A Toxicological Evaluation of a Standardized Hydrogenated Extract of Curcumin (CuroWhite™)
A series of toxicological investigations were conducted in order to evaluate the genotoxic potential and repeated-dose oral toxicity of CuroWhite, a proprietary extract of curcumin that has been hydrogenated and standardized to not less than 25% hydrogenated curcuminoid content. All tests were condu...
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2018-01-01
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Series: | Journal of Toxicology |
Online Access: | http://dx.doi.org/10.1155/2018/5243617 |
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doaj-4855c06e640b4b4f9f22e119d9e16d312020-11-25T02:21:32ZengHindawi LimitedJournal of Toxicology1687-81911687-82052018-01-01201810.1155/2018/52436175243617A Toxicological Evaluation of a Standardized Hydrogenated Extract of Curcumin (CuroWhite™)Alastimmanahalli Narasimhiah Ravikumar0Joby Jacob1Sreeraj Gopi2Tumkur Subbarao Jagannath3Liveon Biolabs (P) Ltd., Tumkur, Karnataka 572106, IndiaR&D Centre, Aurea Biolabs (P) Ltd., Kolenchery, Cochin, Kerala 682311, IndiaR&D Centre, Aurea Biolabs (P) Ltd., Kolenchery, Cochin, Kerala 682311, IndiaLiveon Biolabs (P) Ltd., Tumkur, Karnataka 572106, IndiaA series of toxicological investigations were conducted in order to evaluate the genotoxic potential and repeated-dose oral toxicity of CuroWhite, a proprietary extract of curcumin that has been hydrogenated and standardized to not less than 25% hydrogenated curcuminoid content. All tests were conducted in general accordance with internationally accepted standards. The test item was not mutagenic in the bacterial reverse mutation test or in vitro mammalian chromosomal aberration test, and no in vivo genotoxic activity was observed in rat bone marrow in the micronucleus test. A 90-day repeated-dose study was conducted in male and female Sprague-Dawley rats. Two mortalities occurred in the main and satellite high-dose groups and were determined due to gavage error. No organ specific or other toxic effects of the test item were observed up to the maximum dose of 800 mg/kg bw/day, administered by gavage. NOAEL was, therefore, estimated as 800 mg/kg bw/day.http://dx.doi.org/10.1155/2018/5243617 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Alastimmanahalli Narasimhiah Ravikumar Joby Jacob Sreeraj Gopi Tumkur Subbarao Jagannath |
spellingShingle |
Alastimmanahalli Narasimhiah Ravikumar Joby Jacob Sreeraj Gopi Tumkur Subbarao Jagannath A Toxicological Evaluation of a Standardized Hydrogenated Extract of Curcumin (CuroWhite™) Journal of Toxicology |
author_facet |
Alastimmanahalli Narasimhiah Ravikumar Joby Jacob Sreeraj Gopi Tumkur Subbarao Jagannath |
author_sort |
Alastimmanahalli Narasimhiah Ravikumar |
title |
A Toxicological Evaluation of a Standardized Hydrogenated Extract of Curcumin (CuroWhite™) |
title_short |
A Toxicological Evaluation of a Standardized Hydrogenated Extract of Curcumin (CuroWhite™) |
title_full |
A Toxicological Evaluation of a Standardized Hydrogenated Extract of Curcumin (CuroWhite™) |
title_fullStr |
A Toxicological Evaluation of a Standardized Hydrogenated Extract of Curcumin (CuroWhite™) |
title_full_unstemmed |
A Toxicological Evaluation of a Standardized Hydrogenated Extract of Curcumin (CuroWhite™) |
title_sort |
toxicological evaluation of a standardized hydrogenated extract of curcumin (curowhite™) |
publisher |
Hindawi Limited |
series |
Journal of Toxicology |
issn |
1687-8191 1687-8205 |
publishDate |
2018-01-01 |
description |
A series of toxicological investigations were conducted in order to evaluate the genotoxic potential and repeated-dose oral toxicity of CuroWhite, a proprietary extract of curcumin that has been hydrogenated and standardized to not less than 25% hydrogenated curcuminoid content. All tests were conducted in general accordance with internationally accepted standards. The test item was not mutagenic in the bacterial reverse mutation test or in vitro mammalian chromosomal aberration test, and no in vivo genotoxic activity was observed in rat bone marrow in the micronucleus test. A 90-day repeated-dose study was conducted in male and female Sprague-Dawley rats. Two mortalities occurred in the main and satellite high-dose groups and were determined due to gavage error. No organ specific or other toxic effects of the test item were observed up to the maximum dose of 800 mg/kg bw/day, administered by gavage. NOAEL was, therefore, estimated as 800 mg/kg bw/day. |
url |
http://dx.doi.org/10.1155/2018/5243617 |
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