Article

Novel dry powder formulation of ovalbumin for development of COPD-like animal model: Physicochemical characterization and biomarker profiling in rats.

Department of Pharmacokinetics and Pharmacodynamics and Global Center of Excellence (COE) Program, School of Pharmaceutical Sciences, University of Shizuoka, 52-1, Yada, Suruga-ku, Shizuoka, 422-8526, Japan.
European journal of pharmaceutical sciences: official journal of the European Federation for Pharmaceutical Sciences (impact factor: 2.61). 07/2009; 37(3-4):469-76. DOI:10.1016/j.ejps.2009.04.002 pp.469-76
Source: PubMed

ABSTRACT This study was directed toward the development of novel ovalbumin dry powder inhalation system (OVA-DPI) for preparing experimental animal models of chronic obstructive pulmonary disease, with the aim of aiding the drug discovery. OVA-DPI, prepared with jet mill, showed high dispersion and emission from capsule as evaluated by cascade impactor. Based on the results from long term stability studies employing scanning electron microscopy, UPLC/ESI-MS analysis, powder X-ray diffraction and TG/DTA analyses, the OVA-DPI, stored at room temperature, was found to be stable for more than 3 years as evidenced by no significant degradation and crystal polymorphism. Intratracheal administration of OVA-DPI in OVA-sensitized rats resulted in 11-fold increase of infiltrated granulocytes, especially neutrophil, which would be characteristics of severe asthma/COPD symptoms. Of all plasma biomarkers monitored, myeloperoxidase activity and lactate dehydrogenase leakage into blood seemed to be sensitive indicators of lung injury in this model. In addition, biphasic increase of LDH was observed with peak responses at 3 and 24h after antigen challenge, suggesting that OVA-DPI could cause both acute and delayed inflammatory reactions. Upon these findings, OVA-DPI can be useful and reproducible research tool for the development of experimental asthma/COPD model.

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Keywords

3 years
 
cascade impactor
 
chronic obstructive pulmonary disease
 
experimental animal models
 
experimental asthma/COPD model
 
inflammatory reactions
 
Intratracheal administration
 
jet mill
 
lactate dehydrogenase leakage
 
lung injury
 
OVA-sensitized rats
 
peak responses
 
plasma biomarkers
 
powder X-ray diffraction
 
reproducible research tool
 
scanning electron microscopy
 
severe asthma/COPD symptoms
 
significant degradation
 
term stability studies
 
UPLC/ESI-MS analysis
 

Shingen Misaka