کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1384358 | 982401 | 2013 | 6 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Microwave synthesis and in vitro stability of diclofenac-β-cyclodextrin conjugate for colon delivery Microwave synthesis and in vitro stability of diclofenac-β-cyclodextrin conjugate for colon delivery](/preview/png/1384358.png)
The aim of this work was to synthesize an ester prodrug of diclofenac and β-cyclodextrin suitable for colonic delivery. The synthesis of an ester linkage between diclofenac and β-cyclodextrin was conducted by the nucleophilic substitution of mono-6-tosyl-β-cyclodextrin under microwaves irradiation. After purification, the conjugate was characterized by matrix-assisted laser desorption/ionization-time of flight (MALDI-TOF) mass spectrometry; infrared (IR) spectroscopy; proton nuclear magnetic resonance (1H NMR) spectroscopy; and two-dimensional rotating frame nuclear overhauser effect (ROESY) spectroscopy. The purity was qualified by high pressure liquid chromatography (HPLC). To assess its potential for colonic delivery, the conjugate was evaluated for stability in simulated gastric and small intestinal fluids, and in fecal material from humans processed within a slurry under anaerobic conditions. The conjugate was successfully synthesized with a yield of 20% following purification. The mass spectra showed the parent peak m/z 1434 corresponding to [conjugate+Na] adduct. IR and NMR results confirmed that the carboxyl group of diclofenac is covalently bound to one of the hydroxyl groups of cyclodextrin by an ester linkage. Moreover, ROESY data indicated that the formation of the conjugate is not accompanied by the inclusion of diclofenac within the cyclodextrin. The conjugate was otherwise stable in simulated gastric and small intestinal conditions, but was also readily hydrolyzed liberating diclofenac in less than 2 h within the human fecal slurry. This confirmed the potential for this new prodrug as a carrier for colonic delivery.
► Novel cyclodextrin conjugate synthesised using microwave irradiation.
► Conjugates fully characterized using spectroscopic methods and HPLC analysis.
► The conjugate was stable in simulated gastric and small intestinal fluids.
► Conjugate readily hydrolyzed in human colonic conditions.
Journal: Carbohydrate Polymers - Volume 93, Issue 2, 2 April 2013, Pages 512–517