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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 preparation of methyl-β-cyclodextrin from dimethyl carbonate and β-cyclodextrin

TL;DR: The results show that the average degree of substitution of methyl-β-cyclodextrin can be dependent on the reaction temperature and the molar ratio of raw material primarily.
Journal ArticleDOI

Effect of preparation processes and structural insight into the supermolecular system: Bisacodyl and β-cyclodextrin inclusion complex.

TL;DR: It was found that acid solution and low temperature were unfavorable for formation of bisacodyl · β- CD and the pyridine moiety was suggested to be enclosed in the hydrophobic cavity of β-CD.
Journal ArticleDOI

Synergistic effect of Cu-nanoparticles and β-cyclodextrin functionalized reduced graphene oxide nanocomposite on the adsorptive remediation of tetracycline antibiotics.

TL;DR: In this article, copper nanoparticles immobilized-β-cyclodextrin functionalized reduced graphene oxide (Cu/β-CD/rGO) were successfully prepared as an efficient extractor of tetracycline (TC), oxytetracyCLine (OTC) and doxycycline (DC) antibiotics from different environmental water samples.
Journal ArticleDOI

Properties of Cassava Starch Modified by Amylomaltase from Corynebacterium glutamicum

TL;DR: Amylomaltase (α-1,4-glucanotransferase, AM; EC 2.4.1.25) from Corynebacterium glutamicum expressed in Escherichia coli was used to prepare the enzyme-modified cassava starch for food application and showed an improvement in the thermo-reversibility property.
Journal ArticleDOI

Overview of intranasally delivered peptides: key considerations for pharmaceutical development.

TL;DR: The goals of this undertaking were to build a database of the key physicochemical and pharmacokinetic properties of peptide delivered by the nasal route, to evaluate formulation attributes applied to IN peptide delivery systems, and to provide key considerations for IN delivery of peptides.
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.