Washington | Scientists have for the first time developed a technique that coats anti-cancer drugs in membranes made from patient’s own platelets, allowing the drugs to last longer in the body and attack tumours. The technique was tested successfully in an animal model, researchers said. There are two key advantages to using platelet membranes to coat anticancer drugs, said Zhen Gu, assistant professor in the joint biomedical engineering program at North Carolina State University and the University of North Carolina at Chapel Hill.
First, the surface of cancer cells has an affinity for platelets, they stick to each other. Second, because the platelets come from the patient’s own body, the drug carriers aren’t identified as foreign objects, so last longer in the bloodstream, said Gu, corresponding author of research paper. This combination of features means that the drugs can not only attack the main tumour site, but are more likely to find and attach themselves to tumour cells circulating in the bloodstream essentially attacking new tumours before they start, said Quanyin Hu.
In the process, blood is taken from a patient then a lab mouse in the case of this research and the platelets are collected from that blood. The isolated platelets are treated to extract the platelet membranes, which are then placed in a solution with a nanoscale gel containing the anticancer drug doxorubicin (Dox), which attacks the nucleus of a cancer cell. The solution is compressed, forcing the gel through the membranes and creating nanoscale spheres made up of platelet membranes with Dox-gel cores.
These spheres are then treated so that their surfaces are coated with the anticancer drug TRAIL, which is most effective at attacking the cell membranes of cancer cells. When released into a patient’s bloodstream, these pseudo platelets can circulate for up to 30 hours, as compared to approximately six hours for the nanoscale vehicles without the coating.
When one of the pseudo-platelets comes into contact with a tumour, three things happen more or less at the same time. First, the P-Selectin proteins on the platelet membrane bind to the CD44 proteins on the surface of the cancer cell, locking it into place. Second, the TRAIL on the pseudo-platelet’s surface attacks the cancer cell membrane. Third, the nanoscale pseudo-platelet is effectively swallowed by the larger cancer cell. The acidic environment inside the cancer cell then begins to break apart the pseudo-platelet – freeing the Dox to attack the cancer cell’s nucleus.
In mice, the researchers found that using Dox and TRAIL in the pseudo-platelet drug delivery system was significantly more effective against large tumours and circulating tumour cells than using Dox and TRAIL in a nano-gel delivery system without the platelet membrane.
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