Environmental Science-Nano
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2025
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IF 5.1
Guillaume Crosset-Perrotin,Angélique Moraz,Raquel Portela,Victor Alcolea-Rodriguez,David Burrueco-Subirà,Casey Smith,Miguel A. Bañares,Hosein Foroutan,D. Howard Fairbrother
Challenges inherent to the extraction of micro- and nanoplastics (MNPs) from the environment, combined with the limited range of commercially available MNPs, have prompted an increasing number of researchers to generate in-house reference and test MNPs. The first part of this review provides a comprehensive overview of existing MNP production methods, including top-down and bottom-up fabrication techniques. Strengths and weaknesses of different methods are compared and contrasted, and the potential for optimization and control over MNP properties is discussed. Methods to label and to artificially weather MNPs before, during, or after production, as well as appropriate dispersion protocols for introducing MNPs into different media, are also covered. The second part of this review focuses on how reference and test MNPs have been implemented in different types of studies, categorized as toxicity, uptake, fate, and monitoring. Given the wide range of properties needed to fully define MNPs, we propose a set of essential properties that need to be characterized depending on the study type. Looking forward, we suggest future needs, not only in the creation of reference MNPs, but also in experimental protocols that would help to better understand the behavior and impacts of MNPs. Overall, this review aims to provide the necessary information to guide researchers in decision-making regarding which reference MNPs are most appropriate to answer their specific research questions and to serve as a framework that will contribute to obtaining reliable, benchmarked data urgently needed to develop consensus on the fate and risk posed by MNPs.
研究领域:
环境科学
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材料科学
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生物学
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DOI
高影响因子
ANALYTICA CHIMICA ACTA
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2013
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IF 4.387
Debin Wan,Hongmei Yang,Fengrui Song,Zhiqiang Liu,Shuying Liu
1-Phenyl-3-methyl-5-pyrazolone (PMP) labeling technique has hitherto proved to be a convenient and sensitive method for separating and detecting oligosaccharides. However, the detailed fragmentation of the derivatives by tandem mass spectrometry has been reported limitedly and no characteristic fragment ions for isomers have been detected. In this study, eight disaccharide isomers were labeled with PMP and analyzed by positive ion electrospray ionization multi-stage tandem mass spectrometry (ESI-MS n ). In comparison with the native disaccharides, PMP labeled disaccharides gave rise to more fragment ions in the tandem mass spectra. The distinctive diagnostic fragment ions formed from cleavage of C C bonds have been detected in the fragmentation of PMP-labeled disaccharide linkage isomers, allowing unambiguous assignment of the position of the glycosidic linkages. This feature is particularly useful for the structural determination of unknown isomeric disaccharides mixed together. In addition, the anomeric configurations can also be easily assigned based on the relative abundance ratios of the selected ion pairs. To verify the feasibility of the method used in the analysis of natural product, water soluble Panax Ginseng extract has been further investigated to identify its unknown disaccharides. The results confirmed that the PMP labeling technique in conjunction with ESI-MS n could offer a powerful and convenient tool for differentiation of structurally closely related isomers, even the unknown mixtures of isomeric disaccharides with different linkage types.
研究领域:
分析化学
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生物化学
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DOI
高影响因子
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
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2024
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IF 5.7
Tong Zhou,Meigui Huang,Heping Cui,Shahzad Hussain,Khizar Hayat,Xiaoming Zhang,Chi-Tang Ho
The formation pathway and mechanism of various pyrazines were investigated during the thermal treatment of the alanine-xylose Amadori compound (Ala-ARP) and exogenous alanine (Ala). 15N-labeled Ala was used to coheated with Ala-ARP to clarify the nitrogen sources and the respective contributions of exogenous Ala and the regenerated Ala released from Ala-ARP to different pyrazine formation. It was found that exogenous Ala exhibited a priority in capturing glyoxal (GO) to form pyrazine during the thermal degradation of ARP. Compared to the Ala-methylglyoxal (MGO) model, a lower activation energy was required for the Ala-GO reaction, where the reaction dynamics of Ala-GO followed a zero-order model. In addition to forming pyrazine, the interaction between existing exogenous Ala and GO would accelerate the thermal degradation of Ala-ARP and retro-aldolization reaction of deoxyxylosones (DXs) to α-dicarbonyls. During this process, the release of regenerated Ala and MGO was promoted. Accordingly, as GO was expended by exogenous Ala during the initial stage of ARP-Ala degradation, the condensation between regenerated Ala and MGO became intensified, leading to the generation of methylpyrazine and 2,5-dimethylpyrazine. As a result, in the thermally treated mixture of Ala-ARP and exogenous Ala, 55% of the formed pyrazine originated from exogenous Ala, while 63% of the formed methylpyrazine and 57% of the formed 2,5-dimethylpyrazine were derived from regenerated Ala (120 °C, 30 min).
研究领域:
食品科学
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化学
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产品关联
DOI
PubMed
高影响因子
Journal of Advanced Research
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2025
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IF 13
Ruomeng Li,Xueyin Wu,Jing Yao,Jiawen Chen,Xindong Shui,Xiaoqing Zheng,Wujin Tian,Long Wang,Ying Zhou,Tao Zhang,Dongmei Chen,Yang Liu,Tae Ho Lee
Introduction The upregulation of death-associated protein kinase 1 (DAPK1) is involved in tau hyperphosphorylation, neuronal apoptosis and cognitive dysfunction, which are key pathological features of Alzheimer’s disease (AD). This result suggests that DAPK1 is novel therapeutic target for AD. Objectives This study aimed to evaluate the efficacy and mechanism of action of CJ1, a novel hydrophobic tagging (HyT)-based degrader, in targeting DAPK1 and alleviating in AD. Methods A library of HyT-based bifunctional molecules was synthesized and systematically screened for their ability to degrade DAPK1 in vitro . CJ1 emerged as the most potent candidate degrader of DAPK1, and its capacity to induce DAPK1 degradation via the proteasome system was further evaluated. Its effects on tau phosphorylation and neuronal viability were evaluated in multiple cellular models. The in vivo efficacy of systemic CJ1 administration was assessed in two tau-related pathology (tauopathy) mouse models, AAV-hTau-P301L and hTau transgenic mice. Behavioral, biochemical, and histological analyses were performed to evaluate cognitive function, tau pathology, neuroinflammation, neurodegeneration, and safety. Results CJ1 selectively promoted the posttranslational degradation of DAPK1 by the proteasome system without affecting DAPK1 mRNA expression. In vitro studies demonstrated that CJ1 significantly reduced tau phosphorylation at multiple AD-related sites. In vivo , CJ1 effectively penetrated the BBB, decreased the levels of both the soluble and insoluble forms of hyperphosphorylated tau, and suppressed the formation of neurofibrillary tangles. Additionally, CJ1 treatment restored synaptic and dendritic structures, enhanced spatial learning and memory, attenuated neuroinflammatory responses, preserved neuronal populations, and produced no evidence of systemic toxicity. Conclusion CJ1 functions as a potent and selective degrader of DAPK1, exerting neuroprotective effects by reducing tau hyperphosphorylation and preserving neuronal structural integrity. These findings support DAPK1 as a promising therapeutic target and suggest that further preclinical studies are warranted to evaluate CJ1 as a potential treatment for tauopathies associated with AD.
✓ 已验证
DOI
PubMed
高影响因子
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