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1.
Psychol Health Med ; 27(1): 265-279, 2022 01.
Article in English | MEDLINE | ID: mdl-33573426

ABSTRACT

The prevalence of and risk factors for uncertainty stress among residents during the COVID-19 pandemic remain unclear. An online cross-sectional survey was conducted to explore and identify the risk factors for high perceived uncertainty stress among the general public in China during the COVID-19 outbreak. Information about the respondents' socioeconomic characteristics, knowledge of and attitudes towards COVID-19, perceived uncertainty stress, social capital, anxiety, and depressive symptoms was collected and analysed. Among the 1205 respondents, 45.3% (546) reported a high level of uncertainty stress. Multiple linear regression analysis indicated that anxiety (ß=3.871,P<0.001) and depression symptoms (ß=2.458, P<0.001), family residence (in towns or rural areas) (ß=0.947, P<0.001), lack of support for local epidemic control strategies (ß=1.253, P<0.001), worry about the pandemic (ß=1.191, P<0.001), and symptoms of weakness among family members (ß=1.525, P=0.002) were positively associated with perceived uncertainty stress. Cognitive social capital (ß=-0.883, P<0.001) and social networks (ß=-0.726, P<0.001) were negatively, but social participation (ß=0.714, P<0.001) was positively associated with perceived uncertainty stress. Our findings identify factors associated with a higher level of uncertainty stress and should be helpful in the consideration of effective policies and interventions for uncertainty stress during the initial phases of public health emergencies.


Subject(s)
COVID-19 , Pandemics , Anxiety/epidemiology , China/epidemiology , Cross-Sectional Studies , Depression/epidemiology , Humans , SARS-CoV-2 , Surveys and Questionnaires , Uncertainty
2.
Front Public Health ; 9: 659871, 2021.
Article in English | MEDLINE | ID: mdl-34295865

ABSTRACT

Background: An organ donation coordinator plays an important role in the process of organ donation and transplant. Therefore, investigating and analyzing the current situation in organ donation and examining the correlation between professional identity and psychological resilience of human organ donation coordinator, provides a reference for promoting stable development of organ donation. Methods: A total of 48 coordinators of organ donation in Zhejiang Province were recruited for the study by using the method of convenience sampling. The psychological resilience scale and professional identity questionnaire were used to collect data. Results: The results revealed that the total average score of the professional identity of organ donation coordinators was 34.92 ± 8.57. Compared with the median professional identity score of 34.50, the professional identity of the coordinator in this survey was at a moderate level. The total average score of psychological resilience was 64.44 ± 11.91. There was a significant positive correlation between the professional identity of the coordinator and the total score of psychological resilience (r = 0.641, P < 0.01). Conclusion: The professional identity and psychological resilience of the coordinators in Zhejiang Province were found to be in the middle level and the higher the psychological resilience score, the stronger the professional identity of the coordinators. It is important to improve the level of psychological resilience among organ donation coordinators to enhance their professional identity.


Subject(s)
Organ Transplantation , Resilience, Psychological , Tissue and Organ Procurement , China , Humans , Surveys and Questionnaires
3.
Neurosci Lett ; 704: 45-49, 2019 06 21.
Article in English | MEDLINE | ID: mdl-30946930

ABSTRACT

Alpha-synuclein (α-SYN) is found in peripheral autonomic neuronal network apart from brain in Parkinson's disease (PD). Nitrated α-SYN is an undesirable modification associated with oxidative and nitrative damage and has been found extensively in brain, gastrointestinal(GI) tract and blood cells in PD. We aim to investigate the presence of nitrated α-SYN in minor salivary gland biopsy in PD. Patients with PD and age-matched controls underwent minor salivary gland biopsy. Motor impairment was assessed by Hoehn-Yahr (H-Y) stage and Unified Parkinson's Disease Rating Scale (UPDRS) Part III in off-state. 11C-methyl-N-2b-carbomethoxy-3b-(4-fluorophenyl) tropane (11C-CFT) DAT-PET scan was performed in all subjects. Immunohistochemical staining for nitrated α-SYN was performed in the minor salivary gland tissues. The minor salivary gland tissues of 8 PD cases and 7 controls with early stage (H-Y stage 1-2) were detected. All PD patients showed asymmetrical and reduction of 11C-CFT uptake in the caudate, anterior and posterior putamen, while all control subjects showed normal DAT-PET scan. Positive nitrated α-SYN immunostaining was observed in all PD patients (8/8,100%) but not in control subjects (0/7). The results were consistent well with that of DAT-PET. These nitrated alpha-synuclein positive structures were mainly located in the periacinar stroma in PD patients. Our result suggests that nitrated α-SYN exists in the early stage and is probably a promising biomarker for PD. Minor salivary gland is an ideal site for α-SYN nitration detection. Despite of the small number of subjects, attention should be given to α-SYN nitration in PD and more investigations on nitrated α-SYN in different sites and large sample using should be explored in future.


Subject(s)
Nitro Compounds/metabolism , Parkinson Disease/metabolism , Salivary Glands, Minor/metabolism , alpha-Synuclein/metabolism , Adult , Aged , Biomarkers/metabolism , Biopsy , Case-Control Studies , Female , Humans , Male , Middle Aged , Young Adult
4.
Guang Pu Xue Yu Guang Pu Fen Xi ; 36(2): 331-5, 2016 Feb.
Article in Chinese | MEDLINE | ID: mdl-27209725

ABSTRACT

This paper introduces the methods improving the performance and stability of copper-phthalocyanine(CuPc) / fullerene (C60) small molecule solar cells by using tris-(8-hydroxyquinoline) aluminum(Alq3): cesium fluoride(CsF) composite cathode buffer layer. The device with Alq3:CsF composite cathode buffer layer with a 4 wt. % CsF at a thickness of 5 nm exhibits a power conversion efficiency (PCE) of up to 0.76%, which is an improvement of 49%, compared to a device with single Alq3 cathode buffer layer and half-lifetime of the cell in air at ambient circumstance without any encapsulation is almost 9.8 hours, 6 times higher than that of without buffer layer, so the stability is maintained. The main reason of the device performance improvement is that doping of CsF can adjust the interface energy alignment, optimize the electronic transmission characteristics of Alq3 and improve the short circuit current and the fill factor of the device using ultraviolet-visible absorption, external quantum efficiency and single-electron devices. Placed composite cathode buffer layer devices with different time in the air, by comparing and analyzing current voltage curve, Alq3:CsF can maintain a good stability as Alq3. Alq3:CsF layer can block the diffusion of oxygen and moisture so completely as to improve the lifetime of the device.

5.
Neuroreport ; 27(7): 476-80, 2016 May 04.
Article in English | MEDLINE | ID: mdl-26981712

ABSTRACT

Chronic pain is categorized as inflammatory and neuropathic, and there are common mechanisms underlying the generation of each pain state. Such pain is difficult to treat and the treatment at present is inadequate. Corydalis yanhusuo is a traditional Chinese medicine with demonstrated analgesic efficacy in humans. The potential antihyperalgesic effect of its active component is L-tetrahydropalmatine (L-THP). L-THP has been used for the treatment of headache and other mild pain. However, little is known about its analgesic effect on chronic pain and its mechanism. Here, we report that L-THP exerts remarkable antihyperalgesic effects on neuropathic and inflammatory pain in animal models. Neuropathic hypersensitivity was induced by segmental spinal nerve ligation and inflammatory hypersensitivity was induced by an intraplantar injection of complete Freund's adjuvant. To determine the receptor mechanism underlying the antihyperalgesic actions of L-THP, we used SCH23390, an antagonist of a dopamine D1 receptor, in an attempt to block the antihyperalgesic effects of L-THP. We found that L-THP (1-4 mg/kg, i.p.) produced a dose-dependent antihyperalgesic effect in spinal nerve ligation and complete Freund's adjuvant models. The antihyperalgesic effects of L-THP were abolished by a dopamine D1 receptor antagonist SCH23390 (0.02 mg/kg). Furthermore, L-THP (4 mg/kg, i.p.) did not influence motor function. These findings suggest that L-THP may ameliorate mechanical hyperalgesia by enhancing dopamine D1 receptor-mediated dopaminergic transmission.


Subject(s)
Analgesics/administration & dosage , Berberine Alkaloids/administration & dosage , Chronic Pain/prevention & control , Hyperalgesia/prevention & control , Inflammation/complications , Neuralgia/prevention & control , Animals , Chronic Pain/etiology , Corydalis , Freund's Adjuvant , Inflammation/chemically induced , Ligation , Male , Mice , Spinal Nerves/injuries , Spinal Nerves/surgery
6.
Eur J Pharmacol ; 777: 129-35, 2016 Apr 15.
Article in English | MEDLINE | ID: mdl-26945820

ABSTRACT

It is well established that taurine shows potent protection against glutamate-induced injury to neurons in stroke. The neuroprotection may result from multiple mechanisms. Increasing evidences suggest that NADPH oxidases (Nox), the primary source of superoxide induced by N-methyl-d-aspartate (NMDA) receptor activation, are involved in the process of oxidative stress. We found that 100µM NMDA induced oxidative stress by increasing the reactive oxygen species level, which contributed to the cell death, in vitro. Neuron cultures pretreated with 25mM taurine showed lower percentage of death cells and declined reactive oxygen species level. Moreover, taurine attenuated Nox2/Nox4 protein expression and enzyme activity and declined intracellular calcium intensity during NMDA-induced neuron injury. Additionally, taurine also showed neuroprotection against H2O2-induced injury, accompanying with Nox inhibition. So, we suppose that protection of taurine against reactive oxygen species during NMDA-induced neuron injury is associated with Nox inhibition, probably in a calcium-dependent manner.


Subject(s)
Enzyme Inhibitors/pharmacology , NADPH Oxidases/antagonists & inhibitors , Neurons/drug effects , Neurons/metabolism , Neuroprotective Agents/pharmacology , Reactive Oxygen Species/metabolism , Taurine/pharmacology , Animals , Calcium/metabolism , Cell Death/drug effects , Hydrogen Peroxide/pharmacology , Mice , Mice, Inbred ICR , N-Methylaspartate/pharmacology , Neurons/cytology , Neurons/enzymology , Oxidative Stress/drug effects , Up-Regulation/drug effects
7.
CNS Neurosci Ther ; 21(10): 855-66, 2015 Oct.
Article in English | MEDLINE | ID: mdl-26387576

ABSTRACT

AIMS: Postural instability/gait difficulty (PIGD) and tremor-dominant (TD) subtypes of Parkinson's disease (PD) show different clinical manifestations; however, their underlying neural substrates remain incompletely understood. This study aimed at investigating the subtype-specific patterns of spontaneous brain activity in PD. METHODS: Thirty-one patients with PD (12 TD/19 PIGD) and 22 healthy gender- and age-matched controls were recruited. Resting-state functional magnetic resonance imaging data were collected, and amplitude of low-frequency fluctuations (ALFF) was measured. Voxelwise one-way analysis of covariance and post hoc analyses of ALFF were performed among the three groups, with age and gender as covariates (levodopa daily dosage and gray matter volume as additional covariates for validation analysis). Correlations of clinical variables (e.g., disease duration and PIGD/tremor subscale score) with ALFF values were examined. RESULTS: Compared with controls, patients with TD exhibited higher ALFF in the right cerebellar posterior lobe and patients with PIGD exhibited lower ALFF in the bilateral putamen and cerebellar posterior lobe, and higher values primarily in several cortical areas including the inferior and superior temporal gyrus, superior frontal, and parietal gyrus. Compared with patients with PIGD, patients with TD had higher ALFF in the bilateral putamen and the cerebellar posterior lobe, as well as lower ALFF in the bilateral temporal gyrus and the left superior parietal lobule. In all patients, ALFF in the bilateral cerebellar posterior lobe positively correlated with tremor score and ALFF in the bilateral putamen negatively correlated with PIGD score. CONCLUSION: Different patterns of spontaneous neural activity in the cerebellum and putamen may underlie the neural substrate of PD motor subtypes.


Subject(s)
Brain/physiopathology , Gait Disorders, Neurologic/physiopathology , Parkinson Disease/physiopathology , Tremor/physiopathology , Adult , Aged , Antiparkinson Agents/therapeutic use , Brain/drug effects , Brain/pathology , Brain Mapping , Female , Gait Disorders, Neurologic/drug therapy , Gait Disorders, Neurologic/pathology , Gray Matter/drug effects , Gray Matter/pathology , Gray Matter/physiopathology , Humans , Levodopa/therapeutic use , Magnetic Resonance Imaging/methods , Male , Middle Aged , Neural Pathways/drug effects , Neural Pathways/pathology , Neural Pathways/physiopathology , Organ Size , Parkinson Disease/drug therapy , Parkinson Disease/pathology , Rest , Tremor/drug therapy , Tremor/pathology
8.
Stroke ; 46(5): 1352-8, 2015 May.
Article in English | MEDLINE | ID: mdl-25851770

ABSTRACT

BACKGROUND AND PURPOSE: Previous studies reported that Tat-NR2B9c, a peptide disrupting the N-methyl-d-aspartate receptor-postsynaptic density protein-95 interaction, reduced ischemic damage in the acute phase after stroke. However, its effect in the subacute phase is unknown. The aim of this study is to determine whether disrupting the N-methyl-d-aspartate receptor-postsynaptic density protein-95 interaction in the subacute phase promotes recovery after stroke. METHODS: Studies were performed on Sprague-Dawley rats or nNOS(-/-) mice, and experimental ischemic stroke was induced by middle cerebral artery occlusion. Animals were treated with drugs starting at day 4 after ischemia. Sensorimotor functions and spatial learning and memory ability were assessed after drug treatment. Then, rats were euthanized for morphological observation and biochemical tests. RESULTS: Disrupting the N-methyl-d-aspartate receptor-postsynaptic density protein-95 interaction with Tat-HA-NR2B9c significantly ameliorated the ischemia-induced impairments of spatial memory and sensorimotor functions in rats during subacute stage but did not improve stroke outcome in nNOS(-/-) mice. Consistent with the functional recovery, Tat-HA-NR2B9c substantially increased neurogenesis in the dentate gyrus and dendritic spine density of mature neurons in the motor cortex of rats, meanwhile, reversed the ischemia-induced formation of S-nitrosylation-cyclin-dependent kinase 5 and increased cyclin-dependent kinase 5 activity in ipsilateral hippocampus. However, directly blocking N-methyl-d-aspartate receptors with MK-801 or Ro 25-6981 did not show the beneficial effects above. CONCLUSIONS: Dissociating N-methyl-d-aspartate receptor-postsynaptic density protein-95 coupling by Tat-HA-NR2B9c in the subacute phase after stroke promotes functional recovery, probably because of that it increases neurogenesis and dendritic spine density of mature neurons via regulating cyclin-dependent kinase 5 in the ischemic brain.


Subject(s)
Neuroprotective Agents/therapeutic use , Peptides/therapeutic use , Stroke/drug therapy , Animals , Brain Ischemia/drug therapy , Brain Ischemia/pathology , Cognition/drug effects , Cyclin-Dependent Kinase 5/metabolism , Dendritic Spines/ultrastructure , Dentate Gyrus/pathology , Disks Large Homolog 4 Protein , Intracellular Signaling Peptides and Proteins/antagonists & inhibitors , Male , Maze Learning/drug effects , Membrane Proteins/antagonists & inhibitors , Motor Cortex/pathology , Neurogenesis/drug effects , Neuroprotective Agents/administration & dosage , Nitric Oxide Synthase Type I/metabolism , Peptides/administration & dosage , Psychomotor Performance/drug effects , Rats , Rats, Sprague-Dawley , Recovery of Function , Sensation/drug effects , Stroke/prevention & control
9.
Nat Med ; 20(9): 1050-4, 2014 Sep.
Article in English | MEDLINE | ID: mdl-25129479

ABSTRACT

Anxiety disorders are highly prevalent psychiatric diseases. There is need for a deeper understanding of anxiety control mechanisms in the mammalian brain and for development of new anxiolytic agents. Here we report that the coupling between neuronal nitric oxide synthase (nNOS) and its carboxy-terminal PDZ ligand (CAPON) can serve as a target for developing new anxiolytic agents. Augmenting nNOS-CAPON interaction in the hippocampus of mice by overexpressing full-length CAPON gave rise to anxiogenic-like behaviors, whereas dissociating CAPON from nNOS by overexpressing CAPON-125C or CAPON-20C (the C-terminal 125 or 20 amino acids of CAPON) or delivering Tat-CAPON-12C (a peptide comprising Tat and the 12 C-terminal amino acids of CAPON) in the hippocampus of mice produced anxiolytic-like effects. Mice subjected to chronic mild stress (CMS) displayed a substantial increase in nNOS-CAPON coupling in the hippocampus and a consequent anxiogenic-like phenotype. Disrupting nNOS-CAPON coupling reversed the CMS-induced anxiogenic-like behaviors. Moreover, small-molecule blockers of nNOS-CAPON binding rapidly produced anxiolytic-like effects. Dexamethasone-induced ras protein 1 (Dexras1)-extracellular signal-regulated kinase (ERK) signaling was involved in the behavioral effects of nNOS-CAPON association. Thus, nNOS-CAPON association contributes to the modulation of anxiety-related behaviors via regulating Dexras1-ERK signaling and can serve as a target for developing potential anxiolytics.


Subject(s)
Adaptor Proteins, Signal Transducing/metabolism , Anti-Anxiety Agents/pharmacology , Nitric Oxide Synthase Type I/metabolism , Humans
10.
Eur J Pharmacol ; 740: 522-31, 2014 Oct 05.
Article in English | MEDLINE | ID: mdl-24975100

ABSTRACT

Free radical production contributes to the early ischemic response and the neuroinflammatory response to injury initiates the second wave of cell death following ischemic stroke. Edaravone is a free radical scavenger, and borneol has shown anti-inflammatory effect. We investigated the synergistic effect of these two drugs in the rat model of transient cerebral ischemia. Edaravone scavenged OH, NO and ONOO─ concentration-dependently, and borneol inhibited ischemia/reperfusion-induced tumor necrosis factor-α (TNF-α), inducible nitric oxide synthase (iNOS), interleukin-1ß (IL-1ß) and cyclooxygenase-2 (COX-2) expressions. In the rat model of transient cerebral ischemia and reperfusion, the combination of edaravone and borneol significantly ameliorated ischemic damage with an optimal proportion of 4:1. Emax (% inhibition) of edaravone, borneol and two drugs in combination was 55.7%, 65.8% and 74.3% respectively. ED50 of edaravone and borneol was 7.17 and 0.36 mg/kg respectively. When two drugs in combination, ED50 was 0.484 mg/kg, in which edaravone was 0.387 mg/kg (ineffective dose) and borneol was 0.097 mg/kg (ineffective dose). Combination index (CI)<1 among effects observed in experiments, suggesting a significant synergistic effect. Reduced levels of pro-inflammatory mediators and free radicals were probably associated with the synergistic effect of edaravone and borneol. The combination exhibited a therapeutic time window of 6h in ischemia/reperfusion model, and significantly ameliorated damages in permanent ischemia model. Moreover, two drugs in combination promoted long-term effect, including improved elemental vital signs, sensorimotor functions and spatial cognition. Our results suggest that the combination of edaravone and borneol have a synergistic effect for treating ischemic stroke.


Subject(s)
Anti-Inflammatory Agents/therapeutic use , Antipyrine/analogs & derivatives , Brain Ischemia/drug therapy , Camphanes/therapeutic use , Free Radical Scavengers/therapeutic use , Stroke/drug therapy , Animals , Anti-Inflammatory Agents/pharmacology , Antipyrine/pharmacology , Antipyrine/therapeutic use , Brain/drug effects , Brain/metabolism , Brain/pathology , Brain Ischemia/metabolism , Brain Ischemia/pathology , Camphanes/pharmacology , Cell Survival/drug effects , Cells, Cultured , Coculture Techniques , Cyclooxygenase 2/metabolism , Disease Models, Animal , Drug Synergism , Drug Therapy, Combination , Edaravone , Free Radical Scavengers/pharmacology , Interleukin-1beta/metabolism , Maze Learning/drug effects , Neuroglia , Neurons/drug effects , Rats, Sprague-Dawley , Stroke/metabolism , Stroke/pathology , Tumor Necrosis Factor-alpha/metabolism
11.
Biomed Pharmacother ; 67(1): 58-65, 2013 Feb.
Article in English | MEDLINE | ID: mdl-23201007

ABSTRACT

This study investigated the in vitro and in vivo antitumor effects of 5-[2,3-Dichloro-4-(2-methylene-1-oxobutyl) phenoxymethyl]-3-methyl-1,2,4- oxadiazole (6r), a novel ethacrynic acid (EA) derivative. The in vitro effect of 6r on cell proliferation of human colon, leukemia, prostate, lung, breast, ovarian and cervical tumor cell lines was assessed using MTT assay and the in vivo effect was determined with an SW620 xenografts nude mice model. The effect of 6r on expressions of GST P1-1 and apoptosis-related proteins were measured by western blotting and the effect on cell apoptosis was analysed by Hoechst 33258 nuclear staining as well as by cell surface staining of annexin V/propidium iodide. The effect on cell cycle was assessed by flow cytometry. Results showed that 6r inhibit proliferation of a range of human cancer cells in vitro and growth of SW620 tumor xenografts in vivo. The anti-proliferative effect of 6r is associated with cell apoptosis as a result of increased ratio of cellular Bax/bcl-2 expression and subsequent cytochrome-c and caspase-3 activation. Unlike EA, 6r did not show any influence on cellular GST P1-1 expression and its anti-proliferative action was associated with cell cycle arrest in G1/S-phase. In conclusion, 6r has the potential to be developed as a chemotherapeutic agent by induction of cell apoptosis but not regulating GST P1-1.


Subject(s)
Antineoplastic Agents/pharmacology , Apoptosis/drug effects , Neoplasms/drug therapy , Oxadiazoles/pharmacology , Animals , Blotting, Western , Cell Line, Tumor , Cell Proliferation/drug effects , Colonic Neoplasms/drug therapy , Colonic Neoplasms/pathology , Female , Flow Cytometry , G1 Phase Cell Cycle Checkpoints/drug effects , Gene Expression Regulation, Neoplastic , Glutathione S-Transferase pi/genetics , Humans , Mice , Mice, Inbred BALB C , Mice, Nude , Neoplasms/pathology , S Phase Cell Cycle Checkpoints/drug effects , Xenograft Model Antitumor Assays
12.
Int J Mol Sci ; 13(10): 13398-413, 2012 Oct 18.
Article in English | MEDLINE | ID: mdl-23202959

ABSTRACT

The relationship between chromosome deletion in wheat and protein expression were investigated using Chinese Spring and fine deletion line 3BS-8. Through 2-DE (2-D electrophoresis) analysis, no differentially expressed proteins (DEPs) were found in leaf samples; however, 47 DEPs showed at least two-fold abundance variation (p < 0.05) in matured wheat grains and 21 spots were identified by tandem MALDI-TOF/TOF-MS. Among the identified spots, four were cultivar-specific, including three (spots B15, B16, and B21) in Chinese Spring and one in 3BS-8 (spot B10). Among variety-different DEPs between Chinese Spring and 3BS-8, most spots showed a higher express profile in CS; only four spots showed up-regulated expression tendency in 3BS-8. An interesting observation was that more than half of the identified protein spots were involved in storage proteins, of which 11 spots were identified as globulins. According to these results, we can presume that the encoded genes of protein spots B15, B16, and B21 were located on the chromosome segment deleted in 3BS-8.


Subject(s)
Albumins/analysis , Globulins/analysis , Plant Proteins/analysis , Proteomics , Triticum/metabolism , Electrophoresis, Gel, Two-Dimensional , Plant Leaves/metabolism , Proteome/analysis , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization , Up-Regulation
13.
Guang Pu Xue Yu Guang Pu Fen Xi ; 31(9): 2328-31, 2011 Sep.
Article in Chinese | MEDLINE | ID: mdl-22097820

ABSTRACT

In the present work, the photoluminescence (PL) and electroluminescence (EL) characteristics of Tris[2-(2,4-difluorophenyl)pyridine]iridium(III) (Ir(Fppy)3) doped poly(n-vinylcarbazole) (PVK) with different doping concentrations were investigated. And a blue phosphorescent organic light-emitting diode (OLED) with the structures of ITO/PEDOT : PSS/PVK : Ir(Fppy)3/BCP/Alq3/LiF/Al was fabricated. The experimental results show that the luminescence performances of devices are different as the doping concentration of Ir(Fppy)3 is different. When the doping concentration of Ir(Fppy)3 is lower, the luminescence of PVK can be found in EL spectra. When the doping concentration is too high, concentration quenching may occur. As the doping concentration is suitable, the luminescence of PVK can not be found, only the luminescence of Ir(Fppy)3 can be found in EL spectra. It is concluded that the device with doping concentration of 4% has the best photoelectric performance according to its current density-voltage-luminance curve.

14.
Guang Pu Xue Yu Guang Pu Fen Xi ; 31(7): 1729-33, 2011 Jul.
Article in Chinese | MEDLINE | ID: mdl-21942012

ABSTRACT

Series of organic light emitting devices with basic structure of ITO/PCBM: PVK(x Wt%, approximately 40 nm)/DPVBi(30 nm)/Alq3 (30 nm)/Al were fabricated in order to investigate the carrier recombination region movement in these devices. The carrier injection-dependent, the carrier transport-dependent and the voltage-dependent carrier recombination region movements were investigated respectively by modifying cathode with lithium fluoride, by changing the doping concentration of PCBM and by changing the voltage on the devices. The physical mechanism behind the voltage-dependent carrier recombination region movement was discussed.

15.
Guang Pu Xue Yu Guang Pu Fen Xi ; 31(4): 886-9, 2011 Apr.
Article in Chinese | MEDLINE | ID: mdl-21714221

ABSTRACT

The present work investigates the effects of different buffer layers on the performance of blue organic light-emitting diodes (OLEDs), and compares them with the device with no buffer layer. Two kinds of blue OLEDs with 4,4'-bis(2,2'-diphenyl vinyl)-1,1'-biphenyl (DPVBi) as the emitting layer, N, N'-bis-(1-naphthyl)-N, N'-1-diphenyl-1,1 '-biphenyl-4, 4'-diamine (NPB) as the hole transporting layer, and copper phthalocyanine (CuPc) and poly(3,4-ethylenedioxythiophene) : poly (styrenesulphonate) PEDOT : PSS as the hole injection layer respectively were fabricated with the structures of ITO/CuPc/NPB/DPVBi/BCP/Alq3 /Al and ITO/PEDOT : PSS/NPB/DPVBi/BCP/Alq3/Al. Moreover, the effects of different preparation technology of CuPc on the performance of OLEDs were also investigated. It was found that the performance of the devices with a hole injection layer is better than that of the device without any hole-injection layer. Although the luminance and efficiency of the water-soluble CuPc based device are worse than that of the device with thermally evaporated CuPc, but better than that of the device with water-soluble PEDOT : PSS. So the water-soluble CuPc is a good hole injection material because it is easier to fabricate the film than traditional CuPc.

16.
Guang Pu Xue Yu Guang Pu Fen Xi ; 31(10): 2676-9, 2011 Oct.
Article in Chinese | MEDLINE | ID: mdl-22250533

ABSTRACT

The present work investigates the photoluminescence (PL) and electroluminescence (EL) characteristics of Eu-complex Eu (UVA)3Phen doped PVK with different doping concentrations. The results indicate that there exists Forster energy transfer from PVK to Eu(UVA)3 phen in the mixed system. It can get good color purity by optimizing the doping concentration of host and guest materials. And the authors can obtain the best doping concentration to be 4% in EL device.

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