Literature DB >> 1510450

Comparison of nephrotoxicities of different polyoxyethyleneglycol formulations of amphotericin B in rats.

C Tasset1, V Preat, A Bernard, M Roland.   

Abstract

The aim of the present study was to assess whether amphotericin B (AmB)-Myrj 59, AmB-polyoxyethyleneglycol 24 cholesterol (PC), and AmB-Synperonic A50 (SA50) were less nephrotoxic than AmB-deoxycholate (DC). Rats were treated with the different AmB formulations (10 mg/kg of body weight) intraperitoneally or with the surfactants alone. A group of control rats receiving the vehicle was also examined. After 6 days of daily intraperitoneal injections of AmB-DC, decreased body weight and glomerular filtration rate as well as increased degree of diuresis, uremia, microalbuminuria, and N-acetyl-beta-D-glucosaminidase excretion in urine were noted. Urinary excretion of potassium and sodium was also decreased in AmB-DC-treated rats. Most of these effects were more pronounced with AmB-PC and AmB-SA50. In contrast, AmB-Myrj 59 was less nephrotoxic than AmB-DC. Indeed, after 6 days of treatment with AmB-Myrj 59, the natriuria, kaliuria, albuminuria, and glomerular filtration rates were unchanged compared with those of controls. Moreover, the body weight loss and uremia increase of the rats treated by AmB-Myrj 59 were less than those of the rats treated with the commercial preparation. Among the surfactants, only PC was toxic for the rats. The intrinsic toxicity of PC and the higher systemic exposure to AmB could contribute to increased toxicities of AmB-PC and AmB-SA50, respectively. AmB-Myrj 59 was less nephrotoxic than AmB-DC at equivalent areas under the plasma concentration-time curves. These preliminary results suggest that this formulation could be a good alternative to the commercial product.

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Year:  1992        PMID: 1510450      PMCID: PMC191615          DOI: 10.1128/AAC.36.7.1525

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  55 in total

1.  NEPHROTOXICITY OF AMPHOTERICIN B; EARLY AND LATE EFFECTS IN 81 PATIENTS.

Authors:  W T BUTLER; J E BENNETT; D W ALLING; P T WERTLAKE; J P UTZ; G J HILL
Journal:  Ann Intern Med       Date:  1964-08       Impact factor: 25.391

2.  ELECTROCARDIOGRAPHIC AND ELECTROLYTE ABNORMALITIES CAUSED BY AMPHOTERICIN B IN DOG AND MAN.

Authors:  W T BUTLER; J E BENNETT; G J HILL
Journal:  Proc Soc Exp Biol Med       Date:  1964 Aug-Sep

3.  Studies on glucosaminidase. 4. The fluorimetric assay of N-acetyl-beta-glucosaminidase.

Authors:  D H LEABACK; P G WALKER
Journal:  Biochem J       Date:  1961-01       Impact factor: 3.857

4.  High-performance liquid chromatographic determination of amphotericin B in human serum.

Authors:  C Brassinne; C Laduron; A Coune; J P Sculier; C Hollaert; N Collette; F Meunier
Journal:  J Chromatogr       Date:  1987-08-07

5.  Continuous-flow system for automation of latex immunoassay by particle counting.

Authors:  A M Bernard; R R Lauwerys
Journal:  Clin Chem       Date:  1983-06       Impact factor: 8.327

6.  [Prevention of nephrotoxicity of amphotericin B during the treatment of deep candidiasis].

Authors:  E Jacqz; R A Branch; H Heidemann; Y Aujard
Journal:  Ann Biol Clin (Paris)       Date:  1987       Impact factor: 0.459

7.  Molecular basis for the selective toxicity of amphotericin B for yeast and filipin for animal cells.

Authors:  J Kotler-Brajtburg; H D Price; G Medoff; D Schlessinger; G S Kobayashi
Journal:  Antimicrob Agents Chemother       Date:  1974-04       Impact factor: 5.191

8.  Leukoencephalopathy in patients treated with amphotericin B methyl ester.

Authors:  W G Ellis; R A Sobel; S L Nielsen
Journal:  J Infect Dis       Date:  1982-08       Impact factor: 5.226

9.  The influence of sodium status and furosemide on canine acute amphotericin B nephrotoxicity.

Authors:  J F Gerkens; R A Branch
Journal:  J Pharmacol Exp Ther       Date:  1980-08       Impact factor: 4.030

10.  Pilot study of amphotericin B entrapped in sonicated liposomes in cancer patients with fungal infections.

Authors:  J P Sculier; A Coune; F Meunier; C Brassinne; C Laduron; C Hollaert; N Collette; C Heymans; J Klastersky
Journal:  Eur J Cancer Clin Oncol       Date:  1988-03
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  6 in total

1.  A chemically modified tetracycline (CMT-3) is a new antifungal agent.

Authors:  Yu Liu; Maria E Ryan; Hsi-Ming Lee; Sanford Simon; George Tortora; Carol Lauzon; Michael K Leung; Lorne M Golub
Journal:  Antimicrob Agents Chemother       Date:  2002-05       Impact factor: 5.191

2.  Comparative pharmacokinetics, tissue distributions, and effects on renal function of novel polymeric formulations of amphotericin B and amphotericin B-deoxycholate in rats.

Authors:  I Echevarría; C Barturen; M J Renedo; I F Trocóniz; M C Dios-Viéitez
Journal:  Antimicrob Agents Chemother       Date:  2000-04       Impact factor: 5.191

3.  Cholesterol induces renal vasoconstriction and anti-natriuresis by inhibiting nitric oxide production in anesthetized rats.

Authors:  Libor Kopkan; Md Abdul H Khan; Agnieszka Lis; Mouhamed S Awayda; Dewan S A Majid
Journal:  Am J Physiol Renal Physiol       Date:  2009-09-23

4.  Formulation and evaluation of microemulsion based delivery system for amphotericin B.

Authors:  Pradnya S Darole; Darshana D Hegde; Hema A Nair
Journal:  AAPS PharmSciTech       Date:  2008-01-18       Impact factor: 3.246

5.  Oral administration of amphotericin B nanoparticles: antifungal activity, bioavailability and toxicity in rats.

Authors:  Mahasen A Radwan; Bushra T AlQuadeib; Lidija Šiller; Matthew C Wright; Benjamin Horrocks
Journal:  Drug Deliv       Date:  2017-11       Impact factor: 6.419

6.  Evaluation of hypokalemia and potassium supplementation during administration of liposomal-amphotericin B.

Authors:  Eiseki Usami; Michio Kimura; Tetsufumi Kanematsu; Shinya Yoshida; Takayuki Mori; Keiji Nakashima; Tomoko Matsuoka; Tomoaki Yoshimura; Hiromi Mori; Tadashi Sugiyama; Hitomi Teramachi
Journal:  Exp Ther Med       Date:  2014-02-11       Impact factor: 2.447

  6 in total

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