Intranasal immunization with dry powder vaccines

Eur J Pharm Biopharm. 2018 Jan:122:167-175. doi: 10.1016/j.ejpb.2017.11.001. Epub 2017 Nov 6.

Abstract

Vaccination represents a cost-effective weapon for disease prevention and has proven to dramatically reduce the incidences of several diseases that once were responsible for significant mortality and morbidity worldwide. The nasal cavity constitutes the initial stage of the respiratory system and the first contact with inhaled pathogens. The intranasal (IN) route for vaccine administration is an attractive alternative to injection, due to the ease of administration as well as better patient compliance. Many published studies have demonstrated the safety and effectiveness of IN immunization with liquid vaccines. Currently, two liquid IN vaccines are available and both contain live attenuated influenza viruses. FluMist® was approved in 2003 in the United States, and Nasovac® H1N1 vaccine was approved in India in 2010. Preclinical studies showed that IN immunization with dry powder vaccines (DPVs) is feasible. Although there is not a commercially available DPV yet, DPVs have the inherent advantage of being relatively more stable than liquid vaccines. This review focuses on recent developments of DPVs as next-generation IN vaccines.

Keywords: Devices; Dry powder; Mucoadhesives; Mucosal immune responses; NALT.

Publication types

  • Review

MeSH terms

  • Administration, Intranasal
  • Animals
  • Humans
  • Immunization / methods
  • Nasal Cavity / immunology*
  • Powders / administration & dosage*
  • Vaccination / methods
  • Vaccines, Attenuated / administration & dosage*
  • Vaccines, Attenuated / immunology*

Substances

  • Powders
  • Vaccines, Attenuated