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本文引用的文献

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Light-scattering techniques for characterization of synthetic gene therapy vectors.用于合成基因治疗载体表征的光散射技术
Methods Mol Med. 2001;65:349-76. doi: 10.1385/1-59259-139-6:349.
2
Non-viral gene delivery carrier and its three-dimensional transfection system.非病毒基因传递载体及其三维转染系统。
Int J Pharm. 2010 Feb 15;386(1-2):232-42. doi: 10.1016/j.ijpharm.2009.11.006. Epub 2009 Nov 14.
3
Balancing protection and release of DNA: tools to address a bottleneck of non-viral gene delivery.平衡 DNA 的保护与释放:解决非病毒基因传递瓶颈的工具。
J R Soc Interface. 2010 Feb 6;7 Suppl 1(Suppl 1):S67-82. doi: 10.1098/rsif.2009.0260. Epub 2009 Sep 4.
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Nanocarriers' entry into the cell: relevance to drug delivery.纳米载体进入细胞:与药物递送的相关性。
Cell Mol Life Sci. 2009 Sep;66(17):2873-96. doi: 10.1007/s00018-009-0053-z. Epub 2009 Jun 5.
5
Discarded free PEG-based assay for obtaining the modification extent of pegylated proteins.用于获取聚乙二醇化蛋白质修饰程度的废弃游离聚乙二醇检测法。
Talanta. 2007 Jan 15;71(1):381-4. doi: 10.1016/j.talanta.2006.04.010. Epub 2006 May 16.
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Nonviral vectors for gene delivery.用于基因递送的非病毒载体。
Chem Rev. 2009 Feb;109(2):259-302. doi: 10.1021/cr800409e.
7
Quantitative comparison of intracellular unpacking kinetics of polyplexes by a model constructed from quantum dot-FRET.通过基于量子点-荧光共振能量转移构建的模型对多聚体的细胞内解包动力学进行定量比较。
Mol Ther. 2008 Feb;16(2):324-32. doi: 10.1038/sj.mt.6300392. Epub 2008 Jan 8.
8
Gene therapy clinical trials worldwide to 2007--an update.截至2007年全球基因治疗临床试验——最新情况
J Gene Med. 2007 Oct;9(10):833-42. doi: 10.1002/jgm.1100.
9
Preparation of N-succinimidyl 3-[*I]iodobenzoate: an agent for the indirect radioiodination of proteins.N-琥珀酰亚胺基-3-[¹²⁵I]碘苯甲酸酯的制备:一种用于蛋白质间接放射性碘化的试剂。
Nat Protoc. 2006;1(2):707-13. doi: 10.1038/nprot.2006.99.
10
Overall interaction of cytosolic proteins with the PEI/DNA complex.胞质蛋白与聚乙烯亚胺/DNA复合物的整体相互作用。
J Control Release. 2007 Apr 23;118(3):364-9. doi: 10.1016/j.jconrel.2006.12.027. Epub 2007 Jan 9.

与转染效率相关的基于 PEI 的聚电解质纳米粒的性质。

Properties of PEI-based polyplex nanoparticles that correlate with their transfection efficacy.

机构信息

Department of Molecular Genetics of Intracellular Transport, Institute of Gene Biology, RAS, Moscow, Russia.

出版信息

Mol Ther. 2011 Jan;19(1):103-12. doi: 10.1038/mt.2010.233. Epub 2010 Nov 2.

DOI:10.1038/mt.2010.233
PMID:21045811
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3017456/
Abstract

We have evaluated the key properties of the polyethylenimine (PEI)-polyethylene glycol (PEG)-TAT peptide polyplex nanoparticles including their behavior in cells and compared them with the transfection efficacy (TE) using 11 different cell lines. We found statistically significant positive correlation between TE and the share of 50-75 nm fraction in the whole mixture of nanoparticles estimated with atomic force microscopy. Variations in PEG/PEI and N/P ratios (PEI nitrogen to DNA phosphate ratio) enabled us to find their optimal combinations, which resulted in up to 100% TE for several cell lines. Surfaces of the TE dependence of both PEG/PEI and N/P turned out to be similar in appearance for all investigated cell lines, while maximum TEs were different. We investigated subcellular transport kinetics and unpacking of the polyplex nanoparticles labeled with quantum dots (plasmid DNA) and AlexaFluor647 (block-copolymer part) using Förster Resonance Energy Transfer approach. The results demonstrated clear and statistically significant positive correlation of TE with the cellular uptake rate of the nanoparticles and negative correlation with the rate constant of their unpacking within endo/lysosomal compartments in the living cells.

摘要

我们评估了聚乙烯亚胺(PEI)-聚乙二醇(PEG)-TAT 肽聚合物纳米粒的关键性质,包括它们在细胞中的行为,并将其与使用 11 种不同细胞系的转染效率(TE)进行了比较。我们发现,使用原子力显微镜估计的整个纳米颗粒混合物中 50-75nm 部分的比例与 TE 之间存在统计学上显著的正相关。PEG/PEI 和 N/P 比(PEI 氮与 DNA 磷酸比)的变化使我们能够找到最佳组合,这导致几种细胞系的 TE 高达 100%。对于所有研究的细胞系,PEG/PEI 和 N/P 的 TE 依赖性表面在外观上似乎相似,而最大 TE 则不同。我们使用Förster 共振能量转移方法研究了用量子点(质粒 DNA)和 AlexaFluor647(嵌段共聚物部分)标记的聚合物纳米粒的亚细胞转运动力学和解包。结果表明,TE 与纳米颗粒的细胞摄取率之间存在明显且统计学上显著的正相关,与活细胞内内体/溶酶体隔间中纳米颗粒的解包速率常数之间存在负相关。