Abstract:
Interpenetrating polymer network (IPN) hydrogels of polyacrylamide
(PAAm) and sodium carboxymethyl cellulose (NaCMC) were prepared by free radical
polymerization and crosslinking. Potassium persulfate, citric acid and N,N-
methylenebisacrylamide (MBAAm) were used as an initiator for acrylamide monomer,
and crosslinking agents for NaCMC and PAAm, respectively. The non-porous and
porous PAAm/NaCMC IPN hydrogels were prepared and characterized for controlled
release application. The properties of hydrogels were studied in terms of gel content,
swelling, water-holding capacity, thermal stability, morphology and porosity. The
results from gel fraction and Attenuated total reflection-Fourier transform infrared
(ATR-FTIR) analysis suggested that the hydrogels were successfully prepared and
crosslinked. The swelling was studied in distilled water and buffer solutions at pH 5.5
and pH 10.0. The results showed that the swelling ratio of hydrogels increased with
increasing NaCMC composition and pH value. On the other hand, the swelling profiles
of porous hydrogels were faster than those of the dense samples at the same
compositions. To evaluate the possibility of hydrogels for wound dressing application,
mangiferin was used as a model drug and loaded in the IPNs. The release behavior of
hydrogels were studied in both pH 5.5 (pH of normal skin) and 10.0 (pH of wound
infection) buffer solutions. It was found that all samples showed higher amount of
released mangiferin in pH 10.0 than those in pH 5.5 buffer solution. Moreover, the
NaCMC composition and porosity played an important role in controlled release of
mangiferin from hydrogels. According to the kinetic models, the release of mangiferin
was controlled by diffusion mechanism with swelling of the matrix. These findings
v
indicated that the hydrogels could be a potential alternative for wound dressing
material.
To develop the pH-sensitive character of PAAm/NaCMC IPNs for oral drug
delivery, the pH-sensitive hydrogels were obtained after alkaline hydrolysis. The
conversion of amide (-CONH2) to carboxylate groups (-COO-
) after hydrolysis was
confirmed by ATR-FTIR spectroscopy. Swelling ability of the hydrolyzed hydrogels
was investigated as a function of time and pH in different buffer solutions similar to
that of simulated gastrointestinal fluid. It was found that the swelling ratio in pH 7.4
buffer solution was considerably higher than in pH 1.2 buffer solution. This change in
swelling behavior was attributed to the presence of carboxylate anion groups in
hydrogels that either protonated or deprotonated in response to the pH media. The
release profiles showed that low amount of mangiferin was release in pH 1.2 buffer
solution. On the other hand, the release rate increased rapidly in pH 7.4 environment
because the ionization of carboxylate groups caused the repulsion between the polymer
molecules and significant swelling of hydrogels. As a result, diffusion of mangiferin
out of the hydrogels was facilitated. According to the kinetic model, the release of
mangiferin from hydrolyzed hydrogels was controlled by diffusion mechanism with
matrix swelling, in which the release rate dependent on concentration of drug. The
results indicated that the hydrolyzed hydrogels were potential for the application of oral
controlled drug delivery system