New sporopollenin-based β-cyclodextrin functionalized magnetic hybrid adsorbent for magnetic solid-phase extraction of nonsteroidal anti-inflammatory drugs from water samples

被引:18
|
作者
Yaacob, Syed Fariq Fathullah Syed [1 ]
Kamboh, Muhammad Afzal [3 ]
Ibrahim, Wan Aini Wan [4 ]
Mohamadu, Sharifah [1 ,2 ]
机构
[1] Univ Malaya, Fac Sci, Dept Chem, Kuala Lumpur, Malaysia
[2] Univ Malaya, UMCiL, Kuala Lumpur, Malaysia
[3] Shaheed Benazir Bhutto Univ, Dept Chem, Shaheed Benazirabad, Sindh, Pakistan
[4] Univ Teknol Malaysia, Fac Sci, Dept Chem, Separat Sci & Technol Grp SepSTec, Johor Baharu, Johor, Malaysia
来源
ROYAL SOCIETY OPEN SCIENCE | 2018年 / 5卷 / 07期
关键词
sporopollenin; magnetic nanoparticles; beta-cyclodextrin; NSAIDs; magnetic solid-phase extraction; POLYCYCLIC AROMATIC-HYDROCARBONS; ORGANOPHOSPHORUS PESTICIDES; ENVIRONMENTAL WATER; AQUEOUS-SOLUTION; HUMAN URINE; NANOPARTICLES; CHROMATOGRAPHY; REMOVAL; MICROEXTRACTION; SEPARATION;
D O I
10.1098/rsos.171311
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A magnetic solid-phase extraction (MSPE) procedure on the newly synthesized magnetic beta-cyclodextrin functionalized wi th toluene diisocyanate (TDI) as a linker arid further modified with bio-polymeric spores of sporopollenin (MSp-TDI-beta CD), 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-beta CD was comprehensibly characterized using FT-IR, XRD, SEM-EDX, BET and VSM analyses. The separation of selected NSAIDs on MSp-TDI-beta CD 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 do sage, 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%).
引用
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页数:14
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