In vitro uptake of polystyrene microspheres: effect of particle size, cell line and cell density
Uptake of polycation–DNA particles is the first step in achieving gene delivery with non-viral vehicles. One of the important characteristics determining uptake of DNA particles is their size. Here we have characterized the ability of several cell lines to internalise labelled polystyrene microspher...
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Veröffentlicht in: | Journal of controlled release 2001-03, Vol.71 (1), p.39-51 |
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description | Uptake of polycation–DNA particles is the first step in achieving gene delivery with non-viral vehicles. One of the important characteristics determining uptake of DNA particles is their size. Here we have characterized the ability of several cell lines to internalise labelled polystyrene microspheres of different sizes. All the cell lines tested ingested 20-nm microspheres avidly. With larger microspheres (93, 220, 560 and 1010 nm) cell type as well as growth related differences were observed. Whereas some cell lines (HUVEC, ECV 304 and HNX 14C) took up microspheres up to 1010 nm even when the cells were confluent, others did not take up many microspheres larger than 93 nm (Hepa 1–6 and HepG2). In one cell line (KLN 205), uptake of 93-, 220- and 560-nm microspheres was avid in growing cells, but not detectable when they were confluent. In KLN 205 cells, a good correlation was found between the uptake of 560-nm microspheres and the uptake of a peptide–DNA polyplex formulation, when it was prepared under conditions leading to small particle sizes. Little correlation was found when the polyplex formulation was allowed to aggregate. |
doi_str_mv | 10.1016/S0168-3659(00)00358-8 |
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One of the important characteristics determining uptake of DNA particles is their size. Here we have characterized the ability of several cell lines to internalise labelled polystyrene microspheres of different sizes. All the cell lines tested ingested 20-nm microspheres avidly. With larger microspheres (93, 220, 560 and 1010 nm) cell type as well as growth related differences were observed. Whereas some cell lines (HUVEC, ECV 304 and HNX 14C) took up microspheres up to 1010 nm even when the cells were confluent, others did not take up many microspheres larger than 93 nm (Hepa 1–6 and HepG2). In one cell line (KLN 205), uptake of 93-, 220- and 560-nm microspheres was avid in growing cells, but not detectable when they were confluent. In KLN 205 cells, a good correlation was found between the uptake of 560-nm microspheres and the uptake of a peptide–DNA polyplex formulation, when it was prepared under conditions leading to small particle sizes. Little correlation was found when the polyplex formulation was allowed to aggregate.</description><identifier>ISSN: 0168-3659</identifier><identifier>EISSN: 1873-4995</identifier><identifier>DOI: 10.1016/S0168-3659(00)00358-8</identifier><identifier>PMID: 11245907</identifier><identifier>CODEN: JCREEC</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Amino Acid Sequence ; Animals ; Biological and medical sciences ; Cell Line ; Collagenases ; DNA ; DNA - chemistry ; Extracellular Matrix ; General pharmacology ; Humans ; Hydrolysis ; Medical sciences ; Mice ; Microspheres ; Molecular Sequence Data ; Oligopeptides - administration & dosage ; Oligopeptides - metabolism ; Particle Size ; Pharmaceutical technology. Pharmaceutical industry ; Pharmacology. Drug treatments ; Polyplex ; polystyrene ; Polystyrene microspheres ; Polystyrenes ; Uptake</subject><ispartof>Journal of controlled release, 2001-03, Vol.71 (1), p.39-51</ispartof><rights>2001 Elsevier Science B.V.</rights><rights>2001 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c420t-3d8a9719c3b5fd826f0882ab4296486fb10c85a9524bcbabbe2e891428bde9313</citedby><cites>FETCH-LOGICAL-c420t-3d8a9719c3b5fd826f0882ab4296486fb10c85a9524bcbabbe2e891428bde9313</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0168-3659(00)00358-8$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=938453$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11245907$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zauner, Wolfgang</creatorcontrib><creatorcontrib>Farrow, Neil A</creatorcontrib><creatorcontrib>Haines, Adrian M.R</creatorcontrib><title>In vitro uptake of polystyrene microspheres: effect of particle size, cell line and cell density</title><title>Journal of controlled release</title><addtitle>J Control Release</addtitle><description>Uptake of polycation–DNA particles is the first step in achieving gene delivery with non-viral vehicles. One of the important characteristics determining uptake of DNA particles is their size. Here we have characterized the ability of several cell lines to internalise labelled polystyrene microspheres of different sizes. All the cell lines tested ingested 20-nm microspheres avidly. With larger microspheres (93, 220, 560 and 1010 nm) cell type as well as growth related differences were observed. Whereas some cell lines (HUVEC, ECV 304 and HNX 14C) took up microspheres up to 1010 nm even when the cells were confluent, others did not take up many microspheres larger than 93 nm (Hepa 1–6 and HepG2). In one cell line (KLN 205), uptake of 93-, 220- and 560-nm microspheres was avid in growing cells, but not detectable when they were confluent. In KLN 205 cells, a good correlation was found between the uptake of 560-nm microspheres and the uptake of a peptide–DNA polyplex formulation, when it was prepared under conditions leading to small particle sizes. Little correlation was found when the polyplex formulation was allowed to aggregate.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cell Line</subject><subject>Collagenases</subject><subject>DNA</subject><subject>DNA - chemistry</subject><subject>Extracellular Matrix</subject><subject>General pharmacology</subject><subject>Humans</subject><subject>Hydrolysis</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Microspheres</subject><subject>Molecular Sequence Data</subject><subject>Oligopeptides - administration & dosage</subject><subject>Oligopeptides - metabolism</subject><subject>Particle Size</subject><subject>Pharmaceutical technology. Pharmaceutical industry</subject><subject>Pharmacology. Drug treatments</subject><subject>Polyplex</subject><subject>polystyrene</subject><subject>Polystyrene microspheres</subject><subject>Polystyrenes</subject><subject>Uptake</subject><issn>0168-3659</issn><issn>1873-4995</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkV1rFTEQhoNY7LH2J1QCgih0dfK1m3hTSqm1UPBCe50m2QlG9-xukz2F46_vng_ay97MMPC8M8P7EnLC4AsDVn_9NRddiVqZTwCfAYTSlX5FFkw3opLGqNdk8YQckrel_AUAJWTzhhwyxqUy0CzI3XVPH9KUB7oaJ_cP6RDpOHTrMq0z9kiXKeShjH8wY_lGMUYM05ZxeUqhQ1rSfzylAbuOdmkWuL7dTS32JU3rd-Qguq7g8b4fkdvvl78vflQ3P6-uL85vqiA5TJVotTMNM0F4FVvN6whac-clN7XUdfQMglbOKC598M575KgNk1z7Fo1g4oh83O0d83C_wjLZZSqbR1yPw6rYpjYNGP0yyBoDNePNDKoduHGgZIx2zGnp8toysJsM7DYDuzHYAthtBlbPuvf7Ayu_xPZZtTd9Bj7sAVeC62J2fUjliTNCSyVm6mxH4ezaQ8JsS0jYB2xTnkOw7ZBeeOQR1lijAw</recordid><startdate>20010312</startdate><enddate>20010312</enddate><creator>Zauner, Wolfgang</creator><creator>Farrow, Neil A</creator><creator>Haines, Adrian M.R</creator><general>Elsevier B.V</general><general>Elsevier</general><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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20010312</creationdate><title>In vitro uptake of polystyrene microspheres: effect of particle size, cell line and cell density</title><author>Zauner, Wolfgang ; Farrow, Neil A ; Haines, Adrian M.R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c420t-3d8a9719c3b5fd826f0882ab4296486fb10c85a9524bcbabbe2e891428bde9313</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cell Line</topic><topic>Collagenases</topic><topic>DNA</topic><topic>DNA - chemistry</topic><topic>Extracellular Matrix</topic><topic>General pharmacology</topic><topic>Humans</topic><topic>Hydrolysis</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Microspheres</topic><topic>Molecular Sequence Data</topic><topic>Oligopeptides - administration & dosage</topic><topic>Oligopeptides - metabolism</topic><topic>Particle Size</topic><topic>Pharmaceutical technology. Pharmaceutical industry</topic><topic>Pharmacology. Drug treatments</topic><topic>Polyplex</topic><topic>polystyrene</topic><topic>Polystyrene microspheres</topic><topic>Polystyrenes</topic><topic>Uptake</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zauner, Wolfgang</creatorcontrib><creatorcontrib>Farrow, Neil A</creatorcontrib><creatorcontrib>Haines, Adrian M.R</creatorcontrib><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>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of controlled release</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zauner, Wolfgang</au><au>Farrow, Neil A</au><au>Haines, Adrian M.R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In vitro uptake of polystyrene microspheres: effect of particle size, cell line and cell density</atitle><jtitle>Journal of controlled release</jtitle><addtitle>J Control Release</addtitle><date>2001-03-12</date><risdate>2001</risdate><volume>71</volume><issue>1</issue><spage>39</spage><epage>51</epage><pages>39-51</pages><issn>0168-3659</issn><eissn>1873-4995</eissn><coden>JCREEC</coden><abstract>Uptake of polycation–DNA particles is the first step in achieving gene delivery with non-viral vehicles. One of the important characteristics determining uptake of DNA particles is their size. Here we have characterized the ability of several cell lines to internalise labelled polystyrene microspheres of different sizes. All the cell lines tested ingested 20-nm microspheres avidly. With larger microspheres (93, 220, 560 and 1010 nm) cell type as well as growth related differences were observed. Whereas some cell lines (HUVEC, ECV 304 and HNX 14C) took up microspheres up to 1010 nm even when the cells were confluent, others did not take up many microspheres larger than 93 nm (Hepa 1–6 and HepG2). In one cell line (KLN 205), uptake of 93-, 220- and 560-nm microspheres was avid in growing cells, but not detectable when they were confluent. In KLN 205 cells, a good correlation was found between the uptake of 560-nm microspheres and the uptake of a peptide–DNA polyplex formulation, when it was prepared under conditions leading to small particle sizes. Little correlation was found when the polyplex formulation was allowed to aggregate.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>11245907</pmid><doi>10.1016/S0168-3659(00)00358-8</doi><tpages>13</tpages></addata></record> |
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subjects | Amino Acid Sequence Animals Biological and medical sciences Cell Line Collagenases DNA DNA - chemistry Extracellular Matrix General pharmacology Humans Hydrolysis Medical sciences Mice Microspheres Molecular Sequence Data Oligopeptides - administration & dosage Oligopeptides - metabolism Particle Size Pharmaceutical technology. Pharmaceutical industry Pharmacology. Drug treatments Polyplex polystyrene Polystyrene microspheres Polystyrenes Uptake |
title | In vitro uptake of polystyrene microspheres: effect of particle size, cell line and cell density |
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