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poly(vinylpyrrolidone-co-vinyl-acetate)

Known as: Copovidone, poly(V-co-V-Ac), poly(vinyl pyrrolidone-co-vinyl acetate) 
 
National Institutes of Health

Papers overview

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2017
2017
Co-amorphous drug-amino acid systems have gained growing interest as an alternative to common amorphous formulations which… Expand
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2013
2013
Abstract The objective of the study was to prepare solid dispersions containing a thermally unstable drug by hot-melt extrusion… Expand
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2012
2012
Hot-melt extrusion was applied to improve dissolution behavior of poorly soluble model drug fenofibrate. Blends of polymers were… Expand
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2012
2012
The purposes of this study were to assess the efficiency of different nifedipine amorphous solid dispersions (ASDs) in achieving… Expand
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Highly Cited
2011
Highly Cited
2011
Tumor segmentation in PET and CT images is notoriously challenging due to the low spatial resolution in PET and low contrast in… Expand
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Highly Cited
2011
Highly Cited
2011
We present a dynamical model incorporating both physiological and psychological factors that predicts changes in body mass and… Expand
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Highly Cited
2009
Highly Cited
2009
This study tested the hypothesis that bioactive coating glass (SiO(2)-CaO-P(2)O(5)-MgO-K(2)O-Na(2)O system), used for implant… Expand
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2009
2009
BackgroundIsobaric Tags for Relative and Absolute Quantitation (iTRAQ™) [Applied Biosystems] have seen increased application in… Expand
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Highly Cited
2007
Highly Cited
2007
Role of various water-soluble carriers was studied for dissolution enhancement of a poorly soluble model drug, rofecoxib, using… Expand
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Highly Cited
2000
Highly Cited
2000
17Beta-estradiol hemihydrate (17beta-E2) is a poorly water-soluble drug. Physical methods for improving the solubility and… Expand
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