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Biodistribution and In Vivo Antileishmanial Activity of 1,2-Distigmasterylhemisuccinoyl- sn -Glycero-3-Phosphocholine Liposome-Intercalated Amphotericin B.
- Source :
-
Antimicrobial agents and chemotherapy [Antimicrob Agents Chemother] 2017 Aug 24; Vol. 61 (9). Date of Electronic Publication: 2017 Aug 24 (Print Publication: 2017). - Publication Year :
- 2017
-
Abstract
- 1,2-Distigmasterylhemisuccinoyl- sn -glycero-3-phosphocholine (DSHemsPC) is a new lipid in which two molecules of stigmasterol (an inexpensive plant sterol) are covalently linked via a succinic acid to glycerophosphocholine. Our previous study revealed that liposome (Lip)-intercalated amphotericin B (AMB) prepared from DSHemsPC (DSHemsPC-AMB-Lip) possesses excellent colloidal properties and in vitro antifungal and antileishmanial activities similar to those of the liposomal AMB preparation AmBisome. The aim of this study was to determine the biodistribution and evaluate the antileishmanial effects of DSHemsPC-AMB-Lip in Leishmania major -infected BALB/c mice. The serum profile and tissue concentrations of AMB were similar in DSHemsPC-AMB-Lip- and AmBisome-treated mice after intravenous (i.v.) injection. Multiple i.v. doses of the micellar formulation of AMB (Fungizone; 1 mg/kg of body weight), DSHemsPC-AMB-Lip (5 mg/kg), and AmBisome (5 mg/kg) were used in L. major -infected BALB/c mouse models of early and established lesions. In a model of the early lesions of cutaneous leishmaniasis (CL), the results indicated that the level of footpad inflammation was significantly ( P < 0.001) lower in mice treated with DSHemsPC-AMB-Lip and AmBisome than mice treated with empty liposomes or 5% dextrose. The splenic and footpad parasite load was also significantly ( P < 0.001) lower in these groups of mice than in control mice that received 5% DW or free liposome. The in vivo activity of DSHemsPC-AMB-Lip was comparable to that of AmBisome, and both provided improved results compared to those achieved with Fungizone at the designated doses. The results suggest that systemic DSHemsPC-AMB-Lip administration may be useful for the treatment of leishmaniasis, and because it costs less to produce DSHemsPC-AMB-Lip than AmBisome, DSHemsPC-AMB-Lip merits further investigation.<br /> (Copyright © 2017 American Society for Microbiology.)
- Subjects :
- Animals
Antiprotozoal Agents pharmacokinetics
Disease Models, Animal
Drug Administration Routes
Drug Carriers therapeutic use
Female
Leishmania major pathogenicity
Leishmaniasis, Cutaneous parasitology
Liposomes therapeutic use
Mice
Mice, Inbred BALB C
Parasite Load
Spleen parasitology
Stigmasterol pharmacokinetics
Stigmasterol therapeutic use
Amphotericin B pharmacokinetics
Amphotericin B therapeutic use
Antiprotozoal Agents therapeutic use
Leishmania major drug effects
Leishmaniasis, Cutaneous drug therapy
Phosphatidylcholines pharmacokinetics
Phosphatidylcholines therapeutic use
Stigmasterol analogs & derivatives
Subjects
Details
- Language :
- English
- ISSN :
- 1098-6596
- Volume :
- 61
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- Antimicrobial agents and chemotherapy
- Publication Type :
- Academic Journal
- Accession number :
- 28630182
- Full Text :
- https://doi.org/10.1128/AAC.02525-16