Author/Authors :
Ebrahimian, Mahboubeh Nanotechnology Research Center - Pharmaceutical Technology Institute - Mashhad University of Medical Sciences, Mashhad, Iran , Shahgordi, Sanaz Department of Immunology - School of Medicine - Golestan University of Medical Sciences, Gorgan, Iran , Yazdian-Robati, Rezvan Molecular and Cell Biology Research Center - Faculty of Medicine - Mazandaran University of Medical Sciences, Sari, Iran , Etemad, Leila Pharmaceutical Research Center - Pharmaceutical Technology Institute - Mashhad University of Medical Sciences, Mashhad, Iran , Hashemi, Maryam Department of Pharmaceutical Biotechnology - School of Pharmacy - Mashhad University of Medical Sciences, Mashhad, Iran , Salmasi, Zahra Department of Pharmaceutical Nanotechnology - School of Pharmacy - Mashhad University of Medical Sciences, Mashhad, Iran
Abstract :
Objective: The aim of this study was to investigate the efficacy of mesenchyme stem cells (MSCs) derived from human adipose tissue (hMSCs) as carriers for delivery of galbanic acid (GBA), a potential anticancer agent, loaded into poly (lactic-co-glycolic acid) (PLGA) nanoparticles (nano-engineered hMSCs) against tumor cells.
Materials and Methods: GBA-loaded PLGA nanoparticles (PLGA/GBA) were prepared by single emulsion method and their physicochemical properties were evaluated. Then, PLGA/GBA nanoparticles were incorporated into hMSCs (hMSC/PLGA-GBA) and their migration ability and cytotoxicity against colon cancer cells were investigated.
Results: The loading efficiency of PLGA/GBA nanoparticles with average size of 214±30.5 nm into hMSCs, was about 85 and 92% at GBA concentration of 20 and 40 μM, respectively. Nano-engineered hMSCs showed significant higher migration to cancer cells (C26) compared to normal cells (NIH/3T3). Furthermore, nano-engineered hMSCs could effectively induce cell death in C26 cells in comparison with non-engineered hMSCs.
Conclusion: hMSCs could be implemented for efficient loading of PLGA/GBA nanoparticles to produce a targeted cellular carrier against cancer cells. Thus, according to minimal toxicity on normal cells, it deserves to be considered as a valuable platform for drug delivery in cancer therapy.
Keywords :
Nano-engineered mesenchymal , stem cells , Targeted delivery , Cellular carrier , Galbanic acid , PLGA , Cancer