Department of Bioengineering, Henry Samueli School of Engineering and Applied Science, University of California Los Angeles, Los Angeles, CA 90095, USA; Crump Institute for Molecular Imaging and Department of Molecular and Medical Pharmacology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA 90095, USA.
Crump Institute for Molecular Imaging and Department of Molecular and Medical Pharmacology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA 90095, USA; Physics & Biology in Medicine Interdepartmental Graduate Program, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA 90095, USA.
Anal Chim Acta. 2017 Sep 8;985:129-140. doi: 10.1016/j.aca.2017.05.037. Epub 2017 Jun 19.
A novel injector for microchip electrophoresis (MCE) has been designed and evaluated that achieves very high repeatability of injection volume suitable for quantitative analysis. It eliminates the injection biases in electrokinetic injection and the dependence on pressure and sample properties in hydrodynamic injection. The microfluidic injector, made of poly(dimethylsiloxane) (PDMS), operates similarly to an HPLC injection valve. It contains a channel segment (chamber) with a well-defined volume that serves as an "injection loop". Using on-chip microvalves, the chamber can be connected to the sample source during the "loading" step, and to the CE separation channel during the "injection" step. Once the valves are opened in the second state, electrophoretic potential is applied to separate the sample. For evaluation and demonstration purposes, the microinjector was connected to a 75 μm ID capillary and UV absorbance detector. For single compounds, a relative standard deviation (RSD) of peak area as low as 1.04% (n = 11) was obtained, and for compound mixtures, RSD as low as 0.40% (n = 4) was observed. Using the same microchip, the performance of this new injection technique was compared to hydrodynamic injection and found to have improved repeatability and less dependence on sample viscosity. Furthermore, a non-radioactive version of the positron-emission tomography (PET) imaging probe, FLT, was successfully separated from its known 3 structurally-similar byproducts with baseline resolution, demonstrating the potential for rapid, quantitative analysis of impurities to ensure the safety of batches of short-lived radiotracers. Both the separation efficiency and injection repeatability were found to be substantially higher when using the novel volumetric injection approach compared to electrokinetic injection (performed in the same chip). This novel microinjector provides a straightforward way to improve the performance of hydrodynamic injection and enables extremely repeatable sample volume injection in MCE. It could be used in any MCE application where volume repeatability is needed, including the quantitation of impurities in pharmaceutical or radiopharmaceutical samples.
一种用于微芯片电泳(MCE)的新型注射器已经被设计和评估,该注射器能够实现非常高的注射体积重复性,适用于定量分析。它消除了电动注射中的注射偏差以及液压注射中对压力和样品性质的依赖性。微流体注射器由聚二甲基硅氧烷(PDMS)制成,其工作原理类似于高效液相色谱(HPLC)注射阀。它包含一个具有明确定义体积的通道段(腔室),用作“注射环”。使用芯片上的微阀,在“加载”步骤中可以将腔室连接到样品源,在“注射”步骤中可以将腔室连接到 CE 分离通道。一旦在第二状态下打开阀门,就施加电泳电势以分离样品。为了评估和演示目的,将微注射器与 75μm ID 毛细管和紫外吸收检测器相连。对于单一化合物,获得了低至 1.04%(n=11)的峰面积相对标准偏差(RSD),对于化合物混合物,观察到低至 0.40%(n=4)的 RSD。使用相同的微芯片,将这种新的注射技术的性能与液压注射进行了比较,发现其重复性更好,对样品粘度的依赖性更小。此外,成功地将放射性药物正电子发射断层扫描(PET)成像探针 FLT 与其已知的 3 种结构相似的副产品分离,基线分辨率高,证明了快速、定量分析杂质以确保短寿命放射性示踪剂批次安全性的潜力。与电动注射(在同一芯片上进行)相比,新型体积注射方法的分离效率和注射重复性都显著提高。它可以用于任何需要体积重复性的 MCE 应用,包括药物或放射性药物样品中杂质的定量。