Wang Wei-Hao, Yan Ping-Zhen, Yang Bin
Institute of Chinese Material Medica,China Academy of Chinese Medical Sciences Beijing 100700,China.
Institute of Chinese Material Medica,China Academy of Chinese Medical Sciences Beijing 100700,China School of Pharmaceutical Engineering,Shenyang Pharmaceutical University Shenyang 110016,China.
Zhongguo Zhong Yao Za Zhi. 2021 Mar;46(5):1179-1190. doi: 10.19540/j.cnki.cjcmm.20201012.203.
To demonstrate the fragmentation patterns of simple coumarins furanocourmarin(C_7-C_8), furanocourmarin(C_6-C_7) and dihydrofuran coumarin by mass spectrometry, with fraxin, scopoletin, isopsoralen, pimpinellin, isoimperatorin, notopterol and noda-kenin as study subjects, so as to provide a basis for rapid identification of compounds in different subtypes of coumarins. Ultrahigh performance liquid chromatography combined with quardrupole time-of-flight mass spectrometry(UPLC-Q-TOF-MS) was implemented in both positive and negative ion modes. Masslynx software was employed to provide the elemental constituents of each detected ion based on its accurate molecular weight. Chemdraw 2014 was used to cultivate mass number of each inferred structure. The fragment pattern of each compound was determined based on the structures inferred from all the relevant ions. And the patterns were drawn by Chemdraw 2014. The deviation between the calculated molecular weight of the inferred structure and the detected value of the ions was used to assess the correctness of the inferred structures in the fragmentation patterns. The results showed that with UPLC-Q-TOF, neutral loss of CO_2 and CO was reflected in lactone and furan skeletons from the courmarin structure. An even mass was attributed to the loss of an odd number of methyl radicals from compounds with a methoxy substituent. Furanocourmarin(C_7-C_8) produced a protonated molecular ion([M+H]+), while the other courmarin subtypes produced either a sodium adduct of the molecular ion([M+Na]+) or a sodium adduct of the molecular ion([M+Na]+) with a protonated molecular ion([M+H]+). The m/z 203.03 was a diagnostic ion for furanocourmarin(C_6-C_7), and the m/z 147.04 was supplementary evidence for furanocourmarin(C_6-C_7) identification. The characteristic ion of furanocourmarin(C_7-C_8) was m/z 131.05, while m/z 187.04 was the characteristic ion of dihydrofuran coumarin. The m/z 203.03 ion for furanocourmarin(C_7-C_8) was pretty weak. In negative ion mode, furanocourmarin(C_7-C_8) did not have any signals that were different from the other subtypes of courmarins. The fragmentation patterns in negative ion mode for the other subtypes of courmarins were similar to those in positive ion mode. Four types of fragmentation patterns were identified as forcourmarins from Notopterygium inchum. This study provides the basis for the rapid identification of courmarin subtypes by mass spectrometry.
以秦皮素、东莨菪内酯、异补骨脂素、茴芹内酯、异欧前胡素、羌活醇和紫花前胡苷元为研究对象,通过质谱法展示简单香豆素、呋喃香豆素(C₇-C₈)、呋喃香豆素(C₆-C₇)和二氢呋喃香豆素的裂解模式,为快速鉴定不同亚型香豆素中的化合物提供依据。采用超高效液相色谱-四极杆飞行时间质谱联用仪(UPLC-Q-TOF-MS)在正离子和负离子模式下进行分析。利用Masslynx软件根据每个检测离子的精确分子量提供其元素组成。使用Chemdraw 2014计算每个推断结构的质量数。根据从所有相关离子推断出的结构确定每种化合物的裂解模式,并由Chemdraw 2014绘制这些模式。通过比较推断结构的计算分子量与离子检测值之间的偏差,评估裂解模式中推断结构的正确性。结果表明,采用UPLC-Q-TOF时,香豆素结构中的内酯和呋喃骨架会出现CO₂和CO的中性丢失。具有甲氧基取代基的化合物失去奇数个甲基会导致质量数为偶数。呋喃香豆素(C₇-C₈)产生质子化分子离子([M+H]⁺),而其他香豆素亚型产生分子离子的钠加合物([M+Na]⁺)或同时产生分子离子的钠加合物([M+Na]⁺)和质子化分子离子([M+H]⁺)。m/z 203.03是呋喃香豆素(C₆-C₇)的诊断离子,m/z 147.04是鉴定呋喃香豆素(C₆-C₇)的补充证据。呋喃香豆素(C₇-C₈)的特征离子为m/z 131.05,而m/z 187.04是二氢呋喃香豆素的特征离子。呋喃香豆素(C₇-C₈)的m/z 203.03离子非常弱。在负离子模式下,呋喃香豆素(C₇-C₈)没有与其他香豆素亚型不同的信号。其他香豆素亚型在负离子模式下的裂解模式与正离子模式下相似。确定了羌活中香豆素的四种裂解模式。本研究为通过质谱法快速鉴定香豆素亚型提供了依据。