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Selective killing of cells triggered by their mRNA signature in the presence of smart nanoparticles.
Heuer-Jungemann, Amelie; El-Sagheer, Afaf H; Lackie, Peter M; Brown, Tom; Kanaras, Antonios G.
Affiliation
  • Heuer-Jungemann A; Physics and Astronomy, Faculty of Physical Sciences and Engineering, UK.
  • El-Sagheer AH; Department of Chemistry, University of Oxford, Chemistry Research Laboratory, 12 Mansfield Road, Oxford, OX1 3TA, UK and Chemistry Branch, Department of Science and Mathematics, Faculty of Petroleum and Mining Engineering, Suez University, Suez 43721, Egypt.
  • Lackie PM; Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, SO16 6YD, UK.
  • Brown T; Department of Chemistry, University of Oxford, Chemistry Research Laboratory, 12 Mansfield Road, Oxford, OX1 3TA, UK.
  • Kanaras AG; Physics and Astronomy, Faculty of Physical Sciences and Engineering, UK and Institute for Life Sciences, University of Southampton, Southampton, SO171BJ, UK. A.Kanaras@soton.ac.uk.
Nanoscale ; 8(38): 16857-16861, 2016 Sep 29.
Article in En | MEDLINE | ID: mdl-27714148
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.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: RNA, Messenger / Drug Carriers / Nanoparticles / Antineoplastic Agents Limits: Humans Language: En Journal: Nanoscale Year: 2016 Document type: Article Affiliation country:
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: RNA, Messenger / Drug Carriers / Nanoparticles / Antineoplastic Agents Limits: Humans Language: En Journal: Nanoscale Year: 2016 Document type: Article Affiliation country:
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