Department of Chemistry, Chung Yuan Christian University 200 Chung Pei Road, Chung Li District, Taoyuan City, 320, Taiwan, R.O.C.
Langmuir. 2016 Nov 8;32(44):11465-11473. doi: 10.1021/acs.langmuir.6b03067. Epub 2016 Oct 24.
In this study, we first demonstrated the effect of two types of metal-organic framework-polymer (MOF-polymer) monoliths on in-tube solid-phase microextraction (IT-SPME) of sulfonamides. Sulfonamides were successfully adsorbed onto MIL-101(Cr)-polymer but were difficult to elute due to these sulfonamides could interact via Lewis acid-base interaction with the presence of Cr(III) coordinatively unsaturated metal sites (CUS). Moreover, the cage-type topology of MIL-101(Cr) that could produce multiple pathways thus complicates the desorption of the test analytes from the sorbent. Contrastingly, MIL-53(Al)-polymer provided weaker Al(III) CUS, and its one-dimensional channel pore structure could provide an unhindered pathway for sulfonamides transfer during elution. After optimizing the IT-SPME condition such as MOF content, pH of sample matrix, column length, extraction flow rate, and elution volume, the calculated extraction recovery of sulfonamides in MIL-53(Al)-polymer as analyzed by microemulsion electrokinetic chromatography (MEEKC) were in the range of 40%-90% with relative standard deviations (RSDs) below 5% and a reusability of at least 30 times.
在这项研究中,我们首先展示了两种类型的金属有机骨架-聚合物(MOF-聚合物)整体柱对磺酰胺类药物的管内固相微萃取(IT-SPME)的影响。磺酰胺类药物成功地被 MIL-101(Cr)-聚合物吸附,但由于这些磺酰胺类药物可以通过路易斯酸碱相互作用与存在的 Cr(III)配位不饱和金属位(CUS)相互作用,因此难以洗脱。此外,MIL-101(Cr)的笼型拓扑结构可以产生多种途径,从而使测试分析物从吸附剂上解吸变得复杂。相比之下,MIL-53(Al)-聚合物提供了较弱的 Al(III)CUS,其一维通道孔结构可以在洗脱过程中为磺酰胺类药物的转移提供无障碍途径。在优化 IT-SPME 条件,如 MOF 含量、样品基质 pH 值、柱长、萃取流速和洗脱体积后,通过微乳液电动色谱(MEEKC)分析,MIL-53(Al)-聚合物对磺酰胺类药物的计算萃取回收率在 40%-90%之间,相对标准偏差(RSD)低于 5%,至少可重复使用 30 次。