Czauderna Marian, Białek Małgorzata, Molik Edyta, Zaworski Kamil
The Kielanowski Institute of Animal Physiology and Nutrition, Polish Academy of Sciences, 05-110 Jabłonna, Poland.
Faculty of Animal Science, University of Agriculture in Cracow, 30-239 Kraków, Poland.
Animals (Basel). 2021 Nov 9;11(11):3196. doi: 10.3390/ani11113196.
Ultra-fast liquid chromatography (UFLC) with a photodiode array detector (DAD) for simple and rapid determination of orotic acid (OAc) in milk of sheep and cows is described. Milk samples are treated with acetonitrile (1:1, ) and then centrifuged at 4 °C. To 1 mL of the obtained supernatant 9 mL of ultrapure water was added. Subsequently, 0.5-6 µL of the resulting solution was injected into the UFLC-DAD system. Separation and quantification of OAc in milk samples was achieved using two Kinetex C18 columns (1.7 µm, 150 mm × 2.1 mm, i.d., 100 Å; Phenomenex) fitted with a pre-column of 4 mm × 2 mm, i.d. (Phenomenex) containing C packing material. All separations were performed at a column temperature of 35 °C while the ambient temperature was 21-24 °C. Satisfactory separation of OAc from endogenous species of milk can be achieved using the binary gradient elution program and UV detection at wavelengths 278 nm. Our original procedure resulted in suitable separation and quantification of OAc in milk samples; OAc eluted at 6.44 ± 0.03 min. The total run time of OAc analysis (including re-equilibration) was 27 min. As expected, the OAc peak was absent from the blank when the proposed gradient elution program and UV detection at 278 nm was used. The average recoveries of OAc standards added to milk samples were satisfactory (96.7-105.3%). The low inter-and intra-assay coefficient of variation derived from the measurements of OAc in cow and ovine milk samples (i.e., 0.784%, 1.283% and 0.710%, 1.221%, respectively) and in O-Ac standards (i.e., 0.377% and 0.294%, respectively), as well as high recoveries of OAc added to ovine and cows' milk (~100%) and the low detection (0.04 ng) and quantification (0.12 ng) limits point to satisfactory accuracy, precision and sensitivity of the reported method. OAc concentrations in ovine milk samples were within the range from 25 to 36 mg/L, while OAc levels in cows' milk samples was found in the range of 32-36 mg/L. Our original procedure is suitable for routine quantification of OAc in milk of ewes and cows.
描述了一种采用光电二极管阵列检测器(DAD)的超快速液相色谱法(UFLC),用于简单快速地测定绵羊奶和牛奶中的乳清酸(OAc)。牛奶样品用乙腈(1:1, )处理,然后在4℃下离心。向1mL获得的上清液中加入9mL超纯水。随后,将0.5 - 6μL所得溶液注入UFLC - DAD系统。使用两根Kinetex C18柱(1.7μm,150mm×2.1mm,内径,100Å;Phenomenex)和一根4mm×2mm内径的预柱(Phenomenex,含C填充材料)实现牛奶样品中OAc的分离和定量。所有分离均在柱温35℃下进行,环境温度为21 - 24℃。使用二元梯度洗脱程序和278nm波长的紫外检测可实现OAc与牛奶内源性物质的良好分离。我们原来的方法能够对牛奶样品中的OAc进行合适的分离和定量;OAc在6.44±0.03分钟洗脱。OAc分析的总运行时间(包括重新平衡)为27分钟。正如预期的那样,当使用所提出的梯度洗脱程序和278nm紫外检测时空白中没有OAc峰。添加到牛奶样品中的OAc标准品的平均回收率令人满意(96.7 - 105.3%)。牛和羊牛奶样品中OAc测量值的低批间和批内变异系数(即分别为0.784%,1.283%和0.710%,1.221%)以及O - Ac标准品中的低变异系数(即分别为0.377%和0.294%),以及添加到羊和牛奶中的OAc的高回收率(~100%)和低检测限(0.04ng)及定量限(0.12ng)表明所报道方法具有令人满意的准确性、精密度和灵敏度。绵羊奶样品中OAc浓度在25至36mg/L范围内,而牛奶样品中OAc水平在32 - 36mg/L范围内。我们原来的方法适用于常规定量测定母羊和奶牛奶中的OAc。