Drug delivery method for targeting cancer stem cells
Systems and methods for targeting specific cancer cell subpopulations present in tumor tissue are described. A system can include a first component for specifically targeting cancer stem cells and a second component for specifically targeting differentiated cancer cells. A system can include a drug conjugated to small (e.g., 5-20 nm) nanoparticles, e.g., polyhedral oligomeric silsesquioxane nanoparticles. The small nanoparticles can be preferentially taken up by cancer stem cells via macropinocytosis and can release a toxic payload within the cancer stem cells without triggering the efflux pump. A system can include a second component that targets differentiated cancer cells, e.g., a free drug or a drug encapsulated in nanoparticles.
1. A method for targeting cancer stem cells, the method comprising:
delivering a first nanoparticle to an area containing the cancer stem cells and differentiated cancer cells, the first nanoparticle having a size of from about 5 nanometers to about 20 nanometers, wherein the first nanoparticle is conjugated to a first biologically active agent that directly or indirectly affects the cancer stem cells; and
delivering a second biologically active agent to the area, wherein the second biologically active agent directly or indirectly affects the differentiated cancer cells, wherein the second biologically active agent is encapsulated in or conjugated to a second nanoparticle having a size of from about 100 nanometers to about 200 nanometer or is in the form of a free drug.
2. The method of claim 1 , wherein the first nanoparticle comprises a polyhedral oligomeric silsesquioxane.
3. The method of claim 1 , wherein the area comprises tumor tissue and tumor vasculature.
4. The method of claim 1 , wherein the second biologically active agent is released from the second nanoparticle in the area upon degradation of the nanoparticle.
5. The method of claim 1 , wherein the second biologically active agent is directly or indirectly conjugated to an antibody, the second biologically active agent binding to the to the differentiated cancer cells via the antibody.
6. The method of claim 5 , wherein the antibody specifically binds a differentiated cancer cell surface receptor.
7. The method of claim 1 , wherein the first nanoparticle comprises a polyhedral oligomeric silsesquioxane.
8. The method of claim 7 , the polyhedral oligomeric silsesquioxane comprising a structure of RSiO 1.5 , in which R is a hydrogen, an alkyl group, an aryl group, a halogen, an alkenyl group, or a combination thereof.
9. The method of claim 7 , the polyhedral oligomeric silsesquioxane comprising a structure of (RSiO 1.5 ) n in which n has a value of 6, 8, 10, or 12.
10. The method of claim 1 , wherein the second biologically active agent is the same as the first biologically active agent.
11. The method of claim 1 , wherein the second biologically active agent is different from the first biologically active agent.