The importance of obtaining new compounds with improved
antimicrobial
activity is a current trend and challenge. Some polymers such as chitosan
have shown promising bactericidal properties when they are structurally
modified, which is due to the binding versatility provided by their
free amines. Likewise, antimicrobial peptides (AMPs) have received
attention in recent years because of their bactericidal activity that
is similar to or even better than that of conventional drugs, and
they exhibit a low induction rate of antimicrobial resistance. Herein,
the modified AMP Ctx(Ile
21
)-Ha-Ahx-Cys was conjugated to
chitosan using
N
-acetylcysteine as an intermediate
by the carbodiimide method. Films were prepared using protonated chitosan
in 1% acetic acid and Ctx(Ile
21
)-Ha-Ahx-Cys AMP dissolved
in
N
-acetylcysteine-chitosan; 1.6 mmol of ethylcarbodiimide
hydrochloride, 1.2 mmol of
N
-hydroxysulfosucchimide,
and 0.1 mol L
–1
of
N
-morpholino)ethanesulfonic
acid buffer at pH 6.5 by continuous stirring at 100 × g for 10
min at 37 °C. Physicochemical properties were evaluated by Fourier-transform
infrared spectroscopy, differential scanning calorimetry/thermogravimetric
analysis, and X-ray diffraction to determine the mechanical properties,
solubility, morphology, and thickness. Furthermore, the antimicrobial
activities of chitosan-based conjugated films were evaluated against
Staphylococcus aureus
,
Pseudomonas
aeruginosa
,
Salmonella
Typhimurium, and
Escherichia coli
.
The results showed that the conjugation of a potent AMP could further
increase its antibacterial activity and maintain its stable physicochemical
properties. Therefore, the developed peptide–chitosan conjugate
could be applied as an additive in surgical procedures to prevent
and combat bacterial infection.