ArticleArchives of toxicology2025
Concentration-time profiles of the nerve agent VX and the pesticide parathion in five different cell culture plates.
Article in Archives of toxicology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Cell cultivation tools are usually not considered the primary factors influencing research results. In this study, we selected two organophosphorus compounds (OP) to examine possible compound absorption in five different commercially available cell culture plates. In addition, compound degradation processes were studied. The plates were exposed to the nerve agent VX or the OP pesticide parathion. Using analytical methods such as LC-ESI-MS/MS or GC-MS, the respective concentrations of VX and its degradation products O-ethyl methylphosphonic acid (EMPA) and S-[2-(diisopropylamino)ethyl]methylphosphonothioic acid (EA-2192) as well as parathion, paraoxon, diethyl thiophosphate (DETP), and diethyl phosphate (DEP) were determined up to 72 h. Our data showed that the choice of the cell culture plate can have an impact on the OP concentration and the degradation products. The balance of VX, EMPA, and EA-2192 resulted in about the initial VX concentration at all evaluated time points, indicating that VX absorption was not likely to occur in the cell culture plates. In contrast, relevant parathion concentrations were unaccounted for after 72 h suggesting absorption to the plates. In conclusion, it was shown for the model substance parathion that it is important to characterize cell culture tools, i.e., the respective plates, regarding possible compound interaction. The suitability of the cell cultivation tool for investigations with an OP should be evaluated in advance to obtain a high quality of the study and to improve the concordance with in vivo data.
Indexed as
Identifiers
40261328What OpenQuestion holds
Registered trials
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.