Magnetite nanoparticles: an emerging adjunctive tool for the improvement of cancer immunotherapy.

Cancer immunotherapy has emerged as a groundbreaking field, offering promising and transformative tools for oncological research and treatment. However, it faces several limitations, including variations in cancer types, dependence on the tumor microenvironments (TMEs), immune cell exhaustion, and adverse reactions. Magnetic nanoparticles, particularly magnetite nanoparticles (MNPs), with established pharmacodynamics and pharmacokinetics for clinical use, hold great promise in this context and are now being explored for therapeutic aims. Numerous preclinical studies have illustrated their efficacy in enhancing immunotherapy through various strategies, such as modulating leukocyte functions, creating favorable TMEs for cytotoxic T lymphocytes, combining with monoclonal antibodies, and stimulating the immune response via magnetic hyperthermia (MHT) treatment (Front Immunol. 2021;12:701485. doi: 10.3389/fimmu.2021.701485). However, the current clinical trials of MNPs are mostly for diagnostic aims and as a tool for generating hyperthermia for tumor ablation. With concerns about the adverse effects of MNPs in the in vivo systems, clinical translation and clinical study of MNP-boosted immunotherapy remains limited. The lack of extensive clinical investigations poses a current barrier to patient application. Urgent efforts are needed to ascertain both the efficacy of MNP-enhanced immunotherapy and its safety profile in combination therapy. This article reviews the roles, potential, and challenges of using MNPs in advancing cancer immunotherapy. The application of MNPs in boosting immunotherapy, and its perspective role in research and development is also discussed.

Copper and chromium removal from industrial sludge by a biosurfactant-based washing agent and subsequent recovery by iron oxide nanoparticles.

Industrial wastewater treatment generates sludge with high concentrations of metals and coagulants, which can cause environmental problems. This study developed a sequential sludge washing and metal recovery process for industrial sludge containing > 4500 mg/kg Cu and > 5000 mg/kg Cr. The washing agent was formulated by mixing glycolipid, lipopeptide, and phospholipid biosurfactants from Weissella cibaria PN3 and Brevibacterium casei NK8 with a chelating agent, ethylenediaminetetraacetic acid (EDTA). These biosurfactants contained various functional groups for capturing metals. The optimized formulation by the central composite design had low surface tension and contained relatively small micelles. Comparable Cu and Cr removal efficiencies of 37.8% and 38.4%, respectively, were obtained after washing the sludge by shaking with a sonication process at a 1:4 solid-to-liquid ratio. The zeta potential analysis indicated the bonding of metal ions on the surface of biosurfactant micelles. When 100 g/L iron oxide nanoparticles were applied to the washing agent without pH adjustment, 83% Cu and 100% Cr were recovered. In addition, X-ray diffraction and X-ray absorption spectroscopy of the nanoparticles showed the oxidation of nanoparticles, the reduction of Cr(V) to the less toxic Cr(III), and the absorption of Cu. The recovered metals could be further recycled, which will be beneficial for the circular economy.

Influence of organic ligands on the stoichiometry of magnetite nanoparticles.

Magnetite, a ubiquitous mineral in natural systems, is of high interest for a variety of applications including environmental remediation, medicine, and catalysis. If the transformation of magnetite to maghemite through the oxidation of Fe2+ has been well documented, mechanisms involving dissolution processes of Fe2+ in aqueous solutions have been overlooked. Here, the effect of dissolved organic ligands (EDTA (ethylenediaminetetraacetic acid), acetic, lactic and citric acids) on Fe2+ solubility and on the stoichiometry (Fe(ii)/Fe(iii)) of magnetite-maghemite nanoparticles (∼10 nm) was investigated. These ligands were chosen because of their environmental relevance and because they are widely used as coating agents for nanotechnology applications. Results show an insignificant effect of 2 organic ligands (acetate and lactate) on the dissolution of Fe. By contrast, citrate and EDTA enhanced Fe solubility because of the formation of dissolved Fe(ii)- and Fe(iii)-ligand complexes. Both ligands selectively bound Fe(ii) over Fe(iii), but EDTA was much more selective than citrate. The combined effects of oxidation and H+- and ligand-promoted dissolution of Fe from magnetite were predicted using a magnetite-maghemite solid solution model, accounting for the formation of dissolved Fe(ii)- and Fe(iii)-ligand complexes. Therefore, these results show that citrate and EDTA (i) enhance Fe solubility in the presence of magnetite nanoparticles and (ii) modify magnetite stoichiometry, which affects its environmental behavior and its properties for nanotechnology applications.