Drug intelligence / Profile preview

Chitodex gel

Development stage
Unknown
Lead developer
Chitogel
Modality
Hydrogel Systems → Drug Delivery Systems
Administration
Topical, Intranasal, Otic
01

Overview

Chitodex gel is an innovative topical surgical gel developed by the University of Adelaide in collaboration with The Queen Elizabeth Hospital and the University of Otago. Its active ingredient is a chitosan-dextran (CD) biopolymer matrix, which functions as a biodegradable, biocompatible nasal dressing and hemostatic agent. Applied locally following functional endoscopic sinus surgery (FESS), Chitodex gel controls postoperative bleeding, promotes wound healing, reduces adhesion and scar formation, and prevents infection. The gel naturally biodegrades and dissolves over approximately 10 days, eliminating the need for painful nasal packing removal. In clinical trials, Chitodex gel has been evaluated alone, in combination with adjuvant antibiofilm agents (such as deferiprone and gallium-protoporphyrin), and with anti-inflammatory or analgesic agents (such as budesonide and ropivacaine) to improve postoperative outcomes in patients with chronic rhinosinusitis. It is also being investigated as a middle ear and external auditory canal packing agent in tympanoplasty surgery.

Brand names
Chitodex
Other names
Chitosan-dextran gelChitosan-dextranCD gel
02

Targets

Negatively charged bacterial cell wall and membrane componentsHost tissue and plasma proteins with accessible primary amines

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