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采用液相色谱-串联质谱法(LC-MS/MS)和高效液相色谱法(HPLC)对他莫昔芬及其代谢物进行评估。

Evaluation of tamoxifen and metabolites by LC-MS/MS and HPLC methods.

作者信息

Heath D D, Flat S W, Wu A H B, Pruitt M A, Rock C L

出版信息

Br J Biomed Sci. 2014;71(1):33-9. doi: 10.1080/09674845.2014.11669960.

Abstract

Epidemiological and laboratory evidence suggests that quantification of serum or plasma levels of tamoxifen and its metabolites, 4-hydroxy-N-desmethyl-tamoxifen (endoxifen), Z-4-hydroxytamoxifen (4HT), N-desmethyl-tamoxifen (ND-tam), is a clinically useful tool in the assessment and monitoring of breast cancer status in patients taking adjuvant tamoxifen. A liquid chromatographic mass spectrometric method (LC-MS/MS) was used to measure the blood levels of tamoxifen and its metabolites. This fully automated analytical method is specific, accurate and sensitive. The LC-MS/MS automated technique has now become a widely accepted reference method. This study analysed a randomly selected batch of blood samples from participants enrolled in a breast cancer study to compare results from this reference method in 40 samples with those obtained from a recently developed high-performance liquid chromatography (HPLC) method with fluorescence detection. The mean (SD) concentrations for the LC-MS/MS method (endoxifen 12.6 [7.5] ng/mL, tamoxifen 105 [44] ng/mL, 4-HT 1.9 [1.0] ng/mL, ND-tam 181 [69] ng/mL) and the HPLC method (endoxifen 13.1 [7.8] ng/mL, tamoxifen 108 [55] ng/mL, 4-HT 1.8 [0.8] ng/mL, ND-tam 184 [81] ng/mL) did not show any significant differences. The results confirm that the HPLC method offers an accurate and comparable alternative for the quantification of tamoxifen and tamoxifen metabolites.

摘要

流行病学和实验室证据表明,对他莫昔芬及其代谢产物4-羟基-N-去甲基他莫昔芬(内昔芬)、Z-4-羟基他莫昔芬(4HT)、N-去甲基他莫昔芬(ND-他莫昔芬)的血清或血浆水平进行定量,是评估和监测接受辅助性他莫昔芬治疗的乳腺癌患者病情的一种临床有用工具。采用液相色谱-质谱联用方法(LC-MS/MS)测定他莫昔芬及其代谢产物的血药浓度。这种全自动分析方法具有特异性、准确性和灵敏性。LC-MS/MS自动化技术现已成为一种广泛接受的参考方法。本研究分析了从一项乳腺癌研究的参与者中随机选取的一批血样,以比较该参考方法在40份样本中的结果与最近开发的具有荧光检测功能的高效液相色谱(HPLC)方法所获得的结果。LC-MS/MS方法(内昔芬12.6 [7.5] ng/mL,他莫昔芬105 [44] ng/mL,4-HT 1.9 [1.0] ng/mL,ND-他莫昔芬181 [69] ng/mL)和HPLC方法(内昔芬13.1 [7.8] ng/mL,他莫昔芬108 [55] ng/mL,4-HT 1.8 [0.8] ng/mL,ND-他莫昔芬184 [81] ng/mL)的平均(标准差)浓度没有显示出任何显著差异。结果证实,HPLC方法为他莫昔芬及其代谢产物的定量提供了一种准确且可比的替代方法。

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本文引用的文献

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Determination of tamoxifen and five metabolites in plasma.
J Pharm Biomed Anal. 1988;6(6-8):1065-8. doi: 10.1016/0731-7085(88)80136-5.

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