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高效液相色谱-质谱法测定大鼠不同脑区的硫酸酯型神经甾体
引用本文:任进民,侯艳宁.高效液相色谱-质谱法测定大鼠不同脑区的硫酸酯型神经甾体[J].色谱,2004,22(6):575-578.
作者姓名:任进民  侯艳宁
作者单位:白求恩国际和平医院,河北,石家庄,050082;河北医科大学,河北,石家庄,050017
摘    要:应用高效液相色谱-质谱联用技术,以雌酮硫酸酯为内标,建立了大鼠不同脑区硫酸酯型神经甾体的测定方法。甾体分两步萃取,第一步用氯仿-仲丁醇(体积比为1∶1)提取甾体硫酸酯,然后经固相萃取纯化。溶剂解使甾体硫酸酯形成游离型甾体,然后用衍生化试剂进行衍生化,再用液相色谱-质谱分离测定。初步研究发现,雄性SD大鼠不同脑区神经甾体孕烯醇酮硫酸酯和脱氢表雄酮硫酸酯的含量分别为(4.14±1.33) ng/g和(2.26±0.76) ng/g(垂体),(1.98±1.13) ng/g和(1.80±0.93) ng/g(下

关 键 词:大鼠  高效液相色谱-质谱  脑区  脱氢表雄酮硫酸酯  孕烯醇酮硫酸酯  
文章编号:1000-8713(2004)06-0575-04
修稿时间:2004年6月9日

Determination of Neurosteroids in Rat Brain Regions by Liquid Chromatography/Negative Atomspheric Pressure Ionization Mass Spectrometry
REN Jinmin.Determination of Neurosteroids in Rat Brain Regions by Liquid Chromatography/Negative Atomspheric Pressure Ionization Mass Spectrometry[J].Chinese Journal of Chromatography,2004,22(6):575-578.
Authors:REN Jinmin
Institution:Bathune International Peace Hospital, Shijiazhuang 050082, China.
Abstract:A simplified method has been established using liquid chromatography-negative atomspheric pressure ionization mass spectrometry (LC-MS) to simultaneously determine two conjugated neurosteroids from rat brain regions. Neurosteroids were separately isolated in a two-step procedure using chloroform/2-butanol (50: 50, v/v) where the first step was to extract sulfated steroids, then steroid fractions were purified by solid phase extraction (SPE), and finally the sulfated steroid was solvolyzed. Estrogen sulfate was chosen as internal standard. All steroids were derivatized with 2-nitro-4-trifluoromethylphenylhydrazine (2NFPH) and analyzed by LC-MS using selected-ion monitoring. LC-MS was performed on an Agilent 1100 liquid chromatograph-mass spectrometer with atmospheric pressure chemical ionization (APCI) interface, and the hydrazones of oxosteroids was analyzed in a negative-ion mode. A Zorbax SB C18 column was used with a flow rate of 1 mL/min at 40 degrees C. The mobile phase consisted of acetonitrile and distilled water. The concentrations of PREGS and DHEAS in male rat brain regions were (4.14 +/- 1.33 ) ng/g and (2.26 +/- 0.76) ng/g (pituitary gland), (1.98 +/- 1.13) ng/g and (1.80 +/- 0.93) ng/g (hypothalamus), (1.08 +/- 0.48 ) ng/g and (0.81 +/- 0.23) ng/g (frontal cortex), (0.72 +/- 0.19) ng/g and (0.77 +/- 0.12) ng/g (hippocampus), (1.70 +/- 0.45) ng/g and (1.44 +/- 0.71 ) ng/g (amygdale), (0.92 +/- 0.27) ng/g and (0.85 +/- 0.44) ng/g (striatum), (3.62 +/- 1.77) ng/g and (3.17 +/- 2.11) ng/g (nucleus accumbens), respectively. Good linearity and accuracy were observed for each steroid. The procedure was suitable for measuring concentrations of the sulfated steroids in rat brain regions simultaneously.
Keywords:high performance liquid chromatography-mass spectrometry  pregnenolone sulfate  dihydroepiandrosterone sulfate  brain region  rat  
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