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An HPLC method is described for separation of TNT and its main reduction metabolites. Two columns(LC-C(18) and LC-CN)are connected in series and operated isocratically at 1.0mL/min with water-methanol-tetrahydrofuran(60+ 35+ 5 ). The baseline separation of 4-amino-2,6-dinitrotoluene(4A) and 2-amino-4,6-dinitrotoluene(2A) ,which are main metabolites of TNT,is obtained(Rs=2.1). 相似文献
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固相萃取富集-高效液相色谱分离和测定邻甲苯胺和邻硝基甲苯 总被引:5,自引:0,他引:5
建立了以固相萃取技术进行富集 ,高效液相色谱进行分离和检测邻甲苯胺和邻硝基甲苯的方法。污染水中的邻甲苯胺和邻硝基甲苯采用Sep pakC1 8萃取柱进行固相萃取。色谱分离条件是 :Shim PackCLCODS(1 5 0mm× 4 .6mmid ,5 μm)柱为分析柱 ,甲醇 水 =60∶4 0 (V V)为流动相 ,流速为 1 .0mL min,邻甲苯胺和邻硝基甲苯的紫外检测波长分别为 2 3 0nm和 2 5 4nm ,本法具有良好的灵敏度和重现性。 相似文献
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HPLC has been successfully used to the separation of protamines in sperm cells of fertile and infertilemen. The separation was carried out with TSK G3000 SW column,2mol/L ureaand UV detector at 216nm. From these chromatographic tests here it is shown that there haven’t been enough protamines in sperm cellsof infertile men by compared with fertile men. And this method can be used for assay of protamines in spermcells and is proved to be simple,accurate and sensitive. 相似文献
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高效液相色谱法测定血浆中表阿霉素浓度 总被引:3,自引:0,他引:3
报道了高效液相色谱法测定血浆中表阿霉素浓度的实验方法。采用μBondapakC_(18)色谱柱,正磷酸、甲醇、乙腈、异丙醇为流动相。荧光检测器检测,激发波长为450nm,发射波长为530nm。血浆经离心后,取血清,用甲醇沉淀蛋白。方法的平均相对回收率为99.4%±4.6%,日内和日间平均RSD小于5%和6%。最低检测限为3ng。本方法快速、准确,灵敏度高。 相似文献
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高效液相色谱法测定人血清中格列齐特 总被引:2,自引:0,他引:2
A rapid and simple HPLC method was developed for the quantitative analysis of gliclazide in humanserum. After being extracted with benzene, gliclazide was analyzed by reversedphase HPLC colurnn (YWG-C(18)H(37)) and UV-detector(229nm) with tolbutamide as internal standard. The mobile phase was a mixture ofmethyl alcohol and 0.2%glacial acetic acid solution(5: 4 ) at a rate of 1mL/min. Over the concentrationrange of 0.25~32μmol/L, the linear regression equation was : Y=-0. 008412+0.1817X(n=8,r=0. 9996). 相似文献
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高效液相色谱测定人血清中鬼臼乙叉甙 总被引:2,自引:0,他引:2
A rapid and simple HPLC method was developed for the quantitative analysis of etopo-side in human serum. After being extracted with ethyl acetate, etoposide was analyzed by re-versed-phase HPLC column(YWG-C_(18)H_(37)) and UV-detector(230nm).The mobile phase wasamixture of water-acetonitrile-glacial acetic acid(64: 35 :1),with a flow rate of 1mL/min. Over the concentration range of 0. 085~85μmol/L, the linear regression equation was:Y=292.17X+29.50(n=8,γ=0. 9902). 相似文献
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高效液相色谱法测定人血浆中甲磺酸培氟沙星浓度 总被引:5,自引:0,他引:5
建立了一种测定人血浆中甲磺酸培氟沙星的匠相液相色谱方法,用的是ZorbaxODSC_(18)柱和用三乙醇胺调节成pH为3.0的甲醇-0.04mol/LH_3PO_4溶液(80:20,V/V)的流动相,检测在276nm处进行,流量为1mL/min,线性范围是6.01×10 ̄(-8)~3.01×10 ̄(-5)mol/L(γ=0.9998),检测极限为6.01×10 ̄(-8)mol/L,平均回收率为97.57±3.04%,日内与日间的CV分别为3.29%和5.08%。 相似文献
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固相萃取-高效液相色谱法测定人血浆中的川芎嗪 总被引:7,自引:0,他引:7
建立了高效液相色谱测定人血浆中川芎嗪浓度的方法。色谱条件:分析柱为Luna C18(150 mm×4.6 mm i.d.,5 μ
m),流动相为甲醇-乙腈-醋酸盐缓冲液(pH 5.0)(体积比为50∶8∶42),流速1.0 mL/min,柱温40 ℃,检测波长280 nm。
血浆样品预处理采用C8固相小柱萃取法。方法的线性范围为25~5000 μg/L,线性相关系数为0.9999。高、中、低浓度
的川芎嗪在标准血浆样品中的平均提取回收率为96.72%~100.90%,日内和日间相对标准偏差(RSD)小于8.64%,准确度
为99.59%~103.26%,检测限为10 μg/L。该方法的各项效能指标符合生物样品的分析要求,可用于川芎嗪制剂的人体药
代动力学研究。 相似文献