Journal of Bioequivalence & Bioavailability

Bioanalytical method development and validation for the simultaneous estimation of active metabolite thiocolchicoside and diclofenac in human plasma by LCMS/MS with a special emphashis to bioequivalence study

4^th World Congress on Bioavailability and Bioequivalence: Pharmaceutical R&D Summit

May 20-22, 2013 DoubleTree by Hilton, Beijing, China

Tapan Kumar Pal

AcceptedAbstracts: J Bioequiv Availab

Abstract:

Ulcerative colitis (UC) causes inflammation and ulceration of mucosa of colon and rectum. Literature reports involvement of mast cell activation & increased histamine secretion in the pathogenesis of colitis. Due to this reason, antihistaminic H1 blocker fexofenadine is currently under investigation in the management of colitis. D-glucosamine, an anti-inflammatory nutraceutical aminosugar is involved in biosynthesis of glucosaminoglycan, a major component of intestinal mucus that maintains integrity of gut wall. Levels of N-acetyl glucosamine and glucosamine synthetase go down during the attacks of UC. The present work was focused on design, kinetic studies & screening of colon-specific mutual prodrug of fexofenadine with D-glucosamine in TNBS-induced colitis. Fexofenadine and D-glucosamine were chemically linked through an amide linkage. Spectral analysis confirmed the structure of the prodrug (FG1).Highly hydrophilic nature of prodrug (log P: 0.046) enabled efficient delivery of fexofenadine to colon. FG1 was stable in stomach homogenates negligible release of fexofenadine in small intestinal homogenates. 82 % release of fexofenadine was observed in rat fecal matter at the end of 12 h (t 1/2: 260 min). The prodrug was twice as effective in lowering the quantifying parameters of colonic inflammation in TNBS- induced colitis than fexofenadine, D-glucosamine, their physical mixture and interestingly oral 5-amino salicylic acid while 2.7 times less effective than sulfasalazine. The prodrug restored the disrupted colonic architecture to normal and the results were comparable to sulfasalazine. Prodrug had no adverse effect on stomach, liver and pancreas. The results of the present work support the hypothesis of involvement of histamine in the pathogenesis of UC. This novel, dual acting colon- specific prodrug of fexofenadine could be used in combination with sulfasalazine as a maintenance therapy to counteract the relapse of UC