Food Technology Department, XaRTA-TPV, Escola Tècnica Superior d'Enginyeria Agrària, Universitat de Lleida, Av/Alcalde Rovira Roure 191, 25198 Lleida, Spain.
Talanta. 2012 May 15;93:293-300. doi: 10.1016/j.talanta.2012.02.036. Epub 2012 Feb 23.
An improved method, based on ultra-performance liquid chromatography (UPLC) coupled to tandem mass spectrometry (MS/MS), has been developed to determine the bioactive dipeptides carnosine (CAR) and anserine (ANS) in chicken broth. These analytes are hydrophilic (polar) and in order to improve their retention, the chromatographic mode used was hydrophilic interaction chromatography (HILIC) (1.7 μm particle size). In order to remove the salt before the chromatographic analysis of the chicken broth (0.8%, w/w), an exhaustive sample pre-treatment strategy was necessary since the salt is not volatilized and could block the ionization source and lead to signal suppression. The chicken broth was firstly centrifuged to remove the fat and chicken proteins, and then was pretreated by off-line solid-phase extraction (SPE), using traditional cartridges, or off-line μElution plate (μSPE), using microplates, and the results were compared. Due to the high polar character of the dipeptides studied and the sample matrix, these compounds were not retained in the sorbent hydrophilic-lipophilic balanced (HLB) and were eluted in the load step, whereas the salt was retained in the sorbent. This fact was observed by the addition of silver nitrate in the chicken broth extract, where before the SPE or μSPE a white precipitate (silver chloride) was formed and after the SPE or μSPE this precipitate was not observed. By using these sample pre-treatment strategies, the extraction recoveries were higher than 80%, and the matrix effect was lower than 12%. Once the improved method was developed, the quality parameters of the method were studied. The LODs and LOQs of the CAR and ANS were lower than 6 and 1.8 μg/l, respectively. Then, the method was applied to analyse a commercial chicken broth. This improved method allowed determining CAR and ANS between 6 and 10mg dipeptide/l chicken broth in 10 min (sample pre-treatment and chromatographic analysis). Therefore, the proposed improved method is concluded to be rapid, sensitive and selective for the determination of polar compounds by MS in samples that contain salt.
一种基于超高效液相色谱(UPLC)与串联质谱(MS/MS)联用的改进方法已被开发出来,用于测定鸡汤中的生物活性二肽肌肽(CAR)和鹅肌肽(ANS)。这些分析物具有亲水性(极性),为了提高它们的保留,所采用的色谱模式是亲水相互作用色谱(HILIC)(1.7μm 粒径)。为了去除盐,然后对鸡汤(0.8%,w/w)进行色谱分析,需要进行详尽的样品前处理策略,因为盐不会挥发,会堵塞离子源,导致信号抑制。首先,将鸡汤离心以去除脂肪和鸡肉蛋白,然后通过离线固相萃取(SPE)进行预处理,使用传统的小柱,或通过离线μ洗脱板(μSPE),使用微板,对结果进行比较。由于研究的二肽具有很高的极性特征和样品基质,这些化合物没有保留在亲水性-疏水性平衡(HLB)的吸附剂上,而是在加载步骤中被洗脱,而盐则保留在吸附剂上。通过在鸡汤提取物中加入硝酸银可以观察到这一点,在 SPE 或 μSPE 之前,形成了白色沉淀(氯化银),而在 SPE 或 μSPE 之后,没有观察到这种沉淀。通过使用这些样品前处理策略,提取回收率高于 80%,基质效应低于 12%。一旦开发了改进的方法,就研究了方法的质量参数。CAR 和 ANS 的 LODs 和 LOQs 分别低于 6 和 1.8μg/l。然后,该方法被应用于分析一种商业鸡汤。该改进方法允许在 10 分钟内(样品前处理和色谱分析)测定 6 至 10mg 二肽/升鸡汤中的 CAR 和 ANS。因此,该方法被认为是快速、灵敏和选择性的,适用于含有盐的样品中通过 MS 测定极性化合物。