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Dose escalation of a curcuminoid formulation
BACKGROUND: Curcumin is the major yellow pigment extracted from turmeric, a commonly-used spice in India and Southeast Asia that has broad anticarcinogenic and cancer chemopreventive potential. However, few systematic studies of curcumin's pharmacology and toxicology in humans have been perform...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1434783/ https://www.ncbi.nlm.nih.gov/pubmed/16545122 http://dx.doi.org/10.1186/1472-6882-6-10 |
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author | Lao, Christopher D Ruffin, Mack T Normolle, Daniel Heath, Dennis D Murray, Sandra I Bailey, Joanne M Boggs, Martha E Crowell, James Rock, Cheryl L Brenner, Dean E |
author_facet | Lao, Christopher D Ruffin, Mack T Normolle, Daniel Heath, Dennis D Murray, Sandra I Bailey, Joanne M Boggs, Martha E Crowell, James Rock, Cheryl L Brenner, Dean E |
author_sort | Lao, Christopher D |
collection | PubMed |
description | BACKGROUND: Curcumin is the major yellow pigment extracted from turmeric, a commonly-used spice in India and Southeast Asia that has broad anticarcinogenic and cancer chemopreventive potential. However, few systematic studies of curcumin's pharmacology and toxicology in humans have been performed. METHODS: A dose escalation study was conducted to determine the maximum tolerated dose and safety of a single dose of standardized powder extract, uniformly milled curcumin (C(3 )Complex™, Sabinsa Corporation). Healthy volunteers were administered escalating doses from 500 to 12,000 mg. RESULTS: Seven of twenty-four subjects (30%) experienced only minimal toxicity that did not appear to be dose-related. No curcumin was detected in the serum of subjects administered 500, 1,000, 2,000, 4,000, 6,000 or 8,000 mg. Low levels of curcumin were detected in two subjects administered 10,000 or 12,000 mg. CONCLUSION: The tolerance of curcumin in high single oral doses appears to be excellent. Given that achieving systemic bioavailability of curcumin or its metabolites may not be essential for colorectal cancer chemoprevention, these findings warrant further investigation for its utility as a long-term chemopreventive agent. |
format | Text |
id | pubmed-1434783 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-14347832006-04-08 Dose escalation of a curcuminoid formulation Lao, Christopher D Ruffin, Mack T Normolle, Daniel Heath, Dennis D Murray, Sandra I Bailey, Joanne M Boggs, Martha E Crowell, James Rock, Cheryl L Brenner, Dean E BMC Complement Altern Med Research Article BACKGROUND: Curcumin is the major yellow pigment extracted from turmeric, a commonly-used spice in India and Southeast Asia that has broad anticarcinogenic and cancer chemopreventive potential. However, few systematic studies of curcumin's pharmacology and toxicology in humans have been performed. METHODS: A dose escalation study was conducted to determine the maximum tolerated dose and safety of a single dose of standardized powder extract, uniformly milled curcumin (C(3 )Complex™, Sabinsa Corporation). Healthy volunteers were administered escalating doses from 500 to 12,000 mg. RESULTS: Seven of twenty-four subjects (30%) experienced only minimal toxicity that did not appear to be dose-related. No curcumin was detected in the serum of subjects administered 500, 1,000, 2,000, 4,000, 6,000 or 8,000 mg. Low levels of curcumin were detected in two subjects administered 10,000 or 12,000 mg. CONCLUSION: The tolerance of curcumin in high single oral doses appears to be excellent. Given that achieving systemic bioavailability of curcumin or its metabolites may not be essential for colorectal cancer chemoprevention, these findings warrant further investigation for its utility as a long-term chemopreventive agent. BioMed Central 2006-03-17 /pmc/articles/PMC1434783/ /pubmed/16545122 http://dx.doi.org/10.1186/1472-6882-6-10 Text en Copyright © 2006 Lao et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Lao, Christopher D Ruffin, Mack T Normolle, Daniel Heath, Dennis D Murray, Sandra I Bailey, Joanne M Boggs, Martha E Crowell, James Rock, Cheryl L Brenner, Dean E Dose escalation of a curcuminoid formulation |
title | Dose escalation of a curcuminoid formulation |
title_full | Dose escalation of a curcuminoid formulation |
title_fullStr | Dose escalation of a curcuminoid formulation |
title_full_unstemmed | Dose escalation of a curcuminoid formulation |
title_short | Dose escalation of a curcuminoid formulation |
title_sort | dose escalation of a curcuminoid formulation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1434783/ https://www.ncbi.nlm.nih.gov/pubmed/16545122 http://dx.doi.org/10.1186/1472-6882-6-10 |
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