Affiliations 

  • 1 Department of Pharmacology, SRM College of Pharmacy, SRM Institute of Science and Technology, Kattankulathur, Chengalpattu, Tamil Nadu 603203, India
  • 2 Department of Biological Sciences, School of Medical and Life Sciences, Sunway University Jalan University, Bandar Sunway, Darul Ehsan, Selangor 47500, Malaysia
  • 3 School of Pharmacy, Monash University Malaysia, Bandar Sunway, Subang Jaya, Selangor 47500, Malaysia
  • 4 Department of Pharmaceutical Chemistry, JSS College of Pharmacy, JSS Academy of Higher Education & Research, The Nilgiris, Ooty, Tamil Nadu 643001, India
  • 5 National Brain Research Centre, Manesar, Haryana, India
  • 6 Department of Pharmaceutical Quality Assurance, SRM College of Pharmacy, SRM Institute of Science and Technology, Kattankulathur, Chengalpattu, Tamil Nadu 603203, India
  • 7 Centre for Pre-University Studies, MAHSA University Malaysia, Malaysia
Toxicol Rep, 2025 Jun;14:101956.
PMID: 40059963 DOI: 10.1016/j.toxrep.2025.101956

Abstract

Natural polyphenols have gained greater attention for their potent medicinal properties and potential benefits in addressing various health concerns. Resveratrol, a polyphenolic compound known for its therapeutic properties, has shown limitations in bioavailability, which the novel derivative resveratrol surrogate molecule (RSM5) aims to improve. The present study evaluates the oral toxicity and safety profile of a novel resveratrol derivative through acute and subacute assessments. Acute toxicity was assessed following a single oral administration, while subacute toxicity was evaluated after repeated doses over 28 days in BALB/c mice. Various physiological, biochemical, and histopathological parameters were monitored to determine potential adverse effects. The findings indicate that the RSM5 exhibits no significant toxic effects at the tested doses (15, 30, 60 mg/kg), with both acute and subacute studies showing a favourable safety profile. These results suggest that the novel resveratrol derivative may be safe for further pharmacological development, supporting its potential for therapeutic applications.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.