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Supersaturable self-emulsifying drug delivery system: A strategy for improving the loading and oral bioavailability of quer ... 1 1 Introduction 1 2 Materials 2 3 Methods 2 3.1 Optimizing QT loaded superstaurable self-emulsifying delivery system (QT-sSEEDS) 2 3.1.1 Saturation solubility of QT 2 3.1.2 Formulating SEDDS and determining the QT pay load 2 3.1.3 Screening of precipitation inhibitor (PI) 2 3.1.4 Optimizing the concentration of PI 2 3.2 Characterization of QT-sSEDDS 2 3.2.1 Physicochemical characterization 2 3.2.2 Functional stability 3 3.3 In vitro precipitate characterization 3 3.4 Stability study QT-sSEDDS 3 3.4.1 Stability study in simulated gastro-intestinal fluids 3 3.4.2 Drug content determination 3 3.4.3 Storage stability 3 3.5 In vitro drug release 3 3.6 pH stat lipolysis 4 3.7 Caco-2 cell culture experiments 4 3.7.1 Cell uptake 4 3.7.2 Quantitative uptake 4 3.7.3 Cell viability 4 3.8 In vivo studies 4 3.9 Pharmacokinetics 4 3.10 Statistical analysis 5 4 Results & discussion 5 4.1 Optimization of formulation parameters 5 4.1.1 Solubility of QT in excipients 5 4.1.2 Effect of QT payload on SEDDS 5 4.1.3 Screening of PI 6 4.1.4 Optimizing the concentration of PI 6
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