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Safety profile of RNAi nanomedicines

Journal

ADVANCED DRUG DELIVERY REVIEWS
Volume 64, Issue 15, Pages 1730-1737

Publisher

ELSEVIER
DOI: 10.1016/j.addr.2012.06.007

Keywords

Small interfering RNA; Nanotoxicology; SNALP; Preclinical toxicology; Immunostimulation; Complement activation

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The emerging class of RNA interference (RNAi) therapeutics is a fundamentally novel approach to treating human disease by enabling the pursuit of molecular targets considered undruggable by small molecules and traditional protein therapeutics. A key challenge toward realizing the full potential of this technology is the safe and efficient delivery of siRNA to target tissues. The physical chemical properties of siRNAs preclude passive diffusion across most cell membranes. For systemic administration, novel delivery systems are required to confer drug-like pharmacokinetic and pharmacodynamic properties. Engineered nanomaterials and the emerging field of nanomedicine are important drivers of turning the promise of RNAi therapeutics into reality. The current clinical progress of systemically administered siRNA therapeutics is reviewed, with special attention to the toxicity profiles associated with RNAi nanomedicines. As a case study, the preclinical development of ALN-VSP, the first lipid nanoparticle (LNP)-formulated siRNA therapeutic to be tested in cancer patients, is reviewed to broadly highlight some of the preclinical safety challenges and areas of investigation for next generation LNP systems. (C) 2012 Elsevier B.V. All rights reserved.

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