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- W2921492276 abstract "There is a current void in efficient, cell-specific, retinal drug delivery systems, thus developing a safe, effective, selective drug delivery system would open novel therapeutic avenues. We previously demonstrated that femtosecond (fs) laser irradiation can selectively transfect DNA plasmids into cultured cells in the presence of functionalised gold nanoparticles (AuNPs) (1). Here, we sought out to selectively optoporate retinal cells in vivo with functionalized AuNPs and a 800nm fs laser. The cell-surface Kv1.1 voltage-gated channel was chosen to target retinal ganglion cells (RGCs) in the rat retina. The eyes of anesthetized rats were placed in the beam path of an optical system consisting of a fs laser and an ophthalmoscope for fundus visualization. Following Kv1.1-AuNP and FITC-dextran intravitreal injection and incubation, irradiation resulted in FITC uptake by retinal cells. In addition, similar experiments with Cy3-siRNA clearly show that the technique can effectively deliver siRNA into RGCs. Importantly, neither AuNP intravitreal injection nor irradiation resulted in RGC death, as determined by RBPMS quantification 1 week following AuNP injection and/or irradiation. Since living biological tissues absorb energy very weakly at 800nm, this non-invasive tool may provide a safe, cost effective approach to selectively target retinal cells and limit complications associated with surgical interventions, and potential biological hazards associated with viral-based gene therapy. In addition, given the extensive use of lasers in ophthalmic practice, our proposed technology may be seamlessly inserted to current clinical setups. (1) E. Bergeron et al, Nanoscale, 7, 17836 (2015)." @default.
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- W2921492276 date "2019-03-13" @default.
- W2921492276 modified "2023-10-17" @default.
- W2921492276 title "In vivo laser targeted gene therapy of retina ganglion cells (Conference Presentation)" @default.
- W2921492276 doi "https://doi.org/10.1117/12.2509870" @default.
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