Grant: Discovery Grants Program - Individual
University of Regina
$27,000.00
Supramolecular organic photochemistry: incorporating function through molecular design
EF 2009-10
Résumé
Supramolecular organic photochemistry examines the interaction of light with supramolecular assemblies composed of organic molecules. Supramolecular assemblies that undergo light-induced processes are continually being developed to custom-tailor functions in areas such as drug delivery, catalysis, and optoelectronic molecular devices. The functionality achieved by supramolecular assemblies is a consequence of complementary intermolecular interactions that direct their formation and the photochemical properties of the molecular components. We are developing innovative, functional liposomes through the integration of photochromic compounds with elements of lipid complementarity and reversible photocontrols. These photochromic liposomes will undergo reversible changes in membrane permeability that will restore membrane integrity following the release of encapsulated compounds. We will achieve this objective by incorporating photochromes that span the entire lipid bilayer. Thus far, photochromic systems have lacked this aspect of organization, and the extent of their photoinduced release has been small, except when liposome stability is irreversibly compromised. By spanning the bilayer, isomerization will produce permeable channels through which entrapped molecules will diffuse, resulting from changes in photochrome structure. Charged tethers will anchor the disruptive, photochromic units in place until isomerization back to their more complementary form restores the local lipid order. This approach will be developed through the integration of lipid analogues with two photochromic moieties. These dimers will not only produce larger increases in membrane permeability than previous systems, but also restore membrane integrity. In addition, we will develop similar photochromes with improved two-photon absorption to enhance the spatial and temporal selectivity of these liposomes in practical applications such as photoregulated drug delivery where the delivered dosage will be precisely and reversibly controlled with light. This strategy will benefit public health through a reduction in hospitalization time, lead to patentable technologies, and generate an overall savings to Canada's health care system.
Programme
Discovery Grants Program - Individual
Bénéficiaire
Emplacement
Saskatchewan, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data
Tel que publié
Application id
262002-2007
Name nom
Murphy, Scott
Department département
Chemistry and Biochemistry
Organization id
17
Institution établissement
University of Regina
Province en
Saskatchewan
Province fr
Saskatchewan
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2009
Competition year année de concours
2007
Award amount
27000
Program id
RGPIN
Program nane 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
24
Committee name en
Inorganic & Organic Chemistry
Committee name fr
Chimie inorg. et org.
Area of application code
1202
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Physical sciences
Area of application fr
Sciences physiques
Research subject code
3706
Research subject group en
Organic chemistry
Research subject group fr
Chimie organique
Research subject en
Organic photochemistry
Research subject fr
Photochimie organique
Partie
3
Nb partie
3
Application title
Supramolecular organic photochemistry: incorporating function through molecular design
Keyword
NA
Application summary
Supramolecular organic photochemistry examines the interaction of light with supramolecular assemblies composed of organic molecules. Supramolecular assemblies that undergo light-induced processes are continually being developed to custom-tailor functions in areas such as drug delivery, catalysis, and optoelectronic molecular devices. The functionality achieved by supramolecular assemblies is a consequence of complementary intermolecular interactions that direct their formation and the photochemical properties of the molecular components. We are developing innovative, functional liposomes through the integration of photochromic compounds with elements of lipid complementarity and reversible photocontrols. These photochromic liposomes will undergo reversible changes in membrane permeability that will restore membrane integrity following the release of encapsulated compounds. We will achieve this objective by incorporating photochromes that span the entire lipid bilayer. Thus far, photochromic systems have lacked this aspect of organization, and the extent of their photoinduced release has been small, except when liposome stability is irreversibly compromised. By spanning the bilayer, isomerization will produce permeable channels through which entrapped molecules will diffuse, resulting from changes in photochrome structure. Charged tethers will anchor the disruptive, photochromic units in place until isomerization back to their more complementary form restores the local lipid order. This approach will be developed through the integration of lipid analogues with two photochromic moieties. These dimers will not only produce larger increases in membrane permeability than previous systems, but also restore membrane integrity. In addition, we will develop similar photochromes with improved two-photon absorption to enhance the spatial and temporal selectivity of these liposomes in practical applications such as photoregulated drug delivery where the delivered dosage will be precisely and reversibly controlled with light. This strategy will benefit public health through a reduction in hospitalization time, lead to patentable technologies, and generate an overall savings to Canada's health care system.