Canada Spends Logo

Explore our Budget 2026 analysis

Grant: Engage Grants Program

University of Prince Edward Island

$25,000.00

Modification of pseudoteroxazoles with biodegradable polymers: Improving patient compliance and drug delivery for a potent potential tuberculosis drug

FY 2011-12

Summary
Over one in three people globally is infected with M. tuberculosis, resulting in nearly 2 million deaths per year. Multi-drug resistant tuberculosis has increased the danger of this deadly infection and prompted extensive research into new treatments. Nautilus Biosciences Canada, Inc. has developed pseudoteroxazoles with high activity against the disease. Challenges remain, however, in improving patient compliance, as treatment regimens are long and arduous. Research in the Shaver group has focused on control of macrostructure and microstructure in the ring-opening polymerization of lactide and other cyclic esters to create biodegradable and bioassimilable polymeric materials. The goal of this collaboration is to use hydroxy-functionalized pseudoteroxazoles as initiators for the ring-opening polymerization of lactide with variable chain lengths and microstructure properties. These polymer-modified bioactives will degrade hydrolytically and release the active material, potentially offering controlled release of the drug. Over a six-month project, twelve prototype materials will be prepared and characterized for their physical and degradation properties. By controlling chain length and polymer microstructure by judicious choice of catalyst we hope to be able to tune the release of the pseudoteroxazoles, provide for a sustained release of the drug and eventually improve patient compliance.
Program
Engage Grants Program
Location
Prince Edward Island, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data

As published

Application id
419328-2011
Name nom
Shaver, Michael
Department département
Chemistry
Organization id
88
Institution établissement
University of Prince Edward Island
Province en
Prince Edward Island
Province fr
?le-du-Prince-Édouard
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2011
Competition year année de concours
2011
Award amount
25000
Program id
EGP
Program nane en
Engage Grants Program
Program name fr
Programme de subventions d'engagement partenariat
Group en
Research partnerships programs
Group fr
Programmes de partenariat
Committee code
1551
Committee name en
Atlantic Internal Decision Committee
Committee name fr
Comité de décision interne pour l'Atlantique
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
3751
Research subject group en
Polymer chemistry
Research subject group fr
Chimie des polymères
Research subject en
Polymer synthesis
Research subject fr
Synthèse des polymères
Partie
1
Nb partie
1
Application title
Modification of pseudoteroxazoles with biodegradable polymers: Improving patient compliance and drug delivery for a potent potential tuberculosis drug
Keyword
NSERC
Application summary
Over one in three people globally is infected with M. tuberculosis, resulting in nearly 2 million deaths per year. Multi-drug resistant tuberculosis has increased the danger of this deadly infection and prompted extensive research into new treatments. Nautilus Biosciences Canada, Inc. has developed pseudoteroxazoles with high activity against the disease. Challenges remain, however, in improving patient compliance, as treatment regimens are long and arduous. Research in the Shaver group has focused on control of macrostructure and microstructure in the ring-opening polymerization of lactide and other cyclic esters to create biodegradable and bioassimilable polymeric materials. The goal of this collaboration is to use hydroxy-functionalized pseudoteroxazoles as initiators for the ring-opening polymerization of lactide with variable chain lengths and microstructure properties. These polymer-modified bioactives will degrade hydrolytically and release the active material, potentially offering controlled release of the drug. Over a six-month project, twelve prototype materials will be prepared and characterized for their physical and degradation properties. By controlling chain length and polymer microstructure by judicious choice of catalyst we hope to be able to tune the release of the pseudoteroxazoles, provide for a sustained release of the drug and eventually improve patient compliance.