Department of Analytical Chemistry, University of Barcelona, Barcelona, Spain.
J Sep Sci. 2010 May;33(9):1294-304. doi: 10.1002/jssc.200900669.
In this study, we investigated the performance of several commercial sorbents (Sep-pack) C18, (t)C18, C8 and (t)C2, Oasis HLB, Isolute ENV+, Strata-X and Oasis MCX) for the determination of opioid peptides by solid-phase extraction coupled on-line to capillary electrophoresis (SPE-CE). First, standard solutions were analyzed in order to achieve the lowest LOD and the best electrophoretic separations using UV detection. The best results were obtained using C18, C8 and (t)C2 sorbents, which were examined for the analysis of spiked human plasma samples. A double-step sample clean-up pretreatment, which consisted of precipitation with acetonitrile and filtration, was needed to prevent saturation of the on-line SPE microcartridge. The filtration step was critical to obtain optimum analyte recovery and to clean up the sample matrix. A range of centrifugal filters and filtration conditions were tested and the recoveries of the sample pretreatment were evaluated by CE-ESI-MS. The LODs attained through SPE-CE-UV were approximately ten-fold better with C18 than with C8 and (t)C2. The 0.1 microg/mL LODs achieved by C18-SPE-CE-UV were further improved until we could detect 1 ng/mL concentrations of opioid peptides in plasma samples by C18-SPE-CE-ESI-MS, due to the outstanding selectivity of the MS detection.
在这项研究中,我们考察了几种商用吸附剂(Sep-pack C18、(t)C18、C8 和 (t)C2、Oasis HLB、Isolute ENV+、Strata-X 和 Oasis MCX)在固相萃取-在线毛细管电泳(SPE-CE)联用测定阿片肽中的性能。首先,分析了标准溶液,以使用 UV 检测获得最低的 LOD 和最佳的电泳分离。使用 C18、C8 和 (t)C2 吸附剂获得了最佳的结果,并用其分析了加标人血浆样品。需要两步样品净化预处理,包括乙腈沉淀和过滤,以防止在线 SPE 微柱饱和。过滤步骤对于获得最佳的分析物回收率和净化样品基质至关重要。测试了一系列离心过滤器和过滤条件,并通过 CE-ESI-MS 评估了样品预处理的回收率。与 C8 和 (t)C2 相比,C18 可通过 SPE-CE-UV 获得约十倍更好的 LOD。通过 C18-SPE-CE-UV 达到的 0.1μg/mL LOD 进一步提高,直到我们能够通过 C18-SPE-CE-ESI-MS 检测到血浆样品中浓度为 1ng/mL 的阿片肽,这要归功于 MS 检测的出色选择性。