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柱切换

柱切换的相关文献在1991年到2022年内共计128篇,主要集中在药学、化学、化学工业 等领域,其中期刊论文81篇、会议论文11篇、专利文献746846篇;相关期刊40种,包括浙江大学学报(理学版)、药物分析杂志、药学实践杂志等; 相关会议8种,包括第13届离子色谱学术报告会、中华中医药学会中药分析分会第三届学术交流会、第十一次全国临床药理学学术大会等;柱切换的相关文献由290位作者贡献,包括朱岩、贾正平、李章万等。

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期刊论文>

论文:81 占比:0.01%

会议论文>

论文:11 占比:0.00%

专利文献>

论文:746846 占比:99.99%

总计:746938篇

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柱切换

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  • 贾正平
  • 李章万
  • 王荣
  • 谢华
  • 钟莺莺
  • 张强
  • 张玉荣
  • 梁晨
  • 汪蓉
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    • 姚永青; 王立萍; 刘英
    • 摘要: 目的 建立柱切换高效液相色谱-蒸发光散射检测法(HPLC-ELSD)测定硫酸庆大霉素颗粒中庆大霉素C组分含量,并对2017年国家评价性抽验190批次样品进行检测.方法 采用配置切换六通阀的高效液相色谱仪,GRACE Apollo C18色谱柱( 250mm×4.6mm,5μm),流动相为0.2mol/L三氟乙酸溶液∶甲醇(96∶4,V/V),柱温35°C,流速0.6mL/min,进样量25μL,ELSD漂移管温度110°C,载气流量2.5L/min,增益1.结果 采用新建的柱切换HPLC-ELSD法可有效去除辅料蔗糖等对测定的干扰,庆大霉素C组分(C1、C1a、C2、C2a)的平均回收率分别为98.9%、102.0%、100.1%和98.6%,RSD(n=9)分别为0.5%、0.4%、0.3%和0.6%,线性范围分别为0.0517~0.6465、0.0538~0.6729、0.0651~0.8136和0.0299~0.3738mg/mL.190批次样品中12批次样品的庆大霉素C,偏低,2批次样品的庆大霉素总C组分含量偏低,3批次样品的庆大霉素总C组分含量偏高.结论 新建方法准确简便,专属性良好,可为硫酸庆大霉素颗粒中庆大霉素C组分的控制提供参考.
    • 李进; 姚尚辰; 胡昌勤
    • 摘要: 目的:对注射用头孢美唑钠中的杂质结构进行分析.方法:采用Phenomenex Gemini C18(250 mm ×4.6 mm,5μm)色谱柱,以磷酸二氢铵溶液-甲醇-四氢呋喃-20%四丁基氢氧化铵(700∶ 280∶ 25∶6.4,v/v,pH =4.5)为流动相分离杂质;对注射用头孢美唑钠进行强制降解实验,归属杂质来源;采用柱切换-LC/MSn技术采集杂质的质谱数据,根据头孢菌素类抗生素的质谱裂解规律和降解反应机制,推定相关杂质的化学结构.结果:在制剂中共检出并推断了6种杂质的化学结构,包括3种降解杂质和3种工艺杂质,未检出聚合物类杂质.结论:采用柱切换-LC/MSn技术可快速推定注射用头孢美唑钠中相关杂质的化学结构,《中华人民共和国药典》(ChP)2015年版的注射用头孢美唑钠有关物质检测方法需要进一步优化和提高.
    • 梁剑锋; 李亚; 梁峰
    • 摘要: 烧烤肉制品由于富含动物油脂,在炭火高温烧烤熟制品过程中,容易出现苯并(a)芘超标问题,具有较高安全隐患.建立二维液相色谱仪检测烧烤肉制品中苯并(a)芘的方法.第1维为分离、富集柱,采用Inertsil ODS柱(4.6 mm×150 mm,5μm),流动相为乙腈-水(85:15,V/V),流速1.0 mL/min,可以实现500μL样品中目标物苯并(a)芘的富集与分离;第2维采用ChromSpher Pi柱(3.0 mm×80 mm,5μm),流动相为异丙醇-乙腈(60:40,V/V),流速1.2 mL/min,可以有效分离、测定样品中的苯并(a)芘.结果表明:烧烤肉制品中苯并(a)芘在1.0~20.0 ng/mL范围内呈线性关系,其线性回归方程为y=1.8471x-0.1033(r=0.999),检出限为0.08μg/kg,在1.00、3.00、5.00、10.00μg/kg加标水平下,加标回收率为97.1%~105.2%,相对标准偏差为1.55%~2.77%.
    • 杜小弟; 李俊升; 郭丽萍; 雷家珩
    • 摘要: 通过2台高压恒流泵、1台紫外检测器、1个手动进样阀、1个高压切换阀和2根色谱柱组建了二维液相色谱系统,建立了在线富集测定银杏叶提取物(EGB)及其制剂中微量银杏酸的方法.第一维色谱柱为富集柱,采用ZORBAX Eclipse Plus-C18(2.1 mmx12.5mm,5μm),流动相为甲醇-水-三氟乙酸混合液(体积比80:20:0.01),流速为0.25 mL/min,可实现300μL样品的富集,有效降低了基体干扰.第二维色谱柱为分析柱,采用ZORBAX Eclipse Plus-C18(2.1 mmx150mm,5 μm),流动相为甲醇-水-三氟乙酸混合液(体积比90: 10:0.01),流速为0.25 miymin,可有效分离银杏酸.使用紫外检测器在310 nm处检测,可实现对银杏酸的准确定量.研究了试样的溶剂对富集效果的影响,当试样溶剂与第一维流动相一致时可获得较好的富集效果.该方法对试样中5种银杏酸在0.200-100.0 mg/kg范围内具有良好的线性关系,相关系数均大于0.998,检出限达0.02~0.06 mg/kg.对实际样品测定结果的相对标准偏差均不大于5.0%,在5、 10 mg/kg加标水平下,加标回收率为94.0%~101.3%.%A method of two-dimensional liquid chromatography with online enrichment was established for the determination of trace ginkgolic acids in Ginkgo biloba extract(EGB) and their preparations. The liquid chromatography system was composed of two LC pumps, an UV detector, a manual sampling valve, a switching valve and two columns. The ginkgolic acids were enriched on the first dimensional column of ZORB AX Eclipse Plus-C18 (2.1 mm x 12. 5 mm, 5μm) using a methanol-water-trifluoroacetic acid mixture (80:20:0.01) as mobile phase at a flow rate of 0.25 mL/min, then separated on the second dimensional column of ZORBAX Eclipse Plus-C18(2.1 mm x 150 mm, 5 μm) using a methanol-water-trifluoroacetic acid mixture (90:10-0.01) as mobile phase at a flow rate of 0.25 mL/min, finally detected with a UV detector at 310 nm. The effects of sample solvent and sample volume on the enrichment were investigated. When the sample solvent was consistent with the first dimension mobile phase, the enrichment on 300 μL sample could be achieved. There existed good linear responses for 5 kinds of ginkgolic acids in the range of 0.200-100.0 mg/kg, with correlation coefficients greater than 0.998 and detection limits of 0.02-0.06 mg/kg. The recoveries at two spiked levels of 5 mg/kg and 10 mg/kg were between 94.0% and 101.3% with relative standard deviations not more than 5.0%.
    • 范艳璇; 何沛
    • 摘要: A fast determination method for salt content in crude oil by ion chromatography was de-veloped. The samples were extracted by high frequency oscillation extraction using mixture of water, ethanol,and xylene. The column-switching technique was then used on line to eliminate the interference of ethanol in extraction solution in chromatography analysis. Then the chloride was detected by ion chro-matography. The results show a great linear relationship in the concentration range from 0. 1 to 100 mg-NaCl/L,the correlation coefficient is greater than 0. 999. The detection limit for ion chromatography is 0. 01 mgNaCl/L based on signaloise ratio of 3. The difference between this method and the coulometry method is not significant. The column-switching ion chromatography can meet the analysis requirement of salt content in crude oil but much fast and simple.%建立了用离子色谱方法快速批量测定原油中盐含量的方法,通过手动高频震荡萃取后,利用柱切换技术在线消除萃取液中乙醇对离子色谱系统的干扰,然后经过离子色谱柱对无机氯化物进行分离分析,在优化的色谱条件下,盐质量浓度在0. 1~100 mgNaCl/L范围内线性相关系数均大于0. 999,离子色谱检出限为0. 01 mgNaCl/L(信噪比为3).该方法与现行标准方法电量法之间的差异不显著,可满足原油中盐含量的分析要求.
    • 李进; 张培培; 姚尚辰; 胡昌勤
    • 摘要: 目的 对阿莫西林钠克拉维酸钾复方原料中的杂质结构进行分析.方法 采用BDS Hypersil C18色谱柱,以0.01mol/L磷酸二氢钾溶液(pH6.0)-乙腈为流动相进行梯度洗脱分离杂质;对阿莫西林钠克拉维酸钾(5∶1)原料进行强力实验,归属杂质来源;采用柱切换-LC/MSn技术采集杂质的质谱数据,根据青霉素类抗生素的质谱裂解规律和降解反应机理,推定相关杂质的化学结构.结果 在原料中共检出并推断出11种杂质的化学结构,均为阿莫西林相关杂质,未检出与克拉维酸钾相关的杂质.结论 采用柱切换-LC-MSn技术可快速推定阿莫西林钠克拉维酸钾复方原料中相关杂质的化学结构,为《中国药典》中该类药品标准的提高提供了基础数据.%Objective To study the impurity structures in co-amoxicillin and potassium clavulanate bulk material.Methods Impurities in bulk material were eluted in gradients on a BDS Hypersil C18 column,with 0.01moL/L potassium dihydrogen phosphate (pH6)-acetonitrile as the mobile phase.Stress tests were designed and performed on the bulk material to specify those impurities.The impurities were analyzed by the application of the on-line column-switching LC-MSn method and their structures were characterized based on the degradation mechanism and the mass fragmentation regularity of penicillin.Results Eleven impurities were detected and characterized in the raw material.All of them were related to amoxicillin including seven degradation products and four derived impurities from synthesis process.Impurities related to potassium clavulanate were not detected.Conclusion This research can rapidly identify the structures of related impurities in co-amoxicillin and potassium clavulanate bulk material,and provide the basic data for the specification improvement of co-amoxicillin and potassium clavulanate product in China Pharmacopeia.
    • 赵振东; 谢艳丽
    • 摘要: 以十二烷基苯磺酸钠(SDBS)和脂肪醇聚氧乙烯醚(AEO)进行表面活性剂的复配,应用柱切换离子色谱法,通过测定草甘膦含量评价其热贮稳定性.草甘膦的质量浓度在0.02~5 mg/L范围内与色谱峰面积呈良好的线性,相关系数r=0.9996,检出限为0.009 mg/L(S/N=3),保留时间和峰面积重复性分别为0.72%,1.63%(n=6),回收率为97.96%~102.23%.配制的阴/非离子二元表面活性剂复合体系-草甘膦微乳剂在(54±2)°C条件下贮藏14 d后,分解率小于5%,为合格,配方热贮稳定性良好.该方法简单、准确,灵敏度高,可用于二元表面活性剂-草甘膦微乳剂的热稳定性研究.%Sodium dodecyl benzene sulfonate(SDBS) and fatty alcohol-polyoxyethylene ethe(AEO) were used for making a mixture of surfactants. Thermal storage stability was studied in binary ioniconionic surfactants-glyphosate microemulsion by ion chromatography coupled with column-switching, through detection of glyphosate. The results exhibited good linearity in the range of 0.02-5 mg/L. The limit of detection was 0.009 mg/L. The repeatability of retention time and peak area was 0.72%,1.63%,respectively. The standard addition recoveries between 97.96% and 102.23%. The dissociation of the binary ioniconionic surfactants-glyphosate microemulsion was below 5% after being stored for 14 days at (54±2)°C. This method is simple,reliable and sensitive, it can be used for researchment of thermal stability of binary surfactants-glyphosate microemulsion.
    • 曾冬伟
    • 摘要: 柱切换指的是在对多通道切换阀应用的基础上,使得进样阀和色谱柱、色谱柱和检测器之间呈现出来的相互关系发生一定程度的变化的技术措施,针对在样品当中使用到的多组分待检测物质净化和分离分析,柱切换高效液相色谱法是一种有效性比较强的分析措施,样品需要经过预期性处理之后再开展进样工作.待检测物质可以开展富集、净化以及衍生等操作,以此为基础自然也就可以使得有机溶液的使用量得到有效的控制,并使得回收率得到一定程度的提升,因此对柱切换高效液相色谱法在食品检验领域中得到应用具有一定的现实意义,希望能够给从事食品检验的相关工作人员在对这个问题分析时起到一定程度的借鉴作用,最终为推动我国社会经济向前发展做出一定的贡献.
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