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Utilizing ‘molecular jackhammers’ to advance cancer treatment 

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Just as jackhammers can penetrate concrete, molecular jackhammers (MJH) are nanoscopic machines capable of creating blows so strong that they can crack or rupture the cell membrane, decompensating and killing the cell. The MJHs are turned on by near-infrared (NIR) light that stimulates synchronized delocalized vibrations throughout the cell — a mechanical action that can be exploited to rapidly kill cancer cells. 

Researchers from Texas A&M University, Rice University, and the University of Texas-MD Anderson Cancer Center tested this method using lab cultures of human melanoma cells and mice with melanoma tumors. They found that the molecular jackhammers had a 99% efficiency in killing the cancer cells in vitro and that 50% of the mice treated with this method became cancer-free. This development is the first of its kind and offers a much safer and more effective alternative to current cancer treatments. 

Stimulating vibronic modes in cell membranes works by activating aminocyanine molecules (the MJHs), which can easily adhere to the outside of cells due to their positive charge, opposite to the cell’s phospholipid bilayer. 

Once attached, MJH is activated by exposing these molecules to invisible infrared light (IR) frequency or energy, slightly lower than the energy of visible red light. Since red radiation has the lowest energy in the visible spectrum, any light below red is invisible and this band or range of frequencies is called near-infrared (NIR). 

When activated with NIR, electrons within the MJH create plasmons — an excitation of the entire molecule that causes vibrations at an extremely fast rate. Driven by the NIR radiation, MJHs hit as if they were continually hammering the cell’s surface. These collective hammer blows of the MJHs are strong enough to rupture or crack the cell’s membrane creating a decompensation sufficient to destroy it.

According to Dr. Jorge Seminario, professor in the Artie McFerrin Department of Chemical Engineering at Texas A&M University, one of the critical benefits of this theoretical approach is that it can predict, from first principles theory, how the MJH will behave in an experimental test. This previous knowledge is valuable, making the technique more cost- and time-effective while avoiding risky and expensive trial-and-error experiments. 

This study was recently published in Nature Chemistry