[用HS-GC-IMS、HS-SPME-GC-MS、UPLC-Q-Orbitrap-MS联合化学计量学对当归酒加工前后化学成分的比较]。

Q3 Pharmacology, Toxicology and Pharmaceutics
Xue-Hao Sun, Jia-Xuan Chen, Jia-Xin Yin, Xiao Han, Zhi-Ying Dou, Zheng Li, Li-Ping Kang, He-Shui Yu
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引用次数: 0

摘要

采用顶空-气相色谱-离子迁移谱法(HS-GC-IMS)、顶空-固相微萃取-气相色谱-质谱法(HS-SPME-GC-MS)、超高效液相色谱-四极杆-轨道阱质谱法(UPLC-Q-Orbitrap-MS)联合化学计量学研究了当芪在葡萄酒加工过程中物质基础的内在变化。建立当归炮制前后的HS-GC-IMS指纹图谱,分析其挥发性成分的变化趋势,并对炮制前后挥发性小分子物质进行表征。采用主成分分析(PCA)和正交偏最小二乘判别分析(OPLS-DA)进行差异性分析。利用HS-GC-IMS技术共鉴定出当归挥发物89种,包括14种不饱和烃、16种醛类、13种酮类、9种醇类、16种酯类、6种有机酸和15种其他化合物。HS-SPME-GC-MS检测到118种挥发性成分,包括42种不饱和烃、11种芳香族化合物、30种醇类、8种烷烃、6种有机酸、4种酮类、7种醛类、5种酯类和5种其他挥发性化合物。UPLC-Q-Orbitrap-MS鉴定出76种非挥发性化合物。主成分分析显示,三种检测方法中,生当归和酒制当归的聚类明显不同。PCA和OPLS-DA均能有效区分两组,145个化合物(VIP>1)被鉴定为评价加工质量的关键标志物,包括HS-GC-IMS检测的4-甲基-3-戊烯-2- 1、2-甲基戊酸乙酯和2,4-二甲基-1,3-二氧索烷,HS-SPME-GC-MS检测的天使酸、β-蒎烯和germacene B, UPLC-Q-Orbitrap-MS检测的l-色氨酸、甘草酮和angenomalin。综上所述,三种检测方法与化学计量学相结合,阐明了生当归与酒制当归化学物质基础的差异,为了解酒制当归的炮制机理及临床应用提供了科学依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Comparison on chemical components of Angelicae Sinensis Radix before and after wine processing by HS-GC-IMS, HS-SPME-GC-MS, and UPLC-Q-Orbitrap-MS combined with chemometrics].

The study investigated the intrinsic changes in material basis of Angelicae Sinensis Radix during wine processing by headspace-gas chromatography-ion mobility spectrometry(HS-GC-IMS), headspace-solid phase microextraction-gas chromatography-mass spectrometry(HS-SPME-GC-MS), and ultra-high performance liquid chromatography-quadrupole-orbitrap mass spectrometry(UPLC-Q-Orbitrap-MS) combined with chemometrics. HS-GC-IMS fingerprints of Angelicae Sinensis Radix before and after wine processing were established to analyze the variation trends of volatile components and characterize volatile small-molecule substances before and after processing. Principal component analysis(PCA) and orthogonal partial least squares-discriminant analysis(OPLS-DA) were employed for differentiation and difference analysis. A total of 89 volatile components in Angelicae Sinensis Radix were identified by HS-GC-IMS, including 14 unsaturated hydrocarbons, 16 aldehydes, 13 ketones, 9 alcohols, 16 esters, 6 organic acids, and 15 other compounds. HS-SPME-GC-MS detected 118 volatile components, comprising 42 unsaturated hydrocarbons, 11 aromatic compounds, 30 alcohols, 8 alkanes, 6 organic acids, 4 ketones, 7 aldehydes, 5 esters, and 5 other volatile compounds. UPLC-Q-Orbitrap-MS identified 76 non-volatile compounds. PCA revealed distinct clusters of raw and wine-processed Angelicae Sinensis Radix samples across the three detection methods. Both PCA and OPLS-DA effectively discriminated between the two groups, and 145 compounds(VIP>1) were identified as critical markers for evaluating processing quality, including 4-methyl-3-penten-2-one, ethyl 2-methylpentanoate, and 2,4-dimethyl-1,3-dioxolane detected by HS-GC-IMS, angelic acid, β-pinene, and germacrene B detected by HS-SPME-GC-MS, and L-tryptophan, licoricone, and angenomalin detected by UPLC-Q-Orbitrap-MS. In conclusion, the integration of the three detection methods with chemometrics elucidates the differences in the chemical material basis between raw and wine-processed Angelicae Sinensis Radix, providing a scientific foundation for understanding the processing mechanisms and clinical applications of wine-processed Angelicae Sinensis Radix.

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来源期刊
Zhongguo Zhongyao Zazhi
Zhongguo Zhongyao Zazhi Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.50
自引率
0.00%
发文量
581
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