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1.
Food Chem ; 171: 32-9, 2015 Mar 15.
Article in English | MEDLINE | ID: mdl-25308639

ABSTRACT

The objective of this study was to produce and characterise xylitol microcapsules for use in foods, in order to prolong the sweetness and cooling effect provided by this ingredient. Complex coacervation was employed as the microencapsulation method. A preliminary double emulsion step was performed due to the hydrophilicity of xylitol. The microcapsules obtained were characterised in terms of particle size and morphology (optical, confocal and scanning electron microscopy), solubility, sorption isotherms, FTIR, encapsulation efficiency and release study. The microcapsules of xylitol showed desirable characteristics for use in foods, such as a particle size below 109 µm, low solubility and complete encapsulation of the core by the wall material. The encapsulation efficiency ranged from 31% to 71%, being higher in treatments with higher concentrations of polymers. Release of over 70% of the microencapsulated xylitol in artificial saliva occurred within 20 min.


Subject(s)
Food Industry/methods , Sweetening Agents/chemistry , Xylitol/chemistry , Capsules , Chewing Gum , Emulsions , Microscopy, Confocal , Microscopy, Electron, Scanning , Models, Biological , Particle Size , Saliva/chemistry , Solubility , Surface Properties
2.
Food Chem ; 139(1-4): 72-8, 2013 Aug 15.
Article in English | MEDLINE | ID: mdl-23561080

ABSTRACT

The objective of this work was to microencapsulate aspartame by double emulsion followed by complex coacervation, aiming to protect it and control its release. Six treatments were prepared using sunflower oil to prepare the primary emulsion and gelatin and gum Arabic as the wall materials. The microcapsules were evaluated structurally with respect to their sorption isotherms and release into water (36°C and 80°C). The microcapsules were multinucleated, not very water-soluble or hygroscopic and showed reduced rates of equilibrium moisture content and release at both temperatures. FTIR confirmed complexation between the wall materials and the intact nature of aspartame. The results indicated it was possible to encapsulate aspartame with the techniques employed and that these protected the sweetener even at 80°C. The reduced solubility and low release rates indicated the enormous potential of the vehicle developed in controlling the release of the aspartame into the food, thus prolonging its sweetness.


Subject(s)
Aspartame/chemistry , Food Technology/methods , Sweetening Agents/chemistry , Capsules/chemistry , Emulsions/chemistry , Food Technology/instrumentation , Hot Temperature , Kinetics , Solubility
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