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超高效液相色谱-四极杆/轨道阱高分辨质谱法测定15种危害药品分析方法的建立与验证

Establishment and validation of analytical methods for 15 hazardous drugs by UPLC-Q/Orbitrap-HRMS.

作者信息

Yu Bo, Wang Yang, Geng Zhou, Qu Yuchen, Pan Jie, Zhai Qing

机构信息

Department of Pharmacy, Shanghai Cancer Center, Fudan University, Shanghai, China.

Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China.

出版信息

Ann Transl Med. 2022 Jun;10(12):686. doi: 10.21037/atm-22-2330.

Abstract

BACKGROUND

Cytotoxic drug residues in pharmacy intravenous admixture services (PIVAS) have always been a major problem for pharmaceutical workers and the PIVAS environment,which is not only pollutes the PIVAS environment, but also causes serious harm to the life and health of the staff. This study aimed to establish an ultra-high performance liquid chromatography quadrupole orbitrap high resolution mass spectrometry (UPLC-Q/Orbitrap-HRMS) method for the rapid detection and monitor of 15 cytotoxic drugs.

METHODS

UPLC-Q/Orbitrap-HRMS method was used to establish a rapid detection method for 15 cytotoxic drugs such as cytarabine, gemcitabine and so on. The daily precision and accuracy of this method were verified by injecting four concentrations of standard solution on the same day, and the same four concentrations of standard solution were injected within three days respectively to verify the daily precision of this method. The signal-to-noise ratio (SNR) of 10:1 was calculated as the limit of quantity. The mixed standard solution of 15 cytotoxic drugs with concentrations of 0.5, 1, 3, 10, 30, 100, 300, and 1,000 ng/mL was configured and detected by this method for linearity and range.The stability of this method was investigated using a mixture of 15 drugs (15MIX) standard solutions at high concentration (300 ng/mL) and low concentration (10 ng/mL) at room temperature for 12 and 24 hours, respectively. A standard solution of each drug, 15MIX and blank solution were taken to verify the exclusivity of the method.

RESULTS

The results showed that the method had good specificity, and the intraday precision of all drugs was less than 10% and the intraday precision was less than 15%. At the same time, the standard curve had good linearity, R was greater than 0.99, and the limit of quantification of most drugs was about 1 ng/mL.

CONCLUSIONS

In this study, an UPLC-Q/Orbitrap-HRMS method was established for the rapid detection of 15 cytotoxic drugs, providing technical support for the monitoring of cytotoxic drug residues in PIVAS, which is of great significance for environmental contamination mornitoring as well as occupational exposure alert.

摘要

背景

医院静脉药物配置中心(PIVAS)中的细胞毒性药物残留一直是药学工作者和PIVAS环境面临的主要问题,这不仅污染PIVAS环境,还会对工作人员的生命健康造成严重危害。本研究旨在建立一种超高效液相色谱-四极杆-轨道阱高分辨率质谱(UPLC-Q/Orbitrap-HRMS)方法,用于快速检测和监测15种细胞毒性药物。

方法

采用UPLC-Q/Orbitrap-HRMS方法建立对阿糖胞苷、吉西他滨等15种细胞毒性药物的快速检测方法。通过在同一天内进样4种浓度的标准溶液来验证该方法的日间精密度和准确度,在三天内分别进样相同的4种浓度标准溶液来验证该方法的日内精密度。以信噪比(SNR)为10:1计算定量限。配制浓度为0.5、1、3、10、30、100、300和1000 ng/mL的15种细胞毒性药物的混合标准溶液,用该方法进行线性和范围检测。分别在室温下,采用高浓度(300 ng/mL)和低浓度(10 ng/mL)的15种药物混合标准溶液(15MIX)考察该方法在12小时和24小时的稳定性。取各药物标准溶液、15MIX和空白溶液验证该方法的专属性。

结果

结果表明,该方法具有良好的特异性,所有药物的日内精密度均小于10%,日间精密度小于15%。同时,标准曲线具有良好的线性,R大于0.99,大多数药物的定量限约为1 ng/mL。

结论

本研究建立了一种UPLC-Q/Orbitrap-HRMS方法用于快速检测15种细胞毒性药物,为PIVAS中细胞毒性药物残留监测提供技术支持,对环境污染监测及职业暴露预警具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ee4/9279804/4a2a3b7768a2/atm-10-12-686-f1.jpg

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