Abstract

Cancer is one of the deadliest diseases in human history with extremely poor prognosis. Although many traditional therapeutic modalities—such as surgery, chemotherapy, and radiation therapy—have proved to be successful in inhibiting the growth of tumor cells, their side effects may vastly limited the actual benefits and patient acceptance. In this context, a nanomedicine approach for cancer therapy using functionalized nanomaterial has been gaining ground recently. Considering the ability to carry various anticancer drugs and to act as a photothermal agent, the use of carbon-based nanomaterials for cancer therapy has advanced rapidly. Within those nanomaterials, reduced graphene oxide (rGO), a graphene family 2D carbon nanomaterial, emerged as a good candidate for cancer photothermal therapy due to its excellent photothermal conversion in the near infrared range, large specific surface area for drug loading, as well as functional groups for functionalization with molecules such as photosensitizers, siRNA, ligands, etc. By unique design, multifunctional nanosystems could be designed based on rGO, which are endowed with promising temperature/pH-dependent drug/gene delivery abilities for multimodal cancer therapy. This could be further augmented by additional advantages offered by functionalized rGO, such as high biocompatibility, targeted delivery, and enhanced photothermal effects. Herewith, we first provide an overview of the most effective reducing agents for rGO synthesis via chemical reduction. This was followed by in-depth review of application of functionalized rGO in different cancer treatment modalities such as chemotherapy, photothermal therapy and/or photodynamic therapy, gene therapy, chemotherapy/phototherapy, and photothermal/immunotherapy.

Highlights

  • The results suggested that reduced graphene oxide (rGO) exhibits high DOX loading, good stability, and pH-sensitive sustained drug release, which is evident from the effective cytotoxicity against MCF-7 and A549 cancer cells in vitro [64]

  • Due to improved photothermal response by absorbing light in the near infrared (NIR) range and the potential for high loading of chemotherapeutic drugs, photosensitizers and small interfering RNA (siRNA), rGO synthesized by means of various reducing agents is well suited for applications in single or multi-mode cancer therapy

  • Based on the reducing agent used for rGO synthesis, and the moieties conjugated with it, rGO-based nanocomposite is endowed with triggered drug release capability after intracellular uptake, by pH change or hyperthermia

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Summary

Introduction

The lateral dimensions and thickness of graphene family nanomaterials, such as graphene oxide (GO), reduced graphene oxide (rGO), graphene quantum dots, and graphene nanoribbons can be fine-tuned from original two-dimensional (2D) structure into zero-, one-, or three-dimensional assemblies [27], which provide improved accumulation as drug vehicles and contrast agents at specific target sites [28] Such unique and tunable features have promised their new applications in drug delivery [29]. With its facile synthesis, high water dispersibility, easy surface functionalization, and good biocompatibility, rGO has emerged as an excellent multifunctional nanomaterial for PTT [33] After combining this unique characteristic with the high loading capacity of anticancer drugs, rGO reveals itself as a promising nanomaterial for chemo-photothermal therapy [34].

Schematic diagram illustrating the preparation fromGO
Hydrazine Hydrate
Resveratrol
Chitosan
Sodium Borohydride
Green Tea Polyphenols
Chemotherapy
Gene Therapy
Findings
Conclusions and Outlook
Full Text
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