Assisting PNA transport through cystic fibrosis human airway epithelia with biodegradable hybrid lipid-polymer nanoparticles

Cystic fibrosis (CF) is characterized by an airway obstruction caused by a thick mucus due to a malfunctioning Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) protein. The sticky mucus restricts drugs in reaching target cells limiting the efficiency of treatments. The development of new a...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:Sci Rep
Autors principals: Comegna, Marika, Conte, Gemma, Falanga, Andrea Patrizia, Marzano, Maria, Cernera, Gustavo, Di Lullo, Antonella Miriam, Amato, Felice, Borbone, Nicola, D’Errico, Stefano, Ungaro, Francesca, d’Angelo, Ivana, Oliviero, Giorgia, Castaldo, Giuseppe
Format: Artigo
Idioma:Inglês
Publicat: Nature Publishing Group UK 2021
Matèries:
Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7973768/
https://ncbi.nlm.nih.gov/pubmed/33737583
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-021-85549-z
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars