Literature DB >> 33430262

Biocompatible Lipid Polymer Cationic Nanoparticles for Antigen Presentation.

Yunys Pérez-Betancourt1, Bianca de Carvalho Lins Fernandes Távora2, Eliana L Faquim-Mauro2, Ana Maria Carmona-Ribeiro1.   

Abstract

Biocompatible lipid polymer nanoparticles (NPs) previously used as antimicrobial agents are explored here as immuno-adjuvants. Poly (methyl methacrylate) (PMMA)/dioctadecyldimethylammonium bromide (DODAB)/poly (diallyldimethylammonium chloride) (PDDA) nanoparticles (NPs) were prepared by emulsion polymerization of methyl methacrylate (MMA) in the presence of DODAB and PDDA, with azobisisobutyronitrile (AIBN) as the initiator. NPs characterization after dialysis by dynamic light-scattering yielded 225 ± 2 nm hydrodynamic diameter (Dz), 73 ± 1 mV zeta-potential (ζ), and 0.10 ± 0.01 polydispersity (P). Ovalbumin (OVA) adsorption reduced ζ to 45 ± 2 mV. Balb/c mice immunized with NPs/OVA produced enhanced OVA-specific IgG1 and IgG2a, exhibited moderate delayed type hypersensitivity reaction, and enhanced cytokines production (IL-4, IL-10, IL-2, IFN-γ) by cultured spleen cells. There was no cytotoxicity against cultured macrophages and fibroblasts. Advantages of the PMMA/DODAB/PDDA NPs were high biocompatibility, zeta-potential, colloidal stability, and antigen adsorption. Both humoral and cellular antigen-specific immune responses were obtained.

Entities:  

Keywords:  biocompatible polymer; cationic lipid; cationic nanoparticles toxicity; cationic polymer; humoral and cellular immune responses; hybrid nanoparticles; ovalbumin; protein delivery; vaccine adjuvants

Year:  2021        PMID: 33430262      PMCID: PMC7825723          DOI: 10.3390/polym13020185

Source DB:  PubMed          Journal:  Polymers (Basel)        ISSN: 2073-4360            Impact factor:   4.329


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