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. 2021 Mar 5;26(5):1397. doi: 10.3390/molecules26051397

Table 5.

Analytical methods for the determination of the main components of Mitragyna speciosa.

Compounds Sample (Amount) Sample Preparation Analytical Technique Limits of Detection Limits of Quantitation Recovery (%) Reference
Mitragynine, 7-hydroxymitragynine, Speciociliatine, Speciogynine
and Paynantheine
Urine (1 mL) SPE (PolyChrom ClinII 3 cm3 (35 mg)) LC-Q/TOF-MS 0.25–1 μg/L 0.5–1 μg/L - [122]
Mitragynine, 7-hydroxy-mitragynine, 5-desmethyl-mitragynine, 17-desmethyldihydromitragynine and mitraphylline Urine (0.2 mL) Hydrolysis (β-Glucuronidase) and LLE (methyl tert-butyl ether) LC-MS/MS (ESI) - 1 μg/L - [123]
Mitragynine, 16-carboxy mitragynine and 9-O-demethyl mitragynine Urine (1 mL) Hydrolysis (β-glucuronidase/arylsulfatase) and SPE (Bond Elut Certify
(200 mg, 3 mL) and Abs Elut-Nexus SPE (60 mg, 3 mL))
LC-MS/MS (ESI) - 1–50 μg/L - [121]
Mitragynine and 7-hydroxymitragynine Urine (1 mL) Dilution (water with 0.1% formic acid) LC-MS/MS (ESI) 0.012–0.069 μg/L 0.0356–0.215 μg/L - [124]

Caption: ESI (electrospray ionization); LC (liquid chromatography); LLE (liquid-liquid extraction); MS (mass spectrometry); MS/MS (tandem mass spectrometry); SPE (solid-phase extraction); Q/ToF (time of flight).