Effects of synthetic lipids on solubilization and colloid stability of hydrophobic drugs (original) (raw)

Assembly of a model hydrophobic drug into cationic bilayer fragments

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Synthetic Bilayer Fragments for Solubilization of Amphotericin B

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Amphiphile-Induced Stabilization of Hydrophobic Colloidal Particles in Aqueous Solutions

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Solubilization of Itraconazole by Surfactants and Phospholipid-Surfactant Mixtures: Interplay of Amphiphile Structure, pH and Electrostatic Interactions

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Nanoparticles Methods for Hydrophobic Drugs — A Novel Approach: Graphical Abstract

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Think Beyond the Core: The Impact of the Hydrophilic Corona on the Drug Solubilization Using Polymer Micelles

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Nanosized bilayer disks: Attractive model membranes for drug partition studies

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Size-dependent interaction of hydrophilic/hydrophobic ligand functionalized cationic and anionic nanoparticles with lipid bilayers

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A Novel One-Step Drug-Loading Procedure for Water-Soluble Amphiphilic Nanocarriers

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Techniques to Enhance Solubility of Hydrophobic Drugs: An Overview

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Entrapment of Hydrophobic Drugs in Nanoparticle Monolayers with Efficient Release into Cancer Cells

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Effect of Lipophilicity of Dispersed Drugs on the Physicochemical and Technological Properties of Solid Lipid Nanoparticles

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The Open Drug Delivery Journal, 2008

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SOLUBILITY AND BIOAVAILABILITY ENHANCEMENT STRATEGIES FOR EFFECTIVE DELIVERY OF POORLY WATER SOLUBLE DRUGS BY NANO FORMULATIONS AND SOLID DISPERSIONS

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Substrate effects on interactions of lipid bilayer assemblies with bound nanoparticles

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Biomimetic Particles: Optimization of Phospholipid Bilayer Coverage on Silica and Colloid Stabilization

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Formation of Lipid Sheaths around Nanoparticle-Supported Lipid Bilayers

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The effective encapsulation of a hydrophobic lipid-insoluble drug in solid lipid nanoparticles using a modified double emulsion solvent evaporation method

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Drug Delivery Using Nanoparticle-Stabilized Nanocapsules

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Drug delivery strategies for poorly water-soluble drugs

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Structure of Self-Organized Multilayer Nanoparticles for Drug Delivery

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Langmuir, 2008

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