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Investigations into the stabilisation of drugs by sugar glasses

Source :
International Journal of Pharmaceutics. 257(1-2):273-281
Publication Year :
2003
Publisher :
Elsevier Bedrijfsinformatie b.v., 2003.

Abstract

In this study the possibility to deliver the acid-sensitive enzyme alkaline phosphatase (AP) from calf intestine (CIAP) to the intestinal system by oral administration was investigated. Tablets were prepared and in vitro evaluated. Final proof of concept studies were performed in rats. This acid labile enzyme is potentially useful in the treatment of sepsis, a serious condition during which endotoxins can migrate into the blood stream. The CIAP was freeze-dried with inulin and subsequently compacted into round biconvex tablets with a diameter of 4mm and a weight of 25-30mg per tablet. The tablets were coated with an enteric coating in order to ensure their survival in the stomach. In vitro evaluation of tablets containing alkaline phosphatase from bovine intestine (BIAP) was the first step in the development. It was found that tablets without enteric coating dissolved rapidly in 0.10M HCl with total loss of enzymatic activity of the alkaline phosphatase. Tablets that were coated were stable for at least 2h in 0.10M HCl, but dissolved rapidly when the pH was increased to 6.8. Furthermore, it was shown that the enzymatic activity of the released BIAP was fully preserved. The in vivo test clearly showed that the oral administration of enteric coated tablets resulted in the release of enzymatically active CIAP in the intestinal lumen of rats. The location of the enhanced enzymatic activity of AP in the intestines varied with the time that had passed between the administration of the tablets and the sacrificing of the rats. Also, the level of enzymatic activity increased with an increasing number of tablets that were administered. © 2003 Elsevier Science B.V. All rights reserved.

Details

Language :
English
ISSN :
18733476 and 03785173
Volume :
257
Issue :
1-2
Database :
OpenAIRE
Journal :
International Journal of Pharmaceutics
Accession number :
edsair.dris...01423..bfe682cf4847d2a101126366d712ae62