Department of Chemistry, University of South Florida, 4202 E. Fowler Avenue, CHE 205, Tampa, FL, 33620-5250, USA.
J Am Soc Mass Spectrom. 2019 Apr;30(4):595-604. doi: 10.1007/s13361-018-02127-w. Epub 2019 Feb 22.
Providing rapid and sensitive sample cleanup, sol-gel capillary microextraction (CME) is a form of solid phase microextraction (SPME). The capillary format of CME couples easily with mass spectrometry (MS) by employing sol-gel sorbent coatings in inexpensive fused silica capillaries. By leveraging the syringe pump and six-port valve readily available on the commercial MS, we can obviate the need for chromatography for samples as complex as urine in quantitative assays. Two different sol-gel materials were studied as microextraction sorbents: one with a single ligand of octadecyl (C) and the other with a dual-ligand combination of C and phenyl (Phe) groups. The CME-MS method was optimized for flow rate and solvent desorption and studied for overall microextraction performance between the two sorbents studied. We extract illicit drugs including cocaine, heroin, amphetamine, methamphetamine, 3,4-methylenedioxymethamphetamine, and oxycodone, proving good run-to-run reproducibility (RSD% < 10%) and low detection limits (< 10 ng mL). The dual-ligand sorbent demonstrated superior performance due to typical hydrophobic properties of C as well as potential π-π interactions of the Phe functionality and the aromatic moiety common to many drugs. This study demonstrates the advantage of fine-tuning sol-gel sorbents for application-specific CME-MS. We apply our method to the analysis of various drugs in synthetic and human urine samples and show low carryover effect (~ 5%) and low matrix effect in the presence of the urine matrix. Thus, the sol-gel CME-MS technique described herein stands to be an attractive alternative to other SPME-MS techniques.
提供快速和灵敏的样品净化,溶胶-凝胶毛细管微萃取(CME)是固相微萃取(SPME)的一种形式。CME 的毛细管形式通过在廉价的熔融石英毛细管中使用溶胶-凝胶吸附剂涂层,很容易与质谱(MS)结合。通过利用商业 MS 上 readily available 的注射器泵和六通阀,我们可以避免对复杂样品(如尿液)进行色谱分离,实现定量分析。研究了两种不同的溶胶-凝胶材料作为微萃取吸附剂:一种具有单一配体十八烷基(C),另一种具有 C 和苯基(Phe)基团的双配体组合。优化了 CME-MS 方法的流速和溶剂解吸,并研究了两种吸附剂之间的整体微萃取性能。我们提取了包括可卡因、海洛因、安非他命、甲基苯丙胺、3,4-亚甲基二氧基甲基苯丙胺和羟考酮在内的非法药物,证明了良好的运行重复性(RSD%<10%)和低检测限(<10ng mL)。双配体吸附剂由于 C 的典型疏水性以及 Phe 官能团和许多药物共有的芳香部分之间的潜在π-π相互作用,表现出优异的性能。本研究证明了为特定应用调整溶胶-凝胶吸附剂的优势。我们将我们的方法应用于合成和人尿液样品中各种药物的分析,并显示出在尿液基质存在下低的携带效应(~5%)和低的基质效应。因此,本文描述的溶胶-凝胶 CME-MS 技术有望成为其他 SPME-MS 技术的替代方法。