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   <subfield code="a">HPLC Determination of Lactulose in Heat Treated Milk</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Pamela Manzi, Laura Pizzoferrato]</subfield>
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   <subfield code="a">Lactulose (4-O-β-d-galactopyranosyl-d-fructose), formed from lactose (4-O-β-d-galactopyranosyl-d-glucose) by the Lobry de Bruyn-Alberda van Ekenstein rearrangement during severe heat treatments, is considered a useful indicator of heat-induced modifications in milk. Its chromatographic determination in milk is particularly troublesome due to the concomitant presence of a lactose amount two orders of magnitude larger than the lactulose amount and to a similar retention time of the two compounds. In this work, four HPLC methods have been compared with the aim to develop a more accurate analytical procedure to determine lactulose in milk, together with lactose. The developed method is based on a Carrez precipitation followed by a HPLC separation on two in-series amino-based columns, using CH3CN:H2O 75:25 (v:v) as the mobile phase at 1ml/min flow rate and a refractive index as the detector. The linearity test for the quantitation of lactulose has been carried out over the range 0.060-1.006mg/ml, the limit of detection, is 0.013mg/ml (256ng injected) and the limit of quantitation is 0.028mg/ml (556ng injected). The proposed method, simple, cheap and time-saving, allows an accurate lactulose-lactose separation, with conventional HPLC equipment.</subfield>
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