Stable Dry Powder Formulation for Nasal Delivery of Anthrax Vaccine
| Autor: | Shaun M. Kirwan, Herman F. Staats, Sheena H. Wang, Soman N. Abraham, Anthony J. Hickey |
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| Jazyk: | angličtina |
| Rok vydání: | 2011 |
| Předmět: |
Chemistry
Pharmaceutical Drug Storage Pharmaceutical Science Mucous membrane of nose Anthrax Vaccines Neutralization Article Microbiology Anthrax Immune system Antigen Adjuvants Immunologic Drug Stability Spectroscopy Fourier Transform Infrared Animals Particle Size Administration Intranasal Antigens Bacterial Anthrax vaccines biology Chemistry Circular Dichroism Antibody titer Antibodies Bacterial Nasal Mucosa Freeze Drying biology.protein Nasal administration Female Rabbits Antibody Powders |
| Popis: | There is a current biodefense interest in protection against anthrax. Here, we developed a new generation of stable and effective anthrax vaccine. We studied the immune response elicited by recombinant protective antigen (rPA) delivered intranasally with a novel mucosal adjuvant, a mast cell activator compound 48/80 (C48/80). The vaccine formulation was prepared in a powder form by spray-freeze-drying (SFD) under optimized conditions to produce particles with a target size of D(50) = 25 μm, suitable for delivery to the rabbit nasal cavity. Physicochemical properties of the powder vaccines were characterized to assess their delivery and storage potential. Structural stability of rPA was confirmed by circular dichroism and attenuated total reflectance-Fourier transform infrared spectroscopy, whereas functional stability of rPA and C48/80 was monitored by cell-based assays. Animal study was performed using a unit-dose powder device for direct nasal application. Results showed that C48/80 provided effective mucosal adjuvant activity in rabbits. Freshly prepared SFD powder vaccine formulations or powders stored for over 2 years at room temperature elicited significantly elevated serum PA-specific and lethal toxin neutralization antibody titers that were comparable to that induced by intramuscular immunization with rPA. Nasal delivery of this vaccine formulation may be a viable alternative to the currently licensed vaccine or an attractive vaccine platform for other mucosally transmitted diseases. |
| Databáze: | OpenAIRE |
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