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Development of a non-viral multifunctional envelope-type nano device by a novel lipid film hydration method

机译:新型脂膜水合法的非病毒多功能包膜型纳米装置的研制

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The development of a multifunctional envelope-type nano device (MEND) for use in a non-viral gene delivery system using a novel lipid film hydration method is described. This packaging method involves three steps: (i) DNA condensation with a polycation, (ii) lipid film hydration for the electrostatic binding of the condensed DNA, and (iii) sonication to package the condensed DNA with lipids. For DNA condensation, the optimum ratio of DNA to poly-L-lysine (PLL) was determined by titrating DNA and PLL. The condensed DNA/PLL complex (DPC) was coated with a lipid bilayer by lipid film hydration followed by sonication, which was confirmed by sucrose density gradient centrifugation. Packaging of DPC with lipids increased the transfection activity 10-fold over that of DPC. MEND, having octaarginine on the envelope as a device for membrane penetration to enhance cellular uptake, showed a 1000-fold higher transfection activity than DPC. The MEND developed in this study represents a promising non-viral gene delivery system. (C) 2004 Elsevier B.V. All rights reserved.
机译:描述了一种用于使用新型脂膜水化方法的非病毒基因递送系统的多功能包膜型纳米装置(修补)的开发。该包装方法涉及三个步骤:(i)与聚阳离子的DNA缩合,(ii)脂肪膜水合用于静电结合的静电结合,(iii)超声处理用脂质包装稠合的DNA。对于DNA缩合,通过滴定DNA和PLL测定DNA与聚-L-赖氨酸(PLL)的最佳比率。通过脂膜水合用脂质膜水合涂覆凝聚的DNA / PLL复合物(DPC),然后通过蔗糖密度梯度离心证实。 DPC与脂质的包装增加了DPC的转染活性10倍。在封套上具有八曲脉的修补程序作为膜渗透以增强细胞摄取的装置,表现出比DPC高1000倍的转染活性。本研究开发的修复代表了有前途的非病毒基因递送系统。 (c)2004年elestvier b.v.保留所有权利。

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