| Literature DB >> 15501699 |
Chiara Casolari1, Tiziana Rossi, Giosué Baggio, Andrea Coppi, Ginevra Zandomeneghi, Antonio Ippazio Ruberto, Claudio Farina, Giuliana Fabio, Andrea Zanca, Mario Castelli.
Abstract
Candidiasis and cryptococcosis are the most common fungal diseases among patients suffering from HIV infection. In the present work we assess whether the combined therapies, proteinase inhibitors and antimycotic drugs, could modify the therapeutic effect of antimycotics. An in vitro study to evaluate the antifungal effect of saquinavir and antimycotic drugs combination on yeast growth was performed. Strains of C. albicans and C. neoformans from HIV-seropositive patients were used. Susceptibility tests of yeasts to amphotericin B, 5-fluorocytosine, miconazole and fluconazole, singly and in combination with saquinavir, were performed in two different media. In the combinations the antimycotic agents and saquinavir were tested at sub-inhibitory concentrations: 0.1-10 microg ml(-1) and 12.50 microg ml(-1), respectively. The fractionary inhibitory concentration (FIC) index was also calculated. The results show that the interaction between saquinavir and all the antimycotic drugs never resulted in antagonism. Fluconazole acts in more synergistic way, no matter which medium is used. The combined therapy miconazole/saquinavir results in synergism, especially in Sabouraud. The total absence of antagonism and the presence of synergism suggest that a combined therapy could be proposed in the treatment of HIV-seropositive patients to reduce side effects, thanks to the use of lower doses of antimycotic drugs.Entities:
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Year: 2004 PMID: 15501699 DOI: 10.1016/j.phrs.2004.06.008
Source DB: PubMed Journal: Pharmacol Res ISSN: 1043-6618 Impact factor: 7.658