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A Pilot Cross-Over Study to Evaluate Human Oral Bioavailability of BCM-95(®)CG (Biocurcumax™), A Novel Bioenhanced Preparation of Curcumin
Curcumin, the bioactive component of turmeric, Curcuma longa has an exceptionally wide spectrum of activities including antioxidant, anti-inflammatory and anti-cancer properties, and is currently under different phases of clinical trials for various types of soft tissue cancers. However, although in...
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Formato: | Texto |
Lenguaje: | English |
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Medknow Publications
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2792534/ https://www.ncbi.nlm.nih.gov/pubmed/20046768 http://dx.doi.org/10.4103/0250-474X.44591 |
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author | Antony, B. Merina, B. Iyer, V. S. Judy, N. Lennertz, K. Joyal, S. |
author_facet | Antony, B. Merina, B. Iyer, V. S. Judy, N. Lennertz, K. Joyal, S. |
author_sort | Antony, B. |
collection | PubMed |
description | Curcumin, the bioactive component of turmeric, Curcuma longa has an exceptionally wide spectrum of activities including antioxidant, anti-inflammatory and anti-cancer properties, and is currently under different phases of clinical trials for various types of soft tissue cancers. However, although in vitro and animal studies have shown anticancer activities of curcumin for virtually all types of human cancers, its poor bioavailability in the human body has severely limited its application to these diseases. Methods to increase its oral bioavailability are a subject of intense current research. Reconstituting curcumin with the non-curcuminoid components of turmeric has been found to increase the bioavailability substantially. In the present clinical study to determine the bioavailability of curcuminoids, a patented formulation, BCM-95(®)CG was tested on human volunteer group. Normal curcumin was used in the control group. Curcumin content in blood was estimated at periodical intervals. After a washout period of two weeks the control group and drug group were crossed over BCM-95(®)CG and curcumin, respectively. It was also compared with a combination of curcumin-lecithin-piperine which was earlier shown to provide enhanced bioavailability. The results of the study indicate that the relative bioavailability of BCM-95(®)CG (Biocurcumax™) was about 6.93-fold compared to normal curcumin and about 6.3-fold compared to curcumin-lecithin-piperine formula. BCM-95(®)CG thus, has potential for widespread application for various chronic diseases. |
format | Text |
id | pubmed-2792534 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Medknow Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-27925342009-12-14 A Pilot Cross-Over Study to Evaluate Human Oral Bioavailability of BCM-95(®)CG (Biocurcumax™), A Novel Bioenhanced Preparation of Curcumin Antony, B. Merina, B. Iyer, V. S. Judy, N. Lennertz, K. Joyal, S. Indian J Pharm Sci Research Paper Curcumin, the bioactive component of turmeric, Curcuma longa has an exceptionally wide spectrum of activities including antioxidant, anti-inflammatory and anti-cancer properties, and is currently under different phases of clinical trials for various types of soft tissue cancers. However, although in vitro and animal studies have shown anticancer activities of curcumin for virtually all types of human cancers, its poor bioavailability in the human body has severely limited its application to these diseases. Methods to increase its oral bioavailability are a subject of intense current research. Reconstituting curcumin with the non-curcuminoid components of turmeric has been found to increase the bioavailability substantially. In the present clinical study to determine the bioavailability of curcuminoids, a patented formulation, BCM-95(®)CG was tested on human volunteer group. Normal curcumin was used in the control group. Curcumin content in blood was estimated at periodical intervals. After a washout period of two weeks the control group and drug group were crossed over BCM-95(®)CG and curcumin, respectively. It was also compared with a combination of curcumin-lecithin-piperine which was earlier shown to provide enhanced bioavailability. The results of the study indicate that the relative bioavailability of BCM-95(®)CG (Biocurcumax™) was about 6.93-fold compared to normal curcumin and about 6.3-fold compared to curcumin-lecithin-piperine formula. BCM-95(®)CG thus, has potential for widespread application for various chronic diseases. Medknow Publications 2008 /pmc/articles/PMC2792534/ /pubmed/20046768 http://dx.doi.org/10.4103/0250-474X.44591 Text en © Indian Journal of Pharmaceutical Sciences http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Antony, B. Merina, B. Iyer, V. S. Judy, N. Lennertz, K. Joyal, S. A Pilot Cross-Over Study to Evaluate Human Oral Bioavailability of BCM-95(®)CG (Biocurcumax™), A Novel Bioenhanced Preparation of Curcumin |
title | A Pilot Cross-Over Study to Evaluate Human Oral Bioavailability of BCM-95(®)CG (Biocurcumax™), A Novel Bioenhanced Preparation of Curcumin |
title_full | A Pilot Cross-Over Study to Evaluate Human Oral Bioavailability of BCM-95(®)CG (Biocurcumax™), A Novel Bioenhanced Preparation of Curcumin |
title_fullStr | A Pilot Cross-Over Study to Evaluate Human Oral Bioavailability of BCM-95(®)CG (Biocurcumax™), A Novel Bioenhanced Preparation of Curcumin |
title_full_unstemmed | A Pilot Cross-Over Study to Evaluate Human Oral Bioavailability of BCM-95(®)CG (Biocurcumax™), A Novel Bioenhanced Preparation of Curcumin |
title_short | A Pilot Cross-Over Study to Evaluate Human Oral Bioavailability of BCM-95(®)CG (Biocurcumax™), A Novel Bioenhanced Preparation of Curcumin |
title_sort | pilot cross-over study to evaluate human oral bioavailability of bcm-95(®)cg (biocurcumax™), a novel bioenhanced preparation of curcumin |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2792534/ https://www.ncbi.nlm.nih.gov/pubmed/20046768 http://dx.doi.org/10.4103/0250-474X.44591 |
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