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学者姓名:陈红青
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Abstract :
A highly selective and sensitive electrochemical sensor for ascorbic acid (AA) assay has been prepared through Cu(I) catalyzed azide-alkyne cycloaddition reaction (CuAAC). The catalyst, Cu(I) species, is acquired from the reduction of Cu(II) by AA in situ. In the presence of Cu(I) catalyst, the azide modified Au electrode surface is shown to react quantitatively with terminal propargyl-functionalized ferrocene forming 1,2,3-triazoles. The electrochemical response of propargyl-functionalized ferrocene modified Au electrode surface can be monitored using differential pulse voltammetry (DPV) technique. Under optimal conditions, it is found that the current intensity has a linear relationship with the logarithm of AA concentration in the range of 5.0 x 10(-12) to 1.0 x 10(-9) M. Furthermore, the proposed electrochemical sensor shows a good stability (RSD 4.2%), high selectivity and low detection limit for AA detection. In addition, it also demonstrates that the proposed sensor can be applied to detect AA in real urine samples with satisfactory results.
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GB/T 7714 | Qiu, Suyan , Gao, Sen , Xie, Lidan et al. An ultra-sensitive electrochemical sensor for ascorbic acid based on click chemistry [J]. | ANALYST , 2011 , 136 (19) : 3962-3966 . |
MLA | Qiu, Suyan et al. "An ultra-sensitive electrochemical sensor for ascorbic acid based on click chemistry" . | ANALYST 136 . 19 (2011) : 3962-3966 . |
APA | Qiu, Suyan , Gao, Sen , Xie, Lidan , Chen, Hongqin , Liu, Qida , Lin, Zhenyu et al. An ultra-sensitive electrochemical sensor for ascorbic acid based on click chemistry . | ANALYST , 2011 , 136 (19) , 3962-3966 . |
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目的:建立HPLC法测定梅花入骨丹中没食子酸和槲皮素含量的方法。 方法:采用HPLC法,以SinoChrom C18(4.6mm×250mm,5μm)为色谱柱,乙腈-0.2%磷酸溶液为流动相,梯度洗脱(0min,乙腈-0.2%磷酸溶液比例为5:95;10min,比例为10:90;40min,比例为50:50);流速为1mL/min;检测波长为255nm;柱温为30℃。 结果:没食子酸在0.162~3.24μg(r=0.99995),槲皮素在0.002052~0.041μg(r=0.9997)内呈良好的线性关系,没食子酸平均回收率为103.86%,RSD为1.20%,槲皮素平均回收率为100.54%,RSD为0.97%。 结论:该方法简便可行,重复性好,分离效果好,可用于梅花入骨丹中没食子酸和槲皮素的含量测定。
Keyword :
HPLC法 HPLC法 梅花入骨丹 梅花入骨丹 槲皮素 槲皮素 没食子酸 没食子酸
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GB/T 7714 | 叶蕻芝 , 陈鹏程 , 陈红青 et al. HPLC法测定梅花入骨丹中的没食子酸和槲皮素含量 [C] //第六届全国中西医结合基础理论研究学术研讨会暨第二届湖南省中西医结合学会肝病专业学术年会论文集 . 2010 : 125-130 . |
MLA | 叶蕻芝 et al. "HPLC法测定梅花入骨丹中的没食子酸和槲皮素含量" 第六届全国中西医结合基础理论研究学术研讨会暨第二届湖南省中西医结合学会肝病专业学术年会论文集 . (2010) : 125-130 . |
APA | 叶蕻芝 , 陈鹏程 , 陈红青 , 徐两军 , 林薇 , 郑春松 et al. HPLC法测定梅花入骨丹中的没食子酸和槲皮素含量 第六届全国中西医结合基础理论研究学术研讨会暨第二届湖南省中西医结合学会肝病专业学术年会论文集 . (2010) : 125-130 . |
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目的 测定梅花入骨丹多糖含量. 方法 采用苯酚-硫酸法. 结果 本法建立的标准曲线为Y=8.1249X-0.0067(r2=0.9991),检测波长为490 nm,多糖含量为2.98%,平均回收率为99.15%,RSD为1.73%(n=5). 结论 此方法 简便可行,重现性较好,可作为梅花入骨丹的质量评价依据,为合理开发该药提供参考.
Keyword :
多糖 多糖 梅花入骨丹 梅花入骨丹 苯酚-硫酸法 苯酚-硫酸法
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GB/T 7714 | 叶蕻芝 , 杨名平 , 林薇 et al. 梅花入骨丹多糖含量的测定 [J]. | 福建中医学院学报 , 2009 , 19 (4) : 22-24 . |
MLA | 叶蕻芝 et al. "梅花入骨丹多糖含量的测定" . | 福建中医学院学报 19 . 4 (2009) : 22-24 . |
APA | 叶蕻芝 , 杨名平 , 林薇 , 郑春松 , 陈红青 , 刘献祥 . 梅花入骨丹多糖含量的测定 . | 福建中医学院学报 , 2009 , 19 (4) , 22-24 . |
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A high-performance CE with amperometric detection (CE-AD) was employed for the kinetic study of keto-enol tautomerism of p-hydroxyphenylpyruvic acid (pHPP). Several factors (concentration of beta-cyclodextrin (beta-CD), concentration and pH of running buffer, separation voltage and injection time) affecting CE-AD were investigated and separation conditions were optimized. The kinetics of pHPP was performed in water solution and phosphate solution under different pH and temperature, the homologous ketonization rate constants and half-life were obtained. Also, the activation energy was calculated according to the rate constants under different temperature. The experimental results indicated that beta-CD played an important role in the separation, therefore UV spectrometric method was applied for the study of complexation interaction between ketonic pHPP and beta-CD. The results indicated that the stoichiometric ratio of the pHPP-beta-CD complex was 1:1 and formation constant was determined. The obtained kinetic results are in correspondence with those reported by our group with CE-UV.
Keyword :
CE with amperometric detection CE with amperometric detection Keto-enol tautomerism Keto-enol tautomerism p-Hydroxyphenylpyruvic acid p-Hydroxyphenylpyruvic acid
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GB/T 7714 | Huang, Ying , Zhang, Xiaoli , Xu, Liangjun et al. Characterization of keto-enol tautomerism of p-hydroxyphenylpyruvic acid using CE with amperometric detection and spectrometric analysis [J]. | JOURNAL OF SEPARATION SCIENCE , 2009 , 32 (23-24) : 4155-4160 . |
MLA | Huang, Ying et al. "Characterization of keto-enol tautomerism of p-hydroxyphenylpyruvic acid using CE with amperometric detection and spectrometric analysis" . | JOURNAL OF SEPARATION SCIENCE 32 . 23-24 (2009) : 4155-4160 . |
APA | Huang, Ying , Zhang, Xiaoli , Xu, Liangjun , Chen, Hongqing , Chen, Guonan . Characterization of keto-enol tautomerism of p-hydroxyphenylpyruvic acid using CE with amperometric detection and spectrometric analysis . | JOURNAL OF SEPARATION SCIENCE , 2009 , 32 (23-24) , 4155-4160 . |
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A room temperature ionic liquid (IL), 1-butyl-3-methylimidazolium hexafluorophosphate (BMIMPF6) was used as a binder to prepare the electrically heated ionic liquid/carbon paste electrode (IL-HCPE). It has been found that N6-isopentenyl-adenine (2-ip) can enhance the electrochemiluminescent (ECL) intensity of Ru(bpy)(3)(2+). The electrode surface temperature (T-e) has great effect on the ECL intensity of Ru(bpy)(3)(2+)/2-ip system. The ECL intensities has a linear relationship with the concentration of 2-ip in the range of 1.0 x 10(-7)-1.2 x 10(-6) mol/L with a detection limit of 3.6 x 10(-8) mol/L (S/N = 3) when T-e was 58 degrees C, while the linear range was of 5.0 x 10(-7)-1.0 x 10(-6) mol/L with a detection limit of 1.8 x 10(-7) mol/L under 27 degrees C. It was also found that the reproducibility of this ECL system would be better at elevating temperature, the RSD were 7.2% and 1.5% for 8.0 x 10(-7) mol/L of 2-ip at 27 and 58 degrees C, respectively. The possible mechanism of the Ru(bpy)(3)(2+)/2-ip ECL system has been proposed also. (C) 2009 Elsevier B.V. All rights reserved.
Keyword :
Electrically heated carbon paste electrode Electrically heated carbon paste electrode Electrochemiluminescence Electrochemiluminescence N6-isopentenyl-adenine N6-isopentenyl-adenine Room temperature ionic liquid Room temperature ionic liquid
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GB/T 7714 | Lin, Zhenyu , Chen, Xiaoping , Chen, Hongqin et al. Electrochemiluminescent behavior of N6-isopentenyl-adenine/Ru(bpy)(3)(2+) system on an electrically heated ionic liquid/carbon paste electrode [J]. | ELECTROCHEMISTRY COMMUNICATIONS , 2009 , 11 (10) : 2056-2059 . |
MLA | Lin, Zhenyu et al. "Electrochemiluminescent behavior of N6-isopentenyl-adenine/Ru(bpy)(3)(2+) system on an electrically heated ionic liquid/carbon paste electrode" . | ELECTROCHEMISTRY COMMUNICATIONS 11 . 10 (2009) : 2056-2059 . |
APA | Lin, Zhenyu , Chen, Xiaoping , Chen, Hongqin , Qiu, Bin , Chen, Guonan . Electrochemiluminescent behavior of N6-isopentenyl-adenine/Ru(bpy)(3)(2+) system on an electrically heated ionic liquid/carbon paste electrode . | ELECTROCHEMISTRY COMMUNICATIONS , 2009 , 11 (10) , 2056-2059 . |
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拟肾上腺素药物是一类化学结构与药理作用和肾上腺素相似的胺类药物,与肾上腺素受体结合后可激动受体,产生肾上腺素一样的作用。目前测定拟肾上腺素药物的方法有流动注射化学发光法,高效液相色谱法,毛细管区带电泳-紫外检测法。而有关用毛细管电泳-安培检测方法的报道较少。本文利用毛细管电泳.安培检测的方法对三种拟肾上腺素药物去氧肾上腺素(PHE),间羟胺(MR),异丙肾上腺素(IP)进行了分离分析。在0.950V的检测电位下,以50mmol/L,磷酸盐溶液(pH10.0)-3mmo/lβ环糊精(β-CD)为运行液,分离电压18kV,三种物质在60cm×251μmi.d毛细管中可达到基线分离。利用上述方法测定了PHE和MR针剂及尿样,回收率测定结果满意。
Keyword :
拟肾上腺素药物 拟肾上腺素药物 样品富集 样品富集 毛细管电泳 毛细管电泳
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GB/T 7714 | 张晓丽 , 黄颖 , 徐两军 et al. 拟肾上腺素药物的毛细管电泳-安培检测研究 [C] //第十七届全国色谱学术报告会论文集 . 2009 : 733-734 . |
MLA | 张晓丽 et al. "拟肾上腺素药物的毛细管电泳-安培检测研究" 第十七届全国色谱学术报告会论文集 . (2009) : 733-734 . |
APA | 张晓丽 , 黄颖 , 徐两军 , 肖佳 , 陈红青 , 陈国南 . 拟肾上腺素药物的毛细管电泳-安培检测研究 第十七届全国色谱学术报告会论文集 . (2009) : 733-734 . |
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在pH 5.0的Britton-Robinson缓冲溶液中,马兜铃酸在玻碳电极上产生不可逆的还原波(Vc,p=-0.51 V vs.Ag/AgCl),具有吸附控制特性.利用马兜铃酸的电化学还原性质建立微分脉冲伏安法测定体系.马兜铃酸浓度在8.0×10-7~6.0×10-6 mol/L范围内与还原峰电流呈良好的线性关系,检出限达1.6×10-8mol/L.测定方法简便灵敏,应用于关木通中马兜铃酸总酸含量的快速测定,结果令人满意.
Keyword :
关木通 关木通 微分脉冲伏安法 微分脉冲伏安法 马兜铃酸 马兜铃酸
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GB/T 7714 | 吴晓苹 , 卢杰山 , 陈红青 . 马兜铃酸的电化学性质及其在关木通中的含量测定 [J]. | 分析测试学报 , 2007 , 26 (5) : 736-738,741 . |
MLA | 吴晓苹 et al. "马兜铃酸的电化学性质及其在关木通中的含量测定" . | 分析测试学报 26 . 5 (2007) : 736-738,741 . |
APA | 吴晓苹 , 卢杰山 , 陈红青 . 马兜铃酸的电化学性质及其在关木通中的含量测定 . | 分析测试学报 , 2007 , 26 (5) , 736-738,741 . |
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利用循环伏安法(CV)、线性扫描伏安法(LSV)、方波伏安法(OSWV)等电化学技术研究了隐丹参酮在玻碳电极(GCE)上的电化学氧化过程,并用计时电量法和恒电位库仑电解法等对其在电极表面的吸附行为及氧化还原机理进行了探讨.此外利用自组装DNA修饰玻碳电极研究了隐丹参酮与DNA之间的相互作用.
Keyword :
DNA DNA 修饰电极 修饰电极 电化学 电化学 相互作用 相互作用 隐丹参酮 隐丹参酮
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GB/T 7714 | 刘薇 , 吴晓苹 , 郑国森 et al. 隐丹参酮的电化学性质及其与DNA相互作用的研究 [J]. | 分析测试技术与仪器 , 2007 , 13 (4) : 246-252 . |
MLA | 刘薇 et al. "隐丹参酮的电化学性质及其与DNA相互作用的研究" . | 分析测试技术与仪器 13 . 4 (2007) : 246-252 . |
APA | 刘薇 , 吴晓苹 , 郑国森 , 张兰 , 陈红青 , 陈国南 . 隐丹参酮的电化学性质及其与DNA相互作用的研究 . | 分析测试技术与仪器 , 2007 , 13 (4) , 246-252 . |
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采用毛细管电泳安培检测法对厚朴酚及和厚朴酚的分离测定进行了详细研究.工作电极为0.3 mm碳圆盘电极,30 mmol/L、pH 10.0的硼砂-氢氧化钠为运行缓冲液,分离电压21 kV,检测电位0.95 V.在最优化实验条件下,两待测物在6 min以内完全基线分离.厚朴酚及和厚朴酚的线性范围分别为0.2~50 μg/mL和0.4~60 μg/mL,检测限分别为0.06和0.2 μg/mL.应用于中药厚朴以及中成药霍香正气水和保济丸中厚朴酚及和厚朴酚的检测.
Keyword :
厚朴酚 厚朴酚 和厚朴酚 和厚朴酚 安培检测 安培检测 毛细管电泳 毛细管电泳
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GB/T 7714 | 陈颖 , 段建平 , 陈红青 et al. 毛细管电泳安培检测法同时测定厚朴酚与和厚朴酚 [J]. | 福州大学学报(自然科学版) , 2007 , 35 (4) : 612-615 . |
MLA | 陈颖 et al. "毛细管电泳安培检测法同时测定厚朴酚与和厚朴酚" . | 福州大学学报(自然科学版) 35 . 4 (2007) : 612-615 . |
APA | 陈颖 , 段建平 , 陈红青 , 陈国南 . 毛细管电泳安培检测法同时测定厚朴酚与和厚朴酚 . | 福州大学学报(自然科学版) , 2007 , 35 (4) , 612-615 . |
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以荧光素异硫氰酸盐柱前衍生了3种激肽类生物活性肽,较为详细地研究了衍生反应条件以及毛细管电泳的分离条件,建立了毛细管电泳激光诱导荧光法分离检测舒缓激肽、胰激肽、神经激肽A的方法。
Keyword :
异硫氰酸盐 异硫氰酸盐 毛细管电泳 毛细管电泳 生物活性肽 生物活性肽 神经激肽A 神经激肽A 胰激肽 胰激肽 舒缓激肽 舒缓激肽 荧光检测 荧光检测 荧光素 荧光素
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GB/T 7714 | 陈颖 , 段建平 , 徐两军 et al. 激肽类生物活性肽的毛细管电泳激光诱导荧光检测 [C] //中国化学会第十四届有机分析及生物分析学术研讨会论文集 . 2007 : 199 . |
MLA | 陈颖 et al. "激肽类生物活性肽的毛细管电泳激光诱导荧光检测" 中国化学会第十四届有机分析及生物分析学术研讨会论文集 . (2007) : 199 . |
APA | 陈颖 , 段建平 , 徐两军 , 陈红青 , 陈国南 . 激肽类生物活性肽的毛细管电泳激光诱导荧光检测 中国化学会第十四届有机分析及生物分析学术研讨会论文集 . (2007) : 199 . |
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