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采用液相色谱-离子阱质谱法鉴定和定量白术中苍术内酯I和苍术内酯III的含量。

Identification and quantification of atractylenolide I and atractylenolide III in Rhizoma Atractylodes Macrocephala by liquid chromatography-ion trap mass spectrometry.

作者信息

Chen Qinhua, He Hongsheng, Li Peng, Zhu Jun, Xiong Min

机构信息

Institute of Pharmaceutical Analysis and Drug Screening, Affiliated Dongfeng Hospital, Hubei University of Medicine, Hubei Shiyan, 442008, China.

出版信息

Biomed Chromatogr. 2013 Jun;27(6):699-707. doi: 10.1002/bmc.2847. Epub 2012 Nov 23.

DOI:10.1002/bmc.2847
PMID:23175447
Abstract

Rhizoma Atractylodes Macrocephala (RAM) is an important traditional Chinese medicinal herb that is used for treatment of dyspepsia and anorexia. The active ingredients, atractylenolide I (AO-I) and atractylenolide III (AO-III), were identified by direct-injection ion trap-mass spectrometry (IT-MS) for collecting MS(n) spectra. The major fragment ions of AO-I and AO-III were confirmed by MS(n) both in negative ion mode and in positive ion mode. The possible main cleavage pathway of fragment ions was studied. The determinations of AO-I and AO-III were accomplished by liquid chromatography (LC) with UV and MS. The analytes provided good signals corresponding to the protonated molecular ions M + H and product ions. The precursor ions and product ions for quantification of AO-III and AO-I were m/z 249 → 231 and m/z 233 → 215, respectively, using selected ion monitoring by LC-IT-MS. Two methods were evaluated for a number of validation characteristics (repeatability, limit of detection, calibration range, and recovery). MS provides a high selectivity and sensitivity for determination of AO-III and AO-I in positive mode. After optimization of the methods, separation, identification and quantification of the two components in RAM were comprehensively tested by HPLC with UV and MS.

摘要

白术是一种重要的传统中草药,用于治疗消化不良和食欲不振。通过直接进样离子阱质谱(IT-MS)收集MS(n) 谱图,鉴定了其活性成分白术内酯I(AO-I)和白术内酯III(AO-III)。在负离子模式和正离子模式下,均通过MS(n) 确认了AO-I和AO-III的主要碎片离子。研究了碎片离子可能的主要裂解途径。通过液相色谱(LC)结合紫外和质谱对AO-I和AO-III进行测定。分析物产生了与质子化分子离子M + H 和产物离子相对应的良好信号。使用LC-IT-MS的选择离子监测,AO-III和AO-I定量的前体离子和产物离子分别为m/z 249 → 231和m/z 233 → 215。对两种方法的多项验证特性(重复性、检测限、校准范围和回收率)进行了评估。质谱在正模式下对AO-III和AO-I的测定具有高选择性和灵敏度。方法优化后,采用HPLC结合紫外和质谱对白术中这两种成分进行了分离、鉴定和定量的综合测试。

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