Comparison of nephrotoxicities of different polyoxyethyleneglycol formulations of amphotericin B in rats
- PMID: 1510450
- PMCID: PMC191615
- DOI: 10.1128/AAC.36.7.1525
Comparison of nephrotoxicities of different polyoxyethyleneglycol formulations of amphotericin B in rats
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.
Similar articles
-
Potassium depletion potentiates amphotericin-B-induced toxicity to renal tubules.Nephron. 1995;70(2):235-41. doi: 10.1159/000188590. Nephron. 1995. PMID: 7566310
-
Pharmacokinetics and Renal Toxicity of Monomeric Amphotericin B in Rats after a Multiple Dose Regimen.Pharm Nanotechnol. 2016;4(1):16-23. doi: 10.2174/2211738504666160301233754. Pharm Nanotechnol. 2016. PMID: 27774409 Free PMC article.
-
Plasma protein binding of amphotericin B and pharmacokinetics of bound versus unbound amphotericin B after administration of intravenous liposomal amphotericin B (AmBisome) and amphotericin B deoxycholate.Antimicrob Agents Chemother. 2002 Mar;46(3):834-40. doi: 10.1128/AAC.46.3.834-840.2002. Antimicrob Agents Chemother. 2002. PMID: 11850269 Free PMC article. Clinical Trial.
-
Carrier effects on biological activity of amphotericin B.Clin Microbiol Rev. 1996 Oct;9(4):512-31. doi: 10.1128/CMR.9.4.512. Clin Microbiol Rev. 1996. PMID: 8894350 Free PMC article. Review.
-
Amphotericin-B colloidal dispersion. A review of its use against systemic fungal infections and visceral leishmaniasis.Drugs. 1998 Sep;56(3):365-83. doi: 10.2165/00003495-199856030-00008. Drugs. 1998. PMID: 9777313 Review.
Cited by
-
A chemically modified tetracycline (CMT-3) is a new antifungal agent.Antimicrob Agents Chemother. 2002 May;46(5):1447-54. doi: 10.1128/AAC.46.5.1447-1454.2002. Antimicrob Agents Chemother. 2002. PMID: 11959581 Free PMC article.
-
Comparative pharmacokinetics, tissue distributions, and effects on renal function of novel polymeric formulations of amphotericin B and amphotericin B-deoxycholate in rats.Antimicrob Agents Chemother. 2000 Apr;44(4):898-904. doi: 10.1128/AAC.44.4.898-904.2000. Antimicrob Agents Chemother. 2000. PMID: 10722488 Free PMC article.
-
Formulation and evaluation of microemulsion based delivery system for amphotericin B.AAPS PharmSciTech. 2008;9(1):122-8. doi: 10.1208/s12249-007-9022-8. Epub 2008 Jan 18. AAPS PharmSciTech. 2008. PMID: 18446472 Free PMC article.
-
Oral administration of amphotericin B nanoparticles: antifungal activity, bioavailability and toxicity in rats.Drug Deliv. 2017 Nov;24(1):40-50. doi: 10.1080/10717544.2016.1228715. Drug Deliv. 2017. PMID: 28155565 Free PMC article.
-
Cholesterol induces renal vasoconstriction and anti-natriuresis by inhibiting nitric oxide production in anesthetized rats.Am J Physiol Renal Physiol. 2009 Dec;297(6):F1606-13. doi: 10.1152/ajprenal.90743.2008. Epub 2009 Sep 23. Am J Physiol Renal Physiol. 2009. PMID: 19776170 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources