“…The system comprises of a polysaccharide in the tablet core acting as a triggering agent for site specific release of drug in the colon. The system is first coated with acid soluble polymer [11] , followed with or without a barrier layer [12] and final coating of enteric polymer which releases the drug at targeted site i.e. colon.…”
“…The system comprises of a polysaccharide in the tablet core acting as a triggering agent for site specific release of drug in the colon. The system is first coated with acid soluble polymer [11] , followed with or without a barrier layer [12] and final coating of enteric polymer which releases the drug at targeted site i.e. colon.…”
“…E NE30D is insoluble polymer with low permeability which is often used in development of different formulation with time-controlled, pHindependent drug release [25][26][27][28]. It poses excellent film forming properties and it can be used for the preparation of different matrix-type drug delivery systems [29]. During the preparation of the spray-drying feed, E NE30D was added into the alkaline E S100 , prior the addition of the ethanolic solution of ZAL.…”
Section: Technological Properties Of the Microspheres Preparedmentioning
“…Polysaccharidegel-based colon cancer therapy was studied recently using 5-fluorouracil in CHT micro- [107] and nanospheres [102] or paclitaxel in chitin nanoparticles [132]. Protein delivery from polysaccharide gels was also studied: BSA, used as a model, was investigated by Zeng et al [162], Cwp84-loaded pectin beads were tested for oral vaccination against Clostridium difficile [118], while a review reporting some examples of the use of polysaccharide gels for insulin oral admistration was recently published by Maroni et al [82]. Numerous studies on delivery of probiotic bacteria by means of their entrapment in polysaccharide gels were also carried out [20].…”
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