The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Polysaccharides for Colon Targeted Drug Delivery
Open accessAbstract
Colon targeted drug delivery has the potential to deliver bioactive agents for the treatment of a variety of colonic diseases and to deliver proteins and peptides to the colon for their systemic absorption. Various strategies, currently available to target the release of drugs to colon, include formation of prodrug, coating of pH-sensitive polymers, use of colon-specific biodegradable polymers, timed released systems, osmotic systems, and pressure controlled drug delivery systems. Among the different approaches to achieve targeted drug release to the colon, the use of polymers especially biodegradable by colonic bacteria holds great promise. Polysaccharidases are bacterial enzymes that are available in sufficient quantity to be exploited in colon targeting of drugs. Based on this approach, various polysaccharides have been investigated for colon-specific drug release. These polysaccharides include pectin, guar gum, amylose, inulin, dextran, chitosan, and chondroitin sulphate. This family of natural polymers has an appeal to drug delivery as it is comprised of polymers with a large number of derivatizable groups, a wide range of molecular weights, varying chemical compositions, and, for the most part, low toxicity and biodegradability yet high stability. The most favorable property of these materials is their approval as pharmaceutical excipients.
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Cites
Wong, D., Larrabee, S., Clifford, K., Tremblay, J., & Friend, D. R. (1997) · Journal of Controlled Release · doi:10.1016/s0168-3659(97)01633-7 · Cited by 110
Chiu, H.-C., Hsiue, G.-H., Lee, Y.-P., & Huang, L.-W. (1999) · Journal of Biomaterials Science Polymer Edition · doi:10.1163/156856299x00504 · Cited by 88
Simonsen, L., Hovgaard, L., Mortensen, P. B., & Brøndsted, H. (1995) · European Journal of Pharmaceutical Sciences · doi:10.1016/0928-0987(95)00023-6 · Cited by 75
Cited by
Gut microorganisms, mammalian metabolism and personalized health care
Nicholson, J. K., Holmes, E., & Wilson, I. D. (2005) · Nature Reviews Microbiology · doi:10.1038/nrmicro1152 · Cited by 945
Crosslinked ionic polysaccharides for stimuli-sensitive drug delivery
Alvarez-Lorenzo, C., Blanco-Fernandez, B., Puga, A. M., & Concheiro, A. (2013) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2013.04.016 · Cited by 532
Gyles, D. A., Castro, L. D., Silva, J. O. C., & Ribeiro-Costa, R. M. (2017) · European Polymer Journal · doi:10.1016/j.eurpolymj.2017.01.027 · Cited by 527
Benalaya, I., Alves, G., Lopes, J., & Silva, L. R. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25021322 · Cited by 482
Choonara, B. F., Choonara, Y. E., Kumar, P., Bijukumar, D., du Toit, L. C., & Pillay, V. (2014) · Biotechnology Advances · doi:10.1016/j.biotechadv.2014.07.006 · Cited by 311
Metadata
- Authors
- Chourasia, M. K., & Jain, S. K.
- Venue
- Drug Delivery
- Publisher
- Informa UK Limited
- Published
- 2004-01
- Volume
- 11
- Issue
- 2
- Pages
- 129-148
- ISSN
- 1071-7544 (ISSN-L)
- 1521-0464
- OpenAlex
- W2131698002
- Cited by
- 349
- References
- 3
- FWCI
- 7.60
- Type
- journal article
- Language
- en
- Open access
- bronze
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Data sources
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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