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In vitro and in vivo safety evaluation of Nephure™

Nephure™ is a proprietary oxalate decarboxylase (OxDC) enzyme being developed as a food ingredient. In this study, the safety of Nephure™ was evaluated in a bacterial mutagenicity assay and in a sub-chronic (13-week) oral toxicity study in rats. Nephure™ did not show any mutagenic properties in the...

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Autores principales: Cowley, Helena, Yan, Qin, Koetzner, Lee, Dolan, Laurie, Nordwald, Erik, Cowley, Aaron B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Authors. Published by Elsevier Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5500298/
https://www.ncbi.nlm.nih.gov/pubmed/28322893
http://dx.doi.org/10.1016/j.yrtph.2017.03.016
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author Cowley, Helena
Yan, Qin
Koetzner, Lee
Dolan, Laurie
Nordwald, Erik
Cowley, Aaron B.
author_facet Cowley, Helena
Yan, Qin
Koetzner, Lee
Dolan, Laurie
Nordwald, Erik
Cowley, Aaron B.
author_sort Cowley, Helena
collection PubMed
description Nephure™ is a proprietary oxalate decarboxylase (OxDC) enzyme being developed as a food ingredient. In this study, the safety of Nephure™ was evaluated in a bacterial mutagenicity assay and in a sub-chronic (13-week) oral toxicity study in rats. Nephure™ did not show any mutagenic properties in the mutagenicity assay. In the 13-week sub-chronic oral toxicity study in which 10 Sprague Dawley rats per sex were administered 0, 118, 235 and 475 mg/kg bw/day (8260, 16450 and 33,250 Units/kg bw/day, respectively) of Nephure™ by gavage, male and female rats did not show any test article-related clinical observations or effects on body weight, body weight gain, food consumption, food efficiency, ophthalmology, functional observational battery parameters or motor activity. Furthermore, there were no changes in coagulation, clinical chemistry, urinalysis or hematology parameters, macroscopic/microscopic findings or organ weights that could be attributed to the test article. Based on these results, Nephure™ was not mutagenic and the no-adverse-effect level (NOAEL) in the 13-week study was determined to be 475 mg/kg bw/day (33,250 Units/kg bw/day). Evaluation of the estimated consumption of Nephure™, generation of the metabolite formate, and the current safety studies resulted in a conclusion of a tolerable upper limit of 3450 Units of OxDC activity/day (57.5 Units activity/kg bw/day), when Nephure™ is added to food to decrease dietary oxalate.
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spelling pubmed-55002982018-06-01 In vitro and in vivo safety evaluation of Nephure™ Cowley, Helena Yan, Qin Koetzner, Lee Dolan, Laurie Nordwald, Erik Cowley, Aaron B. Regul Toxicol Pharmacol Article Nephure™ is a proprietary oxalate decarboxylase (OxDC) enzyme being developed as a food ingredient. In this study, the safety of Nephure™ was evaluated in a bacterial mutagenicity assay and in a sub-chronic (13-week) oral toxicity study in rats. Nephure™ did not show any mutagenic properties in the mutagenicity assay. In the 13-week sub-chronic oral toxicity study in which 10 Sprague Dawley rats per sex were administered 0, 118, 235 and 475 mg/kg bw/day (8260, 16450 and 33,250 Units/kg bw/day, respectively) of Nephure™ by gavage, male and female rats did not show any test article-related clinical observations or effects on body weight, body weight gain, food consumption, food efficiency, ophthalmology, functional observational battery parameters or motor activity. Furthermore, there were no changes in coagulation, clinical chemistry, urinalysis or hematology parameters, macroscopic/microscopic findings or organ weights that could be attributed to the test article. Based on these results, Nephure™ was not mutagenic and the no-adverse-effect level (NOAEL) in the 13-week study was determined to be 475 mg/kg bw/day (33,250 Units/kg bw/day). Evaluation of the estimated consumption of Nephure™, generation of the metabolite formate, and the current safety studies resulted in a conclusion of a tolerable upper limit of 3450 Units of OxDC activity/day (57.5 Units activity/kg bw/day), when Nephure™ is added to food to decrease dietary oxalate. The Authors. Published by Elsevier Inc. 2017-06 2017-03-18 /pmc/articles/PMC5500298/ /pubmed/28322893 http://dx.doi.org/10.1016/j.yrtph.2017.03.016 Text en © 2017 The Authors. Published by Elsevier Inc. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Cowley, Helena
Yan, Qin
Koetzner, Lee
Dolan, Laurie
Nordwald, Erik
Cowley, Aaron B.
In vitro and in vivo safety evaluation of Nephure™
title In vitro and in vivo safety evaluation of Nephure™
title_full In vitro and in vivo safety evaluation of Nephure™
title_fullStr In vitro and in vivo safety evaluation of Nephure™
title_full_unstemmed In vitro and in vivo safety evaluation of Nephure™
title_short In vitro and in vivo safety evaluation of Nephure™
title_sort in vitro and in vivo safety evaluation of nephure™
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5500298/
https://www.ncbi.nlm.nih.gov/pubmed/28322893
http://dx.doi.org/10.1016/j.yrtph.2017.03.016
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