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      Micro/nanotechnology-inspired rapid diagnosis of respiratory infectious diseases

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          Abstract

          Humans have suffered from a variety of infectious diseases since a long time ago, and now a new infectious disease called COVID-19 is prevalent worldwide. The ongoing COVID-19 pandemic has led to research of the effective methods of diagnosing respiratory infectious diseases, which are important to reduce infection rate and help the spread of diseases be controlled. The onset of COVID-19 has led to the further development of existing diagnostic methods such as polymerase chain reaction, reverse transcription polymerase chain reaction, and loop-mediated isothermal amplification. Furthermore, this has contributed to the further development of micro/nanotechnology-based diagnostic methods, which have advantages of high-throughput testing, effectiveness in terms of cost and space, and portability compared to conventional diagnosis methods. Micro/nanotechnology-based diagnostic methods can be largely classified into (1) nanomaterials-based, (2) micromaterials-based, and (3) micro/nanodevice-based. This review paper describes how micro/nanotechnologies have been exploited to diagnose respiratory infectious diseases in each section. The research and development of micro/nanotechnology-based diagnostics should be further explored and advanced as new infectious diseases continue to emerge. Only a handful of micro/nanotechnology-based diagnostic methods has been commercialized so far and there still are opportunities to explore.

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          Most cited references193

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          Identification of a Novel Coronavirus in Patients with Severe Acute Respiratory Syndrome

          The severe acute respiratory syndrome (SARS) has recently been identified as a new clinical entity. SARS is thought to be caused by an unknown infectious agent. Clinical specimens from patients with SARS were searched for unknown viruses with the use of cell cultures and molecular techniques. A novel coronavirus was identified in patients with SARS. The virus was isolated in cell culture, and a sequence 300 nucleotides in length was obtained by a polymerase-chain-reaction (PCR)-based random-amplification procedure. Genetic characterization indicated that the virus is only distantly related to known coronaviruses (identical in 50 to 60 percent of the nucleotide sequence). On the basis of the obtained sequence, conventional and real-time PCR assays for specific and sensitive detection of the novel virus were established. Virus was detected in a variety of clinical specimens from patients with SARS but not in controls. High concentrations of viral RNA of up to 100 million molecules per milliliter were found in sputum. Viral RNA was also detected at extremely low concentrations in plasma during the acute phase and in feces during the late convalescent phase. Infected patients showed seroconversion on the Vero cells in which the virus was isolated. The novel coronavirus might have a role in causing SARS. Copyright 2003 Massachusetts Medical Society
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            COVID-19 infection: Origin, transmission, and characteristics of human coronaviruses

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              Characterization of a novel coronavirus associated with severe acute respiratory syndrome.

              P Rota (2003)
              In March 2003, a novel coronavirus (SARS-CoV) was discovered in association with cases of severe acute respiratory syndrome (SARS). The sequence of the complete genome of SARS-CoV was determined, and the initial characterization of the viral genome is presented in this report. The genome of SARS-CoV is 29,727 nucleotides in length and has 11 open reading frames, and its genome organization is similar to that of other coronaviruses. Phylogenetic analyses and sequence comparisons showed that SARS-CoV is not closely related to any of the previously characterized coronaviruses.
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                Author and article information

                Contributors
                keekyoung.kim@ucalgary.ca
                sskim@ucalgary.ca
                Journal
                Biomed Eng Lett
                Biomed Eng Lett
                Biomedical Engineering Letters
                The Korean Society of Medical and Biological Engineering (Korea )
                2093-9868
                2093-985X
                8 September 2021
                : 1-31
                Affiliations
                [1 ]GRID grid.22072.35, ISNI 0000 0004 1936 7697, Department of Mechanical and Manufacturing Engineering, Schulich School of Engineering, , University of Calgary, ; Calgary, AB T2N 1N4 Canada
                [2 ]GRID grid.22072.35, ISNI 0000 0004 1936 7697, Biomedical Engineering Graduate Program, Schulich School of Engineering, , University of Calgary, ; Calgary, AB T2N 1N4 Canada
                Author information
                http://orcid.org/0000-0001-7735-3582
                Article
                206
                10.1007/s13534-021-00206-8
                8424173
                a9f39c9a-2e21-4c88-b288-9f42a81f10f7
                © Korean Society of Medical and Biological Engineering 2021

                This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.

                History
                : 28 June 2021
                : 17 August 2021
                : 29 August 2021
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100000038, natural sciences and engineering research council of canada;
                Award ID: RGPIN-04559-2020
                Award ID: RGPIN-03943-2020
                Award Recipient :
                Categories
                Review Article

                respiratory infectious diseases,micro/nanotechnology-based diagnostic methods,nanomaterials,micromaterials,micro/nanodevices

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