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1.
Food Chem ; 358: 129856, 2021 Oct 01.
Artículo en Inglés | MEDLINE | ID: mdl-33933975

RESUMEN

W/O/W emulsions were easily prepared by oleogelation of the oil phase using rice bran wax (RBX) and their microstructure, stability, rheology and protection of proanthocyanidins and ß-carotene were investigated. Formation of the W/O/W emulsion was confirmed using confocal laser scanning microscopy and staining of the inner aqueous phase by tartrazine. The average particle size and viscosity of the emulsion increased as the RBX concentration increased. Moreover, RBX increased the stability of the emulsion and the emulsion was the most stable when the RBX concentration was 8.0% or 10.0%. On the other hand, the W/O/W emulsions were used to simultaneously encapsulate proanthocyanidins and ß-carotene. Specifically, proanthocyanidins and ß-carotene in RBX-containing emulsions were more stable and had higher bioaccessibility than in the emulsion without RBX. Besides, both their chemical stability and bioaccessibility reached the maximum value when the RBX concentration was 8.0% or 10.0%. In summary, the optimal RBX concentration was 8.0%.


Asunto(s)
Emulsiones/química , Proantocianidinas/química , Aceite de Salvado de Arroz/química , beta Caroteno/química , Aceite de Maíz/química , Almacenamiento de Alimentos , Tamaño de la Partícula , Proantocianidinas/farmacocinética , Reología , Viscosidad , Agua/química , beta Caroteno/farmacocinética
2.
Int J Nanomedicine ; 14: 9113-9125, 2019.
Artículo en Inglés | MEDLINE | ID: mdl-31819422

RESUMEN

BACKGROUND: Prednisolone (PD) is extremely effective for treating rheumatoid arthritis (RA). However, it distributes nonspecifically throughout the body and its use is associated with serious side effects, which promoted us to compound it into a phytomedicine for greater efficacy and safety. METHODS: We combined PD with curcumin (CU), an effective monomer from traditional Chinese medicine, and human serum albumin (HSA) in a nanoparticulate system (N-PD/CU) to compensate for the poor bioavailability of PD and CU. N-PD/CU was prepared by high-pressure homogenization, and its characteristics were evaluated in vitro. Next, we investigated its toxicity and mechanism of anti-inflammatory to macrophages. Finally, its pharmacokinetics, biodistribution and therapeutic efficacy were assessed in rats with adjuvant-induced arthritis (AIA). RESULTS: N-PD/CU showed a narrow size distribution around 150.4 ± 2.4 nm, a polydispersity index of 0.22 ± 0.02 and drug loading efficiency (DLE) of 88.75 ± 1.82% for PD and 85.79 ± 1.43% for CU. N-PD/CU showed sustained release of both drugs in vitro. N-PD/CU had no toxicity to macrophages in vitro on concentrations between 0.1 and 1.2 µmol/mL. In activated macrophages, N-PD decreased levels of pro-inflammatory cytokines, while N-CU increased levels of anti-inflammatory IL-10, and N-PD/CU exhibited best therapeutic effect in vitro, suggesting co-delivery of PD and CU may synergistically control the course of RA. In AIA rats, N-PD/CU accumulated in inflamed joints through the effect of extravasation through leaky vasculature and subsequent inflammatory cell-mediated sequestration (ELVIS effect) in inflammatory lesion and showed higher therapeutic efficacy than single-loaded nanoparticles, either free drug on its own, or a simple mixture of the two drugs. CONCLUSION: This codelivery system based on HSA is a promising platform for combination chemotherapy in RA.


Asunto(s)
Artritis Reumatoide/tratamiento farmacológico , Curcumina/administración & dosificación , Curcumina/uso terapéutico , Sistemas de Liberación de Medicamentos , Nanopartículas/administración & dosificación , Prednisolona/administración & dosificación , Prednisolona/uso terapéutico , Albúmina Sérica Humana/metabolismo , Animales , Antiinflamatorios/uso terapéutico , Artritis Reumatoide/patología , Disponibilidad Biológica , Citocinas/metabolismo , Liberación de Fármacos , Humanos , Mediadores de Inflamación/metabolismo , Masculino , Ratones , Nanopartículas/ultraestructura , Tamaño de la Partícula , Células RAW 264.7 , Ratas Sprague-Dawley , Distribución Tisular
3.
Zhong Nan Da Xue Xue Bao Yi Xue Ban ; 39(1): 43-8, 2014 Jan.
Artículo en Chino | MEDLINE | ID: mdl-24473384

RESUMEN

OBJECTIVE: To investigate the expression pattern of adapter protein with a Src-homology 2 domain (SH2B1), the suppressor of cytokine signaling-3 (SOCS3), protein-tyrosine phosphatase 1B (PTP1B) and neturopetide Y (NPY) in obese and normal mice hypothalamus and its relation with serum leptin and insulin levels. METHODS: The obesity animal model was prepared with healthy C57/bl6 mice. Lee's index and Homeostasis model assessment-insulin resistance (HOMA-IR) were calculated. The mRNA levels of SH2B1, SOCS3, PTP1B and NPY were measured by fluorescent quantitation RT-PCR. The SH2B1 and NPY protein expressions were detected by Western blot. RESULTS: Compared with the normal mice of the same age, SH2B1 mRNA expression in the obese mice hypothalamus decreased. SOCS3 and PTP1B mRNA expression increased. Western blot showed that SH2B1 protein expression decreased, while NPY protein expression increased in the obese mice. Linear correlation analysis showed that the serum leptin and fasting insulin levels were negatively correlated with SH2B1mRNA expression and positively correlated with SOCS3 and PTP1B mRNA expression. CONCLUSION: SH2B1, SOCS3, PTP1B and NPY are key factors for obesity development.


Asunto(s)
Proteínas Adaptadoras Transductoras de Señales/metabolismo , Hipotálamo/metabolismo , Neuropéptido Y/metabolismo , Obesidad/metabolismo , Proteína Tirosina Fosfatasa no Receptora Tipo 1/metabolismo , Proteínas Supresoras de la Señalización de Citocinas/metabolismo , Animales , Insulina/sangre , Resistencia a la Insulina , Leptina/sangre , Ratones , Ratones Endogámicos C57BL , ARN Mensajero , Proteína 3 Supresora de la Señalización de Citocinas
4.
Zhongguo Zhong Xi Yi Jie He Za Zhi ; 31(7): 988-90, 2011 Jul.
Artículo en Chino | MEDLINE | ID: mdl-21866676

RESUMEN

The new edition of Pharmacology of Chinese Materia Medica has broken through the previous mode of the teaching materials. It classified traditional Chinese medicinal herbs into three categories: the herbs for radical cure depending on syndrome differentiation, the herbs for etiological treatment aimed at pathogenesis, and the herbs for symptomatic treatment, combined diseases differentiation with syndrome differentiation, showing active significance in enlightening, guiding the Chinese medicine theory of combining traditional Chinese and Western medicine's compiling, teaching, learning and research applications.


Asunto(s)
Medicina Tradicional China , Farmacología Clínica/educación , Plantas Medicinales , Medicamentos Herbarios Chinos , Materiales de Enseñanza
5.
Zhong Nan Da Xue Xue Bao Yi Xue Ban ; 32(3): 485-9, 2007 Jun.
Artículo en Chino | MEDLINE | ID: mdl-17611330

RESUMEN

OBJECTIVE: To determine the effects of Tongxinluo on cell viability and tissue factor (TF) in AngII induced vascular endothelial cells and to investigate its mechanism. METHODS: AngII(10(-6)mol/L) was added to human vascular endothelial cells (HUVECs) culture media alone or with various concentration of Tongxinluo drug containing plasma (5%,10%, and 20%) added 30 minutes before AngII. Cell viability was evaluated after 24-hour incubation with AngII in a dose manner. TF, AngII type 1 receptor (AT(1)) mRNA, NO synthase (NOS) and NO were observed after 24-hour incubation with AngII. In addition, NOS inhibitor nomega-nitro-larginine (L-NAME) was added 30 minutes before Tongxinluo and AngII. Cell viability, TF, AT(1)mRNA, the level of NOS and NO were evaluated after 24-hour incubation with Tongxinluo and AngII. RESULTS: Tongxinluo significantly improved AngII induced endothelial cell viability and the effect was the most obvious at 10%. Tongxinluo (10%) decreased the TF and AT(1) mRNA while increased the NOS and NO levels. L-NAME obviously inhibited the effects of Tongxinluo on cell viability, TF, AT(1) mRNA, and NOS and NO levels. CONCLUSION: Up-regulating NOS-NO signaling may be the mechanism of Tongxinluo on cell viability and TF in AngII induced vacular endothelial cells.


Asunto(s)
Angiotensina II/farmacología , Medicamentos Herbarios Chinos/farmacología , Endotelio Vascular/efectos de los fármacos , Tromboplastina/biosíntesis , Línea Celular , Supervivencia Celular/efectos de los fármacos , Células Cultivadas , Endotelio Vascular/citología , Endotelio Vascular/metabolismo , Inhibidores Enzimáticos , Ensayo de Inmunoadsorción Enzimática , Humanos , NG-Nitroarginina Metil Éster/farmacología , Óxido Nítrico Sintasa de Tipo I/antagonistas & inhibidores , Óxido Nítrico Sintasa de Tipo I/biosíntesis , Óxido Nítrico Sintasa de Tipo I/genética , ARN Mensajero/biosíntesis , ARN Mensajero/genética , Receptor de Angiotensina Tipo 1/biosíntesis , Receptor de Angiotensina Tipo 1/genética , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Tromboplastina/genética
6.
Huan Jing Ke Xue ; 28(2): 358-62, 2007 Feb.
Artículo en Chino | MEDLINE | ID: mdl-17489197

RESUMEN

The sorption of methyl parathion by neutral alumina which was modified by ionic surfactants such as SDS, SDBS and CTMAB was studied. It showed that the adsorbability of alumina to methyl parathion were related to the type and concentration of surfactant and pH of the system. The adsorbabilities of alumina on three kinds of surfactants were different. When pH = 7, the adsorbance of SDS was the largest, but the adsorbance of CTMAB was the smallest. When pH = 4, the adsorbance of SDS or SDBS was increased, while the adsorbance of CTMAB was decreased. The adsorbability of alumina was strengthened, not weakened, by the cooperation of pollutant and anionic surfactant, while the sorption of methyl parathion by alumina with cationic surfactant was weakened. These features had the practical value when neutral alumina is used to remove more than one contaminants from wastewater.


Asunto(s)
Óxido de Aluminio/química , Metil Paratión/química , Tensoactivos/química , Adsorción
7.
Zhongguo Zhong Yao Za Zhi ; 31(13): 1103-7, 2006 Jul.
Artículo en Chino | MEDLINE | ID: mdl-17048615

RESUMEN

OBJECTIVE: To observe the protective effects of Denghuang injection on cerebral infarction in animal. METHOD: The study evaluated the protective effects of Denghuang injection on cerebral infarction through 3 experiments: 1. ligating the arteria cerebri media of dog; 2. blocking the internal carotid artery of rat; 3. ligating the common carotiol artery of gerbil. RESULT: The results showed Denghuang injection could reduce the cerebral infarction area after the dog's arteria cerebri media was ligated, and also could restrain the AKP&CK increase. The injection could reduce the cerebral infarction area of rat after the internal carotid artery was bloked by thrombus, and the mark of behavior and nerve symptom was better than that in the control group. Denghuang injection could obviously reduce the water content in pallium of gerbil after the common carotiol artery was ligated, and also could increase the amount of living pyramidal neuron in hippocampus, and reduce the MDA&LDH increase in pallium slurry. CONCLUSION: Denghuang injection can obviously protect animal on cerebral infarction.


Asunto(s)
Astragalus propinquus , Infarto Cerebral/patología , Medicamentos Herbarios Chinos/farmacología , Erigeron , Fármacos Neuroprotectores/farmacología , Fosfatasa Alcalina/sangre , Animales , Astragalus propinquus/química , Conducta Animal/efectos de los fármacos , Encéfalo/metabolismo , Encéfalo/patología , Infarto Cerebral/metabolismo , Creatina Quinasa/sangre , Perros , Combinación de Medicamentos , Medicamentos Herbarios Chinos/administración & dosificación , Medicamentos Herbarios Chinos/aislamiento & purificación , Erigeron/química , Femenino , Flavonoides/administración & dosificación , Flavonoides/aislamiento & purificación , Flavonoides/farmacología , Gerbillinae , L-Lactato Deshidrogenasa/metabolismo , Masculino , Malondialdehído/metabolismo , Fármacos Neuroprotectores/administración & dosificación , Fármacos Neuroprotectores/aislamiento & purificación , Plantas Medicinales/química , Ratas , Ratas Wistar , Saponinas/administración & dosificación , Saponinas/aislamiento & purificación , Saponinas/farmacología
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