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      Surface engineering at the nanoscale: A way forward to improve coronary stent efficacy

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          Abstract

          Coronary in-stent restenosis and late stent thrombosis are the two major inadequacies of vascular stents that limit its long-term efficacy. Although restenosis has been successfully inhibited through the use of the current clinical drug-eluting stent which releases antiproliferative drugs, problems of late-stent thrombosis remain a concern due to polymer hypersensitivity and delayed re-endothelialization. Thus, the field of coronary stenting demands devices having enhanced compatibility and effectiveness to endothelial cells. Nanotechnology allows for efficient modulation of surface roughness, chemistry, feature size, and drug/biologics loading, to attain the desired biological response. Hence, surface topographical modification at the nanoscale is a plausible strategy to improve stent performance by utilizing novel design schemes that incorporate nanofeatures via the use of nanostructures, particles, or fibers, with or without the use of drugs/biologics. The main intent of this review is to deliberate on the impact of nanotechnology approaches for stent design and development and the recent advancements in this field on vascular stent performance.

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          Electrospinning and Electrospun Nanofibers: Methods, Materials, and Applications

          Electrospinning is a versatile and viable technique for generating ultrathin fibers. Remarkable progress has been made with regard to the development of electrospinning methods and engineering of electrospun nanofibers to suit or enable various applications. We aim to provide a comprehensive overview of electrospinning, including the principle, methods, materials, and applications. We begin with a brief introduction to the early history of electrospinning, followed by discussion of its principle and typical apparatus. We then discuss its renaissance over the past two decades as a powerful technology for the production of nanofibers with diversified compositions, structures, and properties. Afterward, we discuss the applications of electrospun nanofibers, including their use as “smart” mats, filtration membranes, catalytic supports, energy harvesting/conversion/storage components, and photonic and electronic devices, as well as biomedical scaffolds. We highlight the most relevant and recent advances related to the applications of electrospun nanofibers by focusing on the most representative examples. We also offer perspectives on the challenges, opportunities, and new directions for future development. At the end, we discuss approaches to the scale-up production of electrospun nanofibers and briefly discuss various types of commercial products based on electrospun nanofibers that have found widespread use in our everyday life.
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            Nanoparticle-based targeted drug delivery.

            Nanotechnology could be defined as the technology that has allowed for the control, manipulation, study, and manufacture of structures and devices in the "nanometer" size range. These nano-sized objects, e.g., "nanoparticles", take on novel properties and functions that differ markedly from those seen from items made of identical materials. The small size, customized surface, improved solubility, and multi-functionality of nanoparticles will continue to open many doors and create new biomedical applications. Indeed, the novel properties of nanoparticles offer the ability to interact with complex cellular functions in new ways. This rapidly growing field requires cross-disciplinary research and provides opportunities to design and develop multifunctional devices that can target, diagnose, and treat devastating diseases such as cancer. This article presents an overview of nanotechnology for the biologist and discusses the attributes of our novel XPclad((c)) nanoparticle formulation that has shown efficacy in treating solid tumors, single dose vaccination, and oral delivery of therapeutic proteins.
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              Atherosclerosis.

              A Lusis (2000)
              Atherosclerosis, a disease of the large arteries, is the primary cause of heart disease and stroke. In westernized societies, it is the underlying cause of about 50% of all deaths. Epidemiological studies have revealed several important environmental and genetic risk factors associated with atherosclerosis. Progress in defining the cellular and molecular interactions involved, however, has been hindered by the disease's aetiological complexity. Over the past decade, the availability of new investigative tools, including genetically modified mouse models of disease, has resulted in a clearer understanding of the molecular mechanisms that connect altered cholesterol metabolism and other risk factors to the development of atherosclerotic plaque. It is now clear that atherosclerosis is not simply an inevitable degenerative consequence of ageing, but rather a chronic inflammatory condition that can be converted into an acute clinical event by plaque rupture and thrombosis.
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                Author and article information

                Contributors
                Journal
                APL Bioeng
                APL Bioeng
                ABPID9
                APL Bioengineering
                AIP Publishing LLC
                2473-2877
                June 2021
                01 June 2021
                01 June 2021
                : 5
                : 2
                : 021508
                Affiliations
                [1 ]Amrita Centre for Nanosciences and Molecular Medicine, Amrita Vishwa Vidyapeetham , Ponekkara P.O. Cochin 682041, Kerala, India
                [2 ]Department of Cardiology, Amrita Institute of Medical Science and Research Centre, Amrita Vishwa Vidyapeetham , Ponekkara P.O. Cochin 682041, Kerala, India
                Author notes
                [a) ] Author to whom correspondence should be addressed: deepthymenon@ 123456aims.amrita.edu and deepsmenon@ 123456gmail.com
                Author information
                https://orcid.org/0000-0002-5102-9116
                https://orcid.org/0000-0002-2648-1813
                https://orcid.org/0000-0003-2772-2276
                Article
                5.0037298 APB20-RV-00185
                10.1063/5.0037298
                8172248
                e3782264-b802-4743-b2aa-6f6e77cbb447
                © 2021 Author(s).

                All article content, except where otherwise noted, is licensed under a Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 12 November 2020
                : 26 April 2021
                Page count
                Pages: 28
                Funding
                Funded by: Indian Council of Medical Research https://doi.org/10.13039/501100001411
                Award ID: 5/3/8/48/ITR-F/2018-ITR
                Funded by: Department of Biotechnology, Ministry of Science and Technology, India https://doi.org/10.13039/501100001407
                Award ID: BT/PR3516/MED/32/192/2011
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