RESUMO
In this study, microcapsules with a magnetic particle as the core and polyelectrolyte multilayers as the shell were fabricated. The cavity of the microcapsules was created by etching the SiO2 layer, which was first coated on the magnetic core particle, and the size of the cavity can be adjusted by the thickness of the SiO2 layer. This magnetically responsive microcapsule deforms upon application of a constant magnetic field and results in the release of the core content, and the release velocity could be controlled by the strength of the magnetic field. This release mechanism is proactive and repeatable, combined with its localized and remote controllability; it can be a powerful tool for delivering medical agents on site.
Assuntos
Compostos Férricos/química , Polímeros/química , Dióxido de Silício/química , Cápsulas/química , Eletrólitos/química , Compostos Férricos/síntese química , Campos Magnéticos , Tamanho da Partícula , Propriedades de SuperfícieRESUMO
Hollow silica microspheres with holes of tunable numbers and sizes on the shell wall were prepared in this study. Clusters with positively charged polystyrene (PS) microspheres as the central spheres (CSs) and negatively charged PS spheres as the "halo" spheres (HSs) were formed via electrostatic interactions and utilized as a template. In the subsequent silica coating process, only CS was selectively coated; hence, after calcination, porous hollow silica microspheres were obtained.
Assuntos
Microesferas , Dióxido de Silício/síntese química , Tamanho da Partícula , Poliestirenos/química , Porosidade , Dióxido de Silício/química , Eletricidade Estática , Propriedades de SuperfícieRESUMO
Accurate determination of nanoplastics (NPs) in aquatic ecosystems constitutes a challenge for which highly sensitive analytical methods are necessitated. Herein, a sample pretreatment based on self-made amino-functionalized activated carbon fibers (ACFs-NH2) dispersive solid-phase extraction (DSPE) allows for high-recovery, followed by high-sensitivity detection of NPs by pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS). The developed methodology allowed low detection limits (20-100 µg/L) to be achieved quickly in a few steps. Under optimal conditions, ACFs-NH2 (12.5 mg) was able to recover ≥98.45 % of polystyrene (PS) nanoplastics at high concentration (100 mg/L) in 10 mL seawater. Based on the high adsorption performance of materials, the adsorption dynamics and isotherms were determined to infer the interaction mechanism of PSNPs on ACFs-NH2. After adsorption, the target on the surface of the adsorbent can be directly pyrolyzed, which can simplify the operation steps and avoid the elution of organic solvents, making the process more environmentally friendly. This strategy is feasible for the analysis of trace NPs in water systems.
Assuntos
Cromatografia Gasosa-Espectrometria de Massas , Limite de Detecção , Água do Mar , Extração em Fase Sólida , Poluentes Químicos da Água , Extração em Fase Sólida/métodos , Cromatografia Gasosa-Espectrometria de Massas/métodos , Poluentes Químicos da Água/análise , Poluentes Químicos da Água/isolamento & purificação , Poluentes Químicos da Água/química , Adsorção , Água do Mar/química , Poliestirenos/química , Carvão Vegetal/químicaRESUMO
Chitosan (CS), the only alkaline polysaccharose available in nature, has always been a promising candidate for drug delivery owing to its excellent biodegradability and biocompatibility. However, inherent solubility and polycationic properties of CS largely hinder electrospinning, which is an efficient method of fabricating nanofibers for drug carriers. To solve this problem and extend the applications of CS, polyamide/chitosan/tetraethyl orthosilicate (PA/CS/TEOS) composite nanofibers were successfully prepared as drug carriers in this study via electrospinning. The PA/CS/TEOS ratios significantly influenced the nanofiber morphology. As the content of each was increased, the beads among the membranes increased initially and then decreased, determined by scanning electron microscopy (SEM). The morphology of the optimum membranes with the ratio of 1:0.13:0.67 was smoother with less beads and uniform fiber diameter. Finally, the membranes with optimum ratios were used as carriers of ofloxacin in the study of drug release performance to identify their future feasibility, which revealed an initial fast release followed by a relatively stable release.
Assuntos
Quitosana , Nanofibras , Portadores de Fármacos , Nylons , SilanosRESUMO
Phytohormones are interrelated by synergistic or antagonistic crosstalk and play important roles in the regulation of plant growth and development. In order to understand the interaction between phytohormones in the plant physiological network, it is necessary to determine trace levels of multiple phytohormones simultaneously in a complex matrix. Here, we synthesized ionic liquids containing different functional groups and modified the surface of carbon fibers with them. Based on these carbon fibers-ionic liquid (CFs-IL) materials, a solid phase microextraction method was developed to enable the simultaneous extraction of phytohormones. The adsorption specificity of multiple phytohormones was studied by identifying the hydrophobic, electrostatic, and π-π interactions, as well as hydrogen bonds, which favor simultaneous extraction of the relevant acidic, alkaline and neutral phytohormones by improving compatibility. The proposed method, coupled with liquid chromatography-tandem mass spectrometry, was applied to the simultaneous determination of 13 acidic, alkaline and neutral phytohormones in tomato. The limits of quantification were found to be in the range of 0.32-54.05 ng mL-1 and 4.6-185.8 pg mL-1, respectively, when measured by QQQ and Q-TOF. All of the relative recoveries were in the range of 94.40-113.37% with RSDs ≤15.36% (n = 3) for spiked tomato samples. This method is expected to be widely applied to multiple phytohormones analysis for in-depth researches concerning the physiological networks of plants.
Assuntos
Líquidos Iônicos , Microextração em Fase Líquida , Solanum lycopersicum , Fibra de Carbono , Cromatografia Líquida de Alta Pressão , Cromatografia Líquida , Limite de Detecção , Reguladores de Crescimento de Plantas/análise , Microextração em Fase SólidaRESUMO
New coated carbon fibers (CCFs) have been synthesized, characterized and used as solid phase microextraction (SPME) matrix for the analysis of phytohormones (jasmonic acid, indole-3-acetic acid, and abscisic acid) in wheat samples. The SPME device, realized inserting CCFs in a pencil-type device, when coupled with gas chromatography-mass spectrometry, provides in few steps high recovery values (79-112%), fast on-fiber derivatization (30â¯s), good method reproducibility (RSDâ¯<â¯20%), low detection limits (0.5-2.1â¯ngâ¯g-1). The pencil-type CCFs-SPME device was successfully employed for the determination of phytohormone in wheat samples, allowing simple and quick extraction/derivatization/injection processes. The proposed device can be then considered as a promising and functional tool for fast and reliable extraction and preconcentration of analytes from real samples, allowing a simple derivatization procedure and direct injection in the chromatographic instrumentation.
Assuntos
Fibra de Carbono/química , Cromatografia Gasosa-Espectrometria de Massas/métodos , Reguladores de Crescimento de Plantas/análise , Microextração em Fase Sólida/instrumentação , Triticum/química , Análise de Alimentos/instrumentação , Análise de Alimentos/métodos , Limite de Detecção , Reprodutibilidade dos Testes , Microextração em Fase Sólida/métodos , Compostos de Trimetilsilil/químicaRESUMO
This communication demonstrates a facile method for naked-eye detection of urea based on the structure color change of pH-sensitive photonic crystals. The insertion of urease provides excellent selectivity over other molecules. The detection of urea in different concentration ranges could be realized by changing the molar ratio between the functional monomer and cross-linker.
Assuntos
Colorimetria , Ureia/análise , Concentração de Íons de Hidrogênio , Impressão Molecular , Fótons , Polímeros/química , Urease/química , Urease/metabolismoRESUMO
UNLABELLED: The potential of rice bran as a bioabsorbent for tea catechins was examined. Defatted rice bran had the highest adsorption capacity for tea catechins and the best selectivity for (-)-epigallocatechin gallate over total catechins among water-washed rice bran and untreated rice bran. The adsorption characteristics of tea catechins onto defatted rice bran were determined over a range of concentration (0.5 to 2.5 g/L) and temperatures (10, 25, and 45 °C). The adsorption of tea catechins onto defatted rice bran showed excellent fitness with the pseudo-second-order model at different temperature. Both the Langmuir and Freundlich models adequately describe the isothermal adsorption of tea catechins onto defatted rice bran. The adsorption of total catechins on rice bran decreased from 10 to 25 °C, whereas was greatly enhanced at 45 °C. The adsorption system of bioadsorbent with multiconstituents may not be as simple as the single-force-driving adsorption system. Protein and cellulose are the main contributors to the adsorption of tea catechins on defatted rice bran. PRACTICAL APPLICATION: Rice bran is regarded as a good fibre source that can be added to various food products and health supplements, which is a potential biocarrier for bioactives. Our study showed that defatted rice bran had a high affinity for tea catechins but caffeine, and provided a promising way for selective enrichment of catechins on defatted rice bran under practical condition. Protein and cellulose are the main contributors to the adsorption of tea catechins on defatted rice bran.