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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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Applications of steroid drugs entrapped in cyclodextrins

TL;DR: The effect of cyclodextrin–steroid interaction on the solubility, stability and bioavailability of the entrapped steroid drugs is highlighted, highlighting the importance of the catalysis and inhibition of various biotransformation reactions of steroids by cyclodesxtrin complexation used in biotechnology.
Journal ArticleDOI

Efficient Encapsulation of Citral in Fast-Dissolving Polymer-Free Electrospun Nanofibers of Cyclodextrin Inclusion Complexes: High Thermal Stability, Longer Shelf-Life, and Enhanced Water Solubility of Citral

TL;DR: Citral was efficiently encapsulated in citral/CD-IC-NFs, and these citrals have been shown to be fast dissolving and have enhanced water solubility of citral along with high-temperature stability and a longer shelf-life.
Journal ArticleDOI

An econazole β-cyclodextrin inclusion complex: an unusual dissolution rate, supersaturation, and biological efficacy example

TL;DR: Toxicity testing on a human buccal epithelium in vitro model — based on TR146 cells — showed that the physical mixture was more toxic than the inclusion complex when TR146 cell mortality was evaluated.
Journal ArticleDOI

Solubility of Clonazepam, Diazepam, Lamotrigine, and Phenobarbital in N-Methyl-2-pyrrolidone + Water Mixtures at 298.2 K

TL;DR: Experimental solubilities of clonazepam, diazepam, lamotrigine, and phenobarbital in binary solvent mixtures of N-methyl-2-pyrrolidone (NMP) + water at 298.2 K were reported.
Journal ArticleDOI

Hybrid liposomal PEGylated calix[4]arene systems as drug delivery platforms for curcumin.

TL;DR: At concentrations exceeding the critical micellization concentration of PEGylated calixarene, the tremendous solubility enhancement of curcumin is attributed to additional solubilization and hydrophobic non-covalent interactions of the drug with supramolecular aggregates.
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