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

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 h...

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Autores principales: Ebrahimian, Mahboubeh, Shahgordi, Sanaz, Yazdian-Robati, Rezvan, Etemad, Leila, Hashemi, Maryam, Salmasi, Zahra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9482708/
https://www.ncbi.nlm.nih.gov/pubmed/36186932
http://dx.doi.org/10.22038/AJP.2022.20022
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author Ebrahimian, Mahboubeh
Shahgordi, Sanaz
Yazdian-Robati, Rezvan
Etemad, Leila
Hashemi, Maryam
Salmasi, Zahra
author_facet Ebrahimian, Mahboubeh
Shahgordi, Sanaz
Yazdian-Robati, Rezvan
Etemad, Leila
Hashemi, Maryam
Salmasi, Zahra
author_sort Ebrahimian, Mahboubeh
collection PubMed
description 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.
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spelling pubmed-94827082022-09-29 Targeted delivery of galbanic acid to colon cancer cells by PLGA nanoparticles incorporated into human mesenchymal stem cells Ebrahimian, Mahboubeh Shahgordi, Sanaz Yazdian-Robati, Rezvan Etemad, Leila Hashemi, Maryam Salmasi, Zahra Avicenna J Phytomed Original Research Article 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. Mashhad University of Medical Sciences 2022 /pmc/articles/PMC9482708/ /pubmed/36186932 http://dx.doi.org/10.22038/AJP.2022.20022 Text en https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research Article
Ebrahimian, Mahboubeh
Shahgordi, Sanaz
Yazdian-Robati, Rezvan
Etemad, Leila
Hashemi, Maryam
Salmasi, Zahra
Targeted delivery of galbanic acid to colon cancer cells by PLGA nanoparticles incorporated into human mesenchymal stem cells
title Targeted delivery of galbanic acid to colon cancer cells by PLGA nanoparticles incorporated into human mesenchymal stem cells
title_full Targeted delivery of galbanic acid to colon cancer cells by PLGA nanoparticles incorporated into human mesenchymal stem cells
title_fullStr Targeted delivery of galbanic acid to colon cancer cells by PLGA nanoparticles incorporated into human mesenchymal stem cells
title_full_unstemmed Targeted delivery of galbanic acid to colon cancer cells by PLGA nanoparticles incorporated into human mesenchymal stem cells
title_short Targeted delivery of galbanic acid to colon cancer cells by PLGA nanoparticles incorporated into human mesenchymal stem cells
title_sort targeted delivery of galbanic acid to colon cancer cells by plga nanoparticles incorporated into human mesenchymal stem cells
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9482708/
https://www.ncbi.nlm.nih.gov/pubmed/36186932
http://dx.doi.org/10.22038/AJP.2022.20022
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