Hydrodynamic Delivery of Chitosan-Folate-DNA Nanoparticles in Rats with Adjuvant-Induced Arthritis
50 kDa chitosan was conjugated with folate, a specific tissue-targeting ligand. Nanoparticles such as chitosan-DNA and folate-chitosan-DNA were prepared by coacervation process. The hydrodynamic intravenous injection of nanoparticles was performed in the right posterior paw in normal and arthritic r...
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description | 50 kDa chitosan was conjugated with folate, a specific tissue-targeting ligand. Nanoparticles such as chitosan-DNA and folate-chitosan-DNA were prepared by coacervation process. The hydrodynamic intravenous injection of nanoparticles was performed in the right posterior paw in normal and arthritic rats. Our results demonstrated that the fluorescence intensity of DsRed detected was 5 to 12 times more in the right soleus muscle and in the right gastro muscle than other tissue sections. β-galactosidase gene expression with X-gal substrate and folate-chitosan-plasmid nanoparticles showed best coloration in the soleus muscle. Treated arthritic animals also showed a significant decrease in paw swelling and IL-1β and PGE2 concentration in serum compared to untreated rats. This study demonstrated that a nonviral gene therapeutic approach using hydrodynamic delivery could help transfect more efficiently folate-chitosan-DNA nanoparticles in vitro/in vivo and could decrease inflammation in arthritic rats. |
doi_str_mv | 10.1155/2011/148763 |
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Nanoparticles such as chitosan-DNA and folate-chitosan-DNA were prepared by coacervation process. The hydrodynamic intravenous injection of nanoparticles was performed in the right posterior paw in normal and arthritic rats. Our results demonstrated that the fluorescence intensity of DsRed detected was 5 to 12 times more in the right soleus muscle and in the right gastro muscle than other tissue sections. β-galactosidase gene expression with X-gal substrate and folate-chitosan-plasmid nanoparticles showed best coloration in the soleus muscle. Treated arthritic animals also showed a significant decrease in paw swelling and IL-1β and PGE2 concentration in serum compared to untreated rats. This study demonstrated that a nonviral gene therapeutic approach using hydrodynamic delivery could help transfect more efficiently folate-chitosan-DNA nanoparticles in vitro/in vivo and could decrease inflammation in arthritic rats.</description><identifier>ISSN: 1110-7243</identifier><identifier>ISSN: 2314-6133</identifier><identifier>EISSN: 1110-7251</identifier><identifier>EISSN: 2314-6141</identifier><identifier>DOI: 10.1155/2011/148763</identifier><identifier>PMID: 21274258</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Puplishing Corporation</publisher><subject><![CDATA[Analysis of Variance ; Animals ; Arthritis ; Arthritis, Experimental - genetics ; Arthritis, Experimental - metabolism ; Arthritis, Experimental - therapy ; beta-Galactosidase - biosynthesis ; beta-Galactosidase - genetics ; Cancer ; Care and treatment ; Chitin ; Chitosan - administration & dosage ; Dinoprostone - metabolism ; Disease Models, Animal ; DNA - administration & dosage ; DNA - genetics ; Drug Delivery Systems - methods ; Female ; Folic Acid - administration & dosage ; Freund's Adjuvant - administration & dosage ; Gene expression ; Gene therapy ; Genetic aspects ; Histocytochemistry ; Humans ; Injections, Intravenous ; Interleukin 1 Receptor Antagonist Protein - genetics ; Interleukin 1 Receptor Antagonist Protein - metabolism ; Interleukin-1beta - metabolism ; Medical research ; Muscle, Skeletal - metabolism ; Nanoconjugates - administration & dosage ; Nanoconjugates - chemistry ; Nanoparticles ; Nanoparticles - administration & dosage ; Nanoparticles - chemistry ; Physiological aspects ; Proteins ; Rats ; Rats, Inbred Lew ; Rodents ; Tarsus, Animal - pathology ; Tissue Distribution]]></subject><ispartof>BioMed research international, 2011-01, Vol.2011 (2011), p.1-9</ispartof><rights>Copyright © 2011 Qin Shi et al.</rights><rights>COPYRIGHT 2011 John Wiley & Sons, Inc.</rights><rights>Copyright © 2011 Qin Shi et al. Qin Shi et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright © 2011 Qin Shi et al. 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c569t-65899597a8e69d1abf5e99bd99c012036a861b2c78b43d0ede965de07fa617903</citedby><cites>FETCH-LOGICAL-c569t-65899597a8e69d1abf5e99bd99c012036a861b2c78b43d0ede965de07fa617903</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3022186/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3022186/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21274258$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Gualillo, Oreste</contributor><creatorcontrib>Fernandes, Julio C.</creatorcontrib><creatorcontrib>Dai, Kerong</creatorcontrib><creatorcontrib>Zhang, Xiaoling</creatorcontrib><creatorcontrib>Winnik, Françoise M.</creatorcontrib><creatorcontrib>Qiu, Xingping</creatorcontrib><creatorcontrib>Tran, Covi</creatorcontrib><creatorcontrib>Wang, Huijie</creatorcontrib><creatorcontrib>Shi, Qin</creatorcontrib><creatorcontrib>Benderdour, Mohamed</creatorcontrib><title>Hydrodynamic Delivery of Chitosan-Folate-DNA Nanoparticles in Rats with Adjuvant-Induced Arthritis</title><title>BioMed research international</title><addtitle>J Biomed Biotechnol</addtitle><description>50 kDa chitosan was conjugated with folate, a specific tissue-targeting ligand. Nanoparticles such as chitosan-DNA and folate-chitosan-DNA were prepared by coacervation process. The hydrodynamic intravenous injection of nanoparticles was performed in the right posterior paw in normal and arthritic rats. Our results demonstrated that the fluorescence intensity of DsRed detected was 5 to 12 times more in the right soleus muscle and in the right gastro muscle than other tissue sections. β-galactosidase gene expression with X-gal substrate and folate-chitosan-plasmid nanoparticles showed best coloration in the soleus muscle. Treated arthritic animals also showed a significant decrease in paw swelling and IL-1β and PGE2 concentration in serum compared to untreated rats. This study demonstrated that a nonviral gene therapeutic approach using hydrodynamic delivery could help transfect more efficiently folate-chitosan-DNA nanoparticles in vitro/in vivo and could decrease inflammation in arthritic rats.</description><subject>Analysis of Variance</subject><subject>Animals</subject><subject>Arthritis</subject><subject>Arthritis, Experimental - genetics</subject><subject>Arthritis, Experimental - metabolism</subject><subject>Arthritis, Experimental - therapy</subject><subject>beta-Galactosidase - biosynthesis</subject><subject>beta-Galactosidase - genetics</subject><subject>Cancer</subject><subject>Care and treatment</subject><subject>Chitin</subject><subject>Chitosan - administration & dosage</subject><subject>Dinoprostone - metabolism</subject><subject>Disease Models, Animal</subject><subject>DNA - administration & dosage</subject><subject>DNA - genetics</subject><subject>Drug Delivery Systems - methods</subject><subject>Female</subject><subject>Folic Acid - administration & dosage</subject><subject>Freund's Adjuvant - administration & dosage</subject><subject>Gene expression</subject><subject>Gene therapy</subject><subject>Genetic aspects</subject><subject>Histocytochemistry</subject><subject>Humans</subject><subject>Injections, Intravenous</subject><subject>Interleukin 1 Receptor Antagonist Protein - genetics</subject><subject>Interleukin 1 Receptor Antagonist Protein - metabolism</subject><subject>Interleukin-1beta - metabolism</subject><subject>Medical research</subject><subject>Muscle, Skeletal - metabolism</subject><subject>Nanoconjugates - administration & dosage</subject><subject>Nanoconjugates - chemistry</subject><subject>Nanoparticles</subject><subject>Nanoparticles - administration & dosage</subject><subject>Nanoparticles - chemistry</subject><subject>Physiological aspects</subject><subject>Proteins</subject><subject>Rats</subject><subject>Rats, Inbred Lew</subject><subject>Rodents</subject><subject>Tarsus, Animal - pathology</subject><subject>Tissue Distribution</subject><issn>1110-7243</issn><issn>2314-6133</issn><issn>1110-7251</issn><issn>2314-6141</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>RHX</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqFktFrFDEQxhdRbK0--aws-qZsm2Q32eRFWK7WFkoF0eeQTWbvcuwlZ5K9cv-9KVsPCweSh4TMb77JTL6ieIvROcaUXhCE8QVueMvqZ8UpxhhVLaH4-eHc1CfFqxjXCOGWM_GyOCGYtA2h_LTor_cmeLN3amN1eQmj3UHYl34oFyubfFSuuvKjSlBd3nXlnXJ-q0KyeoRYWlf-UCmW9zatys6sp51yqbpxZtJgyi6kVbDJxtfFi0GNEd487mfFr6uvPxfX1e33bzeL7rbSlIlUMcqFoKJVHJgwWPUDBSF6I4RGmKCaKc5wT3TL-6Y2CAwIRg2gdlAMtwLVZ8WXWXc79RswGlwKapTbYDcq7KVXVj6NOLuSS7-TNSIEc5YFPjwKBP97gpjk2k_B5TdLThnJIxNthj7O0FKNIK0bfNbSGxu17AhjjAjR4kxVR6glOMiFvYPB5usn_PkRPi8D-V-OJnyeE3TwMQYYDn1iJB9sIR9sIWdbZPr9v6M5sH99kIFPM7Cyzqh7-x-1dzMMGYFBHeCmEazh9R_FYse6</recordid><startdate>20110101</startdate><enddate>20110101</enddate><creator>Fernandes, Julio C.</creator><creator>Dai, Kerong</creator><creator>Zhang, Xiaoling</creator><creator>Winnik, Françoise M.</creator><creator>Qiu, Xingping</creator><creator>Tran, Covi</creator><creator>Wang, Huijie</creator><creator>Shi, Qin</creator><creator>Benderdour, Mohamed</creator><general>Hindawi Puplishing Corporation</general><general>Hindawi Publishing Corporation</general><general>John Wiley & Sons, Inc</general><general>Hindawi Limited</general><scope>ADJCN</scope><scope>AHFXO</scope><scope>RHU</scope><scope>RHW</scope><scope>RHX</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>3V.</scope><scope>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>CWDGH</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope></search><sort><creationdate>20110101</creationdate><title>Hydrodynamic Delivery of Chitosan-Folate-DNA Nanoparticles in Rats with Adjuvant-Induced Arthritis</title><author>Fernandes, Julio C. ; Dai, Kerong ; Zhang, Xiaoling ; Winnik, Françoise M. ; Qiu, Xingping ; Tran, Covi ; Wang, Huijie ; Shi, Qin ; Benderdour, Mohamed</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c569t-65899597a8e69d1abf5e99bd99c012036a861b2c78b43d0ede965de07fa617903</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Analysis of Variance</topic><topic>Animals</topic><topic>Arthritis</topic><topic>Arthritis, Experimental - genetics</topic><topic>Arthritis, Experimental - metabolism</topic><topic>Arthritis, Experimental - therapy</topic><topic>beta-Galactosidase - biosynthesis</topic><topic>beta-Galactosidase - genetics</topic><topic>Cancer</topic><topic>Care and treatment</topic><topic>Chitin</topic><topic>Chitosan - administration & dosage</topic><topic>Dinoprostone - metabolism</topic><topic>Disease Models, Animal</topic><topic>DNA - administration & dosage</topic><topic>DNA - genetics</topic><topic>Drug Delivery Systems - methods</topic><topic>Female</topic><topic>Folic Acid - administration & dosage</topic><topic>Freund's Adjuvant - administration & dosage</topic><topic>Gene expression</topic><topic>Gene therapy</topic><topic>Genetic aspects</topic><topic>Histocytochemistry</topic><topic>Humans</topic><topic>Injections, Intravenous</topic><topic>Interleukin 1 Receptor Antagonist Protein - genetics</topic><topic>Interleukin 1 Receptor Antagonist Protein - metabolism</topic><topic>Interleukin-1beta - metabolism</topic><topic>Medical research</topic><topic>Muscle, Skeletal - 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Nanoparticles such as chitosan-DNA and folate-chitosan-DNA were prepared by coacervation process. The hydrodynamic intravenous injection of nanoparticles was performed in the right posterior paw in normal and arthritic rats. Our results demonstrated that the fluorescence intensity of DsRed detected was 5 to 12 times more in the right soleus muscle and in the right gastro muscle than other tissue sections. β-galactosidase gene expression with X-gal substrate and folate-chitosan-plasmid nanoparticles showed best coloration in the soleus muscle. Treated arthritic animals also showed a significant decrease in paw swelling and IL-1β and PGE2 concentration in serum compared to untreated rats. This study demonstrated that a nonviral gene therapeutic approach using hydrodynamic delivery could help transfect more efficiently folate-chitosan-DNA nanoparticles in vitro/in vivo and could decrease inflammation in arthritic rats.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Puplishing Corporation</pub><pmid>21274258</pmid><doi>10.1155/2011/148763</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analysis of Variance Animals Arthritis Arthritis, Experimental - genetics Arthritis, Experimental - metabolism Arthritis, Experimental - therapy beta-Galactosidase - biosynthesis beta-Galactosidase - genetics Cancer Care and treatment Chitin Chitosan - administration & dosage Dinoprostone - metabolism Disease Models, Animal DNA - administration & dosage DNA - genetics Drug Delivery Systems - methods Female Folic Acid - administration & dosage Freund's Adjuvant - administration & dosage Gene expression Gene therapy Genetic aspects Histocytochemistry Humans Injections, Intravenous Interleukin 1 Receptor Antagonist Protein - genetics Interleukin 1 Receptor Antagonist Protein - metabolism Interleukin-1beta - metabolism Medical research Muscle, Skeletal - metabolism Nanoconjugates - administration & dosage Nanoconjugates - chemistry Nanoparticles Nanoparticles - administration & dosage Nanoparticles - chemistry Physiological aspects Proteins Rats Rats, Inbred Lew Rodents Tarsus, Animal - pathology Tissue Distribution |
title | Hydrodynamic Delivery of Chitosan-Folate-DNA Nanoparticles in Rats with Adjuvant-Induced Arthritis |
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