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Tuesday, June 12, 2007 Nanocurry vs. CancerResearchers hope that curcumin encapsulated in nanospheres will spice up clinical trials for Alzheimer's, cystic fibrosis, and cancer. By Ganapati Mudur
In recent years, laboratory and animal studies have suggested that curcumin--the pigment that gives the Indian curry spice turmeric its bright-yellow hue--may have some power to kill tumors and clear the brain plaques that characterize Alzheimer's disease. But because curcumin is insoluble, it mostly passes through the gut without making it into the bloodstream. While doctors in the United States, Europe, and Asia have conducted more than two-dozen clinical trials using curcumin, most have required patients to swallow up to 12 grams, or even more, of curcumin every day. That's a lot--even for the most ardent lovers of Indian food. Now researchers at the Johns Hopkins University School of Medicine and the University of Delhi, in India, have invented curcumin-carrying nanospheres that could far more easily slip into the bloodstream. Call it nanocurry--a marriage of 21st-century nanotechnology with an ancient ingredient from the East. The nanospheres open up the possibility that low doses of oral curcumin could be used far more widely in clinical trials, a key step toward getting the ingredient from the spice aisle to the pharmacist's shelf. Animal studies to determine whether nanocurcumin has any effect against pancreatic tumors in mice are expected to begin within weeks; the development of the particles was published in the Journal of Nanobiotechnology in April. Anirban Maitra, a professor of pathology and oncology at Johns Hopkins, and his collaborators in Delhi--including his father, Amarnath Maitra, a professor of chemistry--used special polymers to synthesize tiny nanoparticles about 50 nanometers in diameter. The particles have hydrophobic interiors and hydrophilic exteriors. The hydrophobic component holds the curcumin, while the hydrophilic exteriors make the particles soluble. This way, they can pass easily from the gut to the bloodstream. Once in the blood, the curcumin leaks out as the polymers slowly degrade. The Johns Hopkins team has already shown in laboratory experiments with pancreatic cancer cells that nanocurcumin retains its ability to activate key events that destroy tumors. What's more, early animal studies have revealed that the nanoparticles are nontoxic, the team says. There's a big need for these little particles. Over the past five years, evidence of curcumin's clinical potential has steadily mounted. Studies in the United States, India, and elsewhere have shown that curcumin can fight tumor growth in breast, colon, ovarian, and pancreatic cancers. Curcumin has also shown promise beyond fighting cancer: earlier this year, researchers at Massachusetts General Hospital reported that in mice, curcumin cleared and reduced plaques associated with Alzheimer's disease. |
Proton Radiation for All
07/24/2007



Comments
cyberpageman on 06/12/2007 at 1:32 PM
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ccanton on 07/09/2007 at 7:23 PM
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www.pionair.net
Candie
ramaraju_1972 on 07/19/2007 at 6:09 AM
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i am dr.rao from india. i would like to know about the dosage & duration of curcumin u used. is it single peak curcumin or curcuminoids?
Salit58@yahoo.com on 10/13/2007 at 7:00 PM
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DenisL on 11/17/2007 at 6:55 PM
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Interesting abstract:
Curcumin and pancreatic cancer: Phase II clinical trial experience.
Sub-category: Pancreatic Cancer
Category: Gastrointestinal (Noncolorectal) Cancer
Meeting: 2007 ASCO Annual Meeting
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Abstract No: 4599
Citation: Journal of Clinical Oncology, 2007 ASCO Annual Meeting Proceedings Part I. Vol 25, No. 18S (June 20 Supplement), 2007: 4599
Author(s): N. Dhillon, B. B. Aggarwal, R. A. Newman, R. A. Wolff, A. B. Kunnumakkara, J. L. Abbruzzese, D. S. Hong, L. H. Camacho, C. Ng, R. Kurzrock
Abstract: Background: Pancreatic cancer is virtually always lethal, and the only FDA-approved therapies- gemcitabine and erlotinib- produce objective responses in less than 10% of patients. Curcumin (diferuloyl methane) is a plant-derived dietary ingredient that suppresses NF-?B and numerous other pathways relevant to pancreatic cancer and has potent preclinical anti-tumor activity. Herein, we evaluated the safety and potential antitumor activity of curcumin against advanced pancreatic cancer, and its impact on biologic correlates. Methods: Patients received 8 grams of curcumin by mouth daily for two months and were then restaged. Maintenance therapy was continued at the same dose and schedule until disease progression. Results: Twenty-five patients were enrolled as of the date of analysis, with 21 evaluable for response. Circulating curcumin was detectable, albeit at low steady-state levels (about 31 ng/ml), suggesting poor oral bioavailability. To date, two patients have had prolonged stable disease (8 and 12+ months). Interestingly, one patient had a brief, but marked tumor regression (73%) (accompanied by significant increases (4-35-fold) in serum cytokine (interleukin-6 (IL-6), IL-8, IL-10, and IL-1 receptor antagonist (IL-1RA) levels). No toxicities have been observed. Curcumin down-regulated expression of NF-?B, COX-2 and phosphorylated STAT3 in peripheral blood mononuclear cells (PBMC) from patients (most of whom had baseline levels considerably higher than those found in healthy volunteers)although the decrease did not reach statistical significance for p65. Curcumin was determined in patient plasma samples after enzymatic digestion with glucuronidase enzyme. While there was considerable variation in plasma curcumin levels from patient to patient, drug levels peaked at 22-41 ng/ml and remained relatively constant over the entire 4 week experimental period. Conclusions: We conclude that oral curcumin is well tolerated and, despite its limited absorption, has biologic activity in patients with pancreatic cancer. Correlative Serum Markers Correlative Markers Pre-dose Post- dose t-value p-value
p65 74.5±10 65.8±14.2 1.584 0.131
COX- 2 60.8±12.53 44.7±17.37 2.377 0.029
pSTAT3 40.2±15.76 21.1±13.3 2.929 0.009
Mean ± SD
bradleybrokers on 09/06/2007 at 2:42 AM
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