Precise construction of Regorafenib-loaded gold nanoparticles: investigation of antiproliferative activity and apoptosis induction in liver cancer cells
Regorafenib (Reg) inhibits the growth of liver cancer cells in vitro and animal model. However, due to its poor bioavailability, its potential as a chemopreventive or therapeutic drug is severely restricted. In this work, we developed two environmentally friendly delivery systems by synthesizing Reg...
Saved in:
Main Authors: | , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Taylor & Francis Group
2023-12-01
|
Series: | Journal of Experimental Nanoscience |
Subjects: | |
Online Access: | https://www.tandfonline.com/doi/10.1080/17458080.2023.2254006 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
_version_ | 1846157487732948992 |
---|---|
author | Meng Yue Rui Yang Yakun Jiang Xiuhua Yang |
author_facet | Meng Yue Rui Yang Yakun Jiang Xiuhua Yang |
author_sort | Meng Yue |
collection | DOAJ |
description | Regorafenib (Reg) inhibits the growth of liver cancer cells in vitro and animal model. However, due to its poor bioavailability, its potential as a chemopreventive or therapeutic drug is severely restricted. In this work, we developed two environmentally friendly delivery systems by synthesizing Regorafenib-gold nanoparticles conjugates Reg@GNPs1 and Reg@GNPs2, employing a dual role of Reg to reduce Au3+ and stabilize the synthesized GNPs. UV-Vis’s spectroscopy, Fourier transform infrared spectroscopy, and Powder-XRD verified the fabrication of Reg@GNPs. Reg@GNPs1 and Reg@GNPs2 were both found to be spherical and uniform in size (10 ± 2 and 2 ± 33 nm, respectively) using transmission electron microscopy. Similar negative zeta potential (−35.0 ± 2.5 and −37.0 ± 1.6 mV) was observed by dynamic light scattering analysis, even though the hydrodynamic diameter of the nanoconjugates ranged from 65.0 ± 1.7 to 153.0 ± 2.2 nm. Reg@GNPs1 and Reg@GNPs2 were calculated to have a Reg loading of 46% and 48%, respectively. Selectivity towards the non-cancerous cell line (L929) cells, whereas the MTT assay in vitro showed the antiproliferative effects of Reg@GNPs on three liver carcinoma (Hep3B, BEL7402, and HepG2) cell lines. Several fluorescent staining techniques were used to examine liver cancer cell morphology. Flow cytometric analysis confirmed that the effects of the superior Reg@GNPs nanoconjugate on cell proliferation than free Reg. In conclusion, the acquired results show that the novel synthesized GNPs loaded with Reg are stable as an anticancer agent, with minimal toxicity against non-cancerous cells, as determined by cytotoxicity and IC50 evaluations. |
format | Article |
id | doaj-art-edc90d6ec3aa4a888c4e626fda777b77 |
institution | Kabale University |
issn | 1745-8080 1745-8099 |
language | English |
publishDate | 2023-12-01 |
publisher | Taylor & Francis Group |
record_format | Article |
series | Journal of Experimental Nanoscience |
spelling | doaj-art-edc90d6ec3aa4a888c4e626fda777b772024-11-25T10:28:58ZengTaylor & Francis GroupJournal of Experimental Nanoscience1745-80801745-80992023-12-0118110.1080/17458080.2023.2254006Precise construction of Regorafenib-loaded gold nanoparticles: investigation of antiproliferative activity and apoptosis induction in liver cancer cellsMeng Yue0Rui Yang1Yakun Jiang2Xiuhua Yang3Department of Gastroenterology, Central Hospital Affiliated to Shandong First Medical University, Jinan City, Shandong Province, ChinaDepartment of Stomatology, Central Hospital Affiliated to Shandong First Medical University, Jinan City, Shandong Province, ChinaDepartment of Gastroenterology, Central Hospital Affiliated to Shandong First Medical University, Jinan City, Shandong Province, ChinaDepartment of Gastroenterology, Central Hospital Affiliated to Shandong First Medical University, Jinan City, Shandong Province, ChinaRegorafenib (Reg) inhibits the growth of liver cancer cells in vitro and animal model. However, due to its poor bioavailability, its potential as a chemopreventive or therapeutic drug is severely restricted. In this work, we developed two environmentally friendly delivery systems by synthesizing Regorafenib-gold nanoparticles conjugates Reg@GNPs1 and Reg@GNPs2, employing a dual role of Reg to reduce Au3+ and stabilize the synthesized GNPs. UV-Vis’s spectroscopy, Fourier transform infrared spectroscopy, and Powder-XRD verified the fabrication of Reg@GNPs. Reg@GNPs1 and Reg@GNPs2 were both found to be spherical and uniform in size (10 ± 2 and 2 ± 33 nm, respectively) using transmission electron microscopy. Similar negative zeta potential (−35.0 ± 2.5 and −37.0 ± 1.6 mV) was observed by dynamic light scattering analysis, even though the hydrodynamic diameter of the nanoconjugates ranged from 65.0 ± 1.7 to 153.0 ± 2.2 nm. Reg@GNPs1 and Reg@GNPs2 were calculated to have a Reg loading of 46% and 48%, respectively. Selectivity towards the non-cancerous cell line (L929) cells, whereas the MTT assay in vitro showed the antiproliferative effects of Reg@GNPs on three liver carcinoma (Hep3B, BEL7402, and HepG2) cell lines. Several fluorescent staining techniques were used to examine liver cancer cell morphology. Flow cytometric analysis confirmed that the effects of the superior Reg@GNPs nanoconjugate on cell proliferation than free Reg. In conclusion, the acquired results show that the novel synthesized GNPs loaded with Reg are stable as an anticancer agent, with minimal toxicity against non-cancerous cells, as determined by cytotoxicity and IC50 evaluations.https://www.tandfonline.com/doi/10.1080/17458080.2023.2254006Regorafenibgold nanoparticlesliver cancerapoptosis |
spellingShingle | Meng Yue Rui Yang Yakun Jiang Xiuhua Yang Precise construction of Regorafenib-loaded gold nanoparticles: investigation of antiproliferative activity and apoptosis induction in liver cancer cells Journal of Experimental Nanoscience Regorafenib gold nanoparticles liver cancer apoptosis |
title | Precise construction of Regorafenib-loaded gold nanoparticles: investigation of antiproliferative activity and apoptosis induction in liver cancer cells |
title_full | Precise construction of Regorafenib-loaded gold nanoparticles: investigation of antiproliferative activity and apoptosis induction in liver cancer cells |
title_fullStr | Precise construction of Regorafenib-loaded gold nanoparticles: investigation of antiproliferative activity and apoptosis induction in liver cancer cells |
title_full_unstemmed | Precise construction of Regorafenib-loaded gold nanoparticles: investigation of antiproliferative activity and apoptosis induction in liver cancer cells |
title_short | Precise construction of Regorafenib-loaded gold nanoparticles: investigation of antiproliferative activity and apoptosis induction in liver cancer cells |
title_sort | precise construction of regorafenib loaded gold nanoparticles investigation of antiproliferative activity and apoptosis induction in liver cancer cells |
topic | Regorafenib gold nanoparticles liver cancer apoptosis |
url | https://www.tandfonline.com/doi/10.1080/17458080.2023.2254006 |
work_keys_str_mv | AT mengyue preciseconstructionofregorafenibloadedgoldnanoparticlesinvestigationofantiproliferativeactivityandapoptosisinductioninlivercancercells AT ruiyang preciseconstructionofregorafenibloadedgoldnanoparticlesinvestigationofantiproliferativeactivityandapoptosisinductioninlivercancercells AT yakunjiang preciseconstructionofregorafenibloadedgoldnanoparticlesinvestigationofantiproliferativeactivityandapoptosisinductioninlivercancercells AT xiuhuayang preciseconstructionofregorafenibloadedgoldnanoparticlesinvestigationofantiproliferativeactivityandapoptosisinductioninlivercancercells |