Among polymeric polycations, chitosan has emerged as a powerful carrier for gene delivery. Only a few studies have focused on the stability of the chitosan/DNA complex under storage, although this is imperative for nanomedicinal applications. Here, we synthesized polyelectrolyte complexes at a charge ratio of 10 using 50 kDa chitosan and plasmid (p)DNA that encodes a GFP reporter. These preparations were stable up to 3 months at 4 °C and showed reproducible transfection efficiencies in vitro in HEK293 cells. In addition, we developed a methodology that increases the in vitro transfection efficiency of chitosan/pDNA complexes by 150 % with respect to standard procedures. Notably, intracellular pDNA release and transfected cells peaked 5 days following transection of mitotically active cells. These new developments in formulation technology enhance the potential for polymeric nanoparticle-mediated gene therapy.
Improved stability and efficacy of chitosan/pDNA complexes for gene delivery / Cifani, Noemi; Chronopoulou, Laura; Pompili, Barbara; Antonio Di, Martino; Bordi, Federico; Sennato, Simona; DI DOMENICO, Enea Gino; Palocci, Cleofe; Ascenzioni, Fiorentina. - In: BIOTECHNOLOGY LETTERS. - ISSN 0141-5492. - STAMPA. - 37:3(2015), pp. 557-565. [10.1007/s10529-014-1727-7]
Improved stability and efficacy of chitosan/pDNA complexes for gene delivery
CIFANI, NOEMI;CHRONOPOULOU, LAURA;POMPILI, BARBARA;BORDI, FEDERICO;SENNATO, Simona;DI DOMENICO, Enea Gino;PALOCCI, Cleofe;ASCENZIONI, Fiorentina
2015
Abstract
Among polymeric polycations, chitosan has emerged as a powerful carrier for gene delivery. Only a few studies have focused on the stability of the chitosan/DNA complex under storage, although this is imperative for nanomedicinal applications. Here, we synthesized polyelectrolyte complexes at a charge ratio of 10 using 50 kDa chitosan and plasmid (p)DNA that encodes a GFP reporter. These preparations were stable up to 3 months at 4 °C and showed reproducible transfection efficiencies in vitro in HEK293 cells. In addition, we developed a methodology that increases the in vitro transfection efficiency of chitosan/pDNA complexes by 150 % with respect to standard procedures. Notably, intracellular pDNA release and transfected cells peaked 5 days following transection of mitotically active cells. These new developments in formulation technology enhance the potential for polymeric nanoparticle-mediated gene therapy.File | Dimensione | Formato | |
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