The stems of Uncaria rhynchophylla (Miq.) ex Havil have a long history of use in traditional Chinese medicine to treat diseases and improve health. There is evident evidence that alkaloids constituents are mainly responsible for the beneficial effects of this plant medicine. The amounts of the major bioactive alkaloids in this plant vary widely with species, habitat, and as such, and establishment of a high-performance liquid chromatography (HPLC) fingerprint for quality control of this herbal medicine is of particular importance. The most alkaloids are used for medicine treatment and research. On the basis of the chromatographic data, a consistent HPLC fingerprint pattern containing 15 common peaks was obtained. Among these common peaks, four were identified as rhynchophylline, isorhynchophylline, corynoxeine, and isocorynoxeine. On the basis of this HPLC fingerprint and principal-components analysis, the quality of fifteen samples from different producing areas of China was objectively assessed. To summarize, the data described in this study offer valuable information for quality control and proper use of U. rhynchophylla (Miq.) ex Havil.
The heat capacities of chrysanthemic acid in the temperature range from 80 to 400 K were measured with a precise automatic
adiabatic calorimeter. The chrysanthemic acid sample was prepared with the purity of 0.9855 mole fraction. A solid-liquid
fusion phase transition was observed in the experimental temperature range. The melting point, Tm, enthalpy and entropy of fusion, ΔfusHm, ΔfusSm, were determined to be 390.7410.002 K, 14.510.13 kJ mol-1, 37.130.34 J mol-1 K-1, respectively. The thermodynamic functions of chrysanthemic acid, H(T)-H(298.15), S(T)-S(298.15) and G(T)-G(298.15) were reported with a temperature interval of 5 K. The TG analysis under the heating rate of 10 K min-1 confirmed that the thermal decomposition of the sample starts at ca. 410 K and terminates at ca. 471 K. The maximum decomposition
rate was obtained at 466 K. The purity of the sample was determined by a fractional melting method.
Authors:Y. Xu, S. Zhang, H. Ding, X. Lu, W. Yang, S. Yuan, Y. Xiao, and Y. Niu
The neutron-rich target-like isotope 236Th has been produced in the 238U-2p multinucleon transfer reaction between a 60 MeV/u 18O beam and natural 238U targets. The activities of thorium were determined after radiochemical separation of Th from the mixture of uranium and
reaction products. The 236Th isotope was identified by the characteristic γ-rays of 642.2, 687.6 and 229.6 keV. The production cross section of 236Th was determined to be 250±50 μb.
Authors:Z.-C. Tan, B. Xue, S.-W. Lu, S.-H. Meng, X.-H. Yuan, and Y.-J. Song
The heat capacities of fenpropathrin in the temperature range from 80 to 400 K were measured with a precise automatic adiabatic calorimeter. The fenpropathrin sample was prepared with the purity of 0.9916 mole fraction. A solid—liquid fusion phase transition was observed in the experimental temperature range. The melting point, Tm, enthalpy and entropy of fusion,
fusSm, were determined to be 322.48±0.01 K, 18.57±0.29 kJ mol–1 and 57.59±1.01 J mol–1 K–1, respectively. The thermodynamic functions of fenpropathrin, H(T)—H(298.15), S(T)—S(298.15) and G(T)—G(298.15), were reported with a temperature interval of 5 K. The TG analysis under the heating rate of 10 K min–1 confirmed that the thermal decomposition of the sample starts at ca. 450 K and terminates at ca. 575 K. The maximum decomposition rate was obtained at 558 K. The purity of the sample was determined by a fractional melting method.
Authors:J. Lu, G.Z. Ji, G. Li, Y.F. Wu, J. Yang, S.L. Lin, D.L. Yang, J.N. Zhao, and W.M. Xiu
Global rice supplies have been found contaminated with unapproved varieties of genetically modified (GM) rice in recent years, which has led to product recalls in several of countries. Faster and more effective detection of GM contamination can prevent adulterated food, feed and seed from being consumed and grown, minimize the potential environmental, health or economic damage. In this study, a simple, reliable and cost-effective multiplex polymerase chain reaction (PCR) assay for identifying genetic modifications of TT51-1, Kemingdao1 (KMD1) and Kefeng6 (KF6) rice was developed by using the event-specific fragment. The limit of detection (LOD) for each event in the multiplex PCR is approximately 0.1%. Developed multiplex PCR assays can provide a rapid and simultaneous detection of GM rice.