Department of Pharmaceutical Analysis and Analytical Chemistry, College of Pharmacy, Harbin Medical University, No. 157 Baojian Road, Nangang District, Harbin 150081, Heilongjiang, China.
Department of Pharmacy Management Harbin Medical University, Harbin 150086, Heilongjiang, China.
Molecules. 2018 Aug 2;23(8):1927. doi: 10.3390/molecules23081927.
A rapid and sensitive Ultra high-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) method was developed for the simultaneous determination of fourteen alkaloids in beagle dog plasma after a single oral dose of the () extract selected bifendate as the internal standard (IS). The plasma samples were preprocessed by liquid-liquid extraction (LLE) with aether before separation on an Agilent SB-C column (1.8 µm, 150 × 2.1 mm) using a gradient elution program. The mobile phase consists of 0.2% acetic acid and acetonitrile at the flow rate of 0.3 mL/min. In the positive ion mode, the analytes were detected by multiple reaction monitoring (MRM). The results indicated that calibration curves for fourteen analytes have good linearity (² = 0.9904). The lower limits of quantification (LLOQ) of fourteen alkaloids and IS were all over 4.87 ng/mL and the matrix effects ranged from 94.08% to 102.76%. The mean extraction recoveries of Quality control samples at low (LQC), medium (MQC) and high (HQC) and IS were all more than 78.03%. The intra- and inter-day precision (R.S.D.%) also met the criterion, at the same time the deviation of assay accuracies (R.E) ranged from -13.70% to 14.40%. The values of fourteen alkaloids were no more than 1 h. The range of was from 74.16 ± 8.71 to 2256 ± 255.9 ng/mL. The assay was validated in the light of the regulatory bioanalytical guidelines and proved acceptable, which was successfully applied to a pharmacokinetic study of these compounds in beagle dogs after oral administration of extract.
建立了一种快速灵敏的超高效液相色谱-串联质谱(UHPLC-MS/MS)法,用于单次口服()提取物后犬血浆中 14 种生物碱的同时测定。以双呋丁为内标(IS)。血浆样品经乙醚液-液萃取(LLE)预处理,在 Agilent SB-C 柱(1.8 µm,150×2.1 mm)上进行分离,采用梯度洗脱程序。流动相由 0.2%乙酸和乙腈组成,流速为 0.3 mL/min。在正离子模式下,通过多反应监测(MRM)检测分析物。结果表明,14 种分析物的校准曲线具有良好的线性(²=0.9904)。14 种生物碱和 IS 的定量下限(LLOQ)均大于 4.87 ng/mL,基质效应范围为 94.08%-102.76%。低(LQC)、中(MQC)和高(HQC)QC 及 IS 的质控样品平均提取回收率均大于 78.03%。日内和日间精密度(RSD%)也符合标准,同时测定准确度的偏差(RE)范围为-13.70%至 14.40%。14 种生物碱的 t₁/₂ 值均不超过 1 h。AUC₀-t 的范围为 74.16±8.71 至 2256±255.9 ng/mL·h。该测定方法符合监管生物分析指南的要求,可接受性良好,成功应用于犬口服()提取物后这些化合物的药代动力学研究。
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