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气相色谱-质谱联用法定量测定β-榄香烯及其与癌症患者抗肿瘤疗效关系的初步评估

Quantification of β-Elemene by GC-MS and Preliminary Evaluation of Its Relationship With Antitumor Efficacy in Cancer Patients.

作者信息

Hou Juanjuan, Yi Jia, Wang Yan, Cui Lili, Xia Wenwen, Liang Zhengyan, Ye Liya, Wang Zhipeng, Gao Shouhong, Wang Zhan

机构信息

College of Traditional Chinese Medicine, Yunnan University of Traditional Chinese Medicine, Kunming 650500, Yunnan, China.

Department of Pharmacy, Second Affiliated Hospital of Naval Medical University, Shanghai 200003, China.

出版信息

J Anal Methods Chem. 2025 Mar 30;2025:6694947. doi: 10.1155/jamc/6694947. eCollection 2025.

Abstract

To establish and validate a sensitive and robust gas chromatography-mass spectrometry (GC-MS) method for the quantification of β-elemene in human plasma and assess the correlation between antitumor effect and β-elemene concentration . The chromatographic column was HP-5 ms (30 m × 0.25 mm, 0.25 μm, Agilent, United States of America). The carrier gas was helium (purity > 99.5%). The flow rate was 1.0 mL/min and the total run time was 11.0 min. The plasma sample was pretreated with protein precipitation plus liquid-liquid extraction. Cancer patients were enrolled and their samples were collected for analysis. Calibration range of β-elemene was 200.0-20,000.0 ng/mL, with correlation coefficients > 0.99. The intra- and interday precision and accuracy were less than 5.8% and within the range of -10.4%-6.6%. The exposure level of β-elemene in the responder group ranged from 278.13 to 11,886.27 ng/mL, with a median of 3568.91 ng/mL, while in the nonresponder group, the range was from 675.92 to 9716.52 ng/mL, with a median of 3351.94 ng/mL. No difference was found in the β-elemene exposure level between the two groups ( > 0.05). This method was effectively developed, validated, and utilized to quantify β-elemene in cancer patients. The initial findings indicated no significant relationship between therapeutic efficacy and the concentration of β-elemene.

摘要

建立并验证一种灵敏且可靠的气相色谱 - 质谱联用(GC-MS)方法,用于定量测定人血浆中的β-榄香烯,并评估抗肿瘤效果与β-榄香烯浓度之间的相关性。色谱柱为HP-5 ms(30 m×0.25 mm,0.25 μm,美国安捷伦公司)。载气为氦气(纯度>99.5%)。流速为1.0 mL/min,总运行时间为11.0 min。血浆样品采用蛋白沉淀加液 - 液萃取进行预处理。招募癌症患者并采集其样本进行分析。β-榄香烯的校准范围为200.0 - 20,000.0 ng/mL,相关系数>0.99。日内和日间精密度及准确度均小于5.8%,且在 -10.4% - 6.6%范围内。应答组中β-榄香烯的暴露水平为278.13至11,886.27 ng/mL,中位数为3568.91 ng/mL,而无应答组的范围为675.92至9716.52 ng/mL,中位数为3351.94 ng/mL。两组之间的β-榄香烯暴露水平无差异(>0.05)。该方法已有效开发、验证并用于定量测定癌症患者体内的β-榄香烯。初步研究结果表明治疗效果与β-榄香烯浓度之间无显著关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/095a/11972858/e2703add4d17/JAMC2025-6694947.001.jpg

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