Publications by authors named "R Ivkov"

Nanoparticles can exert immune modulating effects in a host depending on composition, mode of administration, and type of disease. Although the specific mechanisms of nanoparticle-induced immune responses remain unclear, their uptake by macrophages and other phagocytic innate immune cells is considered to be a key event. Our objective here was to ascertain if nanoparticle-mediated activation of dendritic cells (DCs) occurs or when exposed to hydroxyethyl starch-coated iron oxide nanoparticles.

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Magnetic particle hyperthermia (MPH) enables the direct heating of solid tumors with alternating magnetic fields (AMFs). One challenge with MPH is the unknown particle distribution in tissue after injection. Magnetic particle imaging (MPI) can measure the nanoparticle content and distribution in tissue after delivery.

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Article Synopsis
  • - Systemic exposure to starch-coated iron oxide nanoparticles (IONPs) has been shown to enhance T cell responses against tumors in mouse models, leading to reduced tumor growth and increased survival, even without significant IONP retention in the tumors
  • - The research indicates that a single injection of IONPs can stimulate immune responses by activating specific pathways (like TLR pathways) that are essential for inhibiting tumor progression and metastases
  • - Analysis suggests that certain immune markers (TLR3 and IRF3) may be associated with better survival rates in breast cancer patients, pointing to the potential of IONP formulations as cancer therapies that work through immune modulation rather than direct tumor targeting
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Purpose: Magnetic particle hyperthermia is an approved cancer treatment that harnesses thermal energy generated by magnetic nanoparticles when they are exposed to an alternating magnetic field (AMF). Thermal stress is either directly cytotoxic or increases the susceptibility of cancer cells to standard therapies, such as radiation. As with other thermal therapies, the challenge with nanoparticle hyperthermia is controlling energy delivery.

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The dynamic nature of perfusion in living tissues, such as solid tumors during thermal therapy, produces challenging spatiotemporal thermal boundary conditions. Changes in perfusion can manifest as changes in convective heat transfer that influence temperature changes during cyclic heating. Herein, we propose a method to actively monitor changes in local convection (perfusion) in vivo by using a transient thermal pulsing analysis.

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