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Review Article


 

Thiolated Chitosans: Novel Polymers for Mucoadhesive Drug Delivery – A Review

 

SA Sreenivas1* and KV Pai2

1Department of Pharmaceutics, KLES’s College of Pharmacy, Vidyanagar, Hubli, Karnataka. 2Department of Industrial Chemistry, Shankaraghatta, Shimoga, Karnataka, India.

*Corresponding author: E-mail: saiseenu7@rediffmail.com;  Tel: 09242892034

 

Tropical Journal of Pharmaceutical Research, September 2008; 7(3): 1077-1088

Abstract

Chitosan is a natural polycationic copolymer consisting of glucosamine and N-acetylglucosamine units. The polymer has valuable properties as a biomaterial because it is considered to be biocompatible, biodegradable and non-toxic. The purpose of this review article is to provide detailed information about thiolated chitosans which are gaining popularity because of their  high mucoadhsiveness and  extended drug release properties. The derivatization of the primary amino groups of chitosan with coupling reagents bearing thiol functions leads to the formation of thiolated chitosans. Various properties of chitosan are improved by the immobilization of thiol groups. Due to the formation of disulfide bonds with mucus glycoproteins, mucoadhesiveness is augmented. The permeation of paracellular markers through mucosa can be enhanced by utilizing thiolated instead of unmodified chitosan. Moreover, thiolated chitosans display in situ gelling features due to the pH-dependent formation of inter- as well as intra-molecular disulfide bonds. This latter process provides, strong cohesion and stability of carrier matrices, being based on thiolated chitosans. The in situ gel formation within the pH range of 5 to 6.8 makes the application of thiolated chitosans on vaginal, nasal and ocular mucosa also possible. Thiolated chitosans can guarantee prolonged controlled release of embedded therapeutic ingredients.  

Keywords: Thiolated chitosan,Thiomers, Mucoadhesion, Permeation enhancement, In situ gelation

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