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纳米晶纤维素作为生物模板制备多孔二氧化钛薄膜作为薄膜微萃取中酮咯酸、美洛昔康、双氯芬酸和甲芬那酸的吸附剂。

Nanocrystalline cellulose as a biotemplate for preparation of porous titania thin film as a sorbent for thin film microextraction of ketorolac, meloxicam, diclofenac and mefenamic acid.

机构信息

Department of Analytical Chemistry, Faculty of Chemistry, University of Mazandaran, Babolsar, Iran.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2020 Apr 1;1142:122039. doi: 10.1016/j.jchromb.2020.122039. Epub 2020 Feb 22.

Abstract

The present study included the procedure of preparing porous titania thin film using a direct nanocrystalline cellulose templating (NCC) as a bio-template. The microextraction applicability of the porous film was investigated by thin film microextraction (TFME) of the nonsteroidal anti-inflammatory drugs (NSAIDs) including ketorolac, meloxicam, diclofenac and mefenamic acid from different types of urine sample. The extracted NSAIDs were analyzed by HPLC-UV. Under optimum conditions, the calibration curves were linear within the range of 1.0-500 µg L (2.0-200 µg L for ketorolac, 2.0-500 µg L for meloxicam, 1.0-200 µg L for diclofenac and 1.0-200 µg L for mefenamic acid). The limit of detection was found to be between 0.2 and 0.5 µg L. The calculated intra- and inter-day relative standard deviations RSDs% (n = 3) at concentration level of 10 µg L were less than 6.3% and 6.0%, respectively. Finally, the method was successfully applied to determine selected NSAIDs in urine samples from different human individuals.

摘要

本研究采用直接纳米纤维素模板(NCC)作为生物模板,制备了多孔二氧化钛薄膜。通过薄膜微萃取(TFME)从不同类型的尿液样本中萃取非甾体抗炎药(NSAIDs),如酮咯酸、美洛昔康、双氯芬酸和甲芬那酸,研究了多孔薄膜的微萃取适用性。用 HPLC-UV 分析提取的 NSAIDs。在最佳条件下,校准曲线在 1.0-500 µg L 范围内呈线性(酮咯酸为 2.0-200 µg L,美洛昔康为 2.0-500 µg L,双氯芬酸为 1.0-200 µg L,甲芬那酸为 1.0-200 µg L)。检测限发现介于 0.2 和 0.5 µg L 之间。在 10 µg L 的浓度水平下,计算得到的日内和日间相对标准偏差(RSD)%(n=3)分别小于 6.3%和 6.0%。最后,该方法成功应用于测定来自不同个体的尿液样本中选定的 NSAIDs。

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