Role of synchronous release of sodium decanoate on sulpiride absorption in the intestine of the rat

Abraham Rubinstein*, Muhammad Baluom, Michael Friedman

*Corresponding author for this work

Research output: Contribution to journalConference articlepeer-review

Abstract

The use of absorption enhancers to increase drug bioavailability after oral administration was demonstrated. Sodium decanoate was employed for the enhancement of drug absorption following rectal administration. The non-synchronous formulations were significantly inferior to the synchronous ones in terms of the absorption enhancement of sulpiride. The extent and duration of the enhancement SD effect could be fine-tuned by manipulating the amounts of Hydroxypropyl methylcellulose in the synchronous oral formulations.

Original languageEnglish
Pages (from-to)263-264
Number of pages2
JournalAmerican Chemical Society, Polymer Preprints, Division of Polymer Chemistry
Volume40
Issue number1
StatePublished - Mar 1999
EventProceedings of the 1999 ACS Anaheim Meeting - Anaheim, CA, USA
Duration: 21 Mar 199925 Mar 1999

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