高内相乳液聚合物复合材料中的碳纳米管用于尿液中氟喹诺酮类药物的填料式微固相萃取

IF 5.2 Q1 CHEMISTRY, ANALYTICAL Advances in Sample Preparation Pub Date : 2024-02-01 DOI:10.1016/j.sampre.2024.100103
Francesca Merlo , Francesca Colucci , Giulia De Soricellis , Francesca Rinaldi , Enrica Calleri , Antonella Profumo , Andrea Speltini
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引用次数: 0

摘要

本研究的目的是评估以碳纳米管为基础的聚合高内相乳液复合材料(CNT/polyHIPE)作为吸附相在生物样品制备中的应用。研究人员开发了一种微固相萃取程序(μSPE),用于痕量检测人体尿液样品中的氟喹诺酮类(FQ)抗菌素,即环丙沙星、左氧氟沙星、洛美沙星、莫西沙星、诺氟沙星和司帕沙星。通过加入不同浓度的纳米管(0.2-0.8 wt %)改性的 PolyHIPEs 被一锅合成并应用于填料盒环境中。在自来水和缓冲水溶液中对药物的吸附亲和力进行了研究,结果表明聚合物中嵌入的纳米管发挥了关键作用。选择 0.5 wt % 的 CNT 复合材料是为了直接在原尿(1 mL 样品)中开发一种简单的 µSPE 程序,然后进行 HPLC-MS/MS。目标物以接近中性的 pH 值保留在吸附剂上,经过水洗(0.1 % v/v 甲酸)后,再用 4 % v/v 氨水溶液(15 % v/v 乙腈)一步洗脱,从而将萃取和净化结合在一起。该方法可准确定量 FQs,在添加 40、75 和 150 µg L-1 的空白混合尿样中的回收率(74-116%,n = 3)证明了这一点,同时该方法还具有良好的日间精密度(RSD < 14 %,n = 3)。为了证实该分析方法的适用性,我们处理了一些真实的盲样作为概念验证。
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Carbon nanotubes in high internal phase emulsion polymer composite for packed-cartridge micro-solid-phase extraction of fluoroquinolones in urine

Aim of this study stands in the evaluation of a carbon nanotubes-based polymerized high internal phase emulsion composite (CNT/polyHIPE) as sorptive phase in biological sample preparation. A micro-solid-phase extraction procedure (µSPE) was developed for trace fluoroquinolone (FQ) antimicrobials, namely Ciprofloxacin, Levofloxacin, Lomefloxacin, Moxifloxacin, Norfloxacin and Sparfloxacin, in human urine samples. PolyHIPEs modified by incorporation of different concentrations of nanotubes (0.2–0.8 wt %) were one-pot synthesized and applied in the packed-cartridge setting. The sorption affinity for the drugs was investigated in tap water and buffered aqueous solutions, demonstrating the key role of the nanotubes embedded in the polymer. The 0.5 wt % CNT composite was selected to develop a straightforward µSPE procedure directly in raw urine (1 mL sample), followed by HPLC-MS/MS. Targets were retained on the sorbent at near neutral pH and, after an aqueous washing (0.1 % v/v formic acid), eluted in a single-step with 4 % v/v ammonia aqueous solution (15 % v/v acetonitrile), thus combining extraction and clean-up. The method allowed accurate quantification of FQs, as evidenced by the recoveries (74–116 %, n = 3) obtained on blank pooled urine samples spiked with 40, 75, 150 µg L−1, accompanied by good inter-day precision (RSD < 14 %, n = 3). To confirm the applicability of the analytical method, some real-life blind samples were processed as a proof of concept.

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