Transfection and intracellular trafficking properties of carbon dot-gold nanoparticle molecular assembly conjugated with PEI-pDNA

聚乙烯亚胺 转染 基因传递 材料科学 纳米材料 荧光 生物物理学 纳米颗粒 生物相容性 纳米技术 细胞内 共轭体系 胶体金 荧光显微镜 聚合物 化学 生物 生物化学 物理 基因 复合材料 冶金 量子力学
作者
Jinhwan Kim,Juhee Park,Hyunwoo Kim,Kaushik Singha,Won Jong Kim
出处
期刊:Biomaterials [Elsevier BV]
卷期号:34 (29): 7168-7180 被引量:167
标识
DOI:10.1016/j.biomaterials.2013.05.072
摘要

The work employs carbon dot (CD) which has been emerging as a fluorescent nanomaterial with excellent biocompatibility and perceived as a promising alternative to quantum dot (QD), to monitor the association/dissociation of polymeric carrier/plasmid DNA (pDNA) complex during transfection. To shed light on the underlying post-endosomal events and provide the insight to design rational and efficient gene delivery vector, the adopted strategy exploited the quenching of the fluorescence of CD by Au nanoparticles. The surface of CD and Au was modified with highly cationic polymer, polyethylenimine (PEI) and subsequent treatment with non-labeled pDNA gave rise to quenched delivery complex. High salt concentration triggered the dissociation of the complex with accompanied fluorescence recovery arising due to the increase in distance between CD and Au. The studies revealed the potential of the developed CD-PEI/Au-PEI/pDNA ternary nano-assembly as a highly efficient hybrid transfecting agent with high cell viability under the optimum condition. The changes occurred at the intracellular level during transfection especially post-endosomal step were monitored by fluorescence measurement using fluorescence microscope. This nano-assembly system was found to be very effective at monitoring the carrier/pDNA dissociation in a non-labeled manner, thus provides efficient strategy to study the mechanistic aspect of polymer-mediated pDNA delivery.
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