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HP 55

Known as: HP-55 
 
National Institutes of Health

Papers overview

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2016
2016
Abstract The aim of present study was to investigate a pH-responsive and mucoadhesive nanoparticle system for oral… Expand
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Highly Cited
2011
Highly Cited
2011
The use of compendial pH 6.8 phosphate buffer to assess dissolution of enteric coated products gives rise to poor in vitro-in… Expand
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2008
2008
Previous attempts to improve the dissolution and absorption properties of itraconazole (ITZ) through advanced formulation design… Expand
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2007
2007
The primary objective of the study is to investigate the influence of composition parameters including drug:polymer ratio and… Expand
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2006
2006
The influence of the acidic film formers Eudragit L 100, HPMCAS-HF, HP-55, and shellac on the stability of the acid-labile proton… Expand
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2004
2004
The purpose of this study was to evaluate the nature of film formation on tablets with different compositions, using confocal… Expand
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2002
2002
A new gastrointestinal mucoadhesive patch system (GI-MAPS) has been designed for the oral delivery of protein drugs. The system… Expand
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2001
2001
Furosemide (frusemide) is a weakly acidic diuretic drug. Its absorption is poor and variable, in part due to its restricted sites… Expand
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1996
1996
A new triazol antifungal agent, (+)-2-(2,4-difluorophenyl)-3-methyl-1-(1H-1, 2,4-triazol-1-yl)-3-[6-(1H-1,2,4-triazol-1-yl… Expand
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1991
1991
A polymer carrier system was developed to reduce the bitterness of erythromycin and its 6-O-methyl derivative, clarithromycin, by… Expand
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