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In vitro biological responses to nanofibrillated cellulose by human dermal, lung and immune cells: surface chemistry aspect

BACKGROUND: Nanocellulose, and particularly nanofibrillated cellulose (NFC), has been proposed for a diversity of applications in industry and in the biomedical field. Its unique physicochemical and structural features distinguish nanocellulose from traditional materials and enable its use as an adv...

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Autores principales: Lopes, Viviana R., Sanchez-Martinez, Carla, Strømme, Maria, Ferraz, Natalia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5223298/
https://www.ncbi.nlm.nih.gov/pubmed/28069023
http://dx.doi.org/10.1186/s12989-016-0182-0
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author Lopes, Viviana R.
Sanchez-Martinez, Carla
Strømme, Maria
Ferraz, Natalia
author_facet Lopes, Viviana R.
Sanchez-Martinez, Carla
Strømme, Maria
Ferraz, Natalia
author_sort Lopes, Viviana R.
collection PubMed
description BACKGROUND: Nanocellulose, and particularly nanofibrillated cellulose (NFC), has been proposed for a diversity of applications in industry and in the biomedical field. Its unique physicochemical and structural features distinguish nanocellulose from traditional materials and enable its use as an advance nanomaterial. However, its nanoscale features may induce unknown biological responses. Limited studies with NFC are available and the biological impacts of its use have not been thoroughly explored. This study assesses the in vitro biological responses elicited by wood-derived NFC gels, when human dermal fibroblasts, lung MRC-5 cells and THP-1 macrophage cells are exposed to the nanomaterial. Furthermore, whether the presence of surface charged groups (i.e. carboxymethyl and hydroxypropyltrimethylammonium groups) on NFC can induce distinct biological responses is investigated. RESULTS: The introduction of surface charged groups resulted in individual nanofibrils, while fibril aggregates predominated in the unmodified NFC gel suspensions as observed by transmission electron microscopy. In the presence of proteins, the surface modified NFCs formed compact agglomerates while the agglomeration pattern of the unmodified NFC was similar in the presence of proteins and in physiological buffer. Unmodified and modified NFC gels did not induce cytotoxicity in human dermal fibroblasts, lung and macrophage cells. No significant ROS production by THP-1 macrophages was found and no cellular uptake was observed. However, an inflammatory response was detected when THP-1 macrophages were treated with unmodified NFC as assessed by an increase in TNF-α and IL1-β levels, an effect that was absent when surface charged groups were introduced into NFC. CONCLUSIONS: Taken together, the data presented here show the absence of cytotoxic effects associated with the exposure to unmodified, carboxymethylated and hydroxypropyltrimethylammonium-modified NFCs. Unmodified NFC presented a pro-inflammatory effect which can be further moderated by introducing surface modifications such as carboxymethyl and hydroxypropyltrimethylammonium groups into the nanofibrils. The present findings suggest that the inflammatory response to NFC might be driven by the material surface chemistry, and thus open up for the possibility of designing safe nanocellulose materials. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12989-016-0182-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-52232982017-01-11 In vitro biological responses to nanofibrillated cellulose by human dermal, lung and immune cells: surface chemistry aspect Lopes, Viviana R. Sanchez-Martinez, Carla Strømme, Maria Ferraz, Natalia Part Fibre Toxicol Research BACKGROUND: Nanocellulose, and particularly nanofibrillated cellulose (NFC), has been proposed for a diversity of applications in industry and in the biomedical field. Its unique physicochemical and structural features distinguish nanocellulose from traditional materials and enable its use as an advance nanomaterial. However, its nanoscale features may induce unknown biological responses. Limited studies with NFC are available and the biological impacts of its use have not been thoroughly explored. This study assesses the in vitro biological responses elicited by wood-derived NFC gels, when human dermal fibroblasts, lung MRC-5 cells and THP-1 macrophage cells are exposed to the nanomaterial. Furthermore, whether the presence of surface charged groups (i.e. carboxymethyl and hydroxypropyltrimethylammonium groups) on NFC can induce distinct biological responses is investigated. RESULTS: The introduction of surface charged groups resulted in individual nanofibrils, while fibril aggregates predominated in the unmodified NFC gel suspensions as observed by transmission electron microscopy. In the presence of proteins, the surface modified NFCs formed compact agglomerates while the agglomeration pattern of the unmodified NFC was similar in the presence of proteins and in physiological buffer. Unmodified and modified NFC gels did not induce cytotoxicity in human dermal fibroblasts, lung and macrophage cells. No significant ROS production by THP-1 macrophages was found and no cellular uptake was observed. However, an inflammatory response was detected when THP-1 macrophages were treated with unmodified NFC as assessed by an increase in TNF-α and IL1-β levels, an effect that was absent when surface charged groups were introduced into NFC. CONCLUSIONS: Taken together, the data presented here show the absence of cytotoxic effects associated with the exposure to unmodified, carboxymethylated and hydroxypropyltrimethylammonium-modified NFCs. Unmodified NFC presented a pro-inflammatory effect which can be further moderated by introducing surface modifications such as carboxymethyl and hydroxypropyltrimethylammonium groups into the nanofibrils. The present findings suggest that the inflammatory response to NFC might be driven by the material surface chemistry, and thus open up for the possibility of designing safe nanocellulose materials. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12989-016-0182-0) contains supplementary material, which is available to authorized users. BioMed Central 2017-01-10 /pmc/articles/PMC5223298/ /pubmed/28069023 http://dx.doi.org/10.1186/s12989-016-0182-0 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Lopes, Viviana R.
Sanchez-Martinez, Carla
Strømme, Maria
Ferraz, Natalia
In vitro biological responses to nanofibrillated cellulose by human dermal, lung and immune cells: surface chemistry aspect
title In vitro biological responses to nanofibrillated cellulose by human dermal, lung and immune cells: surface chemistry aspect
title_full In vitro biological responses to nanofibrillated cellulose by human dermal, lung and immune cells: surface chemistry aspect
title_fullStr In vitro biological responses to nanofibrillated cellulose by human dermal, lung and immune cells: surface chemistry aspect
title_full_unstemmed In vitro biological responses to nanofibrillated cellulose by human dermal, lung and immune cells: surface chemistry aspect
title_short In vitro biological responses to nanofibrillated cellulose by human dermal, lung and immune cells: surface chemistry aspect
title_sort in vitro biological responses to nanofibrillated cellulose by human dermal, lung and immune cells: surface chemistry aspect
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5223298/
https://www.ncbi.nlm.nih.gov/pubmed/28069023
http://dx.doi.org/10.1186/s12989-016-0182-0
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