中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Nanoparticles bearing polyethyleneglycol-coupled transferrin as gene carriers: preparation and in vitro evaluation

文献类型:期刊论文

作者Li, YP; Ogris, M; Wagner, E; Pelisek, J; Ruffer, M
刊名INTERNATIONAL JOURNAL OF PHARMACEUTICS
出版日期2003-06-18
卷号259期号:1-2页码:93-101
关键词pDNA nanoparticles transferrin polyethylene glycol poly(cyanoacrylate)
ISSN号0378-5173
DOI10.1016/S0378-5173(03)00211-4
文献子类Article
英文摘要The aims of this work were to determine the stability of pDNA against various conditions during microencapsulation, prepare transferrin (TF)-conjugated PEGylated polycyanoacrylate nanoparticles (TF-PEG-nanoparticles), and assess its physicochemical characteristics and in vitro targeting cells association. The open circular forms of pDNA obviously increased when pDNA was emulsified into organic solution under sonification. When pDNA solution (pH 7.0) contained 1, 3 or 5% (w/v) PVA, after sonification, average 48.2, 59.4 and 62.1% of double-supercoiled DNA (dsDNA) were preserved, respectively. When medium of pDNA was 0.9% NaCl (pH 7.0), 0.1 M NaHCO3 (pH 8.0) or phosphate buffer (pH 8.0), average 53.1, 69.3 and 56.9% of dsDNA remained after sonification, respectively. Poly(aminopoly(ethylene glycol)cyanoacrylate-co-hexadecyl cyanoacrylate) (poly(H(2)NPEGCA-co-HDCA)) showed a slight influence on pDNA in 0.1 M NaHCO3 (pH 8.0) when its concentration increased from 0.5 to 4% (w/v). TF-PEG-nanoparticles loading pDNA were spherical in shape with size under 200 nm and entrapment efficiency 35-50%. 0.1 M NaHCO3 with 3% PVA (w/v) could largely reduce the damage of pDNA during microencapsulation. TF-PEG-nanoparticles bore 1-3% of the total PEG chains conjugated to TF molecules, and exhibited the burst effect with over 30% drug release within I day. After the first phase, pDNA release profiles displayed a sustained release. The amount of cumulated pDNA release over 7 days was: 86.3, 81.5 and 74.4% for 1, 2 and 4% polymer nanoparticles, respectively. The degree of target K562 cell binding of TF-PEG-nanoparticles was greater than that of non-targeted PEG-nanoparticles at 4 degreesC. The presence of free TF decreased significantly the degree of cell binding of TF-PEG-nanoparticles, which revealed that the binding of TF-PEG-nanoparticles to K562 cells was indeed receptor specific. These results suggested that TF-PEG-nanoparticles were useful for delivery of pDNA to target cells. (C) 2003 Elsevier Science B.V. All rights reserved.
WOS关键词FACTOR-ALPHA CARRIERS ; PLASMID DNA ; IN-VIVO ; POLYCYANOACRYLATE NANOPARTICLES ; DEOXYRIBONUCLEIC ACID ; PROTEIN CARRIERS ; DELIVERY ; LIPOSOMES ; RECEPTOR ; RELEASE
WOS研究方向Pharmacology & Pharmacy
语种英语
WOS记录号WOS:000183510300009
出版者ELSEVIER SCIENCE BV
源URL[http://119.78.100.183/handle/2S10ELR8/274218]  
专题中国科学院上海药物研究所
通讯作者Li, YP
作者单位1.Univ Munich, Ctr Drug Res, Dept Pharm, D-81377 Munich, Germany
2.Chinese Acad Sci, Shanghai Inst Biol Sci, Inst Mat Med, Shanghai 200031, Peoples R China
推荐引用方式
GB/T 7714
Li, YP,Ogris, M,Wagner, E,et al. Nanoparticles bearing polyethyleneglycol-coupled transferrin as gene carriers: preparation and in vitro evaluation[J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS,2003,259(1-2):93-101.
APA Li, YP,Ogris, M,Wagner, E,Pelisek, J,&Ruffer, M.(2003).Nanoparticles bearing polyethyleneglycol-coupled transferrin as gene carriers: preparation and in vitro evaluation.INTERNATIONAL JOURNAL OF PHARMACEUTICS,259(1-2),93-101.
MLA Li, YP,et al."Nanoparticles bearing polyethyleneglycol-coupled transferrin as gene carriers: preparation and in vitro evaluation".INTERNATIONAL JOURNAL OF PHARMACEUTICS 259.1-2(2003):93-101.

入库方式: OAI收割

来源:上海药物研究所

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