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Grant: Collaborative Health Research Projects (NSERC partnered)

McMaster University

$327,657.00

Designing Highly Porous Drug-Impregnated Polymer Scaffolds Using Pressurized Gas Expanded Liquids for the Treatment of Lung Fibrosis and Wound Infections

EF 2018-19

Résumé
Highly porous materials offer significant advantages in many biomedical applications based on their extremely high surface areas. In particular, for the delivery of drugs with low water solubility, the high surface area provided by highly porous scaffolds offers unique opportunities for enhancing drug loading thus improving the efficacy of drug therapy. However, most strategies used to prepare such scaffolds are extremely slow and/or require the use of solvents or other additives that can cause issues when the material is used in the body. Our knowledge user Ceapro (a Edmonton-based biotechnology company) has recently developed a high-throughput and rapid processing technology called pressurized gas expanded liquids (PGX) that overcomes these challenges in addition to offering exceptional control over both the macroscopic size of the materials generated (from large continuous networks to microscale particles) as well as the size of the internal pores. We have also, in partnership, developed methods to (1) convert these biopolymer networks to hydrogels by post-processing the polymer scaffolds and/or performing gelation and PGX processing simultaneously and (2) load multiple drugs via a simple and residual solvent-free process. In this proposed project, we aim to exploit these advantages to address key challenges in treating lung fibrosis and infected wounds. For lung fibrosis, the potential to create a highly porous microparticle delivery vehicles loaded with drug would improve the efficacy of inhalation-based therapy; in addition, one of the key biopolymers produced by Ceapro (beta-glucan) provides desirable cell targeting effects. For wound healing, the capacity of the scaffolds to absorb exudate and load tunable mixtures of drugs offers benefits for delivering synergistic drug combinations to treat antibiotic-resistant infections. Together, this work will leverage a patented Canadian technology (PGX) to address key and emerging health challenges for Canadians.
Programme
Collaborative Health Research Projects (NSERC partnered)
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
396485
Name
Hoare Todd R
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Partnername
Natural Sciences and Engineering Research Council of Canada (NSERC)
Instname2
Aging
Theme2
Biomedical
Prcname2
Collaborative Health Research Projects - NSERC Partnered
Projecttitle
Designing Highly Porous Drug-Impregnated Polymer Scaffolds Using Pressurized Gas Expanded Liquids for the Treatment of Lung Fibrosis and Wound Infections
Programtype2
Operating Grants
Orgnameinp2
McMaster University
Cihramount2
$327,657
Cihrequipment2
$7,500
Programname2
Collaborative Health Research Projects (NSERC partnered)
Keyworddelim
Biopolymers; Drug Delivery; Hydrogels; Lung Fibrosis; Macroporous Materials; Polymer Processing; Pulmonary Disease; Supercritical Fluids; Wound Healing; Wound Infections
Abstract
Highly porous materials offer significant advantages in many biomedical applications based on their extremely high surface areas. In particular, for the delivery of drugs with low water solubility, the high surface area provided by highly porous scaffolds offers unique opportunities for enhancing drug loading thus improving the efficacy of drug therapy. However, most strategies used to prepare such scaffolds are extremely slow and/or require the use of solvents or other additives that can cause issues when the material is used in the body. Our knowledge user Ceapro (a Edmonton-based biotechnology company) has recently developed a high-throughput and rapid processing technology called pressurized gas expanded liquids (PGX) that overcomes these challenges in addition to offering exceptional control over both the macroscopic size of the materials generated (from large continuous networks to microscale particles) as well as the size of the internal pores. We have also, in partnership, developed methods to (1) convert these biopolymer networks to hydrogels by post-processing the polymer scaffolds and/or performing gelation and PGX processing simultaneously and (2) load multiple drugs via a simple and residual solvent-free process. In this proposed project, we aim to exploit these advantages to address key challenges in treating lung fibrosis and infected wounds. For lung fibrosis, the potential to create a highly porous microparticle delivery vehicles loaded with drug would improve the efficacy of inhalation-based therapy; in addition, one of the key biopolymers produced by Ceapro (beta-glucan) provides desirable cell targeting effects. For wound healing, the capacity of the scaffolds to absorb exudate and load tunable mixtures of drugs offers benefits for delivering synergistic drug combinations to treat antibiotic-resistant infections. Together, this work will leverage a patented Canadian technology (PGX) to address key and emerging health challenges for Canadians.
Competitiondate
201810
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Hoare, Todd R; Moquin, Paul H; Ask, Kjetil; Coombes, Brian K
Approvedterm
3 ans 0 mois
Cihrcontribution2
Major Initiatives #2~ $327,657~ $7,500~