Incorporation of Methoxyphenamine into Hair in Early Stage after Intake. Issue 9 (17th October 2020)

• Record Type: Journal Article
• Authors: Nitta, Atsushi; Shima, Noriaki; Kamata, Tooru; Sasaki, Keiko; Matsuta, Shuntaro; Ishikawa, Akari; Asai, Ryutaro; Wada, Misato; Kakehashi, Hidenao; Fujii, Shihoko; Kamata, Hiroe; Nishioka, Hiroshi; Sato, Takako; Tsuchihashi, Hitoshi; Miki, Akihiro; Katagi, Munehiro
• Is Part Of: Journal of analytical toxicology. Volume 45:Issue 9(2021)
• Page Start: 1006
• Page End: 1013
• Publication Date: 2020-10-17
• Subjects: Drugs -- Analysis -- Periodicals; Drugs -- Toxicity testing -- Periodicals; 615.907
• DOI: 10.1093/jat/bkaa165
• Languages: English
• ISSNs: 0146-4760

Abstract

Abstract: In order to investigate the incorporation behavior of drugs into hair in early stage (within 24 h) after intake, time-course changes in drug distribution in black hair were carefully analyzed after a single oral administration of methoxyphenamine (MOP), a non-regulated analog of methamphetamine. Single-hair specimens collected by plucking with the roots intact at appropriate intervals post-intake were each divided into 1-mm segments from the proximal end, and MOP in each segment was determined by a validated liquid chromatography–tandem mass spectrometry procedure. At 10 min after intake, MOP was not detected in any of the segments. MOP became detectable 30 min after intake in the hair bulb (0–1-mm segment from the proximal end) and 1 h after intake in the upper dermis zone (1–2-mm to 4–5-mm segments). The amount of MOP in the hair bulb increased rapidly over 3 h after intake and reached a maximum concentration of ∼100–900 pg/1-mm single hair (11–95 ng/mg) around 3–10 h after intake, whereas that in the upper dermis zone increased at a more gradual pace over 24 h and reached a plateau at ∼30–100 pg/1-mm hair (3–11 ng/mg). These differences can be attributed to the different incorporation mechanisms of the drug. Results from this study can further elucidate the drug incorporation mechanism, which is crucial for accurately interpreting results in hair analyses. Our findings also suggest that hair drug analysis with special attention to the hair root can serve as a useful complementary approach to urine- and blood-based testing in the field of forensic toxicology.