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- W2331873103 abstract "Dexamethasone (DEX) is a well-known anti-inflammatory drug, whose widespread clinical use is nevertheless restricted by its serious side effects. By conjugation of DEX with C60, we found that this nanomedicine retained the anti-inflammatory activity of DEX while reducing side effects in the animal model. In mouse thymocytes, the CCK-8 assay showed that the cytotoxicity of DEX–C60 was significantly lower than that of free DEX. Flow cytometric studies revealed that incubation with DEX–C60 induced much less apoptotic thymocytes. Interestingly, such reduced cytotoxicity and apoptosis were not observed when equal moles of free C60 and free DEX were coincubated with thymocytes, suggesting that the conjugation alters the signal pathway of DEX. Indeed, we found that the binding of DEX–C60 and a glucocorticoid receptor (GR) was partially blocked in the thymocytes, which resulted in down-regulation of several apoptosis-related genes. These findings help understand the mechanism of beneficial effects of this new nanomedicine, DEX–C60, and promote its clinical applications." @default.
- W2331873103 created "2016-06-24" @default.
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- W2331873103 date "2013-05-17" @default.
- W2331873103 modified "2023-10-01" @default.
- W2331873103 title "Conjugation of Dexamethasone to C60 for the Design of an Anti-Inflammatory Nanomedicine with Reduced Cellular Apoptosis" @default.
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- W2331873103 doi "https://doi.org/10.1021/am401153k" @default.
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