Discrimination between internal and external uses by analysis of urine and blood from diphenhydramine users

K. Sasaki, Akari Ishikawa, N. Shima, H. Kamata, Atsushi Nitta, Ryutaro Asai, Misato Wada, Hidenao Kakehashi, Shihoko Nakano, S. Matsuta, Tooru Kamata, H. Nishioka, A. Miki, M. Katagi
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引用次数: 1

Abstract

 STAGE DOI: 10.3408 / jafst.773 ) In order to establish the method for discriminating between oral ingestion ( internal use ) and dermal absorption ( external use ) of diphenhydramine ( DPH ) using biological ‰uids, the excretion proˆles of unchanged DPH and its metabolites in urine as well as time-course changes in blood concentration of DPH have been inves-tigated. Urine and blood specimens were obtained from volunteer users of either the sleep-inducing drug Drewell tablet or the antipruritic drug New Restamin Kowa ointment. Unchanged and its metabolites were identiˆed and quantiˆed using liquid chromatography-tandem mass spectrometry with a C 18 semi-micro column. DPH and its three metabolites, diphenhydramine N -oxide, N -desmethyl diphenhydramine and diphenhydramine N -glucuronide, have been detected, for the ˆrst time, in urine after dermal absorption, and the urinary excretion proˆles of DPH and the metabolites were observed along with those after oral ingestion. Maximum concentration times of DPH and its metabolites in urine were between 21 and 73 hours in dermal absorption, and between 4 and 21 hours in oral ingestion. Maximum concentration times of DPH in blood for dermal absorption were also larger than those for oral ingestion. These results suggested that absorption of DPH through the skin occurs more In addition, the maximum concentrations of DPH and its metabolites in urine after oral ingestion were ten to hundred times higher than those after dermal absorption, which suggests that the urinary concentration of DPH and its metabolites could be applicable as the indexes which allow to discriminate between internal and external uses. The ˆndings obtained in this study will be indispensable as the fundamental in-formation for discussing intake situations of DPH in the forensic ˆelds.
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通过对苯海拉明使用者尿液和血液的分析来区分内服和外服
阶段DOI: 10.3408 / jafst。773)为了建立生物制剂对苯海拉明(DPH)口服(内服)和皮肤吸收(外服)的鉴别方法,研究了未改变的DPH及其代谢产物在尿中的排泄速度和血中DPH浓度的时间变化。尿样和血样取自服用安眠药德雷威尔片或止痒药新利stamin Kowa软膏的志愿者。采用c18半微柱液相色谱-串联质谱法对其进行鉴定和定量分析。首次在皮肤吸收后的尿液中检测到DPH及其三种代谢物苯海拉明N -氧化物、N -去甲基苯海拉明和苯海拉明N -葡萄糖醛酸盐,并观察DPH及其代谢物与口服后尿液排泄的变化。尿中DPH及其代谢物经皮肤吸收的最大浓度时间为21 ~ 73小时,口服摄入的最大浓度时间为4 ~ 21小时。皮肤吸收的DPH在血液中的最大浓度倍也大于口服摄入的DPH。以上结果表明,DPH经皮肤吸收较多,口服后尿液中DPH及其代谢物的最高浓度比经皮肤吸收后的最高浓度高10 ~ 100倍,提示尿液中DPH及其代谢物的浓度可作为区分内服外用的指标。本研究获得的结论将是讨论法医领域DPH摄入情况不可或缺的基本信息。
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