Abstract:
Background:
Carbon nanodots (CNDs) are nanoscale carbon-based particles known for their small size
(typically less than 10 nm), excellent biocompatibility, low toxicity, and strong
photoluminescence. Chitosan, a biopolymer derived from chitin, is notable for its
biocompatibility, biodegradability, and ability to enhance drug solubility and permeability. In
drug delivery, it is possible to use CNDs as fluorescent signals for tracking the delivery
process, while chitosan serves as a versatile carrier that can encapsulate drugs, facilitate their
controlled release, and enhance cellular uptake due to its mucoadhesive properties. Together,
they form an effective composite for targeted drug delivery systems, combining the imaging
capabilities of CNDs with the drug-carrying and release properties of chitosan, potentially
improving therapeutic outcomes.
Methodology:
Algae extract was used for the synthesis of carbon nanodots using hydrothermal method where
algal biomass served as carbon precursor for the synthesis carbon nanodots. The synthesized
carbon dots were studied by imaging microscopy, XRD, EDS, and FTIR in addition to scanning
electron microscopy and ultraviolet-visible spectroscopy. Chitosan was mixed with 2:3
solution of acetic acid and glycerol and carbon nanodots were mixed in this solution during
gelation process. The resulting gel was characterised by swelling and degradation studies and
drug release studies were performed using UV-Vis Spectroscopy.
Results:
UV-Vis analysis revealed the distinct peak at 264nm attributed to Carbon nanodots whereas
SEM analysis demonstrated the characteristic morphology of carbon nanodots with spherical
shapes and some agglomeration. FTIR spectra of carbon nanodots confirmed presence of
similar peaks when compared to algal strain with difference in intensity of peaks. Swelling
studies suggested that with increase in concentration of carbon nanodots swelling properties
are reduced. Degradation studies suggested that with gel with increased carbon nanodots
concentration were less prone to degradation. Drug loading and releasing properties of
hydrogel using Vancomycin as model drug were performed at different two different pH. Drug
releasing properties were greatly enhanced in 2 pH conditions as compared to 7.4 pH.
xiv
Conclusion:
The finding suggested carbon nanodots incorporated chitosan gel could be used as possible
strategy for drug delivery of drugs that have poor absorptions in gastrointestinal tract.