Doxepin and nordoxepin concentrations in body fluids and tissues in doxepin associated deaths

被引:13
作者
Gronewold, Antonia [1 ]
Dettling, Andrea [1 ]
Haffner, Hans T. [1 ]
Skopp, Gisela [1 ]
机构
[1] Univ Hosp, Inst Legal & Traff Med, D-69115 Heidelberg, Germany
关键词
Doxepin; Nordoxepin; Combined concentration; Concentration ratio; LC-MS/MS; Postmortem; TRICYCLIC ANTIDEPRESSANT; POSTMORTEM TOXICOLOGY; PLASMA-CONCENTRATIONS; ANTI-DEPRESSANTS; CYP2D6; DRUG; PHARMACOKINETICS; METHADONE; GENOTYPE; 2D6;
D O I
10.1016/j.forsciint.2009.05.015
中图分类号
DF [法律]; D9 [法律]; R [医药、卫生];
学科分类号
0301 ; 10 ;
摘要
Body fluids and tissues in eight doxepin (Dox)-related deaths were investigated in order to prove whether the individual concentration of Dox, the concentration sum of parent drug and its active metabolite N-desmethyldoxepin (NDox) or the concentration ratio Dox/Ndox valuably contribute to making a cause of death determination. Individual case histories were shortly described. Dox and NDox concentrations were determined by LC-MS/MS. Dox concentration measured from two cases was well within a concentration range considered therapeutic, whereas subtherapeutic dosing may have occurred in another two cases. There were two cases of fatal Dox ingestion, as well as a case of high dosage and advanced putrefaction, respectively. The liver concentration sum may be more useful if a fatal ingestion cannot be clearly separated from a person's medication usage. High concentrations could be observed in lung tissue, and combined concentrations of Dox and NDox may also be helpful in making a cause of death determination. There was a trend to a higher concentration sum in the brain with increasing combined levels in blood. Overall, the sum of the absolute figures allows a more accurate interpretation in Dox-related deaths as compared to the molar concentration ratio which may be helpful in acute ingestion. Determination of the N-desmethyl metabolite along with its parent is recommended and analysis should include more than a single specimen. (C) 2009 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:74 / 79
页数:6
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