The technology of directing nanoparticles to specific locations in the body continues to be an area of great interest in a myriad of research fields. In the present study, we have developed nanoparticles and a method that allows the nanoparticles to move to specific sites by simultaneously utilizing the homing ability and magnetism of stem cells. Polymeric clustered SPIO (PCS) nanoparticles are composed of a superparamagnetic iron oxide nanoparticle (SPION) cluster core coated with poly lactic-co-glycolic acid (PLGA) and labeled with the fluorescent dye Cy5.5 for tracking. PCS is designed to be internalized by stem cells via endocytosis and then moved to the desired subcellular location through magnetism. Here, we investigated the interactions between SPIONs and mesenchymal stem cells (MSCs), including their absorption mechanism and subcellular localization. Exposure to the nanoparticles at 40 μg/mL for over 96 h did not affect cell survival or differentiation. We used a variety of endocytosis inhibitors and identified the potential cellular internalization pathway of SPIONs to be clathrin-mediated endocytosis. Antibodies to organelles were used to accumulate lysosomes through early and late endosomes. PCS at 40 μg/mL was internalized and stored without significant deleterious effects on stem cells, indicating that MSCs can act as an effective nanoparticle carrier. These findings also demonstrate the successful localization of the novel particles using magnetic attraction.
|Number of pages||11|
|Journal||Journal of Controlled Release|
|Publication status||Published - 2020 Oct 10|
Bibliographical noteFunding Information:
This work was supported by the National Research Foundation of Korea grant funded by the Korea government (MSIT) [grant number 2019R1A6A3A01096651 ], [grant number NRF-2020R1A2C1009789 ] and [ 2018R1D1A1B07042339 and 2019K2A9A2A08000123 ].
© 2020 Elsevier B.V.
All Science Journal Classification (ASJC) codes
- Pharmaceutical Science