NMR‐based stability evaluation of (E)‐1‐(3′,4′‐dimethoxyphenyl)butadiene (DMPBD) from Zingiber cassumunar Roxb. rhizome
Boonwiset Seaho, Chatkamon Lekwongphaiboon, Wichayasith Inthakusol, Saisuree Prateeptongkum, Wacharee Harnying, Albrecht Berkessel, Nongnaphat Duangdee - Complementary and alternative medicine
- Drug Discovery
- Plant Science
- Molecular Medicine
- General Medicine
- Biochemistry
- Food Science
- Analytical Chemistry
Abstract
Introduction
The active compound (E)‐1‐(3′,4′‐dimethoxyphenyl)butadiene (DMPBD) isolated from the rhizomes of
Objective
In the present study, we aimed to evaluate the stability of DMPBD under various conditions, including different solvents, temperatures, and lighting conditions, to identify the factors affecting stability and optimize the storage and handling conditions.
Methodology
DMPBD samples subjected to the different conditions tested were monitored by quantitative 1H NMR (qHNMR), using an internal standard for the determination of the absolute quantity of DMPBD as a function of time and the changes thereof within 1 month.
Results
Significant decomposition of DMPBD was observed in chloroform‐d1, whereas its content remained constant in methanol‐d4. The content of DMPBD was maintained upon storage at temperatures below 4°C, both as methanolic solution and in the crude extract. Exposure to light had a slight negative impact on its contents. Some degradation products could be identified as resulting from O2‐induced cleavage of the diene moiety.
Conclusions
For pharmacological/therapeutic applications, DMPBD should be stored in the form of the crude extract or as a purified material in methanolic solution. Ideally, the storage temperature should be below 4°C and O2 should be excluded.