| Literature DB >> 28300411 |
Jeffrey C Foster1, Scott C Radzinski1, Xianlin Zou2, Carla V Finkielstein2, John B Matson1.
Abstract
We report the preparation of S-aroylthiooxime (SATO) functionalized amphiphilic block copolymer micelles that release hydrogen sulfide (H2S), a gaseous signaling molecule of relevance to various physiological and pathological conditions. The micelles release H2S 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 H2S impacts growth and proliferation of cancer cells; however, the limited control over H2S generation from inorganic sulfide sources results in conflicting reports. Therefore, we compare the cellular cytotoxicity of SATO-functionalized micelles, which release H2S in a sustained manner, to Na2S, which releases H2S in a single dose. Our results show that H2S-releasing micelles significantly reduce the survival of HCT116 colon cancer cells relative to Na2S, GYY4137, and a small molecule SATO, indicating that release kinetics may play an important role in determining toxicity of H2S toward cancer cells. Furthermore, H2S-releasing micelles are well tolerated by immortalized fibroblasts (NIH/3T3 cells), suggesting a selective toxicity of H2S toward cancer cells.Entities:
Keywords: H2S donors; RAFT; controlled release; gasotransmitter; polymer amphiphiles
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Year: 2017 PMID: 28300411 DOI: 10.1021/acs.molpharmaceut.6b01117
Source DB: PubMed Journal: Mol Pharm ISSN: 1543-8384 Impact factor: 4.939