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基于低分子量聚乙烯亚胺和油酸的负电性基因载体(英文) 被引量:1

Negatively Charged Lipopolyplex for Gene Delivery Based on Low-Molecular-Weight Polyethylenimine and Oleic Acid
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摘要 构建负电性的基因载体、发展基于低分子量聚乙烯亚胺(PEI)的基因载体对基因传递研究具有重要意义.本文基于低分子量聚乙烯亚胺(2 kDa)和油酸构建了负电性的基因载体.它通过混合聚乙烯亚胺(2 kDa)、dsDNA和油酸胶束而自发形成.该基因载体在血清中很稳定,细胞毒性非常低,可包封80%以上DNA.通过1,2-二硬脂酰-sn-甘油-3-磷酸乙醇胺-N-[甲氧基(聚乙二醇2000)]铵盐(DSPE-PEG)对其表面进行修饰,发现多达90%的基因可被细胞摄取. The development of synthetic vectors based on low-molecular-weight polyethylenimine (PEI) and the construction of negatively charged vectors with high nucleic acid encapsulation are two of the current research trends in gene delivery. In the present study, we developed a stable and negatively charged lipopolyplex based on oleic acid and a low-molecular-weight PEI (2 kDa); it was formed by simultaneously mixing oleic acid micelles and a polyplex produced from PEI (2 kDa) and oligo dsDNA. This lipopolyplex is stable in serum, and because of the low molecular weight of the PEI, the lipopolyplex exhibits very low toxicity. The encapsulation efficiencies of nucleic acids by traditional anionic vectors are low, but very high (more than 80%) by this lipopolyplex. Suitable surface modification with 1,2-distearoryl-sn-glycero-3-phosphoethanolamine-N-methoxy(polyethyleneglycol-2000) ammonium salt enabled the lipopolyplex to bind to cells, and a high cellular uptake efficiency (ca 90%) was observed in vitro.
作者 杨阳 郭霞
出处 《物理化学学报》 SCIE CAS CSCD 北大核心 2014年第2期345-350,共6页 Acta Physico-Chimica Sinica
基金 supported by the National Natural Science Foundation of China(21073155,21373179) NIH grants,USA(CA129835,CA149363,CA151652,CA129421)~~
关键词 聚乙烯亚胺 油酸 基因传递 Polyethylenimine Oleicacid Gene delivery
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  • 1Xu, L.; Anchordoquy, T. J. Pharmaceutical Sci. 2011,100,38. doi: 10.1002/jps.22243.
  • 2Malam, Y.; Lim, E. J.; Seifalian, A. M. Current MedicinalChemistry 2011,18,1067. doi: 10.2174/092986711794940860.
  • 3Guo, X.; Huang, L. Accounts of Chemical Research 2012,45,971. doi: 10.1021/ar200151m.
  • 4Boussif, O.; Lezoualc,h,F.; Zanta, M. A.; Mergny, M. D.;Scherman, D.; Demeneix,B.; Behr, J. P. Proc. Natl. Acad. Sci.U. S. A. 1995, 92, 7297. doi: 10.1073/pnas.92.16.7297.
  • 5Godbey, W. T.; Barry, M. A.; Saggau, P.; Wu, K. K.; Mikos, A.G. J、Biomed Mater. Res. 2000,51y 321.
  • 6Bonner, D. K.; Zhao, X.; Buss, H.; Langer, R.; Hammond, P. T.J. Control. Release 2013,167, 101. doi: 10.1016/j.jconrel.2012.09.004.
  • 7Mahato, M.; Kumar, P.; Sharma, A. K. Molecular Biosystems2013,9, 780. doi: 10.1039/c3mb25444e.
  • 8Patnaik, S.; Gupta, K. C. Expert Opinion on Drug Delivery2013,10, 215. doi: 10.1517/17425247.2013.744964.
  • 9Ogris,M.; Walker, G.; Blessing, T.; Kircheis, R.; Wolschek, M.;Wagner, E. J. Control. Release 2003,91, 173. doi: 10.1016/S0168-3659(03)00230-X.
  • 10Urban-Klein, B.; Werth, S.; Abuharbeid, S.; Czubayko, F.;Aigner, A. Gene Therapy 2005,12, 461. doi: 10.1038/sj.gt.3302425.

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