Article ID Journal Published Year Pages File Type
5433698 Journal of Controlled Release 2017 12 Pages PDF
Abstract

siRNA-based therapeutics possess great potential to treat a wide variety of genetic disorders. However, they suffer from low cellular uptake and short half-lives in blood circulation; issues that remain to be addressed. This work is, to the best of our knowledge, the first to report the production of solid nano-in-nanoparticles, termed double nano carriers (DNCs) by means of the innovative technology of nano spray drying. DNCs (with a median size of 580-770 nm) were produced by spraying at low temperatures (50 °C) to prevent damage to heat-sensitive biomacromolecules like siRNA. DNCs consisting of Poly (d,l-lactide-co-glycolide) used as a wall material, encapsulating 20% human serum albumin primary nanoparticles (PNPs) loaded with siRNA, were obtained as a dry nanoparticulate powder with smooth spherical surfaces and a unique inner morphology. Incubation of pegylated or non-pegylated DNCs under sink conditions at 37 °C, elicited a controlled release profile of the siRNA for up to 12 or 24 h, respectively, with a minimal burst effect. Prolonged incubation of pegylated DNCs loaded with active siRNA (anti EGFR) in an A549 epithelial cell culture monolayer did not induce any apparent cytotoxicity. A slow degradation of the internalized DNCs by the cells was also observed resulting in the progressive release of the siRNA for up to 6 days, as corroborated by laser confocal microscopy. The structural integrity and silencing activity of the double encapsulated siRNA were fully preserved, as demonstrated by HPLC, gel electrophoresis, and potent RNAi activity of siRNA extracted from DNCs. These results demonstrate the potential use of DNCs as a nano drug delivery system for systemic administration and controlled release of siRNA and potentially other sensitive bioactive macromolecules.

Graphical abstractNano in nanoparticles: SEM images of intact double nano carriers (DNCs) (left) and a fractured DNC (following freeze-fracture process), showing the inner structure (right). Left insert shows the general architecture of pegylated DNCs and right insert is a zoom-in of the inner matrix of the DNCs, composed of polymeric PLGA fibers with HSA PNPs (~ 100 nm) embedded within them.Download high-res image (321KB)Download full-size image

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Physical Sciences and Engineering Materials Science Biomaterials
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