| 摘要 |
Natural and recombinant interferons are stabilised with bidistilled water, lactose, albumin, sodium mono- and dihydrophosphates, (C5H10O5)n, such as arabic gum, dissolved and diluted in 20 % ethanol solution to the fourth decimal by homeopathic method. The final solution is sprayed on to an excipient comprising of 20 % arabic gum, 30 % lactose and 50 % starch for manufacturing tablets of 100 mg each containing 200 I.U. of human alfa-interferon. The tablets are sublingually administered to the patient for treatment of viral infections sensitive to interferon. |
