SILICA-CORED CARRIER PARTICLE
A nanoparticulate imaging probe with an oxide core, a biocompatible polymeric shell covalently attached to the oxide core, a dye, and a cleavable spacer that covalently binds the dye to the probe. When the spacer is cleaved, the dye is liberated from the probe. The emissions of the dye are quenched when the dye is bound to the probe and not quenched when the dye is liberated from the probe. The spacer can be, for example, a peptide. The oxide core can be, for example, a silicon oxide core.
1 . A nanoparticulate imaging probe comprising an oxide core, a biocompatible polymeric shell covalently attached to the oxide core, a dye that produces emissions in response to electromagnetic radiation, and a cleavable spacer that covalently binds the dye to the probe such that the dye is liberated from the probe when the spacer is cleaved, wherein the probe has a size of less than 100 nm and the emissions of the dye is quenched when the dye is bound to the probe and not quenched when the dye is liberated from the probe.
2 . The imaging probe as recited in claim 1 , wherein the spacer is comprised of a polypeptide.
3 . The imaging probe as recited in claim 1 , wherein the oxide core is comprised of an oxide of an element selected from the group consisting of silicon, aluminum, iron, zinc, and zirconium.
4 . The imaging probe as recited in claim 1 , wherein the oxide core is comprised of an oxide of silicon.
5 . The imaging probe as recited in claim 1 , wherein the polymeric shell is comprised of a plurality of poly(ethylene glycol) segments.
6 . The imaging probe as recited in claim 1 , wherein the electromagnetic radiation is infrared radiation.
7 . The imaging probe as recited in claim 1 , wherein the dye is bound to the cleavable peptide through a functional group selected from the group consisting of an amine, a carboxylic acid, an activated ester, a 4-fluoro-5-nitro-benzoate, a thiol, and a hydroxyl.
8 . The imaging probe as recited in claim 7 , further comprising an agent covalently bound to the probe wherein the agent is selected from the group consisting of a therapeutic agent, a targeting agent, and a diagnostic agent.
9 . The imaging probe as recited in claim 1 , wherein the cleavable peptide is bound to the oxide core.
10 . The imaging probe as recited in claim 1 , wherein the cleavable peptide is bound to the polymeric shell.
11 . A nanoparticulate imaging probe comprising an oxide core, a biocompatible polymeric shell covalently attached to the oxide core, a dye that produces emissions in response to electromagnetic radiation, a quencher that quenches the emissions of the dye, and a cleavable peptide that covalently binds the probe to a component selected from the group consisting of the dye and the quencher, such that the component is liberated from the probe when the peptide is cleaved, wherein the probe has a size of less than 100 nm and the emission of the dye molecules is quenched when the component is bound to the probe and not quenched when the component is liberated from the probe.
12 . The imaging probe as recited in claim 11 , wherein the oxide core is comprised of an oxide of an element selected from the group consisting of silicon, aluminum, iron, zinc, and zirconium.
13 . The imaging probe as recited in claim 11 , wherein the oxide core is comprised of an oxide of silicon.
14 . The imaging probe as recited in claim 11 , wherein the polymeric shell is comprised of a plurality of poly(ethylene glycol) segments.
15 . The imaging probe as recited in claim 11 , wherein the component is bound to the cleavable peptide through a functional group selected from the group consisting of an amine, a carboxylic acid, an activated ester, a 4-fluoro-5-nitro-benzoate, a thiol, and a hydroxyl.
16 . The imaging probe as recited in claim 15 , further comprising an agent covalently bound to the probe wherein the agent is selected from the group consisting of a therapeutic agent, a targeting agent, and a diagnostic agent.
17 . The imaging probe as recited in claim 11 , wherein the cleavable peptide is bound to the oxide core.
18 . The imaging probe as recited in claim 11 , wherein the cleavable peptide is bound to the polymeric shell.
19 . The imaging probe as recited in claim 11 , wherein the component which is bound to the cleavable peptide is the dye and the quencher is not bound to the cleavable peptide.
20 . The imaging probe as recited in claim 11 , wherein the component which is bound to the cleavable peptide is the quencher and the dye is not bound to the cleavable peptide.
21 . A process for in vivo imaging comprising the steps of:
administering a nanoparticulate imaging probe to an animal which has a targeted tissue and a non-targeted tissue, wherein the probe comprises an oxide core, a biocompatible polymeric shell covalently attached to the oxide core, a dye that produces emissions in response to near-infrared electromagnetic radiation, and a cleavable peptide that covalently binds the probe to the dye such that the dye is liberated from the probe when the peptide is cleaved, wherein the probe has a size of less than 100 nm and the emissions of the dye is quenched when the dye is bound to the probe and not quenched when the dye is liberated from the probe;
waiting for the probe to accumulate in the targeted tissue which includes an enzyme, wherein the cleavable peptide is configured to be cleaved by the enzyme;
irradiating the targeted tissue with near-infrared electromagnetic radiation of a wavelength absorbable by the dye, thus producing the emissions; and
detecting the emissions of the liberated dye.
22 . The process as recited in claim 21 , further comprising the steps of
administering a second nanoparticulate imaging probe to the animal, wherein the second probe comprises a second oxide core, a second biocompatible polymeric shell covalently attached to the second oxide core, a second dye that produces emissions in response to near-infrared electromagnetic radiation, and a second cleavable peptide that covalently binds the second probe to the second dye such that the second dye is liberated from the second probe when the second peptide is cleaved, wherein the second probe has a size of less than 100 nm and the emissions of the second dye is quenched when the second dye is bound to the second probe and not quenched with the second dye is liberated from the second probe;
waiting for the second probe to accumulate in the targeted tissue which includes a second enzyme, wherein the second cleavable peptide is configured to be cleaved by the second enzyme;
irradiating the targeted tissue with electromagnetic radiation of a wavelength absorbable by the second dye, thus producing the emissions; and
detecting the emissions of the second liberated dye.