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Fabrication of Functional bioMOF-100 Prototype as Drug Delivery System for Breast Cancer Therapy

Breast cancer is the most frequent cause of cancer death in women, representing the fifth leading cause of cancer death overall. Therefore, the growing search for the development of new treatments for breast cancer has been developed lately as well as drug delivery systems such as biocompatible meta...

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Autores principales: Alves, Renata Carolina, Perosa Fernandes, Richard, Lira de Farias, Renan, da Silva, Patricia Bento, Santos Faria, Raquel, Quijia, Christian Rafael, Galvão Frem, Regina Célia, Azevedo, Ricardo Bentes, Chorilli, Marlus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9699488/
https://www.ncbi.nlm.nih.gov/pubmed/36432650
http://dx.doi.org/10.3390/pharmaceutics14112458
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author Alves, Renata Carolina
Perosa Fernandes, Richard
Lira de Farias, Renan
da Silva, Patricia Bento
Santos Faria, Raquel
Quijia, Christian Rafael
Galvão Frem, Regina Célia
Azevedo, Ricardo Bentes
Chorilli, Marlus
author_facet Alves, Renata Carolina
Perosa Fernandes, Richard
Lira de Farias, Renan
da Silva, Patricia Bento
Santos Faria, Raquel
Quijia, Christian Rafael
Galvão Frem, Regina Célia
Azevedo, Ricardo Bentes
Chorilli, Marlus
author_sort Alves, Renata Carolina
collection PubMed
description Breast cancer is the most frequent cause of cancer death in women, representing the fifth leading cause of cancer death overall. Therefore, the growing search for the development of new treatments for breast cancer has been developed lately as well as drug delivery systems such as biocompatible metal–organic Frameworks (bio-MOFs). These may be promising and attractive for drug incorporation and release. The present study aims to develop a drug carrier system RCA (bioMOF-100 submitted to the activation process) containing incorporated curcumin (CCM), whose material surface is coated with folic acid molecules (FA) to promote the targeting of drug carrier systems to the tumor region. They were synthesized and characterized using several characterization techniques. The materials were submitted to drug encapsulation tests, whose encapsulation efficiency was 32.80% for CCM@RCA-1D. Using the (1)H nuclear magnetic resonance (NMR) spectroscopy technique, it was possible to verify the appearance of signals referring to folic acid, suggesting success in the functionalization of these matrices. In vitro tests such as cell viability and type of cell death were evaluated in both series of compounds (CCM@RCA-1D, CCM@RCA-1D/FA) in breast tumor lines. The results revealed low toxicity of the materials and cell death by late apoptosis. Thus, these results indicate that the matrices studied can be promising carriers in the treatment of breast cancer.
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spelling pubmed-96994882022-11-26 Fabrication of Functional bioMOF-100 Prototype as Drug Delivery System for Breast Cancer Therapy Alves, Renata Carolina Perosa Fernandes, Richard Lira de Farias, Renan da Silva, Patricia Bento Santos Faria, Raquel Quijia, Christian Rafael Galvão Frem, Regina Célia Azevedo, Ricardo Bentes Chorilli, Marlus Pharmaceutics Article Breast cancer is the most frequent cause of cancer death in women, representing the fifth leading cause of cancer death overall. Therefore, the growing search for the development of new treatments for breast cancer has been developed lately as well as drug delivery systems such as biocompatible metal–organic Frameworks (bio-MOFs). These may be promising and attractive for drug incorporation and release. The present study aims to develop a drug carrier system RCA (bioMOF-100 submitted to the activation process) containing incorporated curcumin (CCM), whose material surface is coated with folic acid molecules (FA) to promote the targeting of drug carrier systems to the tumor region. They were synthesized and characterized using several characterization techniques. The materials were submitted to drug encapsulation tests, whose encapsulation efficiency was 32.80% for CCM@RCA-1D. Using the (1)H nuclear magnetic resonance (NMR) spectroscopy technique, it was possible to verify the appearance of signals referring to folic acid, suggesting success in the functionalization of these matrices. In vitro tests such as cell viability and type of cell death were evaluated in both series of compounds (CCM@RCA-1D, CCM@RCA-1D/FA) in breast tumor lines. The results revealed low toxicity of the materials and cell death by late apoptosis. Thus, these results indicate that the matrices studied can be promising carriers in the treatment of breast cancer. MDPI 2022-11-15 /pmc/articles/PMC9699488/ /pubmed/36432650 http://dx.doi.org/10.3390/pharmaceutics14112458 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
Alves, Renata Carolina
Perosa Fernandes, Richard
Lira de Farias, Renan
da Silva, Patricia Bento
Santos Faria, Raquel
Quijia, Christian Rafael
Galvão Frem, Regina Célia
Azevedo, Ricardo Bentes
Chorilli, Marlus
Fabrication of Functional bioMOF-100 Prototype as Drug Delivery System for Breast Cancer Therapy
title Fabrication of Functional bioMOF-100 Prototype as Drug Delivery System for Breast Cancer Therapy
title_full Fabrication of Functional bioMOF-100 Prototype as Drug Delivery System for Breast Cancer Therapy
title_fullStr Fabrication of Functional bioMOF-100 Prototype as Drug Delivery System for Breast Cancer Therapy
title_full_unstemmed Fabrication of Functional bioMOF-100 Prototype as Drug Delivery System for Breast Cancer Therapy
title_short Fabrication of Functional bioMOF-100 Prototype as Drug Delivery System for Breast Cancer Therapy
title_sort fabrication of functional biomof-100 prototype as drug delivery system for breast cancer therapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9699488/
https://www.ncbi.nlm.nih.gov/pubmed/36432650
http://dx.doi.org/10.3390/pharmaceutics14112458
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