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Targeted delivery of galbanic acid to colon cancer cells by PLGA nanoparticles incorporated into human mesenchymal stem cells

عنوان مقاله: Targeted delivery of galbanic acid to colon cancer cells by PLGA nanoparticles incorporated into human mesenchymal stem cells
شناسه ملی مقاله: JR_AJP-12-3_008
منتشر شده در در سال 1401
مشخصات نویسندگان مقاله:

Mahboubeh Ebrahimian - Nanotechnology Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran
Sanaz Shahgordi - Department of Immunology, School of Medicine, Golestan University of Medical Sciences, Gorgan, Iran
Rezvan Yazdian-Robati - Molecular and Cell Biology Research Center, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran
Leila Etemad - Pharmaceutical Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran
Maryam Hashemi - Department of Pharmaceutical Biotechnology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran
Zahra Salmasi - Department of Pharmaceutical Nanotechnology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran

خلاصه مقاله:
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 ۲۱۴±۳۰.۵ nm into hMSCs, was about ۸۵ and ۹۲% at GBA concentration of ۲۰ and ۴۰ μM, respectively. Nano-engineered hMSCs showed significant higher migration to cancer cells (C۲۶) compared to normal cells (NIH/۳T۳). Furthermore, nano-engineered hMSCs could effectively induce cell death in C۲۶ 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.

کلمات کلیدی:
Nano-engineered mesenchymal stem cells, targeted delivery, Cellular carrier, Galbanic acid, PLGA, Cancer

صفحه اختصاصی مقاله و دریافت فایل کامل: https://civilica.com/doc/1429116/