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Journal ArticleDOI

Quantification of aconitine in post-mortem specimens by validated liquid chromatography-tandem mass spectrometry method: Three case reports on fatal ‘monkshood’ poisoning

TLDR
The diester-diterpene alkaloid aconitine was quantified by liquid chromatography-tandem mass spectrometry in post-mortem specimens of three cases where suicidal ingestion of Aconitum napellus L. ('monkshood') was supposed to provide compelling evidence for acute Aconite poisoning as being the cause of death.
Abstract
The diester-diterpene alkaloid aconitine was quantified by liquid chromatography-tandem mass spectrometry in post-mortem specimens of three cases where suicidal ingestion of Aconitum napellus L. (´monkshood´) was supposed. In an attempt at rationalization, sample preparation and chromatographic conditions of plasma/serum drug analysis routine were utilized. Linearity was established from 0.5 to 20 µg L(-1) using newborn calf serum (NCS) as a surrogate calibration matrix for all sample types and mesaconitine as an internal standard. Validation (selectivity, sensitivity, precision, accuracy, recovery of the extraction procedure, matrix effect, processed sample stability) confirmed the applicability of the analytical method to various post-mortem matrices. Internal standard selection was based on multi-matrix process efficiency data. In human post-mortem peripheral blood a lower limit of quantification of 0.51 µg L(-1) and a limit of detection of 0.13 µg L(-1) were accomplished (0.1 ml sample aliquots). Aconitine was degraded to a large extent in different sample types when being stored at +20 °C for 30 days, while at -20 °C and for some matrices also at +4 °C no appreciable degradation occurred. Aconitine concentrations in real samples were 10.3-17.9 µg L(-1) (peripheral blood, n = 3), 14.9-87.9 µg L(-1) (heart blood, n = 3), 317-481 µg L(-1) (urine, n = 2), 609-4040 µg L(-1) (stomach content, n = 3), 139-240 µg L(-1) (bile, n = 2), 8.4 µg L(-1) (vitreous humor, n = 1), 54.7 µg L(-1) (pericardial fluid, n = 1), 492 µg kg(-1) (liver, n = 1), 15.2-19.7 mg L(-1) (unknown liquids secured onsite, n = 3). Together with concomitant circumstances the analytical data provided compelling evidence for acute Aconitum poisoning as being the cause of death. Copyright © 2013 John Wiley & Sons, Ltd. Language: en

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Citations
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Vitreous humor analysis for the detection of xenobiotics in forensic toxicology: a review

TL;DR: The distribution of xenobiotics in VH samples is discussed and illustrated by a table reporting the concentrations of 106 drugs from more than 300 case reports, and a survey was conducted of publications found in the MEDLINE database from 1969 through April 30, 2015.
Journal ArticleDOI

State of the art in bile analysis in forensic toxicology.

TL;DR: An update on the state of knowledge for the use of bile in forensic toxicology is provided, through a review of the Medline literature from 1970 to May 2015, to highlight specificities and consequences from an analytical and interpretative point of view.
Journal ArticleDOI

Real-time toxicity prediction of Aconitum stewing system using extractive electrospray ionization mass spectrometry

TL;DR: A complete analytical strategy, including data acquisition, data mining, and data evaluation was proposed and implemented with overcoming the usual difficulties in real-time mass spectrometry quantification and showed that the strategy worked perfectly and the toxicity of the systems were evaluated and predicated accordingly.
Journal ArticleDOI

Plasma vs heart tissue concentration in humans – literature data analysis of drugs distribution

TL;DR: The article reviews cardiac surgery and forensic medical studies to provide a reference for drug concentrations in human cardiac tissue and depicts potential problems in defining the active concentration location, what may indirectly suggest multiple mechanisms involved in the drug distribution within the heart.
Journal ArticleDOI

Optimization of the traditional processing method for precision detoxification of CaoWu through biomimetic linking kinetics and human toxicokinetics of aconitine as toxic target marker.

TL;DR: The present study aimed to optimize the traditional processing method for precision detoxification of CaoWu through biomimetic linking kinetics and human toxicokinetics (TK) of AC, with a view of providing insights into the changes of toxic target marker.
References
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Journal Article

Linear regression for calibration lines revisited: weighting schemes for bioanalytical methods

TL;DR: In this article, the relevance of weighting schemes for linear regression analysis and how this approach can be useful in the bioanalytical field is discussed and the steps to be taken in the study of the linear calibration approach are described.
Journal ArticleDOI

Aconitum in traditional Chinese medicine: a valuable drug or an unpredictable risk?

TL;DR: This case study serves as a case study to explore the multidisciplinary implications of botanicals used in TCM, with a stipulation for a maximum level of DDA content of Aconitum highly desirable in order to guarantee the clinical safety and its low toxicity in decoctions.
Journal ArticleDOI

Does a stable isotopically labeled internal standard always correct analyte response? A matrix effect study on a LC/MS/MS method for the determination of carvedilol enantiomers in human plasma.

TL;DR: It was clearly demonstrated that a slight difference in retention time between the analyte and the SIL internal standard, caused by deuterium isotope effect, has resulted in a different degree of ion suppression between these two analogues.
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