This review explores how hydrogels improve localized cancer treatment using graphene-based nanomaterials, suggesting enhanced therapeutic effects.
Graphene-based nanomaterials (GBNs), in particular graphene oxide and reduced graphene oxide, have emerged as promising multifunctional nanomaterials for cancer therapy. The growing interest in these nanostructures lies in their exceptionally high drug-loading and photothermal capacities. Conventionally, these GBNs are administered through intravenous injection. However, this systemic route is often associated with a limited tumor uptake and off-target distribution, diminishing the therapeutic capacity of GBNs. To overcome these limitations, hydrogels are soaring as innovative local delivery systems capable of encapsulating and confining the GBNs (and other therapeutics) into the tumor site. These three-dimensional biocompatible matrices are formed by exploiting natural or synthetic polymers, which are then crosslinked by physical and/or chemical cues. The incorporation of GBNs into hydrogels matrices enhances drug loading, modulates release kinetics, and enables photoinduced hyperthermia. Therefore, several in vitro and in vivo studies have evidenced that the GBNs-incorporated hydrogels can perform a more effective chemotherapy, photothermal therapy or chemo-photothermal therapy, while at the same time, reducing the side-effects or diminishing tumor-recurrence rates. This review delves into the preclinical application of GBNs-incorporated hydrogels for cancer chemotherapy, photothermal therapy, and chemo-photothermal therapy. • GBNs stand out for their high drug-loading and photothermal capabilities. • Hydrogels incorporating GBNs enhance drug loading and modulate release kinetics. • Hydrogels can encapsulate GBNs and confine them at the tumor site. • Hydrogels incorporating GBNs can mediate a localized and improved therapy.
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Melo et al. (2026) studied this question.
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