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1.
Molecules ; 26(23)2021 Nov 29.
Artículo en Inglés | MEDLINE | ID: mdl-34885820

RESUMEN

Sophora flavescens is a regularly used traditional Chinese medicine. In an attempt to discover adequate active agents, the isoprenoid flavonoids from S. flavescens were further investigated. In this work, two new compounds (1-2, kurarinol A-B) together with 26 known ones (3-28) were isolated and elucidated on the basis of extensive NMR, UV and MS analyses. Furthermore, the antioxidant activity of all constituents was assessed through ABTS, PTIO and DPPH methodologies and also were evaluated for cytotoxic activity by three tumor cell lines (HepG2, A549 and MCF7) and one human normal cell line (LO2 cells). As a result, a multitude of components revealed significant inhibitory activity. In particular, compound 1-2 (kurarinol A-B), two new flavanonols derivatives, exhibited the most potent ABTS inhibitory activity with IC50 of 1.21 µg/mL and 1.81 µg/mL, respectively. Meanwhile, the new compound 1 demonstrated remarkable cytotoxicity against three cancer cells lines with IC50 values ranging from 7.50-10.55 µM but showed little effect on the normal cell. The two new isoprenoid flavonoids could be promising antioxidant and anti-tumor nature agents.


Asunto(s)
Antioxidantes/farmacología , Flavonoides/farmacología , Sophora/química , Terpenos/farmacología , Benzotiazoles/química , Espectroscopía de Resonancia Magnética con Carbono-13 , Muerte Celular/efectos de los fármacos , Línea Celular Tumoral , Óxidos N-Cíclicos/química , Flavonoides/química , Depuradores de Radicales Libres/química , Humanos , Imidazoles/química , Espectroscopía de Protones por Resonancia Magnética , Ácidos Sulfónicos/química , Terpenos/química
2.
Int J Biol Macromol ; 188: 678-688, 2021 Oct 01.
Artículo en Inglés | MEDLINE | ID: mdl-34343590

RESUMEN

As high-efficiency, safe, and low-drug resistant antibacterial agents, silver nanoparticles (AgNPs) have been widely applied in food and biomedicine. AgNPs was prepared using mango peel extract (MPE) as green and cheap reducing agent and stabilizer. In addition, a novel of preservative film material was developed with polylactic acid (PLA) as protective and substrate. AgNPs was characterized by XPS, XRD and TEM, and the size of AgNPs were in the range of 2.5-6.5 nm. The addition of AgNPs improved the mechanical properties of the film and its barrier ability to water vapor and oxygen. The film exhibited excellent antibacterial properties, and the inhibition rate against Escherichia coli and Staphylococcus aureus were above 95%. Furthermore, in terms of safety, the silver migration and cytotoxicity of the film met the relevant standards, and the shelf life of strawberries was significantly extended.


Asunto(s)
Embalaje de Alimentos , Mangifera/química , Nanopartículas del Metal/química , Extractos Vegetales/química , Poliésteres/química , Plata/química , Animales , Compuestos de Bifenilo/química , Línea Celular , Supervivencia Celular/efectos de los fármacos , Óxidos N-Cíclicos/química , Escherichia coli/efectos de los fármacos , Fragaria , Humanos , Imidazoles/química , Nanopartículas del Metal/ultraestructura , Pruebas de Sensibilidad Microbiana , Tamaño de la Partícula , Espectroscopía de Fotoelectrones , Picratos/química , Plata/farmacología , Espectroscopía Infrarroja por Transformada de Fourier , Staphylococcus aureus/efectos de los fármacos , Termogravimetría , Agua/química , Difracción de Rayos X
3.
J Am Chem Soc ; 143(28): 10565-10570, 2021 07 21.
Artículo en Inglés | MEDLINE | ID: mdl-34232661

RESUMEN

Aerobic alcohol oxidations catalyzed by transition metal salts and aminoxyls are prominent examples of cooperative catalysis. Cu/aminoxyl catalysts have been studied previously and feature "integrated cooperativity", in which CuII and the aminoxyl participate together to mediate alcohol oxidation. Here we investigate a complementary Fe/aminoxyl catalyst system and provide evidence for "serial cooperativity", involving a redox cascade wherein the alcohol is oxidized by an in situ-generated oxoammonium species, which is directly detected in the catalytic reaction mixture by cyclic step chronoamperometry. The mechanistic difference between the Cu- and Fe-based catalysts arises from the use iron(III) nitrate, which initiates a NOx-based redox cycle for oxidation of aminoxyl/hydroxylamine to oxoammonium. The different mechanisms for the Cu- and Fe-based catalyst systems are manifested in different alcohol oxidation chemoselectivity and functional group compatibility.


Asunto(s)
Alcoholes/química , Óxidos N-Cíclicos/química , Compuestos Férricos/química , Nitratos/química , Compuestos de Amonio Cuaternario/síntesis química , Catálisis , Estructura Molecular , Oxidación-Reducción , Compuestos de Amonio Cuaternario/química
4.
Carbohydr Polym ; 254: 117415, 2021 Feb 15.
Artículo en Inglés | MEDLINE | ID: mdl-33357899

RESUMEN

Grapefruit peel nanofibrillated cellulose (GNFC) was used as fat substitute in ice cream. GNFC was characterized by TEM, SEM, and XRD. The effects of GNFC on textural profiles, rheological properties, melting resistance, sensory properties, microstructure, and gross energy (GE) of ice cream were investigated. The results showed that GNFC was short rod-shaped crystal. Ice cream added with GNFC exhibited elastic-dominated behavior and better textural properties. The sensory evaluation score reached the highest level with desirable three-dimensional network structure at 0.4 % GNFC addition. GE of ice cream significantly decreased with reducing fat with maximal reduction rate of 17.90 %. Furthermore, the results of in vitro simulated digestion showed that GNFC addition and fat reduction significantly inhibited fat digestibility of ice cream due to coalescence of fat droplets on GNFC. This study provides new sustainable perspectives for the application of GNFC prepared from agricultural waste as fat substitute in food products.


Asunto(s)
Celulosa/química , Citrus paradisi/química , Sustitutos de Grasa/química , Helados , Nanofibras/química , Nanopartículas/química , Extractos Vegetales/química , Celulosa/farmacología , Óxidos N-Cíclicos/química , Digestión/efectos de los fármacos , Elasticidad , Sustitutos de Grasa/farmacología , Ácidos Grasos no Esterificados/química , Manipulación de Alimentos/métodos , Congelación , Jugo Gástrico/química , Jugo Gástrico/efectos de los fármacos , Concentración de Iones de Hidrógeno , Leucina/química , Extractos Vegetales/farmacología , Reología/métodos , Gusto
5.
Sci Rep ; 10(1): 14150, 2020 08 25.
Artículo en Inglés | MEDLINE | ID: mdl-32843666

RESUMEN

We herein report the synthesis, antioxidant power and neuroprotective properties of nine homo-bis-nitrones HBNs 1-9 as alpha-phenyl-N-tert-butylnitrone (PBN) analogues for stroke therapy. In vitro neuroprotection studies of HBNs 1-9 against Oligomycin A/Rotenone and in an oxygen-glucose-deprivation model of ischemia in human neuroblastoma cell cultures, indicate that (1Z,1'Z)-1,1'-(1,3-phenylene)bis(N-benzylmethanimine oxide) (HBN6) is a potent neuroprotective agent that prevents the decrease in neuronal metabolic activity (EC50 = 1.24 ± 0.39 µM) as well as necrotic and apoptotic cell death. HBN6 shows strong hydroxyl radical scavenger power (81%), and capacity to decrease superoxide production in human neuroblastoma cell cultures (maximal activity = 95.8 ± 3.6%), values significantly superior to the neuroprotective and antioxidant properties of the parent PBN. The higher neuroprotective ability of HBN6 has been rationalized by means of Density Functional Theory calculations. Calculated physicochemical and ADME properties confirmed HBN6 as a hit-agent showing suitable drug-like properties. Finally, the contribution of HBN6 to brain damage prevention was confirmed in a permanent MCAO setting by assessing infarct volume outcome 48 h after stroke in drug administered experimental animals, which provides evidence of a significant reduction of the brain lesion size and strongly suggests that HBN6 is a potential neuroprotective agent against stroke.


Asunto(s)
Isquemia Encefálica/tratamiento farmacológico , Óxidos N-Cíclicos/química , Depuradores de Radicales Libres/uso terapéutico , Neuronas/efectos de los fármacos , Neuroprotección/efectos de los fármacos , Fármacos Neuroprotectores/uso terapéutico , Óxidos de Nitrógeno/uso terapéutico , Animales , Apoptosis/efectos de los fármacos , Isquemia Encefálica/inducido químicamente , Línea Celular Tumoral , Modelos Animales de Enfermedad , Evaluación Preclínica de Medicamentos , Depuradores de Radicales Libres/síntesis química , Depuradores de Radicales Libres/farmacología , Glucosa/farmacología , Infarto de la Arteria Cerebral Media/tratamiento farmacológico , Peroxidación de Lípido/efectos de los fármacos , Inhibidores de la Lipooxigenasa/farmacología , Masculino , Ratones , Ratones Endogámicos C57BL , Estructura Molecular , Neuroblastoma/patología , Fármacos Neuroprotectores/síntesis química , Fármacos Neuroprotectores/farmacología , Óxidos de Nitrógeno/síntesis química , Óxidos de Nitrógeno/farmacología , Oligomicinas/toxicidad , Oxígeno/farmacología , Rotenona/toxicidad
6.
Carbohydr Polym ; 236: 115999, 2020 May 15.
Artículo en Inglés | MEDLINE | ID: mdl-32172833

RESUMEN

Cellulose nanofibers (CNFs) from kelp were prepared by cellulase treatment with lengths greater than 3 µm. CNFs were further oxidized by TEMPO-oxidized system, and the lengths of the oxidized CNFs (TEMPO-CNFs) were 0.6-1 µm. AFM and TEM images showed that intertwined CNFs fibers were divided into individual nanofibrils. The crystallinity of TEMPO-CNFs increased to 66.5 %. TGA analysis indicated that TEMPO-CNFs were more sensitive to temperature than cellulose and CNFs. FT-IR spectra revealed no changes in the basic cellulose structures of CNFs and TEMPO-CNFs. In the sunflower oil/water (20/80, v/v) model emulsions, the oil droplet sizes were less than 20 µm in CNFs emulsions, which became smaller in TEMPO-CNFs emulsions. Delamination was found in CNFs emulsions after three days of storage. Addition of NaCl increased the volumes of TEMPO-CNFs emulsions but enlarged the oil droplets sizes. TEMPO-CNFs emulsions had the largest volume with smallest and most homogeneous oil droplets at pH 3. TEMPO-CNFs emulsions showed good stability after storage for 30 days. Further, TEMPO-CNFs could also emulsify 50 % (v/v) of sunflower oil. All these results indicated that TEMPO-CNFs can be used in preparing Pickering emulsions.


Asunto(s)
Celulosa Oxidada/química , Emulsiones/química , Kelp/química , Laminaria/química , Nanofibras/química , Óxidos N-Cíclicos/química , Tamaño de la Partícula , Aceite de Girasol/química
7.
Spectrochim Acta A Mol Biomol Spectrosc ; 228: 117702, 2020 Mar 05.
Artículo en Inglés | MEDLINE | ID: mdl-31748160

RESUMEN

In this paper, a unique water-soluble heptamethine cyanine dye as NIR photosensitizer was synthesized to explore its properties associated with potential applications in photodynamic therapy (PDT). In the strategy of designing this photosensitizer, a sulfonic acid was used as a water soluble functional group and linked to the fluorophore through alkyl chains. 4-amino-2,2,6,6-tetramethylpiperidine-N-oxyl(Tempo) moiety was used as the a nitroxide spin label in obtaining biochemical reaction information in vivo due to it could greatly increase the inter-system crossing (ISC) process for triplet-state photosensitizers and low toxicity. As expected, the photosensitizers performed well in vitro photodynamic therapy. There were a remarkable absorbance band located at 692 nm and emission peaks falls at 762 nm, the quantum yield (Φf) was calculated to be 12.12% in pure aqueous solution using ICG as standards. The photosensitizer also has high singlet oxygen quantum yield (Φ△) for 16.96% with NIR LED irradiation. This photosensitizer can rapidly produce singlet oxygen and exhibit high phototoxicity under NIR light irradiation. It has excellent cellular uptake ability and better cell compatibility. It was also successfully applied in Near-infrared fluorescence imaging and AO/EB staining. In a whole, the organic dye based on Heptamethine cyanine used as photosensitizer has great potential in vivo cancer treatment.


Asunto(s)
Carbocianinas/uso terapéutico , Colorantes/química , Fotoquimioterapia , Fármacos Fotosensibilizantes/uso terapéutico , Espectroscopía Infrarroja Corta , Agua/química , Carbocianinas/síntesis química , Carbocianinas/química , Línea Celular Tumoral , Óxidos N-Cíclicos/química , Oscuridad , Humanos , Fármacos Fotosensibilizantes/síntesis química , Fármacos Fotosensibilizantes/química , Oxígeno Singlete/química , Solubilidad , Espectrometría de Fluorescencia , Coloración y Etiquetado
8.
Int J Biol Macromol ; 137: 1278-1285, 2019 Sep 15.
Artículo en Inglés | MEDLINE | ID: mdl-31271795

RESUMEN

Three types of nanocellulose, namely nano-fibrilated cellulose (NFC, also called cellulose nano-fibrils (CNF)), TEMPO (2,2,6,6-tetramethylpiperidine-1-oxyl radical) oxidized cellulose nano-fibrils (TEMPO-CNF), and nano-crystalline cellulose (NCC, also called cellulose nano-crystals (CNC)), were studied in terms of their effects on in vitro milk digestion and mineral adsorption. The effects of anionic NC (TEMPO-CNF and CNC) on in vitro starch digestion and glucose diffusion were also investigated. Results show that TEMPO-CNF and CNC at high concentrations caused significant reductions in glucose diffusion, especially at 0.36% (w/w) TEMPO-CNF and 2-4% (w/w) CNC. In addition, CNF and TEMPO-CNF at 0.30% (w/w) significantly reduced the amount of free fatty acid produced during intestinal digestion of milk fat. CNC at a concentration of 0.3% (w/w) delayed diffusion of free amino nitrogen during intestinal digestion of milk protein. All three types of NC adsorbed significant amount of Fe, and CNC adsorbed significant amount of Zn, while no significant adsorption was observed on other minerals (Ca, Mg, Zn, Cu and Ag). Results from this study suggest that all three types of NC, when incorporated in food or supplements as zero-calorie fiber, may affect food digestion and nutrient absorption.


Asunto(s)
Celulosa/química , Digestión , Leche/química , Leche/metabolismo , Minerales/química , Almidón/química , Almidón/metabolismo , Adsorción , Animales , Óxidos N-Cíclicos/química , Difusión , Tracto Gastrointestinal/metabolismo , Glucosa/química , Nitrógeno/química , Reología
9.
BMC Mol Cell Biol ; 20(1): 16, 2019 06 20.
Artículo en Inglés | MEDLINE | ID: mdl-31221093

RESUMEN

BACKGROUND: Colon cancer affects 1.23 million people worldwide and is the third most common malignant disease in men and the second in women. The only curative treatment is surgical resection, but a significant number of patients develop local recurrence or distant metastases. One of the alternative treatment methods for colon cancer is photodynamic therapy (PDT). In recent years, hypericin (HYP) derived from Hypericum perforatum has been suggested as a strong candidate photosensitizer for PDT. Our interest is focused on the biophysical changes in colon cancer cells in relation to HYP-mediated PDT. RESULTS: In this study, HYP-mediated PDT at 0.04, 0.08 or 0.15 µM HYP concentrations was performed in HT-29 colon adenocarcinoma cells and the Electron Paramagnetic Resonance (EPR) spectra of the spin labeled cells were obtained. Plasma membranes are already heterogeneous structures; the presence of cancer cells increased the heterogeneity and also fluidity of the plasma membranes. Therefore, the obtained spectra were evaluated by EPRSIMC program, which provides the calculation of heterogeneous structures up to four spectral components with different fluidity characteristics. Generally, two motional patterns were obtained from calculations and the number of them increased at the highest concentration. As the order parameters of the most populated components compared, an increase was observed depending on the HYP concentration. However, because of the heterogeneous structure of membrane, the order parameters of the less populated components did not exhibit a regular distribution. CONCLUSION: After HYP-mediated PDT, concentration dependent changes were observed in the domain parameters indicating an increase in the HYP accumulation.


Asunto(s)
Adenocarcinoma/tratamiento farmacológico , Neoplasias del Colon/tratamiento farmacológico , Espectroscopía de Resonancia por Spin del Electrón/métodos , Perileno/análogos & derivados , Fotoquimioterapia , Fármacos Fotosensibilizantes/uso terapéutico , Extractos Vegetales/uso terapéutico , Adenocarcinoma/patología , Antracenos , Membrana Celular/efectos de los fármacos , Neoplasias del Colon/patología , Simulación por Computador , Óxidos N-Cíclicos/química , Células HT29 , Humanos , Interacciones Hidrofóbicas e Hidrofílicas , Hypericum/química , Fluidez de la Membrana/efectos de los fármacos , Recurrencia Local de Neoplasia/tratamiento farmacológico , Perileno/metabolismo , Perileno/farmacología , Perileno/uso terapéutico , Fármacos Fotosensibilizantes/metabolismo , Fármacos Fotosensibilizantes/farmacología , Extractos Vegetales/metabolismo , Extractos Vegetales/farmacología , Marcadores de Spin
10.
Int J Nanomedicine ; 13: 7123-7134, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-30464463

RESUMEN

PURPOSE: This article presents a report of the synthesis, characterization, and biomedical application of nitroxide-radicals-modified gold nanorods (Au-TEMPO NRs) for imaging-guided photothermal cancer therapy. PATIENTS AND METHODS: Au nanorods were synthesized through seed-mediated growth method, 4-Amino-TEMPO was added and the reaction proceeded under magnetic stirring. RESULTS: With a mean length of 39.2 nm and an average aspect ratio of approximately 3.85, Au-TEMPO NRs showed good photothermal ability when they were irradiated by 808-nm laser. Au-TEMPO NRs could be stored in PBS for more than 1 month, showed no cytotoxicity against both tumor and normal cells at a concentration of up to 3 mg/mL, and functioned as a dual-mode contrast agent for CT/magnetic resonance (MR) imaging in vitro and in vivo, due to their high X-ray attenuation of Au and good r1 relaxivity of nitroxide radicals. Further, they had a long retention time (~4 hours) in the main organs, which enabled a long CT/MR imaging time window for diagnosis. Bio-distribution results revealed that these Au-TEMPO NRs passively aggregated in the liver and spleen. After irradiation by 808-nm laser, Au-TEMPO NRs could ablate the solid tumor in 4T1 tumor-bearing mice, which implied they were a potential theranostic agent for dual-mode imaging and photothermal cancer therapy. CONCLUSION: This type of Au-TEMPO NRs with the abilities of CT/MR imaging and photothermal therapy, can play an active role in imaging-guided photothermal cancer therapy.


Asunto(s)
Oro/química , Hipertermia Inducida , Imagen por Resonancia Magnética , Nanotubos/química , Neoplasias/terapia , Óxidos de Nitrógeno/química , Fototerapia , Tomografía Computarizada por Rayos X , Animales , Antineoplásicos/farmacología , Muerte Celular/efectos de los fármacos , Línea Celular Tumoral , Óxidos N-Cíclicos/química , Femenino , Células Endoteliales de la Vena Umbilical Humana/efectos de los fármacos , Células Endoteliales de la Vena Umbilical Humana/metabolismo , Humanos , Hígado , Ratones Endogámicos BALB C , Nanotubos/ultraestructura , Neoplasias/diagnóstico por imagen , Electricidad Estática , Temperatura , Distribución Tisular/efectos de los fármacos , Carga Tumoral/efectos de los fármacos
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