RESUMEN
BACKGROUND: Fiber added to the diet can promote intestinal mucin secretion, relieve intestinal inflammation, and enhance the intestinal barrier function. Glycosylation is the key to mucin function. However, there are few studies on the correlation between dietary fiber and mucin glycosylation, especially two kinds of dietary fiber with different solubility. The aim of this study was to investigate the effects of soluble glucomannan (GM) and insoluble cellulose (CL) treatment on mucin secretion and mucin glycosylation-related gene expression in the colons of mice. RESULTS: The GM group significantly increased the goblet cell number, crypt depth, and the expression of mucin 2 (Muc2) and mucin 3a (Muc3a) genes in the colon. At the same time, the analysis of the colon transcriptome showed that the GM group changed the expression of genes related to the mucin glycosylation process, and the GM group up-regulated the expression of Gcnt3, Gcnt4, St3gal1, Galnt13, and B3gnt6 genes involved in the O-glycosylation process. Similarly, Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis showed that differentially glycosylated genes in the GM group were mainly related to the biosynthesis of mucin type O-glycans, while the genes in the CL group were related to the biosynthesis of various types of N-glycans. The correlation analysis between colonic microbes and differentially glycosylated genes also showed that the abundance of Alistipes in the GM group was significantly associated with the expression of Gcnt3, a key glycosylation gene. CONCLUSION: Glucomannan treatment was more favorable for colonic Muc2 and Muc3a secretion and mucin O-glycosylation gene expression. © 2023 Society of Chemical Industry.
Asunto(s)
Celulosa , Mucinas , Ratones , Animales , Mucinas/genética , Glicosilación , Celulosa/metabolismo , Colon/metabolismo , Polisacáridos/metabolismo , Fibras de la Dieta/metabolismo , Expresión Génica , Mucosa Intestinal/metabolismoRESUMEN
BACKGROUND: Pathogenic microorganism pollution has been a challenging public safety issue, attracting considerable scientific interest. A more problematic aspect of this phenomenon is that planktonic bacteria exacerbate biofilm formation. There is an overwhelming demand for developing ultra-efficient, anti-drug resistance, and biocompatibility alternatives to eliminate stubborn pathogenic strains and biofilms. RESULTS: The present work aims to construct a visible light-induced anti-pathogen agents to ablate biofilms using the complementary merits of ROS and cationic polymers. The photosensitizer chlorin e6-loaded polyethyleneimine-based micelle (Ce6-TPP-PEI) was constructed by an amphiphilic dendritic polymer (TPP-PEI) and physically loaded with photosensitizer chlorin e6. Cationic polymers can promote the interaction between photosensitizer and Gram-negative bacteria, resulting in enhanced targeting of PS and lethality of photodynamic therapy, and remain active for a longer duration to prevent bacterial re-growth when the light is turned off. As expected, an eminent antibacterial effect was observed on the Gram-negative Escherichia coli, which is usually insensitive to photosensitizers. Surprisingly, the cationic polymer and photodynamic combination also exert significant inhibitory and ablative effects on fungi and biofilms. Subsequently, cell hemolysis assessments suggested its good biocompatibility. CONCLUSIONS: Given the above results, the platform developed in this work is an efficient and safe tool for public healthcare and environmental remediation.
Asunto(s)
Fotoquimioterapia , Fármacos Fotosensibilizantes , Fármacos Fotosensibilizantes/farmacología , Polímeros/farmacología , Fotoquimioterapia/métodos , Biopelículas , Luz , Cationes/farmacologíaRESUMEN
Ultratrace quantitative detection based on fluorescence is highly desirable for many important applications such as environmental monitoring or disease diagnosis, which however has remained a great challenge because of limited and irregular fluorescence responses to analytes at ultralow concentrations. Herein the problem is circumvented via local enrichment and detection of analytes within a microsensor, that is, photonic porous microspheres grafted with aggregation-induced emission gens (AIEgens). The obtained microspheres exhibit dual structural and molecular functions, namely, bright structural colors and strong fluorescence. Large fluorescence quenching induced by nitrophenol compounds in an aqueous environment is observed at ultralow concentrations (10-12-10-8 mol/L), enabling quantitative detection at a ppb level (ng/L). This is achieved within a porous structure with good connectivity between the nanopores to improve analyte diffusion, an internal layer of poly(ethylene oxide) (PEO) for analyte enrichment via hydrogen bonding, and homogeneous distribution of AIEgens within the PEO layer for enhanced fluorescence quenching. The fluorescent porous microspheres can be readily obtained in a single step templated by well-ordered water-in-oil-in-water double emulsion droplets with AIE amphiphilic bottlebrush block copolymers as the effective stabilizer.
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Polietilenglicoles , Polímeros , Emulsiones , Fluorescencia , MicroesferasRESUMEN
Copper nanoclusters (CuNCs) exhibit susceptibility to oxidation in the subnanometer size range. In this work, a facile and green protocol is reported for the successful synthesis of water soluble CuNCs, with poly(vinylpyrrolidone) as a template and ascorbic acid as a mild reducing agent. The as-prepared CuNCs exhibit a green fluorescence and high quantum yield (QY = 44.67%) in water, which is the highest among the reported water soluble CuNCs. The origin of their highly luminescent nature was also investigated. In addition, the obtained CuNCs show good tolerability to high ionic strength, superior antioxidation properties, good photostability, time-stability, a large Stokes shift and ultralow cytotoxicity, laying the foundation for living cell imaging in THP-1 macrophages. A bright green fluorescence can be observed from the cells, indicating the potential practicality of CuNCs as a fluorescence marker in bioapplications. Interestingly, the as-prepared CuNCs exhibit a good selective fluorescence quenching response towards trinitrophenol over other nitro compounds. Furthermore, CuNCs were employed for sensing trinitrophenol based on the inner filter effect. A good linear relationship was obtained in the low concentration range of trinitrophenol, with a limit of detection of 3.91 × 10-7 M in aqueous medium. This result suggests the potential application of CuNCs as a probe in sensing and monitoring toxic trinitrophenol in the field of environmental security.
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Cobre/química , Nanopartículas del Metal/química , Picratos/análisis , Povidona/química , Ácido Ascórbico/química , Línea Celular , Supervivencia Celular/efectos de los fármacos , Humanos , Macrófagos/citología , Macrófagos/patología , Nanopartículas del Metal/toxicidad , Microscopía Fluorescente , Picratos/química , Espectrometría de FluorescenciaRESUMEN
The Maillard reaction is a well known chemical reaction in the food industry, in which melanoidins are generally considered as the final product. However, the exact final products of the Maillard reaction are far from being well understood. The conversion mechanism of melanoidins is of importance for explanation of the whole process of the Maillard reaction. In this paper, the conversion of melanoidins in the Maillard reaction was studied using glucose and lysine as raw materials. Our results showed that fluorescent nanoparticles (FNPs) can be formed after the hydrothermal reaction of melanoidins at 180 °C for 2, 4, 6 and 8 hours, respectively. Unlike melanoidins, the FNPs are highly water-soluble and strongly fluorescent and have a particle size of around 0.7-6.8 nm. X-ray photoelectron spectroscopy and 1H NMR spectroscopy analysis demonstrated that there are many functional structures like carboxyl, hydroxyl, aldehyde, amine and aromatic groups produced on the surface of the FNPs. Total elemental analysis indicated that the oxidization of the FNPs was intensified with the extension of reaction time. The thermogravimetric kinetics of the FNPs were significantly different from those of melanoidins. More heterocyclic and aromatic compounds were found in the pyrolysis products of the FNPs with the extension of reaction time. The results of this paper provided new insights into the conversion of melanoidins for further understanding of the Maillard reaction.
Asunto(s)
Colorantes Fluorescentes/química , Reacción de Maillard , Nanopartículas/química , Polímeros/química , Glucosa/química , Compuestos Heterocíclicos , Cinética , Lisina , Espectroscopía de Resonancia Magnética , Tamaño de la PartículaRESUMEN
A biocompatible and novelly-defined adsorption membrane for rapid removal of fluoride was prepared. Both adsorption and membrane techniques were used in this research. Al(OH)3 nanoparticles modified hydroxyapatite (Al-HAP) nanowires were developed and made into Al-HAP membrane. The adsorption data of Al-HAP adsorbent could be well described by Freundlich isotherm model while the adsorption kinetic followed pseudo-second-order model. The maximum of adsorption capacity was 93.84mg/g when the fluoride concentration was 200mg/L. The adsorption mechanism was anion exchanges and electrostatic interactions. The contribution rates of HAP nanowires and Al(OH)3 nanoparticles in fluoride removal were 36.70% and 63.30%, respectively. The fixed-bed column test demonstrate that the Al-HAP was biocompatible and in a good stability during the process of water treatment. The fluoride removal abilities of Al-HAP membrane with 0.3mm thickness could reach 1568L/m2 when fluoride concentrations were 5mg/L. This study indicated that the Al-HAP membrane could be developed into a very viable technology for highly effective removal of fluoride from drinking water.
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Hidróxido de Aluminio/química , Agua Potable/análisis , Durapatita/química , Fluoruros/aislamiento & purificación , Membranas Artificiales , Contaminantes Químicos del Agua/aislamiento & purificación , Purificación del Agua/métodos , Adsorción , Nanopartículas/química , Nanopartículas/ultraestructura , Nanocables/química , Nanocables/ultraestructuraRESUMEN
A biocompatible and uniquely defined hydroxyapatite (HAP) adsorption membrane with a sandwich structure was developed for the removal of organic micropollutants for the first time. Both the adsorption and membrane technique were used for the removal of organic micropollutants. The hydrophilicity and hydrophobicity of the HAP adsorbent and membrane were tunable by controlling the surface structure of HAP. The adsorption of organic micropollutants on the HAP adsorbent was studied in batch experiments. The adsorption process was fit with the Freundlich model, while the adsorption kinetics followed the pseudo-second-order model. The HAP membrane could remove organic micropollutants effectively by dynamic adsorption in both aqueous and ethanol solutions. The removal efficiencies of organic micropollutants depended on the solution composition, membrane thickness and hydrophilicity, flow rate, and the initial concentration of organic micropollutants. The adsorption capacities of the HAP membrane with a sandwich structure (membrane thickness was 0.3 mm) were 6700, 6510, 6310, 5960, 5490, 5230, 4980 and 4360 L m-2 for 1-naphthyl amine, 2-naphthol, bisphenol S, propranolol hydrochloride, metolachlor, ethinyl oestradiol, 2,4-dichlorophenol and bisphenol A, respectively, when the initial concentration was 3.0 mg L-1. The biocompatible HAP adsorption membrane can be easily regenerated by methanol and was thus demonstrated to be a novel concept for the removal of organic micropollutants from both aqueous and organic solutions.