Targeted Delivery of Polyclustered-SPION Labeled Mesenchymal Stem Cells in Ototoxic Hearing Loss Mouse Model

Abstract

Abstract Background Highly specialized cells with self-renewal and differentiation potentials are known to as stem cells. These cells can keep their stemness or develop into more specialized cells. Mesenchymal stem cell (MSC)-based cell treatment has caught researchers' interest due to its lack of ethical problems, simplicity of isolation, and abundance. The use of stem cell treatment in regenerative medicine has recently been a subject of great interest. In vitro and in vivo, MSCs have been shown to have anti-inflammatory and immunomodulatory properties. The ability of MSCs to decrease T-cell proliferation and reduce T-cell functioning is responsible for their potent immunosuppressive effects. They possess potential to home to injury site and stimulate indigenous cells to repair and rebuild it, despite their homing ability delivering the stem cell to the anatomically complex area such as inner is still remains as challenge. Studies on enhancing the delivery of stem cells has been emerging. Method The Superparamagnetic iron oxide nanoparticles (SPION) with an iron oxide-based nanoparticle cluster core covered with PLGA-Cy5.5 has been developed. To allow PCS nanoparticles to be transported into MSCs by endocytosis, we modified the nanoparticles for internalization. Nanoparticle labeled mesenchymal stem cells are administered in ototoxic mouse model with or without magnetic field. Results As an outcome, when compared to the control groups, the intratympanic administration with magnet group had the most cells in the brain, followed by the liver, cochlea, and kidney. The magnetic interaction between the produced PCS (poly clustered superparamagnetic iron oxide) nanoparticles and MSCs may increase stem cell delivery effectively. In a variety of experimental models examining cell responsiveness in vitro and in situ, the potential use of SPION to increase the spatial control of stem cells by the application of magnetic fields was examined. The application of the magnetic field has significantly increased the number of cells that migrate toward the area of magnet application in vitro. However, in in vivo settings the quantification of the effect of magnetic field was yet solved. Conclusion The visualization of delivered MSCs, as well as quantitative and qualitative analysis of the processes, will contribute in the formulation of an assessment system for a powerful delivery system in the inner ear, which will aid in the treatment of hearing loss