ArticleForensic science, medicine, and pathology2026
Forensic implication of Zinc sulfide and Zinc sulfide Nanoparticles toxicity on muscle histopathology and postmortem changes in rats.
Article in Forensic science, medicine, and pathology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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
1 citing paper in PubMed.
- Comment on "forensic implication of zinc sulfide and zinc sulfide nanoparticles toxicity on muscle histopathology and postmortem changes in rats".Forensic science, medicine, and pathology · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The current study aimed to investigate the molecular toxic effects of zinc sulfide (ZnS) and zinc sulfide nanoparticles (ZnS-NPs) on rat skeletal muscle tissue. It also explored the forensic implications of ZnS toxicity on postmortem carrion infestation, particularly its potential impact on postmortem interval (PMI) estimation. ZnS nanoparticles were synthesized and characterized using X-ray diffraction (XRD) and scanning electron microscopy (SEM). Thirty Wistar rats were divided into three groups: control, ZnS-treated, and ZnS-NP–treated (both administered at the LD50 dose of 2000 mg/kg). Muscle tissues were harvested for histopathological, ultrastructural, and acridine orange staining analysis. Arthropods were collected and identified across five decomposition stages to assess changes in carrion infestation patterns. Histopathological and ultrastructural analysis showed marked deformation, necrosis, and degeneration of muscle fibers, more severe in the ZnS-NP group. Collagen deposition significantly decreased in both treatment groups. Electron microscopy revealed dissociation and degradation of myofibrils with increased interfibrillar spacing. Arthropod analysis indicated altered colonization patterns, with decreased adult abundance and disrupted succession stages, especially during the active decay phase. ZnS and ZnS-NPs induce significant skeletal muscle toxicity that may mimic postmortem autolysis and lead to PMI misinterpretation. ZnS-NPs exert more severe effects than bulk ZnS. The observed entomological disruption highlights the forensic relevance of ZnS exposure and underscores the need for integrated toxicological and entomological analyses in PMI estimation.
Indexed as
Identifiers
40848181What 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.