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Polyethyleneimine-modified calcium carbonate nanoparticles for p53 gene delivery
In this study, calcium carbonate (CaCO(3)) nanoparticles with spherical structure were regulated by arginine and successfully synthesized via a facile co-precipitation method. The average particle size of as-prepared CaCO(3) was about 900 nm. The properties of nanostructured CaCO(3) particles were c...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4723273/ https://www.ncbi.nlm.nih.gov/pubmed/26816656 http://dx.doi.org/10.1093/rb/rbv029 |
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author | Chen, Cen Han, Huafeng Yang, Wei Ren, Xiaoyuan Kong, Xiangdong |
author_facet | Chen, Cen Han, Huafeng Yang, Wei Ren, Xiaoyuan Kong, Xiangdong |
author_sort | Chen, Cen |
collection | PubMed |
description | In this study, calcium carbonate (CaCO(3)) nanoparticles with spherical structure were regulated by arginine and successfully synthesized via a facile co-precipitation method. The average particle size of as-prepared CaCO(3) was about 900 nm. The properties of nanostructured CaCO(3) particles were characterized by scanning electron microscope, Fourier transform infrared spectroscopy, X-ray diffraction and size distribution. After modified with polyethyleneimine (PEI), the ability of PEI-CaCO(3) nanoparticles to carry GFP-marked p53 gene (pEGFP-C1-p53) into cancer cells to express P53 protein were studied. Meanwhile, the cytotoxicity, transfection efficiency, cells growth inhibition and the ability to induce apoptosis by expressed P53 protein were conducted to evaluate the performances of PEI-CaCO(3) nanoparticles. The results show that prepared PEI-CaCO(3) nanoparticles had good biocompatibility and low cytotoxicity in a certain concentration range. PEI-CaCO(3) effectively transfected pEGFP-C1 gene into epithelial-like cancer cells. And with the expression of GFP-P53 fusion protein, pEGFP-C1-p53-gene-loaded PEI-CaCO(3) particles significantly reduced the proliferation of cancer cells. These findings indicate that our PEI-modified CaCO(3) nanoparticles are potential to be successfully used as carriers for gene therapy. |
format | Online Article Text |
id | pubmed-4723273 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-47232732016-01-26 Polyethyleneimine-modified calcium carbonate nanoparticles for p53 gene delivery Chen, Cen Han, Huafeng Yang, Wei Ren, Xiaoyuan Kong, Xiangdong Regen Biomater Research Articles In this study, calcium carbonate (CaCO(3)) nanoparticles with spherical structure were regulated by arginine and successfully synthesized via a facile co-precipitation method. The average particle size of as-prepared CaCO(3) was about 900 nm. The properties of nanostructured CaCO(3) particles were characterized by scanning electron microscope, Fourier transform infrared spectroscopy, X-ray diffraction and size distribution. After modified with polyethyleneimine (PEI), the ability of PEI-CaCO(3) nanoparticles to carry GFP-marked p53 gene (pEGFP-C1-p53) into cancer cells to express P53 protein were studied. Meanwhile, the cytotoxicity, transfection efficiency, cells growth inhibition and the ability to induce apoptosis by expressed P53 protein were conducted to evaluate the performances of PEI-CaCO(3) nanoparticles. The results show that prepared PEI-CaCO(3) nanoparticles had good biocompatibility and low cytotoxicity in a certain concentration range. PEI-CaCO(3) effectively transfected pEGFP-C1 gene into epithelial-like cancer cells. And with the expression of GFP-P53 fusion protein, pEGFP-C1-p53-gene-loaded PEI-CaCO(3) particles significantly reduced the proliferation of cancer cells. These findings indicate that our PEI-modified CaCO(3) nanoparticles are potential to be successfully used as carriers for gene therapy. Oxford University Press 2016-03 2016-01-13 /pmc/articles/PMC4723273/ /pubmed/26816656 http://dx.doi.org/10.1093/rb/rbv029 Text en © The Author(s) 2016. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial reuse, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Research Articles Chen, Cen Han, Huafeng Yang, Wei Ren, Xiaoyuan Kong, Xiangdong Polyethyleneimine-modified calcium carbonate nanoparticles for p53 gene delivery |
title | Polyethyleneimine-modified calcium carbonate nanoparticles for p53 gene delivery |
title_full | Polyethyleneimine-modified calcium carbonate nanoparticles for p53 gene delivery |
title_fullStr | Polyethyleneimine-modified calcium carbonate nanoparticles for p53 gene delivery |
title_full_unstemmed | Polyethyleneimine-modified calcium carbonate nanoparticles for p53 gene delivery |
title_short | Polyethyleneimine-modified calcium carbonate nanoparticles for p53 gene delivery |
title_sort | polyethyleneimine-modified calcium carbonate nanoparticles for p53 gene delivery |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4723273/ https://www.ncbi.nlm.nih.gov/pubmed/26816656 http://dx.doi.org/10.1093/rb/rbv029 |
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