ArticleAnalytical chemistry2026
Toward Sustainable Clinical Analysis: Benchmarking Plastic Use in LC-MS Sample Preparation - Exemplified by Ketamine Analogues in Whole Blood.
Article in Analytical chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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Who cites it
2 citing papers in PubMed.
- Expanded evaluation of a robust on-line sample cleanup-LC-MS platform suited for new approach methodologies (NAM).Analytical and bioanalytical chemistry · 2026Article
- Self-defenestration associated with 3-MeO-PCE ingestion.International journal of legal medicine · 2026Article
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Authors and funding
6 authors.
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Abstract
The aim of this study was to assess and benchmark plastic consumption in sample preparation for forensic analysis, alongside the development of an LC-MS method for ketamine analogues in whole blood, with various sustainability-related scores and parameters examined throughout. Ketamine analogues are emerging psychoactive substances associated with intoxication and fatalities globally. An analytical method was developed for determining ketamine and eight of its analogues in human whole blood. Focus was placed on traditional analytical parameters but also the consumption of plastics and reagents, an overlooked aspect of clinical and forensic chemistry. We evaluated three sample preparation techniques: protein precipitation (PPT), liquid-liquid extraction (LLE), and electromembrane extraction (EME). While PPT and LLE are well-established techniques used in clinical settings, EME (i.e., electrophoresis across an oil membrane) is a less established but highly promising approach. All three sample preparation approaches demonstrated similar performance with recoveries above 85% and matrix effects averaging approximately 100%. The EME approach was subsequently refined using a Box-Behnken-based design of experiments and was validated according to the American Academy of Forensic Sciences guidelines. All validated parameters were within the limits, suggesting that the tunable EME approach is a potentially valuable tool in clinical chemistry. The amount of plastic consumables per 100 samples was calculated as being 511 g for PPT, 864 g for LLE, and 303 g for EME. Correspondingly, the amount of organic solvent consumption per sample was 470, 1570, and 210 μL, respectively. The AGREEprep scores (ranges from 0 to 1, 1 is best) were 0.48 ± 0.04, 0.36 ± 0.04, and 0.55 ± 0.05, respectively. The rounded value of PPT (arguably the most used approach for related samples) is 0.5 kg per 100 samples, and we propose that this number be used as a benchmark for plastic consumption in today's sample preparation. This may serve as a practical reference when developing and evaluating future sample preparation strategies. For example, employing EME here allowed for a 40% reduction in plastics compared to the benchmark, illustrating a significant improvement. However, the investigated approaches have a significant use of single-use consumables, inviting sample preparation approaches that can reduce the plastic footprint.
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