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High Throughput Screening for Stabilizers of Vaccine Antigens

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Book cover Novel Immune Potentiators and Delivery Technologies for Next Generation Vaccines

Abstract

The formulation and stabilization of vaccines remains one of the most problematic steps in their development [1, 2]. Once an antigen has been identified, its conversion into an efficacious, safe, convenient, and stable dosage form that can be effectively delivered to a target population is often beset with numerous difficulties. Not the least of these is the many different types of vaccine antigens, each with its own individual chemical identity, the presence of associated multiple physical characteristics and degradation pathways as well as accompanying delivery problems. Types of vaccine antigens in rough order of their complexity include peptides, peptide conjugates, natural and recombinant proteins, DNA-based systems, carbohydrate and carbohydrate-conjugates, virus-like particles, live-attenuated and inactivated viruses and bacteria among others. Thus biological macromolecules such as proteins, nucleic acids, polysaccharides, and lipids all may play roles as key components in vaccines and require appropriate attention. Furthermore, many vaccine formulations include an adjuvant which itself can be quite complex in nature (e.g., aluminum salts and oil-in-water emulsions) as well as in terms of adjuvant interactions with antigens and other solution components.

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Correspondence to C. Russell Middaugh .

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Middaugh, C.R., Volkin, D.B., Joshi, S.B. (2013). High Throughput Screening for Stabilizers of Vaccine Antigens. In: Singh, M. (eds) Novel Immune Potentiators and Delivery Technologies for Next Generation Vaccines. Springer, Boston, MA. https://doi.org/10.1007/978-1-4614-5380-2_6

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