最新的GADSL将在IMDS里实施
最新的GADSL将在IMDS里实施
日，最新的GADSL(全球汽车申报物质清单)更新将在IMDS里实施，结合了以下基础物质清单的更新。
Substance Name (en)
Current Flag
New Flag（注）
Cyclododecane,hexabromo-(HBCD)
1,2,5,6,9,10-Hexabromocyclododecane
rel-(1R, 2S, 5R, 6S, 9R, 10S)-1,2,5,6,9,10-Hexabromocyclododecane
Not in IMDS
rel-(1R, 2S, 5R, 6S, 9S, 10R)-1,2,5,6,9,10-Hexabromocyclododecane
Not in IMDS
rel-(1R, 2R, 5S, 6R, 9R, 10S)-1,2,5,6,9,10-Hexabromocyclododecane
Not in IMDS
rel-(1R, 2S, 5R, 6R, 9R, 10S)-1,2,5,6,9,10-Hexabromocyclododecane
Not in IMDS
rel-(1R, 2R, 5R, 6S, 9S, 10R)-1,2,5,6,9,10-Hexabromocyclododecane
Not in IMDS
(1R, 2R, 5R, 6S, 9S, 10S)-1,2,5,6,9,10-Hexabromocyclododecane
Not in IMDS
(1R, 2R, 5R, 6S, 9R, 10S)-1,2,5,6,9,10-Hexabromocyclododecane
Not in IMDS
(1R, 2S, 5S, 6R, 9S, 10S)-1,2,5,6,9,10-Hexabromocyclododecane
Not in IMDS
(1R, 2S, 5S, 6S, 9S, 10R)-1,2,5,6,9,10-Hexabromocyclododecane
Not in IMDS
(1R, 2R, 5S, 6R, 9R, 10S)-1,2,5,6,9,10-Hexabromocyclododecane
Not in IMDS
(1R, 2S, 5R, 6S, 9S, 10S)-1,2,5,6,9,10-Hexabromocyclododecane
Not in IMDS
(1R, 2R, 5R, 6S, 9S, 10R)-1,2,5,6,9,10-Hexabromocyclododecane
Not in IMDS
Dibutyltin bis(C8 to C18 unsatd. fatty acyloxy) derivs.
Not flagged
Dibutyltin diisothiocyanate
Not flagged
Dioctyltin bis(dodecylthio)
Not flagged
Mercury, bromo[1-(methoxyphenylmethyl)-2-oxo-2-[(1,7,7-trimethylbicyclo[2.2.1]hept-2-yl)oxy]ethyl]-
Not flagged
Dihexyl phthalate
Trixylyl phosphate
注：在GADSL中
D/P 表示在某些应用中被禁止，但在所有其他情况下须申报
D 表示必须始终申报的物质，但并未在汽车部件中禁止使用
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你可能喜欢2017 Vol.33 No.2
2017 Vol.33 No.2
偶氮胂Ⅲ分光光度法测定药物中的格拉司琼
周清清， 彭
摘& 要：在pH=7.76的弱碱性溶液中，格拉司琼与偶氮胂Ⅲ反应生成具有两个明显正吸收峰的离子缔合物，最大和次大吸收波长分别位于648 nm和602 nm，表观摩尔吸光系数分别为1.44&104、1.01&104 L/(mol&cm)，格拉司琼的质量浓度在0～4.4 mg/L范围内服从比尔定律。方法可用于人体血液及药物中格拉司琼含量的测定。
关键词：格拉司琼；偶氮胂Ⅲ；药物；分光光度法
中图分类号：O657.32&&&&& 文献标识码：A&&&&& 文章编号：17)02?294?03
参考文献：
［1］& Pharmacopoeia Committee for the Ministry of Health of People&s Republic of China.Pharmacopoeia of People&s Republic of China(PartⅡ).Beijing:Chinese Medicine Science and Technology Press(中华人民共和国药典委员会.中华人民共和国药典(第二部).北京:中国医药科技出版社),.
［2］& REN J M,LI Y R,JIANG Y,DING XY,HAO F.The Chinese Journal of Modern Applied Pharmacy(任进民,李艳荣,蒋晔,丁翔宇，郝福.中国现代应用药学杂志),):323.
［3］& LI J,GUO Y,ZHAO J G,ZHAO L,ZHANG LH.Applied Chemical Industry(李江,郭永,赵建国,赵璐，张丽华.应用化工),):711.
［4］& KUANG Y S,YIN Y,YANG Y Y,ZHANG WS,LIU J.West China Journal of Pharmaceutical Sciences(邝毓姗,尹燕,杨莹莹,张文胜，刘进.华西药学杂志),):615.
［5］& LIANG Y F,JIANG Y L,LUO Y H,WEI C Y,WANG Y S.Chinese Pharmaceutical Affairs(梁艳芳,姜亚莉,罗永慧,魏春燕，王延松.中国药事),.
［6］& CHEN X,MUHETAER T E H,SONG H,LI M Y.Northwest Pharmaceutical Journal(陈鑫,木合塔尔&吐尔洪,宋海林,李明月.西北药学杂志),.
［7］& LI H,TAN Z R.Central South Pharmacy(李浩,谭志荣.中南药学),):701.
［8］& CHEN S S,SUN Y Y,WEI Y,WANG K S.Chinese Journal of Pharmaceutical Analysis(陈姗姗,孙莹莹,韦阳,王恪申.药物分析杂志),):576.
Determination of Granisetron in Medicament by
Spectrophotometry with Arsenazo Ⅲ
ZHOU Qing-qing, PENG Jian, JIANG Hong*
(College of Chemistry and Chemical Engineering,Yangtze Normal University,Chongqing 408100)
Abstract:In alkalescent solution of pH=7.76,granisetron reacts with arsenazo Ⅲ to form an ion-association complex with two obvious positive absorption peak.The maximum positive absorption wavelength and sub-major positive absorption wavelength were 648 nm and 602 nm respectively,and apparent molar absorptivity(&) were 1.44&104 and 1.01&104 L/(mol&cm),respectively.Beer&s law was obeyed in the range within 0－4.4 mg/L of granisetron.The method was applied to determine the content of granisetron in commercially available granisetron hydrochloride medicament and human blood with satisfactory results.
Keywords:GArsenazo Ⅲ;MSpectrophotometry
微孔板化学发光法检测碱性磷酸酶技术的建立
欢, 胡亚萍, 高习习, 王
凡, 王钦富*
摘& 要：碱性磷酸酶（ALP）能催化发光底物APLS迅速水解并持续发光，据此建立了化学发光技术检测ALP活性的方法。利用一种新的发光底物APLS，建立微孔板化学发光法检测ALP活性，并对实验条件进行优化。优化后的最适反应条件为：微孔板上每孔加200 &L APLS，在pH=9.5、37℃条件下与ALP反应10 min,多功能酶标仪检测发光光子数（RLU）,检测ALP线性范围是0.01~1 U/L。微孔板化学发光法检测ALP，敏感度更高，且操作简便易行。
关键词：碱性磷酸酶；化学发光法；微孔板
中图分类号：O657.39&&&&& 文献标识码：A&&&&& 文章编号：17)02?291?03
参考文献：
［1］& WANG H.Determination of Alkaline Phosphatase Using Sequeritial Injection Flouorometry Method and Its Application for Evaluation of Milk Product Pasteurization.Dalian：Liaoning Normal University(王欢.顺序注射荧光法测定碱性磷酸酶及其应用.大连:辽宁师范大学)，2012.
［2］& SHEN J S,WANG J Q,BU D P,et al.China Dairy Industry(申军士,王加启,卜登攀,等.中国乳品工业),):31.
［3］& RU P P,WU J,YING Y B,JI F.Chinese Journal of Analytical Chemistry(茹柿平,吴坚,应义斌,季峰.分析化学),):835.
［4］& Nie Fei,Luo Kai,Zheng Xiaohui,Zheng Jianbin,Song Zhenghua.Sensors And Actuators B：Chemical,.
［5］& LEI Yingjie,Ouyang Jie,ZHANG Youlai,et al.Chinese Journal of Chemistry,):2413.
［6］& ZHANG N,BIAN W W,LI Y H.Chinese Journal of Analytical Chemistry(张娜,边玮玮,李耀辉.分析化学),):721.
［7］& HUI Y H,Han L Q,YANG G Y,WANG L.Chemistry & Bioengineering(惠永华,韩立强,杨国宇,王路.化学与生物工程),):74.
［8］& ZHU Y R,WU F C,LIN Y.Spectroscopy and Spectral Analysis(朱元荣,吴丰昌,林樱.光谱学与光谱分析),):1845.
［9］& Hirata S,Kitamura C,Fukushima H,Nakamichi I,Abiko Y,Terashita M,Jimil E.Joumal of Cellular Biochemistry,):1445.
［10］WANG Y,WANG Z L,CUI L G,et al.Chinese Journal of Analytical Chemistry(王宇,王宗良,崔立国,等.分析化学),):1279.
［11］ZHAO Q R,LI M J,LIU J,et al.Progress In Biochemistry and Biophysics(赵启仁,李美佳,刘洁,等.生物化学与生物物理进展),):70.
［12］Albillos S M,Reddy R,Salter R.Journal of Food Protection,):1144.
Microplate Chemiluminescence Method for Alkaline
Phosphatase Detection
LIU Huan, HU Ya-ping, GAO Xi-xi, WANG Peng, DING Fan, WANG Qin-fu*
(Collegeof Life Science and Technology,Dalian University,Dalian 116622)
Abstract:Alkaline phosphatase(ALP) can catalyze its substrate,leading to emit-ting light continuously.In this paper,a new substrate,APLS,was used,and a chemiluminescence technique for detecting alkaline phosphatase on microplate was developed and optimized.The results showed that the linear range for the determination of ALP was 0.01－1 U/L.Compared with other techniques for detecting ALP,this method is more sensitive and simpler.
Keywords:Alkaline PChemiluMicroplate
气相色谱-质谱法测定塑料制品和电子电气产品中氧化苯乙烯
摘& 要：建立了塑料制品和电子电气产品中氧化苯乙烯的气相色谱-质谱(GC-MS)分析方法。样品经甲醇超声萃取，采用GC-MS的全扫描方式和选择离子监测方式（SIM）对氧化苯乙烯进行定性和定量分析、外标法定量。对萃取溶剂、萃取时间以及色谱条件进行了考察。结果表明：氧化苯乙烯在0.05~10 mg/L浓度范围内线性关系良好，相关系数为0.9999，检出限为0.1 mg/kg，在0.5、20、100 mg/kg添加水平下的回收率为90.5%~120.4%，相对标准偏差（RSD）为0.18%~6.95%。该方法简便、准确性好、灵敏度高，能够满足实际检测工作的需要。
关键词：气相色谱-质谱；氧化苯乙烯；塑料制品；电子电气产品
中图分类号：O657.63&&&&& 文献标识码：A&&&&& 文章编号：17)02?287?04
参考文献：
［1］& FAN C Y.Spices and Its Application.Beijing:Chemical Industry Press(范成有.香料及其应用.北京:化学工业出版社),.
［2］& Weihai Weigao Innovation Co Ltd.China Patent(威海威高创新有限公司.中国专利),:2003.
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［5］& JIN H R,YANG W X.Chinese Journal of Industry Medicine(金焕荣,杨文秀.中国工业医学杂志),):168.
［6］& JIN H R,WANG L,FAN L F,ZHAO G.Chin J Ind Hyg Occup Dis(金焕荣,王路,范来富,赵贵.中华劳动卫生职业病杂志),):156.
［7］& CHEN Z Q,YU J H.China Occupational Medicine(陈自强,于继慧.职业医学),):49.
［8］& Tatiana B,Pavel V,Kateǐrina P,Kari H,Bo L.Carcinogenesis,):2357.
［9］& The Global Automotive Stakeholder Group(GASG).Global Automotive Declarable Substance List(GADSL).［］.http://Plastics.Americanchemistry.Com/GADSL-Document.
［10］TSZ0001G.Control Method for Substances of Environmental Concern.Standards of Toyota Motor Corporation.
［11］ZHONG Y,MAO X J,WANG F,WAN Y Q.Journal of Analytical Science(钟瑶,毛雪金,汪玢,万益群.分析科学学报),):87.
Determination of Styrene Oxide in Plastic，Electrical
and Electronic Products by Gas
Chromatography-Mass Spectrometry
LI Zhi-wei*
(Guangzhou GRG METROLOGY & TEST Co.,LTD,Guangzhou 510656)
Abstract:A method has been developed for the determination of styrene oxide(SO) in plastic,electrical and electronic products by gas chromatography-mass spectrometry.The sample was extracted with methanol under ultrasonic assistance,analyzed by GC-MS under full scan and selected ion monitoring(SIM) mode with the external standard method.The result indicated that the calibration curve showed a good linear relationship in range of 0.05 to 10 mg/L with the correlation coefficient of 0.9999.The detection limit for styrene oxide was 0.1 mg/kg.The average recoveries were in the range of 90.5% to 120.4% at three spiked levels of 0.5,20 and 100 mg/kg with the relative standard deviations of 0.18% to 6.95%.With the advantages of simple,quick,low detection limit,good accuracy and high precision,the method could be used for residue surveillance of Styrene oxide in the plastic,electrical and electronic products.
Keywords:Gas chromatography-SPElectrical and electronic products
直接进样-电感耦合等离子体质谱法测定特殊医用配方食品中铬、钼和硒
祥*， 宋蓉蓉， 赵庆珠， 张润何， 王
敏， 邓晓军， 何宇平
摘& 要：本文采用1%四甲基氢氧化铵溶液溶解样品，单氦碰撞池模式直接分析特殊医用配方食品中的铬、钼和硒。研究表明：铬、钼和硒在质量浓度2.0~50.0 &g/L范围内呈良好的线性关系,铬、钼、硒的检出限分别为0.012、0.009和0.009 mg/kg；加标回收率在94%～117%之间，相对标准偏差在1.47%～5.78%之间。本方法对NIST 1849a和FAPAS T07216QC标准物质中铬、钼和硒的测定值与参考值相符。该方法操作简单、快速，适合特殊医用配方食品中铬、钼和硒的同时测定。
关键词：直接进样；电感耦合等离子体质谱法；铬；钼；硒；特殊医用配方食品
中图分类号：O657.63&&&&& 文献标识码：A&&&&& 文章编号：17)02?283?04
参考文献：
［1］& GB .General Formulas For Special Medical purposes(特殊医学用途配方食品通则).
［2］& GB .General Infant Formulas for Special Medical Purposes(特殊医学用途婴儿配方食品通则).
［3］& GB/T 4.Determination of Chromium in Foods(食品中铬的测定).
［4］& GB 0.Determination of Selenium in Foods(食品中硒的测定).
［5］& Poitevin E,Nicolas M,Graveleau L.J AOAC Int,4.
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［7］& Pacquette L H,Szabo A,Thompson J J.J AOAC Int,):1240.
［8］& Pacquette L H,Szabo A,Thompson J J.J AOAC Int,):588.
［9］& ?ozak A,So?tyk K,Ostapczuk P.Die Pharmazie-An International Journal of Pharmaceutical Sciences,):824.
［10］YUAN Y,LIU L P.Chin J Health Lab Tec(袁媛,刘丽萍.中国卫生检验杂志),):1876.
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Determination of Cr,Mo and Se in Formulas for Special
Medical Purpose with Direct Injection-Inductively
Coupled Plasma Mass Spectrometry
FAN Xiang*, SONG Rong-rong, ZHAO Qing-zhu, ZHANG Run-he,
WANG Min, DENG Xiao-jun, HE Yu-ping
(Animals,Plants and Food Inspection & Quarantine Technical center of Shanghai Entry-Exit
Inspection and Quarantine Bureau,Shanghai 200135)
Abstract:Direct injection-inductively coupled plasma mass spectrometry method was used for the simultaneous determination of Cr,Mo,and Se in formulas for special medical purpose.All samples were dissolved by 1% tetramethylammonium hydroxide(TMAH) solution.The study showed that:linear relationship of Cr,Mo and Se were obtained in the range of 2.0－50.0 &g/L,and the detection limits were 0.012,0.009 and 0.009 mg/kg,respectively.Recoveries(n=8) and relative standard deviation(n=8) were 94%－117% and 1.47%－5.78%,respectively.The determination results of NIST 1849a and FAPAS T07216QC standard material are in agreement with the reference values.The method is simple and fast,and suitable for the simultaneous determination of Cr,Mo,and Se in formulas for special medical purpose.
Keywords:DInductively coupled plasCSMFormulas for special medical purpose
常压敞开式质谱离子源发展趋势
张秀丽， 宁录胜， 俞建成*
摘& 要：近年来常压敞开式离子源凭借快速、原位、实时离子化样品等优势，被广泛应用于样品快速筛查、真伪鉴定、质谱成像等领域，已成为当今离子源的研究热点，受到了学术界及仪器制造、化学和生物分析等相关产业界的广泛关注。目前，该类离子源朝着克服基体效应、提高样品表面定位能力及增加离子传输距离等方向发展。本文主要介绍了可以很好解决上述问题并具有代表性的三种常压敞开式离子源：电喷雾萃取离子源(EESI)、介质阻挡放电离子源(DBDI)及空气动力辅助离子源(AFAI)，重点涉及原理以及在此基础上所做的设计改进和应用进展。
关键词：敞开式离子源；质谱；电喷雾萃取；介质阻挡放电；空气动力辅助
中图分类号：O657.63&&&&& 文献标识码：A&&&&& 文章编号：17)02?276?07
参考文献：
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Trends in Ambient Ion Source Mass Spectrometry
ZHANG Xiu-li, NING Lu-sheng, YU Jian-cheng*
(The Research Institute of Advanced Technologies，Ningbo University，Ningbo 315211)
Abstract:Ambient ion source has been widely used in rapid screening of samples,sample identification,mass-spectrometry imaging and other fields in recent years,because of its outstanding features including rapid,in situ,real-time ionization of sample.Consequently,it has attracted lots of attentions,especially in the areas of academia,instrument manufacturing,chemical and biological analysis,etc.Nowadays ambient ion source tends to strengthen the abilities of overcoming the matrix effects,improving positioning capacity of sample surface and increasing the ion transmission distances.This paper mainly introduces three kinds of representative ambient ion sources,i.e.electrospray extraction ionization(EESI),dielectric barrier discharge ion source(DBDI) and air flow assisted ionization(AFAI),emphasizing their principles,design improvements and application progresses.
Keywords:AMExtdielectrAir flow assisted
悬浮固化分散液相微萃取-高效液相色谱/串联质谱法测定环境水样品中6种雌激素
锦1,2， 张丽君1,2， 董南巡1,2， 高仕谦1,2， 顾海东1,2， 张占恩*1,3
摘& 要：本文建立了悬浮固化分散液相微萃取（DLLME-SFO）高效液相色谱-串联质谱法（HPLC-MS/MS）测定环境水样品中壬基雌酚、双酚A、己烯雌酚、雌酮、雌二醇、炔雌醇6种雌激素的分析方法。萃取的最优条件为：以90 &L 1-十二醇为萃取剂，250 &L 0.025 mol/L Triton X-100为分散剂，调节pH至7.0，超声3 min，在室温条件下萃取环境水样中的雌激素残留。最优条件下，该方法在三个浓度水平下的平均加标回收率为93.4%~108.6%，相对标准偏差为1.3%~8.7%，检出限为0.001~0.05 &g/L。将该方法应用于环境水样中雌激素残留分析，获得了较好的回收率。
关键词：悬浮固化分散液相微萃取；高效液相色谱-串联质谱；雌激素；环境水样
中图分类号：O657.63&&&&& 文献标识码：A&&&&& 文章编号：17)02?271?05
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Dispersive Liquid-Liquid Microextraction Based on
Solidification of Floating Organic Droplets Combined
&with High Performance Liquid Chromatography-Tandem
Mass Spectrometry for Determination of Six Estrogens
in Environmental Water Samples
LI Jin1,2, ZHANG Li-jun1,2, DONG Nan-xun1,2, GAO Shi-qian1,2,
GU Hai-dong1,2, ZHANG Zhan-en*1,3
(1.School of Environmental Science and Engineering,Suzhou University of Science and
Technology,Suzhou 215009;
2.Jiangsu Key Laboratory for Environmental Science and Engineering,Suzhou University of
Science and Technology,Suzhou 215009；
3.Jiangsu Collaborative Center of Water Treatment Technology and Material，Suzhou 215009)
Abstract:A method for simultaneous determination of six estrogens(nonyl phenol,bisphenol A,diethylstilbestrol,estrone,estradiol,17&-ethinylestradio) in environmental water samples by dispersive liquid-liquid microextraction based on solidification of floating organic droplets combined with high performance liquid chromatography-tandem mass spectrometry was established.The optimal conditions were 90 &L of extractant(1-dodecanol)，250 &L of dispersant(triton X-100,0.025 mol/L ),pH=7.0,and 3 min extraction.Experiments were carried out at room temperature.Under the optimum conditions,the samples were spiked at three concentration levels and the average recoveries of target compounds ranged from 93.4% to 108.6% with the RSDs from 1.3% to 8.7%.The limits of detection(LOD) of the method for the six target compounds were in the range of 0.001－0.05 &g/L.This new method was successfully applied for the analysis of the estrogens in environmental water sample with satisfying results.
Keywords:Dispersive liquid liquid microextraction based on solidificationHigh performance liquid chromatography-tandEEnvironmental water samples
液相色谱-串联质谱法测定宠物食品中赭曲霉毒素A和B
陈祥准， 李
舟， 黄芙珍， 朱振瓯， 刘
摘& 要：建立了同时测定宠物食品中赭曲霉毒素A和B的液相色谱-串联质谱分析方法。样品经乙腈/水(1∶1,V/V)提取，HLB固相萃取柱净化。采用Agilent ZOBRAX C18柱(150&2.1 mm,5 &m)分离，以0.1%甲酸水溶液-乙腈作为流动相，梯度洗脱。目标化合物在多反应监测模式(MRM)下进行检测，外标法定量。在优化的条件下，赭曲霉毒素A和B在0.1 ~ 10.0 ng&mL-1范围内呈良好的线性关系，相关系数均不低于0.9993，方法定量限分别为0.1 &g&kg-1和0.05 &g&kg-1。方法平均回收率为78.3%~107.5%，相对标准偏差不大于9.5%。该方法前处理简单、选择性好、灵敏度高，可用于宠物食品中赭曲霉毒素A和B的测定。
关键词：宠物食品；赭曲霉毒素A；赭曲霉毒素B；液相色谱-串联质谱法
中图分类号：O657.63&&&&& 文献标识码：A&&&&& 文章编号：17)02?267?04
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Determination of Ochratoxin A and Ochratoxin B in Pet Food
by Liquid Chromatograpy-Tandem Mass Spectrometry
CHENG Xiang-zhun, LI Zhou, HUANG Fu-zhen, ZHU Zhen-ou, LIU Bin,HAN Chao*
（Wenzhou Entry-Exit Inspection and Quarantine Bureau,Wenzhou 325027）
Abstract:A method of& liquid chromatography-tandem mass spectrometry(LC-MS/MS) was used for the simultaneous determination of Ochratoxin A and Ochratoxin B in pet food sample.Samples were extracted with acetonitrile/water(1∶1,V/V) and cleaned up with HLB solid phase extraction.A gradient elution program was applied with the mobile phase of 0.1% formic acid solution and acetonitrile.The analyte was determined in multiple reaction monitoring transitions(MRMs) mode and the quantification was performed by the external standard method.The results indicated that the calibration curves for Ochratoxin A and Ochratoxin B was linear in the range of 0.1－10.0 ng&mL-1,with correlation coefficients more than 0.9993,and the limits of quantification(LOQs) were 0.1 &g&kg-1 and 0.05 &g&kg-1.The average recoveries ranged from 78.3% to 107.5% with the RSDs less than 9.5%.This method is simple,good selectivity and sensitive,and is suitable for the determination of Ochratoxin A and Ochratoxin B in pet food.
Keywords:POchratoxin A;Ochratoxin B;Liquid chromatography-tandem mass spectrometry
新型有机硒化合物的合成及其离子识别研究
罗杰伟1， 母
波1， 秦大斌2， 赵
波1， 张仕禄1， 孙胜富2， 张
摘& 要：设计合成了四个含有氢蒽基团的新型有机硒化合物1,8-二-(2-苄硒基)丙氧基-9,10-二氢蒽(L1)、1,8-氧双（亚乙硒基丙氧基）-9,10-二氢蒽(L2)、1,8-二-(2-苄硒基)乙氧基-9,10-二氢蒽(L3)、1,8-氧双(亚乙硒基亚乙氧基）-9,10-二氢蒽(L4)，利用1H NMR、13C NMR对化合物进行了结构表征，采用荧光光谱法测定了主体对客体阳离子的识别性能。研究结果发现只有化合物L1对Ag+具有选择识别能力,且对Ag+表现出&off-on&开关性能。化合物L2与Ag+和K+络合后荧光略有增强。
关键词：氢蒽；有机硒化合物；银离子识别
中图分类号：O657.39&&&&& 文献标识码：A&&&&& 文章编号：17)02?263?04
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for Ion Recognition
LUO Jie-wei1, MU Bo1, QIN Da-bin2, ZHAO Bo1,
ZHANG& Si-lu1, SUN Sheng-fu2, ZHANG Bo*1
(1.Basic Medical of North Sichuan Medical College,Nanchong 637000;
2.College of Chemistry and Chemical Engineering,China West Normal University,Nanchong 637000)
Abstract:Four organic selenium compounds (1,8-bis-(2-benzylseleno)propoxy-9,10-bis-hydrogen anthracene)(L1),(1,8-oxy bis(ethyleneselenopropoxy)-9,10-bis-hydrogen anthracene)(L2),(1,8-bis-(2-benzyl seleno) ethoxy-9,10-bis-hydrogen anthracene)(L3) and (1,8-oxy bis(ethyleneselenoethoxy)-9,10-bis-hydrogen anthracene)(L4) containing hydrogen anthracene group were synthesied and characterized by 1H NMR,13C NMR spectrum,which were used to study the host-yuest recognition by using fluorescence spectroscopy.The results show that compound L1(1,8-bis-(2-benzylseleno)propoxy-9,10-bis-hydrogen anthracene） only showed selective recognition ability for silver ion,and exhibited &on-off& switching performance to silver.The fluorescence intensity was slightly enhanced when compound L2 complexed with silver ion and potassium ion respectively.
Keywords:HOrganiSilver ion recognition
基于银纳米粒子的荧光增强法测定依诺沙星
磊, 杜丽娟, 贺彩虹
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［9］& WANG Y X,MA H Y,ZHANG X L,et al.Journal of Analytical Science(王奕璇,马红燕,张向亮,等.分析科学学报),）：253.
［10］WANG H,ZHANG P,WANG S.Metallurgical Analysis(王欢,张萍,王珊.冶金分析),）：64.
Determination of Enoxacin Based on Fluorescence
Enhancing of Silver Nanoparticles
LI Man-xiu*,& WANG Lei, DU Li-juan, HE Cai-hong
（Department of Chemistry,Xinzhou Teachers University,Xinzhou 034000）
Abstract:Silver nanoparticles were synthesized in aqueous solution with polyvinylpyrrolidone as stabilizer and sodium borohydride as reductant.Fluorescence and UV spectra were applied to demonstrate the interaction between silver nanoparticles and enoxacin.A new method was established for the determination of enoxacin based on the fluorescence enhancement of silver nanoparticles.Under optimal experimental condition,the relationship between relative fluorescence intensity F/F0 and the concentration of enoxacin was linear well,and the linear range was from 1.0&10-7 to 1.0&10-5 mol/L.The detection limit was 8.0&10-8 mol/L.The developed method was applied to real samples analysis and the recoveries were 94.5% to 99.8%.
Keywords:Polyvinyl EFluorescence enhancement
维生素B6在纳米Au-N，P/石墨烯修饰电极上的电化学行为
摘& 要：将金纳米粒子（AuNPs）电沉积在N,P/石墨烯(N,P/Graphene)修饰的玻碳电极表面，研究了维生素B6(VB6)在该修饰电极上的电化学行为。实验结果表明:VB6在该修饰电极上出现一个良好的氧化峰，在最佳实验条件下，其氧化峰电流与VB6的浓度在2.0&10-5～4.0&10-4 mol /L 范围内呈线性关系，相关系数R=0.998，检出限为9.2&10-6 mol/L。一些常见的物质如K+、Na+、Zn2+、葡萄糖（Glu）不干扰VB6的检测。此方法已用于片剂中VB6含量的检测，获得较好结果。
关键词：维生素B6;金纳米粒子;N，P/石墨烯;电化学方法
中图分类号：O657.1&&&&& 文献标识码：A&&&&& 文章编号：17)02?255?04
参考文献：
［1］& LI S.Chinese Journal of Biochemical and Pharmaceutics（李莎.中国生化药物杂志），)：176.
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［10］Yamamoto M,Nakamoto M J.Mater Chem,4.
Electrochemical Behavior of Vitamin B6& at
a N,P/Grapene Modified Electrode
PANG Jian*1, WU Xiu-juan2, ZHU Xiao-hong3, CHENG Zheng4
(1.Tongling Politechnic，Tongling 244000;
2.College of Chemistry and Materials Science，Anhui Normal University，Wuhu 241000;
3.Hefei Normal University，Hefei 230000;
4.Tongling Food and Drug Inspection Center,Tongling 244000)
Abstract:Au nanoparticles were prepared on the N,P-codoped graphene modified glassy carbon electrode(GCE) by electrodeposition.The electrochemical behavior of Vitamin B6(VB6) was investigated at the as-prepared modified electrode.The results indicate that the electrochemical redox reaction could occur more easily at the modified electrode than the bare and graphene modified GCE.Under the optimum condition,the amperometric currents are linear with the concentration of VB6 in the range of 2.0&10-5－4.0&10-4 mol/L with a correlation coefficient(R) of 0.998.The detection limit is 9.2&10-6 mol/L at a signal-to-noise ratio of 3.The sensor shows good anti-interference performance for the coexistence such as K+,Na+,Zn2+ and glucose.The proposed method was used for determination of VB6 in the tablet with satisfactory results.
Keywords:Vitamin B6;AN,P-Electrochemical methods
β-环糊精包合富集-紫外分光光度法检测猪肉组织中莱克多巴胺的含量
薇*， 陈坦林， 朱雪琴
摘& 要：利用&-环糊精包合富集莱克多巴胺，采用紫外分光光度法对猪肉组织样品中莱克多巴胺的含量进行测定。实验得到最佳富集条件为：超声时间60 min，包合温度30℃，包合体系pH=7.0。结果表明：在1.5~3.0 mg/L范围内，吸光度变化值△A与莱克多巴胺质量浓度呈良好线性关系，相关系数r=0.9998，检出限为0.05 mg/L，日内（n=6）与日间（n=3）的相对标准偏差（RSD）分别为0.87%~1.07%与0.80%~1.28%，回收率为91.91%~102.30%。该方法操作简单、迅速、灵敏，结果可靠。
关键词：莱克多巴胺；紫外分光光度法；&-环糊精
中图分类号：O657.32&&&&& 文献标识码：A&&&&& 文章编号：17)02?251?04
参考文献：
［1］& Boler D D,Shreck A L,Faulkner D K,et al.Meat Science,):458.
［2］& HUANG Y B.Agricultural Technology Service(黄义彬.农技服务),):67.
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［5］& SU L F,HE D T,XU F.Chinese Journal of Veterinary Medicine(苏丽芳，何丹婷，徐飞.中国兽医杂质),):59.
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［10］CHEN S P,FAN W,LIU M Y.Food Research and Development(陈四平，樊薇，刘梦云.食品研究与开发),):114.
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Detection of Ractopamine in Meat by Ultraviolet
Spectrophotometry& Combined with
&-Cyclodextrin Enrichment
JIN Hui, ZHAO Wei*, CHEN Tan-lin, ZHU Xue-qin
(College of Chemistry and Molecular Sciences,Wuhan University,Wuhan 430072)
Abstract:A new spectrophotometric method for the detection of ractopamine was established based on the formation of inclusion compound of &-cyclodextxin with ractopamine.The best conditions of the inclusion formation were as follows:ultrasonic time 60 min,inclusion temperature 30℃,pH=7.0.Under these conditions,the linear range for ractopamine was 1.5－3.0 mg/L with the correlation coefficient(r) of 0.9998,respectively.The limits of detection for ractopamine was 0.05 mg/L.The relative standard deviations(RSD) of ractopamine were 0.87%－1.07% and 0.80%－1.28% for intra-day and inter-day analysis,with the recovery of 91.91%－102.30%.The ultraviolet spectrophotometry is simple,rapid and reliable for detection.
Keywords:RUltraviol&-Cyclodextrin
氮掺杂石墨烯量子点/钯纳米复合材料的研究
郭云芳1， 李忠平*1， 杜丽清1， 李红荣2， 董
摘& 要：铂基催化剂因具有高催化活性、高稳定性而成为极其重要的能源转化催化剂。本文采用水热法合成氮掺杂石墨烯量子点支撑的钯纳米复合材料（），并将其用于碱性介质中甲醇的电催化氧化反应。实验结果表明，相比同类型材料钯负载于石墨烯纳米片（）、钯负载于石墨烯量子点（）和商业钯黑催化剂（），纳米材料具有很高的催化活性和稳定性，并可减少催化剂材料中贵金属的使用量。
关键词：钯纳米；石墨烯量子点；甲醇电化学催化
中图分类号：O657.1&&&&& 文献标识码：A&&&&& 文章编号：17)02?247?04
参考文献：
［1］& Rao C N R,Sood A K,Subrahmanyam K S,Govindaraj A.Angew Chem Int Ed,):7752.
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Study of Nitrogen-Doped Graphene Quantum Dots
Supported Palladuim Nanocomposites
GUO Yun-fang1, LI Zhong-ping*1, DU Li-qing1, LI& Hung-wing2, DONG Chuan1
（1.Institute of Environmental Science,School of Chemistry and Chemical Engineering,
Shanxi University,Taiyuan 030006;
2.Department of Chemistry,Hong Kong Baptist University,Hong Kong)
Abstract:With high catalytic activity and high stability,Platinum-based nanomaterials become important energy conversion catalysts.Herein,we report a facile one-pot hydrothermal approach to prepare a novel nitrogen-doped graphene quantum dots(N-GQDs) supported palladuim nanocomposite.The
nanocomposite demonstrates an excellent assembling nanostructures for the electrocatalytic oxidation of methanol in an alkaline medium when compared with the graphene sheets supported Pd nanocomposites( quantum dots supported Pd nanocomposites() and commercial palladium catalyst(
nanocomposite offers a promising and attractive perspect by reducing the noble metal dosage in electronic materials which possess high catalytic activity and stability.
Keywords:PalGMethanol oxidation
超声萃取-高效液相色谱法同时测定人造革中7种苯并三唑类紫外线吸收剂含量
谢堂堂1， 王成云*1， 林君峰1， 沈雅蕾1， 褚乃清1， 庄佩洁2
摘& 要：建立了超声萃取-高效液相色谱法(HPLC)同时测定人造革中7种苯并三唑类紫外线吸收剂UV-P、UV-326、UV-327、UV-329、UV-350、UV-320和UV-328含量的方法。该方法以甲醇为萃取溶剂，超声萃取人造革中的苯并三唑类紫外线吸收剂，萃取液经处理后直接进行HPLC分析，外标法定量。在信噪比(S/N)=3的条件下，UV-P、UV-326、UV-327、UV-329、UV-350的检出限均为0.05 mg/kg，UV-320、UV-328的检出限均为0.10 mg/kg。在3个不同加标浓度水平下，各组分的平均加标回收率为88?19%~98.32%，相对标准偏差(RSD)为0.61%~3.74%。该方法简便快捷、灵敏度高，可用于人造革中苯并三唑类紫外线吸收剂的测定。采用该方法对市售人造革样品进行测定，结果在6个样品中检出了不同浓度水平的UV-P和UV-329。
关键词：人造革；超声萃取；高效液相色谱；苯并三唑类紫外线吸收剂
中图分类号：O657.7+2&&&&& 文献标识码：A&&&&& 文章编号：17)02?242?05
参考文献：
［1］& WAN Z X.Polyvinyl Chloride(万忠香.聚氯乙烯),):16.
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Simultaneous Determination of Seven Benzotriazole Ultraviolet
Absorbers in Artificial Leathers by High-performance Liquid
Chromatography Coupled with Ultrasonic Extraction
XIE Tang-tang1, WANG Cheng-yun*1, LIN Jun-feng1,& SHEN Ya-lei1,
ZHU Nai-qing1, ZHUANG Pei-jie2
(1.The Testing and Technology for Industrial Products,Shenzhen Entry-Exit Inspection and Quarantine
&Bureau,Shenzhen .Shenzhen Polytechnic,Shenzhen 518055)
Abstract:A high-performance liquid chromatographic method was established for the simultaneous determination of seven benzotriazole ultraviolet absorbers in artificial leathers.Benzotriazole ultraviolet absorbers in artificial leathers were ultrasonically extracted using methanol as the extraction solvent.The extract was then analyzed by high-performance liquid chromatography(HPLC) technique.The concentration of each analyte was calibrated by external standard method.At the condition of signal to noise(S/N) of three,the limits of detection were 0.05 mg/kg for UV-P,UV-326,UV-327,UV-329 and UV-350,0.10 mg/kg for UV-320 and UV-328,respectively.The recoveries changed from 88.19% to 98?32% under three different spiked levels while the relative standard deviation varied from 0.61% to 3?74%.The proposed method was simple,rapid,sensitive,and applicable to the determination of benzotriazole ultraviolet absorbers in artificial leathers.The proposed method was applied in the determination of benzotriazole ultraviolet absorbers in artificial leathers available commercially.UV-P and UV-329 at different content levels were detected in six samples.
Keywords:AUHigh-performance lBenzotriazole ultraviolet absorbers
高效液相色谱法手性拆分（2-戊基-3-苯基-2,3环氧丙烷基）二苯基磷酸酯对映体
舒1， 韦思平1， 王
力1， 陈碧琼2， 张
摘& 要：采用多糖类手性色谱柱，建立了（2-戊基-3-苯基-2,3环氧丙烷基）二苯基磷酸酯对映体的高效液相色谱手性拆分方法。考察了手性柱类型、流动相组成、流速、柱温等对手性拆分的影响，并对分离机制进行了探讨。结果表明，采用Chiralpak AS-H柱（250&4.6 mm,i.d.,5 &m），以正己烷-异丙醇（85∶15，V/V）为流动相，在柱温25℃，流速1?0 mL/min，检测波长210 nm的条件下，（2-戊基-3-苯基-2,3环氧丙烷基）二苯基磷酸酯对映体能达到完全分离，且稳定性和重复性好。该方法也适用于（2-戊基-3-苯基-2,3环氧丙烷基）二苯基磷酸酯类似物的手性拆分。
关键词：（2-戊基-3-苯基-2,3环氧丙烷基）二苯基磷酸酯；多糖类手性色谱柱；手性拆分；高效液相色谱法
中图分类号：O657.7+2&&&&& 文献标识码：A&&&&& 文章编号：17)02?237?05
参考文献：
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Chiral Separation of (2-Pentyl-3-phenyl-2,3-epoxy propyl)
Diphenyl Phosphate Enantiomers by High Performance
Liquid Chromatogramphy
WANG Shu1, WEI Si-ping1, WANG Li1,CHEN Bi-qiong2,
ZHANG Chun1, WANG Qin1, DU Xi*2
（1.School of Pharmaceutical Science,Southwest Medical University,Luzhou 646000;
2.School of Basic Medical Science,Southwest Medical University,Luzhou 646000)
Abstract:A HPLC method was established for chiral separation and analysis of (2-pentyl-3-phenyl-2,3-epoxy propyl)diphenyl phosphate enantiomers using polysaccharide chiral chromatographic columns.The effect of columns,composition of mobile phase,flow rate and column temperature on the enantiomeric separation was investigated in detail and the separation mechanism was also discussed.The results showed that (2-pentyl-3-phenyl-2,3-epoxy propyl)diphenyl phosphate enantiomers could be baselinely separated with good repeatability and stability at 25℃ column temperature,with Chiarlpak AS-H cloum,mobile phase composition of n-hexane:isopropanol=85∶15(V/V),the flow rate of 1.0 mL/min and the detection wavelength at 210 nm.This method could be applied to separate and analyse (2-pentyl-3-phenyl-2,3-epoxy propyl)diphenyl phosphate enantiomers and its analogues.
Keywords:(2-Pentyl-3-phenyl-2,3-epoxy propyl)Polysaccharide chiral chCHPLC
基于氧化石墨烯修饰玻碳电极的多巴胺和尿酸的电化学检测
雷, 李竞草, 沈和平, 宋雪燕, 汪梦迪, 张
摘& 要：将超声分散的氧化石墨烯（GO）悬浮液滴涂于玻碳电极（GCE）表面，制备成GO/GCE，并用扫描电子显微镜（SEM）和电化学阻抗谱（EIS）对GO/GCE进行表征，利用差分脉冲伏安法（DPV）、循环伏安法（CV）对多巴胺（DA）和尿酸（UA）进行了电化学测定。研究了pH对DA和UA电化学行为的影响并计算相关的动力学参数。结果表明：该修饰电极对DA和UA的氧化还原反应具有良好的电化学催化作用，在1.0~98.0 &mol/L和0.5~90.0 &mol/L范围内峰电流与DA和UA浓度呈良好的线性关系，检出限分别为0?50 &mol/L和0.25 &mol/L。而且可以在抗坏血酸（AA）共存下同时测定DA和UA。该传感器具有良好的选择性与稳定性，有望应用于DA和UA的同时测定。
关键词：氧化石墨烯修饰电极；多巴胺；尿酸
中图分类号：O657.1&&&&& 文献标识码：A&&&&& 文章编号：17)02?232?05
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Electrochemical Detection of Dopamine and Uric Acid
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WU Hai, ZHANG Lei, LI Jing-cao, SHEN He-ping, SONG Xue-yan,
WANG Meng-di, ZHANG Hong*
(School of Chemistry and Material Engineering,Anhui Provincial Key Laboratory for
Degradation and Monitoring of Pollution of the Environment,
Fuyang Normal College,Fuyang 236037)
Abstract:The graphene oxide(GO) modified glassy carbon electrode(GO/GCE) was prepared by casting sonicated graphene oxide dispersion on the surface of glassy carbon electrode(GCE),which was characterized by scan electron microscopy(SEM) and electrochemical impedance spectroscopy(EIS).Differential pulse voltammetry(DPV) and cyclic voltammetry(CV) were employed to detect dopamine(DA) and uric acid(UA).The effects of pH on the behaviors of DA and UA were studied and related kinetic parameter was calculated.Results indicated that the GO/GCE could catalyze the redox reaction of DA and UA.The DPV peak currents were liner with concentrations of DA and UA in the range of 1.0－98.0 &mol/L and 0.5－90.0 &mol/L,and the detection limits were 1.0 &mol/L and 0.25 &mol/L,respectively.Furthermore DA and UA can be simultaneously detected without interference of ascorbic acid(AA).The presented sensor has excellent selectivity and stability,which is expected to be applied to detect DA and UA in real samples.
Keywords:Graphene oxidDUric acid
流动注射-抑制化学发光法测定岩白菜素
韫*， 高苏亚， 扈本荃
摘& 要：本文基于岩白菜素对鲁米诺-牛血清白蛋白体系化学发光信号显著的抑制作用，建立了快速灵敏测定岩白菜素的流动注射-化学发光分析新方法。实验发现，化学发光强度的降低值与岩白菜素质量浓度对数值呈良好的线性关系，方法的线性范围为3.0~5.0&105 pg/mL，检出限（3&）为1.0 pg/mL。当溶液流速为2.0 mL/min时，完成一次分析过程仅需30 s，采样频率120/h。本法用于片剂、人血清和尿液中岩白菜素的含量测定，回收率为98.1%~102.7%，相对标准偏差小于2.0%(n=7)。同时对化学发光反应机理进行了探讨。
关键词：岩白菜素；化学发光；流动注射；鲁米诺；牛血清白蛋白
中图分类号：O657.39&&&&& 文献标识码：A&&&&& 文章编号：17)02?227?05
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Determination of Bergenin by Flow Injection Analysis Coupled
with Inhibited Chemiluminescence System
ZHANG Yun*, GAO Su-ya, HU Ben-quan
(School of Pharmacy, Xi&an Medical University, Xi&an 710021)
Abstract:A rapid and sensitive flow injection-chemiluminescence(FI-CL) method for the determination of bergenin was established,based on the inhibition effect of bergenin on luminol-bull serum albumin system.It was found that the decrement of CL intensity was linearly proportional to the logarithm of bergenin concentration ranging from 3.0 to 5.0&105 pg/mL,with the limit of detection of 1.0 pg/mL(3&).At the flow rate of 2.0 mL/min,a typical analytical procedure including sampling and washing was finished within 30 s,which offered sample efficiency of 120/h.The proposed method has been applied to the determination of bergenin in tablets,human serum and urine samples with the recoveries of 98.1%－102.7%,and the RSDs of less than 2.0%(n=7).The possible mechanism of the CL reaction was also proposed.
Keywords:BCFLBovine serum albumin
气相色谱法测定铁皮石斛、浙贝母和人参中嘧菌酯残留
范丽丽， 王
娟， 吴加伦*
摘& 要：本文建立了铁皮石斛、浙贝母和人参三种中药材中嘧菌酯的残留检测方法。样品采用乙腈提取，二氯甲烷液-液萃取，弗罗里硅土-中性氧化铝-活性炭柱层析净化，乙酸乙酯定容，气相色谱-电子捕获检测器（GC-ECD）检测，基质外标法定量。结果表明:在0.01～1.0 mg/L范围内，不同基质中嘧菌酯的峰面积与其质量浓度间呈良好线性关系，相关系数均大于0.999；在0.01、0.1和0.5 mg/kg的添加水平下，嘧菌酯在3种中药材基质中的平均回收率为85.0%～94.9%，日内相对标准偏差（RSD）均小于5?2%（n=5），日间RSD均小于6.7%（n=15）；其在铁皮石斛、浙贝母和人参基质中的检出限（LOD）为0.002～0.004 mg/kg，定量限（LOQ）均为0.01 mg/kg。方法的准确度和精密度均满足残留分析要求，适用于铁皮石斛、浙贝母和人参中嘧菌酯的检测。
关键词：嘧菌酯；中药材；气相色谱；残留
中图分类号：O657.7+1&&&&& 文献标识码：A&&&&& 文章编号：17)02?222?05
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Determination of Azoxystrobin Residues in Dendrobium
officinale,Fritiliariae thunbergii and
Panax ginseng by Gas Chromatography
FAN Li-li, WANG Juan, WU Jia-lun*
(Ministry of Agriculture Key Laboratory of Molecular Biology of Group Pathogens and Insects,
Institute of& Pesticide and Environment Toxicology,Zhejiang University,Hangzhou 310058)
Abstract:A method for determination of azoxystrobin residues in Dendrobium officinale,Fritiliariae thunbergii and Panax ginseng was established.Samples were extracted ultrasonically with acetonitrile,partioned by dichloromethane,and then cleaned up by column chromatography (florisil-neutral alumina-activated charcoal).The sample extracts were determined by GC-ECD with matrix-matched external standard method.The results indicated that the matrix-matched calibration curves showed good linearity in the concentration range of 0.01－1 mg/L with correlation coefficients higher than 0.999.The average recoveries of azoxystrobin in the three matrices were between 85.0% and 94.9% at the spiked levels of 0.01,0.1 and 0.5 mg/kg,with intra-day relative standard deviations lower than 5.2%(n=5) and inter-day relative standard deviations lower than 6.7%(n=15).The limits of detection (LOD) in Dendrobium officinale,Fritiliariae thunbergii and Panax ginseng were 0.002－0.004 mg/kg,the limits of quantification (LOQ) were 0.01 mg/kg.The method was easy,efficient,sensitive and accurate,which can be suitable for determination of azoxystrobin residues.
Keywords:AChinese traditiGResidue
毛细管电泳-激光诱导荧光检测法测定卡托普利和N-乙酰-L-半胱氨酸
甜, 谭小芳, 孟建新
摘& 要：建立了一种高效、快速的毛细管电泳分离-激光诱导荧光(CE-LIF)检测卡托普利(CAP)和N-乙酰-L-半胱氨酸(NAC)的分析方法。采用1,3,5,7-四甲基-8-溴甲基-二氟二硼-二吡咯甲川（TMMB-Br）为柱前衍生试剂，在50 mmol/L磷酸盐缓冲溶液（pH=8.5）中，40℃下进行衍生反应10 min。以荧光素为内标，25 mmol/L硼酸盐缓冲溶液（pH=9.5）为电泳背景电解质，14 min内达到基线分离。CAP和NAC的检出限分别为0.65 nmol/L、0.76 nmol/L。将该方法应用于人体尿液和血清中这两种物质的测定，回收率在97.0%~105.7%之间。
关键词：毛细管电泳分离-激光诱导荧光检测法；卡托普利；N-乙酰-L-半胱氨酸；衍生
中图分类号：O657.8&&&&& 文献标识码：A&&&&& 文章编号：17)02?217?05
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Determination of Captopril and N-Acetylcysteine by Capillary
Electrophoresis-laser Induced Fluorescence Detection
CAO Li-wei*， SHI Yi-hui， WEI Tian， TAN Xiao-fang， MENG Jian-xin
(Department of Chemistry,College of Chemistry and Material Science,Jinan University,Guangzhou 510632)
Abstract:A highly efficient and fast analysis method was developed for the determination of captopril(CAP) and N-acetylcysteine(NAC) by capillary electrophoresis with laser-induced fluorescence detection(CE-LIF).1,3,5,7-tetramethyl-8-bromomethyl-difluoroboradiaza-s-indacene(TMMB-Br) was used for pre-column derivatization.Fluorescein was used as an internal standard(I.S.).The optimum derivative reaction was conducted in 50 mmol/L phosphate buffer solution(pH=8.5) at 40℃ for 10 min.At room temperature,derivatives of captopril and N-acetylcysteine were baseline separated within 14 min using 25 mmol/L boric acid solution(pH=9.5) as the running buffer.The detection limits(S/N=3) of the thiol derivatives were 0.65 nmol/L and 0.76 nmol/L,respectively.The proposed method was tested by analyzing the drugs in human plasma and urine samples with recoveries of 97.0%－105.7%.
Keywords:Capillary electrophoresis-laser induced fluorescence（CE-LIF）;CN-ADerivatization
气相色谱-串联质谱法测定土壤中多环芳烃和多氯联苯
田福林*， 刘成雁， 王志嘉， 赵海波
摘& 要：研究土壤中持久性有机污染物的含量可以为区域环境治理和来源解析提供基础数据。本文通过固相萃取结合气相色谱-串联质谱法建立了16种多环芳烃和15种多氯联苯的检测方法，并优化了固相萃取净化方法、色谱条件以及质谱碰撞能量。结果表明16种多环芳烃和15种多氯联苯的标准曲线线性关系良好，方法线性相关系数r2＞0.999，方法的检出限为0.1～2.5 &g&kg-1，16种多环芳烃的平均加标回收率范围为62.5%～113.5%，相对标准偏差在2.3%～8.2%之间，15种多氯联苯的平均加标回收率范围为62.6%～91.4%，相对标准偏差在5.2%～7.8%之间。方法的准确度和精密度较高，通过对实际样品的测定，说明该方法具有较低的检出限及较强的抗干扰能力，能满足土壤中多环芳烃和多氯联苯的检测要求。
关键词：土壤；多环芳烃；多氯联苯；串联质谱
中图分类号：O657.63&&&&& 文献标识码：A&&&&& 文章编号：17)02?212?05
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