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- W2132446533 abstract "Curcumin and S-trans, trans-farnesylthiosalicylic acid (FTS) are two promising anticancer agents. In this study, we demonstrated that the two agents exerted significant synergy in antitumor activity in various types of cancer cells with combination indices ranging from 0.46 to 0.98 (a value of less than unity indicates synergism). We have further shown that synergistic-targeted co-delivery of the two agents can be achieved via formulating curcumin in polyethylene glycol (PEG)-derivatized FTS-based nanomicellar system. Curcumin formulated in PEG-FTS micelles had small size of around 20 nm. The nanomicellar curcumin demonstrated enhanced cytotoxicity towards several cancer cell lines in vitro. Intravenous application of curcumin-loaded micelle (20 mg kg−1 curcumin) led to a significantly more effective inhibition of tumor growth in a syngeneic mouse breast cancer model (4T1.2) than curcumin formulated in Cremophor/EL (P < 0.05)." @default.
- W2132446533 created "2016-06-24" @default.
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- W2132446533 date "2014-04-05" @default.
- W2132446533 modified "2023-10-17" @default.
- W2132446533 title "Targeted Delivery of Curcumin to Tumors via PEG-Derivatized FTS-Based Micellar System" @default.
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- W2132446533 doi "https://doi.org/10.1208/s12248-014-9595-6" @default.
- W2132446533 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4012035" @default.
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