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BIOLOGICALLY ACTIVE SUBSTANCE, PROCESS FOR PREPARING THE SAME, PHARMACEUTICAL COMPOSITION FOR THE TREATMENT OF HERPETIC INFECTIONS AND UTILIZATION OF SAID BIOLOGICALLY ACTIVE SUBSTANCE
BIOLOGICALLY ACTIVE SUBSTANCE, PROCESS FOR PREPARING THE SAME, PHARMACEUTICAL COMPOSITION FOR THE TREATMENT OF HERPETIC INFECTIONS AND UTILIZATION OF SAID BIOLOGICALLY ACTIVE SUBSTANCE
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机译:生物活性物质,制备相同的过程,药物组合物,用于治疗疱疹感染和利用所述生物活性物质
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摘要
The invention relates to a biologically active substance, to a process for preparing said substance, to a pharmaceutical composition for treating herpetic infections and to the utilization of said biologically active substance. According to the invention, the biologically active substance comprises 4.5 mg Glu/ 100 mg, 1.47 mg Tre/100 mg, 1.27 mg Cer/100 mg, 1.53 mg Pro/100 mg, 0.25 mg Cis/ 100 mg, 1.39 mg Gly/ 100 mg, 1.71 mg Ala/ 100 mg, 1.24 mg Val/ 100 mg, 0.10 mg Met/ 100 mg, 1. 26 mg Izo/ 100 mg, 1.77 mg :Ley/ 100 mg, 1.11 mg Pir/ 100 mg, 3.17 mg Fen/ 100 mg, 2. 99 mg Asp/ 100 mg, 1.99 mg Arg/ 100 mg, 0.63 mg His/ 100 mg, 0.12 mg Tri / 100 mg. The process for preparing the biologically active substance consists in the steps of: a) growing on a large scale the Galeria mellonella insect in artificial culturing environments, under laboratory conditions; b) selecting one kilo of larvae in a last stadium of development, when insects do not feed themselves and their intestine becomes sterile; c) disinfecting the larvae surface with a detergent in a concentration of 15 ... 20 ml to 2 l of warm water at a temperature ranging from 30 to 35 degree C, washing the larvae three-four times, rinsing the larvae two-three times with double distilled water, subjecting the surface of the bodies of the larvae to UV radiation from a distance of 1 to 1.5 m for 2 to 2.5 min for a total disinfection; d) grinding the sterile larvae for 10 to 15 min till an homogeneous mass of grey light colour is obtained; e) filtering the suspension by means of a very fine mesh with orifices ranging from 200-300 micro in order to remove the larvae tissues remaining from the grinding; f) centrifuging the suspension at a speed of 5, 000 -5, 500 rpm, for 30 -35 min until there do not settle all the proteins any longer; g) lyophilizing or atomizing the suspension at a temperature ranging from -150 ... 160 degree C or at a temperature ranging from 170 ... 180 degree C at the input and 85 ...90 degree C at the output; h) collecting 250 g dry powder and preserving the same at a temperature ranging from 15 to 20 degree C.
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