化学
检出限
核磁共振波谱
定量分析(化学)
分析化学(期刊)
线性
色谱法
光谱学
校准曲线
质子核磁共振
立体化学
量子力学
物理
作者
Zhuoni Hou,Xinmiao Liang,Liangcheng Du,Shengyu Feng,Weike Su
摘要
Nuclear magnetic resonance is defined as a quantitative spectroscopic tool that enables a precise determination of the number of substances in liquids as well as in solids. There is few report demonstrating the application of NMR in the quantification of avermectin B 1a (AVB 1a ); here, a proton nuclear magnetic resonance spectroscopy ( 1 H NMR) using benzene [1‐methoxy‐4‐(2‐nitroethyl) (PMN)] as an internal standard and deuterochloroform as an NMR solvent was tested for the quantitative determination of AVB 1a . The integrated signal of AVB 1a at 5.56 ppm and the signal of PMN at 8.14 ppm in the 1 H NMR spectrum were used for quantification purposes. Parameters of specificity, linearity, accuracy, precision, intermediate precision, range, limit of detection (LOD), limit of quantification (LOQ), stability and robustness were validated. The established method was accurate and precise with good recovery (98.86%) and relative standard deviation (RSD) of assay (0.34%) within the linearity of the calibration curve ranging from 5.08 to 13.58 mg/ml ( R 2 = 0.9999). The LOD and LOQ were 0.009 and 0.029 mg/ml, which indicated the excellent sensitivity of the method. The stability of the method was testified by a calculated RSD of 0.11%. The robustness was testified by modification of four different parameters, and the differences among each parameter were all less than 0.1%. Comparing with the assay described by the manufacturer of avermectin tablets, there was no significant difference between the assay obtained by HPLC and quantitative NMR (qNMR), which indicated qNMR was a simple and efficient method for the determination of AVB 1a in commercial formulation products. Copyright © 2014 John Wiley & Sons, Ltd.
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