Keywords
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Nanohydrogel, Chitosan, Polyethylene glycol, Curcumin, Diabetic wounds
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Abstract
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Nanohydrogels are cross-linked networks of macromolecules that swell in water or
biological fluids. They are swollen, a good system for controlling drug delivery, wound healing
and the transfer of biologically active macromolecules [1]. The reason for focusing on
nanohydrogels is their behavior in response to minor environmental changes such as pH,
temperature, ionic strength and soluble compounds that cause controlled changes in their
volume [2]. A wide range of materials, such as natural and synthetic polymers, are used as
effective drug carriers. Chitosan, a natural polymer, stands out as a first choice material for
hydrogels elaboration in biomedical, cosmetic, and health related applications, owing to its
interesting properties as biocompatibility, biodegradability, antimicrobial capacity, and
mucoadhesive [3]. Also, chitosan has been found to promote cell proliferation, stimulate tissue
reorganization, promote collagen deposition and enhance increased production of hyaluronic
acid at the wound site and also acts as hemostatic agent, thus helps in wound healing with
minimal scar formation [4]. Polyethylene glycol is also a synthetic polymer, which can be used
in the preparation of hybrid nanohydrogels. Curcumin, a natural product of the rhizomes of
Curcuma longa, has been widely used as coloring agent and spice in food. But studies have
shown that curcumin could significantly accelerate the healing of wounds and enhance wound
repair in diabetic impaired healing [5]. In this study, first, chitosan nanohydrogels (CSNH) and
chitosan-polyethylene glycol nanohydrogels (CS-PEGNH) were made by ionic gelation
method. During the production of nanohydrogels, curcumin was trapped in nanohydrogels.
Then, spectrophotometric and SEM analysis were used to confirm the production of
nanohydrogels and entrapment of curcumin. According to the results of SEM images, the
average diameter of CSNH were below 50 nm and the average diameter of CS-PEGNH were
approximately 50 nm. Also, t
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