Accelerated Achilles tendon healing by PDGF gene delivery with mesoporous silica nanoparticles

Abstract We report the ability of amino- and carboxyl-modified MCM-41 mesoporous silica nanoparticles (MSN) to deliver gene in vivo in rat Achilles tendons, despite their inefficiency to transfect primary tenocytes in culture. We show that luciferase activity lasted for at least 2 weeks in tendons i...

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Veröffentlicht in:Biomaterials 2010-07, Vol.31 (19), p.5237-5245
Hauptverfasser: Suwalski, Arnaud, Dabboue, Hinda, Delalande, Anthony, Bensamoun, Sabine F, Canon, Francis, Midoux, Patrick, Saillant, Gérard, Klatzmann, David, Salvetat, Jean-Paul, Pichon, Chantal
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container_end_page 5245
container_issue 19
container_start_page 5237
container_title Biomaterials
container_volume 31
creator Suwalski, Arnaud
Dabboue, Hinda
Delalande, Anthony
Bensamoun, Sabine F
Canon, Francis
Midoux, Patrick
Saillant, Gérard
Klatzmann, David
Salvetat, Jean-Paul
Pichon, Chantal
description Abstract We report the ability of amino- and carboxyl-modified MCM-41 mesoporous silica nanoparticles (MSN) to deliver gene in vivo in rat Achilles tendons, despite their inefficiency to transfect primary tenocytes in culture. We show that luciferase activity lasted for at least 2 weeks in tendons injected with these MSN and a plasmid DNA (pDNA) encoding the luciferase reporter gene. By contrast, in tendons injected with naked plasmid, the luciferase expression decreased as a function of time and became hardly detectable after 2 weeks. Interestingly, there were neither signs of inflammation nor necrosis in tendon, kidney, heart and liver of rat weekly injected with pDNA/MSN formulation during 1.5 months. Our main data concern the acceleration of Achilles tendons healing by PDGF-B gene transfer using MSN. Biomechanical properties and histological analyses clearly indicate that tendons treated with MSN and PDGF gene healed significantly faster than untreated tendons and those treated with pPDGF alone.
doi_str_mv 10.1016/j.biomaterials.2010.02.077
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We show that luciferase activity lasted for at least 2 weeks in tendons injected with these MSN and a plasmid DNA (pDNA) encoding the luciferase reporter gene. By contrast, in tendons injected with naked plasmid, the luciferase expression decreased as a function of time and became hardly detectable after 2 weeks. Interestingly, there were neither signs of inflammation nor necrosis in tendon, kidney, heart and liver of rat weekly injected with pDNA/MSN formulation during 1.5 months. Our main data concern the acceleration of Achilles tendons healing by PDGF-B gene transfer using MSN. 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Dabboue, Hinda ; Delalande, Anthony ; Bensamoun, Sabine F ; Canon, Francis ; Midoux, Patrick ; Saillant, Gérard ; Klatzmann, David ; Salvetat, Jean-Paul ; Pichon, Chantal</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c552t-9abb261b40e424a55b4f94f4a617bfc2d7db9542b1456c52d4321e52fc0ee2cd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Achilles Tendon - drug effects</topic><topic>Achilles Tendon - pathology</topic><topic>Advanced Basic Science</topic><topic>Animals</topic><topic>Dentistry</topic><topic>Drug Carriers - administration &amp; dosage</topic><topic>Drug Carriers - chemistry</topic><topic>Gene therapy</topic><topic>Growth factor</topic><topic>Life Sciences</topic><topic>Nanoparticles - administration &amp; dosage</topic><topic>Nanoparticles - chemistry</topic><topic>Nanoparticles - ultrastructure</topic><topic>Non viral gene delivery</topic><topic>Platelet-Derived Growth Factor - administration &amp; dosage</topic><topic>Platelet-Derived Growth Factor - chemistry</topic><topic>Platelet-Derived Growth Factor - genetics</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Silica nanoparticle, MCM-41</topic><topic>Silicon Dioxide - chemistry</topic><topic>Tendon</topic><topic>Tendon Injuries - drug therapy</topic><topic>Tendon Injuries - pathology</topic><topic>Transfection - methods</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Suwalski, Arnaud</creatorcontrib><creatorcontrib>Dabboue, Hinda</creatorcontrib><creatorcontrib>Delalande, Anthony</creatorcontrib><creatorcontrib>Bensamoun, Sabine F</creatorcontrib><creatorcontrib>Canon, Francis</creatorcontrib><creatorcontrib>Midoux, Patrick</creatorcontrib><creatorcontrib>Saillant, Gérard</creatorcontrib><creatorcontrib>Klatzmann, David</creatorcontrib><creatorcontrib>Salvetat, Jean-Paul</creatorcontrib><creatorcontrib>Pichon, Chantal</creatorcontrib><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><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Biomaterials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Suwalski, Arnaud</au><au>Dabboue, Hinda</au><au>Delalande, Anthony</au><au>Bensamoun, Sabine F</au><au>Canon, Francis</au><au>Midoux, Patrick</au><au>Saillant, Gérard</au><au>Klatzmann, David</au><au>Salvetat, Jean-Paul</au><au>Pichon, Chantal</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Accelerated Achilles tendon healing by PDGF gene delivery with mesoporous silica nanoparticles</atitle><jtitle>Biomaterials</jtitle><addtitle>Biomaterials</addtitle><date>2010-07-01</date><risdate>2010</risdate><volume>31</volume><issue>19</issue><spage>5237</spage><epage>5245</epage><pages>5237-5245</pages><issn>0142-9612</issn><eissn>1878-5905</eissn><abstract>Abstract We report the ability of amino- and carboxyl-modified MCM-41 mesoporous silica nanoparticles (MSN) to deliver gene in vivo in rat Achilles tendons, despite their inefficiency to transfect primary tenocytes in culture. We show that luciferase activity lasted for at least 2 weeks in tendons injected with these MSN and a plasmid DNA (pDNA) encoding the luciferase reporter gene. By contrast, in tendons injected with naked plasmid, the luciferase expression decreased as a function of time and became hardly detectable after 2 weeks. Interestingly, there were neither signs of inflammation nor necrosis in tendon, kidney, heart and liver of rat weekly injected with pDNA/MSN formulation during 1.5 months. Our main data concern the acceleration of Achilles tendons healing by PDGF-B gene transfer using MSN. 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identifier ISSN: 0142-9612
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subjects Achilles Tendon - drug effects
Achilles Tendon - pathology
Advanced Basic Science
Animals
Dentistry
Drug Carriers - administration & dosage
Drug Carriers - chemistry
Gene therapy
Growth factor
Life Sciences
Nanoparticles - administration & dosage
Nanoparticles - chemistry
Nanoparticles - ultrastructure
Non viral gene delivery
Platelet-Derived Growth Factor - administration & dosage
Platelet-Derived Growth Factor - chemistry
Platelet-Derived Growth Factor - genetics
Rats
Rats, Wistar
Silica nanoparticle, MCM-41
Silicon Dioxide - chemistry
Tendon
Tendon Injuries - drug therapy
Tendon Injuries - pathology
Transfection - methods
Treatment Outcome
title Accelerated Achilles tendon healing by PDGF gene delivery with mesoporous silica nanoparticles
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