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基于银杏内酯B水解产物的生成、检测、鉴定及半定量,了解其在生理环境下的区域选择性水解。

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

作者信息

Li Xue-Jing, Yang Kui, Du Gang, Xu Liang, Lan Ke

机构信息

Key laboratory of Drug Targeting and Drug Delivery System, Ministry of Education, West China School of Pharmacy, Sichuan University, Chengdu, 610041, China.

Chengdu BaiKang Institute of Pharmacology and Toxicology, Chengdu, 610046, China.

出版信息

Anal Bioanal Chem. 2015 Oct;407(26):7945-56. doi: 10.1007/s00216-015-8963-0. Epub 2015 Aug 25.

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.

摘要

开发了一种结合特殊样品制备策略的液相色谱 - 质谱(LC - MS)方法,用于研究银杏内酯B(GB)在生理环境中的水解情况,并与银杏内酯A(GA)进行比较。通过直接注入在挥发性缓冲液中制备的样品,捕捉到了快速水解过程。获得了水解产物的LC - MS行为,包括三种单羧酸盐和三种二羧酸盐。通过碎片分析鉴定了单羧酸盐,并通过反应序列相应地初步鉴定了二羧酸盐。在4°C、pH 7.0 - 10.7的条件下对GB和GA的碱催化水解进行了表征。通过在pH 6.8和7.4下的热力学研究揭示了内酯 - C和内酯 - F上的区域选择性反应。结果表明,GB骨架上的1 - 羟基阻碍了内酯 - E的反应性。基于这些结果,在人、大鼠和狗的血浆中证实了GB独特的水解现象,即三内酯快速降解,同时仅产生内酯 - F水解产物。这种现象也与1 - 羟基密切相关,因为在GA中未观察到。更有趣的是,揭示了潜在机制与任何典型的酶催化过程无关,而是可能涉及完整或断裂的内酯 - C部分与血浆中内源性小分子反应物的选择性反应。对GB与GA水解的深入了解不仅有助于理解它们的药理机制,还为研究银杏内酯的构效关系提供了潜在途径。图形摘要:银杏内酯B在pH 7.4缓冲液和血浆中的区域选择性水解。

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