Guan F, Watanabe K, Ishii A, Seno H, Kumazawa T, Hattori H, Suzuki O
Department of Legal Medicine, Hamamatsu University School of Medicine, Japan.
J Chromatogr B Biomed Sci Appl. 1998 Sep 4;714(2):205-13. doi: 10.1016/s0378-4347(98)00234-5.
Solid-phase microextraction (SPME) is a unique extraction and sampling technique, and it has been used for separation of volatile organics from water or other simple matrices. In this study, we have used SPME to separate dinitroaniline herbicides from complicated matrices of human urine and blood in order to broaden its application to biomedical analysis. The SPME conditions were optimized for water, urine and blood samples, in terms of pH, salt additives, extraction temperature, and fiber exposure time. Urine or water (1.0 ml) spiked with herbicides and 0.28 g of anhydrous sodium sulfate was preheated at 70 degrees C for 10 min, and a polydimethylsiloxane-coated fiber for SPME was exposed to the headspace at 70 degrees C for another 30 min; while spiked blood (0.5 ml) diluted with water (0.5 ml) was treated at 90 degrees C in the same way. The herbicides were extractable under these conditions, and could be determined by gas chromatography-electron capture detector (GC-ECD). The recoveries of the herbicides, measured at the concentrations of 0.50 and 1.0 ng/ml urine or water, or 6.0 and 20 ng/0.5 ml blood, ranged from 35 to 64% for different herbicides from water or urine, and from 3.2 to 7.2% from blood. The headspace SPME yielded clean extracts of dinitroaniline herbicides from urine, blood or water, which could be directly analyzed by GC-ECD without further purification. The peak areas of the extracted herbicides were proportional to their concentrations in the range 0.1-10 ng/ml in water or urine, or 1-60 ng/0.5 ml in blood. The lowest detectable concentration of the herbicides lay in 0.1 ng/ml water or urine, or in 0.5 ng/0.5 ml blood. The intra- and inter-day coefficients of variation were within 14% for most of the analytes. Although the recoveries of the herbicides were rather low, the linearity of calibration curve and the precision were good. The developed method is more sensitive and much simpler in sample preparation than previously reported ones. With the established SPME method, a dosed herbicide was successfully separated and determined in rats' blood.
固相微萃取(SPME)是一种独特的萃取和采样技术,已被用于从水或其他简单基质中分离挥发性有机物。在本研究中,我们使用SPME从人尿液和血液的复杂基质中分离二硝基苯胺类除草剂,以扩大其在生物医学分析中的应用。针对水、尿液和血液样本,在pH值、盐添加剂、萃取温度和纤维暴露时间方面对SPME条件进行了优化。将添加了除草剂的尿液或水(1.0 ml)和0.28 g无水硫酸钠在70℃预热10分钟,然后将用于SPME的聚二甲基硅氧烷涂层纤维在70℃下暴露于顶空30分钟;而用水(0.5 ml)稀释的加标血液(0.5 ml)以同样的方式在90℃处理。在这些条件下除草剂是可萃取的,并且可以通过气相色谱 - 电子捕获检测器(GC - ECD)进行测定。在尿液或水中浓度为0.50和1.0 ng/ml,或血液中浓度为6.0和20 ng/0.5 ml时测定的除草剂回收率,对于来自水或尿液的不同除草剂范围为35%至64%,来自血液的回收率为3.2%至7.2%。顶空SPME从尿液、血液或水中得到了二硝基苯胺类除草剂的纯净萃取物,无需进一步纯化即可直接通过GC - ECD进行分析。萃取的除草剂的峰面积在水或尿液中0.1 - 10 ng/ml范围内,或在血液中1 - 60 ng/0.5 ml范围内与它们的浓度成正比。除草剂的最低可检测浓度为0.1 ng/ml水或尿液,或0.5 ng/0.5 ml血液。大多数分析物的日内和日间变异系数在14%以内。虽然除草剂的回收率相当低,但校准曲线的线性和精密度良好。所开发的方法比先前报道的方法更灵敏,且样品制备更简单。使用已建立的SPME方法,成功地在大鼠血液中分离并测定了一剂除草剂。