Demonstrates controlled ibuprofen release in breast cancer cells, indicating potential for targeted therapy.
Ibuprofen (IBU), a widely used nonsteroidal anti‐inflammatory drug, is therapeutically important but is limited by its poor aqueous solubility and bitter taste. Pectin, a natural biopolymer, has gained considerable attention for its biocompatibility and encapsulation efficiency, making it suitable for controlled drug delivery. In this study, we present a green synthesis route for magnetic iron oxide nanoparticles (Fe 3 O 4 NPs) using Opuntia humifusa fruit extract, which functions as both a reducing and stabilizing agent. The synthesized Fe 3 O 4 NPs were subsequently functionalized with pectin and loaded with ibuprofen to obtain Fe 3 O 4 @Pectin‐IBU nanocomposites (Fe 3 O 4 @Pectin‐IBU‐NPs). Comprehensive physicochemical characterization using spectroscopic and microscopic techniques confirmed the successful formation of the nanocomposites. Drug release studies demonstrated that up to 84.54 ± 2.45% of ibuprofen was released at pH 4.2 under an external magnetic field, indicating a magnetically responsive and pH‐sensitive release behavior. The Fe 3 O 4 @Pectin‐IBU‐NPs also exhibited notable cytotoxicity against MCF‐7 breast cancer cells (IC 50 = 92.7 µg/mL) and significant anti‐inflammatory activity (IC 50 = 25.10 µg/mL). Overall, these results underscore the potential of Fe 3 O 4 @Pectin‐IBU‐NPs as a promising nanoplatform for targeted drug delivery and breast cancer therapy, offering an eco‐friendly and effective alternative to conventional treatment strategies.
No takes yet. Share an insight, caveat, or question.
Sasikala et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: