Roig M G, Bello J F, Kennedy J F, Rivera Z S, Lloyd L L
Departamento de Química Física, Facultad de Farmacia, Universidad de Salamanca, Spain.
Bioseparation. 1992;3(2-3):177-84.
An HPLC method using a reversed-phase macroreticular PLRP-S column and phosphate buffer as eluent is described for the analysis of L-ascorbic acid degradation products, 5-hydroxymethyl furfuraldehyde and furfuraldehyde, in processed fruit juices. Measurement of the levels of 5-HMF and furfuraldehyde in citrus juices against time showed the presence of 5-HMF (0.45 mg l-1) even at zero time. An assessment on the effect of the additives on the formation of 5-HMF of reconstituted single-strength orange juice showed virtually the same results for all the samples stored at 4 degrees C and 20 degrees C, irrespective of the additive. For citrus juice samples which had been subjected to accelerated degradation, those that showed the highest decomposition of L-ascorbic acid, produced the highest level of 5-HMF. The presence of furfuraldehyde in any of the samples was not detected, probably due to the fact that furfuraldehyde was formed in such small amounts which are below the minimum detectability limit of the method (0.050 mg l-1).
本文描述了一种采用反相大孔PLRP-S柱和磷酸盐缓冲液作为洗脱剂的高效液相色谱法,用于分析加工果汁中L-抗坏血酸的降解产物5-羟甲基糠醛和糠醛。对柑橘汁中5-羟甲基糠醛和糠醛含量随时间的测定表明,即使在零时刻也存在5-羟甲基糠醛(0.45 mg l-1)。对添加剂对复原单倍浓缩橙汁中5-羟甲基糠醛形成的影响进行的评估表明,对于所有在4℃和20℃下储存的样品,无论添加何种添加剂,结果几乎相同。对于经过加速降解的柑橘汁样品,那些L-抗坏血酸分解程度最高的样品,产生的5-羟甲基糠醛含量也最高。在任何样品中均未检测到糠醛,这可能是因为糠醛的生成量极少,低于该方法的最低检测限(0.050 mg l-1)。