Jianping Zhao , Mei Wang , Joseph Lee , Zulfiqar Ali , Ikhlas A. Khan
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Characterization, differentiation, and adulteration detection of peppermint essential oil: An NMR approach
Peppermint essential oil (PEO) is a valuable natural product widely used in food, cosmetics, and therapeutics. However, its quality and authenticity are frequently compromised by adulteration and compositional variability. This study explored the application of Nuclear Magnetic Resonance (NMR) technique for the characterization and differentiation of PEO, as well as for the identification of adulterants in commercial PEO samples. Comprehensive analyses of 1D and 2D NMR spectra allowed for the identification of characteristic ¹H NMR signals associated with the key components of PEO, and significant compositional variations between PEOs from different geographical origins were revealed. To facilitate differentiation, a straightforward indicator ratio method was developed to distinguish between PEOs from the United States and India, the two primary production regions. A total of 50 commercial PEO samples were evaluated using NMR in combination with chemometric tools, uncovering a high adulteration rate (42 %). Adulterants, including synthetic chemicals, de-mentholized cornmint oil, and lower-cost oils, were identified. This work demonstrates the potential of NMR as a useful tool for quality assessment and authenticity testing of essential oils. The methodology presented may also be extended to other essential oils to ensure product integrity.
期刊介绍:
This journal is an international medium directed towards the needs of academic, clinical, government and industrial analysis by publishing original research reports and critical reviews on pharmaceutical and biomedical analysis. It covers the interdisciplinary aspects of analysis in the pharmaceutical, biomedical and clinical sciences, including developments in analytical methodology, instrumentation, computation and interpretation. Submissions on novel applications focusing on drug purity and stability studies, pharmacokinetics, therapeutic monitoring, metabolic profiling; drug-related aspects of analytical biochemistry and forensic toxicology; quality assurance in the pharmaceutical industry are also welcome.
Studies from areas of well established and poorly selective methods, such as UV-VIS spectrophotometry (including derivative and multi-wavelength measurements), basic electroanalytical (potentiometric, polarographic and voltammetric) methods, fluorimetry, flow-injection analysis, etc. are accepted for publication in exceptional cases only, if a unique and substantial advantage over presently known systems is demonstrated. The same applies to the assay of simple drug formulations by any kind of methods and the determination of drugs in biological samples based merely on spiked samples. Drug purity/stability studies should contain information on the structure elucidation of the impurities/degradants.