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In Vitro Toxicity Study of a Porous Iron(III) Metal‒Organic Framework
A MIL series metal‒organic framework (MOF), MIL-100(Fe), was successfully synthesized at the nanoscale and fully characterized by TEM, TGA, XRD, FTIR, DLS, and BET. A toxicological assessment was performed using two different cell lines: human normal liver cells (HL-7702) and hepatocellular carcinom...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6480057/ https://www.ncbi.nlm.nih.gov/pubmed/30925694 http://dx.doi.org/10.3390/molecules24071211 |
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author | Chen, Gongsen Leng, Xin Luo, Juyuan You, Longtai Qu, Changhai Dong, Xiaoxv Huang, Hongliang Yin, Xingbin Ni, Jian |
author_facet | Chen, Gongsen Leng, Xin Luo, Juyuan You, Longtai Qu, Changhai Dong, Xiaoxv Huang, Hongliang Yin, Xingbin Ni, Jian |
author_sort | Chen, Gongsen |
collection | PubMed |
description | A MIL series metal‒organic framework (MOF), MIL-100(Fe), was successfully synthesized at the nanoscale and fully characterized by TEM, TGA, XRD, FTIR, DLS, and BET. A toxicological assessment was performed using two different cell lines: human normal liver cells (HL-7702) and hepatocellular carcinoma (HepG2). In vitro cytotoxicity of MIL-100(Fe) was evaluated by the MTT assay, LDH releasing rate assay, DAPI staining, and annexin V/PI double staining assay. The safe dose of MIL-100(Fe) was 80 μg/mL. It exhibited good biocompatibility, low cytotoxicity, and high cell survival rate (HL-7702 cells’ viability >85.97%, HepG2 cells’ viability >91.20%). Therefore, MIL-100(Fe) has a potential application as a drug carrier. |
format | Online Article Text |
id | pubmed-6480057 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64800572019-04-30 In Vitro Toxicity Study of a Porous Iron(III) Metal‒Organic Framework Chen, Gongsen Leng, Xin Luo, Juyuan You, Longtai Qu, Changhai Dong, Xiaoxv Huang, Hongliang Yin, Xingbin Ni, Jian Molecules Article A MIL series metal‒organic framework (MOF), MIL-100(Fe), was successfully synthesized at the nanoscale and fully characterized by TEM, TGA, XRD, FTIR, DLS, and BET. A toxicological assessment was performed using two different cell lines: human normal liver cells (HL-7702) and hepatocellular carcinoma (HepG2). In vitro cytotoxicity of MIL-100(Fe) was evaluated by the MTT assay, LDH releasing rate assay, DAPI staining, and annexin V/PI double staining assay. The safe dose of MIL-100(Fe) was 80 μg/mL. It exhibited good biocompatibility, low cytotoxicity, and high cell survival rate (HL-7702 cells’ viability >85.97%, HepG2 cells’ viability >91.20%). Therefore, MIL-100(Fe) has a potential application as a drug carrier. MDPI 2019-03-28 /pmc/articles/PMC6480057/ /pubmed/30925694 http://dx.doi.org/10.3390/molecules24071211 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Chen, Gongsen Leng, Xin Luo, Juyuan You, Longtai Qu, Changhai Dong, Xiaoxv Huang, Hongliang Yin, Xingbin Ni, Jian In Vitro Toxicity Study of a Porous Iron(III) Metal‒Organic Framework |
title | In Vitro Toxicity Study of a Porous Iron(III) Metal‒Organic Framework |
title_full | In Vitro Toxicity Study of a Porous Iron(III) Metal‒Organic Framework |
title_fullStr | In Vitro Toxicity Study of a Porous Iron(III) Metal‒Organic Framework |
title_full_unstemmed | In Vitro Toxicity Study of a Porous Iron(III) Metal‒Organic Framework |
title_short | In Vitro Toxicity Study of a Porous Iron(III) Metal‒Organic Framework |
title_sort | in vitro toxicity study of a porous iron(iii) metal‒organic framework |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6480057/ https://www.ncbi.nlm.nih.gov/pubmed/30925694 http://dx.doi.org/10.3390/molecules24071211 |
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