RESEARCH

Research in our lab is focused on the development of nanomedicine for diagnosis and combinatorial treatment of cancer, endometriosis, pregnancy complications, and other diseases. Particularly, we are developing theranostic nano-agents for application in chemotherapy, hyperthermia, gene therapy, phototherapy, fluorescence, and photoacoustic detection and treatment of diseases.

Financial Support

National Institute of Health: OSU College of Pharmacy

NIH/NCI 1 R37 CA234006-01A1 PhRMA Foundation

NIH/NCI 1 R01CA237569-01A1 OHSU Knight Cancer Institute

NIH/NICHD R21HD098642 Friends of Doernbecher

NIH/NIBIB 1R15EB020351-01A1 OHSU National Primate Research Center

NIH/NCATS KL2 TR002370 Medical Research Foundation of Oregon

Oregon Nanoscience and Microtechnologies Institute OSU Division of Health Sciences

OSU Venture Development Fund OSU Research Equipment Reserve Fund

Photo-Theranostic Nano-Probes

Combining the capability of real-time imaging and therapy into a single agent has high translational potential for disease treatment, including cancer and endometriosis. Presently, our lab is focused on the development of photo-theranostic nanoscale agents for use in optical/photoacoustic imaging, image-guided phototherapy, image-guided surgery, and intraoperative therapy. Near-infrared (NIR) light is not significantly absorbed by bodily tissue and fluid allowing for uninterrupted NIR light to penetrate further within the body. This capability is paired with the dye-loaded nanoparticles that absorb specifically in the NIR region to generate fluorescence, photoacoustic signal or/and heat under NIR light. The main goal is to develop nano-agents for assistance in the accurate location/ diagnosis of diseased tissue, with subsequent immediate treatment. Moses et al. Small 2020   Li et al. Theranostics 2018

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Development of photo-responsive nanomaterials for image-guided combinatorial phototherapy

  Taratula et al. J Vasc Interv Radiol 2019

Nanoparticles-Mediated Magnetic Hyperthermia

Hyperthermia therapy for cancer treatment is a very promising approach. However, the issue with hyperthermia is the difficulty in heating only the local tumor area to the required temperature without harming surrounding healthy tissue. Despite its promising therapeutic potential, nanoparticle-mediated magnetic hyperthermia is currently limited to treatment of localized and relatively accessible cancer tumors because the required therapeutic temperatures above 40 °C can only be achieved by direct intratumoral injection of conventional iron oxide nanoparticles. Our goal is to develop efficient nanoparticles with high heating capacity that can efficiently accumulate at tumor sites following systemic administration and generate desirable intratumoral temperatures upon exposure to an alternating magnetic field (AMF). We are also evaluating hyperthermia treatment efficacy in combination with chemotherapy, gene therapy, and phototherapy.  This approach is also being tested for endometriosis treatment in our lab.

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Development of biocompatible nanoclusters with high heating efficiency for systemically delivered magnetic hyperthermia

Albarqi et al. ACS Nano 2019

Nanomedicine-Based Gene Therapy

Muscle wasting is a debilitating syndrome that occurs in numerous disease states and is an especially common consequence of cancer. We have focused our efforts on the development of a safe therapy that combats muscle wasting in cancer patients without the need for special dietary and exercise requirements. Currently, we are developing an effective nanoplatform for messenger RNA (the genetic blueprint that cells use to manufacture numerous proteins) delivery, with the aim to increase a protein inside the body that is responsible for muscular growth. Results of the ongoing pilot study reveal that overexpressed follistatin is also capable of modulating tumor cell activity, particularly regarding proliferation and migration. We show that, in addition to inducing muscle preservation via myostatin inhibition, follistatin also suppresses tumor cell activity by binding activin A, which was previously shown to be a driver of both tumor proliferation and cancer cachexia. The developed polymeric delivery platform could be an efficient therapeutic option for the safe and efficacious treatment of muscle wasting in cancer patients and could potentially inhibit cancer progression.

In addition, DJ-1 is a multifunctional protein that has recently been implicated as a key oncogenic driver and biomarker for various cancers, including ovarian cancer. It was also documented that increased DJ-1 expression positively correlates with lower survival in ovarian cancer patients. We have recently discovered that DJ-1 suppression in combination with a low dose of chemotherapeutic drug provides a superior therapeutic response as compared to each therapy alone.          Schumann et al. Nanomedicine 2018

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Development of nanomedicine-based gene delivery approaches to treat muscle wasting disorders including cancer cachexia