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Phase solubility techniques

T K Higuchi, +1 more
- Vol. 4, pp 212-217
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The article was published on 1965-01-01 and is currently open access. It has received 2515 citations till now. The article focuses on the topics: Phase (matter) & Solubility.

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Hygroscopicity, phase solubility and dissolution of various substituted sulfobutylether β-cyclodextrins (SBE) and danazol–SBE inclusion complexes

TL;DR: The dissolution of the complexes was significantly greater than that of the corresponding physical mixtures indicating that the formation of amorphous complex increased the solubility of poorly soluble danazol.
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Inclusion complex of usnic acid with β -cyclodextrin: characterization and nanoencapsulation into liposomes

TL;DR: Interestingly, the encapsulation of UA:βCD into the liposomes resulted in a modulation of in vitro kinetics of release of UA, which presented a more prolonged release profile of free usnic acid compared to usnic Acid-loaded liposome.
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Physicochemical properties of the fluoroquinolone antimicrobials. III. Complexation of lomefloxacin with various metal ions and the effect of metal ion complexation on aqueous solubility

TL;DR: In this paper, the stability constants and stoichiometries of lomefloxacin were determined by measuring the change of aqueous solubility as a function of metal ion concentration.
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Inclusion complex of ellagic acid with β-cyclodextrin: Characterization and in vitro anti-inflammatory evaluation

TL;DR: In this article, a freeze-dried inclusion complex of ellagic acid/β-cyclodextrin (EACD) was investigated both in solution and solid state by means of aqueous solubility, in-vitro dissolution, absorption, fluorescence, Fourier transform infrared spectroscopy (FTIR), powder X-ray diffractometry (XRD), scanning electron microscopy (SEM), nuclear magnetic resonance (NMR) and molecular modeling methods.
Journal ArticleDOI

The effects of cyclodextrins on drug absorption II. In vivo observations

TL;DR: Complex formation of diazepam and of naproxen with β-cyclodextrin results in increased aqueous solubility of the drug and the ability of mucus and bile samples to displace eomplexed drug was shown in vitro in displacement studies with phenolphthalein.
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