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Gelucire 50-02

Known as: G 50-02 
 
National Institutes of Health

Papers overview

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2019
2019
To improve the dissolution and oral bioavailability of valsartan (VST), we previously formulated a supersaturable self… Expand
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2018
2018
ABSTRACT Lipid based‐formulations can enhance the bioavailability of poorly water‐soluble lipophilic drugs through enhanced… Expand
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2018
2018
PurposeMethotrexate (MTX), a potent anticancer drug, shows low oral bioavailability due to its low aqueous solubility and… Expand
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2016
2016
In this present study, the secretory transport of P-gp substrates, rhodamine 123 and digoxin, was evaluated using a Caco-2/HT29… Expand
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Highly Cited
2015
Highly Cited
2015
BACKGROUND Curcumin has a wide range of pharmacological activities including antioxidant, anti-inflammatory, antidiabetic… Expand
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2015
2015
Hybrid lipid-polymer particles are gaining increasing interest to be applied as drug delivery systems due to their greater… Expand
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2013
2013
Poor water-solubility is becoming the leading hurdle for novel drug molecules to reach the market. Enhancing the surface-to… Expand
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2004
2004
  • O. Chambina, V. Janninb, D. Championc, C. Chevaliera, M.-H. Rochat-Gonthiera, Y. Pourcelota
  • 2004
  • Corpus ID: 7911661
Recently, self-emulsifying drug delivery systems (SEDDS) have been developed as a method to deliver lipophilic drugs. Gelucire… Expand
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1999
1999
Theophylline extended-release spheres were prepared by extrusion-spheronization of matrix granulations previously obtained by… Expand
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Highly Cited
1991
Highly Cited
1991
Abstract— Release of D&C Yellow No. 10 and anhydrous theophylline have been determined from a thermosoftening, hydrophilic matrix… Expand
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