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AIM:To establish the method of fingerprint analysis on Shuangbai Powder(Radix et Rhizoma rhei,Cacumen platycladi,Cortex phellodendri amurensis,Herba lycopi and Herba menthae)to distinguish the characteristic fingerprint.METHODS:HPLC with ZORBAX Eclipse XDB-C_(18) was used,acetonitrile-0.1% H_3PO_4 solution(gradient elution)as a mobile phase and detection wavelength at 254 nm,flow rate was 1 mL/min,and column temperature was 40℃.RESULTS:Thirty-seven common peaks were separated from 10 batches of Shuangbai Powder.The characteristic peaks were the summation,22 peaks were from Radix et Rhizoma Rhei,6 peaks were from Cortex phellodendri Amurensis,4 peaks were from Cacumen Platycladi,3 peaks were from Herba Lycopi,and 2 peaks were from Herba Menthae,there was one new characteristic peak.CONCLUSION:Ten peaks gathered from Shanghai Powder consist of rhein,emodin,chrysophanol,aloe-emodin,physcion,gallic acid,berberine hydrochloride,palmatine;quercitrosid,and linarin.
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OBJECTIVE: To establish the GC fingerprints for Grassleaf sweetflag rhizome aetherolea and to control its quality .METHODS: The temperature at the mouth of the sample injector was 250℃ and that of the detector was 280℃, the carrier gas was nitrogen gas and the flow rate was 1.3ml/min, the GC of aetherolea in 10 batches of Grassleaf sweetflag rhizome was analyzed by adopting temperature programming.RESULTS:Altogether 6 peaks were marked out,the sum total of the average peak area of which made up(75.4?13.7)% of the total.CONCLUSION: The method is of high degree of precision, reproducibility,stability,the resolving of each component in the aetherolea is good,the established fingerprints can be used as one of the quality control index for Grassleaf sweetflag rhizome.
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OBJECTIVE:To study the chief chemical components of the ethyl acetate part of Angelicae Sinensis Decoction for Supplementing Blood Apozem.METHODS:The HPLC was adopted in which Hypersil ODS was taken as the chromato?graphic column,the Methanol-0.5%glacial acetic acid was taken as the mobile phase(gradient elution),the detective wave?length was280nm,the flow rate was1ml/min and with the column temperature set at room temperature.RESULTS:There were7characteristic peaks in the ethyl acetate part of Angelicae Sinensis Decoction for Supplementing Blood Decoction,6of which come from isoflavone of Radix Astragali and1come from ferulic acid of Angelicae Sinensis.CONCLUSION:The chief characteristic peak of the ethyl acetate part of Angelicae Sinensis Decoction for Supplementing Blood Apozem was the building up of Radix Astragali peak and angelicae sinensis peak,no other significant composition peaks were emerged.
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[Objective] To develop a method for the determination of thiamazole content in Yingqi Ling Tablets. [Methods] High performance liquid chromatography (HPLC) was used. The chromatographic conditions were: C18 Gravity Column (4.6mm ? 250mm), methanol - water (10:90 ) as mobile phase, flow rate being 1.0mL/min and the detection wavelength at 258nm. [Results] The calibration curve was linear in the range of 0.16 - 0.64?g. The average recovery was 101.01% (relative standard deviation sr = 2.21%). Relative standard deviation of precision test was 1.04% and the content of the sample was 0.4841 mg per tablet (sR = 0.78%). [ Conclusion] HPLC is effective for the determination of thiamazole content in Yingqi Ling Tablets.
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OBJECTIVE: To establish a method for the content determination of calycosin-7-O-?-D-glucoside,prim-o-glucosyl cimifugin and 4′ -O-?-D-glucosyl-5-O-methylvisammin in Yupingfeng decoction and to study the influence of different combination on the content of three compositions.METHODS:HPLC was applied and the determination was performed on Hypersil ODS(250 mm?4.0 mm,5 ?m)column.The mobile phase consisted of acetonitrile-water(gradient elution)with detection wavelength of 254 nm.RESULTS: The content of the three compositions represented little change or different deceasing tendency in the decoctions of various compatibilities.The biggest deceasing tendency of content was found in the decoctions containing Astragalus membranaceus,Saposhnikovia divaricata,and Atractylodes macrocephala.CONCLUSIONS: The content of the three compositions of different combination shows a dynamic course,which provides a reference for the rules of the compatibility and material basis of Yupingfeng decoction.
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Objective To establish the fingerprint of Yuanshi Shengmai Chenggu (YSC)Tablets by HPLC.Methods Chromatographic conditions of HPLC were as follows: Hypersil ODS2 column with temperature at 20 ℃; methanol and 1 %acetic acid glacial(gradient elution)as a mobile phase; detection wavelength at 268 nm;analytical time being 55 min and flowing rate being 1.0 mL/min.Results Twenty-five peaks were indicated on the HPLC-fingerprint of YSC Tablets. The peak area of vitexin was the biggest area in different batches of YSC Tablets, the area being 22 %～25 %. The differences of fingerprint in different batches of YSC Tablets were not obvious, which indicated the fingerprint characteristics of YSC Tablets.Conclusion The method is simple and accurate and with a good reproducibility and can be used for the quality control of YSC Tablets.
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Objective To establish a fingerprint analysis method for the medicinal slices of Radix et Rhizoma Rhei.Methods HPLC with ZORBAX Eclipse XDB-C18 was applied.The chromatographic conditions were as follows:acetonitrile-0.1 %H3PO4 solution(gradient alution) as a mobile phase and detection wavelength at 254 nm,flow rate at 1 mL?min-1,and column temperature being 40 ℃.Results Twenty-five common peaks were separated from 10 batches of medicinal slices of Radix et Rhizoma Rhei.Conclusion The method is reliable and accurate,and can be used as a quality control method for the medicinal material of Radix et Rhizoma Rhei.
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Objective To investigate the applicability of the digitized standard of GC-MS characteristic fingerprint in GC. Methods The GC-MS and GC were used to analyze the essential components of thirteen batches of Amomum villosum samples. The digitized standard of characteristic fingerprint of Amomum villosum essential oil was compared with the result of the samples detected by GC-MS and GC. Results Ten essential characteristic components have been identified in thirteen batches of Amomum villosum samples,and their relative content was (88.15?2.97)%,which are the representative components. The main components were ?-pinene,camphene,?-pinene,?-myrcene,limonene,linalol,camphor,isoborneol,borneol and borneol acetate. With the ten components as indexes,the sample similarity calculated by cosin method was 0.994～1.000 when analyzed by GC-MS and GC,0.978～0.999 when analyzed by GC-MS and the digitized standard of GC-MS characteristic fingerprint,and 0.986～0.998 when analyzed by GC and the digitized standard of GC-MS characteristic fingerprint. Conclusion The digitized standard of GC-MS characteristic fingerprint of Amomum villosum can be used in GC,which will ensure the comparison of results obtaining at different time by different types of machines,on different chromatographic columns and under different conditions. The method can be used for quality evaluation of Amomum villosum.
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Objective To establish the method for fingerprint analysis of Pericarpium Citri Reticulatae(PCR) by HPLC, and to compare the quality of PCR from different places of Guangdong. Methods HPLC with Zorbax Esclipe XDB C18 column was used. The mobile phase was composed of methanol-2% acetic acid (gradient elution), the detection wavelength was at 283 nm, the column temperature was maintained at 25 ℃ , and the flow rate was 1.0 mL? min-1. Results Seven common peaks were obtained on HPLC fingerprint of PCR. There existed certain differences in fingerprints of PCR from the different samples, but the similarities of 25 batches of samples were higher. Conclusion The method is reliable and accurate, and provides a reference for the quality control of PCR.
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Objective To develop a quantitative method to determine vitexin in Cajanus cajan (L.) Millsp. Methods The chromatographic conditions were as follows: column C18(250 mm? 4.6 mm, 5 ? m) , mobile phase being MeOH ∶ 1 % HAC (25 ∶ 75) for 20 mins and then being MeOH ∶ 1 % HAC (30 ∶ 70) after 20 mins, flow rate at 1.0 mL/min, and wavelength at 339 nm. Results The good linearity of this method was in the range of 0.104 4～ 0.522 ? g (r=0.999 4), and the average recovery of vitexin was 100.11 % ( RSD =0.63 % ).Conclusion The method is simple and sensitive with good stability, it can be suitable for the quality control of vitexin in Cajanus cajan (L.) Millsp..
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Objective To establish the method of fingerprint analysis on the fruits of Amomum villosum by HPLC and work out the characteristic fingerprint of methanol extracts in the fruits of A.villosum from Yangchun,Guangdong Province as index component which could be used for the accumulation of data to evaluate the inner quality of the fruits of A.villosum.Methods HPLC with Nucleodur C18 Gravity column was used,the methanol-2% acetic acid(gradient elution)as a mobile phase,detection wavelength at 260 nm,column temperature was 30 ℃,and flow rate was 1.0 mL/min.ResultsCommon peaks(20)were separated on HPLC fingerprint in A.villosum.The similarities of 18 batches of samples were higher.Conclusion The method is reliable and accurate,has a better reproducibility,and provides a reference for the quality control to the fruits of A.villosum.
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Object To screen the prescriptions of JIUFEN SPRAY Methods Four prescriptions were primarily obtained from 19 prescriptions of JIUFEN SPRAY on the basis of their stability and spraying effect, then the obtained four prescriptions were screened further according to transdermal rate of them Results Prescription 17th was considered to be the best as its high stability, spraying effect and transdermal rate Conclusion The optimal prescription of JIUFEN SPRAY consisted of 20% alcohol solution of sample, 3% borneol and 5% glycerine
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Objective To establish a fingerprint analysis method for Ganzhixiao Decoction. Methods RP-HPLC was applied with Phenomenex Synergi 4?Hydro-RP 80A as the chromatic column,methanol-0.1 %H3PO4 solution (gradient elution) as the mobile phase,detection wavelength at 280 nm,flow rate being 1.0 mL/min,and column temperature at 30 ℃. Results Twenty common peaks were presented in 10 batches of Ganzhixiao Decoction and the positions of 20 characteristic peaks were identified,including 5-hydroxymethyl furfural,chlorogeni C acid,Salvianolic acid B. Conclusion The method is reliable and accurate,and can provide a reference for the research of Ganzhixiao Decoction.
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Objective To establish the method of fingerprint analysis on Yupingf eng Decoction,and to study the correlation of HPLC fingerprint in Radix Astraga li,Radix Saposhnikovlae,Rhizoma Atractylodis Macrocephalae and Yupingfeng Deco ction. Methods HPLC with Hypersil ODS was used,acetonitrile -water(gradient el ution) as a mobile phase and detection wavelength at 220 nm,flow rate was 1 mL ?min-1,and column temperature was 30 ℃. Results There were 9,8 and 7 common peaks separated from 10 batches of medicinal material of Radix Astragali,Radix Saposhnikovlae,and Rhizoma Atractylodis Macrocephalae,respectively;11 common peaks were separated from 10 batches of Yupingfeng Decoction,of which 6 peaks were shared by Radix Astragali,4 peaks by Radix Saposhnikoviae and 1 peak by Rh izoma Atractylodis Macrocephalae. Conclusion There exists a correlation of Yupin gfeng decoction with the medicinal pieces of Radix Astragali and Radix Saposhnik oviae. The major characteristic fingerprint peaks of Yupingfeng decoction belong to those of the isoflavones from Radix Astragali and chromones from Radix Sapos hnikoviae. This will provide a reference for the rules of the compatibility and component research of Yupingfeng Decoction.
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Objective To determinate the content of quercitrin in Fructus Amomi by HPLC.Methods HPLC with Nucleodur C18 Gravity column was used,the acetonitrile-0.01 mol? L-1 potassium dihydrogen phosphate-acetic acid glacial(18 ∶ 82 ∶ 2)as a mobile phase and detection wavelength at 254 nm.Results The linear range of quercitrin was from 0.029 to 0.464 ? g(r=0.999 9),The average recovery of quercitrin was 99.27 % with a RSD of 1.00 %.Conclusion The method is simple,accurate,and can be used as a quality control method for Amomum villosum Lour.
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Object To establish the fingerprint of isoflavones and ferulic acid of Danggui Buxue decoction.Methods HPLC with Hypersil ODS column was adopted,the methanol-0.2 % acetic acid glacial(gradient elution) as mobile phase with a flow rate of 1mL/min and detecting wavelength at 254 nm.Results There were 10 main peaks in Danggui Buxie decoction,9 of them came from Radix astragali and 3 came from Radix angelicae sinensis.Conclusion This fingerprint can be used as a reference for the stability of the isoflavones and ferulic acid in Danggui Buxue decoction.
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Objective To study the process conditions of purifying the total flavonoids from Cacumen Platycladi by AB-8 resin. Methods Spectrophotometric method was used to detect the total flavonoids,and HPLC was used to determine quercitrin and analyze the characteristic peaks of Fingerprint. Results The purification effect was satisfactory when the concentration of original solution of the extract of Cacumen Platycladi was 0.20 g?mL-1,the loading amount was 0.375 g of Cacumen Platycladi per 1 mL of wet AB-8 resin,the adsorption velocity was 1 mL?min-1,the eluant was 70 %alcohol being 4 times as much as the resin volume,and the elution velocity was 2 mL?min-1. AB-8 resin could be used for 3 times repeatedly after being reproduced by 95 %of ethanol and 1 moL?L-1 of natrium hydroxydatum (NaOH). The remaining rate of the total flavonoids and quercitrin was over 70 %and 95 %respectively,and the remaining rate of peaks 1～3 was over 90 %. After being purified by the B-8 resin,the contents of the total flavonoids and quercitrin were raised 2.48 times and 3.29 times more than those before purification respectively. Conclusion AB-8 resin is fit for separating and purifying the total flavonoids from Cacumen Platycladi.
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AIM:To establish the method of fingerprint analysis on Shuangbai Powder(Radix et Rhizoma rhei,Cacumen platycladi,Cortex phellodendri amurensis,Herba lycopi and Herba menthae) to distinguish the characteristic fingerprint.METHODS:HPLC with ZORBAX Eclipse XDB-C18 was used,acetonitrile-0.1% H3PO4 solution(gradient elution) as a mobile phase and detection wavelength at 254 nm,flow rate was 1 mL/min,and column temperature was 40 ℃.RESULTS:Thirty-seven common peaks were separated from 10 batches of Shuangbai Powder.The characteristic peaks were the summation,22 peaks were from Radix et Rhizoma Rhei,6 peaks were from Cortex phellodendri Amurensis,4 peaks were from Cacumen Platycladi,3 peaks were from Herba Lycopi,and 2 peaks were from Herba Menthae,there was one new characteristic peak.CONCLUSION:Ten peaks gathered from Shangbai Powder consist of rhein,emodin,chrysophanol,aloe-emodin,physcion,gallic acid,berberine hydrochloride,palmatine;quercitrosid,and linarin.
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AIM: To establish a method of fingerprint analysis on Cacumen Platycladi. METHODS: HPLC was adopted with ZORBAX Eclipse XDB-C18,acetonitrile-0. 1% H3PO4 solution (gradient alution) as a mobile phase and detection wavelength at 254 nm,flow rate was 1 mL/min,and colum temperature was at 40 ℃. RESULTS: Eleven common peaks were separated from 14 batches of Cacumen Platycladi. As compared with standard sample,quecitroside and quecitin were checked out. CONCLUSION: The method is reliable,accurate and can be used as a quality control method for Cacumen Platycladi.
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AIM:To establish the method of fingerprint analysis on Yupingfeng Decoction(Radix Astragali,Radix Saposhnikoviae,Rhizoma Atractylodis macrocephalae),work out the characteristic fingerprint,and study the influence of various compatibilities on fingerprint peaks.METHODS:HPLC with Hypersil ODS was used,acetonitrile-water(gradient elution)as a mobile phase and detection wavelength was at 220 nm,flow rate was 1 mL/min,and column temperature was at 30 ℃.RESULTS:11 common peaks were separated in 10 batches of Yupingfeng Decoction.A little influence on characteristic peaks was found in various compatibilities,but there was no new characteristic peak.The characteristic peaks were the summabilty,peak 2,5,6,8,9,10 were from Radix Astragali,peak 1,3,4,7 were from Radix Saposhnikoviae and peak 11 was from Rhizoma Atractylodis macrocephalae.CONCLUSION:The method is reliable,accurate and provides for further reference compatibility and material base of Yupingfeng Decoction.
