Combination therapy is extensively developed for cancer treatment in recent years due to its high efficiency.Herein,we constructed a nanocomposite based on gold nanorods(GNRs)and drug-loaded tetrahedral DNA nanostruct...Combination therapy is extensively developed for cancer treatment in recent years due to its high efficiency.Herein,we constructed a nanocomposite based on gold nanorods(GNRs)and drug-loaded tetrahedral DNA nanostructures(TDN)for chemophotothermal combinational therapy.Anti-tumor drug doxorubicin(DOX)was loaded via the insertion within GC base pairs of TDN.The aptamer AS1411 was attached to the apex of TDN(ATDN)to target tumor cells.The DOX-loaded DNA tetrahedron(ATDN-DOX)was compressed by the GNRs coated with PEI(GNRs@ATDN-DOX)to realize the photothermal function and lysosome escape.GNRs under the illumination of 808nm infrared laser showed high photothermal conversion and stability due to the protection of PEI layer.The drug-loading capacity of ATDN-DOX was as high as 314 DOX molecules in per ATDN.The positive charge of PEI in GNRs@ATDN-DOX nanocomposites was utilized to achieve excellent cell penetration and induce proton sponge effect for lysosomal escape.The nanocomposites presented HeLa and 4T1 cells targeting and resulted in efficient anticancer activity.展开更多
基金supported by the National Natural Science Foundation of China(51873121).
文摘Combination therapy is extensively developed for cancer treatment in recent years due to its high efficiency.Herein,we constructed a nanocomposite based on gold nanorods(GNRs)and drug-loaded tetrahedral DNA nanostructures(TDN)for chemophotothermal combinational therapy.Anti-tumor drug doxorubicin(DOX)was loaded via the insertion within GC base pairs of TDN.The aptamer AS1411 was attached to the apex of TDN(ATDN)to target tumor cells.The DOX-loaded DNA tetrahedron(ATDN-DOX)was compressed by the GNRs coated with PEI(GNRs@ATDN-DOX)to realize the photothermal function and lysosome escape.GNRs under the illumination of 808nm infrared laser showed high photothermal conversion and stability due to the protection of PEI layer.The drug-loading capacity of ATDN-DOX was as high as 314 DOX molecules in per ATDN.The positive charge of PEI in GNRs@ATDN-DOX nanocomposites was utilized to achieve excellent cell penetration and induce proton sponge effect for lysosomal escape.The nanocomposites presented HeLa and 4T1 cells targeting and resulted in efficient anticancer activity.
