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Preparation of hierarchical mesoporous CaCO(3) by a facile binary solvent approach as anticancer drug carrier for etoposide
To develop a nontoxic system for targeting therapy, a new highly ordered hierarchical mesoporous calcium carbonate nanospheres (CCNSs) as small drug carriers has been synthesized by a mild and facile binary solvent approach under the normal temperature and pressure. The hierarchical structure by mul...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3716939/ https://www.ncbi.nlm.nih.gov/pubmed/23849350 http://dx.doi.org/10.1186/1556-276X-8-321 |
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author | Peng, Haibao Li, Kun Wang, Ting Wang, Jin Wang, Jiao Zhu, Rongrong Sun, Dongmei Wang, Shilong |
author_facet | Peng, Haibao Li, Kun Wang, Ting Wang, Jin Wang, Jiao Zhu, Rongrong Sun, Dongmei Wang, Shilong |
author_sort | Peng, Haibao |
collection | PubMed |
description | To develop a nontoxic system for targeting therapy, a new highly ordered hierarchical mesoporous calcium carbonate nanospheres (CCNSs) as small drug carriers has been synthesized by a mild and facile binary solvent approach under the normal temperature and pressure. The hierarchical structure by multistage self-assembled strategy was confirmed by TEM and SEM, and a possible formation process was proposed. Due to the large fraction of voids inside the nanospheres which provides space for physical absorption, the CCNSs can stably encapsulate the anticancer drug etoposide with the drug loading efficiency as high as 39.7 wt.%, and etoposide-loaded CCNS (ECCNS) nanoparticles can dispersed well in the cell culture. Besides, the drug release behavior investigated at three different pH values showed that the release of etoposide from CCNSs was pH-sensitive. MTT assay showed that compared with free etoposide, ECCNSs exhibited a higher cell inhibition ratio against SGC-7901 cells and also decreased the toxicity of etoposide to HEK 293 T cells. The CLSM image showed that ECCNSs exhibited a high efficiency of intracellular delivery, especially in nuclear invasion. The apoptosis test revealed that etoposide entrapped in CCNSs could enhance the delivery efficiencies of drug to achieve an improved inhibition effect on cell growth. These results clearly implied that the CCNSs are a promising drug delivery system for etoposide in cancer therapy. |
format | Online Article Text |
id | pubmed-3716939 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Springer |
record_format | MEDLINE/PubMed |
spelling | pubmed-37169392013-07-22 Preparation of hierarchical mesoporous CaCO(3) by a facile binary solvent approach as anticancer drug carrier for etoposide Peng, Haibao Li, Kun Wang, Ting Wang, Jin Wang, Jiao Zhu, Rongrong Sun, Dongmei Wang, Shilong Nanoscale Res Lett Nano Express To develop a nontoxic system for targeting therapy, a new highly ordered hierarchical mesoporous calcium carbonate nanospheres (CCNSs) as small drug carriers has been synthesized by a mild and facile binary solvent approach under the normal temperature and pressure. The hierarchical structure by multistage self-assembled strategy was confirmed by TEM and SEM, and a possible formation process was proposed. Due to the large fraction of voids inside the nanospheres which provides space for physical absorption, the CCNSs can stably encapsulate the anticancer drug etoposide with the drug loading efficiency as high as 39.7 wt.%, and etoposide-loaded CCNS (ECCNS) nanoparticles can dispersed well in the cell culture. Besides, the drug release behavior investigated at three different pH values showed that the release of etoposide from CCNSs was pH-sensitive. MTT assay showed that compared with free etoposide, ECCNSs exhibited a higher cell inhibition ratio against SGC-7901 cells and also decreased the toxicity of etoposide to HEK 293 T cells. The CLSM image showed that ECCNSs exhibited a high efficiency of intracellular delivery, especially in nuclear invasion. The apoptosis test revealed that etoposide entrapped in CCNSs could enhance the delivery efficiencies of drug to achieve an improved inhibition effect on cell growth. These results clearly implied that the CCNSs are a promising drug delivery system for etoposide in cancer therapy. Springer 2013-07-15 /pmc/articles/PMC3716939/ /pubmed/23849350 http://dx.doi.org/10.1186/1556-276X-8-321 Text en Copyright ©2013 Peng et al.; licensee Springer. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Nano Express Peng, Haibao Li, Kun Wang, Ting Wang, Jin Wang, Jiao Zhu, Rongrong Sun, Dongmei Wang, Shilong Preparation of hierarchical mesoporous CaCO(3) by a facile binary solvent approach as anticancer drug carrier for etoposide |
title | Preparation of hierarchical mesoporous CaCO(3) by a facile binary solvent approach as anticancer drug carrier for etoposide |
title_full | Preparation of hierarchical mesoporous CaCO(3) by a facile binary solvent approach as anticancer drug carrier for etoposide |
title_fullStr | Preparation of hierarchical mesoporous CaCO(3) by a facile binary solvent approach as anticancer drug carrier for etoposide |
title_full_unstemmed | Preparation of hierarchical mesoporous CaCO(3) by a facile binary solvent approach as anticancer drug carrier for etoposide |
title_short | Preparation of hierarchical mesoporous CaCO(3) by a facile binary solvent approach as anticancer drug carrier for etoposide |
title_sort | preparation of hierarchical mesoporous caco(3) by a facile binary solvent approach as anticancer drug carrier for etoposide |
topic | Nano Express |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3716939/ https://www.ncbi.nlm.nih.gov/pubmed/23849350 http://dx.doi.org/10.1186/1556-276X-8-321 |
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