The researchers demonstrated the method in mice in a study published online Aug. 15 in Nature Communications.
Glioblastoma is an aggressive brain cancer that affects about 12,000 people annually in the U.S.; patients have a median survival of 15 to 18 months after diagnosis. Current treatments, which include surgery, chemotherapy and radiation, are largely ineffective. It is difficult to get chemotherapy into glioblastoma tumors because most medications will not pass through the blood-brain barrier, which is a unique property of blood vessels in the brain that restrict and actively prevent substances in the bloodstream from reaching the brain parenchyma.
The barrier acts like a highly selective filter and protective barrier for the brain, said co-corresponding author of the study Dr. Zhenpeng Qin, associate professor of mechanical engineering and Fellow, Eugene McDermott Professor in the Erik Jonsson School of Engineering and Computer Science.
"The biggest challenge to treat any brain disease is this barrier. It’s amazing; it's only a micron thick, but it prevents 98% of molecules from getting inside the brain," Qin said. By comparison, the diameter of human hair is 70 microns.
Qin collaborated with UT Southwestern colleagues Dr. Robert Bachoo, co-corresponding author and associate professor of neurology and internal medicine, and Dr. Elizabeth Maher, professor of internal medicine and neurology. The research involved genetically engineered mice that had mutations found in human glioblastoma patients.
Qin's drug-delivery method relies on co-delivering medication with vessel-targeted gold nanoparticles, which are injected into the bloodstream. From an external source, researchers apply short laser pulses, which pass through the mouse skull and activate the gold nanoparticles. This activation generates thermomechanical waves and briefly makes the blood-brain barrier permeable, allowing medication to reach its target. In their experiments, researchers used paclitaxel, a chemotherapy drug used to treat ovarian, breast and lung cancers, which was abandoned for potential use against brain cancer because, on its own, the drug molecule does not cross the barrier.
The study demonstrated that the new approach overcame the barrier, although years of research will be needed before the method can be tested in humans. Further preclinical studies are ongoing.
"The tumors shrank in size, and we expanded survival by more than 50%," Qin said. "We hope this will lead to expanded therapeutic options for treating diseases in the brain and central nervous system."
Qin has received two grants since 2019 totaling more than $1 million from the Cancer Prevention & Research Institute of Texas to fund his research, which he said "would be impossible without CPRIT's support."
In addition, the work was funded by grants from the Department of Defense, the National Science Foundation (2123971), the National Institutes of Health (RF1NS110499) and the American Heart Association.
Cai Q, Li X, Xiong H, Fan H, Gao X, Vemireddy V, Margolis R, Li J, Ge X, Giannotta M, Hoyt K, Maher E, Bachoo R, Qin Z.
Optical blood-brain-tumor barrier modulation expands therapeutic options for glioblastoma treatment.
Nat Commun. 2023 Aug 15;14(1):4934. doi: 10.1038/s41467-023-40579-1