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      A Novel Top-Down Synthesis of Ultrathin 2D Boron Nanosheets for Multimodal Imaging-Guided Cancer Therapy

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          Abstract

          Single atom non-metal two-dimensional (2D) nanomaterials have shown considerable potential in cancer nanomedicines, owing to their intriguing properties and biocompatibility. Herein, ultrathin boron nanosheets (B NSs) were prepared through a novel top-down approach by coupling thermal oxidation etching and liquid exfoliation technologies, with controlled nanoscale thickness. Based on the PEGylated B NSs, a new photonic drug delivery platform was developed, which exhibited multiple promising features for cancer therapy and imaging, including (i) efficient NIR light to heat conversion with a high photothermal conversion efficiency of 42.5%, (ii) high drug-loading capacity and triggered drug release by NIR light and moderate acidic pH, (iii) strong accumulation at tumor sites, (iv) multimodal imaging properties (photoacoustic, photothermal and fluorescent imaging), and (v) complete tumor ablation and excellent biocompatibility. To the best of our knowledge, this is the first report on the top-down fabrication of ultrathin 2D B NSs by the combined thermal oxidation etching and liquid exfoliation, as well as their application as a multi-modal imaging-guided drug delivery platform. We also expect the newly prepared B NSs to provide a robust and useful 2D nanoplatform for various biomedical applications. Ultrathin 2D boron (B)-based nanosheets (NSs) were fabricated through a novel top-down approach by coupling liquid exfoliating and thermal oxidation etching, and applied to photonic drug delivery for cancer therapy and imaging. The 2D B NS platform exhibits multiple promising features including efficient photothermal conversion, high drug loading, spatiotemporally controlled drug release, strong tumor accumulation, good biocompatibility, and significant potential of multimodal imaging guided-cancer treatment.

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          Most cited references46

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          Graphene-Like Carbon Nitride Nanosheets for Improved Photocatalytic Activities

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            Is Open Access

            Progress and challenges towards targeted delivery of cancer therapeutics

            Targeted delivery approaches for cancer therapeutics have shown a steep rise over the past few decades. However, compared to the plethora of successful pre-clinical studies, only 15 passively targeted nanocarriers (NCs) have been approved for clinical use and none of the actively targeted NCs have advanced past clinical trials. Herein, we review the principles behind targeted delivery approaches to determine potential reasons for their limited clinical translation and success. We propose criteria and considerations that must be taken into account for the development of novel actively targeted NCs. We also highlight the possible directions for the development of successful tumor targeting strategies.
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              Synthesis of borophenes: Anisotropic, two-dimensional boron polymorphs.

              At the atomic-cluster scale, pure boron is markedly similar to carbon, forming simple planar molecules and cage-like fullerenes. Theoretical studies predict that two-dimensional (2D) boron sheets will adopt an atomic configuration similar to that of boron atomic clusters. We synthesized atomically thin, crystalline 2D boron sheets (i.e., borophene) on silver surfaces under ultrahigh-vacuum conditions. Atomic-scale characterization, supported by theoretical calculations, revealed structures reminiscent of fused boron clusters with multiple scales of anisotropic, out-of-plane buckling. Unlike bulk boron allotropes, borophene shows metallic characteristics that are consistent with predictions of a highly anisotropic, 2D metal.
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                Author and article information

                Journal
                Advanced Materials
                Adv. Mater.
                Wiley
                09359648
                September 2018
                September 2018
                July 18 2018
                : 30
                : 36
                : 1803031
                Affiliations
                [1 ]School of Pharmaceutical Sciences (Shenzhen); Sun Yat-sen University; Guangzhou 510275 China
                [2 ]Center for Nanomedicine; Brigham and Women's Hospital; Harvard Medical School; Boston MA 02115 USA
                [3 ]Sir Run Run Shaw Hospital; Zhejiang University School of Medicine; Hangzhou Zhejiang 310000 China
                [4 ]Shenzhen Engineering Laboratory of Phosphorene and Optoelectronics; SZU-NUS Collaborative Innovation Center for Optoelectronic Science and Technology,; and Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province; Shenzhen University; Shenzhen 518060 China
                Article
                10.1002/adma.201803031
                6338531
                30019786
                df50ec00-ca21-41bb-afae-732e7183e1d7
                © 2018

                http://doi.wiley.com/10.1002/tdm_license_1.1

                http://onlinelibrary.wiley.com/termsAndConditions#vor

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