IN-VIVO ACTIVITY AND TOLERANCE OF CONVENTIONAL FORMULATION VERSUS FATEMULSION FORMULATION OF AMPHOTERICIN-B IN EXPERIMENTAL DISSEMINATED CANDIDIASIS IN NEUTROPENIC RABBITS

Citation
P. Chavanet et al., IN-VIVO ACTIVITY AND TOLERANCE OF CONVENTIONAL FORMULATION VERSUS FATEMULSION FORMULATION OF AMPHOTERICIN-B IN EXPERIMENTAL DISSEMINATED CANDIDIASIS IN NEUTROPENIC RABBITS, Journal of antimicrobial chemotherapy, 39(3), 1997, pp. 427-430
Citations number
11
Categorie Soggetti
Microbiology,"Pharmacology & Pharmacy","Infectious Diseases
Journal title
Journal of antimicrobial chemotherapy
ISSN journal
03057453 → ACNP
Volume
39
Issue
3
Year of publication
1997
Pages
427 - 430
Database
ISI
SICI code
Abstract
Amphotericin a can cause significant toxicity but this can be reduced by direct dilution into a fat emulsion (Intralipid). To investigate th e potential use of amphotericin B diluted in Intralipid, a study was m ade of its activity in the treatment of subacute disseminated candidia sis in persistently granulocytopenic rabbits, compared with the same d ose of amphotericin B diluted in dextrose. Amphotericin-B-fat emulsion was at least as effective as amphotericin-B-dextrose. Amphotericin-B- fat emulsion was significantly more effective than amphotericin-B-dext rose therapy in reducing candida colony counts in both kidney and live r tissues (P < 0.05). Furthermore, amphotericin-B-fat emulsion was fou nd less toxic on the renal function than conventional amphotericin B ( P < 0.05). From these experimental results, we conclude that amphoteri cin-B-fat emulsion (Intralipid) was at least as effective and less tox ic than conventional amphotericin B.