Hybrid nanoparticle design based on cationized gelatin and the polyanions dextran sulfate and chondroitin sulfate for ocular gene therapy.

We describe the development of hybrid nanoparticles composed of cationized gelatin and the polyanions CS and DS for gene therapy in the ocular surface. The physicochemical properties of the nanoparticles that impact their bioperformance, such as average size and zeta potential, can be conveniently modulated by changing the ratio of polymers and the crosslinker. These systems associate plasmid DNA and are able to protect it from DNase I degradation. We corroborate that the introduction of CS or DS in the formulation decreases the in vitro toxicity of the nanoparticles to human corneal cells without compromising the transfection efficiency. These nanoparticles are potential candidates for the development of safer and more effective nanomedicines for ocular therapy.

[1]  B. Glasgow,et al.  Endonuclease activity in lipocalins. , 2000, The Biochemical journal.

[2]  D. S. Mcleod,et al.  Ocular nanoparticle toxicity and transfection of the retina and retinal pigment epithelium. , 2008, Nanomedicine : nanotechnology, biology, and medicine.

[3]  M. Spector,et al.  Delivery of plasmid IGF-1 to chondrocytes via cationized gelatin nanoparticles. , 2008, Journal of biomedical materials research. Part A.

[4]  D. Ranney Biomimetic transport and rational drug delivery. , 2000, Biochemical pharmacology.

[5]  P. Weigel,et al.  Characterization of the Recombinant Rat 175-kDa Hyaluronan Receptor for Endocytosis (HARE)* , 2003, Journal of Biological Chemistry.

[6]  C. R. Middaugh,et al.  Formulation and characterization of DNA-polyethylenimine-dextran sulfate nanoparticles. , 2003, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

[7]  J. Pedraz,et al.  Solid lipid nanoparticles for retinal gene therapy: transfection and intracellular trafficking in RPE cells. , 2008, International journal of pharmaceutics.

[8]  A. Elaissari,et al.  Nanotechnology olymer-based nanocapsules for drug delivery , 2009 .

[9]  J. Scott,et al.  Extracellular matrix, supramolecular organisation and shape. , 1995, Journal of anatomy.

[10]  Maria Jose Alonso,et al.  Chitosan-based nanostructures: a delivery platform for ocular therapeutics. , 2010, Advanced drug delivery reviews.

[11]  M. de la Fuente,et al.  Design of novel polysaccharidic nanostructures for gene delivery , 2008, Nanotechnology.

[12]  Shannon M. Conley,et al.  Nanoparticle applications in ocular gene therapy , 2008, Vision Research.

[13]  Ana C. Fonseca,et al.  Drug delivery systems: Advanced technologies potentially applicable in personalized treatments , 2010, EPMA Journal.

[14]  B. Glasgow,et al.  Tear lipocalin is the major endonuclease in tears , 2008, Molecular vision.

[15]  M. di Pietro,et al.  Nuclear aggregates of polyamines are supramolecular structures that play a crucial role in genomic DNA protection and conformation , 2005, The FEBS journal.

[16]  M. Hashida,et al.  The Fate of Plasmid DNA After Intravenous Injection in Mice: Involvement of Scavenger Receptors in Its Hepatic Uptake , 1995, Pharmaceutical Research.

[17]  R. Nussenblatt,et al.  Gene therapy in the treatment of ocular inflammation , 2004, Springer Seminars in Immunopathology.

[18]  Kari B. Green-Church,et al.  Investigation of the human tear film proteome using multiple proteomic approaches , 2008, Molecular vision.

[19]  R. Mohan,et al.  Gene therapy in the cornea , 2005, Progress in Retinal and Eye Research.

[20]  Rahul Raman,et al.  Structural insights into biological roles of protein-glycosaminoglycan interactions. , 2005, Chemistry & biology.

[21]  C. Grimm,et al.  A novel GlcNAcα1-HPO3-6Gal(1-1)ceramide antigen and alkylated inositol-phosphoglycerolipids expressed by the liver fluke Fasciola hepatica , 2003 .

[22]  D. Peer,et al.  Corneal gene therapy. , 2007, Journal of controlled release : official journal of the Controlled Release Society.

[23]  N. Pattabiraman,et al.  Spermine-DNA interactions: a theoretical study. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[24]  M. Kuosmanen,et al.  Inhibition of the activity of restriction endonucleases by spermidine and spermine , 1985, FEBS letters.

[25]  Y. Tabata,et al.  Controlled release of plasmid DNA from cationized gelatin hydrogels based on hydrogel degradation. , 2002, Journal of controlled release : official journal of the Controlled Release Society.

[26]  Y. Tabata,et al.  In vivo release and gene expression of plasmid DNA by hydrogels of gelatin with different cationization extents. , 2003, Journal of controlled release : official journal of the Controlled Release Society.

[27]  S. Franzblau,et al.  Preparation of aminoglycoside-loaded chitosan nanoparticles using dextran sulphate as a counterion , 2009, Journal of microencapsulation.

[28]  M. Alonso,et al.  Hyaluronic Acid/Chitosan-g-Poly(ethylene glycol) Nanoparticles for Gene Therapy: An Application for pDNA and siRNA Delivery , 2010, Pharmaceutical Research.

[29]  Amélie Bochot,et al.  Hyaluronic acid coated poly-epsilon-caprolactone nanospheres deliver high concentrations of cyclosporine A into the cornea. , 2008, Experimental eye research.

[30]  M. de la Fuente,et al.  Novel hyaluronan-based nanocarriers for transmucosal delivery of macromolecules. , 2008, Macromolecular bioscience.

[31]  A. Auricchio,et al.  Ocular gene therapy: current progress and future prospects. , 2009, Trends in molecular medicine.

[32]  D. Sacco,et al.  Interaction of a macromolecular polyanion, dextran sulfate, with human hemoglobin , 1986, FEBS letters.

[33]  A. Bernkop‐Schnürch,et al.  In vitro cytotoxicity testing of non-thiolated and thiolated chitosan nanoparticles for oral gene delivery , 2007 .

[34]  M. Miyasaka,et al.  Identification and characterization of ligands for L-selectin in the kidney. I. Versican, a large chondroitin sulfate proteoglycan, is a ligand for L-selectin. , 1999, International immunology.

[35]  P. Weigel,et al.  The hyaluronan receptor for endocytosis (HARE) is not CD44 or CD54 (ICAM-1). , 2002, Biochemical and biophysical research communications.

[36]  M. de la Fuente,et al.  Novel hyaluronic acid-chitosan nanoparticles for ocular gene therapy. , 2008, Investigative ophthalmology & visual science.

[37]  M. Alonso,et al.  Bioadhesive hyaluronan–chitosan nanoparticles can transport genes across the ocular mucosa and transfect ocular tissue , 2008, Gene Therapy.

[38]  T. Thomas,et al.  Formation of DNA nanoparticles in the presence of novel polyamine analogues: a laser light scattering and atomic force microscopic study. , 2004, Nucleic acids research.

[39]  P. Couvreur,et al.  Cationic Vectors in Ocular Drug Delivery , 2004, Journal of drug targeting.

[40]  Y. Tabata,et al.  Controlled release of plasmid DNA from hydrogels prepared from gelatin cationized by different amine compounds. , 2006, Journal of controlled release : official journal of the Controlled Release Society.

[41]  C. Gualerzi,et al.  Effect of polyamines and basic proteins on cleavage of DNA by restriction endonucleases. , 1984, Biochemistry.