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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

Recognition mechanism of D-and L-tryptophan enantiomers using 2-hydroxypropyl-α-or β-cyclodextrins as chiral selectors

TL;DR: It is determined that, together with charged groups of tryptophan ( NH 3 + and COO−), the indole moiety is the third guest interaction point with the cyclodextrin.
Journal ArticleDOI

Surface treatments on Tencel fabric: Grafting with β‐cyclodextrin

TL;DR: In this article, the grafting of acrylamidomethylated β-cyclodextrin and monochlorotriazinyl-β-cyclodesxtrin to Tencel and the inclusion of different molecules in the free cavities of cyclodextrins were investigated.
Journal ArticleDOI

Inclusion complexes of noscapine in β-cyclodextrin offer better solubility and improved pharmacokinetics

TL;DR: These studies propose for the first time a stable NOS–β-CD inclusion complex as an effective approach to enhance the solubility and bioavailability of NOS for anticancer therapy.
Journal ArticleDOI

Experimental and theoretical analysis of the interaction of (±)-cis-ketoconazole with β-cyclodextrin in the presence of (+)-l-Tartaric acid

TL;DR: Theoretical models of the three-component interaction were built up on the basis of the available NMR data, and the model derived from a folded conformation of ketoconazole turned out to be fully consistent with the molecular assembly found in aqueous solution, as inferred from NOE experiments.
Patent

Sulfoalkyl ether cyclodextrin compositions and methods of preparation thereof

TL;DR: In this article, a particulate SAE-CD composition has been proposed, which has an advantageous combination of physicochemical and morphological properties not found in known solid forms of SAE.
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.