Mezouari S, Liu W Yun, Pace G, Hartman T G
a Department of Food Science, School of Environmental and Biological Sciences , Rutgers University , New Brunswick , NJ , USA.
Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 2015;32(5):768-78. doi: 10.1080/19440049.2015.1010606. Epub 2015 Mar 6.
The objective of this study was to develop an improved analytical method for the determination of 3-chloro-1,2-propanediol (3-MCPD) and 1,3-dichloropropanol (1,3-DCP) in paper-type food packaging. The established method includes aqueous extraction, matrix spiking of a deuterated surrogate internal standard (3-MCPD-d₅), clean-up using Extrelut solid-phase extraction, derivatisation using a silylation reagent, and GC-MS analysis of the chloropropanols as their corresponding trimethyl silyl ethers. The new method is applicable to food-grade packaging samples using European Commission standard aqueous extraction and aqueous food stimulant migration tests. In this improved method, the derivatisation procedure was optimised; the cost and time of the analysis were reduced by using 10 times less sample, solvents and reagents than in previously described methods. Overall the validation data demonstrate that the method is precise and reliable. The limit of detection (LOD) of the aqueous extract was 0.010 mg kg(-1) (w/w) for both 3-MCPD and 1,3-DCP. Analytical precision had a relative standard deviation (RSD) of 3.36% for 3-MCPD and an RSD of 7.65% for 1,3-DCP. The new method was satisfactorily applied to the analysis of over 100 commercial paperboard packaging samples. The data are being used to guide the product development of a next generation of wet-strength resins with reduced chloropropanol content, and also for risk assessments to calculate the virtual safe dose (VSD).
本研究的目的是开发一种改进的分析方法,用于测定纸质食品包装中的3-氯-1,2-丙二醇(3-MCPD)和1,3-二氯丙醇(1,3-DCP)。所建立的方法包括水萃取、氘代替代内标(3-MCPD-d₅)的基质加标、使用埃特拉路特固相萃取进行净化、使用硅烷化试剂进行衍生化,以及将氯丙醇作为其相应的三甲基硅醚进行气相色谱-质谱分析。该新方法适用于采用欧盟委员会标准水萃取和水性食品模拟物迁移试验的食品级包装样品。在这种改进方法中,对衍生化程序进行了优化;与先前描述的方法相比,使用的样品、溶剂和试剂减少了10倍,从而降低了分析成本和时间。总体而言,验证数据表明该方法精确可靠。水提取物中3-MCPD和1,3-DCP的检测限(LOD)均为0.010 mg kg⁻¹(w/w)。分析精密度方面,3-MCPD的相对标准偏差(RSD)为3.36%,1,3-DCP的RSD为7.65%。该新方法成功应用于100多个商业纸板包装样品的分析。这些数据正用于指导下一代氯丙醇含量降低的湿强树脂的产品开发,也用于风险评估以计算虚拟安全剂量(VSD)。