Drugs online research references
IARC Sci Publ. 1978;(19):219-37.
Possible nitrosodimethylamine formation in comparative in vitro nitrosation experiments with six different tetracycline antibiotics.
Roper H, Heyns K.
The hydrochlorides of tetracycline, minocycline, chlorotetracycline, anhydrochlorotetracycline, desmethylchlorotetracycline, oxytetracycline and doxycycline were reacted with sodium nitrite for two hours at 37 degrees C in aqueous buffer solutions at pH 2 and 4 under simulated stomach conditions. NDMA formation was detected from minocycline, doxycycline, oxytetracycline and anhydrochlorotetracycline by GLC and GLC-MS analysis. NDMA formation from minocycline and dodxycycline was blocked by ascorbic acid. The catalytic effect of sodium thiocyanate for NDMA formation from minocycline and nitrite was investigated. The different reactivities of the tested tetracyclines towards nitrite in acidic solutions (NDMA formation from minocycline, doxycycline, oxytetracycline and no NDMA formation from tetracycline, chlorotetracycline and desmethylchlorotetracycline) may be understood from stereochemical considerations. The failure of dealkylative nitrosation reactions in the latter tetracyclines is explained by the formation of intramolecular hydrogen bridge linkages between epidimethylamino groups at C-4 and OH groups at C-6. This hypothesis was proved by the observations of NDMA formation from anhydrochlortetracycline and sodium nitrite at pH 2.
online pharmacy ref source: www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=680727&dopt=Abstract
Antimicrob Agents Chemother. 1982 Oct;22(4):598-603.
In vitro susceptibility and cross-resistance of South African isolates of Neisseria gonorrhoeae to 14 antimicrobial agents.
Liebowitz LD, Ballard RC, Koornhof HJ.
One hundred isolates of Neisseria gonorrhoeae obtained from patients attending clinics in Johannesburg, South Africa, were tested by a broth dilution technique for their minimal inhibitory concentrations (MICs) of benzyl penicillin G, ampicillin, cefoxitin, cefuroxime, cefotaxime, ceftriaxone, ceftazidime, tetracycline, minocycline, doxycycline, spectinomycin, rosaramicin, chloramphenicol, and rosoxacin. None of the isolates tested produced beta-lactamase. The MICs of penicillin ranged from less than or equal to 0.007 to 0.5 micrograms/ml. The isolates were also very susceptible to rosaramicin (minimal concentration at which 50% of isolates were inhibited [MIC50] = 0.02 micrograms/ml) and to the new cephalosporins (cefotaxime MIC50 less than 0.007 micrograms/ml, ceftriaxone MIC50 less than 0.007 micrograms/ml, and ceftazidime MIC50 less than 0.007 micrograms/ml). By using regression analysis, good correlation was observed between the MICs of penicillin and those of the other agents, with the exception of ceftriaxone, spectinomycin, and rosaramicin. The MICs and the minimal bactericidal concentrations were within a log2 concentration of each other.
online pharmacy ref source: www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=6817704&dopt=Abstract
Br J Vener Dis. 1983 Aug;59(4):245-8.
Comparison of tetracycline and minocycline in the treatment of non-gonococcal urethritis.
Oriel JD, Ridgway GL.
The activity of tetracycline hydrochloride and minocycline hydrochloride was compared against 12 strains of Chlamydia trachomatis and Ureaplasma urealyticum; minocycline was more active in vitro against both organisms. A group of 145 men with non-gonococcal urethritis was treated for one week with either tetracycline hydrochloride 500 mg six hourly or minocycline 50 mg twice daily. The clinical results obtained were similar: 61 of 77 (79%) men treated with tetracycline and 53 of 68 (78%) men treated with minocycline were free from urethritis one to two weeks after completing treatment. Both antibiotics were clinically effective against C trachomatis, but activity against U urealyticum was less consistent. Side effects were noted in 14 (18%) men treated with tetracycline and eight (12%) men treated with minocycline; they were predominantly gastrointestinal.
online pharmacy ref source: www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=6871652&dopt=Abstract
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