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Anticryptosporidial activity of ranalexin, lasalocid and azithromycin alone and in combination in cell lines
Author(s) -
Maria Carla Re,
Oscar Cirioni,
Francesco Barchiesi,
Giorgio Scalise
Publication year - 2000
Publication title -
journal of antimicrobial chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.124
H-Index - 194
eISSN - 1460-2091
pISSN - 0305-7453
DOI - 10.1093/jac/45.3.375
Subject(s) - lasalocid , azithromycin , serial dilution , parasite hosting , microbiology and biotechnology , cryptosporidium parvum , incubation , in vitro , incubation period , biology , growth inhibition , minimum inhibitory concentration , chemistry , medicine , biochemistry , antibiotics , ionophore , alternative medicine , pathology , membrane , world wide web , computer science
The in vitro anticryptosporidial activities of ranalexin, lasalocid and azithromycin alone and in combination were investigated against four clinical isolates of Cryptosporidium parvum. Susceptibility was tested by inoculating the isolates on to cell monolayers and determining the parasite count after 48 h incubation at 37 degrees C. The culture medium was supplemented with Dulbecco's modified Eagle's medium containing serial dilutions of the above-mentioned compounds. Ranalexin showed moderate anticryptosporidial activity: at a concentration of 64 mg/L it reduced parasite counts by 33.8%. Azithromycin at a concentration of 8 mg/L gave inhibition comparable to that observed with the highest concentration of ranalexin. Lasalocid showed the highest activity, with a 70.3% reduction in parasite counts at 2 mg/L. The combination of ranalexin 64 mg/L and lasalocid 2 mg/L completely suppressed parasite growth without harming the monolayer.

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