Mucoadhesive chitosan derivatives as novel drug carriers

Abstract

Chitosan on its own is a well-established natural polymer and is widely regarded as a biodegradable, biocompatible and nontoxic material for drug delivery applications. Although unmodified chitosan has some mucoadhesive properties on its own, its bioavailability is limited due to its short retention time in the body. Moreover, the high solubility of chitosan at acidic pH levels limits its use for mucosal drug delivery (especially through the oral route). Chemically-modified mucoadhesive chitosan, especially thiolated chitosan, has arisen as an alternative to create novel mucosal drug delivery systems. The mucoadhesive properties that are conferred to the thiolated chitosan certainly set this novel class of second or third-generation thiomers apart. To understand the significance of mucoadhesive chitosan, we first present the mechanism of mucoadhesion and provide comprehensive coverage of description of a variety of chemical modifications to prepare mucoadhesive thiolated chitosan derivatives. We then present the plethora of applications of these modified chitosan variants in a wide range of drug delivery fields, including the delivery of antigens, proteins and genes through a variety of routes, including oral, nasal, pulmonary, vaginal and others. By presenting the range of applications for mucoadhesive chitosan drug carriers we herein demonstrate that chemically-modified thiolated chitosan is a versatile and effective material for a new class of drug delivery vehicles. © 2015 Bentham Science Publishers

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Keywords

Chemically-modified chitosan, Chitosan nanogel, Chitosan nanoparticle, Drug delivery, Mucoadhesive drug carrier, Adhesiveness, Animals, Chitosan, Drug carriers, Drug delivery systems, Humans, Mucins, Mucous membrane, Nanostructures, 4 mercaptobenzoic acid, 4 thiobutylamidine, 6 mercaptonicotinic acid, Acetylcysteine, Amidine, Antigen, Benzoic acid derivative, Berberine, Chitosan derivative, Cysteine, Drug carrier, Enhanced green fluorescent protein, Glutathione, Insulin, Liposome, Metronidazole benzoate, Mucin, N acetylpenicillamine, Nanoparticle, Nicotinic acid derivative, Paclitaxel, Polyelectrolyte, Prednisolone, Protein, Riboflavin, Small interfering rna, Thioglycolic acid, Unclassified drug, Unindexed drug, Nanomaterial, Antimicrobial activity, Area under the curve, Article, Biocompatibility, Chemical modification, Drug bioavailability, Drug delivery system, Drug formulation, Electron transport, Eye, Gene, Gene silencing, Human, Hybrid, Hydrogel, In vitro study, In vivo study, Luminescence, Lung, Mouth cavity, Mucoadhesion, Mucosa, Mucus, Nonhuman, Nose mucosa, Particle size, Physical chemistry, Polymerization, Priority journal

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