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  • Author or Editor: Jianhua Yin x
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You-Gui-Yin (YGY), a famous traditional Chinese medicine, has been widely used in clinics for the treatment of kidney-yang deficiency, yang deficiency caused by excessive yin, and osteoporosis. A rapid and sensitive ultraperformance liquid chromatography–electrospray ionization–mass spectrometry (UPLC–ESI–MS) method for simultaneous determination of six Aconitum alkaloids including aconitine (AC), hypaconitine (HA), mesaconitine (MA), benzoylaconine (BAC), benzoylhypaconine (BHA), and benzoylmesaconine (BMA) in rat plasma after oral administration of YGY was developed in this study. Chromatographic separation was performed on an ACQUITY UPLC™ BEH C18 column (2.1 × 100 mm, 1.7 μm) using gradient elution with the mobile phase consisting of 2 mmol/L ammonium formate in 0.05% formic acid aqueous solution and 0.05% formic acid methanol solution, at a flow rate of 0.20 mL/min. MS detection was performed in the positive ion mode. The calibration curves were linear in the concentration range of 0.04160–41.60 ng/mL, 0.1070–107.0 ng/mL, 0.07358–73.50 ng/mL, 0.03228–32.28 ng/mL, 0.01809–18.09 ng/mL, and 0.1320–132.0 ng/mL for AC, HA, MA, BAC, BHA, and BMA, respectively. The intra- and inter-day precisions (relative standard deviation [RSD]) were less than 11.6% and 12.6%, respectively. The accuracies Relative Error (RE) ranged from −10.2% to 5.6%, while the recoveries ranged from 70.4% to 99.3%. The method for simultaneous quantitation of Aconitum alkaloids of You-Gui-Yin in rat plasma is accurate and repeatable, and this method was successfully applied to investigate the pharmacokinetics of the six Aconitum alkaloids in rat plasma after oral administration of YGY. For the pharmacokinetic study, the pharmacokinetics of the six Aconitum alkaloids were best described by a two-compartment open model.

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A procedure for labeling of a fullerene derivative 1-[N',N'-bis(2-chloroethyl)-4-aminophenyl]-N-methyl-fullereno-C60-[1,9-c]pyrrolidine (C60-C13H18N2Cl2) with 125I is reported. The compound was first iodinated with a large excess of iodine monochloride and then radiolabeled by isotopic exchange with Na125I in a toluene-water two-phase system. The dependence of the radiolabeling yield on the reaction temperature and exchange time was examined. The radiolabeling yield of the compound was as high as 94% after heating for 2 hours at 130 °C.

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In this work, a simple group separation scheme based on extraction for NAA determination of trace of As, Cd, Hg, Cu and Zn in biological materials is described. For this purpose, zinc-diethyldithiocarbamate, Zn(DDC)2, and methyl isobutyl ketone-iodide have been chosen as reagents. The elements can be extracted successively and quantitatively from strong mineral acids without adjusting pH of the solution, and separated into two groups suitable for gamma-ray spectrometry. Samples of 100–200 mg dry weight were double-sealed into polyethylene bags and irradiated in a swimming pool reactor with a thermal neutron flux of 1013n·cm–2·s–1 for 44 hours. After a cooling period of 1–3 days, the samples were digested with microgram quantities of carrier in concentrated nitric acid and sulfuric acid at 150°C for 3.5 hours in a teflon bomb, then extracted as described above. The reliability of the analytical method was checked using reference materials Horse Kidney IAEA H-8, Human Hair NIES-5 and Tomato Leaves NBS-1573. Most of the results obtained for reference materials agreed with the certified values12. Chinese autopsy samples of hair and liver were presented.

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