Cancer-Cell-Specific Mitochondria-Targeted Drug Delivery by Dual-Ligand-Functionalized Nanodiamonds Circumvent Drug Resistance

Miu Shan Chan*, Pik Kwan L0

*Corresponding author for this work

Research output: Conference PapersPosterpeer-review

Abstract

The application of nanodiamond is rapidly expanded from diagnosis to treatment due to its promising drug loading and non-photo-quenching imaging properties. However, the delivery of sufficient drug amount to the targeted disease site is greatly important in therapeutics. Hence, we developed a cancer-cell-specific sub-cellular organelle-targeted delivery based on photostable Nanodiamond (ND), which is functionalized with folic acid and Mitochondrial Localizing Sequence (MLS) peptides. This dual-ligand-functionalized ND platform does not only distinguish the cancer cells via the overexpression of folate receptors on cell membrane, it also localizes to mitochondria. Importantly, the Doxorubicin (DOX) loaded dual-ligandfunctionalized ND platform induces a significant cytotoxicity in drug resistance cancer cell (MCF-7/ADR) comparing to the free Doxorubicin localized in lysosomes because the localization in mitochondria enhances the retention time of DOX inside the MCF-7/ADR, which has the significant circumvention of P-glycoprotein to pump out the drug inside the cell. This work successfully demonstrates nanodiamond-based nanocarriers for cancer-cell- specific mitochondria-targeted delivery and overcomes drug resistance in Doxorubicin-resistant human breast adenocarcinoma cancer cells.

Conference

Conference2nd International Conference and Exhibition on Nanomedicine and Drug Delivery
PlaceJapan
CityTokyo
Period21/05/1823/05/18
Internet address

Bibliographical note

Research Unit(s) information for this record is provided by the author(s) concerned.

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