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Microplastics and nanoplastics in groundwater: Occurrence, analysis, and identification 地下水中的微塑料和纳米塑料:出现、分析和识别
IF 11.1 2区 化学 Q1 CHEMISTRY, ANALYTICAL Pub Date : 2024-11-09 DOI: 10.1016/j.teac.2024.e00246
Chanhyeok Jeon, Heejung Kim
Microplastics and nanoplastics (MPs/NPs) are a growing environmental concern owing to their widespread distribution and potential adverse effects on ecosystems and human health. Numerous studies on MPs/NPs have focused on their distribution, behavior, and fate; however, there is a lack of knowledge regarding these materials in groundwater, a primary source of drinking water. This is attributed to the difficulties in conducting such studies, the absence of universally accepted standard procedures, and the absence of a global consensus on efficient and accurate analytical protocols. These factors hinder direct data comparison and evaluation. This review provides a summary of the sources of MPs/NPs and their worldwide distribution in groundwater, and categorizes the analytical methods employed for their characterization, including sampling and pretreatment procedures. Finally, promising new technologies for the detection and characterization of MPs/NPs are discussed.
由于微塑料和纳米塑料(MPs/NPs)的广泛分布以及对生态系统和人类健康的潜在不利影响,它们正日益成为环境问题。有关 MPs/NPs 的大量研究都集中在它们的分布、行为和归宿上;然而,人们对作为饮用水主要来源的地下水中的这些材料还缺乏了解。这归因于开展此类研究的困难、缺乏普遍接受的标准程序,以及对高效、准确的分析协议缺乏全球共识。这些因素阻碍了数据的直接比较和评估。本综述概述了 MPs/NPs 的来源及其在地下水中的全球分布情况,并对表征 MPs/NPs 所采用的分析方法进行了分类,包括采样和预处理程序。最后,还讨论了用于检测和表征 MPs/NPs 的前景看好的新技术。
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引用次数: 0
Evaluation of European watch list contaminants in environmental matrices and microplastics: Analytical strategies, mechanisms of adsorption and occurrence 评估环境基质和微塑料中的欧洲观察清单污染物:分析策略、吸附机制和发生机制
IF 11.1 2区 化学 Q1 CHEMISTRY, ANALYTICAL Pub Date : 2024-10-31 DOI: 10.1016/j.teac.2024.e00245
Ludovit Schreiber , Radoslav Halko , Sergio Santana-Viera , Nicolas Milan Michalides , Zoraida Sosa-Ferrera , José Juan Santana-Rodríguez
The European Union requires environmental monitoring to identify potential pollutants suspected of causing adverse effects, affecting not only aquatic organisms but also posing direct and negatively influence to human health. Comprehensive knowledge about their occurrence and impact of these pollutants in environmental matrices, including microplastics, is essential for informed decision regarding their inclusion in surveillance lists. This study focuses on reviewing and assessing the analytical methodologies employed in determine substances listed in the last 4th European Watch List, in various environmental matrices, including water, soils, biota, and microplastics. Additionally, the different interaction mechanisms of adsorption onto microplastics are discussed. A dedicated section is also addressed to examine the occurrence of these substances in diverse environmental matrices. The findings contribute to a better understanding of the presence and effects of these substances, aiding in the development of effective surveillance strategies to mitigate their impact on the environment.
欧盟要求进行环境监测,以确定涉嫌造成不良影响的潜在污染物,这些污染物不仅会影响水生生物,还会对人类健康造成直接和负面的影响。全面了解这些污染物在环境基质(包括微塑料)中的出现和影响,对于在知情的情况下决定是否将其列入监测清单至关重要。本研究的重点是审查和评估用于确定最近第四批欧洲监控清单所列物质的分析方法,这些物质存在于各种环境基质中,包括水、土壤、生物群和微塑料。此外,还讨论了微塑料吸附的不同相互作用机制。还专门用一个章节来研究这些物质在不同环境基质中的出现情况。研究结果有助于更好地了解这些物质的存在和影响,有助于制定有效的监控策略,减轻它们对环境的影响。
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引用次数: 0
Pharmaceuticals and micro(nano)plastics in the environment: Sorption and analytical challenges 环境中的药物和微(纳米)塑料:吸附和分析挑战
IF 11.1 2区 化学 Q1 CHEMISTRY, ANALYTICAL Pub Date : 2024-10-30 DOI: 10.1016/j.teac.2024.e00243
A.L. Patrício Silva , D. Barceló , T. Rocha-Santos
The co-occurrence of pharmaceutical residues and micro(nano)plastics in aquatic environments raises concerns about their potential interactions and consequent fate, transport, bioavailability, and toxicity. While numerous studies have investigated these interactions under laboratory conditions, a significant knowledge gap remains regarding their behaviour in real-world scenarios. This review addresses this gap by critically analysing recent literature on pharmaceutical sorption to micro(nano)plastics in environmental samples or under simulated natural conditions. Key findings underscore the nature of these interactions, influenced by factors such as microplastics’ type, surface area, and biofouling. However, the scarcity of field studies and persistent analytical challenges (including sampling, extraction, and detection limitations), hinder a comprehensive understanding of these processes in real scenarios. Future efforts should prioritise the development of standardised methodologies, advanced analytical techniques, and expanded field-based monitoring to comprehensively assess the environmental and human health risks associated with pharmaceutical-microplastic interactions. This knowledge is crucial for informing effective mitigation strategies and policy decisions to address the growing concern of pharmaceutical and microplastic pollution in aquatic ecosystems.
药物残留和微(纳米)塑料同时出现在水生环境中,引起了人们对它们之间潜在的相互作用以及随之而来的归宿、迁移、生物利用率和毒性的关注。虽然已有大量研究对实验室条件下的这些相互作用进行了调查,但关于它们在现实世界中的行为,仍然存在着巨大的知识差距。本综述通过批判性地分析环境样本或模拟自然条件下药物对微(纳)塑料吸附的最新文献,弥补了这一空白。主要研究结果强调了这些相互作用的性质,它们受到微塑料类型、表面积和生物污垢等因素的影响。然而,实地研究的稀缺性和持续存在的分析难题(包括取样、提取和检测限制)阻碍了对真实场景中这些过程的全面了解。未来的工作应优先发展标准化方法、先进分析技术和扩大实地监测,以全面评估与药物-微塑料相互作用相关的环境和人类健康风险。这些知识对于制定有效的缓解战略和政策决定,解决水生生态系统中日益严重的药物和微塑料污染问题至关重要。
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引用次数: 0
Recent progress on multiplexed detection strategies of heavy metals with emphasis on quantum dots 以量子点为重点的重金属多重检测策略的最新进展
IF 11.1 2区 化学 Q1 CHEMISTRY, ANALYTICAL Pub Date : 2024-10-25 DOI: 10.1016/j.teac.2024.e00244
Juhi Shrivastav, Nishtha Khansili
The rapid industrialization and urbanization of recent decades have intensified the global challenge of heavy metal pollution, necessitating the development of advanced sensing technologies for efficient detection and monitoring. Multiplexed detection, seeking either the simultaneous assessment of multiple analytes in the same experiment or the multi-detection of a single analyte in a complex sample matrix replete of interfering species, has gained, in recent years, a noteworthy interest amidst the analytical community. Evolving from early conventional techniques, multiplexed detection has been able, to deliver reliable and efficient analysis in fields as different as clinical, pharmaceutical, food and environmental analysis. The research on nanomaterials, in particular on photoluminescent quantum dots (QDs), has paved the way for the implementation of innovative and flexible multiplexed assays since their remarkable optical properties and tailored reactivity could be arranged in many configurations, combining different fluorophores and molecular recognition elements and providing the means for the establishment of definite reaction pathways and detection methods. From this particular study it concludes that, the development of QDs -based multiplexed detection techniques, examine the distinct roles they could play at the sensing platform, either alone or combined with other materials, and discuss the emerging developments and trends of QDs based nanosensors for the real-time detection of heavy metal ions. A quest of recent advances, actual issues, and potential futures of QDs-based nanosensors for heavy metals monitoring are provided in this study.
近几十年来,快速的工业化和城市化加剧了重金属污染这一全球性挑战,因此有必要开发先进的传感技术,以实现高效的检测和监测。近年来,多重检测技术受到了分析界的广泛关注,它既可以在同一实验中同时评估多种分析物,也可以在充满干扰物的复杂样品基质中对单一分析物进行多重检测。从早期的传统技术发展而来的多重检测技术已经能够在临床、制药、食品和环境分析等不同领域提供可靠而高效的分析。对纳米材料,特别是光致发光量子点(QDs)的研究为实施创新、灵活的多路复用检测铺平了道路,因为它们具有显著的光学特性和定制的反应活性,可以进行多种配置,结合不同的荧光团和分子识别元素,为建立明确的反应途径和检测方法提供了手段。本研究总结了基于 QDs 的多路复用检测技术的发展,考察了它们在传感平台上单独或与其他材料结合所能发挥的独特作用,并讨论了基于 QDs 的纳米传感器在重金属离子实时检测方面的新兴发展和趋势。本研究对基于 QDs 的重金属监测纳米传感器的最新进展、实际问题和潜在前景进行了探索。
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引用次数: 0
Persulfate-based total oxidizable precursor (TOP) assay approaches for advanced PFAS assessment in the environment – A review 用于环境中全氟辛烷磺酸高级评估的基于过硫酸盐的总可氧化前体(TOP)检测方法--综述
IF 11.1 2区 化学 Q1 CHEMISTRY, ANALYTICAL Pub Date : 2024-10-24 DOI: 10.1016/j.teac.2024.e00242
Frank Thomas Lange , Finnian Freeling , Bernd Göckener
The enormous structural complexity of millions of per- and polyfluorinated alkyl substances (PFASs) poses a major challenge for their chemical analysis. One approach to partially address this challenge is the so-called total oxidizable precursor (TOP) assay. In the past years, however, different laboratories worldwide modified the method in multiple ways leading to a confusingly complex variety of TOP assay approaches. This review aims to provide an overview on this methodological complexity and to identify key parameters and their potential influence on the results and method interpretation. Parameters of all available studies were summarized in a complex table. The amount and concentration of oxidation reagents, the reaction time, temperature and pH value during oxidation, the time of internal standard addition, and the suite of analyzed oxidation products were identified as key factors affecting oxidation efficiency, nature of reaction products, and completeness of precursor assessment. The current complexity of TOP assay approaches demonstrates the need for further method harmonization and standardization, which should include measures to ensure and assess the completeness of precursor oxidation. A further understanding of the chemical reactions during the TOP assay and the inclusion of additional oxidation endpoints were identified as research needs for the future. This review article paves the way for the further implementation of the TOP assay as an important tool to assess the world of PFAS more comprehensively, thereby supporting environmental monitoring, assessment of PFAS contaminations, and the success control of designated PFAS regulations.
数百万全氟和多氟烷基物质(PFASs)的结构非常复杂,这给其化学分析带来了巨大挑战。部分应对这一挑战的方法之一是所谓的总可氧化前体(TOP)测定法。然而,在过去的几年中,全球不同的实验室以多种方式对该方法进行了修改,从而导致了令人困惑的各种 TOP 分析方法。本综述旨在概述这种方法的复杂性,并确定关键参数及其对结果和方法解释的潜在影响。所有可用研究的参数都汇总在一个复杂的表格中。氧化试剂的用量和浓度、反应时间、氧化过程中的温度和 pH 值、内标添加时间以及所分析的氧化产物的种类被确定为影响氧化效率、反应产物性质和前体评估完整性的关键因素。目前 TOP 检测方法的复杂性表明需要进一步协调和标准化方法,其中应包括确保和评估前体氧化完整性的措施。进一步了解 TOP 检测过程中的化学反应以及纳入更多氧化终点被确定为未来的研究需求。这篇综述文章为进一步实施 TOP 分析法铺平了道路,使其成为更全面地评估 PFAS 世界的重要工具,从而为环境监测、PFAS 污染评估和指定 PFAS 法规的成功控制提供支持。
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引用次数: 0
Recent advances in microextraction techniques for sensitive determination of synthetic musks in complex samples 用于灵敏测定复杂样品中合成麝香的微萃取技术的最新进展
IF 11.1 2区 化学 Q1 CHEMISTRY, ANALYTICAL Pub Date : 2024-09-13 DOI: 10.1016/j.teac.2024.e00241
Qian Wang , Yuan Zhang , Yu Zhou , Fang Chen , Xue-song Feng

Synthetic musks (SMs) are commonly found in everyday household items and are introduced into the ecosystem via domestic wastewater, rendering them notable contaminants in both the environment and food sources. Given the intricate nature of sample matrices and the low concentrations of these compounds, the utilization of more sensitive and reliable techniques is imperative for sample preparation. Microextraction, characterized by its high efficiency and stability for environmentally friendly analysis, has demonstrated superiority in various studies and has shown advancements in structural design and the application of novel materials in recent years. This review provides a comprehensive overview of recent advancements in microextraction techniques for the analysis of SMs, focusing on different sample types from 2017 to 2023. The applications of different microextraction techniques in different samples are summarized, highlighting both the major advancements and notable limitations. The discussed techniques include directly immersion solid-phase microextraction, headspace solid-phase microextraction, stir bar sorptive microextraction, thin film microextraction, fabric phase sorptive extraction, and dispersive solid-phase microextraction. Liquid phase microextraction methods, such as hollow fiber liquid-liquid microextraction, dispersive liquid-liquid microextraction, vortex-assisted liquid-liquid microextraction, and ultrasound-assisted electronic membrane extraction, provide alternative approaches for analyzing complex samples. The utilization of modern methodologies and innovative materials underscores the growing emphasis on green chemistry and environmentally friendly practices in the sample preparation of small molecules.

合成麝香 (SM) 常见于日常家居用品中,并通过生活废水进入生态系统,成为环境和食物来源中的重要污染物。鉴于样品基质的复杂性和这些化合物的低浓度,利用更加灵敏可靠的技术进行样品制备势在必行。微萃取技术的特点是高效、稳定,适用于环境友好型分析,在各种研究中都显示出其优越性,近年来在结构设计和新型材料的应用方面也取得了进步。本综述全面概述了从 2017 年到 2023 年用于分析 SMs 的微萃取技术的最新进展,重点关注不同类型的样品。综述了不同微萃取技术在不同样品中的应用,重点介绍了主要的进展和显著的局限性。讨论的技术包括直接浸泡固相微萃取、顶空固相微萃取、搅拌棒吸附微萃取、薄膜微萃取、织物相吸附萃取和分散固相微萃取。液相微萃取方法,如中空纤维液液微萃取、分散液液微萃取、涡流辅助液液微萃取和超声辅助电子膜萃取,为分析复杂样品提供了替代方法。现代方法和创新材料的使用凸显了在小分子样品制备过程中对绿色化学和环保实践的日益重视。
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引用次数: 0
Ion mobility separation coupled to high-resolution mass spectrometry in environmental analysis – Current state and future potential 离子淌度分离与高分辨率质谱联用技术在环境分析中的应用--现状与未来潜力
IF 11.1 2区 化学 Q1 CHEMISTRY, ANALYTICAL Pub Date : 2024-07-29 DOI: 10.1016/j.teac.2024.e00239
Alberto Celma , Nikiforos Alygizakis , Lidia Belova , Lubertus Bijlsma , David Fabregat-Safont , Frank Menger , Rubén Gil-Solsona

The hyphenation of ion mobility separation (IMS) with high-resolution mass spectrometry (HRMS) presents a milestone in the screening of organic micropollutants (OMPs) in complex environmental matrices. Its use has become progressively more widespread in environmental analysis and has led to the development of novel analytical strategies. This work provides a comprehensive overview of the advantages of using IMS-HRMS instrumentation, with a special focus on environmental screening studies. IMS provides an additional parameter for OMP identification, a reduction of spectral background noise and the power to resolve isomeric/isobaric coeluting interferences. These advantages lead to a reduction of false positive identifications. By describing the fundamentals and rationale behind the observed advancements, we highlight areas for further development that will unlock new potential of IMS-HRMS. For example, an enhanced availability of empirical IMS data following the FAIR principles, a better standardization of IMS-HRMS data processing workflows and a higher IMS resolving power are possible ways to advance the use of IMS-HRMS instruments for the analysis of complex environmental samples.

离子淌度分离(IMS)与高分辨质谱(HRMS)的结合是复杂环境基质中有机微污染物(OMPs)筛选的一个里程碑。它在环境分析中的应用日益广泛,并促进了新型分析策略的开发。本研究全面概述了使用 IMS-HRMS 仪器的优势,尤其侧重于环境筛选研究。IMS 为 OMP 鉴定提供了额外的参数,降低了光谱背景噪声,并具有解决异构体/异构体共污染干扰的能力。这些优势可减少假阳性鉴定。通过描述所观察到的进步背后的基本原理和基本原理,我们强调了有待进一步开发的领域,这些领域将释放 IMS-HRMS 的新潜力。例如,遵循 FAIR 原则提高 IMS 经验数据的可用性、更好地标准化 IMS-HRMS 数据处理工作流程以及更高的 IMS 分辨能力,都是推动使用 IMS-HRMS 仪器分析复杂环境样品的可能途径。
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引用次数: 0
Advances in nanohydrolase-based pollutant sensing 基于纳米水解酶的污染物传感技术进展
IF 11.1 2区 化学 Q1 CHEMISTRY, ANALYTICAL Pub Date : 2024-07-18 DOI: 10.1016/j.teac.2024.e00238
Ju Luo, Xue-Yan Gong, Bing-Yi Zhou, Lin Yang, Wen-Chao Yang

Harmful pollutants, such as pesticides, heavy metal ions, and antibiotics, pose significant threats to global food security and ecological safety; seriously damage human health; and hinder the green and sustainable development of modern society. Therefore, there is an urgent need for methods to accurate detect these harmful pollutants. In recent years, significant advancements have been made in nanomimetic research on hydrolases, which are the most common and abundant class of natural enzymes. Researchers have developed a variety of biomimetic hydrolases (also known as nanohydrolases) based on nanomaterials for detecting harmful contaminants (including pesticides, antibiotics, and heavy metal ions) in food and ecological environments. However, to date, there have been few reviews on the use of nanohydrolases for pollutant sensing. Herein, we classify the carrier materials and the types of chemical bonds hydrolyzed by nanohydrolases. Then, we summarize the application of nanohydrolases for sensing harmful pollutants. This study provides guidance for the development of nanohydrolases and contributes to the expansion of nanoenzyme-based sensing of environmental pollutants.

农药、重金属离子和抗生素等有害污染物对全球粮食安全和生态安全构成重大威胁,严重损害人类健康,阻碍现代社会的绿色可持续发展。因此,准确检测这些有害污染物的方法迫在眉睫。近年来,关于水解酶的纳米仿生研究取得了重大进展,水解酶是最常见、最丰富的一类天然酶。研究人员开发了多种基于纳米材料的生物仿生水解酶(也称为纳米水解酶),用于检测食品和生态环境中的有害污染物(包括农药、抗生素和重金属离子)。然而,迄今为止,有关利用纳米水解酶进行污染物传感的综述还很少。在此,我们对纳米水解酶水解的载体材料和化学键类型进行了分类。然后,我们总结了纳米水解酶在有害污染物传感方面的应用。本研究为纳米水解酶的开发提供了指导,并有助于扩大基于纳米酶的环境污染物传感。
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引用次数: 0
Review on unravelling the analytical signatures of fluoroquinolone antibiotics: Exploring diverse matrices through chemometric modelling 关于揭示氟喹诺酮类抗生素分析特征的综述:通过化学计量建模探索不同基质
IF 11.1 2区 化学 Q1 CHEMISTRY, ANALYTICAL Pub Date : 2024-07-08 DOI: 10.1016/j.teac.2024.e00237
Kheerthana Ramesh , Mahdiye Hassanpoor , Padmanaban Velayudhaperumal Chellam

Globally, fluoroquinolones are the third largest antimicrobial category. These molecules can enter natural biota either in unmetabolized or partially metabolised form and undergoes further transformation depending on biotic and abiotic factors in aqueous and terrestrial ecosystems, which can lead to antimicrobial resistance. This requires timely monitoring and prediction of fluoroquinolone and metabolite changes. The physiochemical flexibility of fluoroquinolones, complicated sampling combinations, and matrix interference in sample preparation and detection could give misleading quantifying results. These complex and massive data sets require rigorous statistical and mathematical data processing approaches to detect analytical fingerprints/patterns, and point - nonpoint source discrimination. This paper has critically reviewed the use of predictive and exploratory chemometric models to identify the patterns and resolve overlapping, asymmetric peaks and multicollinearity fluoroquinolone spectrum data raised from several separative and non-separative detection techniques. Moreover, this review also highlights the crucial parameters involved in determining fluoroquinolones in real-time samples, challenges, and research gaps associated with current analytical techniques. The approach also prioritises the integration of clustering, classification and regression-based chemometrics to achieve justifiable accurate results. This review will address fluoroquinolone detection challenges and help the government and research community to develop better regulatory policies, analytical methods, and mitigation strategies to protect life-saving antibiotics.

在全球范围内,氟喹诺酮类药物是第三大抗菌药物类别。这些分子可以未代谢或部分代谢的形式进入天然生物群,并根据水体和陆地生态系统中的生物和非生物因素发生进一步转化,从而导致抗菌药耐药性。这就需要及时监测和预测氟喹诺酮和代谢物的变化。氟喹诺酮类药物的理化性质灵活多变,取样组合复杂,样品制备和检测过程中的基质干扰可能会产生误导性的量化结果。这些复杂而庞大的数据集需要严格的统计和数学数据处理方法来检测分析指纹/模式,并区分点-非点来源。本文对预测性和探索性化学计量学模型的使用进行了批判性评述,以确定模式并解决从几种分离和非分离检测技术中产生的重叠、不对称峰和多共线性氟喹诺酮光谱数据。此外,本综述还强调了在实时样品中确定氟喹诺酮类药物所涉及的关键参数、挑战以及与当前分析技术相关的研究空白。该方法还优先考虑整合聚类、分类和基于回归的化学计量学,以获得合理准确的结果。本综述将解决氟喹诺酮检测难题,帮助政府和研究界制定更好的监管政策、分析方法和缓解策略,以保护拯救生命的抗生素。
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引用次数: 0
Current advances in the implementation of magnetic molecularly imprinted polymers tailored for enrichment of target analytes in different environmental samples: An overview from a comprehensive perspective 磁性分子印迹聚合物用于富集不同环境样品中目标分析物的最新进展:全面概述
IF 11.1 2区 化学 Q1 CHEMISTRY, ANALYTICAL Pub Date : 2024-06-29 DOI: 10.1016/j.teac.2024.e00236
Mohammed Gamal , Mohamed S. Imam , Abdulmajeed Sultan Albugami , Saleh Abdulrahman Hunjur , Ahmed Khalid Aldhalmi , Mohamed AbdElrahman , Mohammed M. Ghoneim , Hazim M. Ali , Nada S. Abdelwahab , Maya S. Eissa

In recent years, advancements in separation techniques have been made by the use of magnetic characteristics in molecularly imprinted polymers (MIPs). Magnetic molecularly imprinted polymers (MMIPs) have benefits over traditional molecular imprinted polymers (MIPs) in sample pretreatment because of their larger specific surface areas and highly accessible particular binding sites, which result in excellent specificity and selectivity toward analytes. MMIPs are easily separated from a variety of complicated matrices and have a high adsorption capability. They play an essential role in the efficient extraction of various analytes from a variety of matrices, including water, soil, food and its derivatives, plant extraction, fruits and vegetables, and various biological samples. Additionally, MMIPs have the major benefit of being a green chemistry approach, whether in synthesis or applications; as a result, they effectively reduce pollution in the environment and minimize the use of resources. A variety of MMIP applications from 2019 to 2023 were reviewed in this work. The various approaches and procedures utilized to create MMIPs are covered in this review. In addition, a brief description of several MMIP-based analytical techniques is provided in this manuscript, along with information on various aspects such as their adsorption capacity, equilibrium time, limit of detection, extraction recovery, and recyclability assessment. The types of porogen and functional monomer used have the greatest effect on the efficiency and reusability of the constructed MMIPs. On the contrary, the cross-linker type has no prominent effect on the efficiency and reusability of the constructed MMIPs. Future opportunities and current obstacles to better promote MMIPs features are also covered. This publication served as a comprehensive assessment of a number of analytes in various matrices recovered by MMIP, including pollutants, dyes, natural components, pesticides, herbicides, and insecticides. As a result, it can serve as a guide for creating new MMIP-based analytical techniques for a range of uses.

近年来,分子印迹聚合物(MIPs)中磁性特征的使用推动了分离技术的发展。磁性分子印迹聚合物(MMIPs)比传统的分子印迹聚合物(MIPs)具有更大的比表面积和高度可访问的特定结合位点,从而对分析物具有极佳的特异性和选择性,因此在样品预处理方面比传统的分子印迹聚合物(MIPs)更有优势。MMIPs 很容易从各种复杂的基质中分离出来,并具有很强的吸附能力。它们在从各种基质(包括水、土壤、食品及其衍生物、植物提取物、水果和蔬菜以及各种生物样品)中高效萃取各种分析物方面发挥着重要作用。此外,无论是在合成还是应用方面,MMIP 都具有绿色化学方法的重大优势;因此,它们能有效减少对环境的污染,并最大限度地减少资源的使用。本研究对 2019 年至 2023 年的各种 MMIP 应用进行了审查。本综述涵盖了用于创建 MMIP 的各种方法和程序。此外,本手稿还简要介绍了几种基于 MMIP 的分析技术,以及吸附容量、平衡时间、检测限、萃取回收率和可回收性评估等各方面的信息。所使用的致孔剂和功能单体类型对所构建 MMIP 的效率和可再利用性影响最大。相反,交联剂类型对构建 MMIP 的效率和可再利用性没有显著影响。此外,还介绍了更好地推广 MMIPs 特性的未来机遇和当前障碍。本出版物全面评估了 MMIP 回收的各种基质中的多种分析物,包括污染物、染料、天然成分、杀虫剂、除草剂和杀虫剂。因此,它可作为创建基于 MMIP 的新分析技术的指南,用于各种用途。
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引用次数: 0
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Trends in Environmental Analytical Chemistry
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