Abstract

Heat effects induced during the storage of enteral formula under laboratory and industrial conditions were evaluated using the following indicators: furosine; loss of available amino groups, measured by decrease in o‐phthaldialdehyde (OPA) reactivity; fluorescence associated with the Maillard reaction (345 nm excitation, 415 nm emission); and colour (absorbance at 420 nm). The storage of formulas A and B (with different protein content) at 4, 20 and 30°C during 12, 24 and 36 weeks produced an increase in furosine values. Under industrial storage conditions at 55°C for between 1 and 12 weeks the behaviour of furosine differed between the two types of formulas. In Formula A (lesser protein content), there was a decrease in furosine level after the third week, whereas in formula B (greater protein content) a decrease was observed after the eighth week.The loss of OPA reactivity reached 18% and 22%, respectively, for formula B and formula A stored at 30°C for 36 weeks. In adverse storage conditions (55°C), the loss of OPA reactivity reached 50%.Fluorescence intensity (FI) and absorbance at 420 nm increased at all time/temperatures assayed. It reached values of 22.5 and 27.5 for FI and 0.161 and 0.173 for A420, respectively, for formula A and B, stored for 36 weeks at 30°C.Furosine, loss of OPA reactivity, fluorescence intensity and colour are useful indicators of nonenzymatic browning during storage of enteral formulas.

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