Monteiro C, Franco J M, Proença P, Castañera A, Claro A, Vieira D N, Corte-Real F
National Institute of Legal Medicine and Forensic Sciences-Centre Branch, Largo da Sé Nova, 3000-213 Coimbra, Portugal; CENCIFOR-Forensic Sciences Centre, Largo da Sé Nova, 3000-213 Coimbra, Portugal.
National Institute of Legal Medicine and Forensic Sciences-Centre Branch, Largo da Sé Nova, 3000-213 Coimbra, Portugal; CENCIFOR-Forensic Sciences Centre, Largo da Sé Nova, 3000-213 Coimbra, Portugal.
Forensic Sci Int. 2014 Oct;243:137-43. doi: 10.1016/j.forsciint.2014.07.016. Epub 2014 Jul 25.
A simple and sensitive procedure, using n-propanol as internal standard (IS), was developed and validated for the qualitative and quantitative analysis of a group of 11 volatile organic substances with different physicochemical properties (1-butanol, 2-propanol, acetaldehyde, ethyl acetate, acetone, acetonitrile, chloroform, diethyl ether, methanol, toluene and p-xylene) in whole blood, urine and vitreous humor. Samples were prepared by dilution with an aqueous solution of internal standard followed by Headspace Gas Chromatography with a Flame-ionization Detector (HS GC-FID) analysis. Chromatographic separation was performed using two capillary columns with different polarities (DB-ALC2: 30m×0.320mm×1.2μm and DB-ALC1: 30m×0.320mm×1.8μm), thus providing a change in the retention and elution order of volatiles. This dual column confirmation increases the specificity, since the risk of another substance co-eluting at the same time in both columns is very small. The method was linear from 5 to 1000mg/L for toluene and p-xylene, 50-1000mg/L for chloroform, and 50-2000mg/L for the remaining substances, with correlation coefficients of over 0.99 for all compounds. The limits of detection (LOD) ranged 1 to 10mg/L, while the limits of quantification (LOQ) ranged from 2 to 31mg/L. The intra-day precision (CV<6.4%), intermediate precision (CV<7.0%) and accuracy (relative error ±10%) of the method were in conformity with the criteria normally accepted in bioanalytical method validation. The method developed has been applied to forensic cases, with the advantages that it uses a small sample volume and does not require any extraction procedure as it makes use of a headspace injection technique.
开发并验证了一种简单且灵敏的方法,该方法以正丙醇作为内标(IS),用于对全血、尿液和玻璃体液中一组11种具有不同理化性质的挥发性有机物质(1-丁醇、2-丙醇、乙醛、乙酸乙酯、丙酮、乙腈、氯仿、乙醚、甲醇、甲苯和对二甲苯)进行定性和定量分析。样品通过用内标水溶液稀释,然后采用带火焰离子化检测器的顶空气相色谱法(HS GC-FID)进行分析来制备。使用两根不同极性的毛细管柱(DB-ALC2:30m×0.320mm×1.2μm和DB-ALC1:30m×0.320mm×1.8μm)进行色谱分离,从而使挥发性物质的保留和洗脱顺序发生变化。这种双柱确证提高了特异性,因为在两根柱中同时出现另一种物质共洗脱的风险非常小。该方法对甲苯和对二甲苯在5至1000mg/L范围内呈线性,氯仿在50 - 1000mg/L范围内呈线性,其余物质在50 - 2000mg/L范围内呈线性,所有化合物的相关系数均超过0.99。检测限(LOD)范围为1至10mg/L,而定量限(LOQ)范围为2至31mg/L。该方法的日内精密度(CV<6.4%)、中间精密度(CV<7.0%)和准确度(相对误差±10%)符合生物分析方法验证中通常接受的标准。所开发的方法已应用于法医案件,其优点是使用的样品体积小,并且由于采用顶空进样技术,不需要任何提取程序。