Synthesis of hybrid polyphenol/hydroxyapatite nanomaterials: adsorption vs. in situ incorporation

29 November 2021, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Plant-derived natural bioactive molecules are of great therapeutic potential but their application in nanomedicine has been so far scarcely studied. This work aimed at comparing two methodologies, i.e. adsorption and in situ incorporation, to prepare hybrid polyphenol/hydroxyapatite nanoparticles. Two flavonoids, baicalin and its aglycone derivative baicalein, and two phenolic acids derived from caffeic acid, rosmarinic and chlorogenic acids, were studied. Adsorption of these polyphenols on pre-formed hydroxyapatite nanoparticles did not modify particles size or shape and loading was less than 10 % (w/w). In contrast, presence of polyphenols during the synthesis of nanoparticles significantly impacted, and sometimes fully inhibited, hydroxyapatite formation, but recovered particles could exhibit higher loadings. Antioxidant properties of the polyphenols were preserved after adsorption but not when incorporated in situ. These results provide fruitful clues for the valorization of natural bioactive molecules in nanomedicine

Keywords

Hydroxyapatite
Polyphenols
Nanoparticles
Antioxidants

Supplementary materials

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S1. N2 sorption isotherm of hydroxyapatite nanoparticle powder S2. TGA analyses of hydroxyapatite nanoparticles before and after adsorption of polyphenols S3. TGA analyses of hydroxyapatite nanoparticles synthesized in presence of polyphenols S4. ESI-MS spectra of baicalin (a) and baicalein (b) in ammonium bicarbonate buffer at pH 7.8 in presence of calcium at ratio BA or BE /Ca = 1:1. BA or BE concentration = 50 µM S5. Stability of (a) RA, (b) CA, (c) BE and (d) BA at pH 12. S6. XRD of powder recovered after 30 min in solution of Ca(OH)2 and Ca(OH)2 + RA, and comparison with XRD of calcite (PDF card 05-0586)
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