4.8 Article

A cerium oxide loaded glycol chitosan nano-system for the treatment of dry eye disease

期刊

JOURNAL OF CONTROLLED RELEASE
卷 315, 期 -, 页码 40-54

出版社

ELSEVIER
DOI: 10.1016/j.jconrel.2019.10.039

关键词

Antioxidant nanoparticles; Reactive oxygen species (ROS); Dry eye disease

资金

  1. Natural Science Foundation of Jiangsu Province [BK20181478]
  2. Edward N. & Della L. Thome Memorial Foundation [138289]
  3. BrightFocus Foundation [M2019063]
  4. Carolina Center of Cancer Nanotechnology Excellence
  5. U.S. National Eye Institute [R01EY026564]

向作者/读者索取更多资源

Dry eye (DE) disease is an uprising health epidemic that directly affects the surface of the eye. We developed a water soluble cerium oxide loaded glycol chitosan nanoparticle as a new type of eye drop, namely GCCNP (glycol chitosan cerium oxide nanoparticles). GCCNP is capable of scavenging cellular reactive oxygen species (ROS) for the treatment of DE disease. The antioxidative effects of GCCNP were assessed in mice primary corneal and conjunctival cells in vitro and in a DE murine model in vivo. GCCNP's effect on the DE models was assessed via histological evaluations, migration assays, cell viability assays, cellular uptake analyses, intracellular ROS scavenging assays, wound healing assays, mitochondrial membrane potential readings, corneal fluorescein staining, tear volume concentrations, tear film break up time analyses, and lastly, analytical/spectroscopic analyses of GCCNP eye drop formulations. Spectroscopic analysis showed that cerium oxide was entrapped into the glycol chitosan (GC). The solubility of cerium in GC (GCCNP) increased to 709.854 +/- 24.3 mu g/ml compared to its original solubility in cerium oxide, which was measured as 0.020 +/- 0.002 mu g/ml. GCCNP had no cytotoxic effect and showed improvements on dry eye disease models by stabilizing the tear film, scavenging ROS, up-regulating SOD, promoting and maintaining corneal and conjunctival cell growth and integrity. We provided convincing evidence that GCCNP is an effective treatment for DE and may represent a potential new class of drug for DE disease.

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