Effects of Dosing Condition on the Oral Bioavailability of Green Tea Catechins after Single-Dose Administration of Polyphenon E in Healthy Individuals
Purpose: Green tea has been shown to exhibit cancer-preventive activities in preclinical studies. Its consumption has been associated with decreased risk of certain types of cancers in humans. The oral bioavailability of the major green tea constituents, green tea catechins, is low, resulting in sys...
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Published in | Clinical cancer research Vol. 11; no. 12; pp. 4627 - 4633 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Philadelphia, PA
American Association for Cancer Research
15.06.2005
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Subjects | |
Online Access | Get full text |
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Summary: | Purpose: Green tea has been shown to exhibit cancer-preventive activities in preclinical studies. Its consumption has been associated
with decreased risk of certain types of cancers in humans. The oral bioavailability of the major green tea constituents, green
tea catechins, is low, resulting in systemic catechin levels in humans many fold less than the effective concentrations determined
in in vitro systems. We conducted this clinical study to test the hypothesis that the oral bioavailability of green tea catechins can
be enhanced when consumed in the absence of food.
Experimental Designs: Thirty healthy volunteers were randomly assigned to one of the following doses of Polyphenon E (a decaffeinated and defined
green tea catechin mixture): 400, 800, or 1,200 mg, based on the epigallocatechin gallate content (10 subjects per dose group).
After an overnight fast, study participants took a single dose of Polyphenon E with or without a light breakfast, which consisted
of one or two 4-oz muffins and a glass of water. Following a 1-week wash-out period, subjects were crossed over to take the
same dose of Polyphenon E under the opposite fasting/fed condition. Tea catechin concentrations in plasma and urine samples
collected after dosing were determined by high-pressure liquid chromatography analysis.
Results: Consistent with previous reports, epigallocatechin gallate and epicatechin gallate were present in plasma mostly as the free
form, whereas epicatechin and epigallocatechin were mostly present as the glucuronide and sulfate conjugates. There was >3.5-fold
increase in the average maximum plasma concentration of free epigallocatechin gallate when Polyphenon E was taken in the fasting
condition than when taken with food. The dosing condition led to a similar change in plasma-free epigallocatechin and epicatechin
gallate levels. Taking Polyphenon E in the fasting state did not have a significant effect on the plasma levels of total (free
and conjugated) epigallocatechin, but resulted in lower plasma levels of total epicatechin. Urinary epigallocatechin gallate
and epicatechin gallate levels were very low or undetectable following Polyphenon E administration with either dosing condition.
Taking Polyphenon E under the fasting state resulted in a significant decrease in the urinary recovery of total epigallocatechin
and epicatechin. Polyphenon E administered as a single dose over the dose range studied was generally well-tolerated by the
study participants. Mild and transient nausea was noted in some of the study participants and was seen most often at the highest
study agent dose (1,200 mg epigallocatechin gallate) and in the fasting condition.
Conclusions: We conclude that greater oral bioavailability of free catechins can be achieved by taking the Polyphenon E capsules on an
empty stomach after an overnight fast. Polyphenon E up to a dose that contains 800 mg epigallocatechin gallate is well-tolerated
when taken under the fasting condition. This dosing condition is also expected to optimize the biological effects of tea catechins. |
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ISSN: | 1078-0432 1557-3265 |
DOI: | 10.1158/1078-0432.CCR-04-2549 |