Supramolecular Nanostructures with Tunable Donor Loading for Controlled H2S Release
Author(s) -
Yin Wang,
John B. Matson
Publication year - 2019
Publication title -
acs applied bio materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.764
H-Index - 17
ISSN - 2576-6422
DOI - 10.1021/acsabm.9b00768
Subject(s) - nanotechnology , supramolecular chemistry , drug delivery , controlled release , hydrogen sulfide , nanostructure , chemistry , payload (computing) , regenerative medicine , biophysics , materials science , molecule , computer science , biochemistry , organic chemistry , computer network , sulfur , network packet , biology , cell
Hydrogen sulfide (H 2 S), 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 H 2 S-releasing compounds (often referred to as H 2 S donors) have been developed for H 2 S delivery, but it is still challenging to make H 2 S donors with tunable payloads in a simple and efficient manner. Herein, a series of peptide-H 2 S donor conjugates (PHDCs) with tunable donor loadings are designed for controlled H 2 S release. The PHDCs self-assemble into nanoribbons with different geometries in aqueous solution. Upon addition of cysteine, these nanostructures release H 2 S, delivering their payload into H9C2 cells, as visualized using an H 2 S-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 H 2 S release profiles. This strategy may enable the development of sophisticated H 2 S-releasing biomaterials for drug delivery and regenerative medicine.
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