Dendrimer-functionalized mesoporous silica as a reversed-phase/anion-exchange mixed-mode sorbent for solid phase extraction of acid drugs in human urine
文献类型:期刊论文
作者 | Li, Yun; Yang, Jiajia; Huang, Chaonan; Wang, Longxing; Wang, Jincheng; Chen, Jiping |
刊名 | journal of chromatography a
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出版日期 | 2015-05-01 |
卷号 | 1392页码:28-36 |
关键词 | Dendrimer functionalization Mesoporous silica Mixed-mode anion-exchanger Solid phase extraction Acidic drugs Human urine |
英文摘要 | a new dendrimer-functionalized mesoporous silica material based on large-pore 3d cubic korea advanced institute of science and technology-6 (kit-6) was synthesized by the growing of dendritic branches inside the mesopores of aminopropyl functionalized kit-6. detailed physical characterizations using transmission electron microscopy, nitrogen adsorption-desorption measurements, fourier transform infrared (ftir) spectroscopy, and elemental analysis reveal that the multifunctional den-drimers have been grown successfully within the confined spaces of mesopores. although the 3d ordered mesoporous architecture of kit-6 was well preserved, there was a significant and continuous decrease in pore size, specific surface area (s-bet) and pore volume when increasing dendrimer generation up to six. in order to get a compromise between the s-bet, pore size and density of functionalities, the dendrimer-functionalized kit-6 (df-kit-6) for generation 2 (s-bet, 314.2 m(2) g(-1); pore size, 7.9 nm; carbon and nitrogen contents, 19.80% and 1.92%) was selected for solid phase extraction (spe) applications. the df-kit-6 was then evaluated as a reversed-phase/anion-exchange mixed-mode sorbent for extraction of the selected acidic drugs (ketoprofen, kep; naproxen, nap; and ibuprofen, ibu), since the dendrimers contained both hydrocarbonaceous and amine functionalities. the effective parameters on extraction efficiency such as sample ph and volume, type and volume of eluent and wash solvents were optimized. under the optimized experimental conditions, the df-kit-6 based spe coupled with hplc-uv method demonstrated good sensitivity (0.4-4.6 ng ml(-1) detection of limits) and linearity (r-2 > 0.990 for 10-2000 ng ml(-1) of kep and ibu, and 1-200 ng ml(-1) of nap). the potential use of df-kit-6 sorbent for preconcentration and cleanup of acid drugs in human urine samples was also demonstrated. satisfactory recoveries at two spiking levels (30 and 300 ng ml(-1) for kep and ibu, 3 and 30 ng ml(-1) for nap) were obtained in the range of 85.7-113.9% with rsd values below 9.3% (n=3). (c) 2015 elsevier b.v. all rights reserved, |
WOS标题词 | science & technology ; life sciences & biomedicine ; physical sciences |
类目[WOS] | biochemical research methods ; chemistry, analytical |
研究领域[WOS] | biochemistry & molecular biology ; chemistry |
关键词[WOS] | performance liquid-chromatography ; tandem mass-spectrometry ; stationary-phase ; waste-water ; sample preparation ; polymeric sorbents ; beta-blockers ; retention ; pharmaceuticals ; metabolites |
收录类别 | SCI |
语种 | 英语 |
WOS记录号 | WOS:000353081900004 |
公开日期 | 2016-05-09 |
源URL | [http://cas-ir.dicp.ac.cn/handle/321008/146174] ![]() |
专题 | 大连化学物理研究所_中国科学院大连化学物理研究所 |
作者单位 | Chinese Acad Sci, Dalian Inst Chem Phys, Key Lab Separat Sci Analyt Chem, Dalian 116023, Liaoning, Peoples R China |
推荐引用方式 GB/T 7714 | Li, Yun,Yang, Jiajia,Huang, Chaonan,et al. Dendrimer-functionalized mesoporous silica as a reversed-phase/anion-exchange mixed-mode sorbent for solid phase extraction of acid drugs in human urine[J]. journal of chromatography a,2015,1392:28-36. |
APA | Li, Yun,Yang, Jiajia,Huang, Chaonan,Wang, Longxing,Wang, Jincheng,&Chen, Jiping.(2015).Dendrimer-functionalized mesoporous silica as a reversed-phase/anion-exchange mixed-mode sorbent for solid phase extraction of acid drugs in human urine.journal of chromatography a,1392,28-36. |
MLA | Li, Yun,et al."Dendrimer-functionalized mesoporous silica as a reversed-phase/anion-exchange mixed-mode sorbent for solid phase extraction of acid drugs in human urine".journal of chromatography a 1392(2015):28-36. |
入库方式: OAI收割
来源:大连化学物理研究所
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