Beetroot extract@chitosan nanocomposite as a promising approach towards cancer therapy

The exceptional antioxidant properties of beetroot (BR) and the cancer antiproliferative effects of chitosan nanoparticles (CS NP) have led to the synthesis of a BR@CS nanocomposite (NC) in this study. The novel BR@CS NC was applied to human epithelial colorectal adenocarcinoma (Caco-2), human epith...

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Veröffentlicht in:International journal of biological macromolecules 2024-03, Vol.261 (Pt 1), p.129700-129700, Article 129700
Hauptverfasser: El-ghannam, Gamal, Moawad, Mahmoud, Abo-Elfadl, Mahmoud T., Elfeky, Souad A.
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Sprache:eng
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Zusammenfassung:The exceptional antioxidant properties of beetroot (BR) and the cancer antiproliferative effects of chitosan nanoparticles (CS NP) have led to the synthesis of a BR@CS nanocomposite (NC) in this study. The novel BR@CS NC was applied to human epithelial colorectal adenocarcinoma (Caco-2), human epithelial ductal breast carcinoma (T-47D), and human epithelial lung carcinoma (A549) cells. SEM characterization of CS NP revealed a variety of particle shapes ranging from 20 to 58 nm in diameter. UV-VIS analysis confirmed the formation of the BR@CS NC, while FTIR analysis demonstrated strong hydrogen bonds between CS NP and BR. These bonds reduced the positive surface charge of CS NP, as indicated by zeta potential analysis. When applied to cancer cell lines at a concentration of 250 μg/mL, the BR@CS NC successfully eradicated 89 % of A549, 88 % of T-47D, and 83 % of Caco-2 cell lines. The cell death mode exhibited extensive, apoptotic, and massive necrotic changes in all cell lines treated with BR@CS NC. Caspase 3 (CasP3) and P53 levels were elevated in BR@CS NC-treated cells. This study merges BR's antioxidant and anti-inflammatory properties with the antiangiogenic mechanism and inhibition of tumors by CS NP, resulting in a unique and innovative strategy for cancer treatment. •Merging the anticancer assets of CS NP and BR created a novel cancer therapy.•BR@CS NC (250 μg/mL) eradicated 89 % of A549, 88 % of T-47D, and 83 % of Caco-2.•Levels of CasP3 and P53 were promoted in all BR@CS NC-treated cells.•BR@CS NC and CS NPs cells uptake shows selectivity towards mucus cells.•BR@CS NC treated cells showed extensive apoptotic and necrotic changes.
ISSN:0141-8130
1879-0003
DOI:10.1016/j.ijbiomac.2024.129700