Shima Noriaki, Nitta Atsushi, Kamata Tooru, Sasaki Keiko, Matsuta Shuntaro, Ishikawa Akari, Asai Ryutaro, Wada Misato, Kakehashi Hidenao, Nakano Shihoko, Kamata Hiroe, Sato Takako, Tsuchihashi Hitoshi, Miki Akihiro, Katagi Munehiro
Forensic Science Laboratory, Osaka Prefectural Police Headquarters, 1-3-18 Hommachi, Chuo-ku, Osaka 541-0053, Japan.
Forensic Science Laboratory, Osaka Prefectural Police Headquarters, 1-3-18 Hommachi, Chuo-ku, Osaka 541-0053, Japan.
Forensic Sci Int. 2019 Aug;301:67-75. doi: 10.1016/j.forsciint.2019.05.013. Epub 2019 May 11.
In order to investigate the influence of pigmentation on the incorporation of drugs into hair, time-course changes in drug distribution along non-pigmented (white) hairs as well as pigmented (black) hairs plucked from the same subject was observed following single administrations of two basic drugs with different properties, zolpidem and methoxyphenamine. These drugs in 1-mm sections of single hair specimens were each determined by a liquid chromatography-tandem mass spectrometric procedure. During the early stage (12-36 h) after intake, for black hairs, both drugs were detected over the entire area of hair root (4-5 mm in length), in which notable concentration of these drugs in the hair bulb (0-1-mm segment from the bottom of hair root, Region 1) and lower concentrations in the upper dermis zone (1-2-mm to 3-4-mm or to 4-5-mm segments, Region 2) were commonly observed. Meanwhile, for white hairs, high drug concentrations in Region 1 as detected in black hairs were not observed although only small amounts of these drugs were detected over Region 2. Subsequent time-course changes in the concentration of drugs in hair demonstrated that the drugs once incorporated into white hair via Region 2 decreased gradually over the period from 24 h to 35 days after intake, but those of black hairs remained almost unchanged. These findings revealed here suggest that hair pigments have two important roles in the distribution of drugs: (1) incorporation of drugs into hair via Region 1, and (2) retention of already incorporated drugs in the hair tissue. These findings would be useful for discussing individual drug-use history based on hair analysis in the forensic fields.
为了研究色素沉着对药物掺入毛发的影响,在单次给予两种性质不同的碱性药物唑吡坦和甲氧那明后,观察了从同一受试者身上拔下的无色素(白色)毛发和有色素(黑色)毛发中药物分布的时间进程变化。通过液相色谱-串联质谱法分别测定单根毛发标本1毫米切片中的这些药物。在摄入后的早期阶段(12 - 36小时),对于黑色毛发,在整个毛根区域(长度为4 - 5毫米)均检测到这两种药物,其中在毛球(从毛根底部起0 - 1毫米段,区域1)中这些药物浓度显著,而在上部真皮区域(1 - 2毫米至3 - 4毫米或至4 - 5毫米段,区域2)中浓度较低,这是常见现象。同时,对于白色毛发,虽然在区域2仅检测到少量这些药物,但未观察到黑色毛发中在区域1所检测到的高药物浓度。随后毛发中药物浓度的时间进程变化表明,一旦通过区域2掺入白色毛发的药物在摄入后24小时至35天内逐渐降低,而黑色毛发中的药物浓度几乎保持不变。此处揭示的这些发现表明,毛发色素在药物分布中具有两个重要作用:(1)通过区域1将药物掺入毛发,以及(2)将已掺入的药物保留在毛发组织中。这些发现对于在法医领域基于毛发分析讨论个体用药史将是有用的。