Self-Assembling Nanoparticles Could Improve Cancer Diagnosis

The IONPs were synthesized and characterized to tether to C-X-C chemokine receptor type 4 (CXCR4, also known as fusin) -targeted peptide ligands.

The nanoparticle is coated bio-orthogonal azide and alkyne surfaces masked by polyethylene glycol (PEG) layers. When it finds a tumor it begins to interact with the cancerous cells, resulting in the stripping off of the PEG coating, causing the nanoparticle to self-assemble into a much larger particle so that it is more visible on the scan. The researchers tested the IONPs in vitro in rats, resulting in T2 signal enhancements of around 160%. Simultaneous systemic administration of the bio-orthogonal IONPs in tumor-bearing mice demonstrated the signal-enhancing ability of the self-assembling nanomaterials. The study was published online on July 15, 2014, in Angewandte Chemie.

“By improving the sensitivity of an MRI examination, our aim is to help doctors spot something that might be cancerous much more quickly, “ said senior author Prof. Nicholas Long, PhD, of the ICL department of chemistry at Imperial College London. “The results show real promise for improving cancer diagnosis. This would enable patients to receive effective treatment sooner, which would hopefully improve survival rates from cancer.”

“We're now looking at fine tuning the size of the final nanoparticle so that it is even smaller but still gives an enhanced MRI image,” added Juan Gallo, MD, of the department of surgery and cancer. “If it is too small the body will just secrete it out before imaging, but too big and it could be harmful to the body. Getting it just right is really important before moving to a human trial.”

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