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Eudragit E PO

 
National Institutes of Health

Papers overview

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2017
2017
Abstract Taste of a pharmaceutical formulation is an important parameter for the effectiveness of pharmacotherapy. Cetirizine… Expand
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2016
2016
This article uses conventional and newly extended solubility parameter (δ) methods to identify polymeric materials capable of… Expand
2015
2015
Orodispersible tablets (ODTs) and orodispersible films (ODFs) are solid oral dosage forms disintegrating or dissolving rapidly… Expand
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2013
2013
PURPOSE Development of a novel, rapid, miniaturized approach to identify amorphous solid dispersions with maximum supersaturation… Expand
2013
2013
Polymethacrylates such as Eudragit® polymers are well established as drug delivery matrix. Here, we synthesize several Eudragit E… Expand
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2011
2011
The aim of this study was to evaluate the influence of Na-bicarbonate as an effervescent agent on the floating and sustained… Expand
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2009
2009
The aim of the present study was to investigate the influence of Eudragit® E PO on the drug release mechanism of Eudragit® L 100… Expand
Highly Cited
2006
Highly Cited
2006
The formation of interpolyelectrolyte complexes (IPEC) between Eudragit E PO (EE) and Eudragit L 100-55 (EL) was investigated… Expand
Highly Cited
2006
Highly Cited
2006
The purpose of this study was to investigate the influence of sodium bicarbonate on the physicochemical properties of controlled… Expand
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Highly Cited
2001
Highly Cited
2001
A transdermal steroidal delivery system usually contains a high concentration of drug to obtain high drug fluxes. The present… Expand