4.8 Article

Surface functionalisation of PLGA nanoparticles for gene silencing

Journal

BIOMATERIALS
Volume 31, Issue 21, Pages 5671-5677

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2010.03.069

Keywords

RNAi; siRNA; PLGA; Cetylated PEI; Drug delivery; Surface modification

Funding

  1. Faculty of Science, Aarhus University
  2. Danish Research Council
  3. EU [LSHB-CT-2004-005276]

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This work presents a method for decorating the surface of poly (lactide-co-glycolide) (PLGA) nanoparticles with polyethyleneimine (PEI) utilising a cetyl derivative to improve surface functionalisation and siRNA delivery. Sub-micron particles were produced by an emulsion-diffusion method using benzyl alcohol. We demonstrate by x-ray photoelectron spectroscopy (XPS), 2.6 times higher surface presentation of amines using the cetyl derivative compared to non-cetylated-PEI formulations (6.5 and 2.5% surface nitrogen, respectively). The modified particles were shown by spectroscopy, fluorescent microscopy and flow cytometry to bind and mediate siRNA delivery into the human osteosarcoma cell line U2OS and the murine macrophage cell line J774.1. Specific reduction in the anti-apoptotic oncogene BCL-w in U2OS cells was achieved with particles containing cetylated-PEI (53%) with no cellular, toxicity. In addition, particles containing cetylated-PEI achieved 64% silencing of TNF alpha in J774.1 cells. This rapid method for surface modification of PLGA nanoparticles promotes its application for alternative cetylated functional derivatives as a strategy to control specific biological properties of nanoparticles. (c) 2010 Elsevier Ltd. All rights reserved.

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