Polysaccharides for Bacterially Triggered System in Colon Targeting

  • P Soni School Of Pharmacy, Devi Aahilya Vishwavidhyalaya ,Indore (M P), India
  • G P Chaudhary School Of Pharmacy, Devi Aahilya Vishwavidhyalaya ,Indore (M P), India
  • LK Soni School Of Pharmacy, Devi Aahilya Vishwavidhyalaya ,Indore (M P), India


Natural polysaccharides are now extensively used for the development of solid dosage forms for delivery of drug to the colon. The rationale for the development of a polysaccharide based delivery system for colon is the presence of large amounts of polysaccharidases in the human colon as the colon is inhabited by a large number and variety of bacteria which secrete many enzymes e.g. β-d-glucosidase, β-d-galactosidase, amylase, pectinase, xylanase, β-d-xylosidase, dextranase, etc. Various major approaches utilizing polysaccharides for colon-specific delivery are fermentable coating of the drug core, embedding of the drug in biodegradable matrix, formulation of drug-saccharide conjugate (prodrugs). A large number of polysaccharides have already been studied for their potential as colon-specific drug carrier systems, such as chitosan, pectin, chondroitin sulphate, cyclodextrin, dextrans, guar gum, inulin, amylose and locust bean gum.. The colon specific delivery systems based on a single polysaccharide do not efficiently permit targeted release. The pH and transit time can vary depending on the individual and the particular disease state. The conventional approaches give rise to premature drug release. The combination/chemically modified forms of polysaccharides eliminated the drawbacks associated with the use of single polysaccharide. Recent efforts and approaches exploiting these polysaccharides in colon-specific drug delivery by bacterially triggered systems. 

Keywords: Colon-specific drug delivery, Colon targeting, Polysaccharides, Carbohydratepolymer, Bacterially triggered system
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How to Cite
Soni, P., G. P. Chaudhary, and L. Soni. “Polysaccharides for Bacterially Triggered System in Colon Targeting”. Current Research in Pharmaceutical Sciences, Vol. 5, no. 3, Oct. 2015, pp. 65-94, https://crpsonline.com/index.php/crps/article/view/144.
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