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基于HPLC指纹图谱及一测多评法评价苓桂术甘汤质量
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作者 林学玉 丁子涵 +6 位作者 周嘉浩 龚佳龄 颜卉 凌菲菲 杨凤林 李玲 张彤 《中成药》 北大核心 2026年第1期1-9,共9页
目的评价苓桂术甘汤质量。方法分析采用BP C_(18)Plus色谱柱(250 mm×4.6 mm,5μm);流动相0.1%磷酸-乙腈,梯度洗脱;体积流量0.8 mL/min;柱温30℃;检测波长220 nm。建立基准样品、现代制剂、传统高压锅代煎样品、智能代煎样品(各3批)... 目的评价苓桂术甘汤质量。方法分析采用BP C_(18)Plus色谱柱(250 mm×4.6 mm,5μm);流动相0.1%磷酸-乙腈,梯度洗脱;体积流量0.8 mL/min;柱温30℃;检测波长220 nm。建立基准样品、现代制剂、传统高压锅代煎样品、智能代煎样品(各3批)HPLC指纹图谱。以甘草苷为内标,计算芹糖甘草苷、肉桂酸、桂皮醛、甘草酸、白术内酯Ⅲ、白术内酯Ⅱ相对校正因子,一测多评法测定其含量。再进行主成分分析、聚类分析。结果12批样品指纹图谱中有26个共有峰,相似度均大于0.95,其中智能代煎样品与基准样品的相似度最高。7种成分在各自范围内线性关系良好(r≥0.9996),平均加样回收率90.72%~104.16%,RSD 0.48%~6.11%,一测多评法所得结果与外标法接近。各批样品聚为2类,现代制剂、智能代煎样品对基准样品的还原度较高。结论该方法稳定可靠,可用于苓桂术甘汤各用药形式的质量控制,其智能代煎样品可最大程度还原基准样品的物质基础分布。 展开更多
关键词 苓桂术甘汤 质量评价 hplc指纹图谱 一测多评 主成分分析 聚类分析
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基于HPLC指纹图谱结合化学模式识别及多成分定量测定的当归酒炙前后质量评价
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作者 赵美茜 姚雪莲 +7 位作者 杨明 祝婧 陆兔林 管咏梅 兰智慧 刘乐灵 赵子波 臧振中 《中草药》 北大核心 2026年第1期64-72,共9页
目的建立生当归Angelicae Sinensis Radix及酒当归HPLC指纹图谱,并结合多元统计分析和定量测定研究当归酒炙前后化学成分的变化,为当归质量评价提供参考。方法采用HPLC法建立生当归及酒当归指纹图谱,并测定其中5-羟甲基糠醛(5-hydroxyme... 目的建立生当归Angelicae Sinensis Radix及酒当归HPLC指纹图谱,并结合多元统计分析和定量测定研究当归酒炙前后化学成分的变化,为当归质量评价提供参考。方法采用HPLC法建立生当归及酒当归指纹图谱,并测定其中5-羟甲基糠醛(5-hydroxymethylfurfural,5-HMF)、绿原酸、香草醛、阿魏酸、藁本内酯的含量。采用中药色谱指纹图谱相似度评价系统计算相似度,标定共有峰并进行指认及归属,以当归酒炙前后共有峰峰面积为指标,运用层次聚类分析(hierarchical cluster analysis,HCA)、主成分分析(principal component analysis,PCA)及正交偏最小二乘-判别分析(orthogonal partial least squares-discriminant analysis,OPLS-DA),评价当归酒炙前后内在质量差异,寻找其主要差异性成分。结果建立了10批次生当归和酒当归HPLC指纹图谱,其中生当归共标定了11个共有峰,酒当归共标定了12个共有峰,生、酒当归指纹图谱相似度均>0.960。化学模式识别筛选出色谱峰12(藁本内酯)、7、11、6号峰(阿魏酸)可能是影响当归酒炙前后质量差异的标志物。含量测定结果表明,当归酒炙后新生成5-HMF成分,阿魏酸、绿原酸、香草醛成分含量整体略微下降,藁本内酯成分含量整体有所上升。结论建立的当归酒炙前后指纹图谱及多成分定量测定方法稳定、可靠,可为生当归及酒当归的质量控制和综合利用提供参考。 展开更多
关键词 当归 酒当归 hplc 指纹图谱 化学计量学 5-羟甲基糠醛 绿原酸 香草醛 阿魏酸 藁本内酯 质量评价 层次聚类分析 主成分分析 正交偏最小二乘-判别分析
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基于HPLC指纹图谱和含量测定的潞党参口服液质量评价
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作者 孙妮妮 刘彩霞 +3 位作者 莫雅丹 杜晨晖 董露露 裴香萍 《中国新药杂志》 北大核心 2026年第1期93-99,共7页
目的:建立潞党参口服液HPLC指纹图谱,同时测定口服液中紫丁香苷、党参炔苷宁、党参炔苷、党参炔醇、白术内酯Ⅲ的含量,并对其进行质量评价。方法:采用DiKMAC_(18)色谱柱(250 mm×4.6 mm,5μm),乙腈-0.1%乙酸溶液为流动相,梯度洗脱;... 目的:建立潞党参口服液HPLC指纹图谱,同时测定口服液中紫丁香苷、党参炔苷宁、党参炔苷、党参炔醇、白术内酯Ⅲ的含量,并对其进行质量评价。方法:采用DiKMAC_(18)色谱柱(250 mm×4.6 mm,5μm),乙腈-0.1%乙酸溶液为流动相,梯度洗脱;体积流量1.0 mL·min^(-1),柱温25℃,检测波长220、215、267 nm,进样量20μL。结果:建立的潞党参口服液指纹图谱中有10个共有峰,各批次样品间相似度>0.981;紫丁香苷、党参炔苷宁、党参炔苷、党参炔醇、白术内酯Ⅲ含量分别为0.032~0.054、0.030~0.041、0.066~0.112、0.006~0.013、0.005~0.010 mg·mL^(-1);5种成分分别在各自范围内线性关系良好(r≥0.9991),精密度、重复性、24 h稳定性试验RSD均<3.000%,5种成分平均加样回收率为97.701%~101.636%,RSD为1.347%~2.551%。结论:该方法稳定性、重复性良好,为完善提升潞党参口服液的质量评价方法提供了科学依据。 展开更多
关键词 潞党参口服液 hplc 指纹图谱 多指标成分定量 质量评价
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Quantitative analysis of astragaloside IV in traditional Chinese medicine‘Huang-Qi-Si-Wu' Capsules by HPLC/UV 被引量:6
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作者 张艳利 杨兴鑫 李晓妮 《Journal of Chinese Pharmaceutical Sciences》 CAS 2010年第3期223-228,共6页
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
关键词 hplc/UV Quantitative analysis Astragaloside IV Radix Astragali 'Huang-Qi-Si-Wu' Capsules
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Chemical analysis of the Hedysarum multijugum root by HPLC fingerprinting
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作者 刘毅 王伟 +3 位作者 赵玉英 陈虎彪 梁鸿 张庆英 《Journal of Chinese Pharmaceutical Sciences》 CAS CSCD 2015年第10期654-659,共6页
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
关键词 Hedysarum multijugum HEDYSARUM hplc fingerprint Quality analysis Species identification
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Correlation analysis between the HPLC fingerprints and in vitro antibacterial activity of ethyl acetate extracts from Radix isatidis
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作者 孔维军 赵艳玲 +2 位作者 山丽梅 肖小河 郭伟英 《Journal of Chinese Pharmaceutical Sciences》 CAS 2007年第4期282-287,共6页
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
关键词 Radix isatidis hplc Fingerprint Antibacterial activity Correlation analysis
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基于UHPLC-Q-Exactive Orbitrap MS、指纹图谱及多成分含量测定的铁线透骨草质量评价与提取工艺优化
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作者 徐梦婷 赵春雨 +4 位作者 周舒 黄文奕 郭彦杰 杜守颖 白洁 《中国现代中药》 2026年第1期74-85,共12页
目的:分析铁线透骨草化学成分,建立其指纹图谱及绿原酸等4个成分的含量测定方法,并结合化学计量学对不同产地的铁线透骨草进行质量评价。方法:基于超高效液相色谱轨道阱质谱法(UHPLC-Q-Exactive Orbitrap MS)对铁线透骨草进行化学成分分... 目的:分析铁线透骨草化学成分,建立其指纹图谱及绿原酸等4个成分的含量测定方法,并结合化学计量学对不同产地的铁线透骨草进行质量评价。方法:基于超高效液相色谱轨道阱质谱法(UHPLC-Q-Exactive Orbitrap MS)对铁线透骨草进行化学成分分析;基于高效液相色谱法(HPLC)建立化学成分指纹图谱并进行相似度评价;结合聚类分析(CA)、主成分分析(PCA)、正交偏最小二乘法-判别分析(OPLS-DA)评价铁线透骨草的质量;以提取溶剂、料液比、超声时间为影响因素,对绿原酸、咖啡酸、芦丁及丹皮酚的含量进行测定,采用L9(34)正交试验法优化提取工艺。结果:从铁线透骨草中鉴别出包括黄酮、苯丙素等类50个化合物,通过对照品比对,指认出其中的5个成分;通过HPLC指纹图谱标定了16批样品中的15个共有峰,绿原酸和芦丁为张家口-保定产区特征性成分,峰5、峰2、峰1和峰15关联承德产区样本。确定的绿原酸、咖啡酸、芦丁、丹皮酚的最佳提取工艺为50%乙醇100 mL,超声提取15 min,4个成分在各自质量浓度范围内线性关系良好,平均加样回收率为92%~104%,RSD<4%,含量检测方法符合《中华人民共和国药典》2025年版要求。结论:建立的铁线透骨草HPLC指纹图谱及多成分含量测定方法合理可靠,结合化学计量学可有效评价河北铁线透骨草质量,可为其质量控制提供参考。 展开更多
关键词 铁线透骨草 化学成分分析 高效液相色谱法指纹图谱 正交试验设计 含量测定 质量评价
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威宁党参HPLC指纹图谱建立及质量评价
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作者 王焱 张蜀 +3 位作者 查钦 周雪 尹胜 唐贵华 《广东药科大学学报》 2026年第1期95-102,共8页
目的建立威宁党参的高效液相色谱(HPLC)指纹图谱,为其质量控制和评价提供科学依据。方法采用Phenomenex lux cellulose-2色谱柱,以乙腈–0.1%甲酸为流动相进行梯度洗脱(流速为1 mL/min,柱温为30℃),测定10批威宁党参与6批其他产地党参... 目的建立威宁党参的高效液相色谱(HPLC)指纹图谱,为其质量控制和评价提供科学依据。方法采用Phenomenex lux cellulose-2色谱柱,以乙腈–0.1%甲酸为流动相进行梯度洗脱(流速为1 mL/min,柱温为30℃),测定10批威宁党参与6批其他产地党参的指纹图谱,结合相似度分析、聚类分析、主成分分析及正交偏最小二乘判别分析进行数据解析。结果成功构建威宁党参对照指纹图谱,鉴定23个共有峰(其中4个峰明确指认);主成分分析提取4种主成分,得分图显示威宁党参质量更优,且党参苷Ⅰ质量分数显著高于对比样本。结论本研究建立的指纹图谱方法可有效区分威宁党参特征成分,为其质量标准完善提供技术支撑。 展开更多
关键词 威宁党参 高效液相色谱法 指纹图谱 质量控制 党参苷Ⅰ 主成分分析
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Qualitative and Quantitative Analysis for the Quality Control of Rhizoma Coptidis by HPLC-DAD and HPLC-ESI-MS 被引量:1
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作者 DOU Sheng-shan ZHU Shuang-lai +3 位作者 DAI Wei-xing ZHANG Wei-dong ZHANG Yi LIU Run-hui 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2010年第5期735-741,共7页
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
关键词 Rhizoma Coptidis hplc-DAD hplc-MS Partial least squares analysis Quality control
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NON-AQUEOUS REVERSED PHASE HPLC WITH LOW-WAVELENGTH UV DETECTION FOR TRIGLYCERIDE ANALYSIS
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作者 Yi Cheng LONG Wan Zhen LU 《Chinese Chemical Letters》 SCIE CAS CSCD 1991年第5期393-396,共4页
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
关键词 hplc TG NON-AQUEOUS REVERSED PHASE hplc WITH LOW-WAVELENGTH UV DETECTION FOR TRIGLYCERIDE analysis NARP UV
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Published the papers of HPLC-MS analysis—Chemical drug
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《Journal of Pharmaceutical Analysis》 SCIE CAS 2011年第1期72-78,共7页
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
关键词 Chemical drug Published the papers of hplc-MS analysis hplc MS
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HPLC指纹图谱、化学模式识别及一测多评法相结合的玫瑰花口服液(无糖型)质量评价研究
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作者 迪娜·努尔火加 蔡晓翠 +4 位作者 郭君婷 赵婷婷 李雷 杨伟俊 刘桂花 《中国药学杂志》 北大核心 2026年第2期197-208,共12页
目的 建立高效液相色谱(HPLC)指纹图谱、化学模式识别及一测多评(quantitative analysis of multi-components by single marker, QAMS)法相结合的方法评价玫瑰花口服液(无糖型)的质量。方法 采用HPLC法建立15批玫瑰花口服液(无糖型)的... 目的 建立高效液相色谱(HPLC)指纹图谱、化学模式识别及一测多评(quantitative analysis of multi-components by single marker, QAMS)法相结合的方法评价玫瑰花口服液(无糖型)的质量。方法 采用HPLC法建立15批玫瑰花口服液(无糖型)的指纹图谱,使用OriginPro 2024、SPSS 27.0及SIMCA14.1软件进行Pearson相关性分析、聚类分析(cluster analysis, CA)、主成分分析(principal component analysis, PCA)、正交偏最小二乘判别分析(orthogonal partial least squares discriminant analysis, OPLS-DA);对玫瑰花口服液(无糖型)中的7种成分[没食子酸、咖啡酸、槲皮素-3-O-葡萄糖基(1→2)半乳糖苷、白麻苷、山柰酚3-O-槐糖苷、金丝桃苷、槲皮苷]进行定量测定并建立QAMS。结果 建立了15批样品的指纹图谱,共标定了24个共有峰,并对12个共有峰进行指认。15批样品的相似度均在0.987及以上。Pearson相关性分析表明各共有峰之间具有复杂的相关性,大部分色谱峰之间呈正相关;CA表明15批样本可聚为3大类,24个共有峰被分为3组;PCA表明4个主成分的累积方差解释率为91.73 2%,综合得分结果显示15批样品整体质量差异较小;OPLS-DA筛选了10个差异性标志物;建立了以金丝桃苷为内参物,同时测定7个成分的QAMS,外标法与QAMS法所得含量结果无明显差异;15批玫瑰花口服液(无糖型)的质量浓度为0.561 5~0.674 8、0.017 6~0.021 9、0.104 1~0.130 7、0.136 2~0.169 2、0.060 2~0.087 8、0.043 2~0.059 2、0.106 5~0.131 4 mg·mL^(-1)。结论 建立的玫瑰花口服液(无糖型)HPLC指纹图谱及QAMS,为玫瑰花口服液(无糖型)的质量控制提供了可靠的分析方法。 展开更多
关键词 玫瑰花口服液(无糖型) 高效液相色谱指纹图谱 一测多评 质量标准
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Published the papers of HPLC-MS analysis—Traditional Chinese medicine
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《Journal of Pharmaceutical Analysis》 SCIE CAS 2011年第1期70-72,共3页
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
关键词 Published the papers of hplc-MS analysis Traditional Chinese medicine hplc MS
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ANALYSIS OF ETHACRYNIC ACID IN URINE BY HPLC-FLUORESEENCE DETECTOR
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作者 Xiu Feng HE Ya Wei LI +2 位作者 Lin LI Yun Ping WANG Tong Hui ZHOU 《Chinese Chemical Letters》 SCIE CAS CSCD 1991年第12期953-956,共4页
A sensitive and selective method has been developed for the detection of free ethacrynic acid in human urine. Using 4-(bromomethyl)-7-methoxycoumarin, ethacrynic acid was transformed into a fluorescent derivative, and... A sensitive and selective method has been developed for the detection of free ethacrynic acid in human urine. Using 4-(bromomethyl)-7-methoxycoumarin, ethacrynic acid was transformed into a fluorescent derivative, and was analysed by HPLC-fluorescence detector. The detection limit is 0.1ug/ml urine. The method is suitable for screening ethacrynic acid in doping control and studying its metabolism. 展开更多
关键词 analysis OF ETHACRYNIC ACID IN URINE BY hplc-FLUORESEENCE DETECTOR hplc ACID
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基于UPLC-Q/TOF-MS技术的蒙药黑云香成分分析及HPLC含量测定研究 被引量:1
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作者 其其格 包晓玲 +3 位作者 李淑艳 乌日吉木斯 韩阿斯如 吴东兴 《中国现代应用药学》 北大核心 2025年第6期941-947,共7页
目的 基于UPLC-Q/TOF-MS技术分析蒙药黑云香成分,并采用HPLC同时测定黑云香中2种成分含量。方法 UPLC-Q/TOF-MS法采用Waters acquity UPLC BEH C_(18)色谱柱(2.1 mm×100 mm,1.7μm),柱温35℃,流动相为甲醇(A)-0.1%甲酸水(B),梯度洗... 目的 基于UPLC-Q/TOF-MS技术分析蒙药黑云香成分,并采用HPLC同时测定黑云香中2种成分含量。方法 UPLC-Q/TOF-MS法采用Waters acquity UPLC BEH C_(18)色谱柱(2.1 mm×100 mm,1.7μm),柱温35℃,流动相为甲醇(A)-0.1%甲酸水(B),梯度洗脱;体积流量0.3 mL·min^(-1);电喷雾离子源,正离子模式下采集质谱数据,质量扫描范围m/z 100~1 000。使用UNIFI Portal软件进行成分分析。HPLC使用Waters SymmetryR C_(18)色谱柱(4.6 mm×250 mm,5μm);流动相为甲醇(A)-0.1%磷酸水(B),梯度洗脱;体积流量1.0 mL·min^(-1);检测波长252 nm;柱温25℃。同时测定黑云香中2-甲氧基-5-乙酰基-呋喃吉玛(10)-烯-6-酮和脱氢松香酸2种成分的含量。结果 基于UPLC-Q/TOF-MS技术在正离子模式下检测出42个化合物;通过化合物的保留时间、母离子、碎片离子等相关信息,并查阅没药属药材的分离等相关文献,初步推测出化合物名称。采用HPLC进行2种成分的含量测定,分别在0.12~0.74、0.04~0.24μg·mL^(-1)内线性关系良好(r>0.999 1),平均加样回收率分别为99.01%、99.46%,RSD分别为0.62%、0.66%。结论 采用UPLC-Q/TOF-MS技术可以快速、准确分析黑云香化学成分;建立的含量测定方法简便可靠,可用于黑云香质量控制。 展开更多
关键词 黑云香 UPLC-Q/TOF-MS hplc 成分分析 含量测定
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基于UHPLC Q-Exactive Plus Orbitrap HRMS和HPLC-UV的川参通注射液化学成分定性和定量研究
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作者 朱星宇 张熊莉 +5 位作者 李华柳 迟明艳 黄勇 郑林 肖海涛 何峰 《中国新药杂志》 北大核心 2025年第23期2541-2551,共11页
目的:基于UHPLC Q-Exactive Plus Orbitrap HRMS联用技术对川参通注射液化学成分进行系统分析,并采用HPLC-UV对其主要化学成分进行含量测定。方法:采用电喷雾电离源(electrospray ionization,ESI),同时获取正、负离子模式下的多级质谱数... 目的:基于UHPLC Q-Exactive Plus Orbitrap HRMS联用技术对川参通注射液化学成分进行系统分析,并采用HPLC-UV对其主要化学成分进行含量测定。方法:采用电喷雾电离源(electrospray ionization,ESI),同时获取正、负离子模式下的多级质谱数据,结合对照品保留时间、质谱离子信息、数据库和文献中相关质谱信息对川参通注射液中的化学成分进行分析;采用HPLC-UV同时测定不同批次川参通注射液中11个成分的含量。结果:在川参通注射液中共鉴定出43个化合物,包括酚酸类10个、氨基酸类8个、有机酸类11个、苯酞类7个、其他类化合物7个,其中14个成分经对照品比对确认;含量测定的11个成分在测定浓度范围内线性关系良好(r≥0.9995),精密度、稳定性、重复性等均符合要求,平均加样回收率为94.89%~98.74%,RSD为0.52%~1.53%。结论:本研究所建立的方法简便、快捷、准确,进一步完善了川参通注射液的质量控制方法,可为该制剂的质量标准提升提供科学依据。 展开更多
关键词 川参通注射液 Uhplc-Q-Exactive Plus Orbitrap HRMS hplc-UV 质量控制 成分分析 含量测定
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Applications of HPLC/MS in the analysis of traditional Chinese medicines 被引量:18
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作者 Miao Li Xiao- Fang Hou Jie Zhang Si-Cen Wang Qiang Fu Lang- Chong He 《Journal of Pharmaceutical Analysis》 SCIE CAS 2011年第2期81-91,共11页
In China, traditional Chinese medicines (TCMs) have been used in clinical applications for thousands of years. The successful hyphenation of high-performance liquid chromatography (HPLC) and mass spectrometry (MS... In China, traditional Chinese medicines (TCMs) have been used in clinical applications for thousands of years. The successful hyphenation of high-performance liquid chromatography (HPLC) and mass spectrometry (MS) has been applied widely in TCMs and biological samples analysis. Undoubtedly, HPLC/MS technique has facilitated the understanding of the treatment mechanism of TCMs. We reviewed more than 350 published papers within the last 5 years on HPLC/MS in the analysis of TCMs. The present review focused on the applications of HPLC/MS in the component analysis, metabolites analysis, and pharmacokinetics of TCMs etc. 50% of the literature is related to the component analysis of TCMs, which show that this field is the most popular type of research. In the metabolites analysis, HPLC coupled with electrospray ionization quadrupole time-of-flight tandem mass spectrometry has been demonstrated to be the powerful tool for the characterization of structural features and fragmentation behavior patterns. This paper presented a brief overview of the applications of HPLC/MS in the analysis of TCMs. HPLC/MS in the fingerprint analysis is reviewed elsewhere. 展开更多
关键词 traditional Chinese medicines (TCMs) hplc/MS component analysis metabolites analysis PHARMACOKINETICS
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基于HPLC指纹图谱、含量测定及酶活性评价不同企业建曲质量
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作者 王瑞生 张振凌 +2 位作者 陈祎甜 孙梦梅 朱建光 《中成药》 北大核心 2025年第9期2848-2855,共8页
目的评价不同企业建曲质量。方法建立HPLC指纹图谱,测定柚皮苷、橙皮苷、新橙皮苷、木犀草素、芹菜素含量,以及淀粉酶、糖化酶、纤维素酶、蛋白酶(中性、酸性、碱性)活性,再进行聚类分析。结果18批样品指纹图谱中有28个共有峰,指认出11... 目的评价不同企业建曲质量。方法建立HPLC指纹图谱,测定柚皮苷、橙皮苷、新橙皮苷、木犀草素、芹菜素含量,以及淀粉酶、糖化酶、纤维素酶、蛋白酶(中性、酸性、碱性)活性,再进行聚类分析。结果18批样品指纹图谱中有28个共有峰,指认出11个,相似度0.697~0.997。5种成分含量分别为0~0.0227%、0.0951%~0.3262%、0~0.0317%、0.0007%~0.0049%、0.0040%~0.0711%,6种酶活性分别为8.71~88.25、17.67~370.13、7.97~61.21、5.21~22.05、5.13~20.66、6.22~20.96 U/g。各批样品聚为4类,不同企业或同一企业不同批次的分类存在交叉。结论不同企业建曲生产工艺不稳定,应尽快规范其炮制工艺,建立其质量标准。 展开更多
关键词 建曲 质量评价 hplc指纹图谱 含量测定 酶活性 聚类分析
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Establishment of HPLC Fingerprint, Cluster Analysis and Principle Component Analysis of Citri Reticulatae Pericarpium Viride 被引量:4
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作者 Beibei JIN Xiangping PEI Huizhen LIANG 《Medicinal Plant》 CAS 2019年第1期69-73,共5页
[Objectives] This study aimed to establish HPLC fingerprint and conduct cluster analysis and principle component analysis for Citri Reticulatae Pericarpium Viride. [Methods] Using the HPLC method, the determination wa... [Objectives] This study aimed to establish HPLC fingerprint and conduct cluster analysis and principle component analysis for Citri Reticulatae Pericarpium Viride. [Methods] Using the HPLC method, the determination was performed on XSelect~&#x00AE; HSS T3-C_(18) column with mobile phase of acetonitrile-0.5% acetic acid solution(gradient elution) at the flow rate of 1.0 mL/min. The detection wavelength was 360 nm. The column temperature was 25℃. The sample size was 10 μL. With peak of hesperidin as the reference, HPLC fingerprints of 10 batches of Citri Reticulatae Pericarpium Viride were determined. The similarity of the 10 batches of samples was evaluated by Similarity Evaluation System for Chromatographic Fingerprint of TCM(2012 edition) to determine the common peaks. Cluster analysis and principal component analysis were performed by using SPSS 17.0 statistical software. [Results] The HPLC fingerprints of the 10 batches of medicinal materials had total 11 common peaks, and the similarity was 0.919-1.000, indicating that the chemical composition of the 10 batches of medicinal materials was consistent. There were 11 common components in the 10 batches of medicinal materials, but their contents were different. When the Euclidean distance was 20, the 10 batches of samples were divided into two categories, S4 in the first category, and the others in the second one. When the Euclidean distance was 5, the second category could be further divided into two sub-categories, S1 and S10 in one sub-category, and S2, S3, S5, S6, S7, S8 and S9 in the other one. The principle component analysis showed that cumulative contribution rate of the two main component factors was 92.797%, and the comprehensive score of S7 was the highest with the best quality. [Conclusions] The results of HPLC fingerprinting, cluster analysis and principle component analysis can provide reference for the quality control of Citri Reticulatae Pericarpium Viride. 展开更多
关键词 Citri Reticulatae Pericarpium Viride hplc FINGERPRINT CLUSTER analysis PRINCIPLE COMPONENT analysis
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Reversed-Phase HPLC Analysis of Steviol Glycosides Isolated from Stevia rebaudiana Bertoni 被引量:5
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作者 Venkata Sai Prakash Chaturvedula Julian Zamora 《Food and Nutrition Sciences》 2014年第17期1711-1716,共6页
High Performance Liquid Chromatography (HPLC) experiments have been performed on nine steviol glycosides namely rebaudioside A, steviolbioside, stevioside, rubusoside, rebaudioside B, rebaudioside C, rebaudioside D, r... High Performance Liquid Chromatography (HPLC) experiments have been performed on nine steviol glycosides namely rebaudioside A, steviolbioside, stevioside, rubusoside, rebaudioside B, rebaudioside C, rebaudioside D, rebaudioside F, and dulcoside A isolated from the leaves of Stevia rebaudiana using Reversed-Phase (RP) column. Using RP-HPLC method, the individual retention times for nine naturally occurring ent-kaurane diterpene glycosides of S. rebaudiana reported in JECFA have been determined at four different temperatures: 20℃, 40℃, 60℃, and 79℃. Also, calculated the relative retention times of the eight steviol glycosides steviolbioside, stevioside, rubusoside, rebaudioside B, rebaudioside C, rebaudioside D, rebaudioside F, and dulcoside A against the major steviol glycoside rebaudioside A. HPLC results suggested that temperatures 40℃ and 60℃ would be ideal conditions for better separation of steviol glycosides. 展开更多
关键词 STEVIA rebaudiana Asteraceae DITERPENE GLYCOSIDES REVERSED-PHASE hplc analysis RETENTION and Relative RETENTION TIMES
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