HPLC methods are described for the determination of furanic compounds (hydr
oxymethylftufural and furfural) in enteral formulas prepared with dextrinom
altose and milk proteins, and in model systems enclosing these ingredients.
These compounds were extracted in aqueous solution, purified with organic
solvents, and separated in a reversed-phase C-18 column with water-acetonit
rile (95:5 v/v). Average recovery rates of HMF and furfural were 99.2% and
71.1%, respectively. The variation coefficients for HMF and furfural were 2
.41% and 1.23%, respectively. The detection limit was 0.01 mg/L for both co
mpounds. HMF and furfural levels in enteral formulas ranged from 0.05 to 19
.1 mg/L and from 0.14 to 0.72 mg/L, respectively.