15
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Nanotechnology for angiogenesis: opportunities and challenges

      Read this article at

      ScienceOpenPublisherPubMed
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          The progress, opportunities, and challenges of nanotechnology-based strategies for angiogenesis inhibition, angiogenesis stimulation, theranostic and imaging purposes are summarized.

          Abstract

          Angiogenesis plays a critical role within the human body, from the early stages of life ( i.e., embryonic development) to life-threatening diseases ( e.g., cancer, heart attack, stroke, wound healing). Many pharmaceutical companies have expended huge efforts on both stimulation and inhibition of angiogenesis. During the last decade, the nanotechnology revolution has made a great impact in medicine, and regulatory approvals are starting to be achieved for nanomedicines to treat a wide range of diseases. Angiogenesis therapies involve the inhibition of angiogenesis in oncology and ophthalmology, and stimulation of angiogenesis in wound healing and tissue engineering. This review aims to summarize nanotechnology-based strategies that have been explored in the broad area of angiogenesis. Lipid-based, carbon-based and polymeric nanoparticles, and a wide range of inorganic and metallic nanoparticles are covered in detail. Theranostic and imaging approaches can be facilitated by nanoparticles. Many preparations have been reported to have a bimodal effect where they stimulate angiogenesis at low dose and inhibit it at higher doses.

          Related collections

          Most cited references541

          • Record: found
          • Abstract: found
          • Article: not found

          Epithelial-mesenchymal transitions in development and disease.

          The epithelial to mesenchymal transition (EMT) plays crucial roles in the formation of the body plan and in the differentiation of multiple tissues and organs. EMT also contributes to tissue repair, but it can adversely cause organ fibrosis and promote carcinoma progression through a variety of mechanisms. EMT endows cells with migratory and invasive properties, induces stem cell properties, prevents apoptosis and senescence, and contributes to immunosuppression. Thus, the mesenchymal state is associated with the capacity of cells to migrate to distant organs and maintain stemness, allowing their subsequent differentiation into multiple cell types during development and the initiation of metastasis.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Stimuli-responsive nanocarriers for drug delivery.

            Spurred by recent progress in materials chemistry and drug delivery, stimuli-responsive devices that deliver a drug in spatial-, temporal- and dosage-controlled fashions have become possible. Implementation of such devices requires the use of biocompatible materials that are susceptible to a specific physical incitement or that, in response to a specific stimulus, undergo a protonation, a hydrolytic cleavage or a (supra)molecular conformational change. In this Review, we discuss recent advances in the design of nanoscale stimuli-responsive systems that are able to control drug biodistribution in response to specific stimuli, either exogenous (variations in temperature, magnetic field, ultrasound intensity, light or electric pulses) or endogenous (changes in pH, enzyme concentration or redox gradients).
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Nanocarriers as an emerging platform for cancer therapy.

              Nanotechnology has the potential to revolutionize cancer diagnosis and therapy. Advances in protein engineering and materials science have contributed to novel nanoscale targeting approaches that may bring new hope to cancer patients. Several therapeutic nanocarriers have been approved for clinical use. However, to date, there are only a few clinically approved nanocarriers that incorporate molecules to selectively bind and target cancer cells. This review examines some of the approved formulations and discusses the challenges in translating basic research to the clinic. We detail the arsenal of nanocarriers and molecules available for selective tumour targeting, and emphasize the challenges in cancer treatment.
                Bookmark

                Author and article information

                Contributors
                (View ORCID Profile)
                (View ORCID Profile)
                (View ORCID Profile)
                (View ORCID Profile)
                (View ORCID Profile)
                Journal
                CSRVBR
                Chemical Society Reviews
                Chem. Soc. Rev.
                Royal Society of Chemistry (RSC)
                0306-0012
                1460-4744
                July 21 2020
                2020
                : 49
                : 14
                : 5008-5057
                Affiliations
                [1 ]Tissue Engineering Research Group (TERG)
                [2 ]Department of Anatomy and Cell Biology
                [3 ]School of Medicine
                [4 ]Mashhad University of Medical Sciences
                [5 ]917794-8564 Mashhad
                [6 ]Institute of Materials Physics and Engineering
                [7 ]Applied Science and Technology Department
                [8 ]Politecnico di Torino
                [9 ]101 29 Torino
                [10 ]Italy
                [11 ]Molecular Pathology and Cytogenetics Laboratory
                [12 ]Ghaem Hospital, Mashhad University of Medical Sciences
                [13 ]Mashhad
                [14 ]Iran
                [15 ]Hematology/Oncology and Stem Cell Transplantation Research Center
                [16 ]Wellman Center for Photomedicine
                [17 ]Massachusetts General Hospital
                [18 ]Boston
                [19 ]USA
                [20 ]Department of Dermatology
                [21 ]Department of Tissue Engineering and Regenerative Medicine
                [22 ]Faculty of Advanced Technologies in Medicine
                [23 ]Iran University of Medical Sciences
                [24 ]Tehran
                Article
                10.1039/C8CS01021H
                32538379
                c6b69e1b-2a1e-4cef-9fbd-93f9a49c8b42
                © 2020

                http://rsc.li/journals-terms-of-use

                History

                Comments

                Comment on this article