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Magnetic transfection with superparamagnetic chitosan-loaded IGFBP(5) nanoparticles and their in vitro biosafety
We prepared the superparamagnetic chitosan nanoparticles (SPCIONPs) to study the application of them as gene vectors using a magnetic transfection system for the targeted treatment of lung metastasis of osteosarcoma. The SPCIONPs were characterized by transmission electron microscopy, Fourier transf...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7890493/ https://www.ncbi.nlm.nih.gov/pubmed/33614075 http://dx.doi.org/10.1098/rsos.201331 |
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author | Tang, Yue Wu, Jun Zhang, Yuan Ju, Lingpeng Qu, Xiangyang Jiang, Dianming |
author_facet | Tang, Yue Wu, Jun Zhang, Yuan Ju, Lingpeng Qu, Xiangyang Jiang, Dianming |
author_sort | Tang, Yue |
collection | PubMed |
description | We prepared the superparamagnetic chitosan nanoparticles (SPCIONPs) to study the application of them as gene vectors using a magnetic transfection system for the targeted treatment of lung metastasis of osteosarcoma. The SPCIONPs were characterized by transmission electron microscopy, Fourier transform infrared spectrometry, superconducting quantum interference device and atomic force microscopy. Their biosafety was determined by cell counting kit-8 (CCK8) and live–dead staining assays. The transfection in vitro was detected by laser confocal microscopy. SPCIONPs, which can bind closely to plasmids and protect them from DNA enzyme degradation, were prepared with an average particle size of approximately 22 nm and zeta potential of 11.3 mV. The results of the CCK8 and live–dead staining assays showed that superparamagnetic chitosan nanoparticles loaded with insulin-like growth factor-binding protein 5 (SPCIONPs/pIGFBP(5)) induced no significant cytotoxicity compared to the control group. The result of transfection in vitro suggested that pIGFBP(5) emitted a greater amount of red fluorescence in the SPCIONPs/pIGFBP(5) group than that in the chitosan-loaded IGFBP(5) (CS/pIGFBP(5)) group. In conclusion, the prepared SPCIONPs had good biosafety and could be effectively used to transfer pIGFBP(5) into 143B cells, and they thus have good application prospects for the treatment of lung metastasis of osteosarcoma. |
format | Online Article Text |
id | pubmed-7890493 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-78904932021-02-18 Magnetic transfection with superparamagnetic chitosan-loaded IGFBP(5) nanoparticles and their in vitro biosafety Tang, Yue Wu, Jun Zhang, Yuan Ju, Lingpeng Qu, Xiangyang Jiang, Dianming R Soc Open Sci Chemistry We prepared the superparamagnetic chitosan nanoparticles (SPCIONPs) to study the application of them as gene vectors using a magnetic transfection system for the targeted treatment of lung metastasis of osteosarcoma. The SPCIONPs were characterized by transmission electron microscopy, Fourier transform infrared spectrometry, superconducting quantum interference device and atomic force microscopy. Their biosafety was determined by cell counting kit-8 (CCK8) and live–dead staining assays. The transfection in vitro was detected by laser confocal microscopy. SPCIONPs, which can bind closely to plasmids and protect them from DNA enzyme degradation, were prepared with an average particle size of approximately 22 nm and zeta potential of 11.3 mV. The results of the CCK8 and live–dead staining assays showed that superparamagnetic chitosan nanoparticles loaded with insulin-like growth factor-binding protein 5 (SPCIONPs/pIGFBP(5)) induced no significant cytotoxicity compared to the control group. The result of transfection in vitro suggested that pIGFBP(5) emitted a greater amount of red fluorescence in the SPCIONPs/pIGFBP(5) group than that in the chitosan-loaded IGFBP(5) (CS/pIGFBP(5)) group. In conclusion, the prepared SPCIONPs had good biosafety and could be effectively used to transfer pIGFBP(5) into 143B cells, and they thus have good application prospects for the treatment of lung metastasis of osteosarcoma. The Royal Society 2021-01-13 /pmc/articles/PMC7890493/ /pubmed/33614075 http://dx.doi.org/10.1098/rsos.201331 Text en © 2021 The Authors. http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/http://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Chemistry Tang, Yue Wu, Jun Zhang, Yuan Ju, Lingpeng Qu, Xiangyang Jiang, Dianming Magnetic transfection with superparamagnetic chitosan-loaded IGFBP(5) nanoparticles and their in vitro biosafety |
title | Magnetic transfection with superparamagnetic chitosan-loaded IGFBP(5) nanoparticles and their in vitro biosafety |
title_full | Magnetic transfection with superparamagnetic chitosan-loaded IGFBP(5) nanoparticles and their in vitro biosafety |
title_fullStr | Magnetic transfection with superparamagnetic chitosan-loaded IGFBP(5) nanoparticles and their in vitro biosafety |
title_full_unstemmed | Magnetic transfection with superparamagnetic chitosan-loaded IGFBP(5) nanoparticles and their in vitro biosafety |
title_short | Magnetic transfection with superparamagnetic chitosan-loaded IGFBP(5) nanoparticles and their in vitro biosafety |
title_sort | magnetic transfection with superparamagnetic chitosan-loaded igfbp(5) nanoparticles and their in vitro biosafety |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7890493/ https://www.ncbi.nlm.nih.gov/pubmed/33614075 http://dx.doi.org/10.1098/rsos.201331 |
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