Collins B J, Slade D, Ryan K, Mathias R, Shan A, Algaier J, Aillon K, Waidyanatha S
Division of the National Toxicology Program, National Institute of Environmental Health Sciences, 111 Alexander Dr., Research Triangle Park, NC, USA.
MRIGlobal, 425 Volker Boulevard, Kansas City, MO, USA.
J Anal Toxicol. 2019 Jan 1;43(1):36-44. doi: 10.1093/jat/bky048.
Tris(chloropropyl)phosphate (TCPP) is an organophosphorus flame retardant (OPFR) and plasticizer increasingly used in consumer products and as a replacement for brominated flame retardants. Commercially available TCPP is a mixture of four structural isomers the most abundant of which is tris(1-chloro-2-propyl)phosphate (TCPP-1). Although there is a widespread use of TCPP and potential for human exposure, there is limited data on the safety or toxicity of TCPP. The National Toxicology Program is conducting long-term studies to examine the toxicity of the TCPP in rats after lifetime exposure, including perinatal oral exposure. Quantitative estimates of internal dose are essential to interpret toxicological findings in rodents. To aid in this, a method was fully validated to quantitate the most abundant isomer, TCPP-1, in female Harlan Sprague Dawley (HSD) rat and B6C3F1 mouse plasma with partial validation in male rat plasma, and male and female mouse plasma. The method used protein precipitation using trichloroacetic acid followed by the extraction with toluene, and analysis by gas chromatography with flame photometric detection. The performance of the method was evaluated over 5-70 ng TCPP-1/mL plasma. The method was linear (r ≥ 0.99), accurate (inter-day relative error: ≤ ± -7.2) and precise (inter-batch relative standard deviation: ≤27.5%). The validated method has lower limits of quantitation and detection of ~5 and 0.9 ng/mL, respectively, in female HSD rat plasma and can be used on samples as small as 50 μL demonstrating the applicability to plasma samples from toxicology studies.
磷酸三(氯丙基)酯(TCPP)是一种有机磷阻燃剂(OPFR)和增塑剂,越来越多地用于消费品中,并作为溴化阻燃剂的替代品。市售的TCPP是四种结构异构体的混合物,其中最主要的是磷酸三(1-氯-2-丙基)酯(TCPP-1)。尽管TCPP被广泛使用且人类有接触的可能性,但关于TCPP安全性或毒性的数据有限。国家毒理学计划正在进行长期研究,以检查大鼠终生暴露(包括围产期口服暴露)后TCPP的毒性。内部剂量的定量估计对于解释啮齿动物的毒理学结果至关重要。为此,一种方法经过了全面验证,可定量雌性哈兰·斯普拉格·道利(HSD)大鼠和B6C3F1小鼠血浆中最主要的异构体TCPP-1,在雄性大鼠血浆以及雄性和雌性小鼠血浆中进行了部分验证。该方法使用三氯乙酸进行蛋白质沉淀,然后用甲苯萃取,并通过气相色谱-火焰光度检测进行分析。该方法在5-70 ng TCPP-1/mL血浆范围内进行了性能评估。该方法具有线性(r≥0.99)、准确(日间相对误差:≤±-7.2)和精密(批间相对标准偏差:≤27.5%)的特点。经过验证的方法在雌性HSD大鼠血浆中的定量下限和检测下限分别约为5和0.9 ng/mL,并且可用于小至50μL的样本,证明了其适用于毒理学研究的血浆样本。