@article {Perkins151, author = {W E Perkins and R G Bianchi and S J Tremont and P W Collins and J J Casler and R L Fenton and G M Wagner and M P McGrath and J C Stolzenbach and D L Kowalski}, title = {Polymer delivery of the active isomer of misoprostol: a solution to the intestinal side effect problem.}, volume = {269}, number = {1}, pages = {151--156}, year = {1994}, publisher = {American Society for Pharmacology and Experimental Therapeutics}, abstract = {SC-53450 is a new polybutadiene-based polymer system with an acid labile diisopropyl silyl ether linker to which the active isomer of misoprostol (SC-30249) is attached covalently at position C-11. It was studied in rats and dogs to define its profile of gastrointestinal effects relative to misoprostol-hydroxypropyl methylcellulose (HPMC) and the systemic availability of prostaglandin from the polymer. Results of rat studies indicate that SC-53450 has a spectrum of mucosal protective activity similar to misoprostol-HPMC, being protective against indomethacin-induced gastric, cysteamine/indomethacin-induced duodenal and indomethacin-induced lower small bowel damage. SC-53450, in contrast to misoprostol-HPMC, was not diarrheagenic in the rat when administered intragastrically. The observation that SC-53450 is more than 4 times more potent than misoprostol-HPMC suggests the possibility of sustained gastric availability of the prostaglandin SC-30249. SC-53450 exhibited gastric antisecretory activity in histamine-stimulated gastric fistula dogs and protected against acidified aspirin-induced gastric damage in normal fasted beagles. Rat and dog experiments indicate that little, if any, polymer-derived prostaglandin is available systemically, suggesting SC-53450 will have reduced abuse potential in abortion induction. SC-53450 is a potential candidate to replace the present misoprostol formulation in the marketplace for the prevention of nonsteroidal anti-inflammatory drug-induced gastric damage.}, issn = {0022-3565}, URL = {https://jpet.aspetjournals.org/content/269/1/151}, eprint = {https://jpet.aspetjournals.org/content/269/1/151.full.pdf}, journal = {Journal of Pharmacology and Experimental Therapeutics} }