Post-mortem concentrations of drugs determined in femoral blood in single-drug fatalities compared with multi-drug poisoning deaths

2016 ◽  
Vol 267 ◽  
pp. 96-103 ◽  
Author(s):  
Alan Wayne Jones ◽  
Anita Holmgren ◽  
Johan Ahlner
2021 ◽  
Vol 36 (3) ◽  
pp. 233-237
Author(s):  
Marek Dziadosz ◽  
Katarina Bolte ◽  
Wolfgang Rosenberger ◽  
Michael Klintschar ◽  
Jörg Teske

Abstract Objectives Since melperone abuse with lethal intoxication is common, expert opinions based on therapeutical and lethal concentration ranges can be considered as important. Because there is a lack of information about fatalities caused by melperone mono-intoxications and data on tissue samples with concentration distribution, the aim of this work is the examination of lethal concentration ranges of melperone and drug quantification in different matrices. Methods An LC-MS/MS method was applied for analyses performed in blood and tissue samples. Quantification based on standard addition and sample preparation on liquid–liquid extraction with 1-chlorobutane. An appropriate tissue homogenization was performed ahead of extraction with an IKA Ultra-Turrax-Tube-Drive®. A Luna 5 µm C18 (2) 100 Å, 150  × 2 mm analytical column was used for chromatographic separation and the elution was performed with two mobile phases consisted of A (H2O/methanol = 95/5, v/v) and B (H2O/methanol = 3/97, v/v) both with 10 mM ammonium acetate and 0.1% acetic acid. Results A multi-drug LC-MS/MS analytical method developed was applied successfully for melperone quantification in different post-mortem matrices. No analytical problems could be identified during method development and analyses of real samples. The melperone lethal concentration calculated in femoral blood of the drug mono-intoxication investigated was 10 mg/L. Melperone concentration distribution was presented for the first time. Conclusions The lethal reference concentration of melperone in femoral blood of 17.1 mg/L pointed out in different reference lists should be used with caution. Instead, a lower lethal melperone concentration should be considered. The post-mortem concentration distribution of the drug presented could be helpful in the interpretation of cases where no blood samples are available.


2020 ◽  
pp. 002580242097381
Author(s):  
Laura J Hikin ◽  
Paul R Smith ◽  
Peter D Maskell ◽  
Hassan Kurimbokus ◽  
Emily Ashong ◽  
...  

Etizolam is a thienodiazepine that although licensed for clinical usage in Japan, India and South Korea is commonly abused and detected in post-mortem cases around the world. To date, there are limited data in the literature to allow for the interpretation of blood concentrations of etizolam in post-mortem cases. A liquid chromatography with tandem mass spectrometry method was used to quantitate etizolam concentrations in 28 post-mortem cases where etizolam was detected. The median concentration of etizolam in femoral blood was 8.5 ng/mL (range 1.0–172.0 ng/mL; n = 24); in antemortem plasma, the etizolam concentration range was 4–44 ng/mL ( n = 4). The mean age of the individuals abusing etizolam was 38.5 ± 8.4 years (median 39 years), with the majority being male (86%). In all of the cases, multiple drugs were detected, with the most common being pregabalin (61%) followed by morphine/heroin (54%), diazepam (54%) and benzoylecgonine (21%), illustrating the increasing problem of poly-substance use in drug abusers. The cause of death in the cases in which etizolam was detected was multi-drug toxicity in 87.5% of the cases, with 12.5% unrelated to drug use (hangings and blunt-force trauma). These data will further help forensic practitioners with the interpretation of post-mortem etizolam concentrations.


2016 ◽  
Vol 33 ◽  
pp. 44-55 ◽  
Author(s):  
Ruth Kerry ◽  
Pierre Goovaerts ◽  
Maureen Vowles ◽  
Ben Ingram

2017 ◽  
Vol 94 (4) ◽  
pp. 572-586 ◽  
Author(s):  
Kathleen Stewart ◽  
Yanjia Cao ◽  
Margaret H. Hsu ◽  
Eleanor Artigiani ◽  
Eric Wish

1975 ◽  
Vol 49 (3) ◽  
pp. 173-177 ◽  
Author(s):  
L. F. Taffs

AbstractA medicated diet containing 0.3% thiabendazole fed continuously to 26 mice for 7 days removed 9 out of 11 (82%) Hymenolepis nana, (one tapeworm remaining in each of two mice), 17 out of 17 (100%) Syphacia obvelata and 8 out of 8 (100%) Aspiculuris tetraptera infections. By contrast in 26 non-treated mice 9 out of 10 Hymenolepis, 17 out of 18 Syphacia and 8 out of 8 Aspiculuris infections persisted through the 7 day treatment period, and at post mortem examination 38 Hymenolepsis, 1,562 Syphacia and 4,911 Aspiculuris worms were recovered. In a second experiment 100% removal of 23 Hymenolepis and 20 Syphacia infections was obtained after 14 days medication of 38 mice. High activity against both roundyvorms and tapeworms of mice was thus obtained using one single drug. Some unexplained deaths amongst inbred strain C3H/Hef Nimr mice occurred within seven day's of the continuous medication.


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