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- Publisher Website: 10.1016/j.biomaterials.2009.06.051
- Scopus: eid_2-s2.0-68549136489
- PMID: 19615741
- WOS: WOS:000270115200060
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Article: The gene transfection efficiency of a folate-PEI600-cyclodextrin nanopolymer
Title | The gene transfection efficiency of a folate-PEI600-cyclodextrin nanopolymer | ||||||
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Authors | |||||||
Keywords | β-Cyclodextrin Biodegradation Folate Gene therapy In vivo test Polyethylenimine | ||||||
Issue Date | 2009 | ||||||
Publisher | Elsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/biomaterials | ||||||
Citation | Biomaterials, 2009, v. 30 n. 29, p. 5793-5803 How to Cite? | ||||||
Abstract | The success of gene therapy relies on a safe and effective gene delivery system. In this communication, we describe the use of folate grafted PEI 600-CyD (H 1) as an effective polyplex-forming plasmid delivery agent with low toxicity. The structures of the polymer and polyplex were characterized, and the in vitro transfection efficiency, cytotoxicity, and in vivo transfection of H 1 were examined. We found that folate molecules were successfully grafted to PEI 600-CyD. At N/P ratios between 5 and 30, the resulting H 1/DNA polyplexes had diameters less than 120 nm and zeta potentials less than 10 mV. In various tumor cell lines examined (U138, U87, B16, and Lovo), the in vitro transfection efficiency of H 1 was more than 50%, which could be improved by the presence of fetal bovine serum or albumin. The cytotoxicity of H 1 was significantly less than high molecular weight PEI-25 kDa. Importantly, in vivo optical imaging showed that the efficiency of H 1-mediated transfection (50 μg luciferase plasmid (pLuc), N/P ratio = 20/1) was comparable to that of adenovirus-mediated luciferase transduction (1 × 10 9 pfu) in melanoma-bearing mice, and it did not induce any toxicity in the tumor tissue. These results clearly show that H 1 is a safe and effective polyplex-forming agent for both in vitro and in vivo transfection of plasmid DNA and its application warrants further investigation. © 2009 Elsevier Ltd. All rights reserved. | ||||||
Persistent Identifier | http://hdl.handle.net/10722/69106 | ||||||
ISSN | 2023 Impact Factor: 12.8 2023 SCImago Journal Rankings: 3.016 | ||||||
ISI Accession Number ID |
Funding Information: We would like to thank Wing-Fu Lai and Ka-Chun William Cheung for critical reading of the manuscript, King-Sun Siu for support in chemical synthesis, Fang Yu and Gao Yi for support in vitro experiments, Zan Shen and Long-Fei Huo for support in animal experiments. This work was supported by the Focus Budget Scheme project at the Chinese University of Hong Kong (Project PI: Hsiangfu Kung) and the National Nature Science Foundation of China (30571068). | ||||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Yao, H | en_HK |
dc.contributor.author | Ng, SS | en_HK |
dc.contributor.author | Tucker, WO | en_HK |
dc.contributor.author | Tsang, YKT | en_HK |
dc.contributor.author | Man, K | en_HK |
dc.contributor.author | Wang, Xm | en_HK |
dc.contributor.author | Chow, BKC | en_HK |
dc.contributor.author | Kung, HF | en_HK |
dc.contributor.author | Tang, GP | en_HK |
dc.contributor.author | Lin, MC | en_HK |
dc.date.accessioned | 2010-09-06T06:10:37Z | - |
dc.date.available | 2010-09-06T06:10:37Z | - |
dc.date.issued | 2009 | en_HK |
dc.identifier.citation | Biomaterials, 2009, v. 30 n. 29, p. 5793-5803 | en_HK |
dc.identifier.issn | 0142-9612 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/69106 | - |
dc.description.abstract | The success of gene therapy relies on a safe and effective gene delivery system. In this communication, we describe the use of folate grafted PEI 600-CyD (H 1) as an effective polyplex-forming plasmid delivery agent with low toxicity. The structures of the polymer and polyplex were characterized, and the in vitro transfection efficiency, cytotoxicity, and in vivo transfection of H 1 were examined. We found that folate molecules were successfully grafted to PEI 600-CyD. At N/P ratios between 5 and 30, the resulting H 1/DNA polyplexes had diameters less than 120 nm and zeta potentials less than 10 mV. In various tumor cell lines examined (U138, U87, B16, and Lovo), the in vitro transfection efficiency of H 1 was more than 50%, which could be improved by the presence of fetal bovine serum or albumin. The cytotoxicity of H 1 was significantly less than high molecular weight PEI-25 kDa. Importantly, in vivo optical imaging showed that the efficiency of H 1-mediated transfection (50 μg luciferase plasmid (pLuc), N/P ratio = 20/1) was comparable to that of adenovirus-mediated luciferase transduction (1 × 10 9 pfu) in melanoma-bearing mice, and it did not induce any toxicity in the tumor tissue. These results clearly show that H 1 is a safe and effective polyplex-forming agent for both in vitro and in vivo transfection of plasmid DNA and its application warrants further investigation. © 2009 Elsevier Ltd. All rights reserved. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Elsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/biomaterials | en_HK |
dc.relation.ispartof | Biomaterials | en_HK |
dc.subject | β-Cyclodextrin | en_HK |
dc.subject | Biodegradation | en_HK |
dc.subject | Folate | en_HK |
dc.subject | Gene therapy | en_HK |
dc.subject | In vivo test | en_HK |
dc.subject | Polyethylenimine | en_HK |
dc.subject.mesh | Cyclodextrins - administration and dosage - chemistry - pharmacokinetics | - |
dc.subject.mesh | DNA - administration and dosage - chemistry - pharmacokinetics | - |
dc.subject.mesh | Drug Carriers - chemistry | - |
dc.subject.mesh | Imines - chemistry | - |
dc.subject.mesh | Melanoma - drug therapy - genetics - metabolism | - |
dc.title | The gene transfection efficiency of a folate-PEI600-cyclodextrin nanopolymer | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0142-9612&volume=30&issue=29&spage=5793&epage=5803&date=2009&atitle=The+gene+transfection+efficiency+of+a+folate-PEI600-cyclodextrin+nanopolymer | en_HK |
dc.identifier.email | Ng, SS: ssmng@hku.hk | en_HK |
dc.identifier.email | Man, K: kwanman@hku.hk | en_HK |
dc.identifier.email | Chow, BKC: bkcc@hku.hk | en_HK |
dc.identifier.email | Lin, MC: mcllin@hkucc.hku.hk | en_HK |
dc.identifier.authority | Ng, SS=rp00767 | en_HK |
dc.identifier.authority | Man, K=rp00417 | en_HK |
dc.identifier.authority | Chow, BKC=rp00681 | en_HK |
dc.identifier.authority | Lin, MC=rp00746 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.biomaterials.2009.06.051 | en_HK |
dc.identifier.pmid | 19615741 | - |
dc.identifier.scopus | eid_2-s2.0-68549136489 | en_HK |
dc.identifier.hkuros | 168606 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-68549136489&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 30 | en_HK |
dc.identifier.issue | 29 | en_HK |
dc.identifier.spage | 5793 | en_HK |
dc.identifier.epage | 5803 | en_HK |
dc.identifier.isi | WOS:000270115200060 | - |
dc.publisher.place | Netherlands | en_HK |
dc.identifier.scopusauthorid | Yao, H=13104506400 | en_HK |
dc.identifier.scopusauthorid | Ng, SS=7403358718 | en_HK |
dc.identifier.scopusauthorid | Tucker, WO=40262670600 | en_HK |
dc.identifier.scopusauthorid | Tsang, YKT=34977619600 | en_HK |
dc.identifier.scopusauthorid | Man, K=7101754072 | en_HK |
dc.identifier.scopusauthorid | Wang, Xm=7501856296 | en_HK |
dc.identifier.scopusauthorid | Chow, BKC=7102826193 | en_HK |
dc.identifier.scopusauthorid | Kung, HF=7402514190 | en_HK |
dc.identifier.scopusauthorid | Tang, GP=7401634016 | en_HK |
dc.identifier.scopusauthorid | Lin, MC=7404816359 | en_HK |
dc.identifier.citeulike | 5372542 | - |
dc.identifier.issnl | 0142-9612 | - |