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991.
992.
建立了五灵脂中原儿茶酸含量的测定方法。利用加速溶剂萃取仪(ASE),以75%乙醇水溶液提取样品中的待测物,用Diamosil C18(4.6 mm×250 mm,5.0μm)色谱柱在梯度洗脱条件下分离待测物,外标法定量。原儿茶酸的线性范围为0.1~10.0 mg/L,相关系数r=0.9998。方法的回收率为83%~107%,测定结果的相对标准偏差为4.6%~10.5%,方法的定量限为1.0 mg/kg。该方法操作简便、快速,提取效率高,适用于检测和分析五灵脂中原儿茶酸的含量。 相似文献
993.
Ik Hyun Kwon Hye Ryoung Park Young Youp Song 《Russian Journal of Electrochemistry》2013,49(3):221-227
LiNi1 ? y Ti y O2 (0.000 ≤ y ≤ 0.100) and LiNi0.990M0.010O2 (M = Zn, Al, and Ti) were synthesized by the combustion method. The effects of Zn, Al and Ti substitution for Ni of LiNiO2 on the electrochemical properties of LiNiO2 were investigated. LiNi0.995Ti0.005O2 has the largest first discharge capacity (188.1 mA h/g) among the Ti-substituted samples. LiNi0.990Ti0.010O2 has a relatively large first discharge capacity (185.5 mA h/g) and a relatively good cycling performance. Among LiNi0.990M0.010O2 (M = Ni, Zn, Al, and Ti), LiNiO2 has the largest discharge capacities at a rate of 0.1 C from n = 1(189.3 mA h/g) to n = 10. LiNi0.990Al0.010O2 has the lowest discharge capacities from n = 1 to n = 10, but it has the best cycling performance. LiNi0.990Zn0.010O2 showed poor crystallinity, LiNi0.990Ti0.010O2 showed high cation mixing, and LiNi0.990Al0.010O2 had good crystallinity and showed low cation mixing. Fewer occurrence of phase transitions and the least change of the ?dx/|dV| vs. voltage curve at the second cycle from the curve at the first cycle of LiNi0.990Al0.010O2 suggest that Al substitution stabilizes the structure and leads to a good cycling performance. 相似文献
994.
995.
A modified glassy carbon (GC) electrode was developed for the amperometric detection of biogenic amines, particularly histamine. The electrode was modified with the co‐enzyme pyrroloquinoline quinone (PQQ) by entrapment during electropolymerziation of pyrrole to form polypyrrole (PPy). This method formed a thin film on the electrode surface possessing very good stability with a shelf‐life exceeding one month without loss of signal. Optimal conditions for the PQQ/PPy electrode were determined and a linear response was found for histamine in phosphate buffer (pH 6) at +550 mV from 40 to 170 mg L?1 with a limit of detection (S/N≥3) of 38 mg L?1. The practical linear range offered by this method suggests ideal use for spoilage detection in fermented foods. 相似文献
996.
The mechanism of cycloaddition reaction between singlet state dichloromethylenegermene (Cl2C=Ge:) and ethene has been investigated with the CCSD(T)//B3LYP/6-31G* method. From the potential energy profile, it could be predicted that the reaction has one dominant reaction channel. The reaction rule presented is that the 4p unoccupied orbital of Ge in dichloromethylenegermene and the π orbital of ethene forming a π → p donor–acceptor bond resulting in the formation of a three-membered ring intermediate. Ring-enlargement effect make the three-membered ring intermediate isomerizes to a four-membered ring germylidene. Because the 4p unoccupied orbital of Ge atom in the four-membered ring germylidene and the π orbital of ethene form a π → p donor–acceptor bond, the four-membered ring germylidene further combines with ethene to form another intermediate. Because the Ge atom in the intermediate happens sp 3 hybridization after transition state, the intermediate isomerizes to a spiro-Ge-heterocyclic ring compound. 相似文献
997.
Wen-Yan Ji Xiao-Li Xia Xiao-Hui Ren Fang Wang Hai-Jun Wang Kai-Sheng Diao 《Structural chemistry》2013,24(1):49-54
Ab initio calculations have been performed on the complexes of CF2Cl2 with NO and SO2, and a set of stable configurations for CF2Cl2–NO and CF2Cl2–SO2 were found with no imaginary frequencies by the MP2 method. In addition, the binding energy and the NBO analysis were used to evaluate the relative stability of the complexes. The calculated results indicate that the weak interactions in the CF2Cl2–NO and CF2Cl2–SO2 systems involved are enhanced with the increase of the number of non-covalent bonds. Further studies predict that the CF2Cl2–SO2 system may play a more important role than the CF2Cl2–NO system in environmental problem because the former offers a stronger interaction than the latter. Furthermore, the non-covalent binding interactions of Cl···N and Cl···O for CF2Cl2–NO system, Cl···O, Cl···S and F···S for CF2Cl2–SO2 system, are the dominant forces, which seem to be very significant as a driving force influencing the arrangement of molecules, especially in CF2Cl2–SO2 system. 相似文献
998.
Sunwoong Bae Chul Woong Kim Jong Seob Choi Ji-Won Yang Tae Seok Seo 《Analytical and bioanalytical chemistry》2013,405(29):9365-9374
This study describes the development of a microfluidic device for the high-throughput screening of culture conditions, such as the optimum sodium acetate concentration for promoting rapid growth and high lipid accumulation of Chlamydomonas reinhardtii. An analysis of the microalgal growth on the microfluidic device revealed an optimum sodium acetate concentration of 5.72 g L?1. The lipid content, determined by the 4,4-Difluoro-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene (BODIPY® 505/515) staining method, increased with the sodium acetate concentration. The results were found to be statistically reproducible with respect to cell growth and lipid production. Other nutrient conditions, including the nitrogen and phosphorus concentrations, can also be optimized on the same microfluidic platform. The microfluidic device performance results agreed well with the results obtained from the flask-scale experiments, validating that the culture conditions were scalable. Finally, we, for the first time, established a method for the absolute quantification of the microalgal lipid content in the picoliter culture volumes by comparing the on-chip and off-chip data. In conclusion, we successfully demonstrated the high-throughput screening of sodium acetate concentrations that induced high growth rates and high lipid contents in C. reinhardtii cells on the microfluidic device. Figure
We have developed a microfluidic device for the high-throughput screening of culture conditions for promoting rapid growth and high lipid accumulation of Chlamydomonas reinhardtii 相似文献
999.
Sooyeun Lee So-young Kang Dajeong Ji Seungkyung Baeck Sangki Lee Seung Min Oh Kyu Hyuck Chung 《Analytical and bioanalytical chemistry》2013,405(10):3185-3194
The chemical castration law, which targets child molesters with recidivism, was introduced in Korea in 2011. For this, leuprolide, a gonadotropin-releasing hormone agonist, is used to decrease testosterone production and suppress libido. In order to achieve efficient law enforcement, it is necessary to monitor intentional ingestion of drugs that antagonize the effect of leuprolide. Therefore, an analytical method for the simultaneous detection of mirodenafil, sildenafil, tadalafil, udenafil, vardenafil, icariin, alprostadil, and yohimbine, which are the major impotence treatment drugs, legitimately or otherwise, in Korea, as well as their selected metabolites, in human urine was established and validated using liquid chromatography–tandem mass spectrometry (LC–MS/MS). First, different sample preparation methods, two solid-phase extractions with different cartridges and protein precipitation, were compared and protein precipitation was chosen for the entire study because it showed better matrix effects and recoveries. Thus, the drugs and metabolites in urine were extracted by protein precipitation and then filtered and analyzed by LC–MS/MS with polarity switching electrospray ionization. The validation results of selectivity, matrix effect, recovery, linearity, intra- and inter-assay precision and accuracy were satisfactory. The limits of detection ranged from 0.25 to 10 ng/mL, and the limits of quantification were 2.5 to 50 ng/mL. The drugs and metabolites in urine did not show any degradation under storage for 7 and 15 days at 4 and ?20 °C as well as after three freeze–thaw cycles. The developed method will be very useful for monitoring the illegal use of impotence treatment drugs. 相似文献
1000.
Kaili Ji Wee Siang Lim Sam Fong Yau Li Kishore Bhakoo 《Analytical and bioanalytical chemistry》2013,405(21):6853-6861
Aptamers are single-stranded oligonucleotides that are capable of binding wide classes of targets with high affinity and specificity. Their unique three-dimensional structures present numerous possibilities for recognizing virtually any class of target molecules, making them a promising alternative to antibodies used as molecular probes in biomedical analysis and clinical diagnosis. In recent years, cell-systematic evolution of ligands by exponential enrichment (SELEX) has been used extensively to select aptamers for various cell targets. However, aptamers that have evolved from cell-SELEX to distinguish the “stimulus-response cell” have not previously been reported. Moreover, a number of cumbersome and time-consuming steps involved in conventional cell-SELEX reduce the efficiency and efficacy of the aptamer selection. Here, we report a “two-step” methodology of cell-SELEX that successfully selected DNA aptamers specifically against “inflamed” endothelial cells. This has been termed as stimulus-response cell-SELEX (SRC-SELEX). The SRC-SELEX enables the selection of aptamers to distinguish the cells activated by stimulus of healthy cells or cells isolated from diseased tissue. We report a promising aptamer, N55, selected by SRC-SELEX, which can bind specifically to inflamed endothelial cells both in cell culture and atherosclerotic plaque tissue. This aptamer probe was demonstrated as a potential molecular probe for magnetic resonance imaging to target inflamed endothelial cells and atherosclerotic plaque detection. Schematic of SRC-SELEX selection
The cells are activated with stimulus and incubated with single-stranded DNA library. The sequences bound on the activated cells are released and amplified to incubate with naïve cells without stimulation. The sequences unbound to the naïve cells are then incubated with activated cells again and go into the next round of selection. After the selection reaches the end point, the single-stranded DNA collected from the last round is cloned and sequenced for identification 相似文献