Molecular Pharmaceutics · 2017 · 88 citations · 34 references
We report the preparation of S-aroylthiooxime (SATO) functionalized amphiphilic block copolymer micelles that release hydrogen sulfide (H<sub>2</sub>S), a gaseous signaling molecule of relevance to various physiological and pathological conditions. The micelles release H<sub>2</sub>S in response to cysteine with a half-life of 3.3 h, which is substantially slower than a related small molecule SATO. Exogenous administration of H<sub>2</sub>S impacts growth and proliferation of cancer cells; however, the limited control over H<sub>2</sub>S generation from inorganic sulfide sources results in conflicting reports. Therefore, we compare the cellular cytotoxicity of SATO-functionalized micelles, which release H<sub>2</sub>S in a sustained manner, to Na<sub>2</sub>S, which releases H<sub>2</sub>S in a single dose. Our results show that H<sub>2</sub>S-releasing micelles significantly reduce the survival of HCT116 colon cancer cells relative to Na<sub>2</sub>S, GYY4137, and a small molecule SATO, indicating that release kinetics may play an important role in determining toxicity of H<sub>2</sub>S toward cancer cells. Furthermore, H<sub>2</sub>S-releasing micelles are well tolerated by immortalized fibroblasts (NIH/3T3 cells), suggesting a selective toxicity of H<sub>2</sub>S toward cancer cells.
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Characterization of a Novel, Water-Soluble Hydrogen Sulfide–Releasing Molecule (GYY4137)
Ling Li, Matthew Whiteman, Yanyi Guan et al. · Circulation · 2008 · 818 citations · Full text