In Vitro Activities of Antibiotics against Plasmodium falciparum Are Inhibited by Iron
Roxithromycin
Spiramycin
DOI:
10.1128/aac.45.6.1746-1750.2001
Publication Date:
2002-07-27T09:56:57Z
AUTHORS (7)
ABSTRACT
ABSTRACT The in vitro activities of cyclines (tetracycline, doxycycline, minocycline, oxytetracycline, and rolitetracycline), macrolides (erythromycin, spiramycin, roxithromycin, lincomycin), quinolones (norfloxacin ofloxacin), rifampin, thiamphenicol, tobramycin, metronidazole, vancomycin, phosphomycin, cephalosporins (cephalexin, cefaclor, cefamandole, cefuroxime, ceftriazone, cefotaxime, cefoxitin) were evaluated on Plasmodium falciparum clones, using an isotopic, micro-drug susceptibility test. Only tetracyclines, macrolides, quinolones, rifampin demonstrated activity against P. , which increased after a prolonged exposure (96 or 144 h). In the presence iron (FeCl 3 ), only tetracyclines norfloxacin decreased. Their intraerythrocytic stages multidrug-resistant their efficacy vivo favor use antibiotics as antimalarial drugs. However, due to slow action fact that they act better contact, probably need be administered conjunction with rapidly acting drug, such short course chloroquine quinine.
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