PAMAM-Calix-Dendrimers: Second Generation Synthesis, Fluorescent Properties and Catecholamines Binding
A convenient method for the synthesis of the second generation of PAMAM dendrimers based on a <i>p-tert</i>-butylthiacalix[4]arene core in <i>cone</i>, <i>partial cone</i> and <i>1,3-alternate</i> conformations was developed. Unusual fluorescence of th...
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Main Authors: | , , , , , , , |
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Format: | Book |
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MDPI AG,
2022-12-01T00:00:00Z.
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Summary: | A convenient method for the synthesis of the second generation of PAMAM dendrimers based on a <i>p-tert</i>-butylthiacalix[4]arene core in <i>cone</i>, <i>partial cone</i> and <i>1,3-alternate</i> conformations was developed. Unusual fluorescence of the obtained PAMAM-calix-dendrimers has been found and explained. The binding ability of the synthesized dendrimers toward catecholamines (dopamine, <i>L</i>-adrenaline and <i>L</i>-noradrenaline) was shown by UV-Vis, fluorescence, 1D and 2D NMR spectroscopy and the binding constants (logK<sub>a</sub> 3.85-4.74) calculated. As was shown, the PAMAM-calix-dendrimers bind catecholamines by the internal cavities. All the studied hormones were most efficiently bound by the dendrimers bearing a macrocyclic core in <i>1,3-alternate</i> conformation. The size of the formed supramolecular systems of dendrimer/catecholamine was established by the DLS method. A decrease in hemolytic activity of the PAMAM-calix-dendrimers with an increase in the generation number of a dendrimer was shown for the dendrimers with a core in <i>1,3-alternate</i> conformation. The prospects for the use of the synthesized dendrimers with the macrocyclic core as drug delivery agents were discussed. |
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Item Description: | 10.3390/pharmaceutics14122748 1999-4923 |