Niosomes loading N-acetyl-L-cysteine for cancer treatment in vivo study

Ebtesam A Mohamad1,2, Abeer A Ali3, Marwa Sharaky4

  • 1Department of Biophysics, Faculty of Science, Cairo University, 12613, Giza, Egypt.

Insights

N-Acetyl-l-cysteine niosomes (NAC-NIO) show promise for tumor treatment by reducing DNA damage and increasing oxidative stress. Oral administration of NAC-NIO demonstrated significant anti-tumor effects in mice, suggesting a potential new therapeutic strategy.

Area of Science:

  • Biomedical Engineering
  • Nanotechnology
  • Pharmacology

Background:

  • Tumor treatment seeks effective, side-effect-free therapies.
  • N-Acetyl-l-cysteine (NAC), a garlic-derived thiol, is explored for therapeutic potential.
  • Niosomes offer a promising drug delivery system for enhanced therapeutic efficacy.

Purpose of the Study:

  • To evaluate N-Acetyl-l-cysteine-loaded niosomes (NAC-NIO) for tumor treatment in a mouse model.
  • To assess the physicochemical properties and in vivo efficacy of NAC-NIO.
  • To investigate the impact of NAC-NIO on tumor progression, DNA damage, oxidative stress, and apoptosis.

Main Methods:

  • Characterization of NAC-NIO (encapsulation efficiency, zeta potential, morphology, size, FTIR).
  • In vivo study involving BALB/c mice divided into control and treatment groups (NAC, NAC-NIO).
  • Evaluation of tumor size, comet assay, oxidative stress markers (GSH, nitric oxide, MDA), western blot (caspase 3 & 9), and histopathology.

Main Results:

  • NAC-NIO exhibited 72±3% encapsulation efficiency and a zeta potential of -5.95 mV, with a spherical shape.
  • Oral NAC-NIO (50 mg/kg) significantly protected against tumor cells, reducing DNA damage (P<0.05).
  • NAC-NIO upregulated caspase 3 and caspase 9 gene expression (P<0.001) and increased oxidative stress in tumor tissue, with histological studies confirming protective effects.

Conclusions:

  • Oral delivery of NAC-NIO formulation demonstrates significant anti-tumor activity in mice.
  • NAC-NIO effectively reduces DNA damage and induces apoptosis in tumor cells.
  • The developed NAC-NIO formulation represents a potential strategy for improved tumor treatment with enhanced antioxidant effects.

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