Therapeutic Delivery of H2S via COS: Small Molecule and Polymeric Donors with Benign Byproducts

被引:112
作者
Powell, Chadwick R. [1 ,2 ]
Foster, Jeffrey C. [1 ,2 ]
Okyere, Benjamin [3 ]
Theus, Michelle H. [3 ]
Matson, John B. [1 ,2 ]
机构
[1] Virginia Tech, Dept Chem, Blacksburg, VA 24061 USA
[2] Virginia Tech, Macromol Innovat Inst, Blacksburg, VA 24061 USA
[3] Virginia Maryland Reg Coll Vet Med, Dept Biomed Sci & Pathobiol, Duck Pond Dr, Blacksburg, VA 24061 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
HYDROGEN-SULFIDE; CARBONYL SULFIDE; NITRIC-OXIDE; SULFUR-DIOXIDE; GEM-DITHIOLS; RELEASE; ACTIVATION; ANHYDRASE; PEPTIDES; ARTERY;
D O I
10.1021/jacs.6b07204
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Carbonyl sulfide (COS) is a gas that may play important roles in mammalian and bacterial biology, but its study is limited by a lack of suitable donor molecules. We report here the use of N-thiocarboxyanhydrides (NTAs) as COS donors that release the gas in a sustained manner under biologically relevant conditions with innocuous peptide byproducts. Carbonic anhydrase converts COS into H2S, allowing NTAs to serve as either COS or H2S donors, depending on the availability of the enzyme. Analysis of the pseudo-first-order H2S release rate under biologically relevant conditions revealed a release half-life of 75 min for the small molecule NTA under investigation. A polynorbornene bearing pendant NTAs made by ring-opening metathesis polymerization was also synthesized to generate a polymeric COS/H2S donor. A half-life of 280 min was measured for the polymeric donor. Endothelial cell proliferation studies revealed an enhanced rate of proliferation for cells treated with the NTA over untreated controls.
引用
收藏
页码:13477 / 13480
页数:4
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