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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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Journal ArticleDOI

Characterization of the host-guest complex of a curcumin analog with β-cyclodextrin and β-cyclodextrin-gemini surfactant and evaluation of its anticancer activity.

TL;DR: The formation of host–guest complexes of NC 2067 with CD or CDgemini surfactant shows good potential to be used as a delivery system for anticancer agents and has been confirmed.
Journal ArticleDOI

Cetirizine release from cyclodextrin formulated compressed chewing gum

TL;DR: Physical mixtures suitable for use in cetirizine/CD formulations instead the complexes with respect to release yield may be avoided, avoiding unnecessary expenses for the complex preformulation.

Dissolution Enhancement of Poorly Soluble Drugs by Using Complexation Technique - A Review

TL;DR: In this paper, a comprehensive literature survey was made collect the rightful utilization of cyclodextrins as complexing, solubility enhancing agents and highlight the applications with these approaches.
Journal ArticleDOI

Kinetic measurements of the hydrolytic degradation of cefixime: effect of Captisol complexation and water-soluble polymers.

TL;DR: A strong stabilizing influence of the cefixime‐Captisol complexation and hypromellose was observed against aqueous mediated degradation, as compared with povidone and macrogol, which may have been due to the steric hindrance.
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.