Literature DB >> 27714148

Selective killing of cells triggered by their mRNA signature in the presence of smart nanoparticles.

Amelie Heuer-Jungemann1, Afaf H El-Sagheer2, Peter M Lackie3, Tom Brown4, Antonios G Kanaras5.   

Abstract

The design of nanoparticles that can selectively perform multiple roles is of utmost importance for the development of the next generation of nanoparticulate drug delivery systems. So far most research studies are focused on the customization of nanoparticulate carriers to maximize their drug loading, enhance their optical signature for tracking in cells or provide photo-responsive effects for therapeutic purposes. However, a vital requirement of the new generation of drug carriers must be the ability to deliver their payload selectively only to cells of interest rather than the majority of various cells in the vicinity. Here we show for the first time a new design of nanoparticulate drug carriers that can specifically distinguish different cell types based on their mRNA signature. These nanoparticles sense and efficiently kill model tumour cells by the delivery of an anti-cancer drug but retain their payload in cells lacking the specific mRNA target.

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Year:  2016        PMID: 27714148     DOI: 10.1039/c6nr06154k

Source DB:  PubMed          Journal:  Nanoscale        ISSN: 2040-3364            Impact factor:   7.790


  2 in total

Review 1.  DNA Nanostructures and DNA-Functionalized Nanoparticles for Cancer Theranostics.

Authors:  Fay Nicolson; Akbar Ali; Moritz F Kircher; Suchetan Pal
Journal:  Adv Sci (Weinh)       Date:  2020-10-15       Impact factor: 16.806

2.  Photocaged amplified FRET nanoflares: spatiotemporal controllable of mRNA-powered nanomachines for precise and sensitive microRNA imaging in live cells.

Authors:  Jing Li; Shiyuan Liu; Jiaoli Wang; Ruiting Liu; Xiaohai Yang; Kemin Wang; Jin Huang
Journal:  Nucleic Acids Res       Date:  2022-04-22       Impact factor: 19.160

  2 in total

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