Fabrication of sea urchin shaped polyaniline-modified magnetic microporous organic network for efficient extraction of non-steroidal anti-inflammatory drugs from animal-derived food samples

被引:2
|
作者
Li, Yan-Hong [1 ]
Li, Xu-Hui [1 ]
Cui, Yuan-Yuan [2 ,3 ]
Abdukayum, Abdukader [1 ]
Yang, Cheng-Xiong [2 ,3 ]
机构
[1] Kashi Univ, Coll Chem & Environm Sci, Xinjiang Key Lab Novel Funct Mat Chem, Lab Xinjiang Native Med & Edible Plant Resources C, Kashgar 844000, Peoples R China
[2] Shandong First Med Univ & Shandong Acad Med Sci, Sch Pharmaceut Sci, Med Sci & Technol Innovat Ctr, Jinan 250117, Shandong, Peoples R China
[3] Shandong First Med Univ & Shandong Acad Med Sci, Inst Mat Med, Med Sci & Technol Innovat Ctr, Jinan 250117, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Microporous organic network; Polyaniline; Nonsteroidal anti-inflammatory drugs; Magnetic solid phase extraction; Sample pretreatment; SOLID-PHASE EXTRACTION; WATER SAMPLES; NANOPARTICLES; FRAMEWORK; ADSORBENT; SORBENT;
D O I
10.1016/j.chroma.2024.465140
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In this work, a novel polyaniline-modified magnetic microporous organic network (MMON-PANI) composite was fabricated for effective magnetic solid phase extraction (MSPE) of five typical nonsteroidal anti-inflammatory drugs (NSAIDs) from animal-derived food samples before high performance liquid chromatography (HPLC) detection. The core-shell sea urchin shaped MMON-PANI integrates the merits of Fe3O4, MON, and PANI, exhibiting large specific surface area, rapid magnetic responsiveness, good stability, and multiple binding sites to NSAIDs. Convenient and effective extraction of trace NSAIDs from chicken, beef and pork samples is realized on MMON-PANI via the synergetic pi-pi, hydrogen bonding, hydrophobic, and electrostatic interactions. Under optimal conditions, the MMON-PANI-MSPE-HPLC-UV method exhibits wide linear ranges (0.2-1000 mu g L-1), low limits of detection (0.07-1.7 mu g L-1), good precisions (intraday and inter-day RSDs < 5.4 %, n = 3), large enrichment factors (98.6-99.9), and less adsorbent consumption (3 mg). The extraction mechanism and selectivity of MMON-PANI are also evaluated in detail. This work proves the incorporation of PANI onto MMON is an efficient way to promote NSAIDs enrichment and provides a new strategy to synthesize multifunctional MON-based composites in sample pretreatment.
引用
收藏
页数:12
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