基于轨道光栅散射和机器学习的表面增强手持拉曼光谱(SERS)技术探索COVID-19疫苗的认证

Megan Watson, D. Al-Jumeily, J. Birkett, Iftikhar Khan, S. Assi
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摘要

COVID-19是一种新型冠状病毒,于2019年12月首次在中国武汉出现,此后在全球迅速蔓延,升级为全球大流行,造成数百万人死亡。对大流行的紧急应对措施包括保持社会距离和隔离措施以及扩大疫苗接种规划。最流行的COVID-19疫苗是以核酸为基础的。病毒的广泛传播和控制工作的艰难使得假冒疫苗在市场上出现了空白。本研究调查了手持式拉曼光谱作为基于核酸的疫苗认证方法的使用,并利用机器学习分析来评估该方法的有效性。传统的拉曼光谱需要很大的工作空间,笨重且耗能,手持式拉曼系统在灵敏度和样品检测方面存在局限性。然而,表面增强拉曼光谱(SERS)显示出作为疫苗认证技术的潜力,允许在光谱中识别特征核酸带。SERS通过波长空间相关性(Correlation in Wavelength Space, CWS)显示出很强的识别潜力,所有疫苗样本与自身对比时的r值约为1。在一些赋形剂和一些选定的基于dna的疫苗之间观察到差异,这可能归因于在不同时间间隔测量胶体-疫苗复合物的SERS胶体的稳定性。该技术的进一步发展将包括SERS方法的优化、稳定性研究以及对更大样本量的更全面的分析和解释。
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Exploring the authentication of COVID-19 vaccines using Surface-enhanced handheld Raman spectroscopy (SERS) equipped with orbital Raster scattering and machine learning
COVID-19 is a novel coronavirus first emerging in Wuhan, China in December 2019 and has since spread rapidly across the globe escalating into a worldwide pandemic causing millions of fatalities. Emergency response to the pandemic included social distancing and isolation measures as well as the escalation of vaccination programmes. The most popular COVID-19 vaccines are nucleic acid-based. The vast spread and struggles in containment of the virus has allowed a gap in the market to emerge for counterfeit vaccines. This study investigates the use of handheld Raman spectroscopy as a method for nucleic acid-based vaccine authentication and utilises machine learning analytics to assess the efficacy of the method. Conventional Raman spectroscopy requires a large workspace, is cumbersome and energy consuming, and handheld Raman systems show limitations with regards to sensitivity and sample detection. Surface Enhanced Raman spectroscopy (SERS) however, shows potential as an authentication technique for vaccines, allowing identification of characteristic nucleic acid bands in spectra. SERS showed strong identification potential through Correlation in Wavelength Space (CWS) with all vaccine samples obtaining an r value of approximately 1 when plotted against themselves. Variance was observed between some excipients and a selected number of DNA-based vaccines, possibly attributed to the stability of the SERS colloid where the colloid-vaccine complex had been measured over different time intervals. Further development of the technique would include optimisation of the SERS method, stability studies and more comprehensive analysis and interpretation of a greater sample size.
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