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荧光测定

荧光测定的相关文献在1986年到2022年内共计186篇,主要集中在化学、预防医学、卫生学、临床医学 等领域,其中期刊论文113篇、会议论文5篇、专利文献142845篇;相关期刊84种,包括生物学杂志、中华预防医学杂志、福建医药杂志等; 相关会议5种,包括2015年度钻井液完井液学组工作会议暨技术交流研讨会、第二届全国试剂与应用技术交流会、第十届全国稀散金属学术会议暨首届国际稀散金属研讨会等;荧光测定的相关文献由533位作者贡献,包括段旭川、俞超、唐庆文等。

荧光测定—发文量

期刊论文>

论文:113 占比:0.08%

会议论文>

论文:5 占比:0.00%

专利文献>

论文:142845 占比:99.92%

总计:142963篇

荧光测定—发文趋势图

荧光测定

-研究学者

  • 段旭川
  • 俞超
  • 唐庆文
  • 开雷
  • 彭花萍
  • 王亮
  • 胡爱玲
  • 苏深广
  • 邓豪华
  • 陈伟
  • 期刊论文
  • 会议论文
  • 专利文献

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    • 张秀蓝; 郭婧; 任立军; 朱超飞; 杨文龙; 刘金林; 吴忠祥; 董亮; 杜兵
    • 摘要: Due to the limiting value of benzidine in water,high performance liquid chromatography with fluorescence detector (HPLC-FLD) was employed to try to meet the monitoring demand.For the pretreatment,two classic methods-both liquid-liquid extraction and solid-phase extraction,were verified and compared.Under the condition of basic (pH =11-12),benzidine was extracted by methylene chloride from 1 L water,and detected by HPLC-FLD,the method detection limit (MDL) was 1.4 ng/L,and the quantitative limit was (QL) 5.5 ng/L;With the same instrument conditions,the MDL and QL were 0.9 and 3.6 ng/L for solid phase extraction method.In order to test the accuracy and precision of these two methods,three kinds of matrix spiking were proceeding.While,the water types were surface water,wastewater and industrial wastewater,and the standard were added 10.0,40.0 and 80.0 ng/L,respectively.According to the results,for both methods had good accuracy and reproducibility,recoveries were between 80%-120%,and relative standard deviations were less than 20%.It' s confirmed that HPLC-FLD was an effective way to monitor benzidine in water.%探讨了利用液相色谱分离,荧光检测器测定地表水中联苯胺的可行性.前处理方法对比验证了液液萃取法和固相萃取法.水样在碱性条件下(pH=11~12)进行提取,当提取体积为1.0L时,液液萃取液相色谱荧光法检测,方法检出限为1.4 ng/L,定量下限为5.5 ng/L;固相萃取液相色谱荧光法检测,方法检出限为0.9 ng/L,定量下限为3.6 ng/L.分别对地表水、生活废水、工业废水3种不同水体进行基体加标试验,加标浓度为10.0、40.0、80.0 ng/L.结果显示,对于3种不同基体和不同加标浓度的水样,两种方法均有较好的准确性和重现性,方法回收率为80% ~ 120%,相对标准偏差均小于20%,满足《地表水环境质量标准》(GB 3838-2002)中对联苯胺的监测需求.
    • 杨旭; 王旭光; 李彬瑶; 杨俊凤; 李昊丰; 黄莹
    • 摘要: 目的 建立简单、快速、灵敏的测定大鼠血浆中阿齐沙坦血药浓度的HPLC-荧光分析方法.方法 色谱柱为Aglient Epilent plus C18 (250 mm×4.6 mm,5 μm),流动相为0.1%磷酸水溶液-甲醇(35∶65),激发波长为265 nm,吸收波长为378nm.结果 血浆中内源性物质对待测物无干扰;线性范围为0.1~100 μg/mL,R2=0.999;定量下限为0.1 μg/mL;高中低浓度样品提取回收率在87.76%~95.65%,批内批间精密度RSD在0.86%~1.87%,相对误差RE均小于5%,符合相关生物样品检测标准.SD大鼠ig给予2.0 g/kg的阿齐沙坦酯钾后,阿齐沙坦在大鼠体内AUC0-t为(5451.94±297.96) μg/L.h,Cmax为(258.01±49.75) μg/mL.结论 建立了专属性强、灵敏度高、重复性好的HPLC-荧光分析方法,可用于阿齐沙坦在大鼠血浆中血药浓度测定.
    • 龚爱琴
    • 摘要: 在pH 7.5体系中,表面活性剂十二烷基硫酸钠( SDS)可以显著增强度他雄胺的荧光强度,从而提出了测定人血清及度他雄胺软胶囊中度他雄胺含量的方法。对实验条件进行了优化,在优化条件下,在0.10~2.56μg·mL-1范围内,度他雄胺的荧光强度与浓度呈良好的线性关系,相关系数R=0.997,方法的检出限为9.0 ng·mL-1,日内和日间精密度分别为0.22%~0.31%、0.28%~0.43%,回收率分别为94.0%~97.6%(胶囊)、93.6%~98.3%(血清)。实验结果表明本方法简便、快速、灵敏、准确,可用于实际样品分析。%A novel spectrofluorimetric method to determine dutasteride in dutasteride soft gelatin capsule and human urine has been developed based on that the fluorescence intensity of dutasteride could be enhanced by surfactant dodecyl sodium sulfate( SDS) in the medium pH=7. 5. The various factors of influencing fluorescence were discussed in detail. Under optimum conditions,a linear calibration curve was obtained in the range of 0. 10~2. 56μg·mL-1 with r=0. 997. The detection limit was 9. 0 ng·mL-1 . The RSD of intraday and interday was 0. 22% ~0. 31%and 0. 28% ~0. 43%,respectively. Obtained values of recoveries ranged from 94. 0%to 97. 6%,from 93. 6%to 98. 3%for dutasteride soft gelatin capsule and human serum,respectively. The method is simple,quick, selective and sensitive,and is suitable for the determination of dutasteride in real samples.
    • 刘延; 陈鑫
    • 摘要: 本文制备了两种硅胶攮质发光纳米粒子以用于水中重金属离子的荧光测定,一种是键合铕配合物的发光纳米粒子,另一种是同时键合荧光素与铕配合物的双发光纳米粒子。第一种首先将氨丙基三乙氧基硅烷与Eu(Ⅲ)配合物BHHBCB-Eu3+结合,通过反相微乳液法制备了内部键合了BHHBCB-Eu3+的硅胶纳米粒子,这种纳米粒子可以在327nm光激发下发出608nm的荧光;第二种首先通过反相微乳法制备了内部键合了荧光素的硅胶纳米粒子,然后将BHHBCB-Eu3+键合到纳米粒子表面得到,这种复合型纳米粒子可以在328nm光激发下发出525nm和607nm的双波长荧光。考察了多种会属离子存在下两种纳米粒子的荧光响应,结果表明这两种新型纳米材料可以作为纳米荧光探针用于水溶液中的Cu2+离子的定量测定。
    • 任建兴; 卢娟娟; 戴平; 闫冉; 赵鹰立; 刘玉兵
    • 摘要: 0引言XRF分析水泥化学成分是GB/T176—2008水泥化学分析方法中的代用法之一,可用于出厂水泥相关化学成分指标的检测。对于硅酸盐水泥,出厂水泥的主要化学成分指标有MgO、SO3、Cl-和碱含量等。标准中采用X射线荧光分析时有熔融法与粉末压片法。采用粉末压片法时,需要化验室自行制备校准样品,而熔融法则可直接使用国家级标准样品或标准物质校准仪器。
    • 张德贵; 冀云柱; 张彦荣
    • 摘要: 介绍了X射线荧光光谱测定铁精粉中高钛量,在没有高钛铁精粉标准物质的情况下,通过自制高钛量铁精粉试样,添加到工作曲线上扩大上限范围来校正曲线,使铁精粉中钛量校正曲线线性范围增宽,线性准确,满足了铁精粉中0.00%~5.00%钛含量测量范围内的分析需求.%X-ray fluorescence spectrometry determinating titanium content in iron powder was introduced, By self-made high titanium content of iron powder sample, to add the curve for extending the range of the curve, so that can determinate 0. 00%-5. 00% titanium content of the i-ron powder.
    • Gianluca Poldi
    • 摘要: 第一个问题意味着需要对一些代表性艺术品进行科学性检查,以确定所使用色素的特点以及它们对最终的颜色有何影响,并考虑到原艺术品的褪色、转暗和重新上色等变化因素。CAV目前开展的一套非介入性分析就是为了解决这个问题。该分析使用轻便仪器进行光谱测定、比色测定和成像测定。特别是光谱测定,它是对可见光进行X射线荧光测定和反射光谱测定,前者是为了认识材料的化学成分,后者是认识表面的色素及其在光线下的表现。这里的操作都按照国际标准进行。
    • 田智勇; 苏雷朋; 王丹; 李亚明; 赵瑾; 王超杰
    • 摘要: The interaction between naphthalimide-polyamine conjugates 1-3 and DNA was investigated by fluorimetry, and the intercalation of compounds 1-3 into DNA was examined. Results show that all the three kinds of tested naphthalimide-polyamine conjugates are able to intercalate into DNA and can act as intercalating agents of DNA.%采用荧光方法研究了DNA与萘酰亚胺-多胺缀合物1-3的作用,并分析了缀合物1-3对DNA的嵌入作用.结果表明,萘酰亚胺多胺缀合物对DNA有嵌入作用,是DNA嵌入剂.
    • 占浔寿; 商燕; 吴芳英
    • 摘要: Water-soluble L-cysteine-modified-ZnS : Mn2+ quantum dots(QDs) were prepared in aqueous solution under the room temperature, and characterized by infrared spectrometry, ultravioletvisible spectrometry, fluorescence spectrometry and X-ray diffraction spectrometry. Based on the flu-orescence quenching of ZnS : Mn2+QDs caused by folic acid (FA) , the prepared QDs were evaluated as a fluorescence probe for FA detection. Factors affecting the fluorescence detection on FA were studied. Under the optimal conditions, the quenched fluorescence intensity was linear with FA con-centration in the range of 1. 0×10-6 - 7.0×10-5 mol L-1 with correlation coefficient of 0.994. The limit of detection for FA was 9. 6× 10 -7 mol L-1. The proposed method was applied in the determination of folic acid in folic acid tablet and urine samples with satisfactory results. The mecha-nism for detection of FA was also investigated.%以L-半胱氨酸为表面修饰剂制备了稳定性和水溶性均优的ZnS:Mn2+纳米晶,并应用于叶酸的检测.在pH 7.4的KH2PO4 - Na2 HPO4缓冲溶液中,叶酸的加入使ZnS:Mn2+体系的荧光发生猝灭,荧光强度的变化与叶酸浓度呈良好的线性关系,其线性范围为1.0 × 10 -6~7.0×10-5mol·L-1(4.4×10-4~3.1 ×10-2g·L-1),方法检出限为9.6×10-7mol·L-1(4.2×10-4 g·L-1).该方法用于叶酸片剂和健康人尿液中叶酸的测定,结果满意.采用荧光光谱、紫外可见吸收光谱及X-ray光谱等研究了ZnS:Mn2+纳米晶及其水溶液的特性,通过热力学参数对叶酸测定的可能机理讲行了探讨.
    • 摘要: 本发明公开了一种X-荧光测定铌铁合金中元素含量的方法,该方法步骤:(1)挂壁;(2)氧化;(3)熔解;(4)荧光强度测量及绘制校准曲线;(5)制备得到待测试样玻璃样片,测定待测试样玻璃样片中铌、铊、硅、
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