Hogendoorn E A, van Zoonen P, Polettini A, Montagna M
National Institute of Public Health and Environmental Protection (RIVM), Bilthoven, The Netherlands.
J Mass Spectrom. 1996 Apr;31(4):418-26. doi: 10.1002/(SICI)1096-9888(199604)31:4<418::AID-JMS315>3.0.CO;2-F.
In a previous work, coupled-column LC (LC/LC) with direct large-volume sample injection for the analysis of beta 2-agonists in bovine urine was investigated, in view of its combination with thermospray (TSP) tandem mass spectrometric (MS/MS) detection. In this work, the potential of both conventional LC and LC/LC coupled to TSP-MS/MS for the rapid determination of beta 2-agonists in bovine urine was evaluated. It was first established that, in order to avoid disturbances in TSP-MS/MS detection due to changes in pressure and flow rate of the mobile phase, LC/LC is preferable to conventional LC. Then, selecting clenbuterol and salbutamol as model compounds for the class of beta 2-agonists, two single-residue LC/LC/TSP-MS/MS methods were developed, permitting the determination of the analytes in bovine urine samples with a limit of quantification of at least 0.1 ng, ml-1, with a sample throughput of 4 h-1. The methods were validated by analysing both spiked urine samples and samples containing clenbuterol or salbutamol residues. Mean recoveries from urine samples spiked with clenbuterol at levels of 5 and 0.22 ng ml-1 were 107% (n = 9, RSD = 7.4%) and 102% (n = 6, RSD = 14%), respectively. A bovine urine sample containing 1.28 ng ml-1 clenbuterol residue (previously quantified by GC/MS) was re-analysed by LC/LC/TSP-MS/MS on four different days (n = 3, each day) and yielded a mean concentration of 1.31 ng ml-1, with a reproducibility of 8.4%. Bovine urine samples spiked with salbutamol at levels of 10.8 and 0.55 ng ml-1 yielded mean recoveries of 101% (n = 3, RSD = 1%) and 89% (n = 3, RSD = 13%), respectively. In bovine urine samples containing salbutamol residues, the concentrations of unconjugated salbutamol were found to be in the range 8-57 ng ml-1.
在之前的一项工作中,鉴于其与热喷雾(TSP)串联质谱(MS/MS)检测相结合,对用于分析牛尿液中β2 - 激动剂的直接大体积进样的耦合柱液相色谱(LC/LC)进行了研究。在这项工作中,评估了常规液相色谱和与TSP - MS/MS联用的LC/LC在快速测定牛尿液中β2 - 激动剂方面的潜力。首先确定,为避免由于流动相压力和流速变化而对TSP - MS/MS检测产生干扰,LC/LC比常规液相色谱更可取。然后,选择克伦特罗和沙丁胺醇作为β2 - 激动剂类别的模型化合物,开发了两种单残留LC/LC/TSP - MS/MS方法,能够测定牛尿液样品中的分析物,定量限至少为0.1 ng·ml-1,样品通量为4 h-1。通过分析加标尿液样品和含有克伦特罗或沙丁胺醇残留的样品对方法进行了验证。在添加了浓度为5和0.22 ng·ml-1克伦特罗的尿液样品中,平均回收率分别为107%(n = 9,RSD = 7.4%)和102%(n = 6,RSD = 14%)。对一份含有1.28 ng·ml-1克伦特罗残留(先前通过气相色谱/质谱法定量)的牛尿液样品在四个不同日期(n = 3,每天)用LC/LC/TSP - MS/MS重新分析,得到平均浓度为1.31 ng·ml-1,重现性为8.4%。添加了浓度为10.8和0.55 ng·ml-1沙丁胺醇的牛尿液样品的平均回收率分别为101%(n = 3,RSD = 1%)和89%(n = 3,RSD = 13%)。在含有沙丁胺醇残留的牛尿液样品中,未结合沙丁胺醇的浓度范围为8 - 57 ng·ml-1。