2000
DOI: 10.1016/s0378-5173(00)00533-0
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Preparation and in-vitro evaluation of poly[N-vinyl-2-pyrrolidone-polyethylene glycol diacrylate]-chitosan interpolymeric pH-responsive hydrogels for oral drug delivery

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Cited by 76 publications
(28 citation statements)
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“…Preparation of these media was described in a previous study [27]. Accurately weighed amounts of beads (ranging from 0.1 to 0.2 g) were immersed in 40 mL of desired solution and, at fixed time intervals, the beads were separated from the medium through filtration.…”
Section: Swelling Measurementsmentioning
confidence: 99%
“…Preparation of these media was described in a previous study [27]. Accurately weighed amounts of beads (ranging from 0.1 to 0.2 g) were immersed in 40 mL of desired solution and, at fixed time intervals, the beads were separated from the medium through filtration.…”
Section: Swelling Measurementsmentioning
confidence: 99%
“…The drug concentration onto the hydrogels disk was measured and it is used as 0.5 mg/ml. All compositions present an initial release effect may be attributed to the diffusion of the drug caused by rapid gel swelling and also the release of drug adsorbed towards the surface of the gel matrix (Shanta and Harding, 2000). As DMAEMA content increase in the copolymer, the release rate and total released drug increases.…”
Section: Release Of Flutamidementioning
confidence: 96%
“…Further cationic polyelectrolyte nature of chitosan could provide a strong electrostatic interaction with mucosal surface. [5] The rank order of mucoadhesion for formulations was to be FC1 > FC2 > FC3 > FC4.…”
Section: Mucoadhesion Studymentioning
confidence: 99%
“…[5,6] A rat stomach mucosa was tied on the glass slide using a thread. About 50 hydrogel pieces were spread on to wet rinsed tissue specimen and prepared slide was hung on to one of the grooves of a USP tablet disintegration apparatus.…”
Section: Mucoadhesion Studymentioning
confidence: 99%