Toxicological effects of ingested nanocellulose in in vitro intestinal epithelium and in vivo rat models

Cellulose is widely used as a thickener and filler in foods and drugs. It has been designated “generally regarded as safe” (GRAS). Nanocellulose (NC) has many additional potential applications designed to improve food quality and safety, but has not yet been designated as GRAS. Here we present resul...

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Main Authors: DeLoid, Glen M., Cao, Xiaoqiong, Molina, Ramon M., Silva, Daniel Imbassahy, Bhattacharya, Kunal, Ng, Kee Woei, Loo, Joachim Say Chye, Brain, Joseph D., Demokritou, Philip
Other Authors: School of Materials Science and Engineering
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Language:English
Published: 2021
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Online Access:https://hdl.handle.net/10356/150824
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spelling sg-ntu-dr.10356-1508242021-07-10T20:11:21Z Toxicological effects of ingested nanocellulose in in vitro intestinal epithelium and in vivo rat models DeLoid, Glen M. Cao, Xiaoqiong Molina, Ramon M. Silva, Daniel Imbassahy Bhattacharya, Kunal Ng, Kee Woei Loo, Joachim Say Chye Brain, Joseph D. Demokritou, Philip School of Materials Science and Engineering Environmental Chemistry and Materials Centre Nanyang Environment and Water Research Institute Engineering::Environmental engineering Cellulose Food Additives Cellulose is widely used as a thickener and filler in foods and drugs. It has been designated “generally regarded as safe” (GRAS). Nanocellulose (NC) has many additional potential applications designed to improve food quality and safety, but has not yet been designated as GRAS. Here we present results of toxicological studies of ingested NC in physiologically relevant in vitro and in vivo systems. In vitro studies employed a gastrointestinal tract simulator to digest two widely-used forms of NC, nanocellulose fibrils (CNF) and cellulose nanocrystals (CNC), at 0.75 and 1.5% w/w, in a fasting diet as well as in a standardized food model based on the average American diet. A triculture model of small intestinal epithelium was used to assess effects of a 24 hour incubation with the digested products (digesta) on cell layer integrity, cytotoxicity and oxidative stress. Other than a 10% increase over controls in reactive oxygen species (ROS) production with 1.5% w/w CNC, no significant changes in cytotoxicity, ROS or monolayer integrity were observed. In vivo toxicity was evaluated in rats gavaged twice weekly for five weeks with 1% w/w suspensions of CNF in either water or cream. Blood, serum, lung, liver, kidney, and small intestine were collected for analysis. No significant differences in hematology, serum markers or histology were observed between controls and rats given CNF suspensions. These findings suggest that ingested NC has little acute toxicity, and is likely non-hazardous when ingested in small quantities. Additional chronic feeding studies are required to assess long term effects, and potential detrimental effects on the gut microbiome and absorbance of essential micronutrients. These studies are underway, and their outcome will be reported in the near future. Nanyang Technological University Accepted version Support for the research reported, including assets and resources required for designing and performing experiments, data analysis, and interpretation, was provided by the Nanyang Technological University-Harvard T. H. Chan School of Public Health Initiative for Sustainable Nanotechnology (NTU-Harvard SusNano; NTU-HSPH 17001). Additional funding for animal studies was provided by the National Institutes of Health (ES-0000002). The engineered nanomaterials used in the research presented in this publication were developed, characterized, and provided by the Engineered Nanomaterials Resource and Coordination Core established at Harvard T. H. Chan School of Public Health (NIH grant # U24ES026946) as part of the Nanotechnology Health Implications Research Consortium. 2021-07-08T06:13:40Z 2021-07-08T06:13:40Z 2019 Journal Article DeLoid, G. M., Cao, X., Molina, R. M., Silva, D. I., Bhattacharya, K., Ng, K. W., Loo, J. S. C., Brain, J. D. & Demokritou, P. (2019). Toxicological effects of ingested nanocellulose in in vitro intestinal epithelium and in vivo rat models. Environmental Science: Nano, 6(7), 2105-2115. https://dx.doi.org/10.1039/c9en00184k 2051-8153 https://hdl.handle.net/10356/150824 10.1039/c9en00184k 32133146 2-s2.0-85069047434 7 6 2105 2115 en NTU-HSPH 17001 Environmental Science: Nano © 2019 The Royal Society of Chemistry. All rights reserved. This paper was published in Environmental Science: Nano and is made available with permission of The Royal Society of Chemistry. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Engineering::Environmental engineering
Cellulose
Food Additives
spellingShingle Engineering::Environmental engineering
Cellulose
Food Additives
DeLoid, Glen M.
Cao, Xiaoqiong
Molina, Ramon M.
Silva, Daniel Imbassahy
Bhattacharya, Kunal
Ng, Kee Woei
Loo, Joachim Say Chye
Brain, Joseph D.
Demokritou, Philip
Toxicological effects of ingested nanocellulose in in vitro intestinal epithelium and in vivo rat models
description Cellulose is widely used as a thickener and filler in foods and drugs. It has been designated “generally regarded as safe” (GRAS). Nanocellulose (NC) has many additional potential applications designed to improve food quality and safety, but has not yet been designated as GRAS. Here we present results of toxicological studies of ingested NC in physiologically relevant in vitro and in vivo systems. In vitro studies employed a gastrointestinal tract simulator to digest two widely-used forms of NC, nanocellulose fibrils (CNF) and cellulose nanocrystals (CNC), at 0.75 and 1.5% w/w, in a fasting diet as well as in a standardized food model based on the average American diet. A triculture model of small intestinal epithelium was used to assess effects of a 24 hour incubation with the digested products (digesta) on cell layer integrity, cytotoxicity and oxidative stress. Other than a 10% increase over controls in reactive oxygen species (ROS) production with 1.5% w/w CNC, no significant changes in cytotoxicity, ROS or monolayer integrity were observed. In vivo toxicity was evaluated in rats gavaged twice weekly for five weeks with 1% w/w suspensions of CNF in either water or cream. Blood, serum, lung, liver, kidney, and small intestine were collected for analysis. No significant differences in hematology, serum markers or histology were observed between controls and rats given CNF suspensions. These findings suggest that ingested NC has little acute toxicity, and is likely non-hazardous when ingested in small quantities. Additional chronic feeding studies are required to assess long term effects, and potential detrimental effects on the gut microbiome and absorbance of essential micronutrients. These studies are underway, and their outcome will be reported in the near future.
author2 School of Materials Science and Engineering
author_facet School of Materials Science and Engineering
DeLoid, Glen M.
Cao, Xiaoqiong
Molina, Ramon M.
Silva, Daniel Imbassahy
Bhattacharya, Kunal
Ng, Kee Woei
Loo, Joachim Say Chye
Brain, Joseph D.
Demokritou, Philip
format Article
author DeLoid, Glen M.
Cao, Xiaoqiong
Molina, Ramon M.
Silva, Daniel Imbassahy
Bhattacharya, Kunal
Ng, Kee Woei
Loo, Joachim Say Chye
Brain, Joseph D.
Demokritou, Philip
author_sort DeLoid, Glen M.
title Toxicological effects of ingested nanocellulose in in vitro intestinal epithelium and in vivo rat models
title_short Toxicological effects of ingested nanocellulose in in vitro intestinal epithelium and in vivo rat models
title_full Toxicological effects of ingested nanocellulose in in vitro intestinal epithelium and in vivo rat models
title_fullStr Toxicological effects of ingested nanocellulose in in vitro intestinal epithelium and in vivo rat models
title_full_unstemmed Toxicological effects of ingested nanocellulose in in vitro intestinal epithelium and in vivo rat models
title_sort toxicological effects of ingested nanocellulose in in vitro intestinal epithelium and in vivo rat models
publishDate 2021
url https://hdl.handle.net/10356/150824
_version_ 1705151318648160256