Chitosan-Based Thermosensitive Hydrogel for Controlled Drug Delivery to the Temporomandibular Joint
Kandile, Nadia; Wael M. Talaat; David R. Harding; Mohamed Haider; Sausan Al Kawas;
Abstract
Intra-articular injections of hyaluronic acid (HA) and
corticosteroids have been extensively used in treating temporoman dibular disorders. However, rapid clearance from the site of injection
is a major concern that is commonly managed by frequent dosing,
which is not without complications. This study aimed to determine
the suitability of thermosensitive chitosan-based hydrogels for intra articular controlled release of drugs in the rabbit temporomandibular
joint (TMJ). A series of hydrogels were prepared using different
chitosan (Ch) to b-glycerophosphate (b-GP) ratios. The gelation
time, swelling ratio, the shape, and surface morphology of the
prepared gels were investigated to select the formulation with
optimum characteristics. The left TMJ in 13 adult male New Zealand
white rabbits was injected with 0.2 mL of Chitosan/b-glyceropho sphate/HA while the right TMJ was injected with 0.2 mL of control
solution of HA. Hyaluronic acid concentrations in experimental and
control groups were measured using Hyaluronan Quantikine
Enzyme-Linked Immunosorbent Assay Kit. In vitro characterization
showed that both the Ch:b-GP ratio and incorporation of HA had a
significant effect on gelation time, degree of swelling, and surface
morphology of the hydrogels. No morphological changes were
observed in the joints in both groups. The mean concentration of
HA in the experimental joints after 7 days (1339.79 244.98mg/g)
was significantly higher than that in the control (474.52 79.36mg/
g). In conclusion, the chitosan-based thermosensitive hydrogel can be
considered as a promising controlled drug release system to the TMJ
in a rabbit model that would potentially overcome many of the current
limitations of intra-articular formulations.
corticosteroids have been extensively used in treating temporoman dibular disorders. However, rapid clearance from the site of injection
is a major concern that is commonly managed by frequent dosing,
which is not without complications. This study aimed to determine
the suitability of thermosensitive chitosan-based hydrogels for intra articular controlled release of drugs in the rabbit temporomandibular
joint (TMJ). A series of hydrogels were prepared using different
chitosan (Ch) to b-glycerophosphate (b-GP) ratios. The gelation
time, swelling ratio, the shape, and surface morphology of the
prepared gels were investigated to select the formulation with
optimum characteristics. The left TMJ in 13 adult male New Zealand
white rabbits was injected with 0.2 mL of Chitosan/b-glyceropho sphate/HA while the right TMJ was injected with 0.2 mL of control
solution of HA. Hyaluronic acid concentrations in experimental and
control groups were measured using Hyaluronan Quantikine
Enzyme-Linked Immunosorbent Assay Kit. In vitro characterization
showed that both the Ch:b-GP ratio and incorporation of HA had a
significant effect on gelation time, degree of swelling, and surface
morphology of the hydrogels. No morphological changes were
observed in the joints in both groups. The mean concentration of
HA in the experimental joints after 7 days (1339.79 244.98mg/g)
was significantly higher than that in the control (474.52 79.36mg/
g). In conclusion, the chitosan-based thermosensitive hydrogel can be
considered as a promising controlled drug release system to the TMJ
in a rabbit model that would potentially overcome many of the current
limitations of intra-articular formulations.
Other data
| Title | Chitosan-Based Thermosensitive Hydrogel for Controlled Drug Delivery to the Temporomandibular Joint | Authors | Kandile, Nadia ; Wael M. Talaat; David R. Harding; Mohamed Haider; Sausan Al Kawas | Keywords | Chitosan glycerophosphate;controlled release;hyaluronic acid;temporomandibular disorders;temporomandibular joint | Issue Date | 2016 | Journal | Journal of Craniofacial Surgery | Volume | 27 | Issue | 3 | Start page | 735 | End page | 740 | DOI | 10.1097/SCS.0000000000002588 |
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