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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
Main Authors: Ulery, Bret D, Phanse, Yashdeep, Sinha, Avanti, Wannemuehler, Michael J, Narasimhan, Balaji, Bellaire, Bryan H
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container_title Pharmaceutical research
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creator Ulery, Bret D
Phanse, Yashdeep
Sinha, Avanti
Wannemuehler, Michael J
Narasimhan, Balaji
Bellaire, Bryan H
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 &amp; 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 &amp; 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&amp;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 &amp; 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. 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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 &amp; 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 &amp; Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Health &amp; 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 &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Nursing &amp; 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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