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Grant: Collaborative Health Research Projects

University of Western Ontario

$54,835.00

Pulmonary delivery of surfactant for treatment of lung diseases

EF 2009-10

Résumé
Exogenous surfactant therapy is successfully used to treat neonatal respiratory distress syndrome (NRDS) and may also be beneficial in the treatment of adult lung diseases such as acute respiratory distress syndrome (ARDS) and asthma. However, results of clinical trials in the latter setting have been disappointing, in part because of the severity of the disease at the time of administration, as well as delivery limitations, as the curreni standard deliver method is by bolus instillation of a saline-surfactant suspension intratracheally. The method is also not suitable for treatment of spontaneously breathing patients, a potential requirement if earlier surfactant treatment strategies proves optimal. Aerosolization of surfactant suspensions via nebulization has not been successful to date due to inactivation of the surfactant via the nebulization process, poor efficiency of delivery as well as more practical difficulties such as foaming due to the low surface tension of the surfactant itself. Dr> powder aerosol delivery of surfactant could avoid these problems, and provide a more feasible, non-invasive and cost-effective method for surfactant delivery and even as a drug delivery vehicle for other lung-targeted therapies. The applicant (Zhu, a powder technology engineer) has developed a novel dry powder inhalation technology for the delivery of medications to the lung, with several granted and pending patents. The proposed research aims at extending this technology to the delivery of lung surfactant, as it is capable of aerosolizing small quantities of respirable dry powder including lung surfactant, for which the co-applicant has done extensive research (Lewis, respirologist). The overall objective the current joint project is to create a new device which meets the clinical requirements for surfactant delivery. The specific objectives of this research proposal are to modify the existing inhaler technology for surfactant delivery, to evaluate the functional integrity and the efficacy of the aerosolized surfactant in-vitro first and then in vivo using a small animal model.
Programme
Collaborative Health Research Projects
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data

Tel que publié

Application id
350806-2008
Name nom
Zhu, Jingxu(Jesse)
Department département
Chemical and Biochemical Engineering
Organization id
36
Institution établissement
University of Western Ontario
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2009
Competition year année de concours
2008
Award amount
54835
Program id
CHRPJ
Program nane en
Collaborative Health Research Projects
Program name fr
Projets de recherche concertée sur la santé
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
360
Committee name en
Collaborative Health Research Projects Selection Panel
Committee name fr
Comité de sélection de projets de recherche concertée sur la santé
Area of application code
518
Area of application group en
Manufacturing processes and products
Area of application group fr
Procédés et produits industriels
Area of application en
Medical equipment and apparatus
Area of application fr
Appareils et instruments médicaux
Research subject code
1805
Research subject group en
Chemical engineering
Research subject group fr
Génie chimique
Research subject en
Transport processes
Research subject fr
Procédés de transfert
Partie
2
Nb partie
3
Application title
Pulmonary delivery of surfactant for treatment of lung diseases
Keyword
NA
Application summary
Exogenous surfactant therapy is successfully used to treat neonatal respiratory distress syndrome (NRDS) and may also be beneficial in the treatment of adult lung diseases such as acute respiratory distress syndrome (ARDS) and asthma. However, results of clinical trials in the latter setting have been disappointing, in part because of the severity of the disease at the time of administration, as well as delivery limitations, as the curreni standard deliver method is by bolus instillation of a saline-surfactant suspension intratracheally. The method is also not suitable for treatment of spontaneously breathing patients, a potential requirement if earlier surfactant treatment strategies proves optimal. Aerosolization of surfactant suspensions via nebulization has not been successful to date due to inactivation of the surfactant via the nebulization process, poor efficiency of delivery as well as more practical difficulties such as foaming due to the low surface tension of the surfactant itself. Dr> powder aerosol delivery of surfactant could avoid these problems, and provide a more feasible, non-invasive and cost-effective method for surfactant delivery and even as a drug delivery vehicle for other lung-targeted therapies. The applicant (Zhu, a powder technology engineer) has developed a novel dry powder inhalation technology for the delivery of medications to the lung, with several granted and pending patents. The proposed research aims at extending this technology to the delivery of lung surfactant, as it is capable of aerosolizing small quantities of respirable dry powder including lung surfactant, for which the co-applicant has done extensive research (Lewis, respirologist). The overall objective the current joint project is to create a new device which meets the clinical requirements for surfactant delivery. The specific objectives of this research proposal are to modify the existing inhaler technology for surfactant delivery, to evaluate the functional integrity and the efficacy of the aerosolized surfactant in-vitro first and then in vivo using a small animal model.