Answers are grounded in this paper and cite their sources.
Present research has been made to reduce frequency of administration and increase therapeutic efficacy by developing sustained release of diclofenac sodium. In this regard, prodrugs have been synthesized by using eco-friendly “green” materials such as cellulose and xylan by activation of carboxylic acid via N,N′-carbonyldiimidazole. The polymer–drug interactions were evaluated by means of FT-IR, powder X-ray diffraction, and thermal analysis techniques. In vitro release study of synthesized prodrugs might be suggested regarding protection of drug in the upper gastrointestinal tract, and, thereby, it is expected to reach the targeted site specifically to colon.
No takes yet. Share an insight, caveat, or question.
Kumar et al. (2013) studied this question.
Synapse has enriched 5 related papers. Consider them for comparative context: