基于两种 MOFs 高效吸附剂的分散微固相萃取用于血浆和废水中尼洛替尼的分析。

IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY DARU Journal of Pharmaceutical Sciences Pub Date : 2024-12-01 Epub Date: 2024-08-13 DOI:10.1007/s40199-024-00531-0
Azra Takhvar, Somaye Akbari, Effat Souri, Reza Ahmadkhaniha, Ali Morsali, Mohammad Reza Khoshayand, Mohsen Amini, Alireza Taheri
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引用次数: 0

摘要

背景:尼罗替尼(NIL)是一种处方药,用于治疗特定类型的白血病,即慢性粒细胞白血病(CML)。测定接受 CML 治疗的患者体内的 NIL 含量对于有效控制治疗和毒性至关重要。此外,监测和控制废水源中的 NIL 水平有助于科学家确定潜在的污染热点,并采取适当措施减轻其对环境和公众健康的影响:本研究首次提出了一种利用两种MOFs作为吸附剂的D-µ-SPE技术,用于高效检测血浆和废水样品中的尼洛替尼:合成并应用两种高效MOFs--MIL-101(Fe)和MIL-53(Al)作为分散微固相萃取(D-µ-SPE)吸附剂,结合高效液相色谱-紫外光谱法在短时间内萃取尼洛替尼。对吸附剂用量、离子强度、pH 值、吸附-解吸时间和洗脱溶剂类型等影响萃取效果的实验参数进行了优化:在最佳实验条件下,人血浆中的线性动态范围为 0.25-5.00 µg/mL ,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)的提取回收率分别为89.18%-91.53%和94.39%-99.60%,尼洛替尼和MIL-53(Al)在人体血浆和废水中的提取回收率分别为91.22%-97.35%和98.14%-100.78%:采用 D-µ-SPE 法测定血浆和废水中的尼洛替尼时,HPLC-UV 显示出了可接受的准确度和精密度。两种吸附剂相比,以 MIL-53(Al)为吸附剂的提取过程更简单、更快速。
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Dispersive micro-solid phase extraction based on two MOFs as highly effective adsorbents for analysis of nilotinib in plasma and wastewater.

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.

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DARU Journal of Pharmaceutical Sciences
DARU Journal of Pharmaceutical Sciences PHARMACOLOGY & PHARMACY-
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期刊介绍: DARU Journal of Pharmaceutical Sciences is a peer-reviewed journal published on behalf of Tehran University of Medical Sciences. The journal encompasses all fields of the pharmaceutical sciences and presents timely research on all areas of drug conception, design, manufacture, classification and assessment. The term DARU is derived from the Persian name meaning drug or medicine. This journal is a unique platform to improve the knowledge of researchers and scientists by publishing novel articles including basic and clinical investigations from members of the global scientific community in the forms of original articles, systematic or narrative reviews, meta-analyses, letters, and short communications.
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