TY - DATA T1 - Profiling and identification of chlorogenic acid metabolites in rats by ultra-high-performance liquid chromatography coupled with linear ion trap-Orbitrap mass spectrometer PY - 2017/08/04 AU - Fei Wang AU - Zhanpeng Shang AU - Lulu Xu AU - Zhibin Wang AU - Wenjing Zhao AU - XiaoDan Mei AU - Jianqiu Lu AU - Jia Yu Zhang UR - https://tandf.figshare.com/articles/journal_contribution/Profiling_and_identification_of_chlorogenic_acid_metabolites_in_rats_by_ultra-high-performance_liquid_chromatography_coupled_with_linear_ion_trap-Orbitrap_mass_spectrometer/5277619 DO - 10.6084/m9.figshare.5277619.v1 L4 - https://ndownloader.figshare.com/files/9035458 KW - Chlorogenic acids KW - Flos Lonicera Japonica KW - metabolites KW - ultra-high-performance liquid chromatography coupled with linear N2 - 1. Chlorogenic acids (CGAs), one kind of major bioactive constituents isolated from Flos Lonicera Japonica, possess many biological activities, such as antibacterial, antioxidant and antiviral activities. In this study, we established an efficient strategy using ultra-high-performance liquid chromatography coupled with linear ion trap-Orbitrap mass spectrometry (UHPLC-LTQ-Orbitrap MS) to profile the in vivo metabolic fate of CGAs in rat urine and plasma. 2. The extract from Flos Lonicera Japonica was orally administrated to Sprague-Dawley (SD) rats at a dose of 1000 mg/kg body weight. Then, a combination of various post-acquisition data mining methods, including high-resolution extracted ion chromatogram (HREIC) and multiple mass defect filters (MMDFs) and diagnostic product ions (DPIs), were adopted to characterize the known and unknown CGA metabolites in SD rats. 3. As a result, a total of 68 CGA metabolites were unambiguously or tentatively screened and characterized. These metabolites, including 18 prototype compounds and 50 metabolites, were deduced to be yielded via methylation, hydrogenation, demethylation, dehydration, sulfate conjugation, glucuronide conjugation, glycosylation conjugation and their composite reactions, which mainly occurred to caffeoylquinic acids, dicaffeoylquinic acids, p-coumaroylquinic acids and feruloylquinic acids. 4. In conclusion, this study profiled CGA metabolites, which are useful in understanding the in vivo metabolic fate, effective forms, and pharmacological and toxic actions of CGAs. ER -