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Biomedical subjects

Z Y Xiao

Publications and source records attributed to Z Y Xiao.

14 recordsLinked to original sources

Preparation of ZnO colloids by aggregation of the nanocrystal subunits.

Colloidal ZnO particles with narrow size distribution were prepared via a sol-gel process by base-catalyzed hydrolysis of zinc acetate. The morphology of ordered arrays of the particles was recorded by SEM. SEM also reveals that these uniform particles were composed of tiny ZnO subunits (singlets) sized of several nanometers. The size of the singlets, which is confirmed by X-ray diffraction and UV-vis absorption spectra, increases as the aging time is prolonged. The size-selective formation of colloids by aggregation of nanosized subunits is proposed to consist of two-stage growth by nucleation of nanosized crystalline primary particles and their subsequent aggregation into polycrystalline secondary colloids. The aggregates are all spherical because the internal rearrangement processes are fast enough. The ZnO colloids, i.e., the aggregates, tend to self-assemble into well-ordered hexagonal close-packed structures. Room-temperature photoluminescence was characterized for green and aged ZnO.

Journal Article↗

The effect of surface properties on visible luminescence of nanosized colloidal ZnO membranes.

Luminescence properties of nanosized zinc oxide (ZnO) colloids depend greatly on their surface properties, which are in turn largely determined by the method of preparation. ZnO nanoparticles in the size range from 3 to 9 nm were prepared by addition of tetramethylammonium hydroxide ((CH3)4NOH) to an ethanolic zinc acetate solution. X-ray diffraction (XRD) indicates nanocrystalline ZnO membranes with polycrystalline hexagonal wurtzite structure. The ZnO membranes have a strong visible-emission intensity and the intensity depends upon hydrolysis time. The infrared spectra imply a variety of forms of zinc acetate complexes present on the surface of ZnO particles. The effect of the ZnO membrane surface properties on photoluminescence is discussed.

Journal Article↗

[Seronegative synovitis syndrome].

3 cases of seronegative synovitis syndrome were reported. Two elderly women and one man presented with symmetrical polysynovitis of acute onset involving most of their appendicular joints and flexor digitorum tendons associated with pitting edema of the dorsum of both hands and both feet. Rheumatoid factor was absent from serum samples in all and no radiologically evident erosions developed. All the three patients had a benign course and the disease resolved completely within 2-18 months after the onset. None had deformities, erosions and/or relapse after being followed for 22-34 months. Literatures on this syndrome were reviewed.

Aged↗

[Chemical constituents of Drynaria propinqua (Wall) J. Sm].

Four compounds isolated from the rhizomes of Drynaria propinqua collected in Sichuan have been identified. One of them was a new natural product, namely propinqualin, whose structure was established as (-)-epiafzelechin-3-O-beta-D-allopyranoside. The other three were 4-O-beta-D-glucopyranosyl caffeic acid, beta-sitosterol-3-O-beta-D-glucopyranoside and sucrose.

Caffeic Acids↗

[Structure of lamiophlomiol C].

A new highly oxygenated iridoid, lamiophlomiol C isolated from the alcohol soluble fraction of the roots of Lamiophlomis rotata (Labiatae), was shown to have the molecular formula C11H14O7. On the basis of UV, IR, MS and NMR spectroscopic data, particularly X-ray crystallographlic analysis, structure I has been assigned to this iridoid.

Drugs, Chinese Herbal↗

[The structures of yiyeliangwanoside III and IV from the bark of Nothopanax davidii (France) Harms].

Two new oleanane type triterpene glycosides, named Yiyeliangwanoside III and IV, were isolated from Nothopanax davidii (France)Harms (Araliaceae). Their chemical structures were elucidated by means of chemical and spectrometric analysis. Yiyeliangwanoside III: C57H88O25, a white powder, mp 206-210 degrees C (dec.), [alpha]D + 2.73 (c 0.1, CH3OH). Its structure was determined as 3-O-alpha (2',4'-O-diacetyl)-L-arabinopyranosyl-3 beta-hydroxyolean-12-ene-28.29- dioicacid-28-O-[alpha-L-rhamnopyranosyl-(1-4)-beta-D-glucopyranosy l-(1-6)- beta-D-glucopyranosyl] ester. Yiyeliangwanoside IV: C37H56O10, a white powder, mp 267-170 degrees C (dec.), [alpha]20D + 31.55 degrees (c 0.1, CH3OH). Its structure was determined as 3-O-alpha-(2'-O-acetyl)-D-xylopyranosyl-3 beta-hydroxyolean-12-ene-28.29-dioic acid.

Drugs, Chinese Herbal↗

[Study on the chemical components from the bark of Nothopanax davidii (Franch) harms].

Two new oleanane type triterpene glycosides, named yiyeliangwanoside I and yiyeliangwanoside II, were isolated from Nothopanax davidii (Franch) Harms (Araliaceae). Their chemical structures were elucidated by means of chemical and spectrometric analysis. Yiyeliangwanoside I: C57H88O25, a white powder, mp 203-205 degrees C (dec.), [alpha]D20-3.47(c 0.1, CH3OH). Its structure was determined as 3-O-alpha-(3',4'-O-dioic-acetyl)-L-arabinopyranosyl-3 beta-hydroxyolean-12-ene-28,29-dioic acid-28-O-[alpha-L-rhamnopyranosyl-(1----6)-beta-D-glycopyranosyl- (1----4)-beta-D-glycopyranosyl] ester. Yiyeliangwanoside II: C37H56O10, a white powder, mp 240-244 degrees C (dec.), [alpha]D20+36.5(c 0.1, CH3OH). Its structure was determined as 3-O-alpha-(3'-O-acetyl)-L-arabinopyranosyl-3 beta-hydroxyolean-12-ene-28,29-dioic acid.

Drugs, Chinese Herbal↗

[Studies on the active constituents of Momordica charantia L].

Five compounds were isolated from the seeds of Momordica charantia. This paper reports their structure determination by spectral (IR, UV, HNMR, CNMR, and MS) and chemical methods. The structures of I, II, III, IV and V were elucidated as vacine, mycose, 3-O-(beta-D-glucopyranosyl)-24 beta-ethyl-5 alpha-cholesta-7, trans-22E, 25 (27)-trien-3 beta-ol, momorcharaside A and momorcharaside B respectively. Mycose was the first time found in this plant and compound III was the first time found in the genus Momordica. IV and V were new compounds. IV exhibited obvious inhibition of DNA and RNA syntheses in S 180 tumor cells in preliminary pharmacological studies.

Animals↗

[Anti-arrhythmic effects and electrophysiological properties of Ophiopogon total saponins].

The arrhythmias induced by chloroform-epinephine, BaCl2, and aconitine were prevented and antagonized by Ophiopogon total saponins (OTS) which were extracted from the root of Ophiopogon japonicus (Thunb) Ker-Gawl. The incidence of ventricular arrhythmia produced by ligation of the left anterior descending coronary artery was effectively decreased without any changes in the hemodynamic indices of dogs. The electrophysiological effects of OTS in vivo and in vitro were studied by means of contact electrode and intracellular microelectrode techniques. The results showed that OTS shortened APD10, APD50, APD90; decreased APA and Vmax of both monophasic and transmembrane action potentials. OTS also increased the ERP/APD ratio and prevented or abolished the arrhythmikinesis provoked by ouabain and aconitine. The anti-arrhythmic properties of OTS lead us to draw an inference that the anti-arrhythmic mechanism may be related to the blocking of sodium and calcium channels.

Aconitine↗

Rapid separation of flavonoids by analytical high-speed counter-current chromatography.

A commercial model of the analytical high-speed counter-current chromatography instrument was used for separation of flavonoids from a crude ethanol extract of dried fruits of sea buckthorn (Hippophae rhamnoides). Using a two-phase solvent system of chloroform-methanol-water (4:3:2), a five-fold increase in flow-rate of the mobile phase from 60 to 300 ml/h resulted in a rapid separation of five components in less than 15 min without significant loss in peak resolution. Major flavonoid component, isorhamnetin, was identified in its pure state by mass spectrometric analysis.

Countercurrent Distribution↗

Multistage evaluation scale, differential threshold steps and equivalent sensation contours of respiratory flow-resistive load sensation.

This paper presents and discusses the methodology and results of studies on respiratory sensation by using a fuzzy set category judgement model and applying the concept of just noticeable difference (JND) step and equivalent sensation. A new kind of category scale, the multistage evaluation scale (MES), based on a fuzzy set category judgement model for quantifying respiratory sensory magnitude has been put forward and verified in 37 subjects. The perceived magnitude of added resistance estimated using MES could reflect properly the difference in sensory perception caused by added loads with equal intensity but applied to different phases of the breathing cycle. In addition, the psychophysical function obtained conforms to the Stevens' power law. On the contrary, the classical category scale does not possess some of these attributes. In 9 subjects, we determined that the sensory continuum corresponding to either inspiratory or expiratory added resistive load, ranging 10-500 mm H2O.1(-1).s, consisted of 6 or 7 JND steps. The sensory magnitude corresponding to each step was estimated by the MES. Relating the results of JND step measurements with that of magnitude estimation using MES, we could elucidate systematically the relationship between perceived magnitude and discrimination for respiratory sensation. In 13 subjects, the equivalent respiratory resistive load sensation contours of 2, 3 and 4 JND step above basal level, respectively, were obtained through experimentation and by quadratic polynomial approximation of experimental data. The results suggest that as regards the human tolerance to various added resistive loads the combined resistive load is the most tolerable among the three; the expiratory, the least. The equivalent sensation contour can be used to predict the changes in respiratory sensation determined by both the intensity of the total added load and the ratio of inspiratory versus expiratory load. In brief, we have proposed a new way to elucidate the physiological and psychophysical effects of various added resistive loads.

Humans↗