4.6 Article

Ocular nanoparticle toxicity and transfection of the retina and retinal pigment epithelium

Journal

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.nano.2008.06.003

Keywords

Chitosan; Magnetic nanoparticle; Gene delivery; Retina; Toxicity

Funding

  1. NEI NIH HHS [R01 EY016151, R03 EY013744, R03 EY013744-03, L40 EY016943-01, R03 EY013744-02, R01 EY009357-13, R01 EY009357-14, R03 EY013744-01, R01 EY016151-02, R01 EY009357-12A1, R01 EY016151-03, EY01765, R03EY013744, R01 EY016151-01A2, R01 EY009357, R01EY09357, P30 EY001765] Funding Source: Medline
  2. NHLBI NIH HHS [T32HL007525, T32 HL007525] Funding Source: Medline

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Chitosan, PCEP (poly{[(cholesteryl oxocarbonylamido ethyl) methyl bis(ethylene) ammonium iodide] ethyl phosphate}), and magnetic nanoparticles (MNPs) were evaluated for the safe delivery of genes in the eye. Rabbits were injected with nanoparticles either intravitreally (IV) or subretinally (SR) and sacrificed 7 days later. Eyes were grossly evaluated for retinal pigment epithelium abnormalities, retinal degeneration, and inflammation. All eyes were cryopreserved and sectioned for analysis of toxicity and expression of either enhanced green or red fluorescent proteins. All of the nanoparticles were able to transfect cells in vitro and in vivo. IV chitosan showed inflammation in 12/13 eyes, whereas IV PCEP and IV MNPs were not inflammatory and did not induce retinal pathology. SR PCEP was nontoxic in the majority of cases but yielded poor transfection, whereas SR MNPs were nontoxic and yielded good transfection. Therefore, we conclude that the best nanoparticle evaluated in vivo was the least toxic nanoparticle tested, the MNP. (c) 2008 Elsevier Inc. All rights reserved.

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