Automated in-line mixing system for large scale production of chitosan-based polyplexes
[Display omitted] Chitosan (CS)-based polyplexes are efficient non-viral gene delivery systems that are most commonly prepared by manual mixing. However, manual mixing is not only poorly controlled but also restricted to relatively small preparation volumes, limiting clinical applications. In order...
Gespeichert in:
Veröffentlicht in: | Journal of colloid and interface science 2017-08, Vol.500, p.253-263 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 263 |
---|---|
container_issue | |
container_start_page | 253 |
container_title | Journal of colloid and interface science |
container_volume | 500 |
creator | Tavakoli Naeini, Ashkan Soliman, Ousamah Younoss Alameh, Mohamad Gabriel Lavertu, Marc Buschmann, Michael D. |
description | [Display omitted]
Chitosan (CS)-based polyplexes are efficient non-viral gene delivery systems that are most commonly prepared by manual mixing. However, manual mixing is not only poorly controlled but also restricted to relatively small preparation volumes, limiting clinical applications. In order to overcome these drawbacks and to produce clinical quantities of CS-based polyplexes, a fully automated in-line mixing platform was developed for production of large batches of small-size and homogeneous CS-based polyplexes. Operational conditions to produce small-sized homogeneous polyplexes were identified. Increasing mixing concentrations of CS and nucleic acid was directly associated with an increase in size and polydispersity of both CS/pDNA and CS/siRNA polyplexes. We also found that although the speed of mixing has a negligible impact on the properties of CS/pDNA polyplexes, the size and polydispersity of CS/siRNA polyplexes are strongly influenced by the mixing speed: the higher the speed, the smaller the size and polydispersity. While in-line and manual CS/pDNA polyplexes had similar size and PDI, CS/siRNA polyplexes were smaller and more homogenous when prepared in-line in the non-laminar flow regime compared to manual method. Finally, we found that in-line mixed CS/siRNA polyplexes have equivalent or higher silencing efficiency of ApoB in HepG2 cells, compared to manually prepared polyplexes. |
doi_str_mv | 10.1016/j.jcis.2017.04.013 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1888959460</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0021979717304058</els_id><sourcerecordid>1888959460</sourcerecordid><originalsourceid>FETCH-LOGICAL-c393t-6f37df205181fe5755c533ec59e11dc209a4a81aca8e9005aeb92a7b2a1e807a3</originalsourceid><addsrcrecordid>eNp9kE1LxDAQQIMoun78AQ-So5fWmaTZNuBFxC8QvCgeQzadapa2WZNW3H9vl1WPnuby5jHzGDtFyBFwfrHMl86nXACWORQ5oNxhMwStshJB7rIZgMBMl7o8YIcpLQEQldL77EBUBWIhxYy9Xo1D6OxANfd91vqeeOe_fP_G0zoN1PEmRN7a-EY8OdsSX8VQj27woeeh4e7dDyHZPlvYNClWoV2vWvqidMz2GtsmOvmZR-zl9ub5-j57fLp7uL56zJzUcsjmjSzrRoDCChtSpVJOSUlOaUKsnQBtC1uhdbYiDaAsLbSw5UJYpApKK4_Y-dY73fUxUhpM55OjtrU9hTEZrKpKK13MYULFFnUxpBSpMavoOxvXBsFsgpql2QQ1m6AGCjMFnZbOfvzjoqP6b-W34ARcbgGavvz0FE1ynnpHtY_kBlMH_5__G3XNh-Q</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1888959460</pqid></control><display><type>article</type><title>Automated in-line mixing system for large scale production of chitosan-based polyplexes</title><source>Elsevier ScienceDirect Journals</source><creator>Tavakoli Naeini, Ashkan ; Soliman, Ousamah Younoss ; Alameh, Mohamad Gabriel ; Lavertu, Marc ; Buschmann, Michael D.</creator><creatorcontrib>Tavakoli Naeini, Ashkan ; Soliman, Ousamah Younoss ; Alameh, Mohamad Gabriel ; Lavertu, Marc ; Buschmann, Michael D.</creatorcontrib><description>[Display omitted]
Chitosan (CS)-based polyplexes are efficient non-viral gene delivery systems that are most commonly prepared by manual mixing. However, manual mixing is not only poorly controlled but also restricted to relatively small preparation volumes, limiting clinical applications. In order to overcome these drawbacks and to produce clinical quantities of CS-based polyplexes, a fully automated in-line mixing platform was developed for production of large batches of small-size and homogeneous CS-based polyplexes. Operational conditions to produce small-sized homogeneous polyplexes were identified. Increasing mixing concentrations of CS and nucleic acid was directly associated with an increase in size and polydispersity of both CS/pDNA and CS/siRNA polyplexes. We also found that although the speed of mixing has a negligible impact on the properties of CS/pDNA polyplexes, the size and polydispersity of CS/siRNA polyplexes are strongly influenced by the mixing speed: the higher the speed, the smaller the size and polydispersity. While in-line and manual CS/pDNA polyplexes had similar size and PDI, CS/siRNA polyplexes were smaller and more homogenous when prepared in-line in the non-laminar flow regime compared to manual method. Finally, we found that in-line mixed CS/siRNA polyplexes have equivalent or higher silencing efficiency of ApoB in HepG2 cells, compared to manually prepared polyplexes.</description><identifier>ISSN: 0021-9797</identifier><identifier>EISSN: 1095-7103</identifier><identifier>DOI: 10.1016/j.jcis.2017.04.013</identifier><identifier>PMID: 28411432</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Bioactivity ; Chitosan ; In-line mixing ; Non-viral gene delivery ; Plasmid ; Polyplex ; siRNA</subject><ispartof>Journal of colloid and interface science, 2017-08, Vol.500, p.253-263</ispartof><rights>2017 Elsevier Inc.</rights><rights>Copyright © 2017 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c393t-6f37df205181fe5755c533ec59e11dc209a4a81aca8e9005aeb92a7b2a1e807a3</citedby><cites>FETCH-LOGICAL-c393t-6f37df205181fe5755c533ec59e11dc209a4a81aca8e9005aeb92a7b2a1e807a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0021979717304058$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28411432$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tavakoli Naeini, Ashkan</creatorcontrib><creatorcontrib>Soliman, Ousamah Younoss</creatorcontrib><creatorcontrib>Alameh, Mohamad Gabriel</creatorcontrib><creatorcontrib>Lavertu, Marc</creatorcontrib><creatorcontrib>Buschmann, Michael D.</creatorcontrib><title>Automated in-line mixing system for large scale production of chitosan-based polyplexes</title><title>Journal of colloid and interface science</title><addtitle>J Colloid Interface Sci</addtitle><description>[Display omitted]
Chitosan (CS)-based polyplexes are efficient non-viral gene delivery systems that are most commonly prepared by manual mixing. However, manual mixing is not only poorly controlled but also restricted to relatively small preparation volumes, limiting clinical applications. In order to overcome these drawbacks and to produce clinical quantities of CS-based polyplexes, a fully automated in-line mixing platform was developed for production of large batches of small-size and homogeneous CS-based polyplexes. Operational conditions to produce small-sized homogeneous polyplexes were identified. Increasing mixing concentrations of CS and nucleic acid was directly associated with an increase in size and polydispersity of both CS/pDNA and CS/siRNA polyplexes. We also found that although the speed of mixing has a negligible impact on the properties of CS/pDNA polyplexes, the size and polydispersity of CS/siRNA polyplexes are strongly influenced by the mixing speed: the higher the speed, the smaller the size and polydispersity. While in-line and manual CS/pDNA polyplexes had similar size and PDI, CS/siRNA polyplexes were smaller and more homogenous when prepared in-line in the non-laminar flow regime compared to manual method. Finally, we found that in-line mixed CS/siRNA polyplexes have equivalent or higher silencing efficiency of ApoB in HepG2 cells, compared to manually prepared polyplexes.</description><subject>Bioactivity</subject><subject>Chitosan</subject><subject>In-line mixing</subject><subject>Non-viral gene delivery</subject><subject>Plasmid</subject><subject>Polyplex</subject><subject>siRNA</subject><issn>0021-9797</issn><issn>1095-7103</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp9kE1LxDAQQIMoun78AQ-So5fWmaTZNuBFxC8QvCgeQzadapa2WZNW3H9vl1WPnuby5jHzGDtFyBFwfrHMl86nXACWORQ5oNxhMwStshJB7rIZgMBMl7o8YIcpLQEQldL77EBUBWIhxYy9Xo1D6OxANfd91vqeeOe_fP_G0zoN1PEmRN7a-EY8OdsSX8VQj27woeeh4e7dDyHZPlvYNClWoV2vWvqidMz2GtsmOvmZR-zl9ub5-j57fLp7uL56zJzUcsjmjSzrRoDCChtSpVJOSUlOaUKsnQBtC1uhdbYiDaAsLbSw5UJYpApKK4_Y-dY73fUxUhpM55OjtrU9hTEZrKpKK13MYULFFnUxpBSpMavoOxvXBsFsgpql2QQ1m6AGCjMFnZbOfvzjoqP6b-W34ARcbgGavvz0FE1ynnpHtY_kBlMH_5__G3XNh-Q</recordid><startdate>20170815</startdate><enddate>20170815</enddate><creator>Tavakoli Naeini, Ashkan</creator><creator>Soliman, Ousamah Younoss</creator><creator>Alameh, Mohamad Gabriel</creator><creator>Lavertu, Marc</creator><creator>Buschmann, Michael D.</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20170815</creationdate><title>Automated in-line mixing system for large scale production of chitosan-based polyplexes</title><author>Tavakoli Naeini, Ashkan ; Soliman, Ousamah Younoss ; Alameh, Mohamad Gabriel ; Lavertu, Marc ; Buschmann, Michael D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c393t-6f37df205181fe5755c533ec59e11dc209a4a81aca8e9005aeb92a7b2a1e807a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Bioactivity</topic><topic>Chitosan</topic><topic>In-line mixing</topic><topic>Non-viral gene delivery</topic><topic>Plasmid</topic><topic>Polyplex</topic><topic>siRNA</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tavakoli Naeini, Ashkan</creatorcontrib><creatorcontrib>Soliman, Ousamah Younoss</creatorcontrib><creatorcontrib>Alameh, Mohamad Gabriel</creatorcontrib><creatorcontrib>Lavertu, Marc</creatorcontrib><creatorcontrib>Buschmann, Michael D.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of colloid and interface science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tavakoli Naeini, Ashkan</au><au>Soliman, Ousamah Younoss</au><au>Alameh, Mohamad Gabriel</au><au>Lavertu, Marc</au><au>Buschmann, Michael D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Automated in-line mixing system for large scale production of chitosan-based polyplexes</atitle><jtitle>Journal of colloid and interface science</jtitle><addtitle>J Colloid Interface Sci</addtitle><date>2017-08-15</date><risdate>2017</risdate><volume>500</volume><spage>253</spage><epage>263</epage><pages>253-263</pages><issn>0021-9797</issn><eissn>1095-7103</eissn><abstract>[Display omitted]
Chitosan (CS)-based polyplexes are efficient non-viral gene delivery systems that are most commonly prepared by manual mixing. However, manual mixing is not only poorly controlled but also restricted to relatively small preparation volumes, limiting clinical applications. In order to overcome these drawbacks and to produce clinical quantities of CS-based polyplexes, a fully automated in-line mixing platform was developed for production of large batches of small-size and homogeneous CS-based polyplexes. Operational conditions to produce small-sized homogeneous polyplexes were identified. Increasing mixing concentrations of CS and nucleic acid was directly associated with an increase in size and polydispersity of both CS/pDNA and CS/siRNA polyplexes. We also found that although the speed of mixing has a negligible impact on the properties of CS/pDNA polyplexes, the size and polydispersity of CS/siRNA polyplexes are strongly influenced by the mixing speed: the higher the speed, the smaller the size and polydispersity. While in-line and manual CS/pDNA polyplexes had similar size and PDI, CS/siRNA polyplexes were smaller and more homogenous when prepared in-line in the non-laminar flow regime compared to manual method. Finally, we found that in-line mixed CS/siRNA polyplexes have equivalent or higher silencing efficiency of ApoB in HepG2 cells, compared to manually prepared polyplexes.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>28411432</pmid><doi>10.1016/j.jcis.2017.04.013</doi><tpages>11</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0021-9797 |
ispartof | Journal of colloid and interface science, 2017-08, Vol.500, p.253-263 |
issn | 0021-9797 1095-7103 |
language | eng |
recordid | cdi_proquest_miscellaneous_1888959460 |
source | Elsevier ScienceDirect Journals |
subjects | Bioactivity Chitosan In-line mixing Non-viral gene delivery Plasmid Polyplex siRNA |
title | Automated in-line mixing system for large scale production of chitosan-based polyplexes |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-10T17%3A29%3A48IST&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=Automated%20in-line%20mixing%20system%20for%20large%20scale%20production%20of%20chitosan-based%20polyplexes&rft.jtitle=Journal%20of%20colloid%20and%20interface%20science&rft.au=Tavakoli%20Naeini,%20Ashkan&rft.date=2017-08-15&rft.volume=500&rft.spage=253&rft.epage=263&rft.pages=253-263&rft.issn=0021-9797&rft.eissn=1095-7103&rft_id=info:doi/10.1016/j.jcis.2017.04.013&rft_dat=%3Cproquest_cross%3E1888959460%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=1888959460&rft_id=info:pmid/28411432&rft_els_id=S0021979717304058&rfr_iscdi=true |