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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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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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Targeted and non-targeted LC-MS analysis of microcystins in Clarias gariepinus from fishponds
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作者 Odo J.Bassey Munyaradzi Mujuru +3 位作者 Mulalo I.Mutoti Adeeyo Adeyemi Farai Dondofema Jabulani Ray Gumbo 《Emerging Contaminants》 2025年第2期286-293,共8页
Cyanotoxins produced by cyanobacteria are formidable threats to aquatic ecosystems and public health worldwide. The potential health risks associated with cyanotoxins from contaminated fishponds are becoming a growing... Cyanotoxins produced by cyanobacteria are formidable threats to aquatic ecosystems and public health worldwide. The potential health risks associated with cyanotoxins from contaminated fishponds are becoming a growing concern, as cyanotoxin production has steadily increased over time in these aquatic environments. Therefore, this study aims to utilize targeted and non-targeted Liquid Chromatography Mass Spectrometer (LC-MS) analytical methods to detect cyanotoxins in catfish (Clarias gariepinus) tissue harvested from fishponds. For detecting cyanotoxins in fish tissue utilizing the non-targeted approach, high-resolution MS/MS spectra data obtained from the analysis were converted to mzML format, analyzed with the Global Natural Product Social (GNPS) Library and CANOPUS annotations for LEVEL 3 metabolite identification, and visualized as a molecular network in Cytoscape. Regarding the targeted method, the toxin identification and quantification were achieved by comparing samples spiked with known concentrations of MC-RR and YR to an authentic toxin standard. The results of the target analysis showed that microcystin variant MC-RR was not detected in the fish tissue. The MC-YR variant was detected in the intestines and gills of Clarias gariepinus at concentrations of 13.2–10.6 μg/g and 1.5–13.9 μg/g, respectively. The muscle tissues across all fish ponds showed MC-YR concentrations between 10.5 and 16.06 μg/g. The highest concentration of MC-YR was found in the liver tissue in pond 6 (20.9 μg/g). The untargeted LC-MS method led to the identification of a larger number of cyanometabolites in the fish tissue, such as aeruginosins, anabaenopeptins, microginins. Non-toxic secondary metabolites like octadecadienoic acid, while phosphocholine (PC), ethanesulfonic acid, pheophorbide A, microcolins, cholic acid, phenylalanine, amyl amine and phosphocholine (PC), triglyceride (TG), phosphocholine (PC) and sulfonic acid derieved from cyanobacteria, fish and anthropogenic sources were also detected in the fish tissues. The non-targeted analysis facilitates the identification of both unexpected and unknown compounds. 展开更多
关键词 Liquid chromatography mass spectrometer CYANOTOXINS CYANOBACTERIA Targeted analysis Metabolites
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Trace analysis of 59 halogenated aromatic disinfection byproducts through the SPE-LC-MS/MS method and their occurrence and transformation during chlorine disinfection
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作者 Shuang Chen Yue Qiao +5 位作者 Youwei Jiang Wei Qiu Shuang Zang Jing Zhang Xianshi Wang Jun Ma 《Journal of Environmental Sciences》 2025年第11期821-832,共12页
Halogenated aromatic disinfection byproducts(DBPs)are gradually receiving attention due to their high detection frequency and usually higher toxicity than regulated DBPs.In this study,we established a solid phase extr... Halogenated aromatic disinfection byproducts(DBPs)are gradually receiving attention due to their high detection frequency and usually higher toxicity than regulated DBPs.In this study,we established a solid phase extraction(SPE)-LC-MS/MS method to simultaneously trace analyze 59 halogenated aromatic DBPs.The limits of detection and limits of quantification of halogenated aromatic DBPs ranged from 0.03 to 135.23 ng/L and from 0.1 to 450.76 ng/L,respectively.The range of recoveries and relative standard deviation(RSD)in river water were between 72.41%to 119.54%and 1.86%to 16.03%,respectively.Therefore,this method can be used to accurately analyze trace levels of halogenated aromatic DBPs in drinking water.The occurrence and transformation of halogenated aromatic DBPs were explored based on this method.In the chlorinated simulated source water and chlorinated river water,20 and 45 halogenated aromatic DBPs were determined,respectively.The active halogen species(HOCl,HOBr,and HOI)first reacted with natural organic matter(NOM)to form halogenated aromatic DBPs.Then,chlorine further reacted with the halogenated aromatic DBPs to convert them into small-molecule halogenated aliphatic DBPs through oxidation,electrophilic substitution,and hydrolysis reaction,etc.In the chlorinated simulated source water,chlorinated river water,and tap water,the toxicity contribution of bromoacetic acids(Br-HAAs)accounted for themajority(>71.16%).Given that halogenated aromatic DBPs are intermediate products of halogenated aliphatic DBPs,controlling the formation of halogenated aromatic DBPs is beneficial in decreasing the formation of halogenated aliphatic DBPs,thereby diminishing the toxicity of drinking water. 展开更多
关键词 Halogenated aromatic disinfection byproducts Trace analysis CHLORINE Drinking water Calculated toxicity
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Comprehensive analysis of phenolic composition and antioxidant mechanisms in Gymnema sylvestre extracts using LC-MS and column chromatography 被引量:1
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作者 Shengjie Hao Yuxin Du +2 位作者 Jianglong He Qian Li Guilin Chen 《Asian Journal of Traditional Medicines》 2024年第4期211-222,共12页
Recent studies have highlighted the potential of plant extracts as therapeutic agents for managing oxidative stress and related disorders.This study aims to elucidate the phenolic composition and antioxidant propertie... Recent studies have highlighted the potential of plant extracts as therapeutic agents for managing oxidative stress and related disorders.This study aims to elucidate the phenolic composition and antioxidant properties of Gymnema sylvestre extracts.Ethanolic reflux extraction followed by column chromatography was employed to isolate phenolic compounds.The total phenolic and flavonoid contents were quantified using the Folin–Ciocalteu and aluminum chloride colorimetric methods,respectively.Antioxidant activities were assessed by DPPH,ABTS scavenging assays and the ferric reducing antioxidant power(FRAP)assay.High-Performance Liquid Chromatography(HPLC)with a C18 column and Thermo TSQ Quantum Access Max(LC-MS)were used to determine the levels of gymnemic acid and identify other potential phenolic compounds.The analysis revealed significant antioxidant activities in the fractions.Fraction A showed the highest DPPH and ABTS scavenging activities,and Fraction C demonstrated the highest ferric reducing power.LC-MS analysis identified several phenolic compounds,indicating that these are major contributors to the antioxidant efficacy of the extract.This study provides a detailed phenolic profile and confirms the strong antioxidant potential of Gymnema sylvestre leaf extract,supporting its therapeutic use and further investigation. 展开更多
关键词 Gymnema sylvestre ANTIOXIDANTS column chromatography phenolic compounds lc-ms
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Comparative metabolite analysis of Piper sarmentosum organs approached by LC-MS-based metabolic profiling
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作者 Ismail Ware Katrin Franke +5 位作者 Andrej Frolov Kseniia Bureiko Elana Kysil Maizatulakmal Yahayu Hesham Ali El Enshasy Ludger A.Wessjohann 《Natural Products and Bioprospecting》 CSCD 2024年第1期527-547,共21页
Piper sarmentosum Roxb.(Piperaceae)is a traditional medicinal and food plant widely distributed in the tropical and subtropical regions of Asia,offering both health and culinary benefits.In this study the secondary me... Piper sarmentosum Roxb.(Piperaceae)is a traditional medicinal and food plant widely distributed in the tropical and subtropical regions of Asia,offering both health and culinary benefits.In this study the secondary metabolites in different organs of P.sarmentosum were identified and their relative abundances were characterized.The metabolic profiles of leaves,roots,stems and fruits were comprehensively investigated by liquid chromatography high-resolution mass spectrometry(LC-HR-MS)and the data subsequently analyzed using multivariate statistical methods.Manual interpretation of the tandem mass spectrometric(MS/MS)fragmentation patterns revealed the presence of 154 tentatively identified metabolites,mostly represented by alkaloids and flavonoids.Principle component analysis and hierarchical clustering indicated the predominant occurrence of flavonoids,lignans and phenyl propanoids in leaves,aporphines in stems,piperamides in fruits and lignan-amides in roots.Overall,this study provides extensive data on the metabolite composition of P.sarmentosum,supplying useful information for bioactive compounds discovery and patterns of their preferential biosynthesis or storage in specific organs.This can be used to optimize production and harvesting as well as to maximize the plant’s economic value as herbal medicine or in food applications. 展开更多
关键词 Piper sarmentosum lc-ms/MS Multivariate analysis Metabolite profiling Secondary metabolites ALKALOIDS
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LC-MS/MS法测定人血浆中艾沙康唑浓度
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作者 赵振寰 荆伟丽 +2 位作者 韩冰 王凯 徐文 《中国新药杂志》 北大核心 2025年第17期1826-1832,共7页
目的:建立并验证了艾沙康唑血药浓度的测定方法,并将该法应用于临床的血药浓度监测。方法:艾沙康唑血浆样本采用甲醇沉淀蛋白预处理,以稳定同位素伏立康唑-d4为内标,采用LC-MS/MS法进行测定。色谱柱为Ultimate AQ-C_(18)反相窄径色谱柱... 目的:建立并验证了艾沙康唑血药浓度的测定方法,并将该法应用于临床的血药浓度监测。方法:艾沙康唑血浆样本采用甲醇沉淀蛋白预处理,以稳定同位素伏立康唑-d4为内标,采用LC-MS/MS法进行测定。色谱柱为Ultimate AQ-C_(18)反相窄径色谱柱,分别采用含量为0.1%甲酸(v/v)的甲醇和含0.1%甲酸的超纯水(v/v)为有机相和水相进行梯度洗脱,流速为0.3 mL·min^(-1),柱温为40℃,处理后的样本进样5.0μL。质谱离子源为电喷雾离子源,以多反应正离子监测模式进行测定,用于质谱分析的离子对分别为m/z 438.2→224.1(艾沙康唑)、m/z 354.2→285.1(伏立康唑-d4)。5例患者给予负荷剂量后分别于开始给药的d 4,d 5,d 6,d 12,d 13,d 14抽取谷浓度血浆样本并测定其血药浓度。结果:艾沙康唑检测质量浓度的线性范围为0.1~10μg·mL^(-1)(r=0.9996),定量下限为0.25μg·mL^(-1);批内、批间RSD均不高于11.9%,相对误差为-4.83%~6.20%;稳定性的相对误差为-2.04%~6.89%,样本和内标的提取回收率、基质效应以及残留效应均不影响待测物的定量分析。5例患者所有样本的谷浓度均大于1μg·mL^(-1)。结论:本研究所提立的测定艾沙康唑的LC-MS/MS法操作简便、快捷,准确度高,可用于真菌感染患者体内艾沙康唑的治疗药物监测。 展开更多
关键词 lc-ms/MS法 艾沙康唑 血药浓度监测
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基于LC-MS济川煎治疗老年慢传输型便秘的作用机制研究
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作者 安明伟 罗嫣嫣 +3 位作者 江喜娟 凌美婷 徐美 唐勇 《江西中医药大学学报》 2025年第4期90-96,共7页
目的:基于液相色谱-质谱联用技术(LC-MS)和网络药理学方法探究济川煎治疗老年慢传输型便秘(STC)的物质基础及其分子机制。方法:采用LC-MS法进行正负离子模式下非靶向代谢物检测,利用Genecards、OMIM、PharmGKB、TTD及DrugBank等数据库... 目的:基于液相色谱-质谱联用技术(LC-MS)和网络药理学方法探究济川煎治疗老年慢传输型便秘(STC)的物质基础及其分子机制。方法:采用LC-MS法进行正负离子模式下非靶向代谢物检测,利用Genecards、OMIM、PharmGKB、TTD及DrugBank等数据库获取慢传输型便秘的作用靶点,并与济川煎对应靶标取交集,获取济川煎治疗STC的对应靶标。使用STRING数据库对济川煎治疗STC作用靶点进行蛋白质相互作用分析并获取核心靶标,通过R语言enrich KEGG包和pathview包,对核心靶标进行KEGG通路富集分析和GO分类富集分析。利用Cytoscape 3.9.1软件,绘制“药物成分-靶标”网络图、核心靶标相互作用网络图。基于网络药理学结果,选择MAPK信号通路进行动物实验验证。结果:从济川煎中共筛选得到60种活性成分、17个核心靶点。经GO注释及KEGG富集分析发现,靶点主要涉及脂多糖代谢、氧化应激、活性氧、类固醇激素等生物过程,参与调节PI3K-Akt、MAPK和cAMP、AMPK等信号通路。动物实验表明,济川煎改善STC模型大鼠粪便含水量和肠道推进率,与模型组比较,济川煎组ERK2蛋白表达水平上调(P<0.05),JNK1蛋白表达水平上调(P<0.05)。结论:济川煎治疗老年STC疗具有多成分-多靶点-多途径共同作用的特点,作用机制可能与其通过调节MAPK通路干预结直肠组织的肠嗜铬细胞、Cajal间质细胞的增殖相关。 展开更多
关键词 济川煎 慢传输型便秘 lc-ms 机制研究
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基于LC-MS/MS结合网络药理学、分子对接及体内外实验探究红花总黄酮抗肝纤维化的作用机制 被引量:1
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作者 李明奇 王映荷 +4 位作者 赵晓璐 包小妹 岳鑫 任贵强 马月宏 《中国临床药理学与治疗学》 北大核心 2025年第5期586-598,共13页
目的:阐明红花总黄酮药效和网络药理学机制,探讨其关键靶点和相关通路,明确其抗肝纤维化的作用机制。方法:对红花总黄酮进行LCMS/MS测定及成分分析;通过TCMSP数据库、SWISS ADME数据库及文献查询筛选出有效成分;在Swiss Target Predict... 目的:阐明红花总黄酮药效和网络药理学机制,探讨其关键靶点和相关通路,明确其抗肝纤维化的作用机制。方法:对红花总黄酮进行LCMS/MS测定及成分分析;通过TCMSP数据库、SWISS ADME数据库及文献查询筛选出有效成分;在Swiss Target Prediction数据库筛选出红花总黄酮相关靶点;在GeneCards数据库筛选出肝纤维化相关靶点;通过Venny.2.1.0取交集获得红花总黄酮抗肝纤维化靶点;通过STRING数据库进行蛋白互作分析;通过Cytoscape软件进行可视化分析;在Metascape平台进行基因本体(GO)功能和京都基因与基因组百科全书(KEGG)通路分析;运用AutoDock软件对核心靶点和活性成分进行分子对接验证;通过动物模型实验和离体细胞实验验证红花总黄酮抗肝纤维化的作用机制。结果:共鉴定出红花黄酮类成分41个。通过网络药理学分析,获得红花总黄酮抗肝纤维化靶点149个,其中核心靶点23个。GO富集分析共涉及生物过程(BP)、细胞组分(CC)、分子功能(MF)三个方面。KEGG富集结果显示,PI3K/Akt、MAPK等是参与肝纤维化发生发展的通路。通过分子对接验证了活性成分Quercetin、Acacetin、Glabridin分别与Akt1、HIFIA紧密结合。在动物模型实验中,通过HE和Masson染色观察到红花总黄酮给药组纤维增生减少,胶原沉积减少,炎性细胞浸润减少,纤维化的肝脏组织得到改善;Western blotting结果提示,红花总黄酮可以使肝纤维化标志因子α-SMA、Collagen I(P<0.01)和PI3K/Akt信号通路标志蛋白PPI3K、PI3K、P-Akt、Akt表达量下降(P<0.01);在离体细胞实验中:Western blotting结果提示,红花总黄酮可以使肝纤维化标志因子α-SMA、Collagen I(P<0.01)和PI3K/Akt信号通路标志蛋白P-PI3K、PI3K、P-Akt、Akt表达量下降(P<0.01)。结论:红花总黄酮通过多成分、多靶点、多通路的形式发挥抗肝纤维化的作用,其作用机制可能是通过调控PI3K/Akt信号通路实现的。 展开更多
关键词 lc-ms/MS 网络药理学 分子对接 肝纤维化 药理实验
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基于UPLC-MS/MS测定重楼皂苷Ⅶ逆转肝癌耐药过程中胆固醇及其关键产物的含量
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作者 李杰 路璐 +2 位作者 刘垚利 丁越 张彤 《中成药》 北大核心 2025年第9期3139-3144,共6页
目的建立UPLC-MS/MS法测定重楼皂苷Ⅶ逆转肝癌耐药过程中胆固醇及其4种合成代谢关键化合物(羊毛甾醇、链甾醇、7-脱氢胆固醇、27-羟基胆固醇)的含量。方法分析采用Zorbax Eclipse plus C_(18)(2.1 mm×50 mm,1.8μm)色谱柱;流动相水... 目的建立UPLC-MS/MS法测定重楼皂苷Ⅶ逆转肝癌耐药过程中胆固醇及其4种合成代谢关键化合物(羊毛甾醇、链甾醇、7-脱氢胆固醇、27-羟基胆固醇)的含量。方法分析采用Zorbax Eclipse plus C_(18)(2.1 mm×50 mm,1.8μm)色谱柱;流动相水(含0.1%甲酸)-甲醇,梯度洗脱;体积流量0.5 mL/min;柱温40℃;大气压化学电离;正离子扫描;多反应监测模式。结果5种成分在各自范围内线性关系良好(r^(2)≥0.992),提取回收率为81.9%~97.1%,基质效应为79.9%~101.6%,日内、日间精密度以及稳定性均符合生物样品分析的要求。重楼皂苷Ⅶ可逆转HepG2细胞的索拉非尼耐药,降低耐药细胞中胆固醇含量,升高27-羟基胆固醇含量。结论该方法简便、准确、灵敏,可用于肿瘤耐药与胆固醇合成代谢相关性研究,为中药成分靶向胆固醇代谢调控逆转肿瘤耐药提供技术支撑。 展开更多
关键词 重楼皂苷Ⅶ 肝癌 耐药性 胆固醇 lc-ms/MS
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LC-MS/MS法同时测定碳青霉烯类抗生素中6种潜在基因毒性杂质 被引量:1
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作者 王梦娜 苗会娟 +2 位作者 高燕霞 徐艳梅 王茉莉 《中国抗生素杂志》 北大核心 2025年第1期58-64,共7页
目的建立一种LC-MS/MS法检测常见碳青霉烯类抗生素(美罗培南、厄他培南和比阿培南)中6种潜在基因毒性杂质的方法。方法采用Agilent Poroshell 120 PFP(100 mm×3 mm,2.7μm)色谱柱;流动相A为含0.1%甲酸的水溶液,流动相B为甲醇,梯度... 目的建立一种LC-MS/MS法检测常见碳青霉烯类抗生素(美罗培南、厄他培南和比阿培南)中6种潜在基因毒性杂质的方法。方法采用Agilent Poroshell 120 PFP(100 mm×3 mm,2.7μm)色谱柱;流动相A为含0.1%甲酸的水溶液,流动相B为甲醇,梯度洗脱;流速为0.3 mL/min,柱温为35℃;采用电喷雾电离(electrospray ionization,ESI)源正/负离子扫描,多反应监测(multi-reaction monitoring,MRM)模式对6种潜在基因毒性杂质同时进行定量检测。结果6种杂质在0.25~100 ng/mL范围内均具有良好的线性关系;在美罗培南中6种杂质,低、中、高3个浓度的加样回收率(n=3)范围为91.4%~103.5%,相对标准偏差(relative standard deviation,RSD)<5.1%;在厄他培南中6种杂质,低、中、高3个浓度的加样回收率(n=3)范围为91.2%~102.7%,RSD<3.9%;在比阿培南中6种杂质,低、中、高3个浓度的加样回收率(n=3)范围为91.3%~102.9%,RSD<4.3%;检测限分别为0.002,0.01,0.008,0.002,0.001和0.08 ng/mL,定量限分别为0.008,0.04,0.02,0.008,0.004和0.2 ng/mL。样品中均未检出上述潜在基因毒性杂质。结论该方法专属性强、灵敏度高、实验操作简便、快速,可用于测定以上常见碳青霉烯类抗生素中6种潜在基因毒性杂质,为常见碳青霉烯类抗生素的质量控制提供技术支持。 展开更多
关键词 碳青霉烯类抗生素 基因毒性杂质 lc-ms/MS 美罗培南 厄他培南 比阿培南
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古茶树优势内生山茶炭疽菌次生代谢产物LC-MS/MS分析
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作者 付晓熳 王卫华 +5 位作者 李楚然 张芷瑜 舒原草 杨晓琴 朱国磊 赵平 《西南林业大学学报(自然科学)》 北大核心 2025年第5期214-220,共7页
采用LC-MS/MS联用技术,对“锦秀茶祖”古茶树叶内生真菌之山茶炭疽菌大米固体发酵物中的次生代谢产物进行分析。结果表明:共鉴定出3309种化合物,包括生物碱类796个、萜类540个、脂肪酸类475个、氨基酸/肽类436个、莽草酸-苯丙素类419个... 采用LC-MS/MS联用技术,对“锦秀茶祖”古茶树叶内生真菌之山茶炭疽菌大米固体发酵物中的次生代谢产物进行分析。结果表明:共鉴定出3309种化合物,包括生物碱类796个、萜类540个、脂肪酸类475个、氨基酸/肽类436个、莽草酸-苯丙素类419个、聚酮类161个、碳水化合物156个、其他类衍生物326个,相对含量分别为24.746%、12.035%、25.739%、14.267%、10.792%、3.813%、2.366%、6.242%。相对含量大于0.5%的化合物共有35个,相对含量合计为37.420%。 展开更多
关键词 古茶树 内生真菌 山茶炭疽菌 次生代谢产物 lc-ms/MS
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基于LC-MS技术分析亚硒酸钠毒害对水稻根系特征及酚酸类、黄酮类化合物积累动态的影响
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作者 杨家琪 吴雪 +5 位作者 刘乃新 周珂 于清涛 陈百翠 李承欣 卜凡珊 《江苏农业科学》 北大核心 2025年第11期261-269,共9页
为了解水稻根系中酚酸类、黄酮类化合物抵抗过量亚硒酸钠的分子机制,采用水培试验,利用不同浓度亚硒酸钠(0、40、80、400 mg/L)对水稻哈育粳十一号进行处理,通过水稻根系参数筛选出对亚硒酸钠浓度敏感处理组,将该处理组与对照组的根系... 为了解水稻根系中酚酸类、黄酮类化合物抵抗过量亚硒酸钠的分子机制,采用水培试验,利用不同浓度亚硒酸钠(0、40、80、400 mg/L)对水稻哈育粳十一号进行处理,通过水稻根系参数筛选出对亚硒酸钠浓度敏感处理组,将该处理组与对照组的根系进行广泛靶向代谢组分析。结果表明,400 mg/L亚硒酸钠处理下水稻幼苗的根长、根鲜/干重、根活性显著受到抑制(P<0.05)。从代谢组测序中鉴定出1 594种差异代谢物,其中包括黄酮类化合物140种、酚酸类化合物129种。其中,在苯丙烷代谢途径中鉴定出10种表达水平变化明显的酚酸类代谢物;在黄酮类生物合成代谢途径、黄酮和黄酮醇生物合成代谢途径检测到的140种中有14个DAM表达水平变化显著,这10种酚酸类化合物和14种黄酮类化合物大部分显著下调表达。对香豆酰奎宁酸不仅参与苯丙烷代谢途径的酚酸合成与代谢,也参与黄酮类生物合成代谢途径,均下调表达。表明高浓度的亚硒酸钠(400 mg/L)能够显著抑制水稻根系中部分酚酸类、黄酮类化合物的合成,削弱水稻根系对过量亚硒酸钠的解毒能力,破坏水稻根系的正常生长。 展开更多
关键词 代谢组 亚硒酸钠 水稻根系 酚酸类化合物 黄酮类化合物 lc-ms
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基于LC-MS/MS技术土壤中14种除草剂残留的检测方法
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作者 常雪淼 王宇欣 +7 位作者 张明 王召 孙楠 陈建华 胡彬 马金海 马栋豪 李劲松 《中国农业大学学报》 北大核心 2025年第7期184-195,共12页
以河南省平顶山市现代农业研发基地为研究对象,建立土壤中苯达松、2甲4氯及氟磺胺草醚和11种磺酰脲类除草剂的快速检测方法,采用液相色谱-串联质谱(LC-MS/MS),通过分步提取结合C_(18)固相萃取净化,使用ACQUITY UPLC®HSS T3柱,以体... 以河南省平顶山市现代农业研发基地为研究对象,建立土壤中苯达松、2甲4氯及氟磺胺草醚和11种磺酰脲类除草剂的快速检测方法,采用液相色谱-串联质谱(LC-MS/MS),通过分步提取结合C_(18)固相萃取净化,使用ACQUITY UPLC®HSS T3柱,以体积分数为1%甲酸水溶液-乙腈为流动相梯度,结合电喷雾正/负离子切换多反应监测模式进行定量分析,采用LC-MS/MS进行定量。试验结果表明:1)14种除草剂的质量分数为0.05~10μg/kg时,进样量与对应的峰面积间呈良好的线性关系,相关系数r≥0.99,加标回收率为88.79%~119.48%;2)非健康生长地块中健康和非健康韭菜根际土中乙草胺的残留量均高于健康生长地块的健康韭菜根际土,表明乙草胺的残留可能与韭菜非健康生长存在潜在关联。本研究为国产LC-MS/MS仪器的应用提供了技术支撑,也为农田除草剂溯源及农产品安全评估提供了技术参考。 展开更多
关键词 lc-ms/MS 除草剂残留 土壤 检测技术
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LC-MS非靶向代谢组学鉴选蓝莓蜜和野蔷薇蜜的特征性物质
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作者 姚丹 詹洪平 +4 位作者 贺兴江 于瀛龙 江兆春 周文才 韦小平 《现代食品科技》 北大核心 2025年第5期267-279,共13页
为了解不同种类蜂蜜中的代谢物组成及特征性物质鉴选。该研究以荆条蜜、野桂花蜜为对照,通过液相色谱-质谱法(Liquid Chromatography-Mass Spectrometry,LC-MS)非靶向代谢组学对39个特色蜂蜜样本的代谢产物进行聚类分析,并对差异代谢物(... 为了解不同种类蜂蜜中的代谢物组成及特征性物质鉴选。该研究以荆条蜜、野桂花蜜为对照,通过液相色谱-质谱法(Liquid Chromatography-Mass Spectrometry,LC-MS)非靶向代谢组学对39个特色蜂蜜样本的代谢产物进行聚类分析,并对差异代谢物(Significant Changed Metabolites,SCMs)鉴定和功能注释,来鉴选特色蜂蜜蓝莓蜜、野蔷薇蜜中的特征性物质。结果显示检测到817个代谢物,富集到氨基酸代谢(14条)、消化系统(10条)等42模块,共364条信号通路上。筛选出蓝莓蜜与荆条蜜、蓝莓蜜与野桂花蜜、蓝莓蜜与野蔷薇蜜、野蔷薇蜜与荆条蜜、野蔷薇与野桂花蜜SCMs分别有336、165、167、270、247个。苯丙氨酸-苏氨酸、3-羟基-4-甲氧基苯乙烯酸独特存在于蓝莓蜜;N1、N5、N10、N14-四反式-对-三甲基亚精胺、半齿泽兰素、2-丙烯酸仅在野蔷薇蜜中检测出,且吲哚及其衍生物类、甘油磷脂类这两类物质在野蔷薇蜜中含量较高。该研究鉴选的蓝莓蜜、野蔷薇蜜的特征性物质,为后期鉴定蜂蜜真伪及溯源识别时提供相应参考依据。 展开更多
关键词 中蜂蜂蜜 液相色谱-质谱法(lc-ms) 非靶向代谢组学 特征性物质
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基于金属有机框架材料结合LC-MS/MS-多肽组学的地龙多肽类成分分析
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作者 刘维清 颜松益 +2 位作者 胡诗筠 李琦 余丽双 《井冈山大学学报(自然科学版)》 2025年第6期24-31,共8页
本实验研究建立了金属有机框架材料结合液相色谱,并串联质谱-多肽组学技术分析地龙及其制剂中的多肽成分。首先利用金属有机框架材料NU-1000富集地龙药材及其制剂中的多肽类成分,然后采用液相色谱串联质谱(LC-MS/MS)对富集的多肽成分进... 本实验研究建立了金属有机框架材料结合液相色谱,并串联质谱-多肽组学技术分析地龙及其制剂中的多肽成分。首先利用金属有机框架材料NU-1000富集地龙药材及其制剂中的多肽类成分,然后采用液相色谱串联质谱(LC-MS/MS)对富集的多肽成分进行分离分析,并利用De novo软件鉴定其多肽成分结构,再结合地龙数据库对特征肽进行对比,最后采用多肽活性预测软件对其活性进行预测。实验结果表明,利用NU-1000结合LC-MS/MS在地龙中药饮片中鉴定到425条多肽,其中141条肽段来自20个前体蛋白,并有四条多肽FAGDDARP、FAGDDARP、FPSLVGR和FAGDDAARP匹配到了5种蛋白质且均为肌动蛋白,具有抗血栓的药理作用。并在多肽地龙蛋白压片中得到15条肽段具有潜在生物活性的新多肽。本研究建立的地龙及其制剂中多肽成分分析方法操作便捷,可快速分析地龙中多肽成分,有望为地龙多肽类活性成分的挖掘和开发提供技术支持。 展开更多
关键词 金属有机框架材料 lc-ms/MS 多肽组学 地龙 多肽
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Genome-wide analysis of the S-phase kinase-association protein1(ClSKP1) family and the role of S-RNase targeting by an SCF(Cullin1-SKP1-F-box) complex in the self-incompatibility of‘Xiangshui' lemon 被引量:1
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作者 Yuze Li Wei Lin +9 位作者 Jiawei Zhu Moying Lan Cong Luo Yili Zhang Rongzhen Liang Liming Xia Wangli Hu Xiao Mo Guixiang Huang Xinhua He 《Horticultural Plant Journal》 2025年第2期593-607,共15页
The SKP1 gene is an important component of the SCF(SKP1-Cullin1-F-box)complex and serves as a bridge connecting the F-box and Cullin1genes(F-box-SKP1-Cullin1).The pattern of S-RNase being ubiquitously labelled by the ... The SKP1 gene is an important component of the SCF(SKP1-Cullin1-F-box)complex and serves as a bridge connecting the F-box and Cullin1genes(F-box-SKP1-Cullin1).The pattern of S-RNase being ubiquitously labelled by the SCF complex and degraded by the 26S protease accounts for the bulk of the available self-incompatibility studies.In this study,15 ClSKP1s from the‘Xiangshui'lemon genome and ubiquitome exist in the same SKP1 conserved domain(CD)as SKP1s in other species.The q PCR results showed that SKP1-6 and SKP1-14 have tissue expression patterns specific for expression in pollen.In addition,SKP1-6 and SKP1-14 in the stigma,style and ovary were significantly upregulated after self-pollination compared to those after cross-pollination.A subcellular location showed that SKP1-6 and SKP1-14 were located in the nucleus.In addition,yeast two-hybrid(Y2H)assays,bimolecular fluorescence complementation(BiFC)and luciferase complementation imaging(LCI)assays showed that SKP1-6 interacted with F-box1,F-box33,F-box34,F-box17,F-box19,Cullin1-2 and 26S proteasome subunit 4 homolog A(26S PS4HA).SKP1-14 interacted with F-box17,F-box19,F-box35,Cullin1-2 and 26S PS4HA.The interaction of Cullin1-2 and the F-box with SKP1 as a bridge was verified by a yeast three-hybrid experiment.The ability of S3-RNase to inhibit pollen and pollen tube growth and development was assessed using in vitro pollen co-culture experiments with recombinant S3-RNase proteins.Overall,this study provides important experimental evidence and theoretical basis for understanding the mechanism of self-incompatibility in plants by revealing the key role of the SCF complex in‘Xiangshui'lemon,which is bridged by ClSKP1-6,in self-incompatibility.The results of this study are of great significance for the future indepth exploration of the molecular mechanism of the SCF complex and its wide application in the self-incompatibility of plants. 展开更多
关键词 LEMON SKP1 SCF SELF-INCOMPATIBILITY Expression analysis Functional analysis
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基于LC-MS及网络药理学鉴定益景汤治疗糖尿病视网膜病变的活性成分及可能机制
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作者 罗丽梅 黄婷 +5 位作者 程艳芳 马煜贺 谢琳 何建忠 刘光辉 郑永征 《国际眼科杂志》 2025年第8期1219-1226,共8页
目的:基于液相色谱-质谱联用(LC-MS)及网络药理学探讨益景汤治疗早期糖尿病视网膜病变的主要活性成分和潜在机制。方法:采用LC-MS技术对益景汤的活性成分进行定性。根据ADME属性明确益景汤中的主要活性成分,结合网络药理学的方法,得到... 目的:基于液相色谱-质谱联用(LC-MS)及网络药理学探讨益景汤治疗早期糖尿病视网膜病变的主要活性成分和潜在机制。方法:采用LC-MS技术对益景汤的活性成分进行定性。根据ADME属性明确益景汤中的主要活性成分,结合网络药理学的方法,得到益景汤潜在治疗糖尿病视网膜病变的靶点,进一步通过疾病蛋白靶点之间蛋白质相互作用(PPI)、基因本体论(GO)富集分析和京都基因与基因组百科全书(KEGG)信号通路分析,预测益景汤治疗糖尿病视网膜病变的核心靶点与网络。最后,对核心靶标及通路进行Western blot实验验证。结果:益景汤中的主要活性成分与疾病靶点互作的核心靶点有TNF、Alb、EGFR、STAT3、PTGS2、ESR1、PPAR、MMP9、TLR4、MAPK等;益景汤治疗糖尿病视网膜病变主要与癌症信号通路、流体剪切应力与动脉粥样硬化、神经退行性变的途径等相关,并集中于炎症反映的调节、程序性细胞死亡的正调控、细胞迁移的正向调节等生物过程。Western blot实验结果显示益景汤可抑制体外高糖环境下大鼠视网膜微血管内皮细胞P-STAT3/STAT3、P-ERK/ERK的表达水平,即抑制STAT3、ERK磷酸化。结论:本研究揭示了益景汤的药效学物质基础及其潜在的多组分、多靶点、多途径的药理作用,益景汤可能通过调节多信号通路,抑制眼底炎症反应,从而保护视网膜血管内皮细胞、维护血-视网膜屏障、促进视网膜神经血管损伤的修复,进而发挥治疗糖尿病视网膜病变的作用。 展开更多
关键词 益景汤 糖尿病视网膜病变 液相色谱-质谱联用(lc-ms) 网络药理学
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Multilevel analysis of the central-peripheral-target organ pathway:contributing to recovery after peripheral nerve injury 被引量:1
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作者 Xizi Song Ruixin Li +6 位作者 Xiaolei Chu Qi Li Ruihua Li Qingwen Li Kai-Yu Tong Xiaosong Gu Dong Ming 《Neural Regeneration Research》 SCIE CAS 2025年第10期2807-2822,共16页
Peripheral nerve injury is a common neurological condition that often leads to severe functional limitations and disabilities.Research on the pathogenesis of peripheral nerve injury has focused on pathological changes... Peripheral nerve injury is a common neurological condition that often leads to severe functional limitations and disabilities.Research on the pathogenesis of peripheral nerve injury has focused on pathological changes at individual injury sites,neglecting multilevel pathological analysis of the overall nervous system and target organs.This has led to restrictions on current therapeutic approaches.In this paper,we first summarize the potential mechanisms of peripheral nerve injury from a holistic perspective,covering the central nervous system,peripheral nervous system,and target organs.After peripheral nerve injury,the cortical plasticity of the brain is altered due to damage to and regeneration of peripheral nerves;changes such as neuronal apoptosis and axonal demyelination occur in the spinal cord.The nerve will undergo axonal regeneration,activation of Schwann cells,inflammatory response,and vascular system regeneration at the injury site.Corresponding damage to target organs can occur,including skeletal muscle atrophy and sensory receptor disruption.We then provide a brief review of the research advances in therapeutic approaches to peripheral nerve injury.The main current treatments are conducted passively and include physical factor rehabilitation,pharmacological treatments,cell-based therapies,and physical exercise.However,most treatments only partially address the problem and cannot complete the systematic recovery of the entire central nervous system-peripheral nervous system-target organ pathway.Therefore,we should further explore multilevel treatment options that produce effective,long-lasting results,perhaps requiring a combination of passive(traditional)and active(novel)treatment methods to stimulate rehabilitation at the central-peripheral-target organ levels to achieve better functional recovery. 展开更多
关键词 central nervous system central peripheral target organ multilevel pathological analysis nerve regeneration peripheral nerve injury peripheral nervous system target organs therapeutic approach
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Sensitivity analysis of the lithospheric magnetic field at satellite altitude:the effects of the inducing field and the shape of the magnetic lithosphere 被引量:1
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作者 JinSong Du YuKun Li +5 位作者 HouPu Li ChangQing Yuan KangAn Zhao JiangSong Gui Pan Zhang ShaoFeng Bian 《Earth and Planetary Physics》 2025年第3期642-652,共11页
As a means of quantitative interpretation,forward calculations of the global lithospheric magnetic field in the Spherical Harmonic(SH)domain have been widely used to reveal geophysical,lithological,and geothermal vari... As a means of quantitative interpretation,forward calculations of the global lithospheric magnetic field in the Spherical Harmonic(SH)domain have been widely used to reveal geophysical,lithological,and geothermal variations in the lithosphere.Traditional approaches either do not consider the non-axial dipolar terms of the inducing field and its radial variation or do so by means of complicated formulae.Moreover,existing methods treat the magnetic lithosphere either as an infinitesimally thin layer or as a radially uniform spherical shell of constant thickness.Here,we present alternative forward formulae that account for an arbitrarily high maximum degree of the inducing field and for a magnetic lithosphere of variable thickness.Our simulations based on these formulae suggest that the satellite magnetic anomaly field is sensitive to the non-axial dipolar terms of the inducing field but not to its radial variation.Therefore,in forward and inverse calculations of satellite magnetic anomaly data,the non-axial dipolar terms of the inducing field should not be ignored.Furthermore,our results show that the satellite magnetic anomaly field is sensitive to variability in the lateral thickness of the magnetized shell.In particular,we show that for a given vertically integrated susceptibility distribution,underestimating the thickness of the magnetic layer overestimates the induced magnetic field.This discovery bridges the greatest part of the alleged gap between the susceptibility values measured from rock samples and the susceptibility values required to match the observed magnetic field signal.We expect the formulae and conclusions of this study to be a valuable tool for the quantitative interpretation of the Earth's global lithospheric magnetic field,through an inverse or forward modelling approach. 展开更多
关键词 lithospheric magnetic field forward calculation spherical harmonic analysis sensitivity analysis satellite magnetism
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