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Nanoparticles are tiny particles – between 1-100 nm – that have unusual properties compared with the same substance at the larger scale. These unusual properties and their tiny size – comprising just a few hundred atoms – makes them useful for working at the cellular and sub-cellular level in biology.
Physicists at The University of Texas at Arlington say they have shown that using microwaves to activate photosensitive nanoparticles produces tissue-heating effects that ultimately lead to cell death within solid tumors.
“Our new method using microwaves can propagate through all types of tissues and target deeply situated tumors,” said Wei Chen, Ph.D., UTA professor of physics and lead author of the study published in the Journal of Biomedical Nanotechnology and titled “A New Modality of Cancer Treatment—Nanoparticle Mediated Microwave Induced Photodynamic Therapy.”
Photodynamic therapy kills cancer cells when a nanoparticle introduced into tumor tissue generates toxic singlet oxygen after being exposed to light. Singlet oxygen is a highly reactive type of oxygen that irreversibly damages cell mitochondria and eventually causes cell death.
“Up to now, photodynamic therapy, which depends on visible, ultraviolet, or near-infrared light, was considered effective for skin cancers or cancers close to the skin surface,” Dr. Chen said. “Our new concept combining microwaves with photodynamic therapy opens up new avenues for targeting deeper tumors and has already proven effective in rapidly and safely reducing tumor size.”
Medicilon boasts nearly 300 tumor evaluation models. At the same time, we are empowering innovative therapies to comprehensively evaluate and study immuno-oncology. We have completed model establishment and efficacy evaluation of immuno-therapies such as CAR-T, TCR-T, CAR-NK, oncolytic virus, antibody (monoclonal antibody, double antibody, polyclonal antibody, etc.), siRNA, AAV.
Tumor Animal Model Medicilon Has Established:
In prior studies, the researchers had identified a novel type of nanoparticle, copper–cysteamine or Cu-Cy, that could be activated by X rays to produce singlet oxygen and slow the growth of tumors. X-ray radiation, however, poses significant risks to patients and can harm healthy tissue.
In the current study, the team demonstrated that the nanoparticle Cu-Cy also can be activated by microwaves, which can be targeted directly at the tumor itself without harming surrounding tissue.
“Our new microwave-induced photodynamic therapy offers numerous advantages, the most significant of which is increased safety,” explained Dr. Chen. “Our nanoparticle Cu-Cy also demonstrates very low toxicity, is easy to make and inexpensive, and also emits intense luminescence, which means it can also be used as an imaging agent.”
The researchers demonstrated that both in vitro and in vivo studies on an osteosarcoma cell line showed significant cell destruction using Cu-Cy nanoparticles under microwave activation. The heating effects and the release of copper ions from copper cysteamine upon activation was the main mechanism for the generation of the reactive oxygen needed for cancer cell destruction.
Alex Weiss, UTA chair of the Physics Department, emphasized the importance of this research in the context of UTA’s increasing focus on health and the human condition within the Strategic Plan 2020: Bold Solutions|Global Impact.
“Dr. Chen’s research into nanoparticle activation has led to important discoveries that could potentially transform cancer treatment,” noted Alex Weiss, Ph.D., UTA chair of the physics department. “This new paper on the possibilities of microwave activation demonstrates yet again how Dr. Chen’s search for new modalities of therapy could play a key role in finding safe, viable, and inexpensive treatments for cancer.”