Synthesis of Novel N-Acyl Thiolated Chitosan Derivatives and their Assessment for Toxicity and Antimicrobial Activity in Vitro
Swapneel Sonone*, Harshal Narkhede, Pramod Shirote and Nilofer Naikwade
Appasaheb Birnale College of Pharmacy, South Shivaji Nagar, Sangli - 416 416 (India).
Chitosan derivative was successively synthesized by initial preparation of acylthiourea reagent using ammonium thiocyanate and making it to react with at primary amino groups of chitosan and then reduced to yield thiolated chitosan. Due to the formation of disulfide bonds with mucus glycoproteins, mucoadhesiveness is augmented. The thiol groups were then quantified using Ellaman’s reagent. The derivatives inherit good swelling property in neutral and alkaline media. The different derivatives containing thiol groups were formulated into tablets using reference drug for evaluation. The thiolated chitosan can guarantee prolonged controlled release of embedded therapeutic ingredients.
KEYWORDS:Thiolated Chitosan; acyl isothiocyanate; Isopropanolol; Mucoadhesion; Matrix tablet
Download this article as:Copy the following to cite this article: Sonone S, Narkhede H, Shirote P, Naikwade N. Synthesis of Novel N-Acyl Thiolated Chitosan Derivatives and their Assessment for Toxicity and Antimicrobial Activity in Vitro. Orient J Chem 2010;26(3). |
Copy the following to cite this URL: Sonone S, Narkhede H, Shirote P, Naikwade N. Synthesis of Novel N-Acyl Thiolated Chitosan Derivatives and their Assessment for Toxicity and Antimicrobial Activity in Vitro. Orient J Chem 2010;26(3). Available from: http://www.orientjchem.org/?p=24539 |
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