首页> 美国卫生研究院文献>Royal Society Open Science >New sporopollenin-based β-cyclodextrin functionalized magnetic hybrid adsorbent for magnetic solid-phase extraction of nonsteroidal anti-inflammatory drugs from water samples
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New sporopollenin-based β-cyclodextrin functionalized magnetic hybrid adsorbent for magnetic solid-phase extraction of nonsteroidal anti-inflammatory drugs from water samples

机译:新型基于孢粉的β-环糊精功能化磁性杂化吸附剂用于磁性固相萃取水样中的非甾体类抗炎药

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摘要

A magnetic solid-phase extraction (MSPE) procedure on the newly synthesized magnetic β-cyclodextrin functionalized with toluene diisocyanate (TDI) as a linker and further modified with bio-polymeric spores of sporopollenin (MSp-TDI-βCD), was developed for the extraction of nonsteroidal anti-inflammatory drugs (NSAIDs), namely, indoprofen (INP), ketoprofen (KTP), ibuprofen (IBP) and fenoprofen (FNP) from water samples prior to their HPLC-DAD determination. The newly synthesized MSp-TDI-βCD was comprehensibly characterized using FT-IR, XRD, SEM-EDX, BET and VSM analyses. The separation of selected NSAIDs on MSp-TDI-βCD from aqueous solution was simply achieved by applying an external magnetic field via a permanent magnet. The MSPE parameters affecting extraction performance, i.e. sorbent dosage, sample volume, extraction and desorption time, type of organic eluent and volume and solution pH were investigated and optimized. The proposed method showed linear range between 0.5 and 500 ng ml−1, low limit of detection at S/N = 3 (0.16–0.37 ng ml−1) and limit of quantification at S/N = 10 (0.53–1.22 ng ml−1). The inter-day (n = 15) and intra-day (n = 5) precision for the proposed methods given by relative standard deviation (RSD%) was in the range of 2.5–4.0 and 2.1–5.5, respectively. The extraction recoveries of NSAIDs from environmental samples (tap, drinking and river water) ranged from 92.5% to 123.6%, with satisfactory precision (RSD% less than 12.4%).
机译:针对新合成的磁性β-环糊精,以甲苯二异氰酸酯(TDI)为连接基进行了功能化,并进一步用孢粉的生物聚合孢子(MSp-TDI-βCD)进行了修饰,制备了磁性固相萃取(MSPE)方法。在测定HPLC-DAD之前,先从水样中提取非甾体抗炎药(NSAIDs),即吲哚洛芬(INP),酮洛芬(KTP),布洛芬(IBP)和非诺洛芬(FNP)。使用FT-IR,XRD,SEM-EDX,BET和VSM分析可全面表征新合成的MSp-TDI-βCD。只需通过永磁体施加外部磁场,即可简单地将MSp-TDI-βCD上选定的NSAID从水溶液中分离出来。研究和优化了影响萃取性能的MSPE参数,即吸附剂剂量,样品量,萃取和解吸时间,有机洗脱液类型,体积和溶液pH值。所提出的方法显示线性范围为0.5至500μngml -1 ,在S / N = 3时的检测下限(0.16-0.37μng−ml -1 )和极限S / N = 10(0.53-1.22ngngml -1 )的定量分析。通过相对标准偏差(RSD%)给出的拟议方法的日间精度(n = 15)和日间精度(n = 5)分别在2.5-4.0和2.1-5.5范围内。从环境样品(自来水,饮用水和河水)中提取非甾体抗炎药的回收率在92.5%至123.6%之间,精确度令人满意(RSD%小于12.4%)。

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