[Objectives]To develop an HPLC fingerprint analysis method for the medicinal material of Lysimachia foenum-graecum Hance,thereby providing a foundation for its quality control.[Methods]Samples of L.foenum-graecum coll...[Objectives]To develop an HPLC fingerprint analysis method for the medicinal material of Lysimachia foenum-graecum Hance,thereby providing a foundation for its quality control.[Methods]Samples of L.foenum-graecum collected from 10 distinct locations in Guangxi were analyzed using HPLC,and chromatographic fingerprints were established.The Similarity Evaluation System for Chromatographic Fingerprint of Traditional Chinese Medicine(2012 Edition)was employed for common peak calibration and similarity evaluation.Additionally,principal component analysis was performed on the common peak area data.[Results]An HPLC fingerprint of L.foenum-graecum was developed,identifying a total of 13 common peaks.Among these,four characteristic components were specifically identified:chlorogenic acid,myricetin,quercetin,and kaempferol.The kaempferol chromatographic peak,exhibiting good resolution and a stable peak shape,was selected as the reference peak.The similarity indices between the fingerprints of the 10 sample batches and the reference fingerprint ranged from 0.954 to 0.995,indicating a relatively high consistency in the chemical composition of L.foenum-graecum from different origins.Principal component analysis identified two principal components,which together accounted for 89.45%of the cumulative variance,effectively capturing the primary chemical differences among the samples.[Conclusions]The established HPLC fingerprint method is straightforward to implement,stable,reliable,and exhibits high specificity.When combined with similarity evaluation and principal component analysis,it offers a scientific basis for developing quality standards for L.foenum-graecum medicinal materials.展开更多
A reliable and accurate HPLC/UV method was developed for the quantitative determination of astragaloside IV in ＇Huang-Qi-Si-Wu＇ Capsules, a widely used prescription of traditional Chinese medicines （TCM）. The chro...A reliable and accurate HPLC/UV method was developed for the quantitative determination of astragaloside IV in ＇Huang-Qi-Si-Wu＇ Capsules, a widely used prescription of traditional Chinese medicines （TCM）. The chromatographic separation conditions employed for HPLC/UV were optimized using a Hypersil-ODS column （250 mm^4.6 mm, 5.0 pm） with isocratic elution. Acetonitrile-water （32：68, v/v） were used as the mobile phase pumped at a flow rate of 1.0 mL/min and a detection wavelength at 203 nm was used. The method was fully validated with respect to linearity, precision, accuracy, specificity and robustness. The validated method was applied successfully to the quantification of astragaloside IV in the extract of ＇Huang-Qi- Si-Wu＇ Capsules from different production batches. The results indicate that the established HPLC/UV method is suitable for the quantitative analysis and quality control of ＇Huang-Qi-Si-Wu＇ Capsules and other related botanical drugs.展开更多
The root of Hedysarum multijugum（RHM） is recorded as a folk herbal medicine in China and is sometimes used as a substitute for Hedysari Radix, which is a famous traditional Chinese medicine derived from the roots of...The root of Hedysarum multijugum（RHM） is recorded as a folk herbal medicine in China and is sometimes used as a substitute for Hedysari Radix, which is a famous traditional Chinese medicine derived from the roots of Hedysarum polybotrys. In the present study, a sensible, reliable, and reproducible HPLC-DAD fingerprint analysis method for RHM was developed and then subsequently applied to analyze RHM samples from different origins. The chemical constituents of the RHM samples were generally consistent, although it was slightly affected by the local environment of the plant. In addition, the chemical constituency of RHM was shown to be significantly different from that of Hedysari Radix, suggesting that RHM is not suitable as a substitute for Hedysari Radix, at least from the chemical point of view.展开更多
Aim To study the correlation between the HPLC fingerprints and in vitro antibacterial activities of EtOAc extracts of Radix isatidis from various sources. Methods Ten batches of Radix isatidis EtOAc extracts were anal...Aim To study the correlation between the HPLC fingerprints and in vitro antibacterial activities of EtOAc extracts of Radix isatidis from various sources. Methods Ten batches of Radix isatidis EtOAc extracts were analyzed with HPLC and the fingerprints were established. The influence of EtOAc extracts on the thermogenic curve of growth of Escherchia coli was obtained by microcalorimetry. The chemical differences of EtOAc extracts of Radix isatidis from various sources in the HPLC fingerprints were probed with hierarchical clustering analysis and similarity analysis. The correlation between the HPLC fingerprints and in vitro antibacterial activities was analyzed with multivafiant correlation analysis. Results Close correlation existed between the HPLC fingerprints and in vitro antibacterial activities of EtOAc extracts of Radix isatidis. Conlusion The combination of HPLC fingerprints and antibacterial activities can be used to discover principle components of Radix isatidis on bioactivity.展开更多
For quality control purpose, an approach of fingerprinting and simultaneous quantification of five major bioactive constituents of Rhizoma Coptidis was established via a high-performance liquid chromatograph coupled w...For quality control purpose, an approach of fingerprinting and simultaneous quantification of five major bioactive constituents of Rhizoma Coptidis was established via a high-performance liquid chromatograph coupled with a photodiode array UV detector（HPLC-DAD） and an electrospray ionization mass spectrometer（HPLC-ESI/MS） The compounds were identified on the basis of the comparison of their mass spectra with literature data and those of standard samples and quantified by the HPLC-DAD method. Baseline separation was achieved on an XTerra C18 column（5 μm, 250 mm×4.6 mm i. d.） with linear gradient elution of formate buffer（consisting of 0.5% formic acid, adjusted to pH=4.5 with ammonia） and acetonitrile（consisting of 0.2% formic acid and 0.2% triethylamine）. The me- thod was validated for linearity（r^2〉0.9995）, repeatability（RSD〈3.1%）, intra- and inter-day precision（RSD〈1.8%） with recovery（99.9%-105.1%）, limits of detection（0.15-0.35 μg/mL）, and limits of quantification（0.53-0.82 μg/mL）. The similarities of 32 batches of Rhizoma Coptidis and their classification according to their manufacturers were based on the retention time and peak areas of the characteristic compounds. The five compounds were selected for quality assessment ofRhizoma coptidis via partial least squares analysis（PLS）.展开更多
Glycerides are first separated to classes of triglycerides(TGs), diglycerides(DGs) and monoglycerides(MGs) by normal phase HPLC on silica gel column. Individual triglyceride separation is then achieved by non-aqueous ...Glycerides are first separated to classes of triglycerides(TGs), diglycerides(DGs) and monoglycerides(MGs) by normal phase HPLC on silica gel column. Individual triglyceride separation is then achieved by non-aqueous reversed phase(NARP) HPLC on C_(18) column with UV detection at 215nm.展开更多
Sun Guoxiang, Ding Nan, Song Yuqing, Wang Zhen, Song Liangwei. Determination of Guaiacol salicylate in Guacetisal by HPLCmethod and qualitative identification of relevant substances by HPLC-MS
Medicinal materials Ma Chenchen, Li Bailin, Ou Jie, Wang Jing, Zhao Junhong. Detection of N-acyl-homoserine lactones class signal molecules of quorum sensing secreted by bacteria using high performance liquid chromato...Medicinal materials Ma Chenchen, Li Bailin, Ou Jie, Wang Jing, Zhao Junhong. Detection of N-acyl-homoserine lactones class signal molecules of quorum sensing secreted by bacteria using high performance liquid chromatography-mass spectrometry/ mass spectrometry展开更多
基金Supported by 2023 Self-funded Research Project of the Guangxi Zhuang Autonomous Region Administration of Traditional Chinese Medicine(GXZYL20230369)2022 Internal Talent Research Project of Affiliated Hospital of Youjiang Medical University for Nationalities(Y202210319).
文摘[Objectives]To develop an HPLC fingerprint analysis method for the medicinal material of Lysimachia foenum-graecum Hance,thereby providing a foundation for its quality control.[Methods]Samples of L.foenum-graecum collected from 10 distinct locations in Guangxi were analyzed using HPLC,and chromatographic fingerprints were established.The Similarity Evaluation System for Chromatographic Fingerprint of Traditional Chinese Medicine(2012 Edition)was employed for common peak calibration and similarity evaluation.Additionally,principal component analysis was performed on the common peak area data.[Results]An HPLC fingerprint of L.foenum-graecum was developed,identifying a total of 13 common peaks.Among these,four characteristic components were specifically identified:chlorogenic acid,myricetin,quercetin,and kaempferol.The kaempferol chromatographic peak,exhibiting good resolution and a stable peak shape,was selected as the reference peak.The similarity indices between the fingerprints of the 10 sample batches and the reference fingerprint ranged from 0.954 to 0.995,indicating a relatively high consistency in the chemical composition of L.foenum-graecum from different origins.Principal component analysis identified two principal components,which together accounted for 89.45%of the cumulative variance,effectively capturing the primary chemical differences among the samples.[Conclusions]The established HPLC fingerprint method is straightforward to implement,stable,reliable,and exhibits high specificity.When combined with similarity evaluation and principal component analysis,it offers a scientific basis for developing quality standards for L.foenum-graecum medicinal materials.
基金Scientific and Technological Innovation Project Foundation of Shanxi,China(Grant No.20090321099)
文摘A reliable and accurate HPLC/UV method was developed for the quantitative determination of astragaloside IV in ＇Huang-Qi-Si-Wu＇ Capsules, a widely used prescription of traditional Chinese medicines （TCM）. The chromatographic separation conditions employed for HPLC/UV were optimized using a Hypersil-ODS column （250 mm^4.6 mm, 5.0 pm） with isocratic elution. Acetonitrile-water （32：68, v/v） were used as the mobile phase pumped at a flow rate of 1.0 mL/min and a detection wavelength at 203 nm was used. The method was fully validated with respect to linearity, precision, accuracy, specificity and robustness. The validated method was applied successfully to the quantification of astragaloside IV in the extract of ＇Huang-Qi- Si-Wu＇ Capsules from different production batches. The results indicate that the established HPLC/UV method is suitable for the quantitative analysis and quality control of ＇Huang-Qi-Si-Wu＇ Capsules and other related botanical drugs.
基金Quality Standards for Chinese Medicines of Chinese Pharmacopeia 2010 edition(Grant No.YZ-029)National Natural Science Foundation of China(Grant No.21372015)
文摘The root of Hedysarum multijugum（RHM） is recorded as a folk herbal medicine in China and is sometimes used as a substitute for Hedysari Radix, which is a famous traditional Chinese medicine derived from the roots of Hedysarum polybotrys. In the present study, a sensible, reliable, and reproducible HPLC-DAD fingerprint analysis method for RHM was developed and then subsequently applied to analyze RHM samples from different origins. The chemical constituents of the RHM samples were generally consistent, although it was slightly affected by the local environment of the plant. In addition, the chemical constituency of RHM was shown to be significantly different from that of Hedysari Radix, suggesting that RHM is not suitable as a substitute for Hedysari Radix, at least from the chemical point of view.
文摘Aim To study the correlation between the HPLC fingerprints and in vitro antibacterial activities of EtOAc extracts of Radix isatidis from various sources. Methods Ten batches of Radix isatidis EtOAc extracts were analyzed with HPLC and the fingerprints were established. The influence of EtOAc extracts on the thermogenic curve of growth of Escherchia coli was obtained by microcalorimetry. The chemical differences of EtOAc extracts of Radix isatidis from various sources in the HPLC fingerprints were probed with hierarchical clustering analysis and similarity analysis. The correlation between the HPLC fingerprints and in vitro antibacterial activities was analyzed with multivafiant correlation analysis. Results Close correlation existed between the HPLC fingerprints and in vitro antibacterial activities of EtOAc extracts of Radix isatidis. Conlusion The combination of HPLC fingerprints and antibacterial activities can be used to discover principle components of Radix isatidis on bioactivity.
基金Supported by the National Natural Science Foundation of China(No.30725045)Shanghai Leading Academic Discipline Project (No.B906)in part by the Scientific Foundation of Shanghai China(Nos.07DZ19728, 06DZ19717 and 06DZ19005)
文摘For quality control purpose, an approach of fingerprinting and simultaneous quantification of five major bioactive constituents of Rhizoma Coptidis was established via a high-performance liquid chromatograph coupled with a photodiode array UV detector（HPLC-DAD） and an electrospray ionization mass spectrometer（HPLC-ESI/MS） The compounds were identified on the basis of the comparison of their mass spectra with literature data and those of standard samples and quantified by the HPLC-DAD method. Baseline separation was achieved on an XTerra C18 column（5 μm, 250 mm×4.6 mm i. d.） with linear gradient elution of formate buffer（consisting of 0.5% formic acid, adjusted to pH=4.5 with ammonia） and acetonitrile（consisting of 0.2% formic acid and 0.2% triethylamine）. The me- thod was validated for linearity（r^2〉0.9995）, repeatability（RSD〈3.1%）, intra- and inter-day precision（RSD〈1.8%） with recovery（99.9%-105.1%）, limits of detection（0.15-0.35 μg/mL）, and limits of quantification（0.53-0.82 μg/mL）. The similarities of 32 batches of Rhizoma Coptidis and their classification according to their manufacturers were based on the retention time and peak areas of the characteristic compounds. The five compounds were selected for quality assessment ofRhizoma coptidis via partial least squares analysis（PLS）.
文摘Glycerides are first separated to classes of triglycerides(TGs), diglycerides(DGs) and monoglycerides(MGs) by normal phase HPLC on silica gel column. Individual triglyceride separation is then achieved by non-aqueous reversed phase(NARP) HPLC on C_(18) column with UV detection at 215nm.
文摘Sun Guoxiang, Ding Nan, Song Yuqing, Wang Zhen, Song Liangwei. Determination of Guaiacol salicylate in Guacetisal by HPLCmethod and qualitative identification of relevant substances by HPLC-MS
文摘Medicinal materials Ma Chenchen, Li Bailin, Ou Jie, Wang Jing, Zhao Junhong. Detection of N-acyl-homoserine lactones class signal molecules of quorum sensing secreted by bacteria using high performance liquid chromatography-mass spectrometry/ mass spectrometry
