soluplus

 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2012-2018
0102020122018

Papers overview

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2016
2016
The aim of this study was to develop a novel drug delivery system using two biocompatible copolymers of Solutol(®)HS15 and… (More)
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2016
2016
The aim of this study was to obtain a stable, amorphous solid dispersion (SD) with Soluplus, prepared by hot-melt extrusion (HME… (More)
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2015
2015
A novel supersaturable self-emulsifying drug delivery system (S-SEDDS) was formulated to improve the oral absorption of… (More)
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2015
2015
The purpose of this study was to apply viscoelastic properties of polymer and drug-polymer mixtures to determine processing… (More)
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2015
2015
Solid dispersions are a useful approach to improve the dissolution rate and bioavailability of poorly water-soluble active… (More)
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2015
2015
The conversion of active pharmaceutical ingredient (API) from amorphous to crystalline form is the primary stability issue in… (More)
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2014
2014
The purpose of this work was to explore the feasibility of using Soluplus(®) in preparing a fenofibrate (FBT) nanosuspension… (More)
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2014
2014
Poor solubility and dissolution of hydrophobic drugs have become a major challenge in pharmaceutical development. Drug… (More)
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2014
2014
Our study aimed to develop an amorphous 9-nitrocamptothecin solid dispersion (9-NC-SD) using polyvinyl caprolactam-polyvinyl… (More)
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2012
2012
For a successful formulation, various formulation parameters that play a crucial role are aqueous solubility; stability at… (More)
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