Altun Zeki, Abdel-Rehim Mohamed
Faculty of Technology and Science, Karlstad University, Karlstad, Sweden.
Anal Chim Acta. 2008 Dec 23;630(2):116-23. doi: 10.1016/j.aca.2008.09.067. Epub 2008 Oct 14.
Microextraction by packed sorbent (MEPS) is a new technique for sample preparation that can be connected on-line with LC or GC. In MEPS, approximately 1-2mg of the solid packing material is inserted into a syringe (100-250 microL) as a plug. Sample preparation takes place on the packed bed. The bed can be packed or coated to provide selective and suitable sampling conditions. The new method is very promising for extraction of drugs and metabolites from biological samples. In this paper, some factors affecting the performance of MEPS such as recovery, carry-over, leakage, washing volume and elution volume were studied using C18 and hydroxylated polystyrene-divinylbenzene copolymer (ENV+) as sorbents. Radioactively labelled bupivacaine in plasma samples was used as test analyte. For the extraction of this drug, using methanol/water 95:5 (v/v) (0.25% ammonium hydroxide) was used as elution solvent. The analyte response increased with increasing the elution volume and it was linear upp up to 100 microL utilizing liquid scintillation counter. Further, for concentrating the sample, we found that MEPS may be used such that the sample can be drawn through the needle, up and down, several times. The analyte leakage increases as the volume washing increases, though higher washing volumes may also result in cleaner extracts. To eliminate analyte carry-over, the sorbents were washed first with 3 x 250 microL elution solution and then with 3 x 250 microL washing solution. In addition, the reproducibility measurements show relatively good relative standard deviation (RSD) % values concerning analyte recovery and analyte leakage. The present study provides an understanding of basic aspects when optimizing methods for MEPS. In this study, MEPS was used off-line with liquid scintillation counter and on-line with LC-MS/MS.
填充吸附剂微萃取(MEPS)是一种用于样品制备的新技术,可与液相色谱(LC)或气相色谱(GC)在线连接。在MEPS中,将约1-2mg的固体填充材料作为塞子插入注射器(100-250μL)中。样品制备在填充床上进行。该床可以进行填充或涂层处理,以提供选择性且合适的采样条件。这种新方法在从生物样品中提取药物和代谢物方面非常有前景。本文以C18和羟基化聚苯乙烯-二乙烯基苯共聚物(ENV+)作为吸附剂,研究了一些影响MEPS性能的因素,如回收率、残留、泄漏、洗涤体积和洗脱体积。血浆样品中放射性标记的布比卡因用作测试分析物。对于该药物的萃取,使用甲醇/水95:5(v/v)(0.25%氢氧化铵)作为洗脱溶剂。利用液体闪烁计数器,随着洗脱体积的增加,分析物响应增强,在高达100μL时呈线性。此外,为了浓缩样品,我们发现可以使用MEPS,使样品通过针头上下抽吸几次。随着洗涤体积的增加,分析物泄漏增加,尽管较高的洗涤体积也可能得到更纯净的提取物。为了消除分析物残留,先用3×250μL洗脱液洗涤吸附剂,然后用3×250μL洗涤液洗涤。此外,重现性测量结果显示,在分析物回收率和分析物泄漏方面,相对标准偏差(RSD)%值相对较好。本研究为优化MEPS方法时的基本方面提供了认识。在本研究中,MEPS与液体闪烁计数器离线使用,并与LC-MS/MS在线使用。