Ochiai Nobuo, Sasamoto Kikuo, Kanda Hirooki, Pfannkoch Edward
Gerstel K.K., Application development, 2-13-18, Nakane, Meguro-ku, Tokyo 152-0031, Japan.
J Chromatogr A. 2008 Jul 18;1200(1):72-9. doi: 10.1016/j.chroma.2008.05.069. Epub 2008 May 29.
A novel extraction procedure for stir bar sorptive extraction (SBSE) termed sequential SBSE was developed. Compared to conventional SBSE, sequential SBSE provides more uniform enrichment over the entire polarity/volatility range for organic pollutants at ultra-trace levels in water. Sequential SBSE consists of a SBSE performed sequentially on a 5-mL sample first without modifier using one stir bar, then on the same sample after addition of 30% NaCl using a second stir bar. The first extraction with unmodified sample is mainly targeting solutes with high Kow (logKow>4.0), the second extraction with modified sample solution (containing 30% NaCl) is targeting solutes with low and medium Kow (logKow<4.0). After extraction the two stir bars are placed in a single glass desorption liner and are simultaneously desorbed. The desorbed compounds were analyzed by thermal desorption and gas chromatography-mass spectrometry (TD-GC-MS). Recovery of model compounds consisting of 80 pesticides (organochlorine, carbamate, organophosphorus, pyrethroid, and others) for sequential SBSE was evaluated as a function of logKow (1.70-8.35). The recovery using sequential SBSE was compared with those of conventional SBSE with or without salt addition (30% NaCl). The sequential approach provided very good recovery in the range of 82-113% for most of the solutes, and recovery less than 80% for only five solutes with low Kow (logKow<2.5), while conventional approaches (with or without salt addition) showed less than 80% recovery for 23 and 41 solutes, respectively. The method showed good linearity (r2>0.9900) and high sensitivity (limit of detection: <10ngL(-1)) for most of the model compounds even with the scan mode in the MS. The method was successfully applied to screening of pesticides at ngL(-1) level in river water samples.
开发了一种称为连续搅拌棒吸附萃取(SBSE)的新型搅拌棒吸附萃取方法。与传统的SBSE相比,连续SBSE能在水中超痕量水平的有机污染物的整个极性/挥发性范围内提供更均匀的富集。连续SBSE包括首先使用一个搅拌棒在5 mL样品上不添加改性剂进行SBSE,然后使用第二个搅拌棒在添加30%氯化钠后的同一样品上进行SBSE。未改性样品的第一次萃取主要针对辛醇-水分配系数(Kow)高(logKow>4.0)的溶质,改性样品溶液(含30%氯化钠)的第二次萃取针对Kow低和中等(logKow<4.0)的溶质。萃取后,将两个搅拌棒置于单个玻璃解吸衬管中并同时解吸。通过热解吸和气相色谱-质谱联用(TD-GC-MS)分析解吸的化合物。评估了由80种农药(有机氯、氨基甲酸酯、有机磷、拟除虫菊酯等)组成的模型化合物在连续SBSE中的回收率与logKow(1.70 - 8.35)的关系。将连续SBSE的回收率与添加或不添加盐(30%氯化钠)的传统SBSE的回收率进行了比较。连续方法对大多数溶质提供了82 - 113%的良好回收率,对于仅五种Kow低(logKow<2.5)的溶质回收率低于80%,而传统方法(添加或不添加盐)分别对23种和41种溶质显示出低于80%的回收率。该方法对大多数模型化合物显示出良好的线性(r2>0.9900)和高灵敏度(检测限:<10 ngL(-1)),即使在质谱的扫描模式下也是如此。该方法成功应用于河水样品中纳克每升水平农药的筛查。