TY - GEN
T1 - Highly specific, NIR fluorescent contrast agent with emission controlled by gold nanoparticle
AU - Wang, Jianting
AU - O'Toole, Martin
AU - Massey, Archna
AU - Biswas, Souvik
AU - Nantz, Michael
AU - Achilefu, Samuel
AU - Kang, Kyung A.
PY - 2011
Y1 - 2011
N2 - Nanoparticles are currently being intensively studied for in vivo molecular imaging because of their unique and beneficial properties. Among these particles, some metal particles possess strong surface plasmon fields that can effectively alter fluorescence. Using this fluorescence alteration, an NIR fluorophore based, nanosized contrast agent for breast cancer diagnosis is being developed. The fluorophore is conjugated to gold nanoparticles (GNP) viaa short spacer whose lengthwas specially adjusted to have the strong plasmon field to quench the fluorescence. The spacer also has a special molecular sequence that can be cleaved by an enzyme secreted by targeted cancer cells. Normally, the entity does not fluoresce. If it is delivered to the cancer site, the short spacer would be cleaved by the enzyme secreted by the cancer cell at which point the fluorescence would be restored. This entity can incorporate a cancer targeting molecule for a cancer specific delivery. The entity specifically targets cancer cells and fluoresce only when the spacer is cleaved by a specific cancer secreting biomolecule, providing dual specificity for cancer diagnosis. In the future, this entity will be combined with cancer drugs for seamless detection and personalized therapy.
AB - Nanoparticles are currently being intensively studied for in vivo molecular imaging because of their unique and beneficial properties. Among these particles, some metal particles possess strong surface plasmon fields that can effectively alter fluorescence. Using this fluorescence alteration, an NIR fluorophore based, nanosized contrast agent for breast cancer diagnosis is being developed. The fluorophore is conjugated to gold nanoparticles (GNP) viaa short spacer whose lengthwas specially adjusted to have the strong plasmon field to quench the fluorescence. The spacer also has a special molecular sequence that can be cleaved by an enzyme secreted by targeted cancer cells. Normally, the entity does not fluoresce. If it is delivered to the cancer site, the short spacer would be cleaved by the enzyme secreted by the cancer cell at which point the fluorescence would be restored. This entity can incorporate a cancer targeting molecule for a cancer specific delivery. The entity specifically targets cancer cells and fluoresce only when the spacer is cleaved by a specific cancer secreting biomolecule, providing dual specificity for cancer diagnosis. In the future, this entity will be combined with cancer drugs for seamless detection and personalized therapy.
UR - http://www.scopus.com/inward/record.url?scp=84934435157&partnerID=8YFLogxK
U2 - 10.1007/978-1-4419-7756-4_21
DO - 10.1007/978-1-4419-7756-4_21
M3 - Conference contribution
C2 - 21445782
AN - SCOPUS:84934435157
SN - 9781441977557
T3 - Advances in Experimental Medicine and Biology
SP - 149
EP - 154
BT - Oxygen Transport to Tissue XXXII
PB - Springer New York LLC
ER -