Suppr超能文献

基于 ZIF67 的多孔碳增强电纺纳米纤维作为提取相,用于在液质联用色谱法之前从生物流体中在线微固相萃取抗真菌药物。

ZIF67-derived porous carbon-reinforced electrospun nanofiber as an extractive phase for on-chip micro-solid-phase extraction of antifungals from biological fluids prior to liquid chromatography tandem mass spectrometry.

机构信息

School of Chemistry, College of Science, University of Tehran, P.O. Box 14155-6455, Tehran, Iran.

Department of Analytical Chemistry, Faculty of Chemistry , K.N. Toosi University of Technology, P.O. Box 16315-1618, Tehran, Postal Code 15418-49611, Iran.

出版信息

Mikrochim Acta. 2023 Dec 6;191(1):10. doi: 10.1007/s00604-023-06103-4.

Abstract

With a view to improving applicability as a sorbent while overcoming the challenges associated with its powdery nature, cobalt-doped zeolitic imidazolate framework (ZIF 67)-derived nanoporous carbon (Co-NPC) was employed as an additive in nanofiber through the process of electrospinning. X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), and Brunauer-Emmett-Teller (BET) surface area analysis were used to characterize the resulting nanocomposite. A microfluidic chip device with four layers, including two layers entailing spiral channels, was designed and employed to assess the analytical performance of the fabricated Co-NPC-reinforced electrospun composite. To do so, a folded piece of electrospun composite was sandwiched between two layers with spiral channels. Therefore, both sides of the folded composite acted as a sorptive phase to extract antifungal drugs as target analytes. The significant factors affecting the efficiency of the extraction process were investigated and optimized. Subsequently, the technique was verified through the utilization of liquid chromatography-tandem mass spectrometry (LC-MS/MS) by employing optimal parameters. The optimal conditions were applied to evaluate the figures of merit. A linear range was obtained for antifungal drugs within the range 0.25-200.0 ng ml with an R value of ≥ 0.9914. The method demonstrated detection limits ranging between 0.08 and 0.40 ng ml. The intra-day and inter-day precisions were less than 6.9%. Relative recoveries exhibited variations between 91.4-106.8%, 95.9-103.6%, and 96.4-109.3% for ketoconazole, clotrimazole, and miconazole, respectively. The proposed approach yielded satisfactory results, demonstrating its efficiency.

摘要

为了提高作为吸附剂的适用性,同时克服其粉末性质带来的挑战,将钴掺杂沸石咪唑酯骨架(ZIF-67)衍生的纳米多孔碳(Co-NPC)作为添加剂通过静电纺丝工艺引入到纳米纤维中。采用 X 射线衍射(XRD)、傅里叶变换红外(FT-IR)光谱、扫描电子显微镜(SEM)、能谱(EDS)和 Brunauer-Emmett-Teller(BET)表面积分析对所得纳米复合材料进行了表征。设计并采用了具有四层结构的微流控芯片装置,其中包括两层螺旋通道,以评估所制备的 Co-NPC 增强型静电纺丝复合材料的分析性能。为此,将折叠的静电纺丝复合材料夹在具有螺旋通道的两层之间。因此,折叠复合材料的两侧都作为吸附相来提取作为目标分析物的抗真菌药物。研究并优化了影响萃取效率的重要因素。随后,通过采用最佳参数的液相色谱-串联质谱(LC-MS/MS)技术对该技术进行了验证。将最佳条件应用于评估衡量指标。在 0.25-200.0ngml 的范围内获得了抗真菌药物的线性范围,R 值≥0.9914。该方法的检测限范围在 0.08-0.40ngml 之间。日内和日间精密度小于 6.9%。酮康唑、克霉唑和咪康唑的相对回收率分别为 91.4-106.8%、95.9-103.6%和 96.4-109.3%。该方法的结果令人满意,证明了其效率。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验