机构地区:[1]中南大学湘雅二医院检验科,湖南长沙410011 [2]湖南省郴州市第一人民医院检验科
出 处:《中华检验医学杂志》2009年第12期1354-1359,共6页Chinese Journal of Laboratory Medicine
基 金:湖南省医药卫生科研计划资助课题(C2005019);湖南省科技计划项目资助课题(05SK3026).
摘 要:目的探讨高效液相色谱-荧光检测法(HPLC-FLD)同时测定血清色氨酸(TRP)和犬尿氨酸(KYN)对诊断类风湿关节炎(RA)的临床意义。方法血清标本加等量5%(V/V)高氯酸溶液去除蛋白,离心取上清液20μl,直接进样分析。色谱柱为Hpersil C8柱(300mm×6.0mm i.d,10μm);流动相为0.25mol/L醋酸锌和50mmol/L醋酸溶液(含3%乙腈),流速为1.5ml/min;0-10min荧光检测器的激发波长和发射波长分别为365nm和480nm,10min后激发波长和发射波长分别变换为254nm和404nm。同时,用该方法测定120名健康成人和110例RA患者血清TRP、KYN和TRP/KYN比值(K/T),并评价其诊断RA的敏感度、特异度和方法学效能。结果血清标本的KYN和TRP保留时间分别为8.1和11.5min,两者分离良好。KYN线性范围为0.098—19.600μmol/L,最低检测浓度为0.04μmol/L;回收率为90.8%—96.2%,日内变异系数为3.68%,日间变异率为4.97%。TRP的线性范围为4.9—196.0μmot/L。最低检测限为0.005μmol/L,回收率为92.6—106.9%,日内变异系数为3.63%,日间变异系数为4.44%。在本试验的色谱条件下测定苯丙氨酸(Phe)、酪氨酸(Tyr)、犬尿喹啉酸(KYNA)、5-羟色胺(5-HT)和Cr均无干扰。RA组患者血清KYN含量和K/T比值[(2.06±0.38)μmol/L和(55.46±5.81)×10^-3]与健康对照组[(1.51±0.35)μmol/L和(32.54±9.00)×10^-3]比较,均显著升高(U=3251.0,t=10741,P均为0.000),而RA组TRP含量[(38.24±5.27)μmol/L]与健康对照组[(47.52±5.79)μmol/L]比较,则显著降低(t=10.399,P=0.000)。K/T比值诊断RA的敏感度、特异度分别为83.6%(92/110)、85.8%(103/120)。结论HPLC-FLD同时测定血清TRP和KYN的方法精密度、回收率、抗干扰能力、线性范围等均符合临床检测要求。K/T比值可作为RA的辅助性诊断指标。Objective To explore the clinical significance of serum kynurenine and tryptophan by HPLC fluorescence detection in patients with rheumatoid arthritis ( RA). Methods Serum samples were deproteinized by equal volume of 5% (V/V) perchloric acid. It employed a Hypersil C8 column and a mobile phase consisted of 0.25 mol/L zinc acetate, 50 mmoL/L acetic acid with 3% (V/V) acetonitrile at a flow rate of 1.5 mL/min. The fluorescence excitation and emission wavelengths were operated at 365 nm and 480 nm respectively at the beginning of the run, and 10 minutes later, the excitation and emission wavelength changed to 254 nm and 404 nm. TRP and KYN of health group and RA group were determined by HPLC-FLD. Results The retention time of KYN was 8.1 min ; the linearity was from 0.098μmol/L to 19.600μmoL/L with the detection limit of 0.04μmol/L , the recovery were 90.8%—96.2% , and the intra-day and inter-day variations were 3.68 % and 4.97%, respectively. The retention time of TRP was 11.5min, the linearity of the assay was from 4.9μmoL/L to 196.0μmol/L, the detection limits was 0.005μmol/L,the recovery of TRP was 92. 6%—106. 9% , the intraday and interday coefficients of variations were 3.63% and 4. 44%, respectively. Phenylalanine, tyrosine, serotonin, kynureuic acid and creatinine didn't interfere in the assay. Compared with healthy subjects, there were significantly increased concentration of serum KYN and K/T Ratio [ (1.51±0. 35 )μmol/L vs ( 2.06±0. 38 )μmol/L, U = 3 251.0, P = 0. 000 ; ( 32. 54±9.00)×10^-3 vs ( 55.46±5.81 ) x 10^-3, t = 10741, P =0. 000] and significantly decreased concentrations of TRP [(47.52±5.79 )μmol/L vs ( 38.24±5.27 )μmol/L ; t = 10. 399, P = 0. 000) ] in the patients with RA. The sensitivity, specificity of K/T ratio for diagnsis RA was 83.6% (92/110) and 85. 8 ( 103/ 120) % respectively. Conclusions A new method is established for simultaneous determination of KYN and TRP in serum by HPLC-FLD with on-column derivatization. The
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