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Article: Octaarginine-modified chitosan as a nonviral gene delivery vector: Properties and in vitro transfection efficiency
Title | Octaarginine-modified chitosan as a nonviral gene delivery vector: Properties and in vitro transfection efficiency | ||||||||
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Authors | |||||||||
Keywords | Chitosan Gene delivery Nanomedicine Octaarginine | ||||||||
Issue Date | 2011 | ||||||||
Publisher | Springer Verlag Dordrecht. The Journal's web site is located at http://springerlink.metapress.com/openurl.asp?genre=journal&issn=1388-0764 | ||||||||
Citation | Journal Of Nanoparticle Research, 2011, v. 13 n. 2, p. 693-702 How to Cite? | ||||||||
Abstract | Protein transduction domains (PTD) have been identified to have the capacity to facilitate molecular cargo to translocate through cell membrane. This study aims to utilize the cell membrane penetrating ability of octaarginine oligopeptide, a simplified prototype of the PTD, to enhance the transfection efficiency of chitosan. Octaarginine-modified chitosan (R 8-CS) was synthesized as a gene transfer carrier by carbodiimide chemistry. The structure and composition of R 8-CSs were characterized using FTIR and 1H NMR. Agarose gel electrophoresis assay showed that R 8-CS could efficiently condense the DNA. The particle size of R 8-CS/DNA complexes were determined to be around 100-200 nm. The nanoparticle complexes exhibited a spherical and compact morphology. R 8-CS demonstrated higher transfection activity and lower cytotoxicity as compared to the unmodified chitosan and also showed good serum resistance. © Springer Science+Business Media B.V. 2010. | ||||||||
Persistent Identifier | http://hdl.handle.net/10722/157634 | ||||||||
ISSN | 2023 Impact Factor: 2.1 2023 SCImago Journal Rankings: 0.416 | ||||||||
ISI Accession Number ID |
Funding Information: This project was partially supported by Hong Kong RGC (HKU7147/07E) and Hong Kong Innovation Technology Commission ITF-GHP 009-06. The authors also acknowledge the support from HKU Seed Funding Programme (200811159133). | ||||||||
References | |||||||||
Grants |
DC Field | Value | Language |
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dc.contributor.author | Zhao, X | en_HK |
dc.contributor.author | Li, Z | en_HK |
dc.contributor.author | Liu, W | en_HK |
dc.contributor.author | Lam, W | en_HK |
dc.contributor.author | Sun, P | en_HK |
dc.contributor.author | Kao, RYT | en_HK |
dc.contributor.author | Luk, KDK | en_HK |
dc.contributor.author | Lu, WW | en_HK |
dc.date.accessioned | 2012-08-08T08:51:50Z | - |
dc.date.available | 2012-08-08T08:51:50Z | - |
dc.date.issued | 2011 | en_HK |
dc.identifier.citation | Journal Of Nanoparticle Research, 2011, v. 13 n. 2, p. 693-702 | en_HK |
dc.identifier.issn | 1388-0764 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/157634 | - |
dc.description.abstract | Protein transduction domains (PTD) have been identified to have the capacity to facilitate molecular cargo to translocate through cell membrane. This study aims to utilize the cell membrane penetrating ability of octaarginine oligopeptide, a simplified prototype of the PTD, to enhance the transfection efficiency of chitosan. Octaarginine-modified chitosan (R 8-CS) was synthesized as a gene transfer carrier by carbodiimide chemistry. The structure and composition of R 8-CSs were characterized using FTIR and 1H NMR. Agarose gel electrophoresis assay showed that R 8-CS could efficiently condense the DNA. The particle size of R 8-CS/DNA complexes were determined to be around 100-200 nm. The nanoparticle complexes exhibited a spherical and compact morphology. R 8-CS demonstrated higher transfection activity and lower cytotoxicity as compared to the unmodified chitosan and also showed good serum resistance. © Springer Science+Business Media B.V. 2010. | en_HK |
dc.language | eng | en_US |
dc.publisher | Springer Verlag Dordrecht. The Journal's web site is located at http://springerlink.metapress.com/openurl.asp?genre=journal&issn=1388-0764 | en_HK |
dc.relation.ispartof | Journal of Nanoparticle Research | en_HK |
dc.subject | Chitosan | en_HK |
dc.subject | Gene delivery | en_HK |
dc.subject | Nanomedicine | en_HK |
dc.subject | Octaarginine | en_HK |
dc.title | Octaarginine-modified chitosan as a nonviral gene delivery vector: Properties and in vitro transfection efficiency | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Kao, RYT:rytkao@hkucc.hku.hk | en_HK |
dc.identifier.email | Luk, KDK:hcm21000@hku.hk | en_HK |
dc.identifier.email | Lu, WW:wwlu@hku.hk | en_HK |
dc.identifier.authority | Kao, RYT=rp00481 | en_HK |
dc.identifier.authority | Luk, KDK=rp00333 | en_HK |
dc.identifier.authority | Lu, WW=rp00411 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1007/s11051-010-0067-3 | en_HK |
dc.identifier.scopus | eid_2-s2.0-79956153879 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-79956153879&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 13 | en_HK |
dc.identifier.issue | 2 | en_HK |
dc.identifier.spage | 693 | en_HK |
dc.identifier.epage | 702 | en_HK |
dc.identifier.isi | WOS:000287860200024 | - |
dc.publisher.place | Netherlands | en_HK |
dc.relation.project | Guanidinylated polyethylenimine (PEI) as nano nonviral vector to transfer human umbilical cord mesenchymal stem cells (UC-hMSC) with BMP2 gene for bone formation | - |
dc.identifier.scopusauthorid | Zhao, X=39162273900 | en_HK |
dc.identifier.scopusauthorid | Li, Z=35784563200 | en_HK |
dc.identifier.scopusauthorid | Liu, W=7408473555 | en_HK |
dc.identifier.scopusauthorid | Lam, W=13403256300 | en_HK |
dc.identifier.scopusauthorid | Sun, P=35254303000 | en_HK |
dc.identifier.scopusauthorid | Kao, RYT=7101675499 | en_HK |
dc.identifier.scopusauthorid | Luk, KDK=7201921573 | en_HK |
dc.identifier.scopusauthorid | Lu, WW=7404215221 | en_HK |
dc.identifier.citeulike | 7815357 | - |
dc.identifier.issnl | 1388-0764 | - |