Copyright (c) 2025 Krishnaveni S, Parvathi K, Ayyanaar S

This work is licensed under a Creative Commons Attribution 4.0 International License.
ROS-Responsive Drug Release from Green Synthesized Silver Nanoparticles Loaded Saponin Nanoarchitectures for Targeted Cancer Therapy
Corresponding Author(s) : Kalyanasundaram Parvathi
Asian Journal of Chemistry,
Vol. 37 No. 12 (2025): Vol 37 Issue 12, 2025
Abstract
Curcumin (CUR), a bioactive polyphenol derived from turmeric, has gained attention in drug delivery systems due to its potent anti-inflammatory, antioxidant and anticancer properties. It can inhibit cancer cell proliferation, metastasis and angiogenesis, while also sensitizing tumor cells to chemotherapy and overcoming drug resistance making it a strong candidate as an adjuvant in cancer therapy. However, curcumin’s clinical translation is hindered by poor bioavailability and rapid metabolism. To address these challenges, a reactive oxygen species (ROS)-responsive nanoparticle system is developed based on green synthesized silver nanoparticles (AgNPs). The AgNPs were fabricated using Phyllanthus niruri leaves extract, serving as both a reducing and capping agent. These biogenic AgNPs were embedded in a saponin (SA) matrix chosen for its ROS-sensitivity due to lipid peroxidation at the double bonds further reinforced with starch and loaded with CUR, resulting in a multifunctional nanocomposite, Ag@SA-Starch-CUR-NPs. This platform leverages the tumor microenvironments acidic pH and elevated ROS levels to trigger targeted drug release. Saponin undergoes oxidative degradation in response to ROS, while starch enhances pH-sensitive CUR release under acidic conditions. The nanocomposites demonstrated high encapsulation efficiency (89.50%), pH and ROS-responsive release kinetics, particularly favouring drug release in tumor-like conditions. Physico-chemical characterization confirmed the composites thermal stability, spherical morphology and uniform elemental distribution. In vitro assays on MCF-7 breast cancer cell lines revealed potent cytotoxic activity (IC50 ≈ 19.5 ± 0.20 µg/mL), while anti-inflammatory testing showed significant activity (IC50 = 20.13 µg/mL), outperforming the standard formulations. Collectively, these findings highlight Ag@SA-Starch-CUR-NPs as a promising, biocompatible and environmentally friendly nanoplatform for targeted cancer therapy, offering improved drug delivery performance and therapeutic outcomes.
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