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Determination of 5-fluorouracil and tegafur in tear fluid of patients treated with oral fluoropyrimidine anticancer agent, S-1

机译:用口服氟嘧啶抗癌患者泪液测定5-氟尿嘧啶和TEGAFUR,S-1

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Purpose To establish a method for the measurement of 5-fluorouracil (5-FU), and tegafur (FT) in tear samples from patients treated with oral fluoropyrimidine anticancer agent S-1. Study design Cross-sectional study. Methods High performance liquid chromatographic (HPLC) method reported for plasma samples was modified for tear samples. Simulated-tear solutions containing lactoferrin, lysozyme and standard solution containing 5-FU or FT were prepared for preliminary measurements. Tear samples from seven patients treated with S-1 were included. The tears were collected following S-1 administration using Schirmer’s strips. Results 5-FU and FT concentrations of pure standard solution without extraction process were detected as original concentration. However, on extraction, FT samples in simulated-tear solution showed a peak for 5-FU but not for FT. FT was converted to 5-FU in the extraction process. Decomposition from FT to 5-FU was suppressed when 50?mg/mL bovine serum albumin was added during extraction. The mean concentrations of 5-FU and FT in tears during S-1 treatment were 0.17?±?0.11 and 1.94?±?0.71?μg/mL, respectively. Conclusion A simple HPLC method to determine 5-FU and FT in tear samples was established.
机译:目的在用口服氟嘧啶抗癌剂S-1处理的患者中建立5-氟尿嘧啶(5-FU)和TEGAFUR(FT)的方法。研究设计横断面研究。方法对血浆样品报告的高效液相色谱(HPLC)方法被修饰用于撕裂样品。制备含有乳铁蛋白,溶菌酶和含有5-FU或FT的标准溶液的模拟撕裂溶液进行初步测量。包括来自S-1治疗的7名患者的撕裂样品。使用Schirmer的条带,在S-1管理后收集泪液。结果纯标准溶液的5-FU和FT浓度无需提取工艺被检测为原始浓度。然而,在萃取时,模拟撕裂溶液中的FT样品显示为5-FU但不是ft的峰值。 FT在提取过程中转化为5-FU。当在提取过程中加入50℃/ mL牛血清白蛋白时,抑制了Ft至5-FU的分解。在S-1处理期间,泪液的平均浓度为0.17Ω±0.11和1.94?±0.71Ω·μg/ ml。结论建立了一种简单的HPLC方法,确定5-FU和撕裂样品中的FT。

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