Sacrificial template synthesis of hollow sulfonate group functionalized microporous organic network for efficient solid phase extraction of sulfonamide antibiotics from milk and honey samples

被引:2
|
作者
Gao, Shuo-Wen [1 ,2 ]
Chen, Li-Hua [3 ,4 ]
Cui, Yuan-Yuan [1 ,2 ]
Yang, Cheng-Xiong [1 ,2 ]
机构
[1] Shandong First Med Univ & Shandong Acad Med Sci, Med Sci & Technol Innovat Ctr, Sch Pharmaceut Sci, Jinan 250117, Shandong, Peoples R China
[2] Shandong First Med Univ & Shandong Acad Med Sci, Med Sci & Technol Innovat Ctr, Inst Mat Med, Jinan 250117, Shandong, Peoples R China
[3] Shandong First Med Univ, Affiliated Hosp 1, Jinan 250014, Shandong, Peoples R China
[4] Shandong Prov Qianfoshan Hosp, Jinan 250014, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Hollow microporous organic network; Solid phase extraction; Sulfonamides; Sample pretreatment; HPLC; WATER SAMPLES; ADSORBENT; FRAMEWORK; RESIDUES; REMOVAL; SPHERES;
D O I
10.1016/j.chroma.2024.464844
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The highly conjugated and hydrophobic characteristics of microporous organic networks (MONs) have largely impeded their broad applications in sample pretreatment especially for the polar or ionic analytes. In this work, a novel uniform hollow shaped sulfonate group functionalized MON (H-MON-SO3H-2) was synthesized via the sacrificial template method for the efficient solid phase extraction (SPE) of sulfonamides (SAs) from environmental water, milk, and honey samples prior to HPLC analysis. H-MON-SO3H-2 exhibited large specific surface area, penetrable space, good stability, and numerous hydrogen bonding, electrostatic, hydrophobic and 7C-7C interaction sites, allowing sensitive SPE of SAs with wide linear range (0.150-1000 mu g L-1), low limit of detection (0.045-0.188 mu g L-1), good precisions (intra-day and inter-day RSD < 7.3%, n = 5), large enrichment factors (95.7-98.5), high adsorption capacities (250.4-545.0 mg g(-1)), and satisfactory reusability (more than 80 times). Moreover, the established method was successfully applied to extract SAs from spiked samples with the recoveries of 86.1-104.3%. This work demonstrated the great potential of H-MON-SO3H-2 in the efficient SPE of trace SAs in complex environmental water and food samples and revealed the prospect of hollow MONs in sample pretreatment.
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页数:13
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