Potential of Chitosan/Alginate Nanoparticles As a Non-Viral Vector for Gene Delivery: Formulation and Optimization Using D-Optimal Design Publisher Pubmed



Zohri M¹ ; Arefian E² ; Akbari Javar H³ ; Gazori T⁴ ; Aghaeebakhtiari SH^{5, 6} ; Taheri M⁷ ; Fatahi Y^{1, 8} ; Azadi A⁹ ; Khoshayand MR¹⁰ ; Ghahremani MH^{1, 11} Show Affiliations
Source: Materials Science and Engineering C Published:2021

Abstract

Chitosan/alginate (Chi/Alg) nanoparticles as a non-viral vector for the Smad4 encoding plasmid were optimized utilizing D-optimal design based on the nanoparticles/plasmid ratio, Chi/Alg MW, and preparation method type. Following the optimization and validation of the best formula, morphology studies and FTIR measurements were performed to evaluate the optimized Chi/Alg/S NPs. Toxicity (MTT assay) and transfection studies were performed for the best formula in comparison with Lipofectamine 2000, and Polyethyleneimine (PEI) and evaluated using Green Fluorescence Protein (GFP) assay, Flow cytometry, and RT-PCR. The model predicted a particle size of 111 nm, loading efficacy (LE) of 43%, cumulative release (CMR) of 39%, the ζ-potential of +50 mV, and PDI of 0.13. The predicted point condition was as follows: NP ratio = 13, Chi/Alg MW ratio = 2.35, and preparation method type = 1. Microscopic findings revealed that the shape of nanoparticles was spherical. The Chi/Alg/S nanoparticles showed no toxicity and transfection efficacy of 29.9% was observed in comparison with Lipofectamine (35.5%) and PEI (30.9%). © 2021 Elsevier B.V.