Hogendoorn E A, van Zoonen P, Polettini A, Marrubini Bouland G, Montagna M
National Institute of Public Health and Environmental Protection (RIVM), Bilthoven, The Netherlands.
Anal Chem. 1998 Apr 1;70(7):1362-8. doi: 10.1021/ac971030w.
This study investigated the potential of restricted access media (RAM) columns used as a first column in coupled-column LC hyphenated to thermospray tandem mass spectrometry (LC/LC-TSP/MS/MS) for the fast, selective, and sensitive determination of target drugs in serum samples. Because of their wide range in polarity, salbutamol and clenbuterol were chosen as model compounds and representatives of the class of beta 2-agonists. Three types of RAM columns were tested: (i) Pinkerton ISRP (internal surface reversed phase, 5 microns), (ii) SPS (semipermeable surface, 5 microns C18), and (iii) RP-18 ADS (alkyl-diol silica, 25 microns). A 3-micron C18 column (50 mm x 4.6 mm i.d.) was chosen as the second column. Tandem mass spectrometric detection was carried out in the selected reaction monitoring (one parent-->one daughter) mode. With regard to retention and, moreover, the peak elution volume of the analytes, the ISRP material was found to perform best: a 50-mm x 4.6-mm i.d. ISRP column in combination with a 100% aqueous buffer (pH of 7.0 +/- 0.2) allowed the injection of large volumes (up to 200 microL) of sample without additional band broadening of the analytes and provided sufficient preseparation between analytes and large-molecule serum constituents. Under the selected conditions, both analytes could be determined in serum samples up to a limit of quantification (LOQ) of 0.5 ng/mL, with a sample throughput of 7 and 5 h-1 for salbutamol and clenbuterol, respectively. Method validation was carried out by analyzing, in the course of several days, calf and human serum samples spiked with the analytes. In the case of salbutamol, the overall recovery from serum samples spiked at levels between 0.5 and 50 ppb (n = 33) was 103.4%, with a repeatability of 12.7% and reproducibility of 14.3%. The overall recovery for clenbuterol was 99.6% (n = 15, spiked level 0.5-5 ppb), with a repeatability of 15.2% and reproducibility of 16.4%. The adopted LC/LC-TSP/MS/ MS analyzer appeared to be very robust under the selected conditions, and, after the period of analysis involving the processing of more than 100 mL of serum, neither loss of chromatographic performance nor pressure increase of columns or of the interface was observed.
本研究考察了在与热喷雾串联质谱联用的柱切换液相色谱(LC/LC-TSP/MS/MS)中,将受限进样介质(RAM)柱用作第一根柱子,用于快速、选择性且灵敏地测定血清样品中目标药物的潜力。由于沙丁胺醇和克伦特罗极性范围广,因此选择它们作为β2-激动剂类别的模型化合物和代表物。测试了三种类型的RAM柱:(i)平克顿内表面反相柱(ISRP,5微米),(ii)半透表面柱(SPS,5微米C18),以及(iii)RP-18二醇基硅胶柱(ADS,25微米)。选择一根3微米的C18柱(50毫米×4.6毫米内径)作为第二根柱子。串联质谱检测在选择反应监测(一个母离子→一个子离子)模式下进行。关于保留情况以及分析物的峰洗脱体积,发现ISRP材料表现最佳:一根50毫米×4.6毫米内径的ISRP柱与100%的水性缓冲液(pH为7.0±0.2)联用,允许进样大量(高达200微升)样品,而不会使分析物的谱带进一步展宽,并且在分析物与大分子血清成分之间提供了足够的预分离。在选定的条件下,两种分析物均可在血清样品中测定,定量限(LOQ)高达0.5纳克/毫升,沙丁胺醇和克伦特罗的样品通量分别为每小时7个和5个。通过在几天内分析添加了分析物的小牛和人血清样品来进行方法验证。对于沙丁胺醇,在添加水平为0.5至50皮克/毫升(n = 33)的血清样品中的总回收率为103.4%,重复性为12.7%,重现性为14.3%。克伦特罗的总回收率为99.6%(n = 15,添加水平0.5至5皮克/毫升),重复性为15.2%,重现性为16.4%。所采用的LC/LC-TSP/MS/MS分析仪在选定条件下似乎非常稳定,并且在涉及处理超过100毫升血清的分析期后,未观察到色谱性能下降、柱子或接口压力增加的情况。