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Journal ArticleDOI

Pharmaceutical Applications of Cyclodextrins. 1. Drug Solubilization and Stabilization

Thorsteinn Loftsson, +1 more
- 01 Oct 1996 - 
- Vol. 85, Iss: 10, pp 1017-1025
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TLDR
The effects of substitution on various cyclodextrins properties and the forces involved in the drug-cyclodextrin complex formation are discussed, and methods which are useful in the optimization of complexation efficacy are reviewed.
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This article is published in Journal of Pharmaceutical Sciences.The article was published on 1996-10-01. It has received 2124 citations till now. The article focuses on the topics: Cyclodextrin & Inclusion compound.

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Citations
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Drug delivery system for poorly water-soluble compounds using lipocalin-type prostaglandin D synthase.

TL;DR: The feasibility of a novel drug delivery system (DDS), utilizing L-PGDS, for poorly water-soluble compounds such as diazepam (DZP), a major benzodiazepine anxiolytic drug, and 6-nitro-7-sulfamoylbenzo-2,3-dione (NBQX), an α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (
Journal ArticleDOI

Effect of external factors on the curcumin/2-hydroxypropyl-β-cyclodextrin: in vitro and in vivo study

TL;DR: Interestingly, it could be concluded that the degrees of curcumin stability improved by HPβCD grew with increasing drug–cyclodextrin binding ability.
Journal ArticleDOI

Investigation of solvent effect and cyclodextrins on fluorescence properties of ochratoxin A.

TL;DR: The fluorescence quenching of OTA by chloroform (aprotic) and water (protic) were studied in methanol as solvent at room temperature and it was inferred that non-linearity can be attributed to fractional accessibility of fluorophore to quencher.
Journal ArticleDOI

Spectrofluorimetric study of eflucimibe-γ-cyclodextrin inclusion complex

TL;DR: In this article, a 1:1 stoichiometric ratio and a 20 M−1 formation constant were obtained for eflucimibe in water containing 10% methanol.
Journal ArticleDOI

Do Cyclodextrins Aggregate in Water? Insights from NMR Experiments.

TL;DR: The question of aggregation of native cyclodextrins (α, β, and γ-) in aqueous solutions is addressed by using (1)H NMR techniques, including NMR diffusometry, relaxometry, and proton peak intensities, and within the detection limit of the NMR experiments, no aggregates ofcyclodextrin were observed.
References
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Journal ArticleDOI

The Determination of Enzyme Dissociation Constants

TL;DR: On the basis of the assumed theory the rate of the observed reaction is directly proportional to the concentration of the enzyme-substrate compound, where (E:l = (ES).
Book

Handbook of Pharmaceutical Excipients

TL;DR: The Handbook of Pharmaceutical Excipients is internationally recognised as the authoritative source of information on pharmaceutical excipients giving a comprehensive guide to uses, properties and safety.
Journal ArticleDOI

Cyclodextrin Inclusion Compounds in Research and Industry

TL;DR: As cyclodextrins catalyze several chemical reactions they and their functionalized derivatives provide useful enzyme models and can be used to advantage in the production of pharmaceuticals, pesticides, foodstuffs, and toilet articles.
Journal ArticleDOI

Stability of Protein Pharmaceuticals

TL;DR: Current methodology to stabilize proteins is presented, including additives, excipients, chemical modification, and the use of site-directed mutagenesis to produce a more stable protein species.
Book

Cyclodextrins in Pharmacy

TL;DR: The present study focused on the development and application of Cyclodextrin Inclusion Compounds in Various Drug Formulations, as well as their applications in Pharmaceutical Applications and Legal Aspects.