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      Rapid analysis technologies with chemometrics for food authenticity field: A review

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          Abstract

          In recent years, the problem of food adulteration has become increasingly rampant, seriously hindering the development of food production, consumption, and management. The common analytical methods used to determine food authenticity present challenges, such as complicated analysis processes and time-consuming procedures, necessitating the development of rapid, efficient analysis technology for food authentication. Spectroscopic techniques, ambient ionization mass spectrometry (AIMS), electronic sensors, and DNA-based technology have gradually been applied for food authentication due to advantages such as rapid analysis and simple operation. This paper summarizes the current research on rapid food authenticity analysis technology from three perspectives, including breeds or species determination, quality fraud detection, and geographical origin identification, and introduces chemometrics method adapted to rapid analysis techniques. It aims to promote the development of rapid analysis technology in the food authenticity field.

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          Highlights

          • This paper summarizes the research progress of rapid analysis technology in the food authenticity field in recent five years.

          • Representative chemometrics methods suitable for rapid analysis techniques are introduced.

          • Problems faced by rapid analysis techniques in the food authenticity field are summarised and countermeasures are proposed.

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          Identifying spiders through DNA barcodes

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            Review: a comprehensive summary of a decade development of the recombinase polymerase amplification

            RPA is a versatile complement or replacement of PCR, and now is stepping into practice. Nucleic acid amplification has permeated every field in the life sciences since the introduction of the classic polymerase chain reaction (PCR) method in 1983. Yet, despite its fundamental reach, PCR has been constrained within the walls of a laboratory, due to its requirement for a sophisticated thermocycling machine, limiting external application in low-resource settings. New isothermal amplification strategies are seeking to break through traditional laboratory boundaries by providing nucleic acid replication at constant temperatures. Of these methods, recombinase polymerase amplification (RPA) is one of the fastest developing, experiencing rapid uptake and market, even though it was introduced comparatively late. Critically, RPA's technology potentiates highly accessible and sensitive nucleic acid amplification outside of laboratory, and even self-testing. Here we provide a comprehensive review of the equipment-free simplicity of RPA over its first decade of development. Our review includes key knowledge of RPA technology, such as its reaction components, mechanism, sensitivities and specificities, and distinctive detection methods. The review also provides know-how for developing RPA assays, and information about commercially available RPA reaction kits and accessories. We summarise critical RPA experimental tips and issues available through data mining the published literature, to assist researchers in mastering the RPA reaction. We also outline influential hotspots of RPA development, and conclude with outlooks for future development and implications for eclipsing PCR and further revolutionising the life sciences.
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              Analytical strategies in metabonomics.

              To perform metabonomics investigations, it is necessary to generate comprehensive metabolite profiles for complex samples such as biofluids and tissue/tissue extracts. Analytical technologies that can be used to achieve this aim are constantly evolving, and new developments are changing the way in which such profiles' metabolite profiles can be generated. Here, the utility of various analytical techniques for global metabolite profiling, such as, e.g., 1H NMR, MS, HPLC-MS, and GC-MS, are explored and compared.
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                Author and article information

                Contributors
                Journal
                Curr Res Food Sci
                Curr Res Food Sci
                Current Research in Food Science
                Elsevier
                2665-9271
                16 January 2024
                2024
                16 January 2024
                : 8
                : 100676
                Affiliations
                [a ]Institute of Food and Nutrition Development, Ministry of Agriculture and Rural Affairs, Beijing, China
                [b ]Institute of Quality Standard & Testing Technology for Agro-Products, Key Laboratory of Agro-Product Quality and Safety, Chinese Academy of Agricultural Sciences, Beijing, China
                [c ]Hangzhou Nutritome Biotech Co., Ltd., Hangzhou, China
                Author notes
                []Corresponding author. Institute of Food and Nutrition Development, Ministry of Agriculture and Rural Affairs, Beijing, 100081, China. liangkehong@ 123456caas.cn
                [∗∗ ]Corresponding author. Institute of Standard &; Testing Technology for Agro-Products, Key Laboratory of Agro-Product Quality and Safety, Chinese Academy of Agricultural Sciences, Beijing, 100081, China. zhaoyan01@ 123456caas.cn
                Article
                S2665-9271(24)00002-9 100676
                10.1016/j.crfs.2024.100676
                10830540
                38303999
                3daac248-6d5f-4e33-ba6e-265a74b82c97
                © 2024 The Authors

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 24 July 2023
                : 15 December 2023
                : 7 January 2024
                Categories
                Review Article

                authenticity,spectroscopic,ambient ionization mass spectrometry,electronic sensors,dna-based technology

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