Development of a Liquid Chromatography–Tandem Mass Spectrometry (LC–MS/MS) Method for Characterizing Linalool Oral Pharmacokinetics in Humans

• Published in: Molecules (Basel, Switzerland) Switzerland), 2023-09, Vol.28 (18), p.6457
• Main Authors: Wang, Yan-Hong, Mondal, Goutam, Stevens, Nicole, Bascoul, Cécile, Osguthorpe, Russell J., Khan, Ikhlas A., Yates, Charles R.
• Format: Article
• Language: English
• Subjects: Accuracy; Acetates; Anxiety; Chromatography; Esters; Gas flow; human; Instrument industry; Ions; LC–MS/MS; linalool; Liquid chromatography; Mass spectrometry; Methods; Oils & fats; Oral administration; Pharmacokinetics; Scientific imaging; Solvents
• ISSN: 1420-3049; 1420-3049
• DOI: 10.3390/molecules28186457

Lavender (Lavandula angustifolia Miller or Lavandula officinalis Chaix) is an ethnopharmacological plant commonly known as English lavender. Linalool and linalyl acetate are putative phytoactives in lavender essential oil (LEO) derived from the flower heads. LEO has been used in aroma or massage therapy to reduce sleep disturbance and to mitigate anxiety. Recently, an oral LEO formulation was administered in human clinical trials designed to ascertain its anxiolytic effect. However, human pharmacokinetics and an LC–MS/MS method for the measurement of linalool are lacking. To address this deficiency, a rapid and sensitive liquid chromatography–tandem mass spectrometry (LC–MS/MS) method was developed for the analysis of linalool in human serum. Prior to the analysis, a simple sample preparation protocol including protein precipitation and liquid–liquid extraction of serum samples was created. The prepared samples were analyzed using a C18 reversed-phase column and gradient elution (acetonitrile and water, both containing 0.1% formic acid). A Waters Xevo TQ-S tandem mass spectrometer (positive mode) was used to quantitatively determine linalool and IS according to transitions of m/z 137.1→95.1 (tR 0.79 min) and 205.2→149.1 (tR 1.56 min), respectively. The method was validated for precision, accuracy, selectivity, linearity, sensitivity, matrix effects, and stability, and it was successfully applied to characterize the oral pharmacokinetics of linalool in humans. The newly developed LC–MS/MS-based method and its application in clinical trial serum samples are essential for the characterization of potential pharmacokinetic and pharmacodynamic interactions.