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1.
Bacterial-derived lipopolysaccharides (LPS) can cause defective intestinal barrier function and play an important role in the development of inflammatory bowel disease. In this study, a nanocarrier based on chitosan and fucoidan was developed for oral delivery of berberine (Ber). A sulfonated fucoidan, fucoidan-taurine (FD-Tau) conjugate, was synthesized and characterized by Fourier transform infrared (FTIR) spectroscopy. The FD-Tau conjugate was self-assembled with berberine and chitosan (CS) to form Ber-loaded CS/FD-Tau complex nanoparticles with high drug loading efficiency. Berberine release from the nanoparticles had fast release in simulated intestinal fluid (SIF, pH 7.4), while the release was slow in simulated gastric fluid (SGF, pH 2.0). The effect of the berberine-loaded nanoparticles in protecting intestinal tight-junction barrier function against nitric oxide and inflammatory cytokines released from LPS-stimulated macrophage was evaluated by determining the transepithelial electrical resistance (TEER) and paracellular permeability of a model macromolecule fluorescein isothiocyanate-dextran (FITC-dextran) in a Caco-2 cells/RAW264.7 cells co-culture system. Inhibition of redistribution of tight junction ZO-1 protein by the nanoparticles was visualized using confocal laser scanning microscopy (CLSM). The results suggest that the nanoparticles may be useful for local delivery of berberine to ameliorate LPS-induced intestinal epithelia tight junction disruption, and that the released berberine can restore barrier function in inflammatory and injured intestinal epithelial. 相似文献
2.
Carlos Montez Wells Emily Carol Coleman Rabeta Yeasmin Zoe Lynn Harrison Mallesh Kurakula Daniel L. Baker Joel David Bumgardner Tomoko Fujiwara Jessica Amber Jennings 《Marine drugs》2021,19(10)
Chitosan nanofiber membranes are recognized as functional antimicrobial materials, as they can effectively provide a barrier that guides tissue growth and supports healing. Methods to stabilize nanofibers in aqueous solutions include acylation with fatty acids. Modification with fatty acids that also have antimicrobial and biofilm-resistant properties may be particularly beneficial in tissue regeneration applications. This study investigated the ability to customize the fatty acid attachment by acyl chlorides to include antimicrobial 2-decenoic acid. Synthesis of 2-decenoyl chloride was followed by acylation of electrospun chitosan membranes in pyridine. Physicochemical properties were characterized through scanning electron microscopy, FTIR, contact angle, and thermogravimetric analysis. The ability of membranes to resist biofilm formation by S. aureus and P. aeruginosa was evaluated by direct inoculation. Cytocompatibility was evaluated by adding membranes to cultures of NIH3T3 fibroblast cells. Acylation with chlorides stabilized nanofibers in aqueous media without significant swelling of fibers and increased hydrophobicity of the membranes. Acyl-modified membranes reduced both S. aureus and P. aeruginosa bacterial biofilm formation on membrane while also supporting fibroblast growth. Acylated chitosan membranes may be useful as wound dressings, guided regeneration scaffolds, local drug delivery, or filtration. 相似文献
3.
Maria Cristina Straccia Giovanna Gomez d’Ayala Ida Romano Adriana Oliva Paola Laurienzo 《Marine drugs》2015,13(5):2890-2908
In this work, a coating of chitosan onto alginate hydrogels was realized using the water-soluble hydrochloride form of chitosan (CH-Cl), with the dual purpose of imparting antibacterial activity and delaying the release of hydrophilic molecules from the alginate matrix. Alginate hydrogels with different calcium contents were prepared by the internal setting method and coated by immersion in a CH-Cl solution. Structural analysis by cryo-scanning electron microscopy was carried out to highlight morphological alterations due to the coating layer. Tests in vitro with human mesenchymal stromal cells (MSC) were assessed to check the absence of toxicity of CH-Cl. Swelling, stability in physiological solution and release characteristics using rhodamine B as the hydrophilic model drug were compared to those of relative uncoated hydrogels. Finally, antibacterial activity against Escherichia coli was tested. Results show that alginate hydrogels coated with chitosan hydrochloride described here can be proposed as a novel medicated dressing by associating intrinsic antimicrobial activity with improved sustained release characteristics. 相似文献
4.
A facile and inexpensive way to prepare self-crosslinkable poly(dimethylsiloxane) (PDMS) for superhydrophobic treatment of cotton fabrics is reported in the study. Through thiol-ene click reaction between mercaptopropyltrimethoxysilane (MPTMOS) and vinyl-containing poly(dimethylsiloxane) (VPDMS), PDMS-g-TMOS can be simply and quickly synthesized. The trimethoxysilane group of PDMS-g-TMOS can react with hydroxyl group on cotton fabric and other -Si(OCH3)3 groups. The synthesized polysiloxane (PDMS-g-TMOS) was identified by FT-IR and 1H-NMR. The morphology of the treated cotton fabric was observed by SEM and XPS was used to analyze the elemental composition on the surface of cotton fabric. The analysis results indicated that the surface was fully covered with PDMS. Due to the low surface energy of PDMS and the rough surfaces of cotton fabric, the optimized water contact angle (WCA) and sliding angle were respectively 154°±0.4° and 14°±0.5°, indicating superhydrophobicity. Moreover, water spray test (AATCC Test Method 22-2010) was also applied to evaluate the water repellency of treated cotton fabric and a score of 90 was assigned according to AATCC Test Method 22-2010. The durability of treated cotton fabric was tested by 50 laundering cycles. The resultant WCA barely decreased and the score of water spray test dropped from 90 to 80, showing the reasonable wash durability. 相似文献
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Electrospun composite fibers of poly-lactic acid (PLA), chitosan (Ch) and paclitaxel (PTX) were fabricated for surface covering of a polymeric prototype PLA stent by means of single nozzle electrospinning approach to prepare a low cytotoxicity drug-eluting stent. Different concentrations of the drug (40 %, 60 %, 80 %, 100 % and 120 %) and chitosan (3 %, 5 %, 7 % and 9 %) were incorporated to reach the optimum composite fibers. The electrospun composite fibers were subjected to detailed analyses including scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), tensile test, MTT assay, cell culture and in vitro drug release. Results have confirmed a proper physical encapsulation of PTX in the polymeric matrix in which no chemical bonding was detected between the polymers and the drug. Among the fabricated composite fibers, specimens including 40 % and 60 % drug also exhibited an excellent cytotoxicity and controlled drug release. SEM images have proved the effect of paclitaxel in resisting cell adhesion and propagation on the fibers. Findings from this study suggest a novel polymer/drug coating that could be potentially applicable in surface covering of polymeric stents e.g. PLA stents. 相似文献
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水稻品种抗褐稻虱的改进筛选法及其应用 总被引:3,自引:1,他引:3
介绍了鉴定水稻抗褐稻虱的改良苗期集团筛选法(MSST),该方法可有效地鉴别中抗品种,同时可在室内进行,用虫量邵,方法简便。采用MSST方法对国际水稻研究所收集保存的部分水稻种质进行了筛选鉴定。 相似文献
8.
Uniform chitosan fibers (CS/PEO) with diameter of 398±76 nm were prepared by electrospinning with merely 5 wt.% of poly(ethylene oxide) (PEO) loading, and then annealed at elevated temperature without the use of additional crosslinker to improve the thermostability and solvent resistance. Swelling test shows that the CS/PEO composite fibers annealed at 200 oC were stable in 50 wt.% acetic acid aqueous solution. The mechanical strength test shows that the annealing temperature can affect the tensile strength of CS/PEO composite fiber mat. The cross-linked CS/PEO composite fibers provide a useful platform for the immobilization of palladium catalyst to catalyze the Mizoroki-Heck reactions of aromatic halides with olefins. Moreover, these CS/PEO composite fibers could be post modified with special ligands to chelate palladium species efficiently to further improve the catalytic activity and stability. 相似文献
9.
Chi Wang Pei-Xu Chen Qiong Xiao Qiu-Ming Yang Hui-Fen Weng Yong-Hui Zhang An-Feng Xiao 《Marine drugs》2021,19(3)
In this work, a non-toxic chitosan-based carrier was constructed via genipin activation and applied for the immobilization of tannase. The immobilization carriers and immobilized tannase were characterized using Fourier transform infrared spectroscopy and thermogravimetric analysis. Activation conditions (genipin concentration, activation temperature, activation pH and activation time) and immobilizations conditions (enzyme amount, immobilization time, immobilization temperature, immobilization pH, and shaking speed) were optimized. The activity and activity recovery rate of the immobilized tannase prepared using optimal activation and immobilization conditions reached 29.2 U/g and 53.6%, respectively. The immobilized tannase exhibited better environmental adaptability and stability. The immobilized tannase retained 20.1% of the initial activity after 12 cycles and retained 81.12% of residual activity after 30 days storage. The catechins composition analysis of tea extract indicated that the concentration of non-ester-type catechins, EGC and EC, were increased by 1758% and 807% after enzymatic treatment. Biological activity studies of tea extract revealed that tea extract treated with the immobilized tannase possessed higher antioxidant activity, higher inhibitory effect on α-amylase, and lower inhibitory effect on α-glucosidase. Our results demonstrate that chitosan activated with genipin could be an effective non-toxic carrier for tannase immobilization and enhancing biological activities of tea extract. 相似文献
10.
Background: The present study aimed to fabricate surface-modified chitosan nanoparticles with two mucoadhesive polymers (sodium alginate and polyethylene glycol) to optimize their protein encapsulation efficiency, improve their mucoadhesion properties, and increase their stability in biological fluids. Method: Ionotropic gelation was employed to formulate chitosan nanoparticles and surface modification was performed at five different concentrations (0.05, 0.1, 0.2, 0.3, 0.4% w/v) of sodium alginate (ALG) and polyethylene glycol (PEG), with ovalbumin (OVA) used as a model protein antigen. The functional characteristics were examined by dynamic light scattering (DLS), X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), and scanning electron microscopy (SEM)/scanning transmission electron microscopy (STEM). Stability was examined in the presence of simulated gastric and intestinal fluids, while mucoadhesive properties were evaluated by in vitro mucin binding and ex vivo adhesion on pig oral mucosa tissue. The impact of the formulation and dissolution process on the OVA structure was investigated by sodium dodecyl-polyacrylamide gel electrophoresis (SDS-PAGE) and circular dichroism (CD). Results: The nanoparticles showed a uniform spherical morphology with a maximum protein encapsulation efficiency of 81%, size after OVA loading of between 200 and 400 nm and zeta potential from 10 to 29 mV. An in vitro drug release study suggested successful nanoparticle surface modification by ALG and PEG, showing gastric fluid stability (4 h) and a 96 h sustained OVA release in intestinal fluid, with the nanoparticles maintaining their conformational stability (SDS-PAGE and CD analyses) after release in the intestinal fluid. An in vitro mucin binding study indicated a significant increase in mucin binding from 41 to 63% in ALG-modified nanoparticles and a 27–49% increase in PEG-modified nanoparticles. The ex vivo mucoadhesion showed that the powdered particles adhered to the pig oral mucosa. Conclusion: The ALG and PEG surface modification of chitosan nanoparticles improved the particle stability in both simulated gastric and intestinal fluids and improved the mucoadhesive properties, therefore constituting a potential nanocarrier platform for mucosal protein vaccine delivery. 相似文献
11.
《Plant Production Science》2013,16(2):152-165
AbstractThe quality of rice grain has been deteriorating as a result of the high temperature during the ripening stage caused by global warming. Easy and effective methods of high-temperature treatment are essential for the analysis of high-temperature tolerance and to screen for tolerant strains. We have improved the open-top chamber (OTC) by adding a solar-heated air introduction tunnel (SAT). The air is warmed by solar radiation as it passes through the tunnel and then flows into the OTC. The increase in temperature in the OTC-SAT was powered by solar radiation. Thereby, the temperature in OTC-SAT rose during the day according to the distance from the air intake (the nearer, the higher). A more uniform increase in temperature of approximately 1.2°C in the daytime was achieved by attaching a sloping wall and funnel-shaped air exhaust tunnel to the OTC-SAT to improve the air flow. The area of the high-temperature treatment was easily increased by increasing the width of the OTC-SAT; this finding might be useful for screening a large number of strains. The increase in the percentage of chalky grains by the use of OTC-SAT was similar to that obtained with the other treatment methods; the OTC-SAT will thus be useful for investigating high-temperature tolerance during the ripening stage, particularly in areas where the wind direction is stable. The use of an OTC with a funnel-shaped tunnel on both the air entrance and the air exit sides might be useful in areas where the wind direction is often reversed. 相似文献
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Summary Potato seed tubers infected withHelminthosporium solani andColletotrichum coccodes were treated with prochloraz (as Omega 450 g a.i. l−1 EC) and/or prochloraz managanese chloride (as Octave 25 g/kg DP), and planted in two separate fields not previously cultivated
with potatoes. Dipping seed 28 d prior to planting in 2,4 or 6 g a.i. l−1 Omega, and dusting with 500 or 750 g Octave per 100 kg seed significantly reduced the incidence of silver scurf and black
dot on progeny tubers. In one field, the higher concentrations of Omega and Octave gave slightly better control than the lower
Omega concentrations. At the second site, postharvest application of 4 g a.i. l−1 Omega or 750 g Octave per 100 kg seed limited development of both diseases on progeny tubers, with slightly better control
when an additional Octave dusting was applied 14 d before planting. None of the prochloraz treatments adversely affected plant
stand or tuber yield. 相似文献
13.
Neurodegenerative diseases are among the most widespread diseases affecting humans, and the number of patients is only rising. Seaweed polysaccharide extracts show significant neuroprotective and reparative activities. Seaweed polysaccharides might provide the next big breakthrough in neurodegenerative disease treatment. This paper reviews the applications of seaweed polysaccharides as potential treatments of neurodegenerative diseases. The particular focus is on fucoidan, ulvan, and their derivatives as potential agents to treat Alzheimer’s disease. This review provides a critical update on the progress in this important research area. 相似文献
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Massimo Genovese Concetta Imperatore Marcello Casertano Anna Aiello Francesco Balestri Lucia Piazza Marialuisa Menna Antonella Del Corso Paolo Paoli 《Marine drugs》2021,19(10)
An in-depth study on the inhibitory mechanism on protein tyrosine phosphatase 1B (PTP1B) and aldose reductase (AR) enzymes, including analysis of the insulin signalling pathway, of phosphoeleganin, a marine-derived phosphorylated polyketide, was achieved. Phosphoeleganin was demonstrated to inhibit both enzymes, acting respectively as a pure non-competitive inhibitor of PTP1B and a mixed-type inhibitor of AR. In addition, in silico docking analyses to evaluate the interaction mode of phosphoeleganin with both enzymes were performed. Interestingly, this study showed that phosphoeleganin is the first example of a dual inhibitor polyketide extracted from a marine invertebrate, and it could be used as a versatile scaffold structure for the synthesis of new designed multiple ligands. 相似文献