Drug against pneumonia


(57) Abstract:

Developed drug against pneumonia - polydisulfide Gallic acid. The drug is more effective than used in practice unithiol. table 2.

The invention relates to biology and medicine and relates to means against pneumonia.

Know the use for the treatment of pneumonia salt drugs [1], acetylcysteine [2], ribonuclease [3].

Wide use for the treatment of pneumonia received the drug unithiol [4] (prototype). However, its effect in the treatment of pneumonia is not effective.

The problem to which the invention is directed, is the extension of the range of products with a therapeutic effect against pneumonia. The problem is solved by the use as a drug against pneumonia polydisulfide Gallic acid formula

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n = 12-16.

Polydisulfide Gallic acid obtained by condensation of Gallic acid with odnoklasniki grey.

Example. In the reaction flask 17.0 g (0.1 M) of Gallic acid, 150-200 ml of previously dried 0-, m-, p-xylene and with vigorous stirring, 13.5 g (8.1 oz) odnoklasniki sulfur within 15-20 is. At the end of the reaction the precipitate of polydisulfide Gallic acid is filtered off, washed with o-, m-, p-kisslola, and then with water until a negative reaction to chlorine ion. The synthesis time of 30 h, the output of 92-95%, So pl. = 260-262oC discrepancies. The reaction scheme

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n = 12-16.

Polydisulfide Gallic acid - substance light yellow color.

The elemental composition, wt. %:

Found: C 38,60; H 1,33; S 24,59;

Calculated: C 36,21; H 1,72; S 27,59.

Molecular weight (cryoscopy in diphenyl) found 3600.

Infrared absorption spectrum (V cm-1):

480 - S-S -, 870-C-H-pentamidine benzene,

1230 - S-C-OH, 1480-benzene ring, 1630-COOH, 3300-OH polymer.

Evaluation of therapeutic action of the drug was carried out on models of inflammation of the lungs at 24 lab rats "Wister" weighing 150-200 g Inflammatory process in the lungs was simulated by introducing a sterile nylon filament with a diameter of 0.25 mm and a length of 2.5 cm into the trachea of laboratory animals. Treatment was started within 14 days after the modeling of the inflammatory process in the lungs. The drugs were injected intraperitoneally for 14 days in 10 injections for treatment. Unithiol was introduced in the form of a 5% solution at a dose of 12.5 mg per 100 g of rat, polydisulfide Gallo is of lungs after treatment the animals were killed by arterial blood-letting from the carotid artery. From blood was isolated serum was prepared hemolysate. After slaughter, the animals were isolated pulmonary-cardiac complex and produced broncho-alveolaris washed away by 6-8 times washing the lungs through the trachea with 10 ml of saline. Wash was centrifuged at 600 rpm for 15 min and supernatant was collected, which was used for biochemical studies. In parallel, we investigated a group of animals in which the inflammatory process was developed without treatment against intraperitoneal administration of saline. As a control used a group of 10 healthy animals. Research methods included the identification of key system components proteolysis and free-radical oxidation of blood and broncho-alveolare secret. Serum was investigated anastasopoulou activity (AEP) [5] , - 1-inhibitorbuying ( -1-MIP) and-2-macroglobulin [6] , lipids phosphoroamidites method, diene conjugates (DC) and dircetory (D) [7], the level of malondialdehyde and TBA-active products (TBCAP) [8], katalizatorow activity [9], ceruloplasmin (CP) [10].

In the hemolysate was determined katalizatorow and peroxidation activity (PA) [11] , in bronchoalveolar secret studied with isopogon activity and CPU usage. Statistical processing of results was performed using criterion Student.

Results therapeutic effect on pneumonia claimed and adverse drug are presented in table. 1 and 2.

In the serum the use of drugs has led to a decrease in the content of products of lipid peroxidation. When using unithiol number of MDA decreased by 30%, and polydisulfide Gallic acid 32% and 40% reduction alactolyticus activity of serum. In bronchoalveolar secret when using polydisulfide Gallic acid observed a threefold reduction in the flushing of diene conjugates, ceruloplasmin more than 2 times, while in the presence of unithiol only 33%.

Thus, polydisulfide Gallic acid is an effective drug that reduces the activation of free radical oxidation and proteolysis in inflammatory lung disease.

Sources of information used in the preparation of the description of the invention

1. Komarov F. I., Danilin, I., Gulyaeva, F. E. Clinical medicine, 1980, No. 4, S. 19-24.

2. Violin R. S., lesser black-backed gull C. E., Kimanis A. A., Pharmacology, 1971, -1, S. 98-100.

3. ASS="ptx2">

5. Ogloblin O. G., Platonov, L. C., L. Myasnikov Century Questions of medical chemistry, 1980, No. 3, S. 387-392.

6. Particula C. F., Pashina ie, Questions of medical chemistry, 1979, No. 4, S. 494-499.

7. Gavrilov Century B. , Meskarune M. Laboratory work, 1983, No. 3, S. 33-35.

8. Asakawa, T., Matsushitus. Lipids 1980, 15, N 3, p. 137-140.

9. Korolyuk M. A., Ivanova L,I., Mayorova, I., Tokarev C. E. Laboratory business, 1986, No. 1, S. 16-19.

10. Kolb Century BC, Kamyshnikov C. S. Handbook of clinical chemistry, Minsk: Belarus, 1982, S. 201-204.

11. Popov, C. , Nalkowska L. A. Hygiene and sanitation, 1971, No. 10, S. 89-91.

Drug against pneumonia, characterized in that it is polydisulfide Gallic acid formula

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where n = 12 to 16.


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