固相萃取-高效液相色谱法测定盐附子中乌头碱含量及大鼠血浆附子类生物碱浓度OA
Determination of Aconite Alkaloids in Yan Fuzi and Rat Plasma by Solid Phase Extraction Coupled with High Performance Liquid Chromatography
目的 建立固相萃取-高效液相色谱法快速测定盐附子中及盐附子水煎液灌胃后30 min大鼠血浆中乌头碱、新乌头碱、次乌头碱、高乌甲素和苯甲酰乌头原碱含量的方法.方法 参考文献方法合成沸石咪唑酯骨架材料8(ZIF-8)材料,并进行表征.通过优化金属有机骨架材料制备工艺和固相萃取条件,开发萃取与液相色谱联用的定量分析方法,检测浓度为0.375 g·kg-1盐附子水煎液灌胃后大鼠血浆中乌头碱、次乌头碱、新乌头碱、高乌甲素和苯甲酰乌头碱的含量.结果 盐附子中5 种乌头碱的含量为:乌头碱 62.78 mg·kg-1,新乌头碱 500.4 mg·kg-1,次乌头碱37.80 mg·kg-1,高乌甲素0.144 mg·kg-1,苯甲酰乌头原碱36.14 mg·kg-1;在大鼠给药后30 min萃取的血浆样本中检测出乌头碱含量为乌头碱2.06 μg·mL-1、新乌头碱11.79 μg·mL-1、次乌头碱1.69 μg·mL-1、高乌甲素1.77 μg·mL-1和苯甲酰乌头原碱23.22 μg·mL-1.方法学考察结果显示,各指标符合含量测定要求.结论 该研究建立的方法可用于盐附子和灌胃后血浆中附子类生物碱含量测定,可为临床检测附子类血浆中附子类生物碱的含量提供参考.
Objective To establish a solid phase extraction-high performance liquid chromatography(SPE-HPLC)method for the rapid determination of aconitine,mesaconitine,hypaconitine,lappaconitine,and benzoylaconine in salt-processed Aconiti Lateralis Radix Praeparata(Yan Fuzi)and rat plasma 30 min after intragastric administration of a Yan Fuzi decoction.Methods Zeolitic imidazolate framework-8(ZIF-8)material was synthesized and characterized according to literature methods.By optimizing the preparation process of metal-organic frameworks and solid-phase extraction conditions,a quantitative analytical method coupling extraction with liquid chromatography was developed.This method was applied to detect the plasma concentrations of aconitine,hypaconitine,mesaconitine,lappaconitine,and benzoylaconine in rat plasma following intragastric administration of Yan Fuzi decoction(0.375 g·kg-1 body weight).Results The contents of five aconite alkaloids in Yan Fuzi were determined as follows:aconitine 62.78 mg·kg-1,mesaconitine 500.4 mg·kg-1,hypaconitine 37.80 mg·kg-1,lappaconitine 0.144 mg·kg-1,and benzoylaconine 36.14 mg·kg-1.In plasma samples collected 30 min post-administration,the concentra-tions detected were:aconitine 2.06 μg·mL-1,mesaconitine 11.79 μg·mL-1,hypaconitine 1.69 μg·mL-1,lappaconitine 1.77 μg·mL-1,and benzoylaconine 23.22 μg·mL-1.Method validation confirmed that all parameters met quantitative determi-nation requirements.Conclusion The established method enables accurate quantification of aconite alkaloids in both Aconiti Lateralis Radix Praeparata and plasma samples after oral administration,providing a valuable reference for clinical monitoring of these compounds in biological matrices.
刘仁炎;朱军;杨洋;冯宝栋;明庭文;辛灵怡;黄嘉欣;绉红海;刘慧敏;陈琴华
湖北医药学院药学院/武当特色中药研究湖北省重点实验室,十堰 442000||湖北医药学院附属国药东风总医院药学部,十堰 442008湖北医药学院药学院/武当特色中药研究湖北省重点实验室,十堰 442000||湖北医药学院附属国药东风总医院药学部,十堰 442008深圳市宝安纯中医治疗医院药学部,深圳 518101湖北医药学院药学院/武当特色中药研究湖北省重点实验室,十堰 442000||湖北医药学院附属国药东风总医院药学部,十堰 442008湖北医药学院药学院/武当特色中药研究湖北省重点实验室,十堰 442000||湖北医药学院附属国药东风总医院药学部,十堰 442008深圳市宝安纯中医治疗医院药学部,深圳 518101深圳市宝安纯中医治疗医院药学部,深圳 518101深圳市宝安纯中医治疗医院药学部,深圳 518101深圳市宝安纯中医治疗医院药学部,深圳 518101深圳市宝安纯中医治疗医院药学部,深圳 518101
医药卫生
盐附子沸石咪唑酯骨架材料附子类生物碱固相萃取-高效液相色谱法
Salt processed Aconiti Lateralis Radix Praeparata(Yan Fuzi)Zeolitic imidazolate framework materialAc-onitum alkaloidsSolid-phase extraction coupled with high performance liquid chromatography
《医药导报》 2026 (3)
389-395,7
武当特色中药研究湖北省重点实验室(湖北医药学院)开放课题(WDCM2024008)深圳医疗卫生三名工程(No.SZZYSM202106004)十堰市科技局引导性项目(24Y152)国药东风总医院创新团队项目(2024C07)国药东风总医院新技术新业务项目(SX20250203).
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