| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1375183 | Bioorganic & Medicinal Chemistry Letters | 2006 | 6 Pages |
The purpose of this study was to synthesize and study the in vitro enzymatic and non-enzymatic hydrolysis of indomethacin–TEG ester and amide prodrugs. It was found that the ester conjugate 10 was comparatively stable between pH 3 and 6 (half-life >90 h), with a half-life equal to 5.2 h in 80% buffered plasma. In contrast, the amide conjugate 12 appeared to be stable over the entire pH range studied with the only observed degradation being cleavage of the indolic N-4-chlorobenzoyl moiety.
Graphical abstractThe purpose of this study was to synthesize and study the in vitro enzymatic and non-enzymatic hydrolysis of indomethacin–TEG ester and amide prodrugs. It was found that the ester conjugate 10 was comparatively stable between pH 3 and 6 (half-life >90 h), with a half-life equal to 5.2 h in 80% buffered plasma. In contrast, the amide conjugate 12 appeared to be stable over the entire pH range studied with the only observed degradation being cleavage of the indolic N-4-chlorobenzoyl moiety.Figure optionsDownload full-size imageDownload as PowerPoint slide
