Zhang Xu, Cai Jibao, Oakes Ken D, Breton François, Servos Mark R, Pawliszyn Janusz
Department of Chemistry, University of Waterloo, Ontario, N2L 3G1, Canada.
Anal Chem. 2009 Sep 1;81(17):7349-56. doi: 10.1021/ac900718q.
To facilitate rapid in situ analyte monitoring within heterogeneous samples, a space-resolved solid phase microextraction (SR-SPME) technique was developed that utilized miniaturized segmented fibers. Initially, a multilayered agarose gel was used to determine the effects of diffusion-based mass transfer and fiber dimension on the space-resolving capability of SPME. For diazepam within agarose gel, the SR-SPME limit of detection was 2.5 ng/mL, with a linear dynamic range up to 500 ng/mL. The efficacy of the SR-SPME technique was further evaluated within diverse biological matrices (onion bulb, fish muscle, and adipose tissues) containing stratified pharmaceutical analytes. Empirically, the results agreed well with established techniques such as microdialysis and liquid extraction, but SR-SPME was simpler to implement, displayed higher spatial resolution, and was more cost-effective than traditional approaches. Additionally, the segmented design of the SPME fibers and stepwise desorption protocols offer potential advantages within high throughput applications.
为便于在异质样品中进行快速原位分析物监测,开发了一种利用小型化分段纤维的空间分辨固相微萃取(SR-SPME)技术。最初,使用多层琼脂糖凝胶来确定基于扩散的传质和纤维尺寸对SPME空间分辨能力的影响。对于琼脂糖凝胶中的地西泮,SR-SPME的检测限为2.5 ng/mL,线性动态范围高达500 ng/mL。在含有分层药物分析物的多种生物基质(洋葱鳞茎、鱼肉和脂肪组织)中进一步评估了SR-SPME技术的功效。根据经验,结果与微透析和液液萃取等既定技术吻合良好,但SR-SPME实施起来更简单,具有更高的空间分辨率,且比传统方法更具成本效益。此外,SPME纤维的分段设计和逐步解吸方案在高通量应用中具有潜在优势。