Your browser doesn't support javascript.
loading
In Vivo Laser-Mediated Retinal Ganglion Cell Optoporation Using KV1.1 Conjugated Gold Nanoparticles.
Wilson, Ariel M; Mazzaferri, Javier; Bergeron, Éric; Patskovsky, Sergiy; Marcoux-Valiquette, Paule; Costantino, Santiago; Sapieha, Przemyslaw; Meunier, Michel.
Afiliação
  • Wilson AM; Department of Engineering Physics , Polytechnique Montréal , Montreal , Quebec , Canada , H3C 3A7.
  • Bergeron É; Department of Engineering Physics , Polytechnique Montréal , Montreal , Quebec , Canada , H3C 3A7.
  • Patskovsky S; Department of Engineering Physics , Polytechnique Montréal , Montreal , Quebec , Canada , H3C 3A7.
  • Marcoux-Valiquette P; Department of Engineering Physics , Polytechnique Montréal , Montreal , Quebec , Canada , H3C 3A7.
  • Meunier M; Department of Engineering Physics , Polytechnique Montréal , Montreal , Quebec , Canada , H3C 3A7.
Nano Lett ; 18(11): 6981-6988, 2018 11 14.
Article em En | MEDLINE | ID: mdl-30285455
ABSTRACT
Vision loss caused by retinal diseases affects hundreds of millions of individuals worldwide. The retina is a delicate central nervous system tissue stratified into layers of cells with distinct roles. Currently, there is a void in treatments that selectively target diseased retinal cells, and current therapeutic paradigms present complications associated with off-target effects. Herein, as a proof of concept, we introduce an in vivo method using a femtosecond laser to locally optoporate retinal ganglion cells (RGCs) targeted with functionalized gold nanoparticles (AuNPs). We provide evidence that AuNPs functionalized with an antibody toward the cell-surface voltage-gated K+ channel subunit KV1.1 can selectively deliver fluorescently tagged siRNAs or fluorescein isothiocyanate-dextran dye into retinal cells when irradiated with an 800 nm 100 fs laser. Importantly, neither AuNP administration nor irradiation resulted in RGC death. This system provides a novel, non-viral-based approach that has the potential to selectively target retinal cells in diseased regions while sparing healthy areas and may be harnessed in future cell-specific therapies for retinal degenerative diseases.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article