Department of Ecology and Marine Resources, IMEDEA (CSIC-UIB) Mediterranean Institute for Advanced Studies, Balearic Islands, Spain.
Anal Chim Acta. 2011 Sep 2;701(1):81-5. doi: 10.1016/j.aca.2011.04.040. Epub 2011 Jun 2.
A high-performance liquid chromatography method was developed for the separation and determination of four cobalamins in seawater. Chromatographic separation was performed on a reversed-phase discovery RP-amide C(16) column with buffer potassium dihydrogenphosphate and acetonitrile as the mobile phases in linear gradients elution mode. Cobalamins were previously preconcentrated in C(18) resins cartridges. Detection was performed using UV-diode array detector in a range of λ of 200-400 nm. The method showed to be linear over a range of 1-300 ng mL(-1) with acceptable precision and accuracy. The detection limits ranged between 0.07 pg mL(-1) for 5'-deoxyadenosylcobalamin and 0.5 pg mL(-1) for hydroxocobalamin. The mean cobalamins recoveries for direct determination ranged between 76 and 93% for hydroxo-, cyano- and methylcobalamin, while the recovery for 5'-deoxyadenosylcobalamin was only 31% suggesting that the preconcentration method was not valid for this cobalamin. The method was successfully applied to coastal seawater where the concentrations ranged from 4.2 to 7.3 ng L(-1) for hydroxo-, 1.4-3.9 ng L(-1) for cyano-, 2.1-4.6 ng L(-1) for 5'-deoxyadenosyl- and 33-83.5 ng L(-1) for methylcobalamin.
建立了一种高效液相色谱法,用于分离和测定海水中的四种钴胺素。采用反相 discovery RP-amide C(16)柱,以磷酸二氢钾缓冲液和乙腈为流动相,在线性梯度洗脱模式下进行色谱分离。钴胺素先前在 C(18)树脂柱中预浓缩。采用紫外二极管阵列检测器在 200-400nm 的λ范围内进行检测。该方法在 1-300ngmL(-1)范围内呈线性,具有可接受的精密度和准确度。检测限范围为 5'-脱氧腺苷钴胺素的 0.07pgmL(-1)至羟钴胺素的 0.5pgmL(-1)。直接测定的钴胺素平均回收率在羟钴胺素、氰钴胺素和甲基钴胺素之间为 76-93%,而 5'-脱氧腺苷钴胺素的回收率仅为 31%,表明预浓缩方法对该钴胺素无效。该方法成功应用于沿海海水,其中羟钴胺素的浓度范围为 4.2-7.3ngL(-1),氰钴胺素的浓度范围为 1.4-3.9ngL(-1),5'-脱氧腺苷钴胺素的浓度范围为 2.1-4.6ngL(-1),甲基钴胺素的浓度范围为 33-83.5ngL(-1)。