缅北强奸

Why drugs don鈥檛 reach cancer cells: 缅北强奸 researchers develop technology to provide answers

From left to right, PhD candidates Abdullah Syed and Shrey Sindhwani discuss their findings with Professor Warren Chan (photo by Neil Ta)

For cancer patients, understanding the odds of a treatment鈥檚 success can be bewildering.

The same drug, applied to the same type of cancer, might be fully successful for one person鈥檚 tumour and do nothing for someone else. Physicians are often unable to explain why.

Now, University of Toronto researchers are beginning to understand one of the reasons. Biomedical engineering students Abdullah Syed and Shrey Sindhwani, and colleagues at the Institute of Biomaterials & Biomedical Engineering (IBBME), have created technology to watch nanoparticles entering into tumours 鈥 revealing barriers that prevent their delivery to targets and the variability between cancers.

鈥淭he biggest thing we鈥檝e noticed is that nanoparticles face multiple challenges posed by the tumour itself on their way to cancer cells,鈥 says Sindhwani, an MD-PhD student working with Professor Warren Chan of IBBME. Syed and Sindhwani  and on the cover of the .

鈥淪o the treatment might work for a while 鈥 or worse, there鈥檚 just enough of the drug for the cancer to develop resistance. This could be prevented if we can figure out the ways in which these barriers stop delivery and distribution of the drug throughout the cancer.鈥

Tiny 鈥渘anoparticles鈥 offer great hope for the treatment of cancer and other diseases because of their potential to deliver drugs to targeted areas in the body, allowing more precise treatments with fewer side-effects. But so far the technology hasn鈥檛 lived up to its promise, due to delivery and penetration problems. 

To dismantle this roadblock, the two graduate students searched for a way to better view the particle鈥檚 journey inside tumours. They discovered that the tough-to-see particles could be illuminated by scattering light off their surfaces.

鈥淭he sensitivity of our imaging is about 1.4 millionfold higher,鈥 says Syed. 鈥淔irst, we make the tissue transparent, then we use the signal coming from the particles to locate them. We shine a light on the particles, and it scatters the light. We capture this scattering light to learn the precise location of the nanoparticles.鈥

It was already understood that nanoparticles were failing to accumulate in tumours, thanks to done by researchers at 缅北强奸. But the researchers have developed technologies to look at nanoparticle distribution in 3D, which provides a much fuller picture of how the particles are interacting with the rest of the tumour biology.

鈥淭he goal is to use this technology to gather knowledge for developing mathematical principles of nanoparticle distribution in cancer, similar to the way principles exist for understanding the function of the heart,鈥 says Syed. 

And because each tumour is unique, this technology and knowledge base should help future scientists to understand the barriers to drug delivery on a personalized basis and to develop custom treatments.

The next step is to understand what, in cancer鈥檚 biology, stops particles from fully penetrating tumours 鈥 and then to develop ways to bypass cancer鈥檚 defences.

But the technology is also useful for diseases other than cancer. With the help of Professor Jennifer Gommerman, a multiple sclerorsis researcher in the department of immunology, Syed and Sindhwani captured 3D images of lesions in a mouse model mimicking multiple sclerosis using nanoparticles.

鈥淭his is going to be very valuable to anyone trying to understand disease or the organ system more deeply,鈥 says Sindhwani.

Syed adds: 鈥淎nd once we understand barriers that don鈥檛 allow drugs to reach their disease site, we can start knocking them down and improving patient health.鈥

The research was supported by the Canadian Institutes of Health Research (CIHR) and the Natural Sciences and Engineering Research Council (NSERC).

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