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Grant: Collaborative Research and Development Grants

Institut national de la recherche scientifique

$145,000.00

Detection and inactivation of porcine parvovirus in pharmaceutical ingredients

FY 2007-08

Summary
To this date, many pharmaceutical products are manufactured from biological sources. When the products are derived from animal sources, it is essential to ensure the safety of the product by demonstrating the absence of viral contaminants.Cystic Fibrosis patients, in addition to suffering from respiratory problems, also suffer from severe digestive problems.  Nowadays, nutrition is considered the key factor to impact the longevity of CF patients.Key products used to enhance the food absorption of CF patients consist of mixtures of lipases, proteases and amylases from porcine pancreas extracts.  Because o f the porcine origin of those products, specific, robust and sensitive methods that can determine the presence of adventitious agents are necessary.This study aims at developing methods to assay for a common pathogen of pigs known as porcine parvovirus (PPV). Although this virus has never been shown to infect humans, it is prudent to ensure its absence from purified materials used in drug products derived from porcine tissues. This study further aims at removing or inactivating residual virus particles found in those pharmaceutical preparations.Additionally, we want to address the problem faced in the preparation of pharmaceuticals from biological extracts that these may be contaminated with viruses that are mutated in the manufacturing process.
Program
Collaborative Research and Development Grants
Location
Quebec, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data

As published

Application id
335018-2005
Name nom
Tijssen, Peter
Department département
INRS-Institut Armand-Frappier
Organization id
56
Institution établissement
Institut national de la recherche scientifique
Province en
Québec
Province fr
Québec
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2007
Competition year année de concours
2005
Award amount
145000
Program id
CRDPJ
Program name en
Collaborative Research and Development Grants
Program name fr
Subventions de recherche et développement coopérative
Group en
Research partnerships programs
Group fr
Programmes de partenariat
Committee code
96
Committee name en
RPP Internal Decision Cttee
Committee name fr
Cté de décision interne - PPR
Area of application code
504
Area of application group en
Manufacturing processes and products
Area of application group fr
Procédés et produits industriels
Area of application en
Human pharmaceuticals
Area of application fr
Produits pharmaceutiques administrables à l'homme
Research subject code
5202
Research subject group en
Microbiology
Research subject group fr
Microbiologie
Research subject en
Virology
Research subject fr
Virologie
Partie
2
Nb partie
3
Application title
Detection and inactivation of porcine parvovirus in pharmaceutical ingredients
Keyword
NA
Application summary
To this date, many pharmaceutical products are manufactured from biological sources. When the products are derived from animal sources, it is essential to ensure the safety of the product by demonstrating the absence of viral contaminants.Cystic Fibrosis patients, in addition to suffering from respiratory problems, also suffer from severe digestive problems.  Nowadays, nutrition is considered the key factor to impact the longevity of CF patients.Key products used to enhance the food absorption of CF patients consist of mixtures of lipases, proteases and amylases from porcine pancreas extracts.  Because o f the porcine origin of those products, specific, robust and sensitive methods that can determine the presence of adventitious agents are necessary.This study aims at developing methods to assay for a common pathogen of pigs known as porcine parvovirus (PPV). Although this virus has never been shown to infect humans, it is prudent to ensure its absence from purified materials used in drug products derived from porcine tissues. This study further aims at removing or inactivating residual virus particles found in those pharmaceutical preparations.Additionally, we want to address the problem faced in the preparation of pharmaceuticals from biological extracts that these may be contaminated with viruses that are mutated in the manufacturing process.