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February 26, 2026Scientific Reports3 citationsOpen Access

Multifunctional hierarchical Ni2CoS4 structures for combating drug-resistant infections and colorectal cancer via piezocatalytic ROS generation

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KQKarzan QurbaniOAOmid AmiriHHHaider Hamzah

Key Points

  • This research aims to develop a multifunctional Ni2CoS4 platform for treating drug-resistant infections and colorectal cancer via ROS generation.
  • Synthesis and optimization of hierarchical Ni₂CoS₄ structures via hydrothermal methods.
  • Characterization by XRD, SEM, and TEM to evaluate morphology and crystallinity.
  • Assessment of piezocatalytic performance in methylene blue degradation.
  • Evaluation of antibacterial activity against MDR Staphylococcus aureus and XDR Pseudomonas aeruginosa.
  • Testing cytotoxic effects in colorectal cancer HCT-116 models.
  • N3 structure achieved 88.57% methylene blue removal within 4 minutes under ultrasonication.
  • Demonstrated antibacterial activity with MIC as low as 5 µg/mL and complete bacterial clearance within 48 hours.
  • Induced dose-dependent cytotoxicity with 91% cell death in HCT-116 cells at LC₅₀ concentration.

Abstract

The global rise of multidrug-resistant infections and cancer underscores the need for multifunctional therapeutic platforms. This study presents the synthesis, optimization, and biomedical assessment of sonicated hierarchical Ni₂CoS₄ structures, with sample N3 identified as optimal among seven hydrothermally synthesized formulations. N3 exhibited uniform morphology, high crystallinity, and redox-active architecture, as confirmed by XRD, SEM, TEM, and BET (8.19 m²/g). Piezocatalytic performance, assessed via methylene blue degradation, showed 88.57% removal within 4 min under 200 W ultrasonication, alongside a 13.27-fold increase in singlet oxygen and superoxide generation. N3 displayed potent antibacterial activity against MDR Staphylococcus aureus and XDR Pseudomonas aeruginosa, with minimum inhibitory concentrations as low as 5 µg/mL and complete bacterial clearance within 48 h. ROS-mediated membrane disruption and > 99% biofilm eradication were confirmed by DiBAC₄(3), TEM, and comparative assays with non-sonicated controls. In colorectal cancer (HCT-116) models, N3 induced dose-dependent cytotoxicity (IC₅₀ = 100 µg/mL; 91% cell death at LC₅₀) with sustained effects over 96 h. These findings position N3 as a promising ROS-generating platform with dual antimicrobial and anticancer efficacy.

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Cite This Study

Qurbani et al. (2026) studied this question.

synapsesocial.com/papers/699f95841bc9fecf3dab34c7https://doi.org/10.1038/s41598-026-41092-3
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