Division of Molecular Pharmaceutics and Drug Delivery, College of Pharmacy, The University of Texas at Austin, Austin, TX 78712, USA.
Division of Molecular Pharmaceutics and Drug Delivery, College of Pharmacy, The University of Texas at Austin, Austin, TX 78712, USA; Inner Mongolia Key Laboratory of Molecular Biology, Inner Mongolia Medical University, Hohhot, Inner Mongolia 010058, China.
Eur J Pharm Biopharm. 2018 Jan;122:167-175. doi: 10.1016/j.ejpb.2017.11.001. Epub 2017 Nov 6.
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.
疫苗接种是预防疾病的一种具有成本效益的手段,已被证明可显著降低几种疾病的发病率,这些疾病曾在全球范围内导致大量死亡和发病。鼻腔构成了呼吸系统的初始阶段,也是与吸入性病原体的首次接触。与注射相比,鼻内(IN)途径给药是一种有吸引力的替代方案,因为其给药容易且患者顺应性更好。许多已发表的研究表明,液体疫苗的 IN 免疫是安全有效的。目前,有两种液体 IN 疫苗可用,均含有减毒活流感病毒。FluMist®于 2003 年在美国获得批准,Nasovac®H1N1 疫苗于 2010 年在印度获得批准。临床前研究表明,干粉疫苗(DPV)的 IN 免疫是可行的。尽管目前尚无市售的 DPV,但 DPV 具有比液体疫苗更稳定的固有优势。本综述重点介绍了作为下一代 IN 疫苗的 DPV 的最新进展。