Responsive
hydrogels have found widespread applications in biomedical
science and engineering fields, especially for drug delivery. Despite
the superior performance of responsive hydrogels, challenges still
exist in drug-delivery efficiency when environmental stimuli are weak.
Recently, the demand in the design of hydrogel-based drug delivery
systems has stimulated considerable interest in the search for new
strategies, for instance, the application of nanocomposite hydrogels
for reinforcing the versatility and flexibility in controlled drug
delivery. In this study, a novel and effective nanocomposite hydrogel
microcapsule drug delivery system, which is composed of poly(N-isopropylacrylamide) (PNIPAM) and alginate interpenetrating
polymer and GO–Fe3O4 nanomaterials, is
developed to achieve NIR light-, magneto-, and pH-responsive drug
release. The GO–Fe3O4 nanomaterials embedded
in the interpenetrating polymer enable the PNIPAM hydrogel deswelling
by raising temperature above the lower critical solution temperature
under NIR light and alternating magnetic field, thus accelerating
the release of doxorubicin. In addition, the introduction of alginate
into PNIPAM hydrogels endows nanocomposite hydrogels (NCHs) with quick
gelation property, enhanced mechanical property, and pH-responsive
performance. The in vitro cytotoxicity assay confirmed that the NCH
platform can effectively kill the cancer cells. This novel multiresponsive
drug delivery system holds great promise for the treatment of diseases.