Microencapsulation of caffeic acid phenethyl ester and caffeic acid phenethyl amide by inclusion in hydroxypropyl-β-cyclodextrin
•Inclusion complexation of CAPE and CAPA with HP-β-CD was studied.•CAPE/HP-β-CD and CAPA/HP-β-CD inclusion complexes are formed at a molar ratio of 1:1.•NMR results showed different modes of encapsulation with CD for CAPE and CAPA.•CDs can be useful to improve biological and chemical properties of C...
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Veröffentlicht in: | Food chemistry 2018-07, Vol.254, p.260-265 |
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Sprache: | eng |
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Zusammenfassung: | •Inclusion complexation of CAPE and CAPA with HP-β-CD was studied.•CAPE/HP-β-CD and CAPA/HP-β-CD inclusion complexes are formed at a molar ratio of 1:1.•NMR results showed different modes of encapsulation with CD for CAPE and CAPA.•CDs can be useful to improve biological and chemical properties of CAPE and CAPA.•Increased aqueous solubility of CAPE/HP-β-CD can expand its industrial applications.
Caffeic acid phenethyl ester (CAPE) is a bioactive polyphenolic compound obtained from propolis extract. Although it has a broad therapeutic potential, the bioavailability of CAPE is limited, due to reduced solubility and poor plasmatic stability. Efforts to reduce these pharmacokinetic drawbacks resulted in the synthesis of caffeic acid phenethyl amide (CAPA). Cyclodextrins have been proved as promising excipients for the formulation of active ingredients. Herein, we report the inclusion complexation behavior and binding ability of CAPE and CAPA with hydroxypropyl-β-cyclodextrin (HP-β-CD). The supramolecular interactions were examined through UV and FTIR spectroscopy, DSC, 1H NMR and 2D ROESY. The CAPE/HP-β-CD and CAPA/HP-β-CD inclusion complexes stability constants were determined to be, respectively, 2911.6 and 584.6 M−1 in water and 2866.2 and 700.1 M−1 at physiological pH. The aqueous solubility increased notably, proving that HP-β-CD can be potentially useful to improve the biological, chemical and physical properties of CAPE and CAPA. |
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ISSN: | 0308-8146 1873-7072 |
DOI: | 10.1016/j.foodchem.2018.02.007 |