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Five methods for detection of Helicobacter pylori in the Turkish population 被引量:1
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作者 Orhan Cem Aktepe ihsan Hakkl +3 位作者 Ciftci Birol Safak ihsan Uslan Fatma Husniye Dilek 《World Journal of Gastroenterology》 SCIE CAS CSCD 2011年第47期5172-5176,共5页
AIM: To compare culture analysis, Helicobacter pylori (H. pylori) stool antigen (HpSA) test, polymerase chain reaction (PCR) and fluorescence in situ hybridization (FISH) for H. pylori detection. METHODS: One hundred ... AIM: To compare culture analysis, Helicobacter pylori (H. pylori) stool antigen (HpSA) test, polymerase chain reaction (PCR) and fluorescence in situ hybridization (FISH) for H. pylori detection. METHODS: One hundred and thirty-two consecutive adult dyspeptic patients receiving diagnostic endoscopy at the department of gastroenterology were enrolled in this study. Culture and histological examination were performed on biopsy specimens. PCR and FISH tests were applied to histopathological samples. Stool samples that were simultaneously collected were tested for the H. pylori antigen using the HpSA test and bacterial DNA using stool PCR. RESULTS: H. pylori was positively identified by histo-logical examination in 85/132 (64.4%) of the patients, while positive samples were found in 56 (42.4%), 64 (48.5%), 98 (74.2%), 28 (21.2%) and 81 (61.4%) of the patients by culture, HpSA, PCR, stool PCR and FISH methods, respectively. The results of the culture, biopsy PCR, HpSA and FISH tests, with the exception of the stool PCR, were found to correlate with the histological examination as a gold standard. CONCLUSION: The HpSA test is a rapid, simple, and noninvasive test for monitoring therapy. FISH is an accurate, rapid, cost-effective, and easy-to-use test for H. pylori detection. 展开更多
关键词 Helicobacter pylori HISTOLOGY Polymerasechain reaction Helicobacter pylori stool antigen fluo-rescence in situ hybridization
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Enhancement of Frster energy transfer from thermally activated delayed fluorophores layer to ultrathin phosphor layer for high color stability in non-doped hybrid white organic light-emitting devices 被引量:1
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作者 王子君 赵娟 +2 位作者 周畅 祁一歌 于军胜 《Chinese Physics B》 SCIE EI CAS CSCD 2017年第4期404-410,共7页
Fluorescence/phosphorescence hybrid white organic light-emitting devices(WOLEDs) based on double emitting layers(EMLs) with high color stability are fabricated.The simplified EMLs consist of a non-doped blue therm... Fluorescence/phosphorescence hybrid white organic light-emitting devices(WOLEDs) based on double emitting layers(EMLs) with high color stability are fabricated.The simplified EMLs consist of a non-doped blue thermally activated delayed fluorescence(TADF) layer using 9,9-dimethyl-9,10-dihydroacridine-diphenylsulfone(DMAC-DPS) and an ultrathin non-doped yellow phosphorescence layer employing bis[2-(4-tertbutylphenyl)benzothiazolato-N,C2']iridium(acetylacetonate)((tbt)_2Ir(acac)).Two kinds of materials of 4,7-diphenyl-1,10-phenanthroline(Bphen) and 1,3,5-tris(2-Nphenylbenzimidazolyl) benzene(TPBi) are selected as the electron transporting layer(ETL),and the thickness of yellow EML is adjusted to optimize device performance.The device based on a 0.3-nm-thick yellow EML and Bphen exhibits high color stability with a slight Commission International de l'Eclairage(CIE) coordinates variation of(0.017,0.009) at a luminance ranging from 52 cd/m^2 to 6998 cd/m^2.The TPBi-based device yields a high efficiency with a maximum external quantum efficiency(EQE),current efficiency,and power efficiency of 10%,21.1 cd/A,and 21.3 lm/W,respectively.The ultrathin yellow EML suppresses hole trapping and short-radius Dexter energy transfer,so that Forster energy transfer(FRET)from DMAC-DPS to(tbt)_2Ir(acac) is dominant,which is beneficial to keep the color stable.The employment of TPBi with higher triplet excited state effectively alleviates the triplet exciton quenching by ETL to improve device efficiency. 展开更多
关键词 white organic light-emitting devices non-doped emitting layers thermally activated delayed fluo-rescence color stability
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Improved Method for Determination of Raspberry Ketone in Fragrance Mist by HPLC-Fluorescence Analysis after Pre-Column Derivatization with 4-(<i>N,N</i>-Dimethylaminosulfonyl)-7-(<i>N</i>-chloroformylmethyl-<i>N</i>-methylamino)-2,1,3-benzoxadiazole 被引量:1
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作者 Yasuhiko Higashi 《Journal of Analytical Sciences, Methods and Instrumentation》 2018年第2期17-24,共8页
Raspberry ketone {RK, 4-(4-hydroxyphenyl)butan-2-one} is structurally resembles 4-(4-hydroxyphenyl)-2-butanol, which causes leukoderma on consumers’ skin. Therefore, it is important to measure in cosmetics for qualit... Raspberry ketone {RK, 4-(4-hydroxyphenyl)butan-2-one} is structurally resembles 4-(4-hydroxyphenyl)-2-butanol, which causes leukoderma on consumers’ skin. Therefore, it is important to measure in cosmetics for quality assessment. Very recently, an HPLC-fluorescence method for determination of RK in a fragrance mist by pre-column derivatization with 4-hydrazino-7-nitro-2,1,3-benzoxadiazole hydrazine was established. However, the derivatization conditions (80&deg;C, 20 min) were severe. In this study, an improved pre-column derivatization with 4-(N,N-dimethylaminosulfonyl)-7-(N-chloro-formylmethyl-N-methylamino)-2,1,3-benzoxadiazole (DBD-COCl) is presented by HPLC-fluorescence method for determination of RK. The DBD-CO-RK derivative was eluted from a reversed-phase ODS column, and detected with excitation at 440 nm and emission at 543 nm. Derivatization was performed at room temperature for 3 min. The retention time of DBD-CO-RK derivative was 16.8 min. The standard curve was linear in the range of 0.05 to 2.5 μg/mL, with a correlation coefficient (r2) value of 0.9988. The lower limit of detection was 0.01 μg/mL (absolute amount of 0.3 pmol). The coefficients of variation were less than 10.0%. The content of RK in fragrance mist (1.00 mL) was 1.20 ± 0.08 mg (range, 1.10 to 1.31 mg, n = 5). Recovery tests were satisfactory (91.8 ± 5.4%;range, 84.2 to 98.2%, n = 5). 展开更多
关键词 Raspberry Ketone High-Performance Liquid Chromatography 4-(N N-Dimethylaminosulfonyl)-7-(N-chloroformylmethyl-N-methylamino)-2 1 3-benzoxadiazole Derivatization fluo-rescence
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The anti-photooxidation of anthocyanins-rich leaves of a purple rice cultivar 被引量:15
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作者 PENG Changlian LIN Zhifang +1 位作者 LIN Guizhu CHEN Shaowei 《Science China(Life Sciences)》 SCIE CAS 2006年第6期543-551,共9页
In the leaf of rice(Oryza sativa L.)cultivar Yunnan purple rice,the anthocyanins with an obvious absorption peak at 530nm were distributed in the cells of upper and lower epidermis,bulliform tissue and bristle.The max... In the leaf of rice(Oryza sativa L.)cultivar Yunnan purple rice,the anthocyanins with an obvious absorption peak at 530nm were distributed in the cells of upper and lower epidermis,bulliform tissue and bristle.The maximal photosynthetic oxygen evolution rate and chlorophyll content in flag leaves were 28%and 23%,respectively,more than the common green leaf rice cultivar Chijiaoru-anzhan.Higher chlorophyll content is probably one of the physiological adaptations for enhancing light harvesting capacity of the antenna in photosystems in this cyanic leaves species.Upon the photooxidation of leaf segments mediated by methyl viologen in weak light for 3 days,the distinct bleaching of anthocyanins in purple rice was associated with the reduction of scavenging ability to DPPH·free radical ability and the increase in membrane leakage rate.But almost no changes in contents of flavonoids and total phenolics were observed.Chlorophyll fluorescence parameters Fv/Fo,qP andφPSⅡdecreased with the increase in NPQ and DES of xanthophylls cycle after photooxidation treatment.Green rice leaves showed more decrease in DPPH·scavenging rate and more increase in cell membrane leakage rate but showed a trace of anthocyanins during photooxidation.It is sug-gested that anthocyanin may be a beneficial and primary antioxidant in sun cyanic rice leaves against oxidative stress induced by environmental adversity.And photooxidation could induce different changing patterns of anthocyanins between the tested purple and green rice leaves. 展开更多
关键词 purple rice anthocyanins PHOTOOXIDATION DPPH·scavenging ability chlorophyll fluo-rescence methyl viologen.
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