GICAPC Research Group, Department of Analytical Chemistry, University of Valencia, Burjassot E-46100, Valencia, Spain.
Affordable and Sustainable Sample Preparation (AS2P) Research Group, Analytical Chemistry Department, Instituto Químico para la Energía y el Medioambiente (IQUEMA), University of Córdoba, Campus of Rabanales, Marie Curie Building, Córdoba E-14071, Spain.
Anal Chem. 2024 Jun 11;96(23):9629-9635. doi: 10.1021/acs.analchem.4c01297. Epub 2024 May 14.
Direct coupling of sample preparation with mass spectrometry (MS) can speed up analysis, enabling faster decision-making. In such combinations, where the analysis time is mainly defined by the extraction procedure, magnetic dispersive solid-phase extraction emerges as a relevant technique because of its rapid workflow. The dispersion and retrieval of the magnetic sorbent are typically uncoupled stages, thus reducing the potential simplicity. Stir bar sorptive dispersive microextraction (SBSDME) is a novel technique that integrates both stages into a single device. Its miniaturization (mSBSDME) makes it more portable and compatible with low-availability samples. This article reports the direct combination of mSBSDME and MS using a needle-based electrospray ionization (NESI) emitter as the interface. This combination is applied to determine tetrahydrocannabinol in saliva samples, a relevant societal problem if the global consumption rates of cannabis are considered. The coupling requires only the transference of the magnet (containing the sorbent and the isolated analyte) from the mSBSDME to the hub of a hypodermic needle, where the online elution occurs. The application of 5 kV on the needle forms an electrospray on its tip, transferring the ionized analyte to the MS inlet. The excellent performance of mSBSDME-NESI-MS/MS relies on the sensitivity (limits of detection as low as 2.25 ng mL), the precision (relative standard deviation lower than 15%), and the accuracy (relative recoveries ranged from 87 to 127%) obtained. According to the results, the mSBSDME-NESI-MS/MS technique promises faster and more efficient chemical analysis in MS-based applications.
直接将样品制备与质谱 (MS) 耦合可以加快分析速度,使决策更加迅速。在这种组合中,分析时间主要由提取程序定义,因此磁性分散固相萃取作为一种相关技术脱颖而出,因为它具有快速的工作流程。磁性吸附剂的分散和回收通常是两个不相关的阶段,因此降低了潜在的简单性。搅拌棒吸附分散微萃取 (SBSDME) 是一种将这两个阶段集成到一个单一设备中的新技术。其微型化 (mSBSDME) 使其更便携,更适合低可用性样品。本文报道了使用基于针的电喷雾电离 (NESI) 发射器作为接口,直接将 mSBSDME 与 MS 结合。该组合应用于唾液样品中四氢大麻酚的测定,如果考虑到大麻的全球消费率,这是一个相关的社会问题。该耦合仅需要将磁铁(含有吸附剂和分离的分析物)从 mSBSDME 转移到皮下注射针的轮毂上,在线洗脱就在那里发生。在针上施加 5 kV 会在其尖端形成电喷雾,将电离的分析物转移到 MS 入口。mSBSDME-NESI-MS/MS 的优异性能依赖于灵敏度(检测限低至 2.25 ng mL)、精密度(相对标准偏差低于 15%)和准确性(相对回收率范围为 87 至 127%)。根据结果,mSBSDME-NESI-MS/MS 技术有望在基于 MS 的应用中实现更快、更高效的化学分析。