Nanocarriers for Cytoplasmic Delivery: Cellular Uptake and Intracellular Fate of Chitosan and Hyaluronic Acid-Coated Chitosan Nanoparticles in a Phagocytic Cell Model

The cellular uptake of hyaluronic‐acid‐coated, negatively charged chitosan/triphosphate nanoparticles and that of uncoated, positively charged ones is investigated by studying cellular localization, uptake kinetics and mechanism of internalization in J774.2 macrophages, using non‐phagocytic L929 fib...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Macromolecular bioscience 2011-12, Vol.11 (12), p.1747-1760
Hauptverfasser: Zaki, Noha M., Nasti, Alessandro, Tirelli, Nicola
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1760
container_issue 12
container_start_page 1747
container_title Macromolecular bioscience
container_volume 11
creator Zaki, Noha M.
Nasti, Alessandro
Tirelli, Nicola
description The cellular uptake of hyaluronic‐acid‐coated, negatively charged chitosan/triphosphate nanoparticles and that of uncoated, positively charged ones is investigated by studying cellular localization, uptake kinetics and mechanism of internalization in J774.2 macrophages, using non‐phagocytic L929 fibroblasts as a control for uncoated nanoparticles. Both kinds of nanoparticles undergo endosomal escape and adopt a similar clathrin‐based endocytic mechanism. The surface decoration with HA profoundly influences the kinetics of cellular uptake, with an at least two orders of magnitude slower kinetics, but also the nature of the binding on the cellular surface. The endocytosis of chitosan nanoparticles (green) with and without hyaluronic acid‐coating is studied in murine macrophages. Both coated and uncoated nanoparticles evade endolysosomal compartments (red), but the hyaluronic acid coating controls stability in media, cellular interactions and uptake kinetics.
doi_str_mv 10.1002/mabi.201100156
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_911937896</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>911937896</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3826-64ab420fabae1908e4057ad39a4661006493a54cefc8b6b6bc14a2a0449434103</originalsourceid><addsrcrecordid>eNqFkc1u1DAUhS0EoqWwZYm8Y5XBThwnZjeEdjpSp-1iCkvrxnGoqRMHOynkhXhOPJ12YIe88M_9zrnyPQi9pWRBCUk_dFCbRUpovNCcP0PHlFOe5FTkzw_nsjhCr0L4HpGiFOlLdJTGOqMFPUa_L6F3Crw32gfcOo-reXSDhdAZhT9ra-61nz_iSls7WfD4ZhjhTmPoG7zuRw_qqXAGo8auxdWtGV2A_gE5n8FO3vXRa6lMk1QuUs1fZtd9AD8aZXXAJorw9S18c2qOTw9N8cY12r5GL1qwQb953E_QzdnptjpPLq5W62p5kaisTHnCGdQsJS3UoKkgpWYkL6DJBDDO44g4ExnkTOlWlTWPS1EGKRDGBMsYJdkJer_3Hbz7Mekwys6E3Reh124KUlAqsjhEHsnFnlTeheB1KwdvOvCzpETuopG7aOQhmih492g91Z1uDvhTFhEQe-CnsXr-j53cLD-t_zVP9loTRv3roAV_J3mRFbn8ermS6Xa72vDtF7nJ_gDSWqwH</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>911937896</pqid></control><display><type>article</type><title>Nanocarriers for Cytoplasmic Delivery: Cellular Uptake and Intracellular Fate of Chitosan and Hyaluronic Acid-Coated Chitosan Nanoparticles in a Phagocytic Cell Model</title><source>MEDLINE</source><source>Access via Wiley Online Library</source><creator>Zaki, Noha M. ; Nasti, Alessandro ; Tirelli, Nicola</creator><creatorcontrib>Zaki, Noha M. ; Nasti, Alessandro ; Tirelli, Nicola</creatorcontrib><description>The cellular uptake of hyaluronic‐acid‐coated, negatively charged chitosan/triphosphate nanoparticles and that of uncoated, positively charged ones is investigated by studying cellular localization, uptake kinetics and mechanism of internalization in J774.2 macrophages, using non‐phagocytic L929 fibroblasts as a control for uncoated nanoparticles. Both kinds of nanoparticles undergo endosomal escape and adopt a similar clathrin‐based endocytic mechanism. The surface decoration with HA profoundly influences the kinetics of cellular uptake, with an at least two orders of magnitude slower kinetics, but also the nature of the binding on the cellular surface. The endocytosis of chitosan nanoparticles (green) with and without hyaluronic acid‐coating is studied in murine macrophages. Both coated and uncoated nanoparticles evade endolysosomal compartments (red), but the hyaluronic acid coating controls stability in media, cellular interactions and uptake kinetics.</description><identifier>ISSN: 1616-5187</identifier><identifier>EISSN: 1616-5195</identifier><identifier>DOI: 10.1002/mabi.201100156</identifier><identifier>PMID: 21954171</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>Animals ; Binding Sites ; Cell Line ; chitosan ; Chitosan - chemistry ; Chitosan - metabolism ; clathrin ; Coated Materials, Biocompatible - chemical synthesis ; Coated Materials, Biocompatible - metabolism ; Coated Materials, Biocompatible - pharmacology ; Drug Carriers - chemical synthesis ; Drug Carriers - metabolism ; Drug Carriers - pharmacology ; endocytosis ; Endocytosis - drug effects ; Endosomes - metabolism ; Fibroblasts - cytology ; Fibroblasts - metabolism ; hyaluronic acid ; Hyaluronic Acid - chemistry ; Hyaluronic Acid - metabolism ; Macrophages - cytology ; Macrophages - metabolism ; Mice ; Microscopy, Fluorescence ; Nanoparticles ; Particle Size ; Static Electricity</subject><ispartof>Macromolecular bioscience, 2011-12, Vol.11 (12), p.1747-1760</ispartof><rights>Copyright © 2011 WILEY‐VCH Verlag GmbH &amp; Co. KGaA, Weinheim</rights><rights>Copyright © 2011 WILEY-VCH Verlag GmbH &amp; Co. KGaA, Weinheim.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3826-64ab420fabae1908e4057ad39a4661006493a54cefc8b6b6bc14a2a0449434103</citedby><cites>FETCH-LOGICAL-c3826-64ab420fabae1908e4057ad39a4661006493a54cefc8b6b6bc14a2a0449434103</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fmabi.201100156$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fmabi.201100156$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21954171$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zaki, Noha M.</creatorcontrib><creatorcontrib>Nasti, Alessandro</creatorcontrib><creatorcontrib>Tirelli, Nicola</creatorcontrib><title>Nanocarriers for Cytoplasmic Delivery: Cellular Uptake and Intracellular Fate of Chitosan and Hyaluronic Acid-Coated Chitosan Nanoparticles in a Phagocytic Cell Model</title><title>Macromolecular bioscience</title><addtitle>Macromol. Biosci</addtitle><description>The cellular uptake of hyaluronic‐acid‐coated, negatively charged chitosan/triphosphate nanoparticles and that of uncoated, positively charged ones is investigated by studying cellular localization, uptake kinetics and mechanism of internalization in J774.2 macrophages, using non‐phagocytic L929 fibroblasts as a control for uncoated nanoparticles. Both kinds of nanoparticles undergo endosomal escape and adopt a similar clathrin‐based endocytic mechanism. The surface decoration with HA profoundly influences the kinetics of cellular uptake, with an at least two orders of magnitude slower kinetics, but also the nature of the binding on the cellular surface. The endocytosis of chitosan nanoparticles (green) with and without hyaluronic acid‐coating is studied in murine macrophages. Both coated and uncoated nanoparticles evade endolysosomal compartments (red), but the hyaluronic acid coating controls stability in media, cellular interactions and uptake kinetics.</description><subject>Animals</subject><subject>Binding Sites</subject><subject>Cell Line</subject><subject>chitosan</subject><subject>Chitosan - chemistry</subject><subject>Chitosan - metabolism</subject><subject>clathrin</subject><subject>Coated Materials, Biocompatible - chemical synthesis</subject><subject>Coated Materials, Biocompatible - metabolism</subject><subject>Coated Materials, Biocompatible - pharmacology</subject><subject>Drug Carriers - chemical synthesis</subject><subject>Drug Carriers - metabolism</subject><subject>Drug Carriers - pharmacology</subject><subject>endocytosis</subject><subject>Endocytosis - drug effects</subject><subject>Endosomes - metabolism</subject><subject>Fibroblasts - cytology</subject><subject>Fibroblasts - metabolism</subject><subject>hyaluronic acid</subject><subject>Hyaluronic Acid - chemistry</subject><subject>Hyaluronic Acid - metabolism</subject><subject>Macrophages - cytology</subject><subject>Macrophages - metabolism</subject><subject>Mice</subject><subject>Microscopy, Fluorescence</subject><subject>Nanoparticles</subject><subject>Particle Size</subject><subject>Static Electricity</subject><issn>1616-5187</issn><issn>1616-5195</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1u1DAUhS0EoqWwZYm8Y5XBThwnZjeEdjpSp-1iCkvrxnGoqRMHOynkhXhOPJ12YIe88M_9zrnyPQi9pWRBCUk_dFCbRUpovNCcP0PHlFOe5FTkzw_nsjhCr0L4HpGiFOlLdJTGOqMFPUa_L6F3Crw32gfcOo-reXSDhdAZhT9ra-61nz_iSls7WfD4ZhjhTmPoG7zuRw_qqXAGo8auxdWtGV2A_gE5n8FO3vXRa6lMk1QuUs1fZtd9AD8aZXXAJorw9S18c2qOTw9N8cY12r5GL1qwQb953E_QzdnptjpPLq5W62p5kaisTHnCGdQsJS3UoKkgpWYkL6DJBDDO44g4ExnkTOlWlTWPS1EGKRDGBMsYJdkJer_3Hbz7Mekwys6E3Reh124KUlAqsjhEHsnFnlTeheB1KwdvOvCzpETuopG7aOQhmih492g91Z1uDvhTFhEQe-CnsXr-j53cLD-t_zVP9loTRv3roAV_J3mRFbn8ermS6Xa72vDtF7nJ_gDSWqwH</recordid><startdate>20111208</startdate><enddate>20111208</enddate><creator>Zaki, Noha M.</creator><creator>Nasti, Alessandro</creator><creator>Tirelli, Nicola</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><scope>BSCLL</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>7X8</scope></search><sort><creationdate>20111208</creationdate><title>Nanocarriers for Cytoplasmic Delivery: Cellular Uptake and Intracellular Fate of Chitosan and Hyaluronic Acid-Coated Chitosan Nanoparticles in a Phagocytic Cell Model</title><author>Zaki, Noha M. ; Nasti, Alessandro ; Tirelli, Nicola</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3826-64ab420fabae1908e4057ad39a4661006493a54cefc8b6b6bc14a2a0449434103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Binding Sites</topic><topic>Cell Line</topic><topic>chitosan</topic><topic>Chitosan - chemistry</topic><topic>Chitosan - metabolism</topic><topic>clathrin</topic><topic>Coated Materials, Biocompatible - chemical synthesis</topic><topic>Coated Materials, Biocompatible - metabolism</topic><topic>Coated Materials, Biocompatible - pharmacology</topic><topic>Drug Carriers - chemical synthesis</topic><topic>Drug Carriers - metabolism</topic><topic>Drug Carriers - pharmacology</topic><topic>endocytosis</topic><topic>Endocytosis - drug effects</topic><topic>Endosomes - metabolism</topic><topic>Fibroblasts - cytology</topic><topic>Fibroblasts - metabolism</topic><topic>hyaluronic acid</topic><topic>Hyaluronic Acid - chemistry</topic><topic>Hyaluronic Acid - metabolism</topic><topic>Macrophages - cytology</topic><topic>Macrophages - metabolism</topic><topic>Mice</topic><topic>Microscopy, Fluorescence</topic><topic>Nanoparticles</topic><topic>Particle Size</topic><topic>Static Electricity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zaki, Noha M.</creatorcontrib><creatorcontrib>Nasti, Alessandro</creatorcontrib><creatorcontrib>Tirelli, Nicola</creatorcontrib><collection>Istex</collection><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><jtitle>Macromolecular bioscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zaki, Noha M.</au><au>Nasti, Alessandro</au><au>Tirelli, Nicola</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nanocarriers for Cytoplasmic Delivery: Cellular Uptake and Intracellular Fate of Chitosan and Hyaluronic Acid-Coated Chitosan Nanoparticles in a Phagocytic Cell Model</atitle><jtitle>Macromolecular bioscience</jtitle><addtitle>Macromol. Biosci</addtitle><date>2011-12-08</date><risdate>2011</risdate><volume>11</volume><issue>12</issue><spage>1747</spage><epage>1760</epage><pages>1747-1760</pages><issn>1616-5187</issn><eissn>1616-5195</eissn><abstract>The cellular uptake of hyaluronic‐acid‐coated, negatively charged chitosan/triphosphate nanoparticles and that of uncoated, positively charged ones is investigated by studying cellular localization, uptake kinetics and mechanism of internalization in J774.2 macrophages, using non‐phagocytic L929 fibroblasts as a control for uncoated nanoparticles. Both kinds of nanoparticles undergo endosomal escape and adopt a similar clathrin‐based endocytic mechanism. The surface decoration with HA profoundly influences the kinetics of cellular uptake, with an at least two orders of magnitude slower kinetics, but also the nature of the binding on the cellular surface. The endocytosis of chitosan nanoparticles (green) with and without hyaluronic acid‐coating is studied in murine macrophages. Both coated and uncoated nanoparticles evade endolysosomal compartments (red), but the hyaluronic acid coating controls stability in media, cellular interactions and uptake kinetics.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><pmid>21954171</pmid><doi>10.1002/mabi.201100156</doi><tpages>14</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1616-5187
ispartof Macromolecular bioscience, 2011-12, Vol.11 (12), p.1747-1760
issn 1616-5187
1616-5195
language eng
recordid cdi_proquest_miscellaneous_911937896
source MEDLINE; Access via Wiley Online Library
subjects Animals
Binding Sites
Cell Line
chitosan
Chitosan - chemistry
Chitosan - metabolism
clathrin
Coated Materials, Biocompatible - chemical synthesis
Coated Materials, Biocompatible - metabolism
Coated Materials, Biocompatible - pharmacology
Drug Carriers - chemical synthesis
Drug Carriers - metabolism
Drug Carriers - pharmacology
endocytosis
Endocytosis - drug effects
Endosomes - metabolism
Fibroblasts - cytology
Fibroblasts - metabolism
hyaluronic acid
Hyaluronic Acid - chemistry
Hyaluronic Acid - metabolism
Macrophages - cytology
Macrophages - metabolism
Mice
Microscopy, Fluorescence
Nanoparticles
Particle Size
Static Electricity
title Nanocarriers for Cytoplasmic Delivery: Cellular Uptake and Intracellular Fate of Chitosan and Hyaluronic Acid-Coated Chitosan Nanoparticles in a Phagocytic Cell Model
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T23%3A58%3A58IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Nanocarriers%20for%20Cytoplasmic%20Delivery:%20Cellular%20Uptake%20and%20Intracellular%20Fate%20of%20Chitosan%20and%20Hyaluronic%20Acid-Coated%20Chitosan%20Nanoparticles%20in%20a%20Phagocytic%20Cell%20Model&rft.jtitle=Macromolecular%20bioscience&rft.au=Zaki,%20Noha%20M.&rft.date=2011-12-08&rft.volume=11&rft.issue=12&rft.spage=1747&rft.epage=1760&rft.pages=1747-1760&rft.issn=1616-5187&rft.eissn=1616-5195&rft_id=info:doi/10.1002/mabi.201100156&rft_dat=%3Cproquest_cross%3E911937896%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=911937896&rft_id=info:pmid/21954171&rfr_iscdi=true