Literature DB >> 26302962

Understanding the regioselective hydrolysis of ginkgolide B under physiological environment based on generation, detection, identification, and semi-quantification of the hydrolyzed products.

Xue-Jing Li1,2, Kui Yang2, Gang Du3, Liang Xu1, Ke Lan4,5.   

Abstract

A liquid chromatography-mass spectrometry (LC-MS) method coupled with specialized sample-preparation strategies was developed to investigate the hydrolysis of ginkgolide B (GB) in physiological environments in comparison with that of ginkgolide A (GA). The rapid hydrolysis processes were captured by the direct injection of samples prepared in the volatile buffers. The LC-MS behavior of the hydrolyzed products, including three monocarboxylates and three dicarboxylates, was acquired. The monocarboxylates were identified by fragmentation analysis, and the dicarboxylates were accordingly tentatively identified by reaction sequences. The base-catalyzed hydrolysis of GB and GA was characterized at 4 °C within pH 7.0-10.7. The regioselective reactions on the lactone-C and lactone-F were revealed by thermodynamic studies at pH 6.8 and 7.4. It was revealed that the 1-hydroxyl group on the skeleton of GB blocks the reactivity of the lactone-E. On the basis of these results, a distinctive hydrolysis phenomenon of GB was confirmed in plasma of humans, rats, and dogs as a rapid degradation of the trilactone along with the only production of the lactone-F-hydrolyzed product. This phenomenon is also closely associated with the 1-hydroxyl group, because it was not observed in GA. More interestingly, the underlying mechanism was revealed not to be associated with any typical enzyme-catalyzed process, but to be potentially involved with a selective reaction of the intact or broken lactone-C moiety with endogenous small-molecule reactants in plasma. This in-depth knowledge of the hydrolysis of GB versus GA not only facilitated understanding of their pharmacological mechanisms but also provided potential routes to study the structure-activity relationships of ginkgolides. Graphical Abstract Regioselective hydrolysis of ginkgolide B in pH 7.4 buffers and plasma.

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Keywords:  Bioanalytical method; Ginkgolide A; Ginkgolide B; Hydrolysis; Lactone; Regioselectivity

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Year:  2015        PMID: 26302962     DOI: 10.1007/s00216-015-8963-0

Source DB:  PubMed          Journal:  Anal Bioanal Chem        ISSN: 1618-2642            Impact factor:   4.142


  2 in total

1.  Factors affecting separation and detection of bile acids by liquid chromatography coupled with mass spectrometry in negative mode.

Authors:  Shanshan Yin; Mingming Su; Guoxiang Xie; Xuejing Li; Runmin Wei; Changxiao Liu; Ke Lan; Wei Jia
Journal:  Anal Bioanal Chem       Date:  2017-07-08       Impact factor: 4.142

2.  Identification of absorbed constituents and evaluation of the pharmacokinetics of main compounds after oral administration of yindanxinnaotong by UPLC-Q-TOF-MS and UPLC-QqQ-MS.

Authors:  Leilei Gong; Haiyu Xu; Huijun Yuan; Lan Wang; Xiaojie Yin; Moqi Fan; Long Cheng; Xiaojing Ma; Rixin Liang; Hongjun Yang
Journal:  RSC Adv       Date:  2018-04-26       Impact factor: 4.036

  2 in total

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