RESUMEN
Group 2 innate lymphoid cells (ILC2s) are crucial in promoting type 2 inflammation that contributes to both anti-parasite immunity and allergic diseases. However, the molecular checkpoints in ILC2s that determine whether to immediately launch a proinflammatory response are unknown. Here, we found that retinoid X receptor gamma (Rxrg) was highly expressed in small intestinal ILC2s and rapidly suppressed by alarmin cytokines. Genetic deletion of Rxrg did not impact ILC2 development but facilitated ILC2 responses and the tissue inflammation induced by alarmins. Mechanistically, RXRγ maintained the expression of its target genes that support intracellular cholesterol efflux, which in turn reduce ILC2 proliferation. Furthermore, RXRγ expression prevented ILC2 response to mild stimulations, including low doses of alarmin cytokine and mechanical skin injury. Together, we propose that RXRγ expression and its mediated lipid metabolic states function as a cell-intrinsic checkpoint that confers the threshold of ILC2 activation in the small intestine.
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Inmunidad Innata , Receptor gamma X Retinoide , Humanos , Alarminas , Linfocitos , Inflamación , Citocinas/metabolismo , Intestino Delgado/metabolismoRESUMEN
As an emerging neurodegenerative disease, Alzheimer's disease (AD) has become a leading cause of dementia in older adults. Visinin-like protein-1 (VILIP-1) is an increasingly used biomarker for AD besides the widely accepted Aß1-40, Aß1-42, and tau. However, significant variations exist in the commercial immuno-based assays for VILIP-1 quantification, underlining the necessity to establish a traceability chain. Certified reference materials (CRMs) located at the top of the traceability chain are traceability sources for relevant matrix standard materials. In this work, VILIP-1 solution CRM with a certified value and uncertainty of 39.82±1.52 µg·g-1 was developed and certified using amino acid-based isotope dilution mass spectrometry (AA-ID-MS) and sulfur-based isotope dilution inductively coupled plasma mass spectrometry (ID-ICP-MS). Certified values from both strategies showed great consistency, with traceability to SI units. Moreover, the candidate VILIP-1 CRM shows excellent homogeneity and can be stable for at least 7 days at -20°C and 12 months at -70°C. The VILIP-1 CRM developed can be used in value assignment to secondary calibrators and clinical matrix CRMs, showing prospects in early diagnosis and disease monitoring for AD.
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Enfermedad de Alzheimer , Enfermedades Neurodegenerativas , Humanos , Anciano , Neurocalcina , Aminoácidos/análisis , Cromatografía Liquida/métodos , Espectrometría de Masas/métodos , Enfermedad de Alzheimer/diagnóstico , Azufre , Isótopos , Estándares de ReferenciaRESUMEN
Herein, we developed a highly sensitive electrochemical sensor for the trace detection of Sudan I (SDI) dye based on composite molecularly imprinted membranes (MIMs). The pentenyl (lipoic acyl)-isoleucyl-chitosan oligosaccharide (P(L)ICO) and pentenyl-asparaginyl-chitosan oligosaccharide (PASCO) served as bifunctional monomer oligomers. After deposition of gold nanoparticles on a glassy carbon electrode (GCE) surface, a P(L)ICO layer successfully self-assembled on the surface. Subsequently, the primary MIM was polymerised on the electrode surface by using SDI as a template, PASCO as a functional monomer oligomer, and ethylene glycol dimethacrylate as a cross-linking agent. Electrochemical polymerisation was then conducted in an N,N'-methylenebisacrylamide solution. After eluting the SDI molecules from the composite MIMs, the fabricated SDI-MIM(PM)/Fn-Au/GCE demonstrated specific adsorption of SDI. Under optimal conditions, the constructed sensor exhibited a linear relationship between decreasing peak current and SDI concentration from 0.02 to 3.5 µM with a low detection limit of 4 nM (S/N = 3). As a proof of concept, SDI-MIM(PM)/Fn-Au/GCE was also applied to detect SDI in chili powder samples, with recoveries ranging from 96.8 to 106.6%.
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Quitosano , Nanopartículas del Metal , Impresión Molecular , Carbono/química , Quitosano/química , Técnicas Electroquímicas , Electrodos , Oro/química , Límite de Detección , Nanopartículas del Metal/química , Naftoles , OligosacáridosRESUMEN
BACKGROUND: Disruption of the postsynaptic density protein-95 (PSD95)-neuronal nitric oxide synthase (nNOS) coupling is an effective way to treat ischemic stroke, however, it still faces some challenges, especially lack of satisfactory PSD95-nNOS uncouplers and the efficient high throughput screening model to discover them. RESULTS: Herein, the multifunctional metal-organic framework (MMOF) nanoparticles as a new screening system were innovatively fabricated via layer-by-layer self-assembly in which His-tagged nNOS was selectively immobilized on the surface of magnetic MOF, and then PSD95 with green fluorescent protein (GFP-PSD95) was specifically bound on it. It was found that MMOF nanoparticles not only exhibited the superior performances including the high loading efficiency, reusability, and anti-interference ability, but also possessed the good fluorescent sensitivity to detect the coupled GFP-PSD95. After MMOF nanoparticles interacted with the uncouplers, they would be rapidly separated from uncoupled GFP-PSD95 by magnet, and the fluorescent intensities could be determined to assay the uncoupling efficiency at high throughput level. CONCLUSIONS: In conclusion, MMOF nanoparticles were successfully fabricated and applied to screen the natural actives as potential PSD95-nNOS uncouplers. Taken together, our newly developed method provided a new material as a platform for efficiently discovering PSD95-nNOS uncouplers for stoke treatment.
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Estructuras Metalorgánicas , Nanopartículas , Accidente Cerebrovascular , Animales , Homólogo 4 de la Proteína Discs Large/metabolismo , Óxido Nítrico Sintasa de Tipo I/metabolismo , Ratas , Ratas Sprague-Dawley , Factores de TranscripciónRESUMEN
Two key concerns exist in contemporary cancer chemotherapy: limited therapeutic efficiency and substantial side effects in patients. In recent years, researchers have been investigating the revolutionary cancer treatment techniques of photodynamic therapy (PDT) and photothermal therapy (PTT) proposed by many scholars. A photothermal treatment of cancer was synthesized using the hydrothermal method which has high photothermal conversion efficiency and can generate reactive oxygen species (ROS) in cells. Photothermal treatment of tumors has a good short-term effect and photodynamic therapy lasts longer. However, both PTT and PDT have their inevitable shortcomings and it is difficult to completely eradicate a tumor using a single mode of treatment. PTT and PDT synergistic treatment not only inherits the advantages of low toxicity and side effects of phototherapy but also enables the two treatment methods to complement each other. It is an effective strategy to improve curative effects and reduce toxic and side effects. Furthermore, gold doped UCNPs have an exceptionally high target recognition for tumor cells. The gold doped UCNPs, in particular, are non-toxic to normal tissues, endowing the as-prepared medications with outstanding therapeutic efficacy and exceptionally low side effects. These findings may encourage the creation of fresh, effective imaging-guided approaches to meet the goal of photothermal cancer therapy.
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Nanopartículas del Metal , Nanopartículas , Nanoestructuras , Neoplasias , Fotoquimioterapia , Oro/farmacología , Humanos , Nanopartículas del Metal/uso terapéutico , Neoplasias/tratamiento farmacológico , Fotoquimioterapia/métodos , Fármacos Fotosensibilizantes/farmacología , Fármacos Fotosensibilizantes/uso terapéutico , FototerapiaRESUMEN
Two key concerns exist in contemporary cancer chemotherapy in clinic: limited therapeutic efficiency and substantial side effects in patients. In recent years, researchers have been investigating a revolutionary cancer treatment technique, and photodynamic therapy (PDT) has been proposed by many scholars. A drug for photodynamic cancer treatment was synthesized using the hydrothermal method, which has a high efficiency to release reactive oxygen species (ROS). It may also be utilized as a clear multi-modality bioimaging platform for photoacoustic imaging (PAI) due to its photothermal effect, computed tomography (CT), and magnetic resonance imaging (MRI). When compared to single-modality imaging, multi-modality imaging delivers far more thorough and precise details for cancer diagnosis. Furthermore, Au-doped up-conversion nanoparticles (UCNPs) have an exceptionally high luminous intensity. The Au-doped UCNPs, in particular, are non-toxic to tissues without laser at an 808 nm wavelength, endowing the as-prepared medications with outstanding therapeutic efficacy but exceptionally low side effects. These findings may encourage fresh effective imaging-guided approaches to meet the goal of photodynamic cancer therapy to be created.
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Oro/química , Nanopartículas del Metal/administración & dosificación , Imagen Multimodal/métodos , Fotoquimioterapia/métodos , Nanomedicina Teranóstica , Neoplasias del Cuello Uterino/tratamiento farmacológico , Animales , Apoptosis , Proliferación Celular , Femenino , Humanos , Nanopartículas del Metal/química , Ratones , Ratones Endogámicos BALB C , Ratones Desnudos , Técnicas Fotoacústicas/métodos , Especies Reactivas de Oxígeno/metabolismo , Células Tumorales Cultivadas , Neoplasias del Cuello Uterino/diagnóstico por imagen , Neoplasias del Cuello Uterino/patología , Ensayos Antitumor por Modelo de XenoinjertoRESUMEN
Two key concerns exist in contemporary cancer chemotherapy in clinics: limited therapeutic efficiency and substantial side effects in patients. In recent years, researchers have been investigating revolutionary cancer treatment techniques and photo-thermal therapy (PTT) has been proposed by many scholars. A drug for photothermal cancer treatment was synthesized using the hydrothermal method, which has a high light-to-heat conversion efficiency. It may also be utilized as a clear multi-modality bioimaging platform for photoacoustic imaging (PAI), computed tomography (CT), and magnetic resonance imaging (MRI). When compared to single-modality imaging, multi-modality imaging delivers far more thorough and precise details for cancer diagnosis. Furthermore, gold-doped upconverting nanoparticles (UCNPs) have an exceptionally high target recognition for tumor cells. The gold-doped UCNPs, in particular, are non-toxic to normal tissues, endowing the as-prepared medications with outstanding therapeutic efficacy but exceptionally low side effects. These findings may encourage the creation of fresh effective imaging-guided approaches to meet the goal of photothermal cancer therapy.
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Oro/química , Nanopartículas del Metal/química , Imagen Multimodal/métodos , Fototerapia/métodos , Animales , Línea Celular Tumoral , Terapia Combinada/métodos , Liberación de Fármacos/fisiología , Femenino , Células HeLa , Humanos , Nanopartículas del Metal/administración & dosificación , Ratones , Ratones Endogámicos BALB C , Nanoestructuras/química , Neoplasias/tratamiento farmacológico , Técnicas Fotoacústicas/métodosRESUMEN
Recently, electrochemistry- and photoelectrochemistry-based biosensors have been regarded as powerful tools for trace monitoring of carcinoembryonic antigen (CEA) due to the fact of their intrinsic advantages (e.g., high sensitivity, excellent selectivity, small background, and low cost), which play an important role in early cancer screening and diagnosis and benefit people's increasing demands for medical and health services. Thus, this mini-review will introduce the current trends in electrochemical and photoelectrochemical biosensors for CEA assay and classify them into two main categories according to the interactions between target and biorecognition elements: immunosensors and aptasensors. Some recent illustrative examples are summarized for interested readers, accompanied by simple descriptions of the related signaling strategies, advanced materials, and detection modes. Finally, the development prospects and challenges of future electrochemical and photoelectrochemical biosensors are considered.
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Técnicas Biosensibles , Antígeno Carcinoembrionario , Técnicas Electroquímicas , Electroquímica , Humanos , InmunoensayoRESUMEN
A split-type photoelectrochemical immunosensor was designed for the ultrasensitive monitoring of prostate-specific antigen (PSA) based on a Cu2+-mediated catalytic reaction for inhibiting the in situ generation of CdS quantum dots (QDs) coupled with the enhancement of the CdS/MoS2 heterojunction; it was constructed by the stepwise modification of MoS2 QDs and CdS QDs onto an ITO electrode surface. In the presence of PSA, CuO NP-labeled anti-PSA antibodies were immobilized onto an anti-PSA antibody-modified 96-well plate via a sandwich immunoreaction and dissolution by hydrochloric acid to obtain a large number of Cu2+ ions. As the Cu2+-triggered catalytic oxidization of glutathione occurred, the in situ growth of CdS QDs as a signal indicator was significantly suppressed, resulting in reduction in the photocurrent response. Under optimal conditions, the biosensor exhibited desirable linearity in the range from 0.5 pg mL-1 to 10 ng mL-1, low detection limit of 0.29 pg mL-1, satisfactory selectivity, and good stability. It was applied to PSA detection in human serum, suggesting a great potential for early diagnostics of some cancers.
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Cobre/química , Antígeno Prostático Específico/sangre , Puntos Cuánticos/química , Anticuerpos Inmovilizados/inmunología , Técnicas Biosensibles/métodos , Compuestos de Cadmio/química , Compuestos de Cadmio/efectos de la radiación , Disulfuros/química , Técnicas Electroquímicas/instrumentación , Técnicas Electroquímicas/métodos , Electrodos , Glutatión/química , Humanos , Inmunoensayo/métodos , Luz , Límite de Detección , Masculino , Molibdeno/química , Oxidación-Reducción , Procesos Fotoquímicos , Antígeno Prostático Específico/inmunología , Puntos Cuánticos/efectos de la radiación , Sulfuros/química , Sulfuros/efectos de la radiación , Compuestos de Estaño/químicaRESUMEN
Photoelectrochemical (PEC) analysis is a new detection technique developed in recent years, which has the advantages of high sensitivity, low background signal and desirable selectivity, obtaining the great progress in sensing applications. Semiconductor nanomaterials with excellent photoelectric activity have played a vital role in the construction of PEC sensing platform. Thus, this Review introduces the recent advances of semiconductor nanomaterials-based PEC analysis, and describes the typical PEC sensing strategies. Some representative nanomaterials, including metallic oxides, metallic sulfides, graphitic carbon nitride, transition-metal dichalcogenides and quantum dots, are summarized for advanced PEC devices, as well as their applications in nucleic acid analysis, immunoassays, cell detection, protein and enzyme sensing, and small biomolecule monitoring. Finally, some future opportunities and challenges of PEC biosensing are also discussed.
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Técnicas Biosensibles/métodos , Técnicas Electroquímicas , Nanoestructuras/química , Semiconductores , Biomarcadores/análisis , Grafito/química , Humanos , Metales/química , Ácidos Nucleicos/análisis , Proteínas/análisisRESUMEN
Based on enzymatic biocatalytic precipitation to quench the amplified photocurrent response generated from WS2 nanosheets-sensitized CdS quantum dots heterostructure, a novel photoelectrochemical immunosensor was constructed for sensitive alpha-fetoprotein (AFP) monitoring. The immunosensor comprised an anti-AFP antibody and a horseradish peroxidase-tagged anti-AFP antibody (HRP-Ab2), which served as a capture unit and a signal indicator, respectively. In the presence of AFP, HRP-Ab2 was immobilized on the electrode surface for establishing a sandwich-type immunocomplex via antigen-antibody interaction, and subsequently catalyzed 4-chloro-1-naphthol to form the nonconductive and insoluble precipitate. This precipitation effectively impeded the diffusion and electron transfer of the electron donor, thus achieving decreased photocurrent. Under optimized conditions, excellent linearity range (1 pg mL-1-20 ng mL-1), satisfactory detection limit (0.43 pg mL-1), desirable selectivity and good stability were obtained for the as-designed immunosensor. Moreover, the application of AFP determination in human serum allowed the immunosensor to hold great potential for early diagnostics of some cancer diseases.
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Técnicas Biosensibles , Compuestos de Cadmio/química , Inmunoensayo , Puntos Cuánticos , Compuestos de Tungsteno/química , alfa-Fetoproteínas/análisis , Técnicas Electroquímicas , Humanos , Límite de Detección , NanoestructurasRESUMEN
Arthropods comprise the majority of all described animal species, and understanding their evolution is a central question in biology. Their developmental processes are under the precise control of distinct hormonal regulators, including the sesquiterpenoids juvenile hormone (JH) and methyl farnesoate. The control of the synthesis and mode of action of these hormones played important roles in the evolution of arthropods and their adaptation to diverse habitats. However, the precise roles of non-coding RNAs, such as microRNAs (miRNAs), controlling arthropod hormonal pathways are unknown. Here, we investigated the miRNA regulation of the expression of the juvenile hormone acid methyltransferase gene (JHAMT), which encodes a rate-determining sesquiterpenoid biosynthetic enzyme. Loss of function of the miRNA bantam in the fly Drosophila melanogaster increased JHAMT expression, while overexpression of the bantam repressed JHAMT expression and resulted in pupal lethality. The male genital organs of the pupae were malformed, and exogenous sesquiterpenoid application partially rescued the genital deformities. The role of the bantam in the regulation of sesquiterpenoid biosynthesis was validated by transcriptomic, qPCR and hormone titre (JHB3 and JH III) analyses. In addition, we found a conserved set of miRNAs that interacted with JHAMT, and the sesquiterpenoid receptor methoprene-tolerant (Met) in different arthropod lineages, including insects (fly, mosquito and beetle), crustaceans (water flea and shrimp), myriapod (centipede) and chelicerate (horseshoe crab). This suggests that these miRNAs might have conserved roles in the post-transcriptional regulation of genes in sesquiterpenoid pathways across the Panarthropoda. Some of the identified lineage-specific miRNAs are potential targets for the development of new strategies in aquaculture and agricultural pest control.
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Factores de Transcripción con Motivo Hélice-Asa-Hélice Básico/genética , Proteínas de Drosophila/genética , Drosophila melanogaster/genética , Metiltransferasas/genética , Transducción de Señal/genética , Animales , Artrópodos/genética , Artrópodos/metabolismo , Factores de Transcripción con Motivo Hélice-Asa-Hélice Básico/metabolismo , Proteínas de Drosophila/metabolismo , Drosophila melanogaster/metabolismo , Metiltransferasas/metabolismo , MicroARNsRESUMEN
A catalytic hairpin assembly (CHA)-programmed porphyrin-DNA complex was designed to trigger the chemiluminescence as photoelectrochemical initiator for DNA sensing. First, the programmed double strand DNA (dsDNA) was formed using two hairpin DNAs as assembly components via target-assisted CHA reaction, and then immobilized on a capture DNA/CdS quantum dots modified electrode. The porphyrin (FeTMPyP) was conveniently assembled on a dsDNA scaffold via the groove interaction. The FeTMPyP@dsDNA complex possessed high catalytic activity toward luminol oxidation to generate the desirable chemiluminescence with high stability under various temperature and alkaline conditions. By integrating the signal amplification capacity of CHA and in situ FeTMPyP-mediated chemiluminescence as excitation light, an amplified photoelectrochemical sensing strategy is proposed for DNA detection. Under optimized conditions, the biosensor shows a wide linear range from 5 to 10000 fM with a detection limit of 2.2 fM. Moreover, the developed photoelectrochemical device exhibits excellent selectivity, high stability, and acceptable fabrication reproducibility. The CHA-programmed porphyrin-DNA strategy not only extends the applications of photoelectrochemistry, but also presents a novel methodology in bioanalysis.
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Técnicas Biosensibles/métodos , ADN/análisis , ADN/química , Secuencias Invertidas Repetidas , Luz , Metaloporfirinas/química , Secuencia de Bases , Compuestos de Cadmio/química , Catálisis , ADN/genética , Electroquímica , Concentración de Iones de Hidrógeno , Límite de Detección , Mediciones Luminiscentes , Modelos Moleculares , Conformación de Ácido Nucleico , Oxidación-Reducción , Puntos Cuánticos/química , Sulfuros/química , TemperaturaRESUMEN
A novel photoelectrochemical sensing strategy is designed for DNA detection on the basis of in situ generation of an electron acceptor via the catalytic reaction of hemin toward H2O2. The photoelectrochemical platform was established by sequential assembly of near-infrared CdTe quantum dots, capture DNA, and a hemin-labeled DNA probe to form a triple-helix molecular beacon (THMB) structure on an indium tin oxide electrode. According to the highly catalytic capacity of hemin toward H2O2, a photoelectrochemical mechanism was then proposed, in which the electron acceptor of O2 was in situ-generated on the electrode surface, leading to the enhancement of the photocurrent response. The utilization of CdTe QDs can extend the absorption edge to the near-infrared band, resulting in an increase in the light-to-electricity efficiency. After introducing target DNA, the THMB structure is disassembled and releases hemin and, thus, quenches the photocurrent. Under optimized conditions, this biosensor shows high sensitivity with a linear range from 1 to 1000 pM and detection limit of 0.8 pM. Moreover, it exhibits good performance of excellent selectivity, high stability, and acceptable fabrication reproducibility. This present strategy opens an alternative avenue for photoelectrochemical signal transduction and expands the applications of hemin-based materials in photoelectrochemical biosensing and clinical diagnosis.
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Técnicas Biosensibles , Técnicas Electroquímicas/métodos , Electrones , Hemina/química , Procesos Fotoquímicos , Secuencia de Bases , Catálisis , Cartilla de ADNRESUMEN
A library of novel chiral biphenol-based diphosphinite (BOP) ligands was designed and created. These BOP ligands were applied to a Pd-catalyzed intermolecular allylic etherification reaction, which provided a key intermediate for the formal total synthesis of (-)-galanthamine with 97% ee in 97% yield.
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Compuestos Alílicos/síntesis química , Galantamina/síntesis química , Paladio/química , Fosfinas/química , Compuestos Alílicos/química , Catálisis , Galantamina/química , Ligandos , Estructura Molecular , EstereoisomerismoRESUMEN
Inhibition of methionine adenosyltransferase 2A (MAT2A) has received significant interest because of its implication as a synthetic lethal target in methylthioadenosine phosphorylase (MTAP)-deleted cancers. Here, we report the discovery of a series of 3H-pyrido[1,2-c]pyrimidin-3-one derivatives as novel MAT2A inhibitors. The selected compound 30 exhibited high potency for MAT2A inhibition and a favorable pharmacokinetic profile. Furthermore, in an HCT-116 MTAP-deleted xenograft model, compound 30 showed better in vivo potency than current clinical compound AG-270.
RESUMEN
In this study. a novel near-infrared fluorescent-driven contrast agent (Ag-doped NaYF4:Yb3+/Er3+@NaYF4:Nd3+@NaGdF4) was synthesized using a coprecipitation-hydrothermal-solvothermal-solvothermal (CHSS) method. The results shows that hexagonal NaYF4:Yb3+/Er3+ with a diameter of 300 nm was successfully synthesized by the CHSS method. The new contrast agent was characterized using scanning electron microscopy, fluorescence spectrometry, transmission electron microscopy, energy-dispersive spectrometry and ultraviolet-visible light diffuse reflectance absorption spectroscopy. Even at low concentrations (0.2 M), this proposed contrast agent can be excited by near-infrared light with a wavelength of 980 nm and emits a dazzling green light with a wavelength of 540 nm, and the comparison of the luminescence intensity proves that doping with silver increases the luminescence intensity of the upconverted nanomaterial by nearly 13 times based on the calculated quantum yield. TEM images show the successful preparation of silver nanoparticles with a diameter of 30 nm, and the energy spectrum shows the successful doping of silver nanoparticles and the successful preparation of the core-shell structure of NaYF4:Yb3+/Er3+@NaYF4:Nd3+@NaGdF4. Furthermore, the mechanism of the increased luminous intensity has been studied using simulation calculations. Finally, cytotoxicity tests were used to test material which was modified by 1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-[amino(polyethylene glycol)-2000] (DSPE-PEG2K), and the biocompatibility was significantly improved, meeting the standard for biological applications.
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In this work, an electrochemical sensor was designed for trace monitoring of bisphenol A (BPA) by decorating a hybrid bilayer molecularly imprinted membrane (MIM) on a multi-walled carbon nanotube-modified glassy carbon electrode. When BPA in the MIM was eluted, a composite molecularly imprinted electrochemical sensor was constructed. Under optimal conditions, the developed sensor showed two linear relationships between ΔI p and BPA concentration in the range of 0.04 µM to 8 µM, as well as good selectivity and stability, and was also applied to detect BPA in water samples with desirable recoveries ranging from 92.0% to 107.0%.
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A novel photoelectrochemical immunosensor was constructed to monitor carcinoembryonic antigen (CEA) based on hybridization chain reaction (HCR)-mediated in situ generation of copper nanoparticles (Cu NPs) and subsequent Cu2+-dependent quenching reaction, in which titanium dioxide nanoparticles-sensitized double-shell zinc cadmium sulfide hollow nanospheres (TiO2/DS-ZnCdS)-modified ITO electrode and anti-CEA antibody-modified 96-well plate served as biological recognition and signal detection platforms, respectively. The synergistic effect of TiO2 NPs and DS-ZnCdS hollow nanospheres contributed to the improvement of photoelectric conversion efficiency, and HCR-mediated signal cascade benefited the enhancement of detection sensitivity. In the presence of CEA, biotin-labelled anti-CEA antibodies were immobilized onto anti-CEA antibody-modified 96-well plate, and triggered HCR process to form long double stranded DNA, which could adsorb a large number of Cu2+ ions and then in situ form Cu NPs on double stranded DNA template by a facile reduction reaction. After acid treatment, the dissolved Cu2+ ions could significantly reduce the photocurrent response due to the generation of CuxS. Under optimal conditions, the immunosensor exhibited a desirable liner range of 1 pg mL-1 - 50 ng mL-1 and a low detection limit of 0.1 pg mL-1, as well as excellent selectivity and stability. Meanwhile, the recoveries of human serum sample analysis ranged from 96.8% to 103.6%, and the relative standard deviation was less than 7.40%, showing a good feasibility in early clinical diagnosis.
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Técnicas Biosensibles , Nanopartículas del Metal , Nanosferas , Antígeno Carcinoembrionario , Técnicas Electroquímicas , Humanos , Inmunoensayo , Límite de Detección , TitanioRESUMEN
ABSTRACT: In the present study, a risk assessment of pesticides, phthalates, and heavy metals in strawberries (n = 335) in recent years was conducted by determining the estimated daily intake, target hazard quotient, and hazard index. The study used 128 pesticides, 18 phthalates, and three heavy metals in this determination. It detected 51 pesticide residues in the strawberry samples, and 97.91% samples had levels of at least 1 of the 51 pesticides above the limit of detection. In addition, 2.39% of samples had pesticides higher than the Chinese maximum residue limit. Multiple pesticide residues were detected in most samples. Bis-2-ethylhexyl phthalate, diisobutyl phthalate, and dibutyl phthalate were detected in the strawberry samples, with a high frequency of detection. Their detectable rates were 100, 100, and 89.9%, respectively. In most samples, lead, cadmium, and nickel were detected, with detectable rates 75.76, 92.93, and 92.93%, respectively. The estimated daily intake of analyzed pesticide, phthalate, and heavy metal residues appears to be relatively low compared with the acceptable daily intake. The average target hazard quotients and hazard indices were less than 1. That means that customers who are exposed to the average contaminant levels may not pose a significant health risk. Our results show that the strawberries may be polluted by many kinds of contaminants. Therefore, monitoring of pesticide, phthalate, and heavy metal residues in strawberries should be increasingly developed to fully protect the health of the consumer.