Abstract
Background: Salvianolic acid A (Sal A) is one of the major water-soluble compounds isolated from the root of Salvia miltiorrhiza, which is widely used as a kind of traditional Chinese medicine. Because of instability of Sal A, the degradation products of Sal A were studied to confirm the conversion of Sal A.
Methods: To elucidate the structures of the degradation products, they were isolated by preparative high performance liquid chromatography (HPLC) and identified by nuclear magnetic resonance (NMR) and mass spectrometry (MS). To understand the formation pathways of the degradation products, stress testing and esterification of Sal A were performed and analyzed on HPLC. Results: Five products were identified as a pair of epimers (products 1 and 2), isosalvianolic acid C (3), salvianolic acid C (4) and salvianolic acid A methyl ester (5). Sal A in high humidity yielded 1 and 2 by electrophilic addition. Sal A in strong basic solution yielded 3 by a free radical intermediate. Sal A in high temperature or base or oxidant in water yielded 4 by an epoxide intermediate. Sal A in methanol yielded 5 by esterification catalyzed by acid. Eight other products were found in heated water solution. Conclusion: According to the formation mechanisms of the products, Sal A could be used in a solid form formulation and should be protected from humidity, oxidant and base when manufacturing, depositing and supplying.Keywords: Salvianolic acid A, degradation products, chemical reactions, formation mechanisms, Salvia miltiorrhiza, HPLC.
Graphical Abstract
Current Analytical Chemistry
Title:Study on the Formation Mechanisms of the Degradation Products of Salvianolic Acid A
Volume: 13 Issue: 2
Author(s): Fengfeng Wang, Dezhi Yang, Guanhua Du and Yang Lv
Affiliation:
Keywords: Salvianolic acid A, degradation products, chemical reactions, formation mechanisms, Salvia miltiorrhiza, HPLC.
Abstract: Background: Salvianolic acid A (Sal A) is one of the major water-soluble compounds isolated from the root of Salvia miltiorrhiza, which is widely used as a kind of traditional Chinese medicine. Because of instability of Sal A, the degradation products of Sal A were studied to confirm the conversion of Sal A.
Methods: To elucidate the structures of the degradation products, they were isolated by preparative high performance liquid chromatography (HPLC) and identified by nuclear magnetic resonance (NMR) and mass spectrometry (MS). To understand the formation pathways of the degradation products, stress testing and esterification of Sal A were performed and analyzed on HPLC. Results: Five products were identified as a pair of epimers (products 1 and 2), isosalvianolic acid C (3), salvianolic acid C (4) and salvianolic acid A methyl ester (5). Sal A in high humidity yielded 1 and 2 by electrophilic addition. Sal A in strong basic solution yielded 3 by a free radical intermediate. Sal A in high temperature or base or oxidant in water yielded 4 by an epoxide intermediate. Sal A in methanol yielded 5 by esterification catalyzed by acid. Eight other products were found in heated water solution. Conclusion: According to the formation mechanisms of the products, Sal A could be used in a solid form formulation and should be protected from humidity, oxidant and base when manufacturing, depositing and supplying.Export Options
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Cite this article as:
Wang Fengfeng, Yang Dezhi, Du Guanhua and Lv Yang, Study on the Formation Mechanisms of the Degradation Products of Salvianolic Acid A, Current Analytical Chemistry 2017; 13 (2) . https://dx.doi.org/10.2174/1573411012666160906154333
DOI https://dx.doi.org/10.2174/1573411012666160906154333 |
Print ISSN 1573-4110 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6727 |

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