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1.
Chinese Journal of Experimental Traditional Medical Formulae ; (24): 138-145, 2022.
Article in Chinese | WPRIM | ID: wpr-940528

ABSTRACT

ObjectiveTo establish an integrated method of fingerprint qualitative, multi-component quantitative analysis and chemometrics, and to evaluate the quality attributes and differences of Aurantii Fructus from different production areas and origins. MethodAnalysis was performed on COSMOSIL 5C18-MS-Ⅱ column (4.6 mm×250 mm, 5 μm) with the mobile phase of acetonitrile-0.2% phosphoric acid solution for gradient elution (0-4 min, 19%A; 4-5 min, 19%-21%A; 5-18 min, 21%A; 18-19 min, 21%-28%A; 19-27 min, 28%A; 27-28 min, 28%-40%A; 28-36 min, 40%A; 36-37 min, 40%-50%A; 37-42 min, 50%-60%A; 42-46 min, 60%-95%A; 46-55 min, 95%-100%A), the flow rate was 1 mL·min-1, the column temperature was 30 ℃, the detection wavelength was set at 320 nm, and the injection volume was 10 μL. High performance liquid chromatography (HPLC) fingerprints of Aurantii Fructus from different production areas and origins were established. Then, the quality of 26 batches of samples was evaluated by cluster analysis (CA), principal component analysis (PCA) and orthogonal partial least squares discriminant analysis (OPLS-DA). A method for the determination of 12 components was developed and verified, and a thermal map-based CA of Aurantii Fructus from different production areas and origins was carried out based on the content difference of samples. ResultThe fingerprint and determination methods were well verified. The similarity of HPLC fingerprint of 12 batches of Aurantii Fructus was 0.85-0.996, 20 common peaks were calibrated and 14 of them were assigned. The resolution and linear relationship of 12 components in quantitative analysis were good. The recovery rates were 99.2%-101.0% with RSD≤2.0%. The results of CA, PCA and OPLS-DA indicated that the differentiation of Aurantii Fructus in different production areas was great, and there were differences among different cultivars. ConclusionThe qualitative analysis of fingerprint and quantitative analysis of multiple indexes based on the same chromatographic analysis conditions are convenient, accurate and reliable, and combined with chemometrics, the identification and quality analysis of Aurantii Fructus from different production areas and origins can be realized, which can provide reference for quality control and evaluation of Aurantii Fructus.

2.
Chinese Journal of Experimental Traditional Medical Formulae ; (24): 130-136, 2021.
Article in Chinese | WPRIM | ID: wpr-905842

ABSTRACT

Objective:To establish a high performance liquid chromatography (HPLC) fingerprint of the substance benchmark of Xiao Chengqitang and evaluate its quality with chemical pattern recognition method. Method:Diamonsil C<sub>18</sub> column (4.6 mm×150 mm, 5 μm) was used, mobile phase was consisted of methanol (A)-0.1% phosphoric acid solution (B) for gradient elution (0-60 min, 20%-90%A; 60-70 min, 90%-100%A), the flow rate was 1 mL·min<sup>-1</sup>, the column temperature was 25 ℃, and the detection wavelength was 254 nm. The similarity evaluation system of chromatographic fingerprint of traditional Chinese medicine (2012 edition) was used to evaluate the similarity of HPLC fingerprint of 15 batches of substance benchmark of Xiao Chengqitang, and the chromatographic data were analyzed by cluster analysis, principal component analysis and orthogonal partial least squares-discriminant analysis, in order to evaluate the quality difference between different batches of substance benchmarks of Xiao Chengqitang and find out the main chemical components that caused the quality difference. Result:The HPLC fingerprint of Xiao Chengqitang substance benchmarks was established, 31 common peaks were identified, and 18 components were identified by comparing with the reference substances. The similarities of 15 batches of HPLC fingerprint of Xiao Chengqitang substance benchmarks were >0.92. The samples could be divided into two categories by three chemical pattern recognition methods. Nine main components leading to the quality discrepancy of samples between batches were screened out, including rhein, chrysophanol-8-<italic>O</italic>-<italic>β</italic>-<italic>D</italic>-glucoside, aloe-emodin-8-<italic>O</italic>-<italic>β</italic>-<italic>D</italic>-glucoside, sennoside A, chrysophanol-1-<italic>O</italic>-<italic>β</italic>-<italic>D</italic>-glucoside, rhein-8-<italic>O</italic>-glucoside and others. Conclusion:The established fingerprint analysis method is accurate, stable and reproducible, which basically reflects the overall chemical composition characteristics of Xiao Chengqitang, and can be used for the quality control of Xiao Chengqitang preparations.

3.
Chinese Journal of Experimental Traditional Medical Formulae ; (24): 241-250, 2020.
Article in Chinese | WPRIM | ID: wpr-872816

ABSTRACT

Xiao Chengqitang, derived from Treatise on Febrile Diseases, is composed of Rhei Radix et Rhizoma, Magnoliae Officinalis Cortex and Aurantii Fructus Immaturus. It is often used to treat Yangming Fushi light syndrome. This formula was included in the Catalogue of Ancient Classical Prescription (The First Batch), which has a high clinical application value. Current researches on the chemical composition, pharmacological effect and clinical application of Xiao Chengqitang have been carried out, but the history of Xiao Chengqitang is unclear and the dose conversation method is vague. It has great difficulties in clinical rational applications of Xiao Chengqitang and the research and development of its compound preparations. In this article, the literature reports on Xiao Chengqitang were summarized from the aspects of historical evolution, literature researching of Chinese herbs, dosage conversation method, modern research in case to clarify the historical context of Xiao Chengqitang and to provide basis for the clinical application and modern scientific research of this formula.

4.
Chinese Journal of Experimental Traditional Medical Formulae ; (24): 161-172, 2020.
Article in Chinese | WPRIM | ID: wpr-872773

ABSTRACT

Objective:To study the serum pharmacochemistry of Aurantii Fructus (AF), and to investigate the pharmacological material basis of AF extract in rats. Method:Rapid identification and speculation of the prototype constituents and their metabolites in vivo were carried out according to the relative retention time, accurate relative molecular mass, cleavage fragments of MS/MS and neutral loss of metabolites with ultrahigh performance liquid chromatography-quadrupole-time-of-flight tandem mass spectrometry (UPLC-Q-TOF/MS) technique by comparing the differences between different samples such as AF extracts, blank plasma, and administered plasma under the same chromatographic and mass spectrometric conditions. Result:After oral administration of the AF extract, 74 transitional constituents absorbed into the blood were detected in serum, in which 49 compounds were prototype constituents and the other 25 were metabolites. The prototype constituents could be divided into dihydroflavones, polymethoxyflavonoids, limonins, coumarins and alkaloids. The identified metabolites included glucuronic acid conjugates, sulfuric acid conjugates, hydroxylated products of flavonoid glycosides and polymethoxyflavonoids, as well as the simultaneous glucuronidation and sulfation products. Conclusion:The constituents absorbed into the blood and their metabolites may be the pharmacodynamic components of AF. Among them, alkaloids, polymethoxyflavonoids and coumarins are mainly introduced into the blood in the prototype form, while naringin and neohesperidin (the index components) exert effect mainly through hydrolysis into aglycones. This work will help to further elucidate the material basis of AF.

5.
Acta Pharmaceutica Sinica ; (12): 256-260, 2012.
Article in Chinese | WPRIM | ID: wpr-323048

ABSTRACT

This study is to investigate the effect of ferulic acid on learning and memory impairments of vascular dementia (VD) rats and its mechanism of action. VD rats model was replicated by permanent bilateral common carotid artery occlusion (2VO). The learning and memory capability of VD rats was evaluated by Morris water maze. The activity of acetylcholinesterase (AChE) and superoxide dismutase (SOD) and the content of glutamic acid (Glu) and malondialdehyde (MDA) in hippocampus of VD rats' brain were determined, separately. The results showed that ferulic acid could alleviate learning and memory deficits of VD rats significantly. Ferulic acid was found to inhibit the activity of AChE and increased the activity of SOD in rat hippocampus. In addition, ferulic acid could also decrease the content of Glu and MDA in rat hippocampus. These results suggested that ferulic acid could alleviate VD rats' learning and memory deficits, which might be due to antioxidation, the improvement of cholinergic system in brain, or the inhibitory of nerve injury by excitatory amino acids.


Subject(s)
Animals , Male , Rats , Acetylcholinesterase , Metabolism , Anticoagulants , Pharmacology , Therapeutic Uses , Coumaric Acids , Pharmacology , Therapeutic Uses , Dementia, Vascular , Metabolism , Glutamic Acid , Metabolism , Hippocampus , Metabolism , Malondialdehyde , Metabolism , Maze Learning , Memory , Memory Disorders , Drug Therapy , Random Allocation , Rats, Sprague-Dawley , Superoxide Dismutase , Metabolism
6.
China Journal of Chinese Materia Medica ; (24): 899-901, 2002.
Article in Chinese | WPRIM | ID: wpr-271845

ABSTRACT

<p><b>OBJECTIVE</b>This paper reports a HPLC method for determinition of strychnine and brucine in Semen Strychni and its processed products of Jiangxi method and innovated methed.</p><p><b>METHOD</b>SiO2 was used as the stationary phase, n-hexane-dichloromethane-methanol-ammonia(47.5:47.5:5:0.35) as the mobile phase, with detection wavelength of 254 nm.</p><p><b>RESULT</b>The contents of strychnine and brucine in the processed products of Jiangxi are lower.</p><p><b>CONCLUSION</b>This method is accurate, simple and reliable.</p>


Subject(s)
Chromatography, High Pressure Liquid , Hot Temperature , Plants, Medicinal , Chemistry , Seeds , Chemistry , Strychnine , Strychnos nux-vomica , Chemistry , Technology, Pharmaceutical , Methods
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