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Supramolecular Nanostructures with Tunable Donor Loading for Controlled H2S Release
被引:20
作者:
Wang, Yin
Matson, John B.
[1
]
机构:
[1] Virginia Tech, Dept Chem, Virginia Tech Ctr Drug Discovery, Blacksburg, VA 24061 USA
基金:
美国国家卫生研究院;
美国国家科学基金会;
关键词:
hydrogen sulfide;
self-assembly;
drug delivery;
controlled release;
peptide;
D O I:
10.1021/acsabm.9b00768
中图分类号:
TB3 [工程材料学];
学科分类号:
0805 ;
080502 ;
摘要:
Hydrogen sulfide ( H2S), an endogenously generated and regulated signaling gas, plays a vital role in a variety of (patho)physiological processes. In the past few years, different kinds of H2S-releasing compounds (often referred to as H2S donors) have been developed for H2S delivery, but it is still challenging to make H2S donors with tunable payloads in a simple and efficient manner. Herein, a series of peptide-H2S donor conjugates (PHDCs) with tunable donor loadings are designed for controlled H2S release. The PHDCs self-assemble into nanoribbons with different geometries in aqueous solution. Upon the addition of cysteine, these nanostructures release H2S, delivering their payload into H9C2 cells, as visualized using an H2S-selective fluorescent probe. Beyond imaging, in vitro studies show that the ability of PHDCs to mitigate doxorubicin-induced cardiotoxicity in H9C2 cardiomyocytes depends on their nanostructures and H2S release profiles. This strategy may enable the development of sophisticated H2S-releasing biomaterials for drug delivery and regenerative medicine.
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页码:5093 / 5098
页数:6
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