Qian Ming-Rong, Chen Zhi-Min, Tao Xue-Xin, Yao Feng, Xu Xiao-Min
key Laboratory of Pollution Exposure and Health Intervention of Zhejiang Province, Interdisciplinary Research Academy, Zhejiang Shuren University, Hangzhou 310015, China.
Lishui Bluetown Agricultural Testing Technology Co., Ltd., Lishui 323000, China.
J Pharm Biomed Anal. 2023 May 10;228:115317. doi: 10.1016/j.jpba.2023.115317. Epub 2023 Feb 27.
As an effective treatment for acute gouty arthritis and cardiovascular disease, colchicine is also a toxic alkaloid and may cause poisoning or even death in overdose. The study of colchicine elimination and the diagnosis of poisoning etiology need the rapid and accurate quantitative analysis method in biological matrix. An analytical method was developed for colchicine in plasma and urine by in-syringe dispersive solid phase extraction (DSPE) followed by liquid chromatography-triple quadrupole mass spectrometry (LC-MS/MS). Sample extraction and protein precipitation were proceeded with acetonitrile. The extract was cleaned by in-syringe DSPE. An XBridge™ BEH C column(100 mm × 2.1 mm, 2.5 µm)was used to separate colchicine by gradient elution with mobile phase of 0.01% (v/v) ammonia-methanol. The amount and filling sequence of magnesium sulfate (MgSO) and primary secondary amine (PSA) suitable for in-syringe DSPE were studied. Scopolamine was screened as the quantitative internal standard (IS) for colchicine analysis according to the consistency of recovery rate, chromatographic retention time and matrix effects. The limits of detection for colchicine in plasma and urine were both 0.06 ng mL and the limits of quantitation were both 0.2 ng mL. The linear range was 0.04 - 20 ng mL (Equivalent to 0.2-100 ng mL in plasma or urine) with a correlation coefficient r > 0.999. By IS calibration, the average recoveries at three spiking levels in plasma and urine were 95.3-102.68% and 93.9-94.8% with the relative standard deviations (RSDs) of 2.9-5.7% and 2.3-3.4%, respectively. The matrix effects, stability, dilution effects and carryover for determination of colchicine in plasma and urine were also evaluated. The elimination of colchicine within 72-384 h post-ingestion was studied for a poisoning patient with the doses of 1 mg d for 39 days and then 3 mg d for 15 days).
秋水仙碱作为治疗急性痛风性关节炎和心血管疾病的有效药物,也是一种有毒生物碱,过量服用可能导致中毒甚至死亡。秋水仙碱消除情况的研究以及中毒病因的诊断需要生物基质中快速准确的定量分析方法。本文建立了一种通过注射器内分散固相萃取(DSPE)结合液相色谱 - 三重四极杆质谱(LC-MS/MS)测定血浆和尿液中秋水仙碱的分析方法。样品萃取和蛋白沉淀采用乙腈进行。萃取液通过注射器内DSPE进行净化。使用XBridge™ BEH C柱(100 mm×2.1 mm,2.5 µm),以0.01%(v/v)氨 - 甲醇为流动相进行梯度洗脱分离秋水仙碱。研究了适用于注射器内DSPE的硫酸镁(MgSO)和伯仲胺(PSA)的用量及填充顺序。根据回收率、色谱保留时间和基质效应的一致性,筛选出东莨菪碱作为秋水仙碱分析的定量内标(IS)。血浆和尿液中秋水仙碱的检测限均为0.06 ng/mL,定量限均为0.2 ng/mL。线性范围为0.04 - 20 ng/mL(相当于血浆或尿液中0.2 - 100 ng/mL),相关系数r > 0.999。通过内标校准,血浆和尿液中三个加标水平的平均回收率分别为95.3 - 102.68%和93.9 - 94.8%,相对标准偏差(RSD)分别为2.9 - 5.7%和2.3 - 3.4%。还评估了血浆和尿液中秋水仙碱测定的基质效应、稳定性、稀释效应和残留。对一名中毒患者(摄入剂量为1 mg/d,持续39天,然后3 mg/d,持续15天)进行了摄入后72 - 384小时内秋水仙碱消除情况的研究。