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The Solubility-Permeability Interplay for Solubility-Enabling Oral Formulations
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The Biopharmaceutical classification system (BCS) classifies the drugs based on their intrinsic
solubility and intestinal permeability. The drugs with good solubility and intestinal permeability
have good bioavailability. The drugs with poor solubility and poor permeability have solubility dependent
and permeability dependent bioavailability, respectively. In the current pharmaceutical field,
most of the drugs have poor solubility. To solve the problem of poor solubility, various solubility enhancement
approaches have been successfully used. The effects of these solubility enhancing approaches
on the intestinal permeability of the drugs are a matter of concern, and must not be overlooked.
The current review article focuses on the effect of various solubility enhancing approaches viz.
cyclodextrin, surfactant, cosolvent, hydrotropes, and amorphous solid dispersion, on the intestinal
permeability of drugs. This article will help in the designing of the optimized formulations having balanced
solubility enhancement without affecting the permeability of drugs.
Bentham Science Publishers Ltd.
Title: The Solubility-Permeability Interplay for Solubility-Enabling Oral Formulations
Description:
The Biopharmaceutical classification system (BCS) classifies the drugs based on their intrinsic
solubility and intestinal permeability.
The drugs with good solubility and intestinal permeability
have good bioavailability.
The drugs with poor solubility and poor permeability have solubility dependent
and permeability dependent bioavailability, respectively.
In the current pharmaceutical field,
most of the drugs have poor solubility.
To solve the problem of poor solubility, various solubility enhancement
approaches have been successfully used.
The effects of these solubility enhancing approaches
on the intestinal permeability of the drugs are a matter of concern, and must not be overlooked.
The current review article focuses on the effect of various solubility enhancing approaches viz.
cyclodextrin, surfactant, cosolvent, hydrotropes, and amorphous solid dispersion, on the intestinal
permeability of drugs.
This article will help in the designing of the optimized formulations having balanced
solubility enhancement without affecting the permeability of drugs.
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