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. 2020 Oct 29;15:8383–8400. doi: 10.2147/IJN.S272495

Figure 1.

Figure 1

Schematic diagram for targeted liver cancer treatment using the nano-drug TLS11a-LB@TATp-MSN/DOX. The nuclear localization peptide (TATp)-mesoporous silica nanoparticle (MSN) complex (TATp-MSN) was synthesized and mixed with doxorubicin (DOX) (I). Liposomes that carried the liver cancer-specific aptamer TLS11a (TLS11a-LB) were produced (II). The nano-drug TLS11a-LB@TATp-MSN/DOX was generated by mixing TLS11a-LB and TATp-MSN/DOX (III). (IV) After intravenous injection, TLS11a-LB@TATp-MSN/DOX was designed to be distributed via blood circulation to liver cancer tissues through TLS11a targeting (a-b), to be localized to the nuclei of the cancer cells through TATp targeting, and to release DOX (c-e).