RESUMO
The facile assembly of three-dimensional (3D) plasmonic substrates has been demonstrated. The assembly is based on the homogeneous decoration of multi-walled carbon nanotube/gold nanoparticle (CNT/AuNP) hybrid nanocomposites on a commercial polyvinylidene difluoride (PVDF) membrane, which is achieved via simple filtration. The CNT/AuNP hybrids with a unique 1D/0D structure remarkably improve the coverage and uniformity of plasmonic nanostructures on the membrane. The effective inter-particle and inter-tube coupling creates a multitude of hot spots within the probe area, and can produce a strong SERS effect. Moreover, the flexible membrane-based scaffold can efficiently collect and concentrate trace targets from large-volume sample solutions at milliliter-scale. The membrane-based SERS sensor shows high sensitivity and good reproducibility. The SERS sensor is employed to detect various molecular contaminants in aqueous samples, demonstrating its excellent field-testing capabilities for applications ranging from food safety to environmental monitoring.
Assuntos
Materiais Revestidos Biocompatíveis/química , Ouro/química , Nanopartículas Metálicas/química , Nanotubos de Carbono/química , Polivinil/química , Análise Espectral Raman , Propriedades de SuperfícieRESUMO
To improve mechanical properties of keratin (KR) porous scaffolds, we prepared a PEGylated keratin through thiol-ene click reaction. Several porous scaffolds were prepared by blending PEGylated keratin with sodium alginate (SA). The surface morphology, mechanical properties, and porosity of scaffolds were detailed studied at different KR/SA proportions. The results showed the content of SA had an effect on pore formation and mechanical properties. When the mass ratio of KR to SA was 2:1, the stress of yield point of the keratin porous scaffold reached 1.24 MPa, and also showed good deformation recovery ability. The PEGylated keratin porous scaffold had a high porosity and great cytocompatibility. Its' porosity is up to 81.7% and the cell viability is about 117.78%. This allows it to absorb the simulated plasma quickly (9.20 ± 0.37 g/g). In addition, the structural stability and acid-base stability of the keratin porous scaffold were also improved after PEGylation. Overall, the PEGylated keratin porous scaffold will be promising in tissue materials due to its great physical, chemical, and biological properties.
Assuntos
Alginatos/química , Materiais Biocompatíveis/química , Queratinas/química , Alicerces Teciduais/química , Lã/química , Animais , Elasticidade , Humanos , Teste de Materiais , Polietilenoglicóis/química , Porosidade , Relação Estrutura-Atividade , Propriedades de Superfície , Engenharia TecidualRESUMO
The fabrication of SERS substrates, which can offer the advantages of strong Raman signal enhancement with good reproducibility and low cost, is still a challenge for practical applications. In this work, a simple three-dimensional (3D) paper-based SERS substrate, which contains plasmonic silver-nanoparticles (AgNPs), has been developed by the silver mirror reaction. This paper strip was characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM), X-ray diffraction (XRD), etc. Pretreatment of the paper as well as the reaction time, temperature, and reagent concentrations for the silver mirror reaction were varied for further studies. With the optimized experimental parameters, the AgNPs synthesized and distributed in-situ on the paper strip could give more favorable SERS performance. The limit of detection (LOD) as low as 10(-11)M for Rhodamine 6G (R6G) and 10(-9)M for p-aminothiophenol (p-ATP) plus wide linear range for the log-log plot of Raman intensity versus analyte concentration were achieved. The detection of R6G in rain water was also carried out successfully. The merits of this protocol include low cost, easy operation, high sensitivity and acceptable stability, which make it ideal for the detection of environmental samples in trace amounts.
Assuntos
Celulose/química , Nanopartículas Metálicas/química , Rodaminas/análise , Prata/química , Compostos de Anilina/análise , Nanopartículas Metálicas/ultraestrutura , Microscopia de Força Atômica , Microscopia Eletrônica de Varredura , Papel , Chuva/química , Espectroscopia de Infravermelho com Transformada de Fourier , Análise Espectral Raman , Compostos de Sulfidrila/análise , Difração de Raios XRESUMO
Paper spray (PS), as a new ambient ionization method, has been applied for direct qualitative and quantitative analysis. The high sensitivity and minimum internal energy (low spray voltage) with optimized paper spray conditions is a significant request for real application in POCT. In this study, a simple and efficient ambient ionization method is developed by spraying from a mesoporous graphene foams (MGFs)-modified paper surface. The good electrical conductivity of MGFs results in obvious spray voltage decrease. Meanwhile, the MGFs-paper substrate has a well improvement in separation and elution efficiency ascribing to ultrahigh specific surface area and π-π electrostatic stacking property of graphene. In combination a commercial triple quadrupole mass spectrometer, the paper spray is successfully used for analysis of amphetamine in saliva. The linear dynamic ranges expand 10 fold in comparison with unmodified chromatography papers and the low limit of quantitation (LOQ) is as low as 1 pg/mL. A small sample volume (0.5 µL) could be analyzed immediately after spotting, without any pretreatment. The performance of this method was demonstrated for application in fast point-of-care mass spectrometry.
Assuntos
Cromatografia em Papel/instrumentação , Cromatografia em Papel/métodos , Monitoramento de Medicamentos/métodos , Grafite/química , Anfetamina/análise , Desenho de Equipamento , Humanos , Modelos Lineares , Saliva/química , Sensibilidade e Especificidade , Espectrometria de Massas por Ionização por Electrospray/métodosRESUMO
A microchip reactor coated with a gold nanoparticle network entrapping trypsin was designed for the efficient on-line proteolysis of low level proteins and complex extracts originating from mouse macrophages. The nanostructured surface coating was assembled via a layer-by-layer electrostatic binding of poly(diallyldimethylammonium chloride) and gold nanoparticles. The assembly process was monitored by UV-visible spectroscopy, atomic force microscopy, and quartz crystal microbalance. The controlled adsorption of trypsin was theoretically studied on the basis of the Langmuir isotherm model, and the fitted Gamma(max) and K values were estimated to be 1.2 x 10(-7) mol/m(2) and 4.1 x 10(5) M(-1), respectively. An enzymatic kinetics assay confirmed that trypsin, which was entrapped in the biocompatible gold nanoparticle network with a high loading capacity, preserved its bioactivity. The maximum proteolytic rate of the adsorbed trypsin was 400 mM/(min.microg). Trace amounts of proteins down to femtomole per analysis were digested using the microchip reactor, and the resulting tryptic products were identified by MALDI-TOF MS/MS. The protein mixtures extracted from the mouse macrophages were efficiently identified by on-line digestion and LC-ESI-MS/MS analysis.