Acute, sub-acute and developmental toxicity studies of molybdenum disulfide nanoflowers in rats, as per OECD guidelines
- PMID: 40855335
- PMCID: PMC12379412
- DOI: 10.1186/s40360-025-00881-8
Acute, sub-acute and developmental toxicity studies of molybdenum disulfide nanoflowers in rats, as per OECD guidelines
Abstract
Background: This study aimed to investigate the potential toxic effects of Molybdenum disulfide nano-flowers (MoS2 NF), which have been suggested as a chemotherapeutic agent, but lack previous toxicity studies.
Methods: Acute, sub-acute and developmental toxicity studies were conducted following OECD guidelines 425, 407 and 414, respectively.
Results: In the acute toxicity study, female Wistar rats received logarithmic doses (1.75-550 mg/kg) of MoS2NF over 14 days. Results indicated a decrease in oxidative stress markers (CAT, SOD and GSH) and increased MDA levels, along with significant decrease in organ weight compared to normal control. Alterations in liver enzymes, CBC profile and lipid profile and histopathological analysis were observed in MoS2 NF groups. Sub-acute toxicity (28-day at 3 and 10 mg/kg in both male and female rats) resulted in increased levels of ALT and AST, decreased levels of CAT, SOD and GSH and increased MDA and urea levels. Sperm analysis in male group showed increased motility and concentration, with more defective morphology. In developmental toxicity studies, a 10 mg/kg dose for 21 days decreased all oxidative markers except MDA, which increased. Fetal crown-to-rump length increased, while uterine SOD, CAT and GSH levels decreased. Histopathology revealed organ damage in both sub-acute and developmental studies. Maternal weight remained unaffected, whereas fetal weight showed an increased.
Conclusion: MoS2 NF exhibited mild-to-moderate toxicity, however, long-term and studies are recommended to assess the safety and therapeutic potential of MoS2NF.
Keywords: Acute toxicity; Developmental toxicity; In vivo; Nano-flowers; Sub-acute toxicity.
© 2025. The Author(s).
Conflict of interest statement
Declaration. Ethical approval: All the procedures and techniques used in this study were approved by the Ethical committee (REC/RIPS/LHR/2023/068) of Riphah International University, Raiwind Campus, Lahore. Pakistan. Consent to participate and consent for publication: Not applicable Competing interests: The authors declare no competing interests.
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