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For a New Phase... A Healthier Experience
Biofemin 2G
PHARMACOKINETICS AND PHARMACODYNAMICS
Once Biofemin 2G has been administered, some components are absorbed by the gastric walls and others by the intestine. Passing to the liver through the lymphatic system, it is absorbed quickly due to the fast metabolism of the phyto-organic compounds that improve the pharmacokinetics and acceptability of cell activity. Maximum plasma levels are reached after 1 to 2 hours, its elimination half-life is approximately 7 hours and it does not accumulate. A small portion of the compound administered is excreted in the urine, but most of it is eliminated in the bile and faeces. The cell extract components are absorbed hepatically and, from there, they are metabolised and transported by mitochondrial self-evaluation to the intracellular fluid which is transmitted to the surrounding cell organisms of the reproductive system. However, there are reports in which no modifications or changes have been noted in the desired direction, without any important consequence. It has zero toxicity and does not create deposits.
