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Methadone, Buprenorphine, Oxycodone, Fentanyl and Tramadol in Multiple Postmortem Matrices.
Stine Marie Havig1, Vigdis Vindenes1,2, Åse Marit Leere Øiestad1
1Department of Forensic Sciences, Oslo University Hospital, Oslo, Norway.
Postmortem toxicology can utilize alternative matrices like pericardial fluid, muscle, and vitreous humor when blood is unavailable. Opioid detection in these samples is possible, but quantitative interpretation requires caution.
Area of Science:
- Forensic Toxicology
- Postmortem Analysis
- Pharmacology
Background:
- Peripheral blood is the preferred matrix for postmortem toxicological interpretation.
- Alternative matrices are needed when blood sampling is not feasible due to decomposition or trauma.
- Limited data exists on postmortem opioid concentrations in non-blood matrices.
Purpose of the Study:
- To investigate the detection and comparability of methadone, buprenorphine, oxycodone, fentanyl, and tramadol concentrations in postmortem pericardial fluid, skeletal muscle, and vitreous humor compared to peripheral blood.
- To assess the utility of these alternative matrices for toxicological interpretation.
Main Methods:
- Analysis of methadone, buprenorphine, oxycodone, fentanyl, and tramadol in peripheral blood, cardiac blood, pericardial fluid, skeletal muscle, and vitreous humor from 54 autopsy cases.
- Comparison of drug concentrations across different matrices.
Main Results:
- Methadone, oxycodone, fentanyl, and tramadol were frequently detected in all alternative matrices.
- Buprenorphine detection was less common.
- Methadone concentrations in alternative matrices (except vitreous humor) were comparable to peripheral blood.
- Significant concentration variations were observed for buprenorphine, oxycodone, and tramadol.
- Quantitative analysis of fentanyl showed promise but was limited by small sample size.
Conclusions:
- Alternative postmortem matrices (pericardial fluid, muscle, vitreous humor) are useful for detecting opioids when blood is unavailable.
- Quantitative interpretation of opioid concentrations in these alternative matrices should be approached with caution due to potential variations.
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