Advances in targeted delivery of small interfering RNA using simple bioconjugates

Publikation: Bidrag til tidsskrift/Konferencebidrag i tidsskrift /Bidrag til avisReviewForskningpeer review

  • Christoffer Nielsen, The Finsen Laboratory, Copenhagen University Hospital
  • ,
  • Jørgen Kjems
  • Kristine Rothaus Sorensen, Department of Veterinary Disease Biology, University of Copenhagen, Graduate School of Health and Medical Sciences, Danmark
  • Lars Henning Engelholm, The Finsen Laboratory, Copenhagen University Hospital, Danmark
  • Niels Behrendt, The Finsen Laboratory, Copenhagen University Hospital, Danmark
Introduction: Development of drugs based on RNA interference by small interfering RNA (siRNA) has been progressing slowly due to a number of challenges associated with the in vivo behavior of siRNA. A central problem is controlling siRNA delivery to specific cell types. Here, we review existing literature on one type of strategy for solving the issue of cell-specific delivery of siRNA, namely delivering the siRNA as part of simple bioconjugate constructs.

Areas covered: This review presents current experience from strategies aimed at targeting siRNA to specific cell types, by associating the siRNA with a targeting moiety, in a simple bioconjugate construct. We discuss the use of different types of targeting moieties, as well as the different conjugation strategies employed for preparing these bioconjugate constructs that deliver the siRNA to target cells. We focus especially on the in-built or passive functionalities associated with each strategy, in order to identify key elements of successful siRNA delivery strategies with potential for further exploration.

Expert opinion: By evaluating the current literature on this subject, we identify strategies and concepts that are suitable for future studies, to enable the development of highly efficient simple bioconjugates for targeted siRNA delivery with therapeutic application.
OriginalsprogEngelsk
TidsskriftExpert Opinion on Drug Delivery
Vol/bind11
Nummer5
Sider (fra-til)791-822
Antal sider32
ISSN1742-5247
DOI
StatusUdgivet - 1 jan. 2014

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