Scientists have created a triple-stage “cluster bomb” technique for delivering the chemotherapy drug cisplatin, through nanoparticles designed to break up when they reach a tumor. The particles have not been tested in humans, although similar ways of packaging cisplatin have been in clinical trials.
What makes these particles distinctive is that they start out relatively large, 100 nanometers wide. This is to allow smooth transport into the tumor through leaky blood vessels. Then, in acidic conditions found close to tumors, the particles release “bomblets” just 5 nanometers in size.
Inside tumor cells, a second chemical step activates the platinum-based cisplatin, which kills by crosslinking and damaging DNA. Doctors have used cisplatin to fight several types of cancer for decades, but toxic side effects – to the kidneys, nerves and inner ear—can limit its effectiveness.
Co-lead author Jinzhi Du said:
“The negative side effects of cisplatin are a long-standing limitation for conventional chemotherapy. In our study, the delivery system was able to improve tumor penetration to reach more cancer cells, as well as release the drugs specifically inside cancer cells through their size-transition property.”
The finding is the result of a collaboration between a team led by professor Jun Wang, PhD at the University of Science and Technology of China, and researchers led by professor Shuming Nie, PhD in the Wallace H. Coulter Department of Biomedical Engineering at Georgia Tech and Emory.
Nie is a member of the Discovery and Developmental Therapeutics research program at Winship Cancer Institute of Emory University. The lead authors are graduate student Hong-Jun Li and postdoctoral fellows Jinzhi Du, PhD and Xiao-Jiao Du, PhD.
Increased Platinum Levels
The researchers showed that their nanoparticles could enhance cisplatin drug accumulation in tumor tissues.
When mice bearing human pancreatic tumors were given the same doses of free cisplatin or cisplatin clothed in pH-sensitive nanoparticles, the level of platinum in tumor tissues was seven times higher with the nanoparticles. This suggests the possibility that nanoparticle delivery of a limited dose of cisplatin could restrain the toxic side effects during cancer treatment.
The researchers also showed that the nanoparticles were effective against a cisplatin-resistant lung cancer model and an invasive metastatic breast cancer model in mice. In the lung cancer model, a dose of free cisplatin yielded just 10 percent growth inhibition, while the same dose clothed in nanoparticles yielded 95 percent growth inhibition, the researchers report.
In the metastatic breast cancer model, treating mice with cisplatin clothed in nanoparticles prolonged animal survival by weeks; 50 percent of the mice were surviving at 54 days with nanoparticles compared with 37 days for the same dose of free cisplatin.
Enhanced efficacy in three different tumor models demonstrate that this strategy may be applicable to several types of cancer, Jinzhi Du says.
Hong-Jun Li et al.
Stimuli-responsive clustered nanoparticles for improved tumor penetration and therapeutic efficacy
Proceedings of the National Academy of Sciences (2016). DOI: 10.1073/pnas.1522080113
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