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猫血浆中莫昔克丁LC-MS/MS检测方法的建立OA

Development an LC-MS/MS method for moxidectin determination in cat plasma

中文摘要英文摘要

旨在研究复方莫昔克丁(moxidectin,Moxi)滴剂在猫体内的药代动力学过程.以Moxi-D3为内标,建立了猫血浆中Moxi 的液相色谱-串联三重四极杆质谱联用(LC-MS/MS)检测方法,以乙腈为提取溶剂,水浴超声辅助提取,提取液浓缩至干后复溶,LC-MS/MS 检测,内标法定量.结果:猫血浆基质对 Moxi 的定量检测干扰较小,检测限(LOD)为 0.5 ng/mL,定量限(LOQ)为 1 ng/mL;基质效应不显著,以溶剂标准溶液制备标准曲线,Moxi 在 1~120 ng/mL 的浓度范围内,线性关系良好(R2>0.99);在不同浓度的添加水平下,批内、批间平均准确度分别在90.15%~114.81%和101.32%~104.10%,批内、批间变异系数均小于11%;-18℃以下放置时,标准储备液 9 个月内稳定,标准工作液 2 个月内稳定;低、高浓度的加标样品,-18℃以下冷冻保存 6 个月,或反复冻融后均稳定,处理液4℃放置72 h 稳定.结论:本方法特异性强,灵敏度高,稳定可靠,可用于复方 Moxi 滴剂在猫体内药代动力学的研究.

To investigate the pharmacokinetics of compound moxidectin(Moxi)drops in cats,a liquid chromatography-tandem mass spec-trometry(LC-MS/MS)method was developed for the determination of Moxi in cat plasma using Moxi-D3 as the internal standard.Acetoni-trile was used as the extraction solvent.The samples were processed by ultrasonication in a water bath,and the extract was concentrated to dryness.Finally,the residue was reconstituted and analyzed by LC-MS/MS,with quantification performed using the internal standard meth-od.The results showed that the cat plasma matrix did not interfere with the quantitative determination of Moxi.The method exhibited high sen-sitivity,with a limit of detection(LOD)of 0.5 ng/mL and a limit of quantification(LOQ)of 1 ng/mL.The Matrix effects were negligible,hence,a standard curve was prepared with solvent standard solution,and the linearity of Moxi was good in the range of 1 to 120 ng/mL(R2>0.99).The intra-batch and inter-batch accuracy ranged from 90.15%to 114.81%and 101.32%to 104.10%at different concentration lev-els of spiked samples,respectively.The coefficients of variation(CV)of intra-batch and inter-batch samples were less than 11%.The standard stock and working solutions stayed stable for 9 and 2 months at-18℃,respectively.The spiked samples with different concentra-tions were stable after 6 months of freezing and storage at-18℃,and still stable after repeated freezing and thawing.The processed solutions of the spiked samples remained stable at 4℃for 72 h.These results indicated that the proposed method had good specificity,high sensitivi-ty,stability and reliability,and could be used for the pharmacokinetics study of the compound moxidectin drops in cats.

过海天;范丽萍;张贺超;杨亚军;李剑勇;周淑贞

中国农业科学院兰州畜牧与兽药研究所/农业农村部兽用药物创制重点实验室/甘肃省新兽药重点实验室,甘肃 兰州 730050||甘肃农业大学动物医学院,甘肃 兰州 730070中国农业科学院兰州畜牧与兽药研究所/农业农村部兽用药物创制重点实验室/甘肃省新兽药重点实验室,甘肃 兰州 730050中国农业科学院兰州畜牧与兽药研究所/农业农村部兽用药物创制重点实验室/甘肃省新兽药重点实验室,甘肃 兰州 730050||甘肃农业大学动物医学院,甘肃 兰州 730070中国农业科学院兰州畜牧与兽药研究所/农业农村部兽用药物创制重点实验室/甘肃省新兽药重点实验室,甘肃 兰州 730050中国农业科学院兰州畜牧与兽药研究所/农业农村部兽用药物创制重点实验室/甘肃省新兽药重点实验室,甘肃 兰州 730050||甘肃农业大学动物医学院,甘肃 兰州 730070佛山市南海东方澳龙制药有限公司,广东 佛山 528234

农业科技

血浆莫昔克丁液相色谱-串联三重四极杆质谱联用内标法

catsplasmamoxidectinLC-MS/MSinternal standard

《畜牧与兽医》 2026 (5)

53-60,8

佛山市自筹经费类科技创新项目(2220001004511)中国农业科技创新工程项目(CAAS-25-LZIHPS-02)

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