The intercalation of flavouring compounds into layered double hydroxides
Three commercial sugar substitutes (acesulfame K, cyclamate and saccharin), a bitterness inhibitor (ferulate) and a flavour potentiator (theobromine) have been intercalated into three common layered double hydroxide (LDH) hosts ([Ca2Al(OH)6]NO3·yH2O, [LiAl2(OH)6]Cl·yH2O and [Mg 2Al(OH)6]NO3·yH2O) by...
| Main Authors: | , , |
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| Format: | Journal article |
| Language: | English |
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2011
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| _version_ | 1826282853331107840 |
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| author | Markland, C Williams, G O'Hare, D |
| author_facet | Markland, C Williams, G O'Hare, D |
| author_sort | Markland, C |
| collection | OXFORD |
| description | Three commercial sugar substitutes (acesulfame K, cyclamate and saccharin), a bitterness inhibitor (ferulate) and a flavour potentiator (theobromine) have been intercalated into three common layered double hydroxide (LDH) hosts ([Ca2Al(OH)6]NO3·yH2O, [LiAl2(OH)6]Cl·yH2O and [Mg 2Al(OH)6]NO3·yH2O) by ion exchange. These LDH-biomolecule nanohybrids have been characterised using powder X-ray diffraction, Fourier transform infrared spectroscopy, thermogravimetric analysis and solid state nuclear magnetic resonance spectroscopy which demonstrate complete intercalation of the anions into the LDH hosts. In vitro studies indicate release of these compounds' anions occurs in both deionised water and simulated saliva. Analysis of the release profiles using a number of kinetic models suggests a solution-dependent release mechanism. In some cases, release occurs at a largely constant rate up to the three-hour timepoint, suggesting that the nanocomposites could be highly suitable as carriers permitting gradual oral release of the guests in edible products. © 2011 The Royal Society of Chemistry. |
| first_indexed | 2024-03-07T00:50:06Z |
| format | Journal article |
| id | oxford-uuid:8614841a-ed1a-4def-9f08-2597d757acfb |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-07T00:50:06Z |
| publishDate | 2011 |
| record_format | dspace |
| spelling | oxford-uuid:8614841a-ed1a-4def-9f08-2597d757acfb2022-03-26T22:01:45ZThe intercalation of flavouring compounds into layered double hydroxidesJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:8614841a-ed1a-4def-9f08-2597d757acfbEnglishSymplectic Elements at Oxford2011Markland, CWilliams, GO'Hare, DThree commercial sugar substitutes (acesulfame K, cyclamate and saccharin), a bitterness inhibitor (ferulate) and a flavour potentiator (theobromine) have been intercalated into three common layered double hydroxide (LDH) hosts ([Ca2Al(OH)6]NO3·yH2O, [LiAl2(OH)6]Cl·yH2O and [Mg 2Al(OH)6]NO3·yH2O) by ion exchange. These LDH-biomolecule nanohybrids have been characterised using powder X-ray diffraction, Fourier transform infrared spectroscopy, thermogravimetric analysis and solid state nuclear magnetic resonance spectroscopy which demonstrate complete intercalation of the anions into the LDH hosts. In vitro studies indicate release of these compounds' anions occurs in both deionised water and simulated saliva. Analysis of the release profiles using a number of kinetic models suggests a solution-dependent release mechanism. In some cases, release occurs at a largely constant rate up to the three-hour timepoint, suggesting that the nanocomposites could be highly suitable as carriers permitting gradual oral release of the guests in edible products. © 2011 The Royal Society of Chemistry. |
| spellingShingle | Markland, C Williams, G O'Hare, D The intercalation of flavouring compounds into layered double hydroxides |
| title | The intercalation of flavouring compounds into layered double hydroxides |
| title_full | The intercalation of flavouring compounds into layered double hydroxides |
| title_fullStr | The intercalation of flavouring compounds into layered double hydroxides |
| title_full_unstemmed | The intercalation of flavouring compounds into layered double hydroxides |
| title_short | The intercalation of flavouring compounds into layered double hydroxides |
| title_sort | intercalation of flavouring compounds into layered double hydroxides |
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