Unusual lipid structures selectively reduce the toxicity of amphotericin B.
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Inhibition of amphotericin B (Fungizone) toxicity to cells by egg lecithin-glycocholic acid mixed micellesIn vitro renal toxicity and in vivo therapeutic efficacy in experimental murine cryptococcosis of amphotericin B (Fungizone) associated with IntralipidComparison of fungizone, Amphotec, AmBisome, and Abelcet for treatment of systemic murine cryptococcosis.Lipid complexing decreases amphotericin B inflammatory activation of human neutrophils compared with that of a desoxycholate-suspended preparation of amphotericin B (Fungizone).Safety, tolerance, and pharmacokinetics of amphotericin B lipid complex in children with hepatosplenic candidiasis.SolEmuls technology: a way to overcome the drawback of parenteral administration of insoluble drugs.Lipid-based amphotericin B for the treatment of fungal infections.In vitro and in vivo antifungal activity of amphotericin B lipid complex: are phospholipases important?Liposomal Formulations in Clinical Use: An Updated Review.Nanodisks derived from amphotericin B lipid complex.Dose-dependent pharmacokinetics of amphotericin B lipid complex in rabbits.A pharmacokinetic study of amphotericin B lipid complex injection (Abelcet) in patients with definite or probable systemic fungal infections.A phospholipid-apolipoprotein A-I nanoparticle containing amphotericin B as a drug delivery platform with cell membrane protective propertiesAmphotericin B and its new formulations: pharmacologic characteristics, clinical efficacy, and tolerability.Stealth Amphotericin B nanoparticles for oral drug delivery: In vitro optimization.Characterization of the colloidal properties, in vitro antifungal activity, antileishmanial activity and toxicity in mice of a di-stigma-steryl-hemi-succinoyl-glycero-phosphocholine liposome-intercalated amphotericin B.The amphotericin B lipid complex or Abelcet: its Belgian connection, its mode of action and specificity: a review.Pharmacokinetics of conventional formulation versus fat emulsion formulation of amphotericin B in a group of patients with neutropenia.Serum pharmacology of amphotericin B applied in lipid emulsions.Comparison of the efficacies of various formulations of amphotericin B against murine visceral leishmaniasis.Recommendations for the treatment of fungal pneumonias.The lipid formulations of amphotericin B.Amphotericin B is cytotoxic at locally delivered concentrationsStudy of the effects of liposomal amphotericin B on Candida albicans, Cryptococcus neoformans, and erythrocytes by using small unilamellar vesicles prepared from saturated phospholipids.Amphotericin B: delivery systems.Carrier effects on biological activity of amphotericin B.Liposomes: realizing their promise.Influence of phospholipid/amphotericin B ratio and phospholipid type on in vitro renal cell toxicities and fungicidal activities of lipid-associated amphotericin B formulations.Immunological effects of amphotericin B and liposomal amphotericin B on splenocytes from immune-normal and immune-compromised mice.Amphotericin B induces interdigitation of apolipoprotein stabilized nanodisk bilayers.Comparative efficacies of four amphotericin B formulations--Fungizone, amphotec (Amphocil), AmBisome, and Abelcet--against systemic murine aspergillosis.Structure-activity study of inhibition of amphotericin B (Fungizone) binding to sterols, toxicity to cells, and lethality to mice by esters of sucrose.Amphotericin B lipid complex therapy of experimental fungal infections in miceLiposomal amphotericin B inhibits in vitro T-lymphocyte response to antigenEfficacy and safety of amphotericin B colloidal dispersion compared with those of amphotericin B deoxycholate suspension for treatment of disseminated murine cryptococcosis.Liposomal nanomedicines.NanoDisk containing super aggregated amphotericin B: a high therapeutic index antifungal formulation with enhanced potencyNovel platforms for vascular carriers with controlled geometry.Factors affecting the pharmacokinetics and pharmacodynamics of liposomal drugs.Bioinspired Calcium Phosphate Nanoparticles Featuring as Efficient Carrier and Prompter for Macrophage Intervention in Experimental Leishmaniasis.
P2860
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P2860
Unusual lipid structures selectively reduce the toxicity of amphotericin B.
description
1988 nî lūn-bûn
@nan
1988 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1988 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
name
Unusual lipid structures selectively reduce the toxicity of amphotericin B.
@ast
Unusual lipid structures selectively reduce the toxicity of amphotericin B.
@en
type
label
Unusual lipid structures selectively reduce the toxicity of amphotericin B.
@ast
Unusual lipid structures selectively reduce the toxicity of amphotericin B.
@en
prefLabel
Unusual lipid structures selectively reduce the toxicity of amphotericin B.
@ast
Unusual lipid structures selectively reduce the toxicity of amphotericin B.
@en
P2093
P2860
P356
P1476
Unusual lipid structures selectively reduce the toxicity of amphotericin B.
@en
P2093
Minchey SR
Popescu MC
Shyamsunder E
Taraschi T
P2860
P304
P356
10.1073/PNAS.85.16.6122
P407
P577
1988-08-01T00:00:00Z