Iron-oxide embemded lipid nanoparticles against ductal infiltration carcinoma as photodynamic therapy using red diode laser irradiation technique: Apoptosis , ferroptosis , EAC model

preprint OA: closed
View at publisher

Abstract

The purpose of the current study is to examine the effectiveness of folic acid-tagged, PLGA/PEGylated iron oxide nanoparticles in overcoming multidrug resistance when used in PDT therapy. The raw medicine and produced nanoparticles were analysed using techniques like FTIR, DSC, XRD, TGA, and Raman spectra. The nanoparticles were produced using the emulsion solvent evaporation method, and they were examined using AFM, SEM, TEM, DLS, in-vitro release, in-vitro cytotoxicity analysis (MTT-assay), cell cycle analysis, in-vitro morphological alterations (PDT), in-vivo research, and other methods.The results of pre-formulation experiments showed that the drug and polymer are compatible, and the nano-formulation makes sure that the drug is well enclosed within the polymer matrix. According to the morphological examination, the nanoparticles had bilayer covering and were round and spherical in shape. Due to their capacity to incorporate into membranes and then translocate into cells where they affect a variety of cellular processes like mitochondrial respiration, ATP synthesis, and activity of drug efflux transporters, MTT-assay results show that PF68-loaded nanoparticles have a higher inhibition rate than other types. Cell cycle analysis research shows that when concentration increases, apoptosis initially increases, and necrosis then increases as concentration increases. According to an in-vitro photodynamic study, nanoparticles treated with lasers cause more cell death than nanoformulations do in a dose- and time-dependent manner. PDT therapy has greater anticancer activity than GANPs, according to an animal study. Conclusion: When compared to polyvinyl alcohol (PVA) loaded nanoparticles, the drug formulated as a nanocarrier with PF68 may have greater bioavailability and anticancer activity. PDT has been used as a co-therapy to ensure that tumour cells undergo morphological changes and to accelerate the rate of cell death. Finally, it was predicted that in the future, it would be a highly effective and well-thought-out treatment for breast cancer.

My notes (saved in your browser only)

Citation neighborhood (no data yet)

We don't have any in-corpus citations linked to this paper yet. The paper's references may be in our DB but unresolved to ``paper_id`` (resolution happens at ingest when the cited DOI matches a row we already have). Run the cross-source citation reconcile pass to retry.

Source provenance

europepmc
last seen: 2026-05-19T01:45:01.086888+00:00