4.6 Article

Enhanced Cytotoxic Effect of Doxorubicin Conjugated to Glutathione-Stabilized Gold Nanoparticles in Canine Osteosarcoma-In Vitro Studies

Journal

MOLECULES
Volume 26, Issue 12, Pages -

Publisher

MDPI
DOI: 10.3390/molecules26123487

Keywords

dogs; doxorubicin; flow cytometry; gold; humans; nanoparticles; osteosarcoma; P-glycoprotein

Funding

  1. Warsaw University of Life Sciences [505-10-023500-N00161-99, 505-10-023500-P00372-99, 505-10-023500-M00249-99]
  2. Ministry of Science and Higher Education [SPUB 505-30-023500-Q00454-99]

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The study showed that the combination of Doxorubicin with gold nanoparticles enhanced cytotoxicity in canine Osteosarcoma cells, bypassing multidrug resistance.
Osteosarcoma (OSA) is the most common malignant bone neoplasia in humans and dogs. In dogs, treatment consists of surgery in combination with chemotherapy (mostly carboplatin and/or doxorubicin (Dox)). Chemotherapy is often rendered ineffective by multidrug resistance. Previous studies have revealed that Dox conjugated with 4 nm glutathione-stabilized gold nanoparticles (Au-GSH-Dox) enhanced the anti-tumor activity and cytotoxicity of Dox in Dox-resistant feline fibrosarcoma cell lines exhibiting high P-glycoprotein (P-gp) activity. The present study investigated the influence of Au-GSH-Dox on the canine OSA cell line D17 and its relationship with P-gp activity. A human Dox-sensitive OSA cell line, U2OS, served as the negative control. Au-GSH-Dox, compared to free Dox, presented a greater cytotoxic effect on D17 (IC50 values for Au-GSH-Dox and Dox were 7.9 mu g/mL and 15.2 mu g/mL, respectively) but not on the U2OS cell line. All concentrations of Au-GSH (ranging from 10 to 1000 mu g/mL) were non-toxic in both cell lines. Inhibition of the D17 cell line with 100 mu M verapamil resulted in an increase in free Dox but not in intracellular Au-GSH-Dox. The results indicate that Au-GSH-Dox may act as an effective drug in canine OSA by bypassing P-gp.

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