Gas Chromatography-Mass Spectrometric Analysis of Essential Oil of Aerial Parts of Glycosmis parviflora (Sims) Little (Rutaceae)

Purpose: To investigate the chemical composition and toxicity of the essential oil of Glycosmis parviflora (Sims) Little aerial parts against root-knot nematode and two grain storage insects (maize weevil and red flour beetle).Methods: Steam distillation of G. parviflora was carried out using Clavenger apparatus in order to extract its volatile oil. Gas chromatography/mass spectrometric (GC/MS) analysis (HP-5MS column) of the essential oil was performed and the toxicity of the oil determined by contact test.Results: A total of 37 components comprising 98.7 % of the essential oil were identified, of which (Z)- caryophyllene (20.6 %), methyl isoeugenol (11.1 %), (Z)-β-ocimene (8.9 %), α-cubebene (6.4 %), nerolidol (5.4 %), aromandendrene (4.9 %) and γ-pyronene (4.7 %) were found to be the major components. The essential oil possessed strong nematicidal activity against M. incognita with an LC50 value of 92.84 μg/ml. The essential oil of G. parviflora exhibited strong contact toxicity against S. zeamais and T. castaneum adults with LD50 values of 41.7 and 22.6 μg/adult,  respectively.Conclusion: The study indicates that the essential oil of G. parviflora aerial parts has a potential for development into a natural insecticide/nematicide for control of nematodes and grain storage insects.Keywords: Glycosmis parviflora, Essential oil, Meloidogyne incognita, Sitophilus zeamais, Triboliumcastaneum, Contact toxicit

From Appearance to Essence

Truth discovery has been widely studied in recent years as a fundamental means for resolving the conflicts in multi-source data. Although many truth discovery methods have been proposed based on different considerations and intuitions, investigations show that no single method consistently outperforms the others. To select the right truth discovery method for a specific application scenario, it becomes essential to evaluate and compare the performance of different methods. A drawback of current research efforts is that they commonly assume the availability of certain ground truth for the evaluation of methods. However, the ground truth may be very limited or even impossible to obtain, rendering the evaluation biased. In this article, we present CompTruthHyp, a generic approach for comparing the performance of truth discovery methods without using ground truth. In particular, our approach calculates the probability of observations in a dataset based on the output of different methods. The probability is then ranked to reflect the performance of these methods. We review and compare 12 representative truth discovery methods and consider both single-valued and multi-valued objects. The empirical studies on both real-world and synthetic datasets demonstrate the effectiveness of our approach for comparing truth discovery methods.Xiu Susie Fang, Quan Z. Sheng, Xianzhi Wang, Wei Emma Zhang, Anne H. H. Ngu, Jian Yan

Temperature modulated solubility and activity alteration for oligo-(N-isopropylacrylamide)-iron tetrasulfonatophthalocyanine conjugates as a new mimetic peroxidase

Iron tetrasulfonatophthalocyanine (FeTSPc) was covalently bound to the terminus of a temperature sensitive oligomer, oligo-N-isopropylacrylamide (ONIPAAm), to form a new mimetic enzyme (ONIPAAm-FeTSPc) to; mimic the peroxidase activity of horseradish peroxidase. This FeTSPc-based mimetic enzyme exhibits a lower critical solution temperature (LCST) of 32 degrees C in neutral solution. It precipitates from water above the LCST and redissolves when the solution temperature is lowered below the LCST. The peroxidase activity of this mimetic enzyme was studied based on its catalytic effect on the reaction of p-hydroxyphenylpropionic acid and H2O2 The results show that the peroxidase activity of the new mimetic enzyme is higher than that of the free FeTSPc. The possibility of its application in the analytical field was also tested by the determination of H2O2 and ONIPAAm-FeTSPc; the detection limits are 8.2 x 10(-9) and 1.7 x 10(-9) mol L-1, respectively

A new red-region substrate, tetra-substituted amino aluminium phthalocyanine, for the fluorimetric determination of H2O2 catalyzed by mimetic peroxidases

A new red-region fluorogenic substrate, tetra-substituted amino aluminium phthalocyanine, was developed for the selective determination of H2O2 based on the catalytic effect of mimetic peroxidases, viz., hemin or iron tetrasulfonatophthalocyanine (FeTSPc). Under the optimum conditions, the linearity of the calibration graph for the determination of H2O2 with hemin (or FeTSPc) as the catalyst was in the range from 0.0 to 3.0 X 10(-7) mol L-1 (or from 0.0 to 2.0 x 10(-6) mol L-1). The detection limits were 3.7 X 10(-9) and 4.9 x 10(-9) mol L-1 H2O2, respectively. The relative standard deviation (n = 7) was within 1.5% in the middle of the linear range. The peroxidase activity of the mimetic enzymes hemin and FeTSPc, the effects of some experimental conditions and the influence of foreign substances were investigated. With this substrate, 0.0-7.5 x 10(-8) mol L-1 hemin and 0.0-2.0 x 10(-6) mol L-1 FeTSPc can be determined with an accuracy and precision of about 1.3%. The potential application of the reagent was tested by the determination of H2O2 in rainwater

Novel spectrofluorimetric method for the determination of thiamine with iron(III) tetrasulfonatophthalocyanine as a catalyst

A sensitive, selective and rapid spectrofluorimetric method is proposed for the determination of thiamine by using mimetic enzyme iron(iii) tetrasulfonatophthalocynanine (FeTSPc) as a catalyst for the oxidation reaction between thiamine and hydrogen peroxide. It is based on the oxidation of thiamine in alkaline medium to give an intensively fluorescent compound, which has an excitation wavelength of 375 nm and an emission wavelength of 440 nm. The determination was found to be activated by fluorogenic substrates with a p-hydroxyphenyl structure such as L-tyrosine, tyramine and p-hydroxyphenylpropionic acid. Under optimum conditions, the responses for thiamine were linear from 1.0 x 10(-8) to 1.0 x 10(-4)mol L-1, with a detection limit of 4.3 x 10(-9) mol L-1. The relative standard deviation was 2.2% for 2.0 X 10(-7) mol L-1 thiamine (n = 6). The activation of the p-hydroxyphenyl substrates, the effects of some experimental conditions and the influence of foreign substances were investigated. The potential application of the method was tested by selectively determining thiamine in commercial vitamin B-1, vitamin B complex and rice

The Effect of Single, Binary and Ternary Anions of Chloride, Carbonate and Phosphate on the Release of 2,4-Dichlorophenoxyacetate Intercalated into the Zn–Al-layered Double Hydroxide Nanohybrid

Intercalation of beneficial anion into inorganic host has lead to an opportunity to synthesize various combinations of new organic–inorganic nanohybrids with various potential applications; especially, for the controlled release formulation and storage purposes. Investigation on the release behavior of 2,4-dichlorophenoxyacetate (2,4-D) intercalated into the interlayer of Zn–Al-layered double hydroxide (ZAN) have been carried out using single, binary and ternary aqueous systems of chloride, carbonate and phosphate. The release behavior of the active agent 2,4-D from its double-layered hydroxide nanohybrid ZANDI was found to be of controlled manner governed by pseudo-second order kinetics. It was found that carbonate medium yielded the highest accumulated release of 2,4-D, while phosphate in combination with carbonate and/or nitrate speeds up the release rate of 2,4-D. These results indicate that it is possible to design and develop new delivery system of latex stimulant compound with controlled release property based on 2,4-D that is known as a substance to increase latex production of rubber tree,Hevea brasiliensis

Interaction of a novel red-region fluorescent probe, Nile Blue, with DNA and its application to nucleic acids assay

A novel fluorimetric method was developed for the rapid determination of DNA and RNA based on their quenching effect on the cationic red-region fluorescent dye Nile Blue (NB) In the investigation of the interaction of NE with DNA by steady-state polarization measurements, thermal denaturing study, determination of absorption and fluorescence characteristics, salt effect study and electrophoresis experiments, the results supported the suggestion that NE served as an intercalator to the stack base pairs of nucleic acids. Further evidence showed that the quenching could be ascribed to the static quenching mode. A binding constant of about 10(6) M-1 and a binding site size of about three base pairs were obtained by spectral methods. Under optimum conditions, the calibration curves for the determination of calf thymus DNA (CT DNA) and yeast RNA were linear over the ranges 3.0 ng mL(-1)-2.0 mu g mL(-1) and 27 ng mL(-1)-10 mu g mL(-1), respectively, The detection limits were 3.0 ng mL(-1) for CT DNA and 27 ng mL(-1) for RNA. The relative standard deviation (n = 6) was within 2.1% in the middle of the linear range. Interferences from some interesting co-existing substances in the determination of DNA were also examined

The Shapes of Cooperatively Rearranging Regions in Glass Forming Liquids

The shapes of cooperatively rearranging regions in glassy liquids change from being compact at low temperatures to fractal or ``stringy'' as the dynamical crossover temperature from activated to collisional transport is approached from below. We present a quantitative microscopic treatment of this change of morphology within the framework of the random first order transition theory of glasses. We predict a correlation of the ratio of the dynamical crossover temperature to the laboratory glass transition temperature, and the heat capacity discontinuity at the glass transition, Delta C_p. The predicted correlation agrees with experimental results for the 21 materials compiled by Novikov and Sokolov.Comment: 9 pages, 6 figure

Strategy Escalation: An emerging paradigm for safe clinical development of T cell gene therapies

Gene therapy techniques are being applied to modify T cells with chimeric antigen receptors (CARs) for therapeutic ends. The versatility of this platform has spawned multiple options for their application with new permutations in strategies continually being invented, a testimony to the creative energies of many investigators. The field is rapidly expanding with immense potential for impact against diverse cancers. But this rapid expansion, like the Big Bang, comes with a somewhat chaotic evolution of its therapeutic universe that can also be dangerous, as seen by recently publicized deaths. Time-honored methods for new drug testing embodied in Dose Escalation that were suitable for traditional inert agents are now inadequate for these novel "living drugs". In the following, I propose an approach to escalating risk for patient exposures with these new immuno-gene therapy agents, termed Strategy Escalation, that accounts for the molecular and biological features of the modified cells and the methods of their administration. This proposal is offered not as a prescriptive but as a discussion framework that investigators may wish to consider in configuring their intended clinical applications