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. 2018 Dec;15(3):298-303.
doi: 10.4274/tjps.38258. Epub 2018 Nov 20.

Simultaneous Determination of Arbutin and Hydroquinone in Different Herbal Slimming Products Using Gas Chromatography-mass Spectrometry

Affiliations

Simultaneous Determination of Arbutin and Hydroquinone in Different Herbal Slimming Products Using Gas Chromatography-mass Spectrometry

Benan Dursunoğlu et al. Turk J Pharm Sci. 2018 Dec.

Abstract

Objectives: The aim of our study was to develop a simple, precise, sensitive and specific method for the simultaneous determination of arbutin and hydroquinone in different herbal slimming products using GC-MS.

Materials and methods: The methanol and aqueous extracts of nine herbal slimming products in Turkey were evaluated for analysis of arbutin and hydroquinone using GC-MS method.

Results: The retention times of arbutin and hydroquinone were found as 11.32 and 5.44 min, respectively. The linear ranges in this method were 5-500 ng/mL for arbutin and hydroquinone, respectively. The intra- and inter-day precisions, expressed as the relative standard deviation, were less than 1.94 and 2.73%, determined from quality control samples for arbutin and hydroquinone, and accuracy was within 1.13 and 2.56% in terms of relative error, respectively. The limit of detection and quantification were 0.555 and 1.665 ng/mL for arbutin, and 0.031 and 0.093 ng/mL for hydroquinone, respectively.

Conclusion: The developed method can be used for routine quality control analysis of arbutin and hydroquinone in different herbal slimming products.

Keywords: Arbutin; Calluna vulgaris; GC-MS; herbal slimming products; hydroquinone.

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Conflict of interest statement

Conflict of Interest: No conflict of interest was declared by the authors.

Figures

Figure 1
Figure 1
Structural formula and derivatization mechanism of arbutin and hydroquinone
Figure 2
Figure 2
Mass spectrometry spectra of arbutin (A) and hydroquinone (B)
Figure 3
Figure 3
Gas chromatography-mass spectrometry chromatograms of arbutin (A) and hydroquinone (B) (500 ng/mL)
Figure 4
Figure 4
Typical chromatograms of methanol (A) and aqueous (B) extracts of product 9 (1.0 mg/mL)

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