In vitro lipolysis models as a tool for the characterization of oral lipid and surfactant based drug delivery systems.
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Pharmacokinetic aspects and in vitro-in vivo correlation potential for lipid-based formulationsEffect of lipolysis on drug release from self-microemulsifying drug delivery systems (SMEDDS) with different core/shell drug location.Effects of PEGylated lipid nanoparticles on the oral absorption of one BCS II drug: a mechanistic investigationIn vitro lipolysis data does not adequately predict the in vivo performance of lipid-based drug delivery systems containing fenofibrate.Improvement of oral availability of ginseng fruit saponins by a proliposome delivery system containing sodium deoxycholateCharacterising lipid lipolysis and its implication in lipid-based formulation development.Biorelevant in-vitro performance testing of orally administered dosage forms.Development of the Digestive System-Experimental Challenges and Approaches of Infant Lipid Digestion.Insights on novel particulate self-assembled drug delivery beads based on partial inclusion complexes between triglycerides and cyclodextrins.Self-assembled structures formed during lipid digestion: characterization and implications for oral lipid-based drug delivery systems.The Precipitation Behavior of Poorly Water-Soluble Drugs with an Emphasis on the Digestion of Lipid Based Formulations.From nanoemulsions to self-nanoemulsions, with recent advances in self-nanoemulsifying drug delivery systems (SNEDDS).Comparison of lipases for in vitro models of gastric digestion: lipolysis using two infant formulas as model substrates.Design of lipid-based formulations for oral administration of poorly water-soluble drug fenofibrate: effects of digestion.The In Vitro Lipolysis of Lipid-Based Drug Delivery Systems: A Newly Identified Relationship between Drug Release and Liquid Crystalline Phase.Insights into drug precipitation kinetics during in vitro digestion of a lipid-based drug delivery system using in-line raman spectroscopy and mathematical modeling.In vitro lipolysis and intestinal transport of β-arteether-loaded lipid-based drug delivery systems.In vitro and in vivo evaluations of the performance of an indirubin derivative, formulated in four different self-emulsifying drug delivery systemsSolid Lipid Particles for Oral Delivery of Peptide and Protein Drugs II – The Digestion of Trilaurin Protects Desmopressin from Proteolytic Degradation
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P2860
In vitro lipolysis models as a tool for the characterization of oral lipid and surfactant based drug delivery systems.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 15 March 2011
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
In vitro lipolysis models as a ...... t based drug delivery systems.
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In vitro lipolysis models as a ...... t based drug delivery systems.
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type
label
In vitro lipolysis models as a ...... t based drug delivery systems.
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In vitro lipolysis models as a ...... t based drug delivery systems.
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In vitro lipolysis models as a ...... t based drug delivery systems.
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In vitro lipolysis models as a ...... t based drug delivery systems.
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P1476
In vitro lipolysis models as a ...... t based drug delivery systems.
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P2093
Anne T Larsen
Philip Sassene
P304
P356
10.1016/J.IJPHARM.2011.03.002
P407
P577
2011-03-15T00:00:00Z