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Development of a novel adjuvanted nasal vaccine: C48/80 associated with chitosan nanoparticles as a path to enhance mucosal immunity.

Publication ,  Journal Article
Bento, D; Staats, HF; Gonçalves, T; Borges, O
Published in: Eur J Pharm Biopharm
June 2015

In a time in which mucosal vaccines development has been delayed by the lack of safe and effective mucosal adjuvants, the combination of adjuvants has started to be explored as a strategy to obtain potent vaccine formulations. This study describes a novel adjuvant combination as an effective approach for a nasal vaccine - the association of the mast cell activator compound 48/80 with chitosan based nanoparticles. It was hypothesized that mucoadhesive nanoparticles would promote the cellular uptake and prolong the antigen residence time on nasal cavity. Simultaneously, mast cell activation would promote a local microenvironment favorable to the development of an immune response. To test this hypothesis, two different C48/80 loaded nanoparticles (NPs) were prepared: Chitosan-C48/80 NP (Chi-C48/80 NP) and Chitosan/Alginate-C48/80 NP (Chi/Alg-C48/80 NP). The potential as a vaccine adjuvant of the two delivery systems was evaluated and directly compared. Both formulations had a mean size near 500nm and a positive charge; however, Chi-C48/80 NP was a more effective adjuvant delivery system when compared with Chi/Alg-C48/80 NP or C48/80 alone. Chi-C48/80 NP activated mast cells at a greater extent, were better internalized by antigen presenting cells than Chi/Alg-C48/80 NP and successfully enhanced the nasal residence time of a model antigen. Superiority of Chi-C48/80 NP as adjuvant was also observed in vivo. Therefore, nasal immunization of mice with Bacillus anthracis protective antigen (PA) adsorbed on Chi-C48/80 NP elicited high levels of serum anti-PA neutralizing antibodies and a more balanced Th1/Th2 profile than C48/80 in solution or Chi/Alg-C48/80 NP. The incorporation of C48/80 within Chi NP also promoted a mucosal immunity greater than all the other adjuvanted groups tested, showing that the combination of a mast cell activator and chitosan NP could be a promising strategy for nasal immunization.

Duke Scholars

Published In

Eur J Pharm Biopharm

DOI

EISSN

1873-3441

Publication Date

June 2015

Volume

93

Start / End Page

149 / 164

Location

Netherlands

Related Subject Headings

  • p-Methoxy-N-methylphenethylamine
  • Time Factors
  • Technology, Pharmaceutical
  • T-Lymphocytes, Helper-Inducer
  • Surface Properties
  • RAW 264.7 Cells
  • Pharmacology & Pharmacy
  • Particle Size
  • Nasal Mucosa
  • Nanoparticles
 

Citation

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Bento, D., Staats, H. F., Gonçalves, T., & Borges, O. (2015). Development of a novel adjuvanted nasal vaccine: C48/80 associated with chitosan nanoparticles as a path to enhance mucosal immunity. Eur J Pharm Biopharm, 93, 149–164. https://doi.org/10.1016/j.ejpb.2015.03.024
Bento, D., H. F. Staats, T. Gonçalves, and O. Borges. “Development of a novel adjuvanted nasal vaccine: C48/80 associated with chitosan nanoparticles as a path to enhance mucosal immunity.Eur J Pharm Biopharm 93 (June 2015): 149–64. https://doi.org/10.1016/j.ejpb.2015.03.024.
Bento, D., et al. “Development of a novel adjuvanted nasal vaccine: C48/80 associated with chitosan nanoparticles as a path to enhance mucosal immunity.Eur J Pharm Biopharm, vol. 93, June 2015, pp. 149–64. Pubmed, doi:10.1016/j.ejpb.2015.03.024.
Bento D, Staats HF, Gonçalves T, Borges O. Development of a novel adjuvanted nasal vaccine: C48/80 associated with chitosan nanoparticles as a path to enhance mucosal immunity. Eur J Pharm Biopharm. 2015 Jun;93:149–164.
Journal cover image

Published In

Eur J Pharm Biopharm

DOI

EISSN

1873-3441

Publication Date

June 2015

Volume

93

Start / End Page

149 / 164

Location

Netherlands

Related Subject Headings

  • p-Methoxy-N-methylphenethylamine
  • Time Factors
  • Technology, Pharmaceutical
  • T-Lymphocytes, Helper-Inducer
  • Surface Properties
  • RAW 264.7 Cells
  • Pharmacology & Pharmacy
  • Particle Size
  • Nasal Mucosa
  • Nanoparticles