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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
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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.

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Design of pharmaceutical cocrystals for drug solubility improvement

TL;DR: In this article, the synthesis and application of cocrystal pharmaceutical systems is described. The solubility and bioavailability of such systems are several orders of magnitude higher than those for the individual compounds and much higher than the respective parameters attainable by other technologies.
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The effect of composition and ageing on the dissolution rates of chlorpropamide-urea solid dispersions.

TL;DR: The optimum dissolution rate composition found was for a melt composed of 30% w/w chlorpropamide which possessed an intrinsic dissolution rate 930 times greater than for the pure drug.
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Enhancement of the dissolution profile of allopurinol by a solid dispersion technique.

TL;DR: To improve the solubility, and therefore the dissolution of poorly water-soluble allopurinol, different methods such as melting and solvent evaporation methods were used to improve dissolution characteristics andsolubility.
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Interplay of formulation and process methodology on the extent of nifedipine molecular dispersion in polymers.

TL;DR: To explore those supersaturation systems for use in drug delivery of poorly water soluble drugs, it is critical to balance drug-polymer interactions and matrix glass transition point and to consider a process technology with a fast solidification rate during formulation and process development of amorphous SD.
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