AAPS PharmSciTech, Journal Year: 2024, Volume and Issue: 25(8)
Published: Nov. 5, 2024
Language: Английский
AAPS PharmSciTech, Journal Year: 2024, Volume and Issue: 25(8)
Published: Nov. 5, 2024
Language: Английский
Journal of Molecular Liquids, Journal Year: 2024, Volume and Issue: 404, P. 124967 - 124967
Published: May 12, 2024
Language: Английский
Citations
4International Journal of Pharmaceutics, Journal Year: 2024, Volume and Issue: 662, P. 124293 - 124293
Published: May 31, 2024
Language: Английский
Citations
4Russian Journal of Organic Chemistry, Journal Year: 2025, Volume and Issue: 61(1), P. 162 - 170
Published: Jan. 1, 2025
Language: Английский
Citations
0Journal of Biomaterials Science Polymer Edition, Journal Year: 2025, Volume and Issue: unknown, P. 1 - 31
Published: May 6, 2025
This study investigates the synthesis, characterization and anticancer efficacy of nerolidol-loaded beta cyclodextrin polymeric nanoparticles (NER-βCD-NPs) against MCF-7 breast cancer cells. Nerolidol, a sesquiterpene with anti-inflammatory, antioxidant, antimicrobial properties, faces challenges poor solubility bioavailability, limiting its therapeutic potential. Breast cancer, leading cause cancer-related deaths in women, necessitates alternative therapies fewer side effects compared to conventional chemotherapy. NER-βCD-NPs were synthesized characterized using UV-visible spectroscopy, fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), dynamic light scattering (DLS), zeta potential analysis differential calorimetry (DSC). Drug encapsulation efficiency vitro release analyzed HPLC, while molecular docking assessed NER-βCD interactions. Characterization confirmed successful nanoparticle synthesis. spectra FTIR indicated encapsulation-specific changes, SEM revealed surface morphology, DLS, DSC analyses demonstrated increased size stability. The was 84.9%, 86% NER at pH 5.4 over 48 h. Docking studies supported strong binding between βCD (binding energy: -3.55 kcal/mol). Cytotoxicity assays showed significant cell inhibition. Mechanistic reactive oxygen species (ROS) generation, mitochondrial dysfunction, nuclear changes cycle arrest G0-G1 phase. Molecular apoptosis through upregulation Bax, Caspase 6, 9 Cytochrome c, alongside Bcl-2 downregulation. These results highlight as promising strategy for therapy, offering targeted delivery enhanced mitigating nerolidol limitations. Further are warranted validate their clinical applications.
Language: Английский
Citations
0International Journal of Biological Macromolecules, Journal Year: 2024, Volume and Issue: 282, P. 136600 - 136600
Published: Oct. 18, 2024
Language: Английский
Citations
1AAPS PharmSciTech, Journal Year: 2024, Volume and Issue: 25(8)
Published: Nov. 5, 2024
Language: Английский
Citations
0