A Charge Reversible Self‐Delivery Chimeric Peptide with Cell Membrane‐Targeting Properties for Enhanced Photodynamic Therapy. (2nd May 2017)

• Record Type: Journal Article
• Authors: Liu, Li‐Han; Qiu, Wen‐Xiu; Zhang, Yao‐Hui; Li, Bin; Zhang, Chi; Gao, Fan; Zhang, Lu; Zhang, Xian‐Zheng
• Is Part Of: Advanced functional materials. Volume 27:Number 25(2017)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2017-05-02
• Subjects: charge reversible peptides -- chimeric peptides -- membrane targets -- photodynamic therapy -- self‐delivery; Materials -- Periodicals; Chemical vapor deposition -- Periodicals; 620.11
• DOI: 10.1002/adfm.201700220
• Languages: English
• ISSNs: 1616-301X

Abstract

Abstract : The cell membrane is the most important protective barrier in living cells and cell membrane targeted therapy may be a high‐performance therapeutic modality for tumor treatment. Here, a novel charge reversible self‐delivery chimeric peptide C16 –PRP–DMA is developed for long‐term cell membrane targeted photodynamic therapy (PDT). The self‐assembled C16 –PRP–DMA nanoparticles can effectively target to tumor by enhanced permeability and retention effect without additional carriers. After undergoing charge reverse in acidic tumor microenvironment, C16 –PRP–DMA inserts into the tumor cell membrane with a long retention time of more than 14 h, which is very helpful for in vivo applications. It is found that under light irradiation, the reactive oxygen species generated by the inserted C16 –PRP–DMA would directly disrupt cell membrane and rapidly induce cell necrosis, which remarkably increases the PDT effect in vitro and in vivo. This novel self‐delivery chimeric peptide with a long‐term cell membrane targeting property provides a new prospect for effective PDT of cancer. Abstract : An easy‐to‐fabricate charge reversible self‐delivery chimeric peptide is developed to realize cell membrane targeted photodynamic therapy (PDT). Under light irradiation, C16 ––PRP–DMA can directly disrupt the cell membrane and rapidly induce cell necrosis, which remarkably increases the PDT effect.