Study on the photostability of guaiazulene by high-performance liquid chromatography/mass spectrometry and gas chromatography/mass spectrometry.
Rapid Commun Mass Spectrom, 2008/9;22(17):2698-706.
Fiori J[1], Gotti R, Albini A, Cavrini V
Affiliations
PMID: 18680092DOI: 10.1002/rcm.3661
Impact factor: 2.586
Abstract
The photostability of guaiazulene (1,4-dimethyl-7-isopropylazulene; GA), a natural azulenic compound used in cosmetic and health-care products, as well as in pharmaceutical preparations, was investigated in solution (methanol, ethanol, acetonitrile), by different techniques: gas chromatography/mass spectrometry (GC/MS) and high-performance liquid chromatography combined with atmospheric pressure chemical ionization mass spectrometry and UV detection (LC/APCI-MS and HPLC/UV). A solar simulator (xenon-arc lamp) was used as UV-A radiation source. The study involved: monitoring compound decomposition, identifying products of photodegradation (PPs), assessing the role of oxygen and evaluating the kinetics of the process. Minor PPs are volatile compounds and were characterized by GC/MS, while oligomeric polyoxygenated compounds, tentatively characterized on the basis of MS and MS/MS spectra, were found to be the main photoproducts. The photodegradation was found to be enhanced by the presence of oxygen; nevertheless, determination of the singlet oxygen quantum yield for GA gave a lower value than that for the reference standard Rose Bengal. The obtained results and the developed stability-indicating methods (GC/MS and LC/MS) are of interest for stability studies and/or quality control purposes of GA as raw material or cosmetic products.
MeSH terms
Antioxidants; Azulenes; Chromatography, High Pressure Liquid; Drug Stability; Gas Chromatography-Mass Spectrometry; Photochemistry; Sesquiterpenes; Sesquiterpenes, Guaiane; Spectrometry, Mass, Electrospray Ionization; Tandem Mass Spectrometry
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