic><topic>Particle Size</topic><topic>Pharmaceutical sciences</topic><topic>Pharmaceutical technology. Pharmaceutical industry</topic><topic>Pharmacology. Drug treatments</topic><topic>Pharmacology/Toxicology</topic><topic>Pharmacy</topic><topic>polyanhydride</topic><topic>Polyanhydrides - chemical synthesis</topic><topic>Polyanhydrides - chemistry</topic><topic>Polyanhydrides - pharmacokinetics</topic><topic>Polyesters - chemical synthesis</topic><topic>Polyesters - chemistry</topic><topic>Polyesters - pharmacokinetics</topic><topic>Polymers</topic><topic>Research Paper</topic><topic>Surface Properties</topic><topic>Vaccines - administration & dosage</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ulery, Bret D</creatorcontrib><creatorcontrib>Phanse, Yashdeep</creatorcontrib><creatorcontrib>Sinha, Avanti</creatorcontrib><creatorcontrib>Wannemuehler, Michael J</creatorcontrib><creatorcontrib>Narasimhan, Balaji</creatorcontrib><creatorcontrib>Bellaire, Bryan H</creatorcontrib><collection>AGRIS</collection><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>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Pharmaceutical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ulery, Bret D</au><au>Phanse, Yashdeep</au><au>Sinha, Avanti</au><au>Wannemuehler, Michael J</au><au>Narasimhan, Balaji</au><au>Bellaire, Bryan H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Polymer Chemistry Influences Monocytic Uptake of Polyanhydride Nanospheres</atitle><jtitle>Pharmaceutical research</jtitle><stitle>Pharm Res</stitle><addtitle>Pharm Res</addtitle><date>2009-03-01</date><risdate>2009</risdate><volume>26</volume><issue>3</issue><spage>683</spage><epage>690</epage><pages>683-690</pages><issn>0724-8741</issn><eissn>1573-904X</eissn><coden>PHREEB</coden><abstract>Purpose To demonstrate that polyanhydride copolymer chemistry affects the uptake and intracellular compartmentalization of nanospheres by THP-1 human monocytic cells. Methods Polyanhydride nanospheres were prepared by an anti-solvent nanoprecipitation technique. Morphology and particle diameter were confirmed via scanning election microscopy and quasi-elastic light scattering, respectively. The effects of varying polymer chemistry on nanosphere and fluorescently labeled protein uptake by THP-1 cells were monitored by laser scanning confocal microscopy. Results Polyanhydride nanoparticles composed of poly(sebacic anhydride) (SA), and 20:80 and 50:50 copolymers of 1,6-bis-(p-carboxyphenoxy)hexane (CPH) anhydride and SA were fabricated with similar spherical morphology and particle diameter (200 to 800 nm). Exposure of the nanospheres to THP-1 monocytes showed that poly(SA) and 20:80 CPH:SA nanospheres were readily internalized whereas 50:50 CPH:SA nanospheres had limited uptake. The chemistries also differentially enhanced the uptake of a red fluorescent protein-labeled antigen. Conclusions Nanosphere and antigen uptake by monocytes can be directly correlated to the chemistry of the nanosphere. These results demonstrate the importance of choosing polyanhydride chemistries that facilitate enhanced interactions with antigen presenting cells that are necessary in the initiation of efficacious immune responses.</abstract><cop>Boston</cop><pub>Boston : Springer US</pub><pmid>18987960</pmid><doi>10.1007/s11095-008-9760-7</doi><tpages>8</tpages></addata></record> |
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subjects | adjuvants Antigen-Presenting Cells Antigens, Surface - administration & dosage Biochemistry Biological and medical sciences Biomedical and Life Sciences Biomedical Engineering and Bioengineering Biomedicine Cell Line Cellular biology Chemical Precipitation chemistry Decanoic Acids - chemical synthesis Decanoic Acids - chemistry Decanoic Acids - pharmacokinetics Dicarboxylic Acids - chemistry Drug Carriers - chemical synthesis Drug Carriers - chemistry Drug Carriers - pharmacokinetics General pharmacology Hexanes - chemistry Humans immune response Immunology Leukocytes Medical Law Medical sciences Microscopy, Confocal Microscopy, Electron, Scanning Monocytes - metabolism Nanoparticles Nanospheres - chemistry Particle Size Pharmaceutical sciences Pharmaceutical technology. Pharmaceutical industry Pharmacology. Drug treatments Pharmacology/Toxicology Pharmacy polyanhydride Polyanhydrides - chemical synthesis Polyanhydrides - chemistry Polyanhydrides - pharmacokinetics Polyesters - chemical synthesis Polyesters - chemistry Polyesters - pharmacokinetics Polymers Research Paper Surface Properties Vaccines - administration & dosage |
title | Polymer Chemistry Influences Monocytic Uptake of Polyanhydride Nanospheres |
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