Intranasal immunization with dry powder vaccines
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. F1uMist(center dot) was approved in 2003 in the United States, and Nasovac(center dot) 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.
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Título según WOS: | ID WOS:000424176300019 Not found in local WOS DB |
Título de la Revista: | EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS |
Volumen: | 122 |
Editorial: | Elsevier |
Fecha de publicación: | 2018 |
Página de inicio: | 167 |
Página final: | 175 |
DOI: |
10.1016/j.ejpb.2017.11.001 |
Notas: | ISI |