Grant: Discovery Grants Program - Individual
Université du Québec à Montréal
$44,000.00
Synthesis of Glycomimetics and Gycodendrimers of Biological Interests
EF 2015-16
Résumé
Cell-surface glycoconjugates are responsible for a wide range of biological interactions at the origin of pathologies. Unfortunately, the nature of the binding interactions is weak and poorly selective. The following integrated research program is aimed at using conceptually novel strategies toward the design of high affinity and specificity carbohydrate dendritic nanomaterials for the targeting of conceptually innovative carriers against cancer, bacterial and viral infections. The concept of dendrimer design will be expanded to include two new features that have been overlooked so far. The conservative and restrictive approaches to dendrimer syntheses will be changed by using different chemical motifs between each layer, thus offering additional controls into the desired biophysical properties. This innovative ""onion-peel"" approach will provide much greater flexibility in the synthetic schemes leading to the novel dendrimer architectures. In addition, the above modifications will be improved by providing dendrimers harboring two different surface moieties to ensure the most efficient bacterial and cancer cell targeting. This will be particularly exemplified with two types of bacteria such as P. aeruginosa and uropathogenic E. coli involved in cystic fibrosis and pyelonephritis. To integrate bactericidal properties within the nanomaterials, we also proposed to simultaneously include antibacterial agents. As an additional level of improvement in the design of novel glycodendrimers, we also propose to use medicinal chemistry methodologies through which, much better ligands candidates will become accessible. Using the above two variables (multivalency and glycomimetic), more reliable, low valency analogs will be secured. A particular emphasis will be given to organometallic and asymmetric chemistry in order to provide access to structures with key chiral centers. Spacer length, distances, hydro/lipo-philicity will all be factors to be optimized. A novel aspect will also concentrate on the syntheses of a new family of self-assembled molecules calles glycodendrimersomes.
Programme
Discovery Grants Program - Individual
Bénéficiaire
Emplacement
Quebec, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data
Tel que publié
Application id
1589-2013
Name nom
Roy, René
Department département
Chimie
Organization id
57
Institution établissement
Université du Québec à Montréal
Province en
Québec
Province fr
Québec
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2015
Competition year année de concours
2013
Award amount
44000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
1504
Committee name en
Chemistry
Committee name fr
Chimie
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
3702
Research subject group en
Organic chemistry
Research subject group fr
Chimie organique
Research subject en
Carbohydrates
Research subject fr
Glucides
Partie
3
Nb partie
5
Application title
Synthesis of Glycomimetics and Gycodendrimers of Biological Interests
Keyword
NSERC
Application summary
Cell-surface glycoconjugates are responsible for a wide range of biological interactions at the origin of pathologies. Unfortunately, the nature of the binding interactions is weak and poorly selective. The following integrated research program is aimed at using conceptually novel strategies toward the design of high affinity and specificity carbohydrate dendritic nanomaterials for the targeting of conceptually innovative carriers against cancer, bacterial and viral infections. The concept of dendrimer design will be expanded to include two new features that have been overlooked so far. The conservative and restrictive approaches to dendrimer syntheses will be changed by using different chemical motifs between each layer, thus offering additional controls into the desired biophysical properties. This innovative ""onion-peel"" approach will provide much greater flexibility in the synthetic schemes leading to the novel dendrimer architectures. In addition, the above modifications will be improved by providing dendrimers harboring two different surface moieties to ensure the most efficient bacterial and cancer cell targeting. This will be particularly exemplified with two types of bacteria such as P. aeruginosa and uropathogenic E. coli involved in cystic fibrosis and pyelonephritis. To integrate bactericidal properties within the nanomaterials, we also proposed to simultaneously include antibacterial agents. As an additional level of improvement in the design of novel glycodendrimers, we also propose to use medicinal chemistry methodologies through which, much better ligands candidates will become accessible. Using the above two variables (multivalency and glycomimetic), more reliable, low valency analogs will be secured. A particular emphasis will be given to organometallic and asymmetric chemistry in order to provide access to structures with key chiral centers. Spacer length, distances, hydro/lipo-philicity will all be factors to be optimized. A novel aspect will also concentrate on the syntheses of a new family of self-assembled molecules calles glycodendrimersomes.