IBBME PhD candidates Abdullah Syed (centre) and Shrey Sindhwani in the lab of Professor Warren Chan (right). The research team has published a paper investigating the biological barriers faced by therapeutic nanoparticles in reaching cancerous tumours. (Photo: Neil Ta).
August 8, 2017 | By Heidi Singer
For cancer patients, understanding the odds of a treatment’s success can be bewildering. The same drug, applied to the same type of cancer, might be fully successful on one person’s tumour and do nothing for another one. Physicians are often unable to explain why.
Now, U of T researchers are beginning to understand one of the reasons. Abdullah Syed and Shrey Sindhwani, both PhD candidates, and their colleagues at the Institute of Biomaterials & Biomedical Engineering (IBBME) have created a technology to watch nanoparticles traveling into tumours — revealing barriers that prevent their delivery to targets and the variability between cancers.
“The biggest thing we’ve noticed is that nanoparticles face multiple challenges posed by the tumour itself on their way to cancer cells,” says Sindhwani, an MD-PhD student in the Integrated Nanotechnology & Biomedical Sciences Laboratory of Professor Warren Chan (IBBME). Syed and Sindhwani co-published their findings online June 22, and on the cover of the Journal of the American Chemical Society. “So the treatment might work for a while — or worse, there’s 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.”
Tiny “nanoparticles” offer great hope for the treatment of cancer and other disease 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’t 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’s journey inside tumours. They discovered that the tough-to-see particles could be illuminated by scattering light off their surfaces.
“The sensitivity of our imaging is about 1.4 millionfold higher,” says Syed. “First, 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.”
It was already understood that nanoparticles were failing to accumulate in tumours, thanks to a meta-analysis of the field done by Chan’s group. 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. “The 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,” 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’s biology stops particles from fully penetrating tumours — and then to develop ways to bypass cancer’s defences.
But the technology is also useful for diseases other than cancer. With the help of Professor Jennifer Gommerman, an researcher in the Department of Immunology who studies multiple sclerosis (MS), Syed and Sindhwani captured 3D images of lesions in a mouse model mimicking MS using nanoparticles.
“This is going to be very valuable to anyone trying to understand disease or the organ system more deeply,” says Sindhwani. “And once we understand barriers that don’t allow drugs to reach their disease site, we can start knocking them down and improving patient health” adds Syed.