| Literature DB >> 27184677 |
Famida G Hoosain1, Yahya E Choonara1, Pradeep Kumar1, Lomas K Tomar1, Charu Tyagi1, Lisa C du Toit1, Viness Pillay2.
Abstract
In this study, an optimized epichlorohydrin-crosslinked semi-interpenetrating polymer network xerogel matrix system (XePoMas) for the controlled delivery of sulpiride was prepared. The ability of XePoMas to sustain drug release was determined by in vitro and in vivo drug release experiments. Swelling of the xerogel over the 24-h experimental period ranged from 346 to 648%; swelling was observed to increase exponentially over the initial 8 h. In vitro drug release depicted a linear zero order drug release profile with an R 2 value of 0.9956. The ability of the fabricated XePoMas to sustain drug release and enhance bioavailability of sulpiride in vivo was investigated by evaluating the plasma drug concentration over 24 h in the large pig model. The optimized XePoMas formulation was shown to increase intestinal absorption of sulpiride to a greater extent than the marketed product in vivo, with a C max of 830.58 ng/mL after 15 h.Entities:
Keywords: bioavailability; gellan gum; poly(ethylene oxide); semi-interpenetrating polymer network; sulpiride; xerogel matrix
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Year: 2016 PMID: 27184677 DOI: 10.1208/s12249-016-0538-7
Source DB: PubMed Journal: AAPS PharmSciTech ISSN: 1530-9932 Impact factor: 3.246