The development of radiation-senstive nanomaterials for in vivo biomedical applications would enable an entirely new class of tools with enhanced detection, diagonosis, and treatment capabilites. Recently, we have investigated a novel class of nanomaterial, X-ray-excitable radioluminescent nanoparticles (RLNPs), also known as nanoscintillators, which are capable of converting X-ray radiation into near infrared (NIR) light. By conjugating these RLNPs with biological targeting agents, such as antibodies, these novel probes can identify molecular signatures a disease or biological processes through imaging. This X-ray-in-NIR-out imaging approach offers several unique advantages over conventional optical imaging including: (1) absence of tissue auto-fluorescent background, leading to better signal-to-noise-ratio (SNR); (2) deep photon penetration of the excitation X-ray source; and (3) the ability to simultaneously multiplex image. In a therapeutic context, these RLNP may serve as energy mediators to optically activate functional ligands for simultaneous multi-therapy delivery when combined with conventional radiation oncology techniques. In this novel strategy, tumor targeted multi-functional RLNPs serve as a link between radiation therapy, photodynamic therapy (PDT), and photochemical internalization (PCI) enhanced drug delivery. We hypothesize that this combined approach possesses several synergies that overcome the individual limitations of each technique. The overall goal of this R35 application is to develop radiation-activated functional nanoparticles for both imaging and therapeutic applications. As a research program development vehicle, this proposal seeks to provide the PI, who is trained in nanotechnology the means to explore this unique nanoscale interaction between materials and biology with the ultimate goal of creating clinically relevant tools. The current application builds logically on the PI's prior work and is focused on applying X-ray stimulated radioluminescence technology toward imaging and radiation therapy. Oregon State University (OSU) and Oregon Health & Science University (OHSU) are ideal settings to undertake this research with strong ties between clinical units at OHSU and basic science and engineering departments at OSU.

Public Health Relevance

The goal of this research program is to investigate novel imaging and therapeutic technologies that exploit the synergistic combination of nanotechnology and radiation in medicine. In this work we seek to utilize well- established techniques, such as X-ray computed tomography and external beam radiation, to advance nanomedicine into clinical applications. The successful implementation of these novel techniques would provide powerful tools for physicians, as well as allow biomedical scientists to interrogate and manipulate various disease states to advance basic research.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Unknown (R35)
Project #
5R35GM119839-03
Application #
9492788
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Smith, Ward
Project Start
2016-09-02
Project End
2021-05-31
Budget Start
2018-06-01
Budget End
2019-05-31
Support Year
3
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Oregon State University
Department
Pharmacology
Type
Schools of Pharmacy
DUNS #
053599908
City
Corvallis
State
OR
Country
United States
Zip Code
97331
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Ashwanikumar, N; Plaut, Justin S; Mostofian, Barmak et al. (2018) Supramolecular self assembly of nanodrill-like structures for intracellular delivery. J Control Release 282:76-89
Brown, Anna L; Winter, Hayden; Goforth, Andrea M et al. (2018) Facile Synthesis of Ligand-Free Iridium Nanoparticles and Their In Vitro Biocompatibility. Nanoscale Res Lett 13:208
Rosch, Justin G; Brown, Anna L; DuRoss, Allison N et al. (2018) Nanoalginates via Inverse-Micelle Synthesis: Doxorubicin-Encapsulation and Breast Cancer Cytotoxicity. Nanoscale Res Lett 13:350
Patel, Siddharth; Ashwanikumar, N; Robinson, Emily et al. (2017) Boosting Intracellular Delivery of Lipid Nanoparticle-Encapsulated mRNA. Nano Lett 17:5711-5718