A method for the determination of protein in human limbs by in vivo neutron activation analysis of their nitrogen content is described. The neutron flux is provided by a collimated 740 GBq (20 Ci) Pu–Be source. The 10.83 MeV thermal neutron capture gamma-rays from14N are detected by a 12.7 cm by 10.2 cm NaI(T1) detector. The nitrogen and hydrogen in an arm, the lower and the upper legs of two volunteers were measured with a statistical error around 3.6%–18% and 0.26%–0.56%, respectively. Also, the ratio of nitrogen to hydrogen in the limbs was compared. For a 1.000 s irradiation the dose equivalent was 0.3 mSv (30 mrem).
The reactions between silicon nitride and carbon take place in two stages, the surface silica of silicon nitride powders reacts
with carbon first followed by the decomposition of silicon nitride and the residual silicon reacting with carbon. The kinetics
of the two stage reactions has been studied by isothermal thermogravimetric analysis. Physico-geometric models for both of
the reaction stages have been proposed, and the kinetic parameters have been calculated. The implications of the kinetic models
and parameters are discussed.
The dehydration process of Co(II), Cu(II)
and Zn(II) methanesulfonates was studied by thermogravimetry/derivative thermogravimetry
(TG/DTG) and differential scanning calorimetry (DSC) techniques in dynamic
N2 atmosphere. The TG/DTG curves show that all of them
contain four crystallization water molecules, which are lost in two steps.
The peak temperature and dehydration enthalpies ΔH
were measured from DSC curves for each compound. The effect of procedural
variables on the TG and DSC curves was investigated. In this work, the procedural
variables included heating rate, Al pan state (unsealed and sealed) and sample
An ultrasensitive and rapid method for the determination of epicatechin, rutin, and quercetin was developed using capillary zone electrophoresis with on-line chemiluminescence detection. Under the optimal conditions, the analytes were baseline separated within 12 min. The limits of detection in turn were 0.60 pg mL−1 for epicatechin, 0.50 pg mL−1 for rutin, and 1.0 pg mL−1 for quercetin. The developed method was an easy and reliable method of determining these analytes concentrations in tea, extract Ginkgo biloba, and rutin tablet, demonstrating the feasibility and reliability of the proposed method.
As a new form of traditional Chinese medicine (TCM), Zuojin pill extract is made containing Coptidis rhizoma (the rhizome of Coptis chinesis Franch. [Ranunculaceae]) and Euodiae fructus (the unripe fruit of Euodia rutaecarpa [Juss.] Benth. [Rutaceae]) at the ratio of 6:1 (w/w) and has been most widely used in TCM to treat gastro-intestinal disorders. However, the quality control is insufficient. For establishing an analysis method for the effective quality control of Zuojin pill extract, the active components of three protoberberine alkaloids (coptisine, palmatine, berberine, components from C. rhizoma) and two indolequinoline alkaloids (evodiamine, rutaecarpine, components from E. fructus) in Zuojin pill extract were determined simultaneously by high-performance liquid chromatography. Chromatographic separations were performed on an Inertsil ODS-3 column (4.6 mm × 250 mm, 5 μm). Elution was carried out at 25°C under isocratic conditions by using 25 mmol L−1 KH2PO4-25 mmol L−1 SDS-acetonitrile (1:1:2, v/v/v, adjusted pH to 3.0 using phosphoric acid) as a mobile phase with a flow rate of 0.5 mL min−1. Detection wavelength was set at 264 nm. Good linearity was obtained with correlation coefficient higher than 0.999 for all the analytes over the investigated concentration ranges. Three batches of Zuojin pill extract were successfully analyzed. The average percentages of coptisine, palmatine, berberine, evodiamine, and rutaecarpine in Zuojin pill extract were 5.35%, 3.92%, 16.64%, 0.03%, and 0.03%, respectively. Consequently, these protoberberine and indolequinoline alkaloids could be identified and determined easily by the established high-performance liquid chromatography (HPLC) method which can be used to evaluate and control the quality of Zuojin pill extract.
The effect of short-term higher ambient temperature (HT) and continuous vibration (CV) treatment was comparatively characterized by sensory evaluation and chemical analysis. Results of quantitative descriptive analysis of modified frequency (MF) showed that HT causes both in red wine and white wine a decrease of fruity and floral characters, an unbalance of taste, and a shortness of aftertaste length. CV wine showed very close sensory characters to control in most terms evaluated. Seventy-four volatile compounds were quantitative analysed by solid phase microextractiongas chromatography-mass spectrometry, and the principal component analysis (PCA) was conducted on the 23 volatiles of highest odour activity value (OAV). The concentrations of potential fruity and floral aroma attributors like isoamyl acetate, ethyl butanoate, ethyl 2-methylbutanoate, ethyl hexanoate, ethyl octanoate, β-damascenone, and linalool were lower in HT wine than that in original wine and CV wine.
This study investigated the influences of drying method (oven-, freeze-, and shade-drying) and extraction solvent (ethanol and water) on the bioactivities of Cirsium setidens. Antioxidant activity was evaluated by DPPH radical scavenging ability, anti-diabetic activity was determined by the inhibitory activity of two enzymes: α-glucosidase and α-amylase, while anti-proliferation activity was assessed by MTT assay of three human cancer cell lines (KB, A549, and PC-3). Results indicated that bioactivities were extremely affected by solvent; water extracts contained more phenolics, exhibited strong anti-diabetic effect, but no activity of anti-proliferation, while the ethanolic extracts rich in flavonoids showed profound DPPH radical scavenging and anti-proliferation ability, yet low activity of antidiabetes. Among the drying methods, freeze-drying extracts preserved more flavonoids and exhibited better activity of anti-proliferation, while shade-drying extracts contained higher phenolics and showed stronger activity on antidiabetes, oven-drying gave the lowest content of phenolics. Hence, antioxidant and anti-diabetic effects were positively related to phenolic content, meanwhile an extremely significant correlation coefficient had been found between anti-proliferation activity and flavonoid content, it can be concluded that drying method and extraction solvent affect bioactivities by phenolic and flavonoid contents.
Phenolic extract from banana peel was extracted with 95% ethanol and characterized by LC-TOF-MS/MS. Epicatechin, rutin, 3,4-dihydroxybenzaldehyde, 3,4-dihydroxybenzoic acid, myricetin, ferulic acid, chlorogenic acid, and gallic acid were detected in the extract. Cholate test was performed for the initial examination of the hypolipidemic effect of the dietary fibres. The dietary fibres prepared by sequential treatment with sulphuric acid then sodium hydroxide (SST) and sodium hydroxide treatment (SHT) had high water-holding capacities (7.48 and 6.91 g g−1) and swelling capacities (4.8 and 4.3 ml g−1). The dietary fibres prepared by sequential treatment with trypsin then sulphuric acid (TST) and sulphuric acid treatment (SAT) had high oil-holding capacities (5.52 and 5.10 g g−1) and enhanced capacities for sodium cholate adsorption. Results indicated the potentials of banana peel as functional ingredient in food applications.
Authors:S. Du, G. Zhang, H. Li, P. Wang, and X. Wang
The free-radical bulk polymerization of 2,2-dinitro-1-butyl-acrylate (DNBA) in the presence of 2,2′-azobisisobutyronitrile
(AIBN) as the initiator was investigated by DSC in the non-isothermal mode. Kissinger and Ozawa methods were applied to determine
the activation energy (Ea) and the reaction order of free-radical polymerization. The results showed that the temperature of exothermic polymerization
peaks increased with increasing the heating rate. The reaction order of non-isothermal polymerization of DNBA in the presence
of AIBN is approximately 1. The average activation energy (92.91±1.88 kJ mol −1) obtained was smaller slightly than the value of Ea=96.82 kJ mol−1 found with the Barrett method.
The detection of characteristic gamma rays emitted promptly by elements after capture of neutrons is used as a means of radioanalytic analysis. Here it is shown that the method can be used for the measurement of the nitrogen (and therefore protein) content of small animals, those with mass around 3 kg.