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Analysis of Monosaccharide Composition of Pu-erh Tea Polysaccaride by Pre-column Derivatization HPLC 被引量:3
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作者 郭威 周斌星 +4 位作者 罗玲 李扬 柴洁 杨超 马存强 《Agricultural Science & Technology》 CAS 2013年第4期556-558,572,共4页
[Objective] This study aimed to establish a pre-column derivatization HPLC method for the identification and analysis of monosaccharide composition of Pu-erh tea polysaccharide. [Method] Pu-erh tea polysaccharide was ... [Objective] This study aimed to establish a pre-column derivatization HPLC method for the identification and analysis of monosaccharide composition of Pu-erh tea polysaccharide. [Method] Pu-erh tea polysaccharide was extracted using the wa- ter extraction method, further isolated and purified by DEAE cellulose-52 columns. The obtained tea polysaccharide and four components TPS1, TPS2, TPS3 and TPS, were first derived by 1-phenyl-3-methyl-5-pyrazolone (PMP), and then the PMP derivatives of monosaccharide were analyzed by high performance liquid chromatog- raphy (HPLC). [Result] Pu-erh tea polysaccharide contained eight kinds of monosac- chaddes (mannose, rhamnose, glucuronic acid, galacturonic acid, grucose, galactose, arabinose, fucose), without xylose; so it was the same with TPS1; each of TPS2, TPS3 and TPS4 contained seven monosaccharides, while no fucose. [Conclusion] This method is simplified and rapid, which can be used to determine the monosac- charide composition of Pu-erh tea polysaccharide and monosaccharide content. 展开更多
关键词 Pu-erh tea POLYSACCHARIDE HPLC pre-column derivatization
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Determination of Sparfloxacin in Human Urine by Reversed-Phase High Performance Liquid Chromatography With Nitrous Acid and Hydroiodic Pre-Column Derivatization 被引量:1
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作者 Li Ming DU Zhe Feng FAN +1 位作者 Jin Li QIAO Jing Ping WANG 《Chinese Chemical Letters》 SCIE CAS CSCD 2001年第11期1007-1010,共4页
Sparfloxacin can be oxidized by nitrous acid, then react with hydroiodic acid to form a fluorescent derivative. Based on this, a reversed-phase high performance liquid chromatographic pre-column derivatization new met... Sparfloxacin can be oxidized by nitrous acid, then react with hydroiodic acid to form a fluorescent derivative. Based on this, a reversed-phase high performance liquid chromatographic pre-column derivatization new method is described for the determination of sparfloxacin in human urine. The linear range is 0.05 mg/L to 4.0 mg/L, the recoveries are 91.5%similar to 95.7% and the RSD is 1.2%similar to4.2%. The results showed that this method is suitable for the determination of sparfloxacin in human urine. 展开更多
关键词 SPARFLOXACIN HPLC pre-column derivatization human urine
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Determination of 18 Kinds of Amino Acids in Fresh Tea Leaves by HPLC Coupled with Pre-column Derivatization 被引量:3
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作者 Shangwen DONG Tengfei LIU Minghui DONG 《Asian Agricultural Research》 2018年第2期55-58,63,共5页
A rapid and accurate quantitative method of high performance liquid chromatography( HPLC) with fluorescence detector has been developed for the analysis of 18 kinds of amino acids in fresh tea leaves. The samples were... A rapid and accurate quantitative method of high performance liquid chromatography( HPLC) with fluorescence detector has been developed for the analysis of 18 kinds of amino acids in fresh tea leaves. The samples were minced and mixed,and extracted with ultra pure water at 90℃ for 20 min. The 6-aminoquinolyl N-hydroxy-succinimidyl carbamate( AQC) was used as pre-column derivatization reagent. Gradient HPLC separation was performed on a C_(18) column( Symmetry C_(18),3. 9 mm × 15 cm,4 μm). Good linearity between concentrations and peak areas was achieved in the concentration range of 5. 0-250 μmol/L for 18 kinds of amino acids. The method was validated by the analysis of five replicates. The 18 kinds of amino acid standards were spiked in fresh tea leaf samples and the average recovery rate was 86. 25%-109. 05% with relative standard deviations( n = 5) ranging from 6. 03% to 10. 56%. The limit of detection( LOD) for the analytes was0. 05-1. 27 μmol/L. The method was successfully applied to the analysis of the 18 kinds of amino acids in fresh tea leaves from east Dongting and west Dongting mountains in Suzhou. The results indicate that the method is simple,rapid,precise and reliable. 展开更多
关键词 Fresh tea leaves Free amino acids pre-column derivatization High performance liquid chromatography(HPLC)
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Enantioresolution of a Series of Chiral Benzyl Alcohols by HPLC on a Dinitrobenzoylphenylglycine Stationary Phase after Achiral Pre-Column Derivatization
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作者 Svilen P. Simeonov Anton P. Simeonov +1 位作者 Aleksandar R. Todorov Vanya B. Kurteva 《American Journal of Analytical Chemistry》 2010年第1期1-13,共13页
High performance liquid chromatography method for the separation of a series of chiral benzyl alcohols on N-(3,5-dinitrobenzoyl)-D-phenylglycine stationary phase (Macherey Nagel, Chiral-2) after pre-column achiral der... High performance liquid chromatography method for the separation of a series of chiral benzyl alcohols on N-(3,5-dinitrobenzoyl)-D-phenylglycine stationary phase (Macherey Nagel, Chiral-2) after pre-column achiral derivatization was developed. Cheap and easy available aromatic acid chlorides were used as derivatization agents. Good to excellent separations of the enantiomers were achieved in all cases in relatively short analytical runs. It was shown that the enantiorecognition depends on the substituents both in the starting alcohol and in the acid chloride. The method presents an efficient alternative to the direct analyses on polysaccharide and cyclodextrine-derived stationary phases. 展开更多
关键词 HPLC DNBPG ENANTIOSEPARATION BENZYL ALCOHOLS Achiral pre-column derivatization BENZOATES Chlorobenzoates Naphthoates
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HPLC of Amino Acids and Oligopeptides by Pre-Column Fluorescence Derivatization with 9-Acridine Formyl Chloride
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作者 Jin Mao YOU Xin Jun FAN Qing Yu OU(Lanzhou Institute of Chemical Physics. Chinese Academy of Sciences 730000) 《Chinese Chemical Letters》 SCIE CAS CSCD 1997年第10期875-878,共4页
A highly sensitive HPLC method for the detection of amino acids and oligopeptides with 9-acridine formyl chloride by pre-column fluorescence derivatization has been developed. Glycine, glycylglycine, histidine, trigly... A highly sensitive HPLC method for the detection of amino acids and oligopeptides with 9-acridine formyl chloride by pre-column fluorescence derivatization has been developed. Glycine, glycylglycine, histidine, triglycine and glutathione were separated on a reversed-phase C-18 column with methanol-water-triethylamine eluent, derivatization and chromatographic conditions were optimized. The five derivatives were eluted in 28 min with a good reproducibility. Linear range of the calibration graph was 0.08-260 nmol/ml(-1). The relative standard deviations(n=6) are < 5%. Detection limits (signal-to-noise ratio=3) for the five derivatives are 20-40 fmol. 展开更多
关键词 HPLC of Amino Acids and Oligopeptides by pre-column Fluorescence derivatization with 9-Acridine Formyl Chloride
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Reversed-phase high-performance liquid chromatographic analysis of seven pairs of chiral drug enantiomers in transport medium after chiral derivatization
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作者 贺瑛 柴晓鹃 曾苏 《Journal of Chinese Pharmaceutical Sciences》 CAS 2010年第2期104-109,共6页
A reversed-phase high-performance liquid chromatographic (RP-HPLC) method was established for the determination of the enantiomers of 7 aryloxy aminopropanol drugs (atenolol, sotalol, celiprolol, carvedilol, metopr... A reversed-phase high-performance liquid chromatographic (RP-HPLC) method was established for the determination of the enantiomers of 7 aryloxy aminopropanol drugs (atenolol, sotalol, celiprolol, carvedilol, metoprolol, propranolol and propafenone) in transport medium. The method involved liquid-liquid extraction of chiral drugs from transport medium, and employed 2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl isothiocyanate (GITC, 1.0 mg/mL in acetonitrile) as a pre-column chiral derivatization reagent. After derivatization, the products were separated on an Agilent Zorbax C8 column (150 min×4.6 mm, 5 μm) at 25 ℃. The mobile phase consisted of a mixture of acetonitrile and 0.01 M phosphate buffer (pH 3.5). The present methods were specific for the determination of enantiomers of each chiral drug. The absolute recoveries of the enantiomers and internal standards were 〉78%. The relative recoveries of the enantiomers were approximately 100%. The intra- and inter-day variations were 〈 15%. The method was reproducible and sufficiently sensitive to determine the enantiomers of seven aryloxy aminopropanol drugs in transport medium. The method could be used to study the transport of atenolol, sotalol, celiprolol, carvedilol, metoprolol, propranolol and propafenone. 展开更多
关键词 Enantiomer separation Aryloxy aminopropanol drugs RP-HPLC pre-column derivatization
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Synthesis and acaricidal activity of strobilurin-pyrimidine derivatives 被引量:4
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作者 Bao-Shan Chai Chang-Ling Liu +4 位作者 Hui-Chao Li Shao-Wu Liu Ying Xu Yu-Quan Song Jun-Biao Chang 《Chinese Chemical Letters》 SCIE CAS CSCD 2014年第1期137-140,共4页
Pyriminostrobin, a new acaricide, was discovered in our previous studies. Because introducing fluorine into organic compounds can increase bioactivity, pyriminostrobin was modified as a series of strobilurin-pyrimidin... Pyriminostrobin, a new acaricide, was discovered in our previous studies. Because introducing fluorine into organic compounds can increase bioactivity, pyriminostrobin was modified as a series of strobilurin-pyrimidine derivatives for biological screening. The compounds were characterized by 1H NMR, MS and elemental analysis. Preliminary bioassays demonstrated that compounds 7e and 7i exhibited significant control against Tetranychus cinnabarinus (Boisd.) at 0.625 mg L^-1, and their acaricidal potencies were higher than pyriminostrobin in a greenhouse. The relationship between structure and acaricidal activity was also studied. 展开更多
关键词 Strobilurin-pyrimidine Acaricidal activity Intermediate derivatization method Pyriminostrohin
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Design, synthesis, and fungicidal activity of novel 1,3,4-oxadiazole derivatives 被引量:1
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作者 Fuqiang Yu Aiying Guan +2 位作者 Mengru Li Lan Hu Xiaowu Li 《Chinese Chemical Letters》 SCIE CAS CSCD 2018年第6期915-918,共4页
Employing the intermediate derivatization method(IDM), twenty novel 1,3,4-oxadiazole derivatives containing arylpyrazoloxyl moiety were designed and synthesized. The structures of the title compounds were identified... Employing the intermediate derivatization method(IDM), twenty novel 1,3,4-oxadiazole derivatives containing arylpyrazoloxyl moiety were designed and synthesized. The structures of the title compounds were identified by1 H NMR,13 C NMR, MS and elemental analyses, compound 4 was further identified by single-crystal X-ray diffraction. Antifungal activities against rice sheath blight(RSB) and sorghum anthracnose(SA) were evaluated by the mycelium linear growth rate method. Compounds 4, 16 and 20 displayed significant activities against RSB(EC50= 0.88 mg/L, 0.91 mg/L and 0.85 mg/L, respectively),higher than the reference tebuconazole; While compound 3 exhibited higher activity against SA(EC50= 1.03 mg/L), equal to commercial pyraclostrobin(EC50= 1.06 mg/L). The study showed that compound 20 is a promising fungicide for further development. 展开更多
关键词 1 3 4-Oxadiazole derivatives Intermediate derivatization method Rice sheath blight Sorghum anthracnose Structure-activity relationship
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Synthesis and bioactivity of novel coumarin derivatives containing(E)-methyl 2-(methoxyimino)-2-phenylacetates
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作者 Ai Ying Guan Chang Ling Liu Zhi Nian Li Ming Xing Zhang 《Chinese Chemical Letters》 SCIE CAS CSCD 2011年第6期663-666,共4页
Ten coumarin derivatives containing(E)-methyl 2-(methoxyimino)-2-phenylacetate were synthesized and bioassayed.The compounds were identified by IR,~1H NMR and elemental analyses.The test results indicated that com... Ten coumarin derivatives containing(E)-methyl 2-(methoxyimino)-2-phenylacetate were synthesized and bioassayed.The compounds were identified by IR,~1H NMR and elemental analyses.The test results indicated that compound 5j(R^1 is methyl and R^2 is n-C_6H_(13)) was the optimal structure in this paper with good fungicidal activity against CDM(85%) at 6.25 mg/L concentration. 展开更多
关键词 COUMARINS Methoxyacrylates Intermediate derivatization method Fungicides
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柱前衍生-气相色谱-质谱法测定鸡蛋中五氯苯酚的含量 被引量:1
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作者 鲁晋南 王丽 +1 位作者 王云 梁杭曦 《理化检验(化学分册)》 北大核心 2025年第2期190-194,共5页
考虑到鸡蛋样品基质复杂,其中五氯苯酚(PCP)检测的相关研究较少,基于PCP和其钠盐可在一定酸度条件下相互转化的特点,提出了题示方法。取鸡蛋样品5.00 g,加入30μL 10.0 mg·L^(-1)2,4,6-三溴苯酚内标溶液、10 mL体积比9∶1的正己烷... 考虑到鸡蛋样品基质复杂,其中五氯苯酚(PCP)检测的相关研究较少,基于PCP和其钠盐可在一定酸度条件下相互转化的特点,提出了题示方法。取鸡蛋样品5.00 g,加入30μL 10.0 mg·L^(-1)2,4,6-三溴苯酚内标溶液、10 mL体积比9∶1的正己烷-乙酸乙酯混合溶液和2.5 mL 5%(体积分数)三氯乙酸溶液,涡旋振荡5 min,超声提取10 min,在0℃下离心5 min。吸取上层有机相,于60℃氮吹至3 mL,加入3 mL 0.1 mol·L^(-1)氢氧化钠溶液,涡旋振荡3 min,在0℃下离心2 min。弃去上层有机相,在水相中加入0.5 mL 6 mol·L^(-1)盐酸溶液和5 mL正己烷,涡旋振荡2 min,在0℃下离心2 min。吸出上层有机相,于60℃氮吹至干,加入1.5 mL乙腈,超声2 min,离心2 min,吸取上层乙腈相,过活化好的SLC固相萃取柱,用4 mL乙腈洗脱柱子,收集洗脱液,于60℃氮吹至0.5 mL,加入0.2 mL体积比1∶1的乙酸酐-吡啶混合溶液,密封后于60℃反应15 min。加入1 mL正己烷和2.0 mL 0.2 mol·L^(-1)碳酸钾溶液,涡旋振荡2 min,离心2 min,吸取有机相,注入气相色谱-质谱仪,在Rtx-5ms色谱柱上以升温程序分离溶液中的PCP,电子轰击(EI)离子源电离,选择离子监测(SIM)模式检测,内标法定量。结果显示:标准曲线的线性范围为10~200 ng,检出限(3S/N)为0.11μg·kg^(-1);按照标准加入法进行回收试验,回收率为83.0%~104%,测定值的相对标准偏差(n=6)为4.2%~9.4%。方法用于18份市售鸡蛋样品的分析,在1份鸡蛋样品中检出PCP,检出量为5.07μg·kg^(-1)。 展开更多
关键词 五氯苯酚 气相色谱-质谱法 内标法 柱前衍生 鸡蛋
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吲哚嗪酮的合成方法及衍生化反应
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作者 黄文宇 傅睿 《发酵科技通讯》 2025年第4期234-242,共9页
吲哚嗪酮属于含氮杂环化合物,其结构中兼具α,β-不饱和烯酮与双烯胺结构单元。作为关键反应前体,吲哚嗪酮可用于合成众多含氮杂环天然产物、药物以及具有生物活性的分子。当前,吲哚嗪酮分子的主流合成方法是借助吡啶、喹啉的环化去芳... 吲哚嗪酮属于含氮杂环化合物,其结构中兼具α,β-不饱和烯酮与双烯胺结构单元。作为关键反应前体,吲哚嗪酮可用于合成众多含氮杂环天然产物、药物以及具有生物活性的分子。当前,吲哚嗪酮分子的主流合成方法是借助吡啶、喹啉的环化去芳构化重排反应。同时,也有少数通过其他途径合成吲哚嗪酮的方法。此外,吲哚嗪酮结构中的双烯胺和α,β-不饱和烯酮结构,能够通过氢化、碘化和环加成等衍生化反应实现进一步的产物转化,从而高效合成更复杂的含氮杂环化合物。 展开更多
关键词 吲哚嗪酮 合成方法 衍生化反应
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衍生气相色谱内标法测定工作场所空气中氯乙酸含量
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作者 孔燕 《质量安全与检验检测》 2025年第3期77-80,85,共5页
建立了作业场所空气中氯乙酸的溶剂解吸衍生毛细管气相色谱检测方法。该方法用硅胶管吸附空气中的氯乙酸,用甲基叔丁基醚解吸,同时添加内标物采用内标法定量,并用HP-5毛细管气相色谱柱分离、ECD检测器检测。结果显示,方法的线性范围在5~... 建立了作业场所空气中氯乙酸的溶剂解吸衍生毛细管气相色谱检测方法。该方法用硅胶管吸附空气中的氯乙酸,用甲基叔丁基醚解吸,同时添加内标物采用内标法定量,并用HP-5毛细管气相色谱柱分离、ECD检测器检测。结果显示,方法的线性范围在5~100μg/mL,回归方程为y=0.0526x-0.0089(r=0.9996),检出限为0.036μg/mL,平均解吸效率为98.4%、97.3%、98.7%,相对标准偏差为1.99%、2.74%、3.11%,平均加标回收率为94.0%~98.8%,衍生效率为95.7%~98.8%。该方法灵敏、便捷、应用范围广,适用于作业场所空气中氯乙酸的检测。 展开更多
关键词 氯乙酸 衍生 毛细管气相色谱 内标法
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柱前衍生化法测定丙氨酰谷氨酰胺异构体
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作者 吴英纪 张亦鸣 《化工与医药工程》 2025年第6期30-34,共5页
丙氨酰谷氨酰胺作为一种二肽,存在异构体结构,且异构体可能会影响丙氨酰谷氨酰胺原料药药效和安全性,所以应严格控制其中异构体的含量,因此应建立柱前衍生化的高效液相色谱法测定丙氨酰谷氨酰胺中的异构体含量。以离子交换型手性柱为色... 丙氨酰谷氨酰胺作为一种二肽,存在异构体结构,且异构体可能会影响丙氨酰谷氨酰胺原料药药效和安全性,所以应严格控制其中异构体的含量,因此应建立柱前衍生化的高效液相色谱法测定丙氨酰谷氨酰胺中的异构体含量。以离子交换型手性柱为色谱柱,用Nα-(2,4-二硝基-5-氟苯基)-L-丙氨酰胺作为衍生化试剂,进行外标法测定,异构体限度按0.1%进行控制。丙氨酰谷氨酰胺异构体(L-丙氨酰-D-谷氨酰胺、D-丙氨酰-D-谷氨酰胺)的线性均在指标的30%~200%(浓度为0.15~1.0μg/mL)范围内符合要求,线性相关系数r均大于0.995,且异构体L-丙氨酰-D-谷氨酰胺和D-丙氨酰-D-谷氨酰胺的含量回收率均在80%~120%范围内,RSD均符合要求。此方法便捷、高灵敏度、高准确、且精密度良好,适用于丙氨酰谷氨酰胺中的异构体含量的检测。 展开更多
关键词 高效液相色谱法 柱前衍生化法 丙氨酰谷氨酰胺 异构体
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全自动免疫磁珠纯化法与免疫亲和柱法对食品中黄曲霉毒素B_(1)检测结果的影响比对
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作者 朱青 曹美萍 +4 位作者 任兴发 陈睿 邵锋伟 胡桂霞 石春红 《食品安全质量检测学报》 2025年第8期93-99,共7页
目的采用全自动免疫磁珠纯化法与免疫亲和柱法对大米、小麦制品、花生制品等多种基质进行前处理,检测其黄曲霉毒素B_(1)(aflatoxin,AFB_(1))含量,并比较两种前处理方法的检测结果。方法样品经甲醇:水(70:30,V:V)提取后,一部分提取液采... 目的采用全自动免疫磁珠纯化法与免疫亲和柱法对大米、小麦制品、花生制品等多种基质进行前处理,检测其黄曲霉毒素B_(1)(aflatoxin,AFB_(1))含量,并比较两种前处理方法的检测结果。方法样品经甲醇:水(70:30,V:V)提取后,一部分提取液采用免疫亲和柱法经AFB_(1)专用免疫亲和柱净化,另取一部分提取液采用搭配免疫磁珠试剂盒的全自动免疫磁珠纯化仪进行前处理,最后都采用高效液相色谱法-柱后衍生法进行检测。结果免疫磁珠纯化试剂盒效能和免疫亲和柱柱效均大于95%,皆能满足实验要求。在质量浓度为1.00~50.00 ng/mL的线性范围内,线性相关系数(r)为0.99993,线性关系良好。在大米基质中进行3水平加标回收率实验(n=6),两种前处理方法回收率范围为98.2%~106.0%,相对标准偏差为1.0%~5.0%;在小麦制品中进行单水平加标回收率实验(n=6),回收率超过80%,相对标准偏差为3.7%~7.2%。AFB_(1)阳性花生制品、玉米粉基质质控样品采用两种前处理方法进行检测,并对结果进行t检验,显示所得结果无显著性差异;对玉米粉基质质控样品采用两种前处理方法进行检测后所得结果进行Bland-Altman统计分析,结果表明在检测该基质AFB_(1)时两种方法可以相互替代。免疫亲和柱法净化步骤耗时长,20批样品耗时约3~4 h;只能人工操作,产生大约1000 mL废液;而免疫磁珠法采用全自动磁珠纯化仪,净化步骤一次40 min,可自动完成20批样品,几乎无废液产生。结论全自动免疫磁珠纯化法与免疫亲和柱法检测多种基质中的AFB_(1)均能取得良好效果,且免疫磁珠纯化法效率高、处理简便、产生废液少,成本可降低大约50%。 展开更多
关键词 黄曲霉毒素B_(1) 免疫磁珠纯化法 免疫亲和柱法 高效液相色谱法-柱后衍生法
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柱后衍生-液相色谱法测定农田灌溉水中5种典型氨基甲酸酯类农药残留
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作者 刘嘉文 《云南化工》 2025年第11期81-83,共3页
以某农业区农田灌溉水为例,选取5种典型氨基甲酸酯类农药为研究对象,灌溉水样品经液液萃取后,提取液浓缩净化,采用柱后衍生-液相色谱法进行测定。结果表明,该方法在0.00~5.00 mg/L的质量浓度范围内线性良好,相关系数可达到0.998;检出限... 以某农业区农田灌溉水为例,选取5种典型氨基甲酸酯类农药为研究对象,灌溉水样品经液液萃取后,提取液浓缩净化,采用柱后衍生-液相色谱法进行测定。结果表明,该方法在0.00~5.00 mg/L的质量浓度范围内线性良好,相关系数可达到0.998;检出限为0.5~0.8μg/L;对实际样品进行低、中、高质量浓度加标测定,农田灌溉水样品加标回收范围为70.1%~106%,相对标准偏差RSD为2.6%~14.8%。通过与标准分析方法比较,5种氨基甲酸酯类农药指标与标准方法相对偏差均在20%以内,具备良好的准确性。证明该方法可适用于水样中氨基甲酸酯类农药的测定。 展开更多
关键词 农田灌溉水 氨基甲酸酯 农药残留 液液萃取 柱后衍生 液相色谱法 方法比对
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柱后衍生-高效液相色谱法测定动物源性食品中氨基甲酸酯类农药的残留
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作者 刘晓燕 龚强 +2 位作者 吴延姣 李强 苗培贞 《市场监管与质量技术研究》 2025年第2期19-24,共6页
文中建立以酸化乙腈提取,使用QuEChERS法对动物源性食品中10种(涕灭威亚砜、涕灭威砜、灭多威、3-羟基克百威、涕灭威、速灭威、克百威、甲萘威、异丙威、仲丁威)氨基甲酸酯类农药残留量进行净化,荧光检测器分析。氨基甲酸酯类标准工作... 文中建立以酸化乙腈提取,使用QuEChERS法对动物源性食品中10种(涕灭威亚砜、涕灭威砜、灭多威、3-羟基克百威、涕灭威、速灭威、克百威、甲萘威、异丙威、仲丁威)氨基甲酸酯类农药残留量进行净化,荧光检测器分析。氨基甲酸酯类标准工作曲线在5.0~200 μg/L内线性范围良好,为外标法定量。动物源性食品中氨基甲酸酯类标准工作溶液添加回收率为85.2 %~93.7 %,测得的相对标准偏差在0.709 %~4.60 %之间。 展开更多
关键词 动物源性食品 QuEChERS方法 氨基甲酸酯类农药 柱后衍生-高效液相色谱仪 荧光检测器
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柱前衍生HPLC分析铁皮石斛多糖中单糖组成的变异规律 被引量:31
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作者 苑鹤 白燕冰 +2 位作者 斯金平 张爱莲 金小丽 《中国中药杂志》 CAS CSCD 北大核心 2011年第18期2465-2470,共6页
通过采集铁皮石斛不同种质、年龄及近缘种的药材,采用柱前衍生HPLC法测定多糖中的单糖组成。结果表明,铁皮石斛与近缘种间,铁皮石斛种质与年龄间各种单糖的绝对量和相对量均存在显著的差异,其中甘露糖绝对峰面积,铁皮石斛近缘种间变幅为... 通过采集铁皮石斛不同种质、年龄及近缘种的药材,采用柱前衍生HPLC法测定多糖中的单糖组成。结果表明,铁皮石斛与近缘种间,铁皮石斛种质与年龄间各种单糖的绝对量和相对量均存在显著的差异,其中甘露糖绝对峰面积,铁皮石斛近缘种间变幅为0.854×107~10.340×107,铁皮石斛种内为1.467×107~8.475×107,一至三年生样品分别为4.411×107(2.577×107~6.516×107),5.528×107(3.179×107~8.475×107),3.601×107(1.467×107~5.888×107);甘露糖与葡萄糖比值(相对峰面积),铁皮石斛近缘种间为0.976~16.599,种内为2.679~7.831,在供试样品中只有肿节石斛、报春石斛的相对峰面积与铁皮石斛重叠。研究结果揭示了铁皮石斛多糖中的单糖组成的变异规律,通过品种选育、采收期的控制可改变铁皮石斛中单糖的组分;利用铁皮石斛甘露糖与葡萄糖的相对峰面积可排除多数铁皮石斛混淆品,为铁皮石斛质量控制、资源培育提供依据。 展开更多
关键词 铁皮石斛 柱前衍生法 HPLC 单糖
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杀菌剂唑菌酯的创制经纬 被引量:14
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作者 李淼 刘长令 +3 位作者 李志念 李林 张弘 司乃国 《农药》 CAS 北大核心 2011年第3期173-174,共2页
概述了运用中间体衍生化方法发现杀菌剂唑菌酯(SYP-3343)的过程:以取代吡唑环替换丁香菌酯结构中的香豆素环,设计并合成了一系列化合物,发现先导化合物(2),通过优化研究发现多个高活性化合物,最终发现了(E)-2-(2-((3-(4-氯苯基)-1-甲基-... 概述了运用中间体衍生化方法发现杀菌剂唑菌酯(SYP-3343)的过程:以取代吡唑环替换丁香菌酯结构中的香豆素环,设计并合成了一系列化合物,发现先导化合物(2),通过优化研究发现多个高活性化合物,最终发现了(E)-2-(2-((3-(4-氯苯基)-1-甲基-1H-吡唑-5-基氧基)甲基)苯基)-3-甲氧基丙烯酸甲酯,即唑菌酯(SYP-3343),其具有广谱的杀菌活性,对蔬菜和作物的多种病害如霜霉病、稻瘟病、白粉病、炭疽病等均有很好的防治效果,同时SYP-3343具有明显的杀虫、杀螨活性,可达到病虫兼治之目的。已于2009年获准临时登记。 展开更多
关键词 中间体衍生化方法 唑菌酯 杀菌活性 霜霉病
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青钱柳叶多糖中单糖组分分析 被引量:8
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作者 蒋向辉 蒋天智 +1 位作者 王翔 苑静 《广西师范大学学报(自然科学版)》 CAS 北大核心 2018年第2期87-93,共7页
采用水提醇沉法提取青钱柳叶中粗多糖,用苯酚-硫酸法测定多糖含量,进一步采用柱前衍生HPLC法测定多糖中的单糖组成,并对3个不同来源的青钱柳叶中多糖和单糖的含量与构成进行比较分析。研究结果显示,青钱柳叶中粗多糖的平均质量分数为4.3... 采用水提醇沉法提取青钱柳叶中粗多糖,用苯酚-硫酸法测定多糖含量,进一步采用柱前衍生HPLC法测定多糖中的单糖组成,并对3个不同来源的青钱柳叶中多糖和单糖的含量与构成进行比较分析。研究结果显示,青钱柳叶中粗多糖的平均质量分数为4.34%,青钱柳叶中多糖主要由木糖、甘露糖、鼠李糖、阿拉伯糖、半乳糖、葡萄糖和核糖等单糖组成,其在粗多糖中的质量分数分别为3.04%、7.35%、8.46%、13.46%、24.32%、24.26%和6.16%。青钱柳叶中多糖因青钱柳叶来源不同而存在单糖组成差异。本研究为青钱柳叶质量控制与药理药效研究提供了依据。 展开更多
关键词 青钱柳 柱前衍生法 HPLC 多糖 单糖组成
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桑叶总生物碱中1-脱氧野尻霉素在大鼠体内的药物动力学研究 被引量:16
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作者 曹旭 欧阳臻 +4 位作者 赵明 裴丹 刘月琴 王吉标 尚磊 《中药新药与临床药理》 CAS CSCD 北大核心 2012年第4期449-452,共4页
目的建立测定大鼠血浆中1-脱氧野尻霉素(DNT)含量的柱前衍生-高效液相色谱荧光法,初步研究桑叶总生物碱中DNJ在大鼠体内的药动学过程。方法大鼠灌胃桑叶总生物碱(给药剂量按DNJ计约为80 mg·kg-1)后不同时间点采集血样,采用柱前衍生... 目的建立测定大鼠血浆中1-脱氧野尻霉素(DNT)含量的柱前衍生-高效液相色谱荧光法,初步研究桑叶总生物碱中DNJ在大鼠体内的药动学过程。方法大鼠灌胃桑叶总生物碱(给药剂量按DNJ计约为80 mg·kg-1)后不同时间点采集血样,采用柱前衍生-高效液相色谱荧光法测定,色谱条件为HiQSiL C18分析柱(4.6 mm×250 mm,5μm),乙腈-0.1%醋酸水溶液(40∶60,V/V)为流动相,荧光检测器激发波长254 nm,发射波长322 nm,流速1.0 mL·min-1,柱温25℃。DNJ血药浓度-时间数据用药动学软件3P97处理。结果 DNJ血浆浓度在1.4~22.4 mg·L-1线性关系良好,血浆中1-脱氧野尻霉素定量下限为1.4 mg·L-1。日内、日间精密度(RSD)分别为3.7%~5.8%和4.6%~6.0%,方法回收率为97.6%~101.5%,提取回收率为76.3%~81.6%。DNJ在大鼠体内的血药浓度-时间过程符合二房室模型,Ka=(4.85±0.95)h-1,AUC=(19.22±1.37)mg·h·L-1,Cmax=(12.98±1.92)mg·L-1,Tmax=(0.50±0.00)h。结论该法准确可靠,专属性强,适用于DNJ在大鼠体内的血药浓度测定及药代动力学研究。 展开更多
关键词 桑叶 总生物碱 1-脱氧野尻霉素 柱前衍生 荧光法 药物动力学
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