A comparative assessment of solubility advantage from glassy and crystalline forms of a water-insoluble drug.
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Nanomilling of Drugs for Bioavailability Enhancement: A Holistic Formulation-Process Perspective.Preformulation study of the inclusion complex irbesartan-beta-cyclodextrinReview: physical chemistry of solid dispersions.Aqueous solubility of crystalline and amorphous drugs: Challenges in measurement.The Role of Configurational Entropy in Amorphous Systems.Dissolution Enhancement of Rosuvastatin Calcium by Liquisolid Compact Technique.Studies on the effect of water-soluble polymers on drug-cyclodextrin complex solubility.Release profile and characteristics of electrosprayed particles for oral delivery of a practically insoluble drug.Solubility advantage from amorphous etoricoxib solid dispersions.Improved dissolution of a poorly water soluble drug in solid dispersions with polymeric and non-polymeric hydrophilic additives.
P2860
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P2860
A comparative assessment of solubility advantage from glassy and crystalline forms of a water-insoluble drug.
description
2007 nî lūn-bûn
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2007年の論文
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2007年学术文章
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2007年学术文章
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2007年学术文章
@zh-cn
2007年学术文章
@zh-hans
2007年学术文章
@zh-my
2007年学术文章
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2007年學術文章
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2007年學術文章
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name
A comparative assessment of so ...... rms of a water-insoluble drug.
@en
A comparative assessment of so ...... rms of a water-insoluble drug.
@nl
type
label
A comparative assessment of so ...... rms of a water-insoluble drug.
@en
A comparative assessment of so ...... rms of a water-insoluble drug.
@nl
prefLabel
A comparative assessment of so ...... rms of a water-insoluble drug.
@en
A comparative assessment of so ...... rms of a water-insoluble drug.
@nl
P1476
A comparative assessment of so ...... rms of a water-insoluble drug.
@en
P2093
Arvind K Bansal
Garima Chawla
P356
10.1016/J.EJPS.2007.05.111
P407
P577
2007-06-02T00:00:00Z