HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Biodistribution of amphotericin B when delivered through cholesterol hemisuccinate vesicles in normal and A. fumigatus infected mice.

AbstractPURPOSE:
This study compared the biodistribution of two amphotericin B formulations in normal and Aspergillus infected mice. Amphotericin B cholesterol hemisuccinate vesicles (ABCV) which reduces the toxicity of amphotericin B and thereby enhances its therapeutic efficacy in a murine model of aspergillosis was compared with conventional amphotericin B deoxycholate suspension (AmB(DOC)).
METHODS:
ABCV (12 mg/kg wt) and AmB(DOC) (2 mg/kg wt) were intravenously administered to normal and A. fumigatus infected mice. The concentration of amphotericin B in plasma and other organs was determined at different time points.
RESULTS:
It was observed that ABCV had a significantly different pharmacokinetic profile compared to conventional amphotericin B. In comparison to AmB(DOC) significantly lower levels of amphotericin B were observed in kidneys and plasma, the major target organs of toxicity. Animals receiving ABCV demonstrated high levels of amphotericin B in liver (38% retention till 48 h) and spleen (2.6% retention till 48 h) in comparison to AmB(DOC) (7.3% and 0.21% retention in liver and spleen respectively till 48 h). Biodistribution studies of ABCV in infected mice demonstrated that there was a moderate enhancement in levels of amphotericin B in liver, spleen, lungs and kidneys as compared to normal mice and the plasma levels were reduced. However, such observations were not made after AmB(DOC) administration to infected mice except for kidneys in which there was a marked increase in uptake as compared to normal mice.
CONCLUSIONS:
Our results suggest that prolonged retention of high concentrations of ABCV in reticuloendothelial system organs is the reason for its reduced toxicity. Enhanced localization of the drug at the infected site may lead to improvement in therapeutic efficacy.
AuthorsS Saxena, P C Ghosh
JournalPharmaceutical research (Pharm Res) Vol. 17 Issue 10 Pg. 1236-42 (Oct 2000) ISSN: 0724-8741 [Print] United States
PMID11145229 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antifungal Agents
  • Buffers
  • Cholesterol Esters
  • Detergents
  • Drug Carriers
  • Suspensions
  • Deoxycholic Acid
  • Amphotericin B
  • cholesteryl succinate
Topics
  • Amphotericin B (administration & dosage, blood, pharmacokinetics)
  • Animals
  • Antifungal Agents (administration & dosage, blood, pharmacokinetics)
  • Aspergillosis (blood, drug therapy, metabolism)
  • Aspergillus fumigatus
  • Buffers
  • Cholesterol Esters (administration & dosage, blood, pharmacokinetics)
  • Deoxycholic Acid (administration & dosage)
  • Detergents (administration & dosage)
  • Drug Carriers
  • Drug Stability
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Suspensions
  • Tissue Distribution

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: