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From frozen shoulders that regain full range of motion after one prolozone, to sore knees that can ski again, to the relaxation of back/neck/shoulder muscles after a biomat session

If your starting material is low-purity, filled with contaminants, or has an incorrect amino acid sequence, your research is doomed from the start

Bioavailability is usually determined by calculating the respective plasma drug exposure assessed as the total area under the drug plasma concentration versus time curve (AUC) after oral and intravenous administration as: In general, determinants of oral drug bioavailability include fraction of dose absorbed in the gastrointestinal tract (GIT) and fraction of dose that escapes elimination by the intestinal tract, liver, and lung

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