PubMed Health⌕ Search

Biomedical subjects

Z A Guo

Publications and source records attributed to Z A Guo.

5 recordsLinked to original sources

[Study on reversed-phase high performance liquid chromatography separation condition and determination method of organic acids].

The pH values of the mobile phase which affect the chromatographic behavior of organic acids in RP-HPLC have been studied. It was considered that the problem of organic acids on an RP-HPLC column was dissociation. The equation for finding the optimum pH of mobile phase was pHlimit of colunm < or = pH < or = pKa -2. In addition the effects of contents of methanol and acetonitrile in mobile phase were studied. By using the formula the mobile phases used for the analysis of organic monobasic acids--formic, acetic, propionic and butyric acid and of organic dibasic acids--propane diacid, butane diacid, pentane diacid and hexane diacid were proposed. For the analysis of the monobasic acids, the wavelength of UV-detector was set at 210 nm and the mobile phase was a mixture of phosphate buffer solution(15 mmol/L, pH 2.1)-methanol(85:15, V/V) and at a rate of 1.5 mL/min and the column was Diamond C18, 150 mm x 4.6 mm i.d.. The average coefficient of correlation was 0.9997 and RSD was less than 0.90%. The mobile phase for organic dibasic acids was a mixture of phosphate buffer solution (20 mmol/L, pH 2.1)-methanol(75:25, V/V). The other conditions were the same as for organic monobasic acids. The average coefficient of correlation was 0.9998 and RSD was less than 0.70%.

Acetic Acid↗

[Study on chemical constituents of the essential oil from Zanthoxylum Bungeanum Maxim by gas chromatography-mass spectrometry].

The essential oil in Zanthoxylum Bungeanum Maxim was extracted by steam distillation and the distilled liquid was collected by passing through chloroform. The aqueous phase was extracted with chloroform sufficiently. The chloroform solution containing the constituents of essential oils was analyzed by gas chromatography-mass spectrometry(GC-MS). Seventeen peaks were separated by gas chromatography, and 16 of them were identified by MS with "Nist98.L" Mass Spectral Data Registry. The structures of the constituents were further verified by manual analysis. The identified constituents accounted for 97% of the peak areas of the essential oils on total ion chromatogram. The major chemical constituents of them are C9, C10 alcohols and alkenes.

Drugs, Chinese Herbal↗

Effects of MN-9202 on platelet aggregation, 5-HT release, TXB2 synthesis, and calcium mobilization in rabbit platelets in vitro.

AIM: To study the effects of MN-9202, a new effective Ca2+ channel blocker, on platelet aggregation, 5-HT and TXB2 release, and calcium transport induced by platelet activators. METHODS: The mobilization of cytosolic-free calcium induced by thrombin in washed platelets was observed by Ca(2+)-sensitive fluorescent indicator, Fura-2 AM and time scan measurement. Aggregation induced by ADP and thrombin in rabbits citrate platelet-rich plasma (PRP) was measured by aggregometer. 5-HT and TXB2 were assayed by HPLC/ECD and RIA, respectively. RESULTS: MN-9202 inhibited platelet aggregation induced by ADP and thrombin in a concentration-dependent manner. MN-9202 1 mumol.L-1 inhibited release of 5-HT in PRP induced by collagen at 15 mg.L-1 (113 +/- 15 vs 178 +/- 18, P < 0.05), however, MN-9202 did not have effect on 5-HT secreted by high dose of collagen. MN-9202 0.1 and 1 mumol.L-1 blocked extracellular calcium influx and sarcoplasmic calcium release, and the suppression on extracellular calcium influx was more obvious. Furthermore, treatment with MN-9202 0.01, 0.1, and 1 mumol.L-1 markedly decreased ADP-induced TXB2 (pg/10(8) platelet) release from PRP (906 +/- 200, 881 +/- 131, and 793 +/- 169 vs 1264 +/- 202, P < 0.01). CONCLUSION: MN-9202 acts as an effective Ca2+ antagonist and blocks platelet activation by inhibiting platelet Ca2+ influx and arachidonic acid metabolism.

Animals↗

[Determination of bentazon and 2,4-D butyl in mixture formulation by HPLC].

Bentazon and 2,4-D butyl(the active ingredients of Cao Di) were determined by reversed phase HPLC aimultancously using methanol/acetonitrile/citrate buffer(pH 3.1) as a mobile phase on Shim-pack clc-CN column. Results showed that the linear correlation and recovery of 2,4-D butyl were 1.000 and (100.2 +/- 0.8)% respectively, and those of bentazon were 1.000 and (98.6 +/- 0.9)% respectively. The coefficients of variation for bentazon and 2,4-D butyl were all was 0.37%.

2,4-Dichlorophenoxyacetic Acid↗

Direct evidence for histamine H3 receptor-mediated inhibition of norepinephrine release from sympathetic terminals of guinea pig myocardium.

AIM: To study the histamine H3 receptors mediated inhibition of norepinephrine (NE) release from cardiac sympathetic terminals of guinea pig isolated atria. METHODS: Release of NE induced by electric field stimulation (50 mA, 5 ms) in the bath solution was measured by HPLC-ECD. RESULTS: The release of NE caused by field stimulation was attenuated by (R)-alpha-methyl-histamine (alpha-MeHA, 0.1 nmol.L-1(-10) mumol.L-1) in a concentration-dependent manner. Thioperamide concentration-dependently antagonized the inhibition of alpha-MeHA. Blockade of H1, H2, alpha 2, beta 2-receptors failed to prevent the inhibitory effect of alpha-MeHA. Thioperamide (1 nmol.L-1(-10) mumol.L-1), when used alone, concentration-dependently facilitated the release of NE evoked by field stimulation. CONCLUSION: The presynaptic histamine H3-receptors inhibited the NE release from cardiac sympathetic terminals.

Adrenergic Fibers↗