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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

A novel solid dosage form of rifampicin and isoniazid with improved functionality.

TL;DR: The problem of rifampicin degradation can be alleviated to a certain extent by this novel dosage form because of the minimization of physical contact between the 2 drugs and controlled release of rIFampic in acidic medium in the modified Rossett-Rice apparatus.
Journal ArticleDOI

Self-assembly Characterization of the β-Cyclodextrin and Hydrochlorothiazide System: NMR, Phase Solubility, ITC and QELS

TL;DR: In this article, the authors characterized the short distance host-guest interactions by NMR techniques such as 1H chemical shift, longitudinal relaxation times, and thermodynamic solubility experiments.
Journal ArticleDOI

Preparation, characterization, and drug release properties of poly(2‐hydroxyethyl methacrylate) hydrogels having β‐cyclodextrin functionality

TL;DR: In this article, a new β-cyclodextrin urethane-methacrylate monomer was synthesized from the reaction of toluene-2,4-diisocyanate, 2-hydroxyethyl methcrylate (HEMA), and β-CD.
Journal ArticleDOI

Role of humic acid on oral drug delivery of an antiepileptic drug.

TL;DR: It could be concluded that HA may be tried as a complexing agent for antiepileptic drug and other classes of low water-soluble drug.
Journal ArticleDOI

Thermodynamics and structure of inclusion compounds of tauro- and glyco-conjugated bile salts and β-cyclodextrin

TL;DR: The interaction between natural beta-cyclodextrin and bile salts common in rat, dog and man was studied using isothermal titration calorimetry, and the structural differences in the interaction were investigated by (1)H-ROESY NMR and molecular modeling.
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.