Rister Alana L, Bidne Katie L, Wood Jennifer R, Dodds Eric D
Department of Chemistry, University of Nebraska - Lincoln, Lincoln, NE, 68588-0304, USA.
Department of Animal Science, University of Nebraska - Lincoln, Lincoln, NE, 68588-0304, USA.
Anal Methods. 2019 Dec 7;11(45):5746-5749. doi: 10.1039/c9ay01757g. Epub 2019 Oct 29.
Corticosterone is an important steroid for the regulation of metabolism and stress response. Existing methods for the measurement of corticosterone include radioimmunoassay (RIA), enzyme linked immunosorbent assay (ELISA), and liquid chromatography-mass spectrometry (LC-MS). While each of these approaches have their advantages, RIAs use radioactive isotopes that necessitate specially regulated usage and disposal. Furthermore, both ELISAs and RIAs require expensive kits and can only measure a single analyte. In this study, we establish a new sample preparation technique based on a modified Folch extraction that allows for the simultaneous isolation of corticosterone and lipids from serum. The extract is then analyzed by LC-MS. Using only 5 µL of serum, quantification of corticosterone was achieved with coefficients of variation at 3% or less and a detection limit of 0.12 µM. Overall, the results of this study should be beneficial to the measurement of circulating corticosterone and lipids for a variety of studies using small volumes of samples.
皮质酮是一种调节新陈代谢和应激反应的重要类固醇。现有的皮质酮测量方法包括放射免疫分析(RIA)、酶联免疫吸附测定(ELISA)和液相色谱-质谱联用(LC-MS)。虽然这些方法各有优点,但放射免疫分析法使用放射性同位素,需要特殊的使用和处置规定。此外,酶联免疫吸附测定法和放射免疫分析法都需要昂贵的试剂盒,并且只能测量单一分析物。在本研究中,我们基于改良的Folch萃取法建立了一种新的样品制备技术,该技术能够同时从血清中分离皮质酮和脂质。然后通过液相色谱-质谱联用对提取物进行分析。仅使用5微升血清,即可实现皮质酮的定量,变异系数在3%或更低,检测限为0.12微摩尔。总体而言,本研究结果应有助于使用少量样品的各种研究中循环皮质酮和脂质的测量。