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Diffusion and Birefringence of Bioactive Dyes in a Supramolecular Guanosine Hydrogel
Transparent self‐standing supramolecular hydrogels were readily prepared by the potassium‐ion‐mediated self‐organization of guanosine and 8‐bromoguanosine whilst the individual components precipitated within a few hours. VT‐NMR spectroscopy showed that bromoguanosine was a superior gelator compared...
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Published in: | Chemistry : a European journal 2012-05, Vol.18 (19), p.6008-6014 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Transparent self‐standing supramolecular hydrogels were readily prepared by the potassium‐ion‐mediated self‐organization of guanosine and 8‐bromoguanosine whilst the individual components precipitated within a few hours. VT‐NMR spectroscopy showed that bromoguanosine was a superior gelator compared to guanosine. XRD analysis showed that gel formation was caused by stacked G‐quartets. AFM analysis revealed dendritic architectures of the nanofibers in the two‐component hydrogel network. DSC profiles showed that the hybrid hydrogels underwent sol–gel transition at lower temperature than the pure guanosine and bromoguanosine hydrogels. Interestingly, bioactive dyes, such as rose bengal, rhodamine‐6‐G, and fluorescein, could be diffused and released in a controlled manner. UV/Vis absorption and fluorescence spectroscopy and CLSM were used to investigate the diffusion behavior of dyes in the hydrogel network. These dyes exhibited strong birefringence in the gel network (0.07–0.1) as a result of the anisotropic organization.
Old before I dye: The K+‐ion‐mediated self‐association of two simple nucleoside building blocks, guanosine and bromoguanosine, produced transparent self‐standing supramolecular hydrogels with dendritic nanoarchitectures (see figure) that diffused and released bioactive small molecules and exhibited strong birefringence in the presence of dyes. |
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ISSN: | 0947-6539 1521-3765 |
DOI: | 10.1002/chem.201103814 |