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基于两种 MOFs 的分散微固相萃取法作为高效吸附剂,用于分析血浆和废水中的 nilotinib。

Dispersive micro-solid phase extraction based on two MOFs as highly effective adsorbents for analysis of nilotinib in plasma and wastewater.

机构信息

Department of Medicinal Chemistry, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.

Department of Human Ecology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Daru. 2024 Dec;32(2):617-630. doi: 10.1007/s40199-024-00531-0. Epub 2024 Aug 13.

Abstract

BACKGROUND

Nilotinib (NIL) is a prescription medication employed in the treatment of specific types of leukemia, namely chronic myelogenous leukemia (CML). The determination of NIL levels in patients undergoing treatment for CML is of paramount importance for effective management of treatment and toxicity. Also, monitoring and controlling its level in wastewater sources could help scientists to identify potential hotspots of contamination and take appropriate measures to mitigate their impact on the environment and public health.

OBJECTIVES

This study presents a D-µ-SPE technique utilizing two MOFs as adsorbents for the efficient detection of nilotinib in plasma and wastewater samples for the first time.

METHODS

Two highly effective MOFs, MIL-101(Fe) and MIL-53(Al), were synthesized and applied as dispersive micro-solid phase extraction (D-µ-SPE) adsorbents for the extraction of nilotinib coupled with HPLC-UV in a short time of analysis. Experimental parameters affecting extraction efficacy such as adsorbent amount, ionic strength, pH value, adsorption-desorption time and type of elution solvent, were optimized.

RESULTS

Under optimal experimental conditions, the linear dynamic was achieved in the range of 0.25-5.00 µg/mL in human plasma and 0.01-0.20 µg/mL in wastewater. The extraction recovery was in the range of 89.18-91.53% and 94.39-99.60% for nilotinib and MIL-101(Fe) and also 91.22-97.35% and 98.14-100.78% for nilotinib and MIL-53(Al) from human plasma and wastewater respectively.

CONCLUSION

HPLC-UV determination of nilotinib after the D-µ-SPE method showed acceptable accuracy and precision in both plasma and wastewater. In comparison between the two adsorbents, the extraction procedure was easier and faster with MIL-53(Al) as the adsorbent.

摘要

背景

尼洛替尼(NIL)是一种用于治疗特定类型白血病(即慢性髓性白血病,CML)的处方药。测定接受 CML 治疗的患者的 NIL 水平对于有效管理治疗和毒性至关重要。此外,监测和控制废水中 NIL 的水平可以帮助科学家识别潜在的污染热点,并采取适当措施减轻其对环境和公众健康的影响。

目的

本研究首次提出了一种 D-µ-SPE 技术,该技术使用两种 MOFs 作为吸附剂,可高效检测血浆和废水中的尼洛替尼。

方法

合成了两种高效 MOFs(MIL-101(Fe)和 MIL-53(Al)),并将其用作分散式微固相萃取(D-µ-SPE)吸附剂,与 HPLC-UV 结合,可在短时间内分析尼洛替尼。优化了影响萃取效率的实验参数,如吸附剂用量、离子强度、pH 值、吸附-解吸时间和洗脱溶剂类型。

结果

在最佳实验条件下,尼洛替尼在人血浆中的线性动态范围为 0.25-5.00 µg/mL,在废水中的线性动态范围为 0.01-0.20 µg/mL。尼洛替尼和 MIL-101(Fe)的提取回收率范围分别为 89.18-91.53%和 94.39-99.60%,尼洛替尼和 MIL-53(Al)从人血浆和废水中的提取回收率范围分别为 91.22-97.35%和 98.14-100.78%。

结论

HPLC-UV 测定经 D-µ-SPE 法处理后的尼洛替尼,在血浆和废水中均具有可接受的准确度和精密度。与两种吸附剂相比,MIL-53(Al)作为吸附剂时,萃取过程更简单、更快。

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