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High Biocompatibility, MRI Enhancement, and Dual Chemo- and Thermal-Therapy of Curcumin-Encapsulated Alginate/Fe(3)O(4) Nanoparticles
(1) Background: Magnetite (Fe(3)O(4)) nanoparticles have great potential for biomedical applications, including hyperthermia and magnetic resonance imaging. In this study, we aimed to identify the biological activity of nanoconjugates composed of superparamagnetic Fe(3)O(4) nanoparticles coated with...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10222081/ https://www.ncbi.nlm.nih.gov/pubmed/37242765 http://dx.doi.org/10.3390/pharmaceutics15051523 |
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author | Do, Xuan-Hai Nguyen, Tu Dac Le, Thi Thu Huong To, Thuy Thanh Bui, Thi Van Khanh Pham, Nam Hong Lam, Khanh Hoang, Thi My Nhung Ha, Phuong Thu |
author_facet | Do, Xuan-Hai Nguyen, Tu Dac Le, Thi Thu Huong To, Thuy Thanh Bui, Thi Van Khanh Pham, Nam Hong Lam, Khanh Hoang, Thi My Nhung Ha, Phuong Thu |
author_sort | Do, Xuan-Hai |
collection | PubMed |
description | (1) Background: Magnetite (Fe(3)O(4)) nanoparticles have great potential for biomedical applications, including hyperthermia and magnetic resonance imaging. In this study, we aimed to identify the biological activity of nanoconjugates composed of superparamagnetic Fe(3)O(4) nanoparticles coated with alginate and curcumin (Fe(3)O(4)/Cur@ALG) in cancer cells. (2) Methods: The nanoparticles were evaluated for the biocompatibility and toxicity on mice. The MRI enhancement and hyperthermia capacities of Fe(3)O(4)/Cur@ALG were determined in both in vitro and in vivo sarcoma models. (3) Results: The results show that the magnetite nanoparticles exhibit high biocompatibility and low toxicity in mice at Fe(3)O(4) concentrations up to 120 mg/kg when administered via intravenous injection. The Fe(3)O(4)/Cur@ALG nanoparticles enhance the magnetic resonance imaging contrast in cell cultures and tumor-bearing Swiss mice. The autofluorescence of curcumin also allowed us to observe the penetration of the nanoparticles into sarcoma 180 cells. In particular, the nanoconjugates synergistically inhibit the growth of sarcoma 180 tumors via magnetic heating and the anticancer effects of curcumin, both in vitro and in vivo. (4) Conclusions: Our study reveals that Fe(3)O(4)/Cur@ALG has a high potential for medicinal applications and should be further developed for cancer diagnosis and treatment. |
format | Online Article Text |
id | pubmed-10222081 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102220812023-05-28 High Biocompatibility, MRI Enhancement, and Dual Chemo- and Thermal-Therapy of Curcumin-Encapsulated Alginate/Fe(3)O(4) Nanoparticles Do, Xuan-Hai Nguyen, Tu Dac Le, Thi Thu Huong To, Thuy Thanh Bui, Thi Van Khanh Pham, Nam Hong Lam, Khanh Hoang, Thi My Nhung Ha, Phuong Thu Pharmaceutics Article (1) Background: Magnetite (Fe(3)O(4)) nanoparticles have great potential for biomedical applications, including hyperthermia and magnetic resonance imaging. In this study, we aimed to identify the biological activity of nanoconjugates composed of superparamagnetic Fe(3)O(4) nanoparticles coated with alginate and curcumin (Fe(3)O(4)/Cur@ALG) in cancer cells. (2) Methods: The nanoparticles were evaluated for the biocompatibility and toxicity on mice. The MRI enhancement and hyperthermia capacities of Fe(3)O(4)/Cur@ALG were determined in both in vitro and in vivo sarcoma models. (3) Results: The results show that the magnetite nanoparticles exhibit high biocompatibility and low toxicity in mice at Fe(3)O(4) concentrations up to 120 mg/kg when administered via intravenous injection. The Fe(3)O(4)/Cur@ALG nanoparticles enhance the magnetic resonance imaging contrast in cell cultures and tumor-bearing Swiss mice. The autofluorescence of curcumin also allowed us to observe the penetration of the nanoparticles into sarcoma 180 cells. In particular, the nanoconjugates synergistically inhibit the growth of sarcoma 180 tumors via magnetic heating and the anticancer effects of curcumin, both in vitro and in vivo. (4) Conclusions: Our study reveals that Fe(3)O(4)/Cur@ALG has a high potential for medicinal applications and should be further developed for cancer diagnosis and treatment. MDPI 2023-05-18 /pmc/articles/PMC10222081/ /pubmed/37242765 http://dx.doi.org/10.3390/pharmaceutics15051523 Text en © 2023 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 Do, Xuan-Hai Nguyen, Tu Dac Le, Thi Thu Huong To, Thuy Thanh Bui, Thi Van Khanh Pham, Nam Hong Lam, Khanh Hoang, Thi My Nhung Ha, Phuong Thu High Biocompatibility, MRI Enhancement, and Dual Chemo- and Thermal-Therapy of Curcumin-Encapsulated Alginate/Fe(3)O(4) Nanoparticles |
title | High Biocompatibility, MRI Enhancement, and Dual Chemo- and Thermal-Therapy of Curcumin-Encapsulated Alginate/Fe(3)O(4) Nanoparticles |
title_full | High Biocompatibility, MRI Enhancement, and Dual Chemo- and Thermal-Therapy of Curcumin-Encapsulated Alginate/Fe(3)O(4) Nanoparticles |
title_fullStr | High Biocompatibility, MRI Enhancement, and Dual Chemo- and Thermal-Therapy of Curcumin-Encapsulated Alginate/Fe(3)O(4) Nanoparticles |
title_full_unstemmed | High Biocompatibility, MRI Enhancement, and Dual Chemo- and Thermal-Therapy of Curcumin-Encapsulated Alginate/Fe(3)O(4) Nanoparticles |
title_short | High Biocompatibility, MRI Enhancement, and Dual Chemo- and Thermal-Therapy of Curcumin-Encapsulated Alginate/Fe(3)O(4) Nanoparticles |
title_sort | high biocompatibility, mri enhancement, and dual chemo- and thermal-therapy of curcumin-encapsulated alginate/fe(3)o(4) nanoparticles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10222081/ https://www.ncbi.nlm.nih.gov/pubmed/37242765 http://dx.doi.org/10.3390/pharmaceutics15051523 |
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