Singh Sheelendra Pratap, Dwivedi Nistha, Raju Kanumuri Siva Rama, Taneja Isha, Wahajuddin Mohammad
Analytical Chemistry Laboratory and Regulatory Toxicology Group, CSIR-Indian Institute of Toxicology Research, Vishvigyan Bhavan, 31, Mahatma Gandhi Marg, Lucknow 226001, Uttar Pradesh, India
Analytical Chemistry Laboratory and Regulatory Toxicology Group, CSIR-Indian Institute of Toxicology Research, Vishvigyan Bhavan, 31, Mahatma Gandhi Marg, Lucknow 226001, Uttar Pradesh, India.
J Anal Toxicol. 2016 Apr;40(3):213-21. doi: 10.1093/jat/bkw002. Epub 2016 Jan 21.
United States Environmental Protection Agency has recommended estimating pyrethroids' risk using cumulative exposure. For cumulative risk assessment, it would be useful to have a bioanalytical method for quantification of one or several pyrethroids simultaneously in a small sample volume to support toxicokinetic studies. Therefore, in the present study, a simple, sensitive and high-throughput ultraperformance liquid chromatography-tandem mass spectrometry method was developed and validated for simultaneous analysis of seven pyrethroids (fenvalerate, fenpropathrin, bifenthrin, lambda-cyhalothrin, cyfluthrin, cypermethrin and deltamethrin) in 100 µL of rat plasma. A simple single-step protein precipitation method was used for the extraction of target compounds. The total chromatographic run time of the method was 5 min. The chromatographic system used a Supelco C18 column and isocratic elution with a mobile phase consisting of methanol and 5 mM ammonium formate in the ratio of 90 : 10 (v/v). Mass spectrometer (API 4000) was operated in multiple reaction monitoring positive-ion mode using the electrospray ionization technique. The calibration curves were linear in the range of 7.8-2,000 ng/mL with correlation coefficients of ≥ 0.99. All validation parameters such as precision, accuracy, recovery, matrix effect and stability met the acceptance criteria according to the regulatory guidelines. The method was successfully applied to the toxicokinetic study of cypermethrin in rats. To the best of our knowledge, this is the first LC-MS-MS method for the simultaneous analysis of pyrethroids in rat plasma. This validated method with minimal modification can also be utilized for forensic and clinical toxicological applications due to its simplicity, sensitivity and rapidity.
美国环境保护局建议使用累积暴露来评估拟除虫菊酯的风险。对于累积风险评估,拥有一种生物分析方法以在小体积样本中同时定量一种或几种拟除虫菊酯,从而支持毒代动力学研究,将是很有用的。因此,在本研究中,开发并验证了一种简单、灵敏且高通量的超高效液相色谱 - 串联质谱法,用于同时分析100μL大鼠血浆中的七种拟除虫菊酯(氰戊菊酯、甲氰菊酯、联苯菊酯、高效氯氟氰菊酯、氟氯氰菊酯、氯氰菊酯和溴氰菊酯)。采用简单的一步蛋白沉淀法提取目标化合物。该方法的总色谱运行时间为5分钟。色谱系统使用Supelco C18柱,采用等度洗脱,流动相由甲醇和5mM甲酸铵按90 : 10(v/v)的比例组成。质谱仪(API 4000)采用电喷雾电离技术,在多反应监测正离子模式下运行。校准曲线在7.8 - 2,000 ng/mL范围内呈线性,相关系数≥0.99。所有验证参数,如精密度、准确度、回收率、基质效应和稳定性,均符合监管指南的验收标准。该方法成功应用于氯氰菊酯在大鼠体内的毒代动力学研究。据我们所知,这是首次用于同时分析大鼠血浆中拟除虫菊酯的液相色谱 - 串联质谱法。由于其简单、灵敏和快速,这种经过验证且只需最少修改的方法也可用于法医和临床毒理学应用。