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The effect of injection using narrow-bore needles on mammalian cells: administration and formulation considerations for cell therapies
Objectives This study focuses on the effect of the injection administration process on a range of cell characteristics. Methods Effects of different ejection rates, needle sizes and cell suspension densities were assessed in terms of viability, membrane integrity, apoptosis and senescence of NIH 3T3...
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Published in: | Journal of pharmacy and pharmacology 2015-05, Vol.67 (5), p.640-650 |
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container_end_page | 650 |
container_issue | 5 |
container_start_page | 640 |
container_title | Journal of pharmacy and pharmacology |
container_volume | 67 |
creator | Amer, Mahetab H. White, Lisa J. Shakesheff, Kevin M. |
description | Objectives
This study focuses on the effect of the injection administration process on a range of cell characteristics.
Methods
Effects of different ejection rates, needle sizes and cell suspension densities were assessed in terms of viability, membrane integrity, apoptosis and senescence of NIH 3T3 fibroblasts. For ratiometric measurements, a multiplex assay was used to verify cell viability, cytotoxicity and apoptosis independent of cell number. Co‐delivery with alginate hydrogels and viscosity‐modifying excipients was also assessed.
Key findings
Ejections at 150 μl/min resulted in the highest percentage of dose being delivered as viable cells among ejection rates tested. The difference in proportions of apoptotic cells became apparent 48 h after ejection, with proportions being higher in samples ejected at slower rates. Co‐delivery with alginate hydrogels demonstrated a protective action on the cell payload.
Conclusions
This study demonstrates the importance of careful consideration of administration protocols required for successful delivery of cell suspensions, according to their nature and cellular responses post‐ejection. |
doi_str_mv | 10.1111/jphp.12362 |
format | article |
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This study focuses on the effect of the injection administration process on a range of cell characteristics.
Methods
Effects of different ejection rates, needle sizes and cell suspension densities were assessed in terms of viability, membrane integrity, apoptosis and senescence of NIH 3T3 fibroblasts. For ratiometric measurements, a multiplex assay was used to verify cell viability, cytotoxicity and apoptosis independent of cell number. Co‐delivery with alginate hydrogels and viscosity‐modifying excipients was also assessed.
Key findings
Ejections at 150 μl/min resulted in the highest percentage of dose being delivered as viable cells among ejection rates tested. The difference in proportions of apoptotic cells became apparent 48 h after ejection, with proportions being higher in samples ejected at slower rates. Co‐delivery with alginate hydrogels demonstrated a protective action on the cell payload.
Conclusions
This study demonstrates the importance of careful consideration of administration protocols required for successful delivery of cell suspensions, according to their nature and cellular responses post‐ejection.</description><identifier>ISSN: 0022-3573</identifier><identifier>EISSN: 2042-7158</identifier><identifier>DOI: 10.1111/jphp.12362</identifier><identifier>PMID: 25623928</identifier><identifier>CODEN: JPPMAB</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Animals ; Apoptosis ; cell injection ; Cell Survival ; cell therapies ; Cell- and Tissue-Based Therapy - instrumentation ; Cell- and Tissue-Based Therapy - methods ; Cellular Senescence ; Injections - adverse effects ; Injections - instrumentation ; Mice ; Needles - adverse effects ; NIH 3T3 ; NIH 3T3 Cells ; Research Paper ; Research Papers ; Suspensions ; viability</subject><ispartof>Journal of pharmacy and pharmacology, 2015-05, Vol.67 (5), p.640-650</ispartof><rights>2015 The Authors Journal of Pharmacy and Pharmacology published by John Wiley & Sons Ltd on behalf of Royal Pharmaceutical Society.</rights><rights>Copyright © 2015 Royal Pharmaceutical Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c6222-63dd386d26bef13042af6c74721e4e7668b31118365678e573e421ccd8deb8df3</citedby><cites>FETCH-LOGICAL-c6222-63dd386d26bef13042af6c74721e4e7668b31118365678e573e421ccd8deb8df3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25623928$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Amer, Mahetab H.</creatorcontrib><creatorcontrib>White, Lisa J.</creatorcontrib><creatorcontrib>Shakesheff, Kevin M.</creatorcontrib><title>The effect of injection using narrow-bore needles on mammalian cells: administration and formulation considerations for cell therapies</title><title>Journal of pharmacy and pharmacology</title><addtitle>J Pharm Pharmacol</addtitle><description>Objectives
This study focuses on the effect of the injection administration process on a range of cell characteristics.
Methods
Effects of different ejection rates, needle sizes and cell suspension densities were assessed in terms of viability, membrane integrity, apoptosis and senescence of NIH 3T3 fibroblasts. For ratiometric measurements, a multiplex assay was used to verify cell viability, cytotoxicity and apoptosis independent of cell number. Co‐delivery with alginate hydrogels and viscosity‐modifying excipients was also assessed.
Key findings
Ejections at 150 μl/min resulted in the highest percentage of dose being delivered as viable cells among ejection rates tested. The difference in proportions of apoptotic cells became apparent 48 h after ejection, with proportions being higher in samples ejected at slower rates. Co‐delivery with alginate hydrogels demonstrated a protective action on the cell payload.
Conclusions
This study demonstrates the importance of careful consideration of administration protocols required for successful delivery of cell suspensions, according to their nature and cellular responses post‐ejection.</description><subject>Animals</subject><subject>Apoptosis</subject><subject>cell injection</subject><subject>Cell Survival</subject><subject>cell therapies</subject><subject>Cell- and Tissue-Based Therapy - instrumentation</subject><subject>Cell- and Tissue-Based Therapy - methods</subject><subject>Cellular Senescence</subject><subject>Injections - adverse effects</subject><subject>Injections - instrumentation</subject><subject>Mice</subject><subject>Needles - adverse effects</subject><subject>NIH 3T3</subject><subject>NIH 3T3 Cells</subject><subject>Research Paper</subject><subject>Research Papers</subject><subject>Suspensions</subject><subject>viability</subject><issn>0022-3573</issn><issn>2042-7158</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><recordid>eNp9Uctu1DAUtRCIDoUNH4AssUNKiR-xExZIVQVT0AgqVFR2lhNfdzwkdrAnlP4A341n0o5gQzaOfR6-xweh56Q8Ifl7vRnX4wmhTNAHaEFLTgtJqvohWpQlpQWrJDtCT1LalGUphRCP0RGtBGUNrRfo9-UaMFgL3RYHi53f5D8XPJ6S89fY6xjDTdGGCNgDmB4SzuCgh0H3TnvcQd-nN1ibwXmXtlHvxdobbEMcpn7ed8EnZ2BG0w7aC_F2nc9GB-kpemR1n-DZ3XqMvr5_d3l2Xqw-Lz-cna6KTtCcRTBjWC0MFS1YwnJUbUUnuaQEOORwdcvyi9RMVELWkJMDp6TrTG2grY1lx-jt7DtO7QCmA59H7tUY3aDjrQraqX8R79bqOvxUvBG84VU2eHlnEMOPCdJWbcIUfZ5ZESF5JSpeisx6NbO6GFKKYA83kFLtOlO7ztS-s0x-8fdMB-p9SZlAZsKN6-H2P1bq48X5xb1pMWtyKfDroNHxuxKSyUpdfVqqZsXF1bL5pr6wPySDtJE</recordid><startdate>201505</startdate><enddate>201505</enddate><creator>Amer, Mahetab H.</creator><creator>White, Lisa J.</creator><creator>Shakesheff, Kevin M.</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><general>John Wiley and Sons Inc</general><scope>BSCLL</scope><scope>24P</scope><scope>WIN</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>7QP</scope><scope>7TK</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>5PM</scope></search><sort><creationdate>201505</creationdate><title>The effect of injection using narrow-bore needles on mammalian cells: administration and formulation considerations for cell therapies</title><author>Amer, Mahetab H. ; White, Lisa J. ; Shakesheff, Kevin M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6222-63dd386d26bef13042af6c74721e4e7668b31118365678e573e421ccd8deb8df3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Apoptosis</topic><topic>cell injection</topic><topic>Cell Survival</topic><topic>cell therapies</topic><topic>Cell- and Tissue-Based Therapy - instrumentation</topic><topic>Cell- and Tissue-Based Therapy - methods</topic><topic>Cellular Senescence</topic><topic>Injections - adverse effects</topic><topic>Injections - instrumentation</topic><topic>Mice</topic><topic>Needles - adverse effects</topic><topic>NIH 3T3</topic><topic>NIH 3T3 Cells</topic><topic>Research Paper</topic><topic>Research Papers</topic><topic>Suspensions</topic><topic>viability</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Amer, Mahetab H.</creatorcontrib><creatorcontrib>White, Lisa J.</creatorcontrib><creatorcontrib>Shakesheff, Kevin M.</creatorcontrib><collection>Istex</collection><collection>Wiley_OA刊</collection><collection>Wiley-Blackwell Open Access Backfiles (Open Access)</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of pharmacy and pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Amer, Mahetab H.</au><au>White, Lisa J.</au><au>Shakesheff, Kevin M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The effect of injection using narrow-bore needles on mammalian cells: administration and formulation considerations for cell therapies</atitle><jtitle>Journal of pharmacy and pharmacology</jtitle><addtitle>J Pharm Pharmacol</addtitle><date>2015-05</date><risdate>2015</risdate><volume>67</volume><issue>5</issue><spage>640</spage><epage>650</epage><pages>640-650</pages><issn>0022-3573</issn><eissn>2042-7158</eissn><coden>JPPMAB</coden><abstract>Objectives
This study focuses on the effect of the injection administration process on a range of cell characteristics.
Methods
Effects of different ejection rates, needle sizes and cell suspension densities were assessed in terms of viability, membrane integrity, apoptosis and senescence of NIH 3T3 fibroblasts. For ratiometric measurements, a multiplex assay was used to verify cell viability, cytotoxicity and apoptosis independent of cell number. Co‐delivery with alginate hydrogels and viscosity‐modifying excipients was also assessed.
Key findings
Ejections at 150 μl/min resulted in the highest percentage of dose being delivered as viable cells among ejection rates tested. The difference in proportions of apoptotic cells became apparent 48 h after ejection, with proportions being higher in samples ejected at slower rates. Co‐delivery with alginate hydrogels demonstrated a protective action on the cell payload.
Conclusions
This study demonstrates the importance of careful consideration of administration protocols required for successful delivery of cell suspensions, according to their nature and cellular responses post‐ejection.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>25623928</pmid><doi>10.1111/jphp.12362</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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language | eng |
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source | Oxford Journals Online |
subjects | Animals Apoptosis cell injection Cell Survival cell therapies Cell- and Tissue-Based Therapy - instrumentation Cell- and Tissue-Based Therapy - methods Cellular Senescence Injections - adverse effects Injections - instrumentation Mice Needles - adverse effects NIH 3T3 NIH 3T3 Cells Research Paper Research Papers Suspensions viability |
title | The effect of injection using narrow-bore needles on mammalian cells: administration and formulation considerations for cell therapies |
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