Graphical abstract Figure. No Caption available. Abstract Although a variety of non‐viral gene delivery systems have been developed, they still suffer from low efficiency and specificity. Herein, we present the… Click to show full abstract
Graphical abstract Figure. No Caption available. Abstract Although a variety of non‐viral gene delivery systems have been developed, they still suffer from low efficiency and specificity. Herein, we present the assembly of a dendrimer complex comprising a DNA cargo and a targeting moiety as a new format for targeted gene delivery. A PAMAM dendrimer modified with histidine and arginine (HR‐dendrimer) was used to enhance the endosomal escape and transfection efficiency. An EGFR‐specific repebody, composed of leucine‐rich repeat (LRR) modules, was employed as a targeting moiety. A polyanionic peptide was genetically fused to the repebody, followed by incubation with an HR‐dendrimer and a DNA cargo to assemble the dendrimer complex through an electrostatic interaction. The resulting dendrimer complex was shown to deliver a DNA cargo with high efficiency in a receptor‐specific manner. An analysis using a confocal microscope confirmed the internalization of the dendrimer complex and subsequent dissociation of a DNA cargo from the complex. The present approach can be broadly used in a targeted gene delivery in many areas.
               
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