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Sensitive and stable pre-calibrated solid-phase extraction columns for environmental and forensic quantification using isotope dilution mass spectrometry

机译:使用同位素稀释质谱法进行环境和法医定量分析的灵敏稳定的预校准固相萃取柱

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A method was developed to pre-load solid-phase extraction columns (SPE) with isotopic calibrant for use with isotope dilution mass spectrometry (IDMS). The pre-calibration method was developed, optimized, and validated for the quantification of the pesticide glyphosate in drinking water using anion-exchange SPE, electrospray-ionization, and time-of-flight mass spectrometry (ESI-TOF-MS). The instrumental method obtained a mass-accuracy of 3 ppm and a limit of quantification (LOQ) of 0.3 ng mL(-1). Quantification of glyphosate by IDMS significantly improved quantitative error and LOQ compared with the calibration curve. The pre-loading methodology was optimized for stability over time and validated in drinking water, exhibiting an accuracy of 1.25%-0.87% error with no significant difference from certified concentrations or traditional SPE. Method LOQ was 0.4 ng mL(-1). Quantifying glyphosate in spiked drinking water sample produced high accuracy up to two-weeks after pre-loading columns, with an accuracy of 6.41%-7.10% error. A potential forensic application was investigated by adapting the pre-loading method to the quantification of seven drugs in synthetic urine using a mixed-mode SPE column. The ESI-TOF-MS method using traditional SPE produced accurate quantification of all seven drugs in synthetic urine with a mean error of 4.16%-3.07% and LOQ of 0.780 ng mL(-1). The pre-loading method produced accurate quantification with 5.36%-4.73% error, with no significant difference from traditional SPE or certified standards. Five of the seven drugs were quantified at high accuracy one week after pre-loading, with 5.40%-4.57% error from certified values. This method may be applicable to analysts seeking to develop methods to improve the transfer of high-accuracy and precision methods between laboratories.
机译:开发了一种使用同位素校正剂预装固相萃取柱(SPE)的方法,该方法可用于同位素稀释质谱(IDMS)。使用阴离子交换SPE,电喷雾电离和飞行时间质谱(ESI-TOF-MS),开发,优化和验证了预校准方法,用于定量饮用水中的农药草甘膦。仪器方法获得的质量准确度为3 ppm,定量极限(LOQ)为0.3 ng mL(-1)。与校正曲线相比,通过IDMS定量草甘膦可显着改善定量误差和LOQ。预加载方法针对时间稳定性进行了优化,并在饮用水中进行了验证,其准确度为1.25%-0.87%,与标准浓度或传统固相萃取无明显差异。方法LOQ为0.4 ng mL(-1)。在预装柱后长达两周的时间内,对加标的饮用水样品中的草甘膦进行定量可产生较高的准确度,准确度为6.41%-7.10%。通过使用混合模式SPE色谱柱将预加载方法调整为合成尿中7种药物的定量方法,研究了潜在的法医学应用。使用传统SPE的ESI-TOF-MS方法可准确定量合成尿中所有七种药物,平均误差为4.16%-3.07%,LOQ为0.780 ng mL(-1)。预加载方法产生的定量准确度为5.36%-4.73%,与传统的SPE或认证标准无明显差异。预加载后一周内,对这七种药物中的五种进行了高精度定量,与认证值的误差为5.40%-4.57%。该方法可能适用于寻求开发方法以改善实验室之间高精度和精密方法转换的分析人员。

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