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Carboxymethyl cellulose/sulfur-functionalized Ti-based MOF composite: synthesis, characterization, antimicrobial, antiviral and anticancer potentiality
Microbial resistance is the first morbidity and mortality cause for patients as usually a secondary infection. Additionally, the MOF is a promising material that shows a nice activity in this field. However, these materials need a good formulation to enhance biocompatibility and sustainability. Cell...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10201485/ https://www.ncbi.nlm.nih.gov/pubmed/37382711 http://dx.doi.org/10.1186/s11671-023-03852-2 |
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author | Abdelhameed, Reda M. Hasanin, Mohamed S. Hashem, Amr H. |
author_facet | Abdelhameed, Reda M. Hasanin, Mohamed S. Hashem, Amr H. |
author_sort | Abdelhameed, Reda M. |
collection | PubMed |
description | Microbial resistance is the first morbidity and mortality cause for patients as usually a secondary infection. Additionally, the MOF is a promising material that shows a nice activity in this field. However, these materials need a good formulation to enhance biocompatibility and sustainability. Cellulose and its derivatives are well as filers for this gap. In this presented work, a novel green active system based on carboxymethyl cellulose and Ti-MOF (MIL-125-NH(2)@CMC) modified with thiophene (Thio@MIL-125-NH(2)@CMC) was prepared by a post-synthetic modification (PSM) route based. FTIR, SEM and PXRD were utilized to characterize nanocomposites. In addition, transmission electron microscopy (TEM) was used to corroborate the nanocomposites' particle size and diffraction pattern as well as the DLS affirmed the size as 50 and 35 nm for MIL-125-NH(2)@CMC and Thio@MIL-125-NH(2)@CMC, respectively. The formulation of the nanocomposites was validated by physicochemical characterization techniques, while morphological analysis confirmed the nanoform of the prepared composites. The antimicrobial, antiviral and antitumor properties of MIL-125-NH(2)@CMC and Thio@MIL-125-NH(2)@CMC were assessed. Antimicrobial testing revealed that Thio@MIL-125-NH(2)@CMC possesses greater antimicrobial activity than MIL-125-NH(2)@CMC. Additionally, Thio@MIL-125-NH(2)@CMC demonstrated promising antifungal activity against C. albicans and A. niger where MICs were 31.25 and 0.97 µg/mL, respectively. Also, Thio@MIL-125-NH(2)@CMC exhibited antibacterial activity against E. coli and S. aureus where MICs were 1000 and 250 µg/mL, respectively. In addition, the results demonstrated that Thio@MIL-125-NH(2)@CMC displayed promising antiviral activity against both HSV1 and COX B4, with antiviral activities of 68.89% and 39.60%, respectively. Furthermore, Thio@MIL-125-NH(2)@CMC exhibited potential anticancer activity against MCF7 and PC3 cancerous cell lines, where IC(50) was 93.16 and 88.45%, respectively. In conclusion, carboxymethyl cellulose/sulfur-functionalized Ti-based MOF composite was successfully synthesized which had antimicrobial, antiviral and anticancer activities. |
format | Online Article Text |
id | pubmed-10201485 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-102014852023-05-23 Carboxymethyl cellulose/sulfur-functionalized Ti-based MOF composite: synthesis, characterization, antimicrobial, antiviral and anticancer potentiality Abdelhameed, Reda M. Hasanin, Mohamed S. Hashem, Amr H. Discov Nano Research Microbial resistance is the first morbidity and mortality cause for patients as usually a secondary infection. Additionally, the MOF is a promising material that shows a nice activity in this field. However, these materials need a good formulation to enhance biocompatibility and sustainability. Cellulose and its derivatives are well as filers for this gap. In this presented work, a novel green active system based on carboxymethyl cellulose and Ti-MOF (MIL-125-NH(2)@CMC) modified with thiophene (Thio@MIL-125-NH(2)@CMC) was prepared by a post-synthetic modification (PSM) route based. FTIR, SEM and PXRD were utilized to characterize nanocomposites. In addition, transmission electron microscopy (TEM) was used to corroborate the nanocomposites' particle size and diffraction pattern as well as the DLS affirmed the size as 50 and 35 nm for MIL-125-NH(2)@CMC and Thio@MIL-125-NH(2)@CMC, respectively. The formulation of the nanocomposites was validated by physicochemical characterization techniques, while morphological analysis confirmed the nanoform of the prepared composites. The antimicrobial, antiviral and antitumor properties of MIL-125-NH(2)@CMC and Thio@MIL-125-NH(2)@CMC were assessed. Antimicrobial testing revealed that Thio@MIL-125-NH(2)@CMC possesses greater antimicrobial activity than MIL-125-NH(2)@CMC. Additionally, Thio@MIL-125-NH(2)@CMC demonstrated promising antifungal activity against C. albicans and A. niger where MICs were 31.25 and 0.97 µg/mL, respectively. Also, Thio@MIL-125-NH(2)@CMC exhibited antibacterial activity against E. coli and S. aureus where MICs were 1000 and 250 µg/mL, respectively. In addition, the results demonstrated that Thio@MIL-125-NH(2)@CMC displayed promising antiviral activity against both HSV1 and COX B4, with antiviral activities of 68.89% and 39.60%, respectively. Furthermore, Thio@MIL-125-NH(2)@CMC exhibited potential anticancer activity against MCF7 and PC3 cancerous cell lines, where IC(50) was 93.16 and 88.45%, respectively. In conclusion, carboxymethyl cellulose/sulfur-functionalized Ti-based MOF composite was successfully synthesized which had antimicrobial, antiviral and anticancer activities. Springer US 2023-05-22 /pmc/articles/PMC10201485/ /pubmed/37382711 http://dx.doi.org/10.1186/s11671-023-03852-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Abdelhameed, Reda M. Hasanin, Mohamed S. Hashem, Amr H. Carboxymethyl cellulose/sulfur-functionalized Ti-based MOF composite: synthesis, characterization, antimicrobial, antiviral and anticancer potentiality |
title | Carboxymethyl cellulose/sulfur-functionalized Ti-based MOF composite: synthesis, characterization, antimicrobial, antiviral and anticancer potentiality |
title_full | Carboxymethyl cellulose/sulfur-functionalized Ti-based MOF composite: synthesis, characterization, antimicrobial, antiviral and anticancer potentiality |
title_fullStr | Carboxymethyl cellulose/sulfur-functionalized Ti-based MOF composite: synthesis, characterization, antimicrobial, antiviral and anticancer potentiality |
title_full_unstemmed | Carboxymethyl cellulose/sulfur-functionalized Ti-based MOF composite: synthesis, characterization, antimicrobial, antiviral and anticancer potentiality |
title_short | Carboxymethyl cellulose/sulfur-functionalized Ti-based MOF composite: synthesis, characterization, antimicrobial, antiviral and anticancer potentiality |
title_sort | carboxymethyl cellulose/sulfur-functionalized ti-based mof composite: synthesis, characterization, antimicrobial, antiviral and anticancer potentiality |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10201485/ https://www.ncbi.nlm.nih.gov/pubmed/37382711 http://dx.doi.org/10.1186/s11671-023-03852-2 |
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