Cargando…
Preparation, Characterization, and In Vitro Release of Curcumin-Loaded IRMOF-10 Nanoparticles and Investigation of Their Pro-Apoptotic Effects on Human Hepatoma HepG2 Cells
Curcumin (CUR) has a bright future in the treatment of cancer as a natural active ingredient with great potential. However, curcumin has a low solubility, which limits its clinical application. In this study, IRMOF-10 was created by the direct addition of triethylamine, CUR was loaded into IRMOF-10...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9228752/ https://www.ncbi.nlm.nih.gov/pubmed/35745062 http://dx.doi.org/10.3390/molecules27123940 |
_version_ | 1784734558122409984 |
---|---|
author | Yin, Dongge Hu, Xueling Cai, Mengru Wang, Kaixin Peng, Hulinyue Bai, Jie Xv, Yvchen Fu, Tingting Dong, Xiaoxv Ni, Jian Yin, Xingbin |
author_facet | Yin, Dongge Hu, Xueling Cai, Mengru Wang, Kaixin Peng, Hulinyue Bai, Jie Xv, Yvchen Fu, Tingting Dong, Xiaoxv Ni, Jian Yin, Xingbin |
author_sort | Yin, Dongge |
collection | PubMed |
description | Curcumin (CUR) has a bright future in the treatment of cancer as a natural active ingredient with great potential. However, curcumin has a low solubility, which limits its clinical application. In this study, IRMOF-10 was created by the direct addition of triethylamine, CUR was loaded into IRMOF-10 using the solvent adsorption method, and the two were characterized using a scanning electron microscope (SEM), X-ray diffraction (XRD), dynamic light scattering (DLS), Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TG) methods, and Brunauer–Emmett–Teller (BET) analysis. We also used the MTT method, 4′,6-diamidino-2-phenylindole (DAPI) staining, the annexin V/PI method, cellular uptake, reactive oxygen species (ROS), and the mitochondrial membrane potential (MMP) to perform a safety analysis and anticancer activity study of IRMOF-10 and CUR@IRMOF-10 on HepG2 cells. Our results showed that CUR@IRMOF-10 had a CUR load of 63.96%, with an obvious slow-release phenomenon. The CUR levels released under different conditions at 60 h were 33.58% (pH 7.4) and 31.86% (pH 5.5). Cell experiments proved that IRMOF-10 was biologically safe and could promote curcumin entering the nucleus, causing a series of reactions, such as an increase in reactive oxygen species and a decrease in the mitochondrial membrane potential, thereby leading to cell apoptosis. In summary, IRMOF-10 is an excellent drug carrier and CUR@IRMOF-10 is an effective anti-liver cancer sustained-release preparation. |
format | Online Article Text |
id | pubmed-9228752 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-92287522022-06-25 Preparation, Characterization, and In Vitro Release of Curcumin-Loaded IRMOF-10 Nanoparticles and Investigation of Their Pro-Apoptotic Effects on Human Hepatoma HepG2 Cells Yin, Dongge Hu, Xueling Cai, Mengru Wang, Kaixin Peng, Hulinyue Bai, Jie Xv, Yvchen Fu, Tingting Dong, Xiaoxv Ni, Jian Yin, Xingbin Molecules Article Curcumin (CUR) has a bright future in the treatment of cancer as a natural active ingredient with great potential. However, curcumin has a low solubility, which limits its clinical application. In this study, IRMOF-10 was created by the direct addition of triethylamine, CUR was loaded into IRMOF-10 using the solvent adsorption method, and the two were characterized using a scanning electron microscope (SEM), X-ray diffraction (XRD), dynamic light scattering (DLS), Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TG) methods, and Brunauer–Emmett–Teller (BET) analysis. We also used the MTT method, 4′,6-diamidino-2-phenylindole (DAPI) staining, the annexin V/PI method, cellular uptake, reactive oxygen species (ROS), and the mitochondrial membrane potential (MMP) to perform a safety analysis and anticancer activity study of IRMOF-10 and CUR@IRMOF-10 on HepG2 cells. Our results showed that CUR@IRMOF-10 had a CUR load of 63.96%, with an obvious slow-release phenomenon. The CUR levels released under different conditions at 60 h were 33.58% (pH 7.4) and 31.86% (pH 5.5). Cell experiments proved that IRMOF-10 was biologically safe and could promote curcumin entering the nucleus, causing a series of reactions, such as an increase in reactive oxygen species and a decrease in the mitochondrial membrane potential, thereby leading to cell apoptosis. In summary, IRMOF-10 is an excellent drug carrier and CUR@IRMOF-10 is an effective anti-liver cancer sustained-release preparation. MDPI 2022-06-20 /pmc/articles/PMC9228752/ /pubmed/35745062 http://dx.doi.org/10.3390/molecules27123940 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Yin, Dongge Hu, Xueling Cai, Mengru Wang, Kaixin Peng, Hulinyue Bai, Jie Xv, Yvchen Fu, Tingting Dong, Xiaoxv Ni, Jian Yin, Xingbin Preparation, Characterization, and In Vitro Release of Curcumin-Loaded IRMOF-10 Nanoparticles and Investigation of Their Pro-Apoptotic Effects on Human Hepatoma HepG2 Cells |
title | Preparation, Characterization, and In Vitro Release of Curcumin-Loaded IRMOF-10 Nanoparticles and Investigation of Their Pro-Apoptotic Effects on Human Hepatoma HepG2 Cells |
title_full | Preparation, Characterization, and In Vitro Release of Curcumin-Loaded IRMOF-10 Nanoparticles and Investigation of Their Pro-Apoptotic Effects on Human Hepatoma HepG2 Cells |
title_fullStr | Preparation, Characterization, and In Vitro Release of Curcumin-Loaded IRMOF-10 Nanoparticles and Investigation of Their Pro-Apoptotic Effects on Human Hepatoma HepG2 Cells |
title_full_unstemmed | Preparation, Characterization, and In Vitro Release of Curcumin-Loaded IRMOF-10 Nanoparticles and Investigation of Their Pro-Apoptotic Effects on Human Hepatoma HepG2 Cells |
title_short | Preparation, Characterization, and In Vitro Release of Curcumin-Loaded IRMOF-10 Nanoparticles and Investigation of Their Pro-Apoptotic Effects on Human Hepatoma HepG2 Cells |
title_sort | preparation, characterization, and in vitro release of curcumin-loaded irmof-10 nanoparticles and investigation of their pro-apoptotic effects on human hepatoma hepg2 cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9228752/ https://www.ncbi.nlm.nih.gov/pubmed/35745062 http://dx.doi.org/10.3390/molecules27123940 |
work_keys_str_mv | AT yindongge preparationcharacterizationandinvitroreleaseofcurcuminloadedirmof10nanoparticlesandinvestigationoftheirproapoptoticeffectsonhumanhepatomahepg2cells AT huxueling preparationcharacterizationandinvitroreleaseofcurcuminloadedirmof10nanoparticlesandinvestigationoftheirproapoptoticeffectsonhumanhepatomahepg2cells AT caimengru preparationcharacterizationandinvitroreleaseofcurcuminloadedirmof10nanoparticlesandinvestigationoftheirproapoptoticeffectsonhumanhepatomahepg2cells AT wangkaixin preparationcharacterizationandinvitroreleaseofcurcuminloadedirmof10nanoparticlesandinvestigationoftheirproapoptoticeffectsonhumanhepatomahepg2cells AT penghulinyue preparationcharacterizationandinvitroreleaseofcurcuminloadedirmof10nanoparticlesandinvestigationoftheirproapoptoticeffectsonhumanhepatomahepg2cells AT baijie preparationcharacterizationandinvitroreleaseofcurcuminloadedirmof10nanoparticlesandinvestigationoftheirproapoptoticeffectsonhumanhepatomahepg2cells AT xvyvchen preparationcharacterizationandinvitroreleaseofcurcuminloadedirmof10nanoparticlesandinvestigationoftheirproapoptoticeffectsonhumanhepatomahepg2cells AT futingting preparationcharacterizationandinvitroreleaseofcurcuminloadedirmof10nanoparticlesandinvestigationoftheirproapoptoticeffectsonhumanhepatomahepg2cells AT dongxiaoxv preparationcharacterizationandinvitroreleaseofcurcuminloadedirmof10nanoparticlesandinvestigationoftheirproapoptoticeffectsonhumanhepatomahepg2cells AT nijian preparationcharacterizationandinvitroreleaseofcurcuminloadedirmof10nanoparticlesandinvestigationoftheirproapoptoticeffectsonhumanhepatomahepg2cells AT yinxingbin preparationcharacterizationandinvitroreleaseofcurcuminloadedirmof10nanoparticlesandinvestigationoftheirproapoptoticeffectsonhumanhepatomahepg2cells |