scispace - formally typeset
Open AccessJournal ArticleDOI

Studies on Absorption of Eutectic Mixture. I. A Comparison of the Behavior of Eutectic Mixture of Sulfathiazole and that of Ordinary Sulfathiazole in Man.

Keiji Sekiguchi, +1 more
- 25 Nov 1961 - 
- Vol. 9, Iss: 11, pp 866-872
Reads0
Chats0
TLDR
In this paper, it was observed that a eutectic mixture of sulfathiazole and urea produces a microcrystalline suspension of the drug in water, which can be used to adjust the therapeutic effect of medical compounds.
Abstract
1) Sulfathiazole forms eutectic mixtures with urea, l-ascorbic acid, acetamide, nicotinic acid, nicotinamide, or succinimide. It was observed that a eutectic mixture of sulfathiazole and urea produces a microcrystalline suspension of sulfathiazole in water. 2) Sulfathiazole in a eutectic mixture with urea shows higher absorption and excretion after oral administration than ordinary sulfathiazole. 3) Since urea does not possess solubilizing action on sulfathiazole and also it does not enhance absorption of the drug physiologically, the accelerated absorption or excretion must be attributed to the physical state of sulfathiazole in its eutectic mixture with easily soluble compound, such as urea. 4) It is assumed that this new form of preparation will give a means of adjusting therapeutic effect of medical compounds.

read more

Citations
More filters
Journal ArticleDOI

Conventional and alternative pharmaceutical methods to improve oral bioavailability of lipophilic drugs

TL;DR: The different approaches discussed to overcome the problem of little or no water solubility, and successfully deliver the lipophilic drug for mankind are reviewed.
Journal ArticleDOI

Preparation and characterization of Domperidone- β-cyclodextrin complexes prepared by kneading method

TL;DR: In this paper, the authors used dispersion complex with β-cyclodextrin and hydroxy propyl cellulose by kneading technique to enhance the solubility and dissolution of domperidone.
Journal ArticleDOI

Fluidity and tableting characteristics of a powder solid dispersion of the low melting drugs ketoprofen and ibuprofen with crospovidone.

TL;DR: An SD of compounds with a low melting point such as KP or IP is suitable for tablet manufacture by direct compression with the addition of 1% MS, which lowered the SP value and eliminated sticking.
Journal ArticleDOI

Conversion of solid dispersion prepared by acid-base interaction into free-flowing and tabletable powder by using Neusilin® US2.

TL;DR: A mesoporous metalosilicate, Neusilin(®) US2, was incorporated in SDs prepared by using malic, tartaric and citric acids, and the addition of silicate converted SDs into powders, which were then characterized for flow properties, bulk and tap density, and tabletability.
DissertationDOI

Nanosuspensions of poorly soluble drugs for oral administration

TL;DR: AAPS abstract of Hesperidin smartCrystals-redispersibility and saturation properties, abstract of 2008 American Association of Pharmaceutical Sciences (AAPS) the Annual Meeting and Exposition, Atlanta, Georgia.
Related Papers (5)