ABSTRACT
In order to provide basic information for the utilization and development of famous classical formulas containing Bletillae Rhizoma, this article systematically analyzes the historical evolution of the name, origin, harvesting and processing of Bletillae Rhizoma by reviewing the ancient materia medica, prescription books, medical books and modern literature. The research results showed that Baiji(白及) was the main name, some scholars took Baiji(白芨) as its main name, and there were many other names such as Baiji(白给), Baigen(白根), Baiji(白苙). The mainstream source of Bletillae Rhizoma was the tubers of Bletilla striata, and drying, large, white, solid, root-free and skin removed completely were the good quality standards. With the promotion of wild to cultivated medicinal materials, there were certain differences between their traits, and the quality evaluation indexes should be adjusted accordingly. The origin of records in the past dynasties was widely distributed, with Guizhou and Sichuan having high production and good quality in modern times. The harvesting period is mostly in spring and autumn, and harvested in autumn was better. The processing and processing technology is relatively simple, and it was used fresh or powdered in past dynasties, while it is mainly sliced for raw use in modern times. Based on the results, it is suggested that the tubers of Bletilla striata of Orchidaceae should be used in the famous classical formulas, and it should be uniformly written as Baiji(白及). And if the original formula indicates the requirement of processing, it should be operated according to the requirement, if the requirement of processing is not indicated, it can be used in raw form as medicine.
ABSTRACT
OBJECTIVE To establis h the method for the simultaneous determination of six iridoids (loganic acid ,loganin, sweroside,dipsanoside B ,dipsanoside A ,sylvestroside Ⅰ)and one triterpene saponin (asperosaponin Ⅵ)in Dipsacus asper . METHODS High performance liquid chromatography (HPLC) method was adopted. The determination was performed on Symmetry® C18 column with mobile phase consisted of acetonitrile- 0.1% phosphoric acid solution (gradient elution )at the flow rate of 1.0 mL/min. The detection wavelengths were set at 212 nm(asperosaponin Ⅵ)and 237 nm(dipsanoside B ,dipsanoside A , sweroside,loganic acid ,sylvestroside Ⅰ,loganin). The column temperature was set at 30 ℃,and sample size was 20 μL. RESULTS The linear range of loganic acid , loganin, sweroside, sylvestroside Ⅰ , dipsanoside B , dipsanoside A and asperosaponin Ⅵ were 399.24-931.56,50.30-150.90,48.24-168.84,27.00-70.20,12.93-38.80,40.64-121.92,42.08-147.28 µg/mL (all r>0.999 0). RSDs of precision ,reproducibility and stability tests (24 h)were all less than 2%. Average recoveries were 104.43%(RSD=0.63%,n=6),101.74%(RSD=1.11%,n=6),100.76%(RSD=1.06%,n=6),98.00%(RSD=1.58%,n=6), 99.03%(RSD=2.31%,n=6),102.93%(RSD=2.26%,n=6),102.31%(RSD=1.00%,n=6),respectively,The contents were 142.5-280.6,5.5-49.0,28.0-112.9,7.2-35.8,4.4-16.9,17.2-79.3,0.8-54.5 mg/g,respectively. CONCLUSIONS Established method is accurate and reliable ,and can be used for the content determination of 7 components in D. asper .
ABSTRACT
OBJECTIVE: To improve the quality standard of Folium Mahoniae. METHODS: TLC was used for qualitative identification. The contents of moisture, ash and ethanol extract were determined. The content of berberine hydrochloride was determined by HPLC. The determination was performed on WondaSil C18 column with mobile phase consisted of acetonitrile-0. 05 mol/L monopotassium phosphate solution (25: 75, V/V) at the flow rate of 1. 0 mL/min. The detection wavelength was 264 nm, column temperature was 30 ℃, and sample size was 10 μL. RESULTS: TLC spots were clear and well-separated. The contents of moisture, total ash, acid-insoluble ash and ethanol extract were 3. 92%-7. 03%, 3. 65%-6. 95%, 0. 05%-1. 03% and 10. 87%-33. 14%, respectively. The linear range of berberine hydrochloride was 0. 183-0. 915 μg(r=0. 999 9); quantitation limit and detection limit was 0. 143, 0. 095 μg, respectively. RSDs of precision, stability and reproducibility tests were lower than 2. 0% (n=6); recovery was 95. 21% -103. 10% (RSD = 2. 95%, n=6). CONCLUSIONS: The content of moisture, total ash and acid-insoluble ash of medicinal materials is not exceed 8. 0%, 6. 0% and 0. 4%, respectively. The content of ethanol extract and berberine hydrochloride is not less than 16. 0% and 1. 0%, respectively. Established standard can be used for quality control of Folium Mahoniae.
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<p><b>OBJECTIVE</b>Seed dormancy mechanisms, breaking dormancy and the optimal germinating conditions were studied to improve reproductive efficiency and quality standard of Pseudostellaria heterophylla.</p><p><b>METHOD</b>The P. heterophylla seeds were stratified into wettish sand for 65 days under the temperature of -2-3 degrees C, embryo length and germination dynamic change of seeds were measured in prophase every other 10 days and in middle every other 5 days. The influences on seed germination and seedling growth under different temperatures, germination beds were investigated.</p><p><b>RESULT</b>The P. heterophylla seeds embryo morphology was unchanged in stratification. The seeds could not germinate at stratification within the first 35 days. The germination rate and germination energy of seeds increased with the stratification time after 35 days. Germination rate, germination energy, plant height and fresh weight under the 10 degrees C were significantly higher than those under other temperatures. Germination rate, germination energy, plant height, fresh weight and dry weight of plant in sand bed were higher than those of plant in other beds, and seed mildew rate and abnormal seedling proportion of plant in sand bed were less than those of plant in other beds.</p><p><b>CONCLUSION</b>The dormancy of P. heterophylla seeds is mainly the physiological post-maturation. The optimal germination conditions of seeds is 10 degrees C the culture of sand. The dormancy was broke under -2-3 degrees C of wettish sand for 45-50 days in practice.</p>