Evidence map›Paper›PMID 41972595›Full record

ArticleAnalytical chemistry2026

Toward Sustainable Clinical Analysis: Benchmarking Plastic Use in LC-MS Sample Preparation - Exemplified by Ketamine Analogues in Whole Blood.

Line Noreng, Åse Marit Leere Øiestad, Frederik André Hansen, Hanne Røberg-Larsen, Steven Ray Wilson, Elisabeth Leere Øiestad

Abstract read
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Self-defenestration associated with 3-MeO-PCE ingestion.International journal of legal medicine · 2026
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Line NorengSection for Chemical Life Sciences, Department of Chemistry, Faculty of Mathematics and Natural Sciences, University of Oslo, 0315 Oslo, Norway.
Åse Marit Leere ØiestadSection of Forensic Toxicological Analytics, Department of Forensic Sciences, Division of Laboratory Medicine, Oslo University Hospital, 0424 Oslo, Norway.
Frederik André HansenDepartment of Pharmacy, Faculty of Mathematics and Natural Sciences, University of Oslo, 0316 Oslo, Norway.
Hanne Røberg-LarsenSection for Chemical Life Sciences, Department of Chemistry, Faculty of Mathematics and Natural Sciences, University of Oslo, 0315 Oslo, Norway.ORCID 0000-0002-4689-6426
Steven Ray WilsonSection for Chemical Life Sciences, Department of Chemistry, Faculty of Mathematics and Natural Sciences, University of Oslo, 0315 Oslo, Norway.ORCID 0000-0002-9755-1188
Elisabeth Leere ØiestadDepartment of Pharmacy, Faculty of Mathematics and Natural Sciences, University of Oslo, 0316 Oslo, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

KetaminePlasticsBenchmarkingHumansLiquid Chromatography-Mass SpectrometryLiquid-Liquid ExtractionKetaminePlastics

Identifiers

PMID41972595
PMCPMC13130169

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.