A UPLC-MS/MS coupled with GC-MS method for quantification of twenty-one chemical ingredients from Suxiao Jiuxin pill in multiple tissue of rat and its application to tissue distribution study.
Ye ShangYameng ZhuShuting ZhouYang LiuShujie WeiHong ZhouYongping JiangYuli WangTong GengQilong WangJun HePublished in: Journal of pharmaceutical and biomedical analysis (2024)
Suxiao Jiuxin pill (SJP) was a commonly-used traditional Chinese medicine for treating cardiovascular diseases. It was composed of the rhizome of Ligusticum chuanxiong Hort. and Borneolum Syntheticum. The distribution of SJP in vivo was still ambiguous. A UPLC-MS/MS coupled with GC-MS method was developed to quantify twenty-one chemical ingredients in multiple tissues from rat after administration of SJP. Protein precipitation and liquid-liquid microextraction were both utilized in sample pretreatment. All analytes were detected under acceptable specificity, linearity (correlation coefficient > 0.992), sensitivity (LLOQ < 12.5 ng/mL), precision (RSD < 14.8 %), accuracy (RE < ±14.6 %), extraction recovery (between 52.8 % and 124.1 %), matrix effect (ranged from 60.5 % and 149.7 %) and stability (RE < ±16.0 %). The established method was successfully applied in the tissue distribution study of SJP in rats. As a result, the distribution characteristics of ten analytes were clearly elucidated, including borneol, isoborneol, ligustilide, senkyunolide A, ferulic acid, senkyunolide I, levistolide A, neocnidilide, senkyunolide H and angelicide. The information provided by this research was greatly meaningful for the active chemical ingredient exploration and clinical application of SJP.
Keyphrases
- ms ms
- cardiovascular disease
- simultaneous determination
- liquid chromatography tandem mass spectrometry
- oxidative stress
- type diabetes
- high performance liquid chromatography
- magnetic resonance
- healthcare
- coronary artery disease
- computed tomography
- metabolic syndrome
- small molecule
- high resolution
- protein protein
- tandem mass spectrometry
- gas chromatography
- molecularly imprinted
- solid phase extraction
- contrast enhanced
- structural basis