Literature DB >> 978408

Solubility of nonelectrolytes in polar solvents IV: nonpolar drugs in mixed solvents.

S H Yalkowsky, S C Valvani, G L Amidon.   

Abstract

The molecular and group surface area approach to solubility is shown to be applicable to mixed aqueous solvent systems. An equation is derived which is consistent with the exponential increase in the aqueous solubility of nonpolar drugs that frequently accompanies the addition of a cosolvent. This equation predicts that: (a) the ability of a drug to be solubilized by a cosolvent is proportional to its hydrophobic surface area per molecule, and (b) the ability of a cosolvent to solubilize any drug is inversely proportional to its interfacial tension against a reference liquid hydrocarbon. These predictions are experimentally verified with solubility studies of several alkyl p-aminobenzoates in propylene glycol-water mixtures and of hexyl p-aminobenzoate in mixtures of water the ethanol, methanol, ethylene glycol, propylene glycol, glycerin, and formamide.

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Year:  1976        PMID: 978408     DOI: 10.1002/jps.2600651018

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  8 in total

1.  Cosolvency and cosolvent polarity.

Authors:  J T Rubino; S H Yalkowsky
Journal:  Pharm Res       Date:  1987-06       Impact factor: 4.200

2.  1,4-Dioxane cosolvency impacts on trichloroethene dissolution and sorption.

Authors:  Justin Milavec; Geoffrey R Tick; Mark L Brusseau; Kenneth C Carroll
Journal:  Environ Pollut       Date:  2019-05-31       Impact factor: 8.071

3.  Triggered in situ drug supersaturation and hydrophilic matrix self-assembly.

Authors:  F Benaouda; M B Brown; G P Martin; S A Jones
Journal:  Pharm Res       Date:  2012-08-30       Impact factor: 4.200

4.  Development and evaluation of a chloramphenicol hypertonic ophthalmic solution.

Authors:  A V Jithan; C Krishna Mohan; M Vimaladevi
Journal:  Indian J Pharm Sci       Date:  2008-01       Impact factor: 0.975

5.  Cosolvency of dimethyl isosorbide for steroid solubility.

Authors:  H Zia; J K Ma; J P O'Donnell; L A Luzzi
Journal:  Pharm Res       Date:  1991-04       Impact factor: 4.200

6.  A quantitative structure-property relationship for predicting drug solubility in PEG 400/water cosolvent systems.

Authors:  Erik Rytting; Kimberley A Lentz; Xue-Qing Chen; Feng Qian; Srini Venkatesh
Journal:  Pharm Res       Date:  2004-02       Impact factor: 4.200

7.  Tools for Early Prediction of Drug Loading in Lipid-Based Formulations.

Authors:  Linda C Alskär; Christopher J H Porter; Christel A S Bergström
Journal:  Mol Pharm       Date:  2015-12-07       Impact factor: 4.939

Review 8.  Models for Predicting Drug Absorption From Oral Lipid-Based Formulations.

Authors:  Linda C Alskär; Christel A S Bergström
Journal:  Curr Mol Biol Rep       Date:  2015-10-07
  8 in total

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