Cerium-oxide nanoparticle based device for the detection of reactive oxygen species and monitoring of chronic inflammation
A polymer-coated cerium oxide based device and system is disclosed for detecting reactive oxygen species and monitoring chronic inflammation. The device and system encapsulate free therapeutic nanoparticle elements not present in a living body in a prosthetic or implantable unit. Embodiment one is a two-chamber structure with a reactive oxygen species (ROS) scavenging component on one end and at the opposite end is an imaging agent consisting of at least one of a fluorophore capable of fluorescence emission, a chemiluminescent agent, a magnetic relaxation agent and an X-ray contrast agent. Embodiment two is a single chamber device consisting of a multifunctional nanocomposite with a ROS-scavenging nanoparticle constituent (nanoceria) and a multimodal reporting nanoparticle component (i.e. Dex-IO-DiR). The device and system are utilized in treatment of diseases with a pro-inflammatory component, including, but not limited to, Crohn's disease, ulcerative colitis, inflammatory bowel disease, cystic fibrosis, arthritis, and cancer chemotherapy.
1. A nanocomposite system encapsulating nanoparticle elements not present in a living body for detection of reactive oxygen species, said nanocomposite system comprising a miniature device in a form of a chamber containing therein nanocomposite including a reactive oxygen species (ROS)-scavenging nanoparticle component and a reporting nanoparticle component that comprises nanoparticles including one or more imaging agent, and having an exterior semi-permeable membrane encapsulating both nanoparticle components within the chamber; said ROS-scavenging nanoparticle component comprising polymer coated cerium oxide nanoparticles, and said nanocomposite comprising a multimodal nanocomposite formed by chemical conjugation of the polymer coated cerium oxide nanoparticles and the reporting nanoparticle component; said (ROS)-scavenging nanoparticle component and said reporting nanoparticle component communicating with an aqueous environment outside of said chamber through the semi-permeable membrane that permits diffusion of the reactive oxygen species therethrough; said ROS-scavenging nanoparticle component of the nanocomposite protecting the reporting nanoparticle component from the reactive oxygen species under the normal physiological condition; said reporting nanoparticle component in the chamber incurring an imaging detectable change in the presence of an elevated non-physiological level of the reactive oxygen species associated with an aberrant clinical condition, thereby indicating the presence of an elevated non-physiological level of the reactive oxygen species.
2. The system of claim 1 , wherein said multimodal nanocomposite is formed by conjugation of propargylated polyacrylic acid coated cerium oxide nanoparticles and azide-carrying indotricarbocyanine polyacrylic acid-coated iron oxide (DiR-PAA-IO).
3. The system of claim 1 , wherein said multimodal nanocomposite is formed by carbodiimide conjugation of polyacrylic acid coated cerium oxide nanoparticles and aminated indotricarbocyanine dextran-coated iron oxide (DiR-Dex-IO).
4. The system of claim 1 , wherein the miniature device is approximately 2 to 4 millimeters (mm) in length and approximately 1 mm in diameter.
5. The system of claim 1 , wherein said polymer-coated cerium oxide nanoparticles are coated with dextran or polyacrylic acid.
6. The system of claim 1 , wherein said imaging agent comprises at least one of a fluorophore capable of fluorescence emission, a chemiluminescent agent, a magnetic relaxation agent, and an X-ray contrast agent.
7. The system of claim 6 , wherein said imaging agent comprises a fluorophore selected from at least one of octodecyl indocarbocyanine (DiI), indodicarbocyanine (DiD), indotricarbocyanine (DiR), cyanine 5.5 (Cy5.5), and indocyanine green (ICG).
8. The system of claim 6 , wherein the reporting nanoparticle component comprises nanoparticles of at least one of iron oxide, bismuth, europium, gadolinium and chelates thereof.
9. The system of claim 6 , wherein the nanoparticles including one or more imaging agent are coated with at least one polymer selected from dextran, polyacrylic acid, hyper-branched polyester, poly-lactic-co-glycolic acid, and mixtures thereof.
10. A nanocomposite system encapsulating nanoparticle elements not present in a living body for detection of reactive oxygen species, said nanocomposite system comprising a miniature device in a form of a chamber containing therein nanocomposite including polymer-coated cerium oxide nanoparticles and imaging nanoparticles and having an exterior semi-permeable membrane encapsulating the nanoparticles within the chamber; said polymer-coated cerium oxide nanoparticles and said imaging nanoparticles communicating with an aqueous environment outside of said chamber through the semi-permeable membrane that permits diffusion of the reactive oxygen species therethrough; said polymer-coated cerium oxide nanoparticles of the nanocomposite protecting the imaging nanoparticles from the reactive oxygen species under the normal physiological condition; said imaging nanoparticles in the chamber incurring an imaging detectable change in the presence of an elevated non-physiological level of the reactive oxygen species associated with an aberrant clinical condition, thereby indicating the presence of an elevated non-physiological level of the reactive oxygen species.
11. The system of claim 10 , wherein said nanocomposite comprises multimodal nanocomposite formed by conjugation of propargylated polyacrylic acid coated cerium oxide nanoparticles and azide-carrying indotricarbocyanine polyacrylic acid-coated iron oxide (DiR-PAA-IO).
12. The system of claim 10 , wherein the imaging nanoparticles are nanoparticles of at least one of iron oxide, bismuth, europium, gadolinium and chelates thereof.
13. The system of claim 10 , wherein the imaging nanoparticles are coated with at least one polymer selected from dextran, polyacrylic acid, hyper-branched polyester, poly-lactic-co-glycolic acid, and mixtures thereof.
14. The system of claim 10 , wherein the imaging nanoparticles are polymer-coated nanoparticles of iron oxide for magnetic resonance imaging detection of the reactive oxygen species, or polymer-coated nanoparticles of iron oxide containing a fluorophore for magnetic resonance imaging and fluorescence imaging detections of the reactive oxygen species.
15. The system of claim 10 , wherein said nanocomposite comprises multimodal nanocomposite formed by carbodiimide conjugation of polyacrylic acid coated cerium oxide nanoparticles and aminated indotricarbocyanine dextran-coated iron oxide (DiR-Dex-IO).
16. The system of claim 15 , wherein the miniature device is approximately 2 to 4 millimeters (mm) in length and approximately 1 mm in diameter.
17. The system of claim 15 , wherein the polymer-coated cerium oxide nanoparticles are coated with dextran or polyacrylic acid.
18. The system of claim 10 , wherein the imaging nanoparticles include one or more imaging agent comprising at least one of a fluorophore capable of fluorescence emission, a chemiluminescent agent, a magnetic relaxation agent, and an X-ray contrast agent.
19. The system of claim 18 , wherein the imaging agent comprises a fluorophore selected from at least one of octodecyl indocarbocyanine (DiI), indodicarbocyanine (DiD), indotricarbocyanine (DiR), cyanine 5.5 (Cy5.5), and indocyanine green (ICG).
20. A nanocomposite system encapsulating nanoparticle elements not present in a living body for detection of reactive oxygen species, said nanocomposite system comprising a miniature device in a form of a chamber containing therein nanocomposite comprising polymer-coated cerium oxide nanoparticles and polymer-coated nanoparticles containing one or more imaging agent, and having an exterior semi-permeable membrane encapsulating the nanoparticles within the chamber; said polymer-coated cerium oxide nanoparticles and said imaging nanoparticles communicating with an aqueous environment outside of said chamber through the semi-permeable membrane that permits diffusion of the reactive oxygen species therethrough; said polymer-coated cerium oxide nanoparticles of the nanocomposite protecting the imaging nanoparticles from the reactive oxygen species under the normal physiological condition; said imaging nanoparticles in the chamber incurring an imaging detectable change in the presence of an elevated non-physiological level of the reactive oxygen species associated with an aberrant clinical condition, thereby indicating the presence of an elevated non-physiological level of the reactive oxygen species.