Vaccine formulation involves the careful design and preparation of vaccines to ensure their safety, stability, and efficacy. Formulation is a critical step in the vaccine development process, influencing factors such as shelf life, administration routes, and immune response. Vaccine formulations consist of antigens, the target components of the pathogen, along with adjuvants that enhance the immune response. Antigens can be inactivated or live attenuated pathogens, subunit proteins, or genetic material like mRNA, depending on the vaccine type. Adjuvants, such as aluminum salts or oil-in-water emulsions, are added to improve the vaccine's immunogenicity. Stabilizers, preservatives, and other excipients are included to maintain vaccine integrity during storage and transportation. Formulation considerations also account for the target population, age groups, and specific disease characteristics. Advances in nanotechnology and liposomal formulations offer new avenues for vaccine delivery and efficacy. Vaccine formulation research continually explores innovative strategies to optimize vaccine stability, increase immunogenicity, and address global health challenges. Careful formulation ensures that vaccines are not only effective but also safe and accessible for diverse populations worldwide.
Title : The importance of post-marketing surveillance and real-world data: For a product to be successful
Regina Au, BioMarketing Insight, United States
Title : A promising novel approach to DNA vaccines
Khursheed Anwer, IMUNON, United States
Title : Prophylactic and molecular approaches for mitigating human influenza A viruses: i. Evaluating influenza vaccine effectiveness in the older population ii. Down-regulation of influenza virus genes with novel sirna-chimeric-ribozyme constructs
Madhu Khanna, University of Delhi, India
Title : Post COVID-19 syndrome is associated with sex and severity of first COVID-19 episode in Honduras
Manuel Antonio Sierra Santos, Central American Technological University, Honduras
Title : Homology analysis of MPXV and VACV peptides underscores the need to consider both MPXV clades for vaccine development
Lara Isis Teodoro, Mayo Clinic, United States
Title : Establishing a platform method for physical appearance assessment of new parenteral pharmaceuticals
Ying Wan, Merck & Co., United States
Title : Development of a novel multi-component vaccine to address the burden of otitis media in high-risk populations
Ayesha Zahid, Griffith University, Australia
Title : High seroprevalence of RSV antibodies in adults indicates potential undetected transmission and requires further public health assessment
Lara Isis Teodoro, Mayo Clinic, United States
Title : New biomarkers in leishmania major vaccine development
Negar Seyed, Pasteur Institute of Iran, Iran (Islamic Republic of)
Title : Development of a platform UPLC-CAD method for high-throughput lipid quantitation and characterization in novel mRNA LNPs
Janet Muzulu, Sanofi, United States