Literature DB >> 19201022

Factors influencing the transfection efficiency of ultra low molecular weight chitosan/hyaluronic acid nanoparticles.

Nicolas Duceppe1, Maryam Tabrizian.   

Abstract

The present work describes nanoparticles made of ultra low molecular weight chitosan (ULMWCh)/hyaluronic acid (HA) as novel potential carriers for gene delivery. Small and monodispersed nanoparticles with high in vitro transfection capabilities have been obtained by the complexation of these two polyelectrolytes. ULMWCh (<10 kDa) presents more advantageous characteristics over the higher molecular weight chitosan for clinical applications, namely increased solubility at physiological pH and improved DNA release. The ULMWCh:HA ratio and the HA molecular weights were varied with the aim of obtaining particles in the 100 nm range. Using chitosan (Ch) with a molecular weight of 5 kDa, HA with a molecular weight of 64 kDa, and a weight ratio of 4:1, nanoparticles with a Z-average size of 146+/-1 nm and narrow size distribution (polydispersity index: 0.073+/-0.030) were obtained. Nanoparticle images taken in dry conditions by SEM and AFM showed spherical particles. The optimal pH for transfection ranged from 6.4 to 6.8 for 0.25 microg of EGFP plasmid per well, with an incubation time of 4 h. Using these optimized parameters, DNA/ULMWCh:HA nanoparticles successfully transfected 25+/-1% of the 293T cells with pEGFP, compared to 0.7% obtained for DNA/ULMWCh under the same conditions. This high transfection efficiency of our non-viral gene delivery system could be attributed to the synergic effect of ULMWCh and low charge density of the HA chain for easy release of DNA which makes the system suitable for targeted gene delivery.

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Year:  2009        PMID: 19201022     DOI: 10.1016/j.biomaterials.2009.01.017

Source DB:  PubMed          Journal:  Biomaterials        ISSN: 0142-9612            Impact factor:   12.479


  18 in total

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Review 3.  Carbohydrate polymers for nonviral nucleic acid delivery.

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5.  Increased in vitro Cell Proliferation by Chitosan/pGM-CSF Complexes.

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Journal:  Indian J Pharm Sci       Date:  2011-03       Impact factor: 0.975

6.  A magnetic nanoparticle-based multiple-gene delivery system for transfection of porcine kidney cells.

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Journal:  PLoS One       Date:  2014-07-21       Impact factor: 3.240

7.  A comparative study of three ternary complexes prepared in different mixing orders of siRNA/redox-responsive hyperbranched poly (amido amine)/hyaluronic acid.

Authors:  Cheng-Jun Chen; Zhi-Xia Zhao; Jian-Cheng Wang; En-Yu Zhao; Ling-Yan Gao; Shu-Feng Zhou; Xiao-Yan Liu; Wan-Liang Lu; Qiang Zhang
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8.  Cellular delivery of quantum dot-bound hybridization probe for detection of intracellular pre-microRNA using chitosan/poly(γ-glutamic acid) complex as a carrier.

Authors:  Yao Geng; Dajie Lin; Lijia Shao; Feng Yan; Huangxian Ju
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9.  Porous chitosan scaffolds with embedded hyaluronic acid/chitosan/plasmid-DNA nanoparticles encoding TGF-β1 induce DNA controlled release, transfected chondrocytes, and promoted cell proliferation.

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Journal:  PLoS One       Date:  2013-07-23       Impact factor: 3.240

10.  Ultrasound treatment increases transfection efficiency of low molecular weight chitosan in fibroblasts but not in KB cells.

Authors:  Ureporn Kedjarune-Leggat; Chanyapat Supaprutsakul; Wilaiwan Chotigeat
Journal:  PLoS One       Date:  2014-03-20       Impact factor: 3.240

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