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作 者:蔺晓娟[1] 黄平[2] 陈进[2] 赵丹[1] 朱丹[1] 丁世家[1]
机构地区:[1]重庆医科大学检验医学院、临床检验诊断学教育部重点实验室,重庆400016 [2]重庆医科大学附属第一医院肝胆外科,重庆400016
出 处:《重庆医科大学学报》2014年第12期1718-1722,共5页Journal of Chongqing Medical University
基 金:国家自然科学基金资助项目(编号:21075141)
摘 要:目的:建立柱前衍生反向高效液相色谱荧光检测法同时对肝癌相关L-酪氨酸(L-tyrosine,L-Tyr)、D-酪氨酸(D-tyrosine,D-Tyr)、L-缬氨酸(L-valine,L-Val)、D-缬氨酸(D-valine,D-Val)进行拆分测定。比较正常人与原发性肝细胞癌(hepatocellular carcinoma,HCC)(以下简称原发性肝癌)患者血浆中酪氨酸与缬氨酸对映体含量的变化,考察它们与原发性肝癌的关系。方法:柱前衍生化试剂:邻苯二甲醛(O-phthaldialdehyde,OPA)和N-乙酰-L-半胱氨酸(N-acetyl-L-cysteine,NAC);色谱柱:菲罗门Gemini C18柱(250 mm×4.6 mm,5μm);流动相:20.0 mmol/L磷酸二氢钠(p H 6.8)-乙腈为流动相的梯度洗脱;荧光检测波长设定:激发波长(λex)为350 nm,发射波长(λem)为450 nm;流速1 ml/min;柱温30℃;进样量10μl。结果:4种物质的回收率在90.74%~106.80%之间,线性关系良好,检出限分别为6.79 pg/ml(L-Tyr),7.81 pg/ml(D-Tyr),1.86 pg/ml(L-Val),1.95 pg/ml(D-Val)。利用该方法,对20名健康志愿者和23名HCC患者的血浆进行测定,统计分析结果表明,L-Tyr明显升高(P=0.011),L-Val(P=0.019)、D-Val(P=0.006)显著性降低,D-Tyr(P=0.973)无明显变化。结论:该方法准确、灵敏、重复性好,适用于实验室研究与临床检测。Objective:To establish reversed-phase high performance liquid chromatography-fluorescence detection (RP-HPLC-FLD) method, to determine hepatoma-associated tyrosine and valine amino acid enantiomers (L-tyrosine (L-Tyr), D-tyrosine (D-Tyr), L- valine (L-Val) and D-valine (D-Val)),to compare changes in tyrosine and v aline amino acid enantiomers concentrations in plasma between hepatocellular carcinoma(HCC) patients and healthy controls and to investigate their possible relationship. Methods:O-ph- thaldialdehyde(OPA) and N-acetyl-L-cysteine(NAC) were served as the pre-column derivatization reagents. Separation was carried out on a Phenomenex Gemini C18 column(250 mm × 4.6 mm,5 μm) with a programmed gradient elution. The mobile phase was con- sisted of 20.0 mmol/L sodium dihydrogen phosphate(pH 6.80) and acetonitrile. The eluted solution was monitored using a fluores- cence detector with excitation wavelength at 350 nm and emission wavelength at 450 nm. Results :The presented method exhibited an excellent linearity for all the analytes over their respective concentration ranges. The recoveries ranged from 90.74% to 106.80%. The detection limits were 6.79 pg/ml, 7.81 pg/ml, 1.86 pg/ml and 1.95 pg/ml for L-Tyr, D-Tyr, L-Val and D-Val, respectively. Twenty plas- ma samples of healthy humans and 23 plasma samples of HCC patients were tested and the HCC patients demonstated higher levels of L-Tyr(P=-0.011) and lower levels of L-Val(P=-0.019) and D-Val(P=-0.006) in plasma while no change was observed in D-Tyr(P= 0.973). Conclusion:This method is simple, accurate and suitable for routine scientific research and clinical measurement.
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