Publication Type:

Journal Article

Source:

Biomaterials, Volume 104, p.119 - 128 (2016)

URL:

http://www.sciencedirect.com/science/article/pii/S0142961216303416

Keywords:

Anti-tumor, hypoxia, Prodrug, Solid tumor, theranostic

Abstract:

Abstract Hypoxia, a distinguished feature of various solid tumors, has been considered as a key marker for tumor progression. Inadequate vasculature and high interstitial pressures result in relatively poor drug delivery to these tumors. Herein, we developed an antitumor theranostic agent, 4, which is activated in hypoxic conditions and can be used for the diagnosis and treatment of solid tumors. Compound 4, bearing biotin, a tumor-targeting unit, and SN38, an anticancer drug, proved to be an effective theranostic agent for solid tumors. \{SN38\} plays a dual role: as an anticancer drug for therapy and as a fluorophore for diagnosis, thus avoids an extra fluorophore and limits cytotoxicity. Compound 4, activated in the hypoxic environment, showed high therapeutic activity in \{A549\} and HeLa cells and spheroids. In vivo imaging of solid tumors confirmed the tumor-specific localization, deep tissue penetration and activation of compound 4, as well as the production of a strong anticancer effect through the inhibition of tumor growth in a xenograft mouse model validating it as a promising strategy for the treatment of solid tumors.

Cite this Research Publication

R. Kumar, Kim, E. - J., Han, J., Lee, H., Shin, W. Sup, Kim, H. Min, Bhuniya, S., Kim, J. Seung, and Hong, K. Soo, “Hypoxia-directed and activated theranostic agent: Imaging and treatment of solid tumor”, Biomaterials, vol. 104, pp. 119 - 128, 2016.

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