Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain
the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in
Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles
and JavaScript.
NPG Asia Materials is proud to present a collection of articles on innovative nanomaterials for advanced therapy of cancer. The collection features a selection of recent articles that report multimodal nanoplatforms for photothermal therapy, 2D nanomaterials and their composites, cell-membrane nanoparticle camouflaging, surface-engineered nanobubbles, or 3D printed scaffolds, as well as a fundamentally novel approach of cell rupturing.
A novel nanoplatform was designed by assembling nano-Se on the surface of NIR-responsive Au@mSiO2/DOX nanoparticles for the effective treatment of metastatic breast cancer (Se@Au@mSiO2/DOX).
Herein, an idea of creating MoS2/GO nanocomposites was brought about, which were constructed to integrate the merits for both materials with additional benefits and shield the mutual weaknesses. It turned out that MoS2/GO nanocomposites manifested beneficial multi-functionalities including favorable lung targeting, enhanced drug loading capacity, increased tumor killing efficacy and improved biosafety as well. This study would open a new path that may lead to desirable use of MoS2/GO nanocomposites in cancer therapeutics.
A batch-by-batch free route for the continuous production black phosphorus nanosheets in a single-pass gas stream was designed, and the resulting nanosheets were directly employed in targeted chemo-phototherapy upon incorporating with doxorubicin, poly-l-lysine, and hyaluronic acid.
Versatile types of self-destructible polysaccharide nanocomposites with adjustable amounts of unlockable Au nanorods were fabricated for highly efficient photothermal cancer therapy systems.
GO can undergo significant physicochemical transformation in two simulated lung fluids–Gamble’s solution and artificial lysosomal fluid (ALF), as the organic acids in lung fluids cause reduction of GO. Biotransformation markedly inhibits the endocytosis of GO by scavenging macrophages. Notably, alterations in Gamble’s solution enhance the aggregation of GO in a layer-to-layer manner, resulting in GO precipitation and reduced interaction with cells, whereas changes in ALF lead to edge-to-edge aggregation of GO, enhancing the adhesion of large sheet-like GO aggregates on plasma membrane without cellular uptake.
Fe-CaSiO3 composite scaffolds (30CS) were designed via 3D printing technique. Firstly, 30CS scaffolds possessed high compressive strength to provide sufficient mechanical support in bone cortical defects; Secondly, a synergistic therapy of photothermal and ROS achieved enhanced tumor therapeutic effect in vitro and in vivo; Thirdly, the presence of CaSiO3 in the composite scaffolds enforced the degradation performance and stimulated proliferation and differentiation of rBMSCs and further promoted bone forming in vivo. Such 30CS scaffolds with high compressive strength can function as versatile and efficient biomaterials for the future regeneration of cortical bone defects and therapy of bone cancer.
Using functionalized particles for treatment of cancer is advantageous because they can access remote parts of the body and is minimally invasive. However, current chemical and biological methods still face challenges. A novel approach that uses the physical force of stimuli-responsive hydrogels is introduced. Temperature-responsive hydrogels were coated with cell-adherent molecules. After attaching cancer cells on its surface and changing the temperature, the force of the expanding stimuli-responsive hydrogel ruptures the cells. Comparing to other chemical and biological methods, this physical approach may be conceptually simpler, technically easier to implement, and more general for different types of cancer cells.
A bifunctional scaffold was successfully prepared by in situ growth of MoS2 nanosheets on the 3D-printed bioceramic scaffolds via a facile hydrothermal process. The prepared scaffolds exhibit an excellent capability for both tumor therapy and tissue regeneration, offering a promising clinical strategy for effective treatment of tumor-induced tissue defects.
Gas filled nanobubbles are fabricated by surface-engineered progress with forming folate-mediated, gadolinium (Gd3+)-labelled and IR-780/5-FU loaded hollow structures. The nanobubbles progress capacity of NIR-/MR-/US-imaging in vitro. Importantly, the nanobubbles present charge-switchable behaviors when pH values changed from 7.4 to 5.0 and demonstrate pH-/light-sensitive drug release behaviors. Coupled with FA-targeting, the nanobubbles can be employed for efficient tri-modal imaging in vivo with selective tumor accumulation, long tumor retention time, and present enhanced anti-tumor activity with combined chemo-/photothermal therapy. Therefore, nanobubbles can act as excellent nanocarriers for active tumor targeting theranostics.
A bioinspired nanosystem of cancer cell membrane-camouflaged SPIO@DOX-ICG nanoparticles was fabricated to realize precise cancer treatment by simultaneous chemotherapy, hyperthermia-therapy, and radiotherapy. The nanosystem achieved synergistic anticancer effects by antagonizing tumor hypoxia and reprograming the polarization of tumor associated macrophages to anti-tumor M1 phenotype, without causing toxic side effects on major organs.