Monday, September 12, 2011 8:18 PM
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jan wexler
http://www.phlebolymphology.org/wp-content/pdf/Phlebolymphology43.pdf Read pages 213-216.
Micronization offers improved efficacy in CVI By acting at the heart of CVI, daflon 500 mg is effective at all stages of disease. However, flavonoids have a poor gastrointestinal absorption. This is overcome, in daflon 500 mg’s case, by the process of micronization: a high-tech process which reduces daflon 500 mg’s mean active particle size by 35 µm with a subsequent faster and better absorption in humans with improved bioavailability. This has been conclusively demonstrated in a single-center, randomized, double-blind, crossover study in 12 healthy male volunteers. Immediately from 24 hours postingestion, daflon 500 mg’s absorption (measured by urinary radioactivity) is almost twice that of simple diosmins (P<0.0001). This improved absorption of daflon 500 mg over simple diosmins is maintained after 2 weeks of treatment (57.9% vs 32.7%; P<0.0004).7 Therefore, evidence that, thanks to micronization, daflon 500 mg’s absorption is almost doubled, leading to significantly improved clinical efficacy.
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