Long-term biophysical stability of nanodiamonds combined with lipid nanocarriers for non-viral gene delivery to the retina
Nanodiamonds were combined with niosome, and resulting formulations were named as nanodiasomes, which were evaluated in terms of physicochemical features, cellular internalization, cell viability and transfection ef ficiency both in in vitro and in in vivo conditions. Such parameters were analyzed a...
| Autores: | , , , , , , , , , , , , , |
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| Tipo de recurso: | artículo |
| Fecha de publicación: | 2023 |
| País: | España |
| Institución: | Universidad Miguel Hernández de Elche |
| Repositorio: | REDIUMH. Depósito Digital de la UMH |
| OAI Identifier: | oai:dspace.umh.es:11000/35179 |
| Acceso en línea: | https://hdl.handle.net/11000/35179 |
| Access Level: | acceso abierto |
| Palabra clave: | nanodiamond niosome non-viral gene delivery stability retina |
| Sumario: | Nanodiamonds were combined with niosome, and resulting formulations were named as nanodiasomes, which were evaluated in terms of physicochemical features, cellular internalization, cell viability and transfection ef ficiency both in in vitro and in in vivo conditions. Such parameters were analyzed at 4 and 25 ◦ C, and at 15 and 30 days after their elaboration. Nanodiasomes showed a particle size of 128 nm that was maintained over time inside the ± 10% of deviation, unless after 30 days of storage at 25 ◦C. Something similar occurred with the initial zeta potential value, 35.2 mV, being both formulations more stable at 4 ◦C. The incorporation of nano diamonds into niosomes resulted in a 4-fold increase of transfection efficiency that was maintained over time at 4 and 25 ◦C. In vivo studies reported high transgene expression of nanodiasomes after subretinal and intravitreal administration in mice, when injected freshly prepared and after 30 days of storage at 4 ◦C. |
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