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1.
Talanta ; 276: 126193, 2024 Aug 15.
Artigo em Inglês | MEDLINE | ID: mdl-38735244

RESUMO

Di(2-ethylhexyl)phthalate (DEHP) is commonly released from plastics in aqueous environment, which can disrupt endocrine system and cause adverse effects on public health. There is a pressing need to highly sensitive detect DEHP. Herein, a near-infrared (NIR) light-driven lab-on-paper cathodic photoelectrochemical aptasensing platform integrated with AgInS2/Cu2O/FeOOH photocathode and "Y"-like ternary conjugated DNA nanostructure-mediated "ON-OFF" catalytic switching of hemin monomer-to-dimer was established for ultrasensitive DEHP detection. Profiting from the collaborative roles of the effective photosensitization of NIR-response AgInS2 and the fast hole extraction of FeOOH, the NIR light-activated AgInS2/Cu2O/FeOOH photocathode generated a markedly enhanced photocathodic signal. The dual hemin-labelled "Y"-like ternary conjugated DNA nanostructures made the hemin monomers separated in space and they maintained highly active to catalyze in situ generation of electron acceptors (O2). The hemin monomers were relocated in close proximity with the help of target-induced allosteric change of DNA nanostructures, which could spontaneously dimerize into catalytically inactive hemin dimers and fail to mediate electron acceptors generation, resulting in a decreased photocathodic signal. Therefore, the ultrasensitive DEHP detection was realized with a linear response range of 1 pM-500 nM and a detection limit of 0.39 pM. This work rendered a promising prototype to construct powerful paper-based photocathodic aptasensing system for sensitive and accurate screening of DEHP in aqueous environment.


Assuntos
Cobre , Dietilexilftalato , Técnicas Eletroquímicas , Eletrodos , Raios Infravermelhos , Processos Fotoquímicos , Cobre/química , Técnicas Eletroquímicas/métodos , Dietilexilftalato/química , Dietilexilftalato/análise , Aptâmeros de Nucleotídeos/química , Técnicas Biossensoriais/métodos , Papel , Prata/química , Limite de Detecção , Índio/química , Poluentes Químicos da Água/análise , Poluentes Químicos da Água/química
2.
Anal Chim Acta ; 1287: 342135, 2024 Jan 25.
Artigo em Inglês | MEDLINE | ID: mdl-38182398

RESUMO

Di(2-ethylhexyl)phthalate (DEHP), as an environmental endocrine disruptor, has adverse effects on eco-environments and health. Thus, it is crucial to highly sensitive on-site detect DEHP. Herein, a double-enzyme active MnO2@BSA mediated dual-modality photoelectrochemical (PEC)/colorimetric aptasensing platform with the cascaded sensitization structures of ZnIn2S4 and TiO2 as signal generators was engineered for rapid and ultrasensitive detection of DEHP using an all-in-one lab-on-paper analytical device. Benefitting from cascaded sensitization effect, the ZnIn2S4/TiO2 photosensitive structures-assembled polypyrrole paper electrode gave an enhanced photocurrent signal. The MnO2@BSA nanoparticles (NPs) with peroxidase-mimic and oxidase-mimic double-enzymatic activity induced multiple signal quenching effects and catalyzed color development. Specifically, the MnO2@BSA NPs acted as peroxidase mimetics to generate catalytic precipitates, which not only obstructed interfacial electron transfer but also served as electron acceptors to accept photogenerated electrons. Besides, the steric hindrance effect from MnO2@BSA NPs-loaded branchy polymeric DNA duplex structures further decreased photocurrent signal. The target recycling reaction caused the detachment of MnO2@BSA NPs to increase PEC signal, realizing the ultrasensitive detection of DEHP with a low detection limit of 27 fM. Ingeniously, the freed MnO2@BSA NPs flowed to colorimetric zone with the aid of fluid channels and acted as oxidase mimetics to induce color intensity enhancement, resulting in the rapid visual detection of DEHP. This work provided a prospective paradigm to develop field-based paper analytical tool for DEHP detection in aqueous environment.


Assuntos
Dietilexilftalato , Polímeros , Compostos de Manganês , Estudos Prospectivos , Óxidos , Pirróis , Peroxidase , Peroxidases , Corantes
3.
Science ; 308(5721): 519-23, 2005 Apr 22.
Artigo em Inglês | MEDLINE | ID: mdl-15845846

RESUMO

The origin of the solar wind in solar coronal holes has long been unclear. We establish that the solar wind starts flowing out of the corona at heights above the photosphere between 5 megameters and 20 megameters in magnetic funnels. This result is obtained by a correlation of the Doppler-velocity and radiance maps of spectral lines emitted by various ions with the force-free magnetic field as extrapolated from photospheric magnetograms to different altitudes. Specifically, we find that Ne7+ ions mostly radiate around 20 megameters, where they have outflow speeds of about 10 kilometers per second, whereas C3+ ions with no average flow speed mainly radiate around 5 megameters. Based on these results, a model for understanding the solar wind origin is suggested.

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