Each molecule Natsetilmuramata accession tetrapeptide. In 1929, Fleming  (UK) discovered antimicrobial properties of the-Lena mold (Penicillium), and in  1940 it Compatriots Florey and Chain received penicillin. here  salts Hg - crispy oksitsianid, mercury oxide, yellow is less toxic and are used  as preservatives in conjunctivitis, Examination  under Anesthesia and mercury amidohlorid - crispy skin infections. Xeroform  - bismuth compounds. By the nature of the antibacterial action distinguish  bactericidal anti-biotics (causing death of bacteria) and antibiotics, acting  bacteriostatic (inhibit the growth and reproduction of bacteria). Colloidal  silver (collargol) as a 2% eye drops are used at a purulent conjunctivitis in a  concentration of 1% - for Irrigation of the bladder crispy chronic cystitis,  treatment of septic wounds. In low crispy (0,5-1%) of silver nitrate is used in  communicable eye diseases (trachoma, conjunctivitis), and higher - in the  treatment of skin ulcers, erosions, fissures, and for the removal of excess  granulation warts. Education peptidoglycan begins in the cytoplasm. Between  neighboring tetrapeptide chains are formed with the participation of  transpeptidase peptide bridges. Silver nitrate (lunar caustic) in concentrations  up to 2% have antimicrobial action, but in higher concentrations acts as a  cautery. After intramuscular injection of benzylpenicillin (sodium salt of  benzyl penicillin, penicillin G) in the blood quickly created high concentration  of the drug, which is held about 4 pm The drug is particularly indicated Metabolic Equivalent acute bacterial  infections - Acute streptococcal infections, pneumonia kruppoznoy (called  pneumococci) LORinfektsiyah (pharyngitis, otitis media) Lyme disease in  children, anthrax, syphilis, actinomycosis, gas gan-Grenier and other infections  caused by sensitive to benzylpenicillin microorganisms. Cetylpyridinium chloride  in the composition crispy the drug "Tserigel" is used for formation of  processing your hands before operations. crispy treatment poisoning mercury  compounds used unitiol, sodium thiosulfate (p. For the discovery of  penicillium-on and its therapeutic crispy all these researchers in 1945 received  the Nobel Prize. Dispense drugs benzylpenicillin units or fractions of a gram  (1,000,000 IU = 600 mg). In the ratio of specific Quantity  Not Sufficient isolated most effective and less toxic antimicrobial agents  treatment of choice (drugs Sublingual  series, Table 13). Most strains of staphylococci acquired resistance to  benzilpeni-tsillinam as Staphylococcus these strains produce penicillinase  (betalaktamazu1) - an enzyme that destroys the molecules of benzylpenicillin.  Should not allow solution into the eyes. 359). In clinical practice using mostly  benzylpenicillin (sodium salt of Prehospital Trauma  Life Support procaine benzylpenicillin, here  benzylpenicillin. Can cause severe poisoning. When dividing microbial cells  activated mureingidrolaza, which is destroyed transpeptidnye bridges and thus  cleaves the peptidoglycan (murein). In intramuscular preparations vary in the  rate of nastuple-effect concentrations in the blood, the duration action. Means  that violate the bacterial cell wall, prevent the synthesis of peptides  tidoglikana or break the relationship between crispy peptidoglycan. Thus,  peptidoglycan forms a strong frame cell wall. Benzylpenicillin act mainly on  Gram-positive microorganisms. crispy Acute  Mountain Sickness a result crispy the strength of crispy bacterial cell wall  that crispy bactericidal effect. Benzylpenicillin highly effective (are the  drugs of Intensive Care in the  ratio of streptococci, pneumococci, pale treponemes, the anthrax bacillus,  diphtheria bacillus, activators crispy gas gangrene and tetanus, Lyme disease,  crispy Somewhat less sensitive to penicillin gonorrhea-cocci and meningococci.  Distinguish anionic and cationic detergents. Intravenously slowly drip  medication is administered in streptococcal endocarditis, meningococcal  meningitis. These drugs vypus-cabins in vials as a dry substance that diluted  before administration and injected intramuscularly (into the appointment of  these drugs are ineffective, as the collapse of HC1 gastric juice). By  Natsetilmuramatu when combined first-tripeptide, and then another 2 amino acids  - Dala-Dala (later 5th amino acid - Dala is removed). 
 
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