硝基咪唑类药物的电化学行为及其与血清白蛋白的相互作用研究
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摘要
第一章:硝基咪唑类药物现已广泛应用于兽药和人医临床,但是由于它们具有潜在的致癌、致突变性,所以其在人体和动物体内的残留对人类健康构成了严重威胁。本章详细介绍了硝基咪唑类药物的性质及其分析方法研究进展。药物与血清白蛋白的相互作用研究是现阶段科学家研究的热点课题,本章综述了药物与血清蛋白质相互作用的研究状况。近年来,电化学分析在方法、技术和应用方面得到了长足的发展,本章对近年来的电化学研究方法,及其优越性做了详细介绍。化学修饰电极与普通电极相比可以增强被测物在电极表面的电化学信号,特别是碳纳米管修饰电极越来越受电化学工作者们的重视,本章详细介绍了化学修饰电极和碳纳米管修饰电极的研究概况。
     第二章:本章主要介绍了甲硝唑在银盘电极上的电化学行为,并对甲硝唑片剂进行了检测,实验证明,该方法可以为甲硝唑药品检验提供一种新的检测手段。并用循环伏安法研究了甲硝唑还原峰的性质,发现电极反应是完全不可逆的,并存在一定的吸附性。
     第三章:碳纳米管修饰电极是现阶段科学家们的研究热点,碳纳米管有其独特的性能,如比表面积大、化学性质稳定、机械性能好、灵敏的电子传递性能,正因为碳纳米管有如此特性,把它用于电极材料时可以加快电极表面的电子传递速度,从而使电极表面的电化学反应充分进行。在本章中,采用多壁碳纳米管修饰的玻碳电极为工作电极来研究奥硝唑在其表面的电化学行为,奥硝唑在该电极上有一灵敏的还原峰,而在裸玻碳电极上则几乎没有峰。
     第四章:研究药物与血清白蛋白的作用有助于阐明药物在体内的存储和转运过程,也能为药物的设计与开发及药理研究提供有价值的信息。本章采用电化学方法研究了甲硝唑与牛血清白蛋白的相互作用,实验结果表明,甲硝唑在-0.57V(vs.SCE)处出现一灵敏的还原峰,而牛血清白蛋白(BSA)在扫描范围为-0.3~-0.8V处没有峰。当牛血清白蛋白加入到甲硝唑溶液中时,甲硝唑的还原峰电流下降,该还原峰电流的下降值与BSA加入量呈线性关系,并对二者的相互作用机理进行了探讨,二者主要通过疏水键相结合。
Chapter 1:5-Nitroimidazoles had been widely used in animal drugs and human clinical medicine,the carcinogensis and mutability of nitroimidazoles damage human health because of its residual drugs,physicochemical property and analytical method research progressivity of nitroimidazolesh have been introduced in this chapter.Scientists are interesting in study of interactivity between drug and serum albumin in present,in this chapter, interactivity between drug and serum albumin has been reviewed.Superiority of electrochemical methodology is developed about method,technology and application widely.The electrochemical methods and its application have been introduced in this chapter.Compared with normal electrode,chemical modified electrode can strengthen electrochemical signal of detected materials,carbon nanotube modified electrodes are attention specially by electrochemical workers.In this chapter,study of chemical modified electrode and carbon nanotube modified electrodes has been introduced.
     Chapter 2:The electrochemical behavior and determination of metronidazole on the silver disk electrode have been studied in this chapter, metronidazole tablets have been detected,the results showed that this method can be used for the determination and pharmacokinetics study of metronidazole.The current property of reduction peak of metronidazole was investigated by the cyclic voltammetry.The characteristic irreversible adsorption of the peak was proved.
     Chapter 3:Electrodes based on carbon nanotubes are an attractive research area now.Carbon nanotubes display remarkable nanostructures in that they combine large surface area、excellent electrical conductivity、good chemical stability and significant mechanical strength.The subtle electronic properties suggest that carbon nanotubes have the ability to promote electron-transfer reactions when used as an electrode material in electrochemical reactions,which represents a new area of application for carbon nanotubes.In this study,the MWNTs were dropped onto the surface of a glassy carbon(GC) electrode to form an MWNT-modified one.The electrochemical behavior of ornidazole at such a modified electrode was investigated in detail,a reduction peak was obtained in ornidazole solution at the MWNT-modified electrode,compared with a bare electrode,the peak current had obviously increased.
     Chapter 4:Study on the interaction drugs and serum albumin help clarify drugs save and operation process,at the same time,it can provide valuable information regarding drug design、development and pharmacology research.In this chapter,the electrochemical methods are used for study on the interaction between metronidazole and bovine serum albumin.The results showed that a sensitive reduction peak of metronidazole has been obtained, the peak potential was-0.57V(vs.SCE).But bovine serum albumin has no reduction peak in the scanning area of-0.3~-0.8V.When bovine serum albumin was added in metronidazole solution,the reduction peak of metronidazole will fall down,the peak current declining value was directly proportional to the bovine serum albumin concentration.In addition,the interaction mechanism between metronidazole and BSA has been studied,the results demonstrate that combination of them mainly by hydrophobicity.
引文
[1]汪纪仓.猪可食组织中硝基咪唑类药物多残留的HPLC法和GC—MS/MS法研究[D].华中农业大学硕士学位论文,2005.
    [2]陈杖榴主编.兽医药理学[M].北京:中国农业出版社,2002,p242-243
    [3]刘世云,李秀红,王东明.甲硝唑在妇产科的临床应用[J].药物与临床,2005,2(21):96
    [4]戴景发,陈新峰,郭文献.奥硝唑的临床应用[J].海峡药学,2005,17(6):143
    [5]赵艳,王少华.塞克硝哗的研究进展[J].中国临床医生,2006,37(7):21
    [6]高小龙.鸡可食组织和蜂产品中硝基咪唑类药物残留检测的HPLC研究[D].华中农业大学硕士学位论文,2002
    [7]Francs J,Roe C.Toxicoiogic evalution of metronidazole with particular reference to carcinogenic,mutagenic and teratogenic potential[J].Surgery,1983,93(1):158-164
    [8]Dibias L,Rossner M C,Sram R.Genotoxicity and Carcinogenicity of Metronidazole[J].Mutation Research,1994,317:177-194
    [9]Voogd C E.On the mutagenicity of nitroimidazoles[J].Mutation Research,1981,86:243-277
    [10]Voogd C E,Stel V D,Jacobs A A.The mutagenic action of nitroimidazoles:Metronidazole,Nimorazole,Dimetronidazole and Ronidazole[J].Mutation Research,1974,26:483-490
    [11]Mudry M D,Carballo M,Labal V M.Mutagenic bioassay of certain pharmacological drugs:ⅢMetronidazole[J].Mutation Research.1994,305:127-132
    [12]Mcclain R M.Effect of metronidazole on fertility and testicular function in male rats[J].Fundamental and Applied Toxicology,1989,12(3):386
    [13]Rustia,Shubik M P.Induction of lung tumors and malignant lymphomas in mice by metronidazole[J].Journal of National Cancer Institute,1972,48:721-729
    [14]Cavaliere A.,Bacci M.,Amorosi A.et al.Induction of lung tumors and lymphomas in BALB/Cmice by metronidazole.Tumori,1983,69:379-382
    [15]罗军玉,曹玉华,廖兰.反相高效液相色谱法测定甲硝哗胶囊中甲硝哗含量[J].药物鉴定,2006,15(6):19
    [16]郝正华.HPLC法测定甲硝唑结肠定位肠溶胶囊含量[J].临床医药实践杂志,2006,15(6):427
    [17]郭利民,任志强.高效液相色谱法测定奥硝唑片的含量[J].医学通报,2005,24(9):822
    [18]李芹,赵焰,梁永广,等.奥硝唑血药浓度的高效液相色谱法测定及其药动学研究[J].临床药学,2003,38(9):690
    [19]丁涛,徐锦忠,沈崇钰,等.高效液相色谱-串联质谱联用测定蜂王浆中的三利,基咪哗类残留[J].色谱,2006,24(4):331-334
    [20]王海,刘素英,单吉浩,吴银良.高效液相色谱-质谱法测定猪组织中硝基咪哗类药物残留量[J].中国兽药杂志,2005,39(12):8-11
    [21]张淑芳,张冬梅,李怀娜.双波长分光光度法测定复方甲硝唑片中甲硝唑和维生素B6的含量[J].曲阜师范大学学报,1997,23(2):77
    [22]钱小蔷.紫外分光光度法测定奥硝唑氯化钠注射液中奥硝唑含量[J].中国药师,2004,7(10):777
    [23]俞英,龙朝阳.甲硝唑片及其伏安行为的示波极谱法测定[J].中国医药工业杂志,2004,35(11):672
    [24]陈勤.牛血清白蛋白与重金属离子相互作用的研究[D].暨南大学硕士学位论文,2007
    [25]Ulrich K H.Molecular aspects of ligand binding to serum albumin[J].Pharmacological Reviews,1981,33(1):17-53.
    [26]易平贵,商志才,俞庆森,等.丝裂霉素C与牛血清白蛋白结合作用的研究[J].化学学报,2000,58(12):1649-1653.
    [27]陶慰孙,李惟,姜涌明.蛋白质分子基础[M].北京:高等教育出版社,1995.85.
    [28]王延华,邹晓莉.蛋白质理论与技术[M].北京:科学出版社,2005.21-35.
    [29]林钧材.血液生物化学[M].北京:人民卫生出版社,1988.32
    [30]薛春霞.药物分子与牛血清白蛋白相互作用的研究。西安建筑科技大学,2006
    [21]Yong Yu,Qilong Li.Studies on the interaction of paclitaxel with tubulin by an electrochemical method[J].Analytica ChimicaActa,2001,436:147-152
    [32]于泳,胡劲波,尚军.抗癌药物长春新碱及其与微管蛋白相互作用的电化学研究[J].化学学报,2004,62(2):137-141
    [33]孙伟,焦奎,刘晓云.电化学法研究蛋白质和茜素红S的相互作用[J].分析化学,2002,30(3):312-314
    [34]Wei Sun,Kui Jiao.Linear sweep voltammetric determination of protein based on its interaction with Alizarin Red S[J].Talanta,2002,56:1073-1080
    [35]邬春华,吕元琦,袁悼斌.大黄酸与牛血清白蛋白相互作用的电化学研究[J].分析测试学报,2004,23(3):73-75
    [36]易平贵,刘俊峰,商志才.荧光光谱法研究亚甲基蓝与蛋白质的结合反应[J].光谱学与光谱分析,2001,21(6):826-828
    [37]王海人,肖思柏,宋功武.荧光素与牛血清白蛋白作用的光谱研究与分析应用[J].分析测试学报,2001,20(4):45-47
    [38]王君,任百祥.药物与蛋白质相互作用的分析测试[J].中国新医药,2003,2(5):47-48
    [39]曹秋娥,李祖碧.偶氮胭脂红B与血清蛋白相互作用的光度法研究及其分析应用[J].分析化学,2002,30(2):222-226
    [40]吴蜻,黄杉生,范忆晶.分光光度法研究牛血清白蛋白与对二甲基亚节罗丹宁的作用[J].分析科学学报,2003,19(2):130-132
    [41]Liu Y,Xie M,Kang J.Studies on the interaction of total saponins of panax notoginseng and human serum albumin by Fourier transform infrared spectroscopy[J].Spectrochimica Acta Part A,2003,59:2747-2758
    [42]谢孟峡,刘媛.红外光谱酞胺Ⅲ带用于蛋白质二级结构的测定研究[J].高等学校化学学报,2003,24(2):226-231
    [43]蒋治良,邹节明,王力生.蛋白质与三氯乙酸相互作用的共振散射光谱研究及分析应用[J].分析化学,2003,31(1):70-73
    [44]杨传孝,李原芳,丽春红.用于人血清样品中总蛋白的共振光散射测定[J].分析化学,2003,31(2):148-152
    [45]周大炜,李发美.盐酸丙咪嗪-人血清白蛋白结合作用的毛细管区带电泳法[J].色谱,2003,21(2):143-146
    [46]郭明,严建伟,俞庆森.加替沙星与牛血清白蛋白的结合反应研究[J].物理化学学报,2004,20(2):202-206
    [47]赵燕燕,杨更亮,范子琳.高效毛细管电泳前沿分析法研究酸性药物那格列奈与人血清白蛋白的结合[J].分析化学,2003,31(7):860-864
    [48]Li B-X,Zhang Z-J,Zhao L-X.Flow-injection chemiluminescence detection for studying protein binding for drug with ultrafiltration sampling[J[.Analytica Chimica Acta,2002,468:65-70
    [49]Huang Y,Zhang Z-J,Zhang D-J.Flow-injection analysis chemiluminescence detection combined with microdialysis sampling for studying protein binding of drug[J].Talanta,2001,53:835-841
    [50]Yang C,Elena H,Babu S.Measurements of drug-protein binding by using immobilized human serum albumin Liquid romatography-mass spectrometry[J].Journal of chromatography B,2004,809:67-73
    [51]Huang Y-M,Zhang Z-J.Binding study of drug with bovine serum album using a combined technique of microdialysis with flow-injection chemiluminescent detection.Journal of Pharmaceutical and Biomedical Analysis,2004,35:1293-1299
    [52]Cao X-N,Lin L,Zhou Y,et al.Study of the interaction of 6-mercaptopurine with protein by microdialysis coupled with LC andelectrochemical detection based on functionalized multi-wall carbon nanotubes modified electrode[J].Journal of Pharmaceutical and Biomedical Analysis,2003,32:505-512
    [53]Fiori M,Fame M,Civitareale C,et al.The Use of Bovine Serum Albumin as a Ligand in Affinity Chromatographic Clean-up of Non-Steroidal Anti-Inflammatory Drugs from Bovine Plasma[J].Chromatographia,2004,60(5-6):253-257
    [54]Xu Y,Yushmanovg Vr E.NMR studies of Drug Interaction with Membranes and Membrane-Associated Proteins[J].Bioscience Reports.2002,22(2):175-196
    [55]Tang K,Qin Y-M,Lin A-H.Interaction of daunomycin antibiotic with humanserum albumin:Investigation by resonant mirror biosensor technique,fluorescence spectroscopy and molecular modeling methods[J].Journal of Pharmaceutical and Biomedical Analysis,2005,39(3-4):404-410
    [56]陈国华.药物分子与主体和生物分子相互作用的电化学方法研究[D].重庆大学硕士学位论文,2003
    [57]李海南.嗪草酮在玻碳电极上的电化学行为及其与DNA相互作用的研究[D].延边大学硕士学位论文.2005
    [58]杨贞,朱世民.卡托普利在汞电极表面的电化学行为[J].分析化学,1999,27(12):1431-1434.
    [59]郭旭明,胡乃非,林树昌.氟呱咙的吸附溶出伏安法研究[J].化学学报,1992,50(4):378-382.
    [60]Gao Z-Q,Siow K S.Catalytic-adsorptive stripping voltammetry of cobalt in the presence of 2,2'-bipyridine and nitrite[J].Talanta,1996,43(2):255-260.
    [61]高鹏,张成孝.金属一毗咤偶氮类试剂配合物的极谱研究[J].分析化学,1988,16(5):441-443.
    [62]赵敬中,孙德志,刘道杰.锢(Ⅲ)-茜红素体系的吸附伏安法[J].分析化学,1996,24(1):101-103.
    [63]Michael T,Carte A J,Bard M T.Carter electrochemical investigations of the interaction of metal chelates with DNA.3.Electrogenerated chemiluminescent investigation of the interaction of tris(1,10-phenanthroline) ruthenium(Ⅱ) with DNA[J],Bioconjugate Chemistry,1990,1:257-263.
    [64]Pang D-W,Bector D,Abrufia.Micromethod for the investigation of the interactions between DNA and redox-active molecules[J].Analytical Chemistry,1998,70:3162-3169.
    [65]Eddowes M J,Hill H A,Vcsakt K J.Electrochemistry of cytochrome C,comparison of the electron transfor at a surface-modified gold glectrode with that to cytochrome oxide[J].Journal of American Chemical Society,1979,101:7113-7118.
    [66]Kudera M,Aitken A,Li J,et al.Electron transfer processes of redor proteins at inherently modified microelectrode array devices[J].Journal of Electroanalytical Chemistry.2000,495:36-41.
    [67]Lojiou E,Bianco P,Bruschi M.Kinetic studies on the electron transfer between various c-type cytochromes and iron(Ⅲ)using a voltammetric approach[J].Talanta,1997,97:2005-2013.
    [68]吴奕辉.几种生物分子在化学修饰电极上的电化学行为研究[D].中南大学硕士学位论文,2007
    [69]竹博万,卢晓泉.化学修饰电极((CME)在水质监测中的应用进展[J].甘肃环境监测与研究,2003,16(4):438-440
    [70]邱东方,赵茜.我国化学修饰电极研究进展[J].南都学坛,1998,18(3):68-72
    [71]策绍俊.化学修饰电极[J].化学通报,1981,12(12):713-721
    [72]Hoyer B,Florence T M,Batley G E.Application of polymer coated glass carbon electrodes in anodic strippingvoltammetry[J].Anal Chem,1987,59(13):1608-1614
    [73]金利通,同威,方禹之.吸附型化学修饰电极在分析化学中的应用[J].分析试验室,1987,6(8):45-47
    [74]土升富,杜丹,邹其超.磷钼钨杂多酸-L-半胱氨酸自组装膜电极的电化学性质[J].物理化学学报,2001,17(12):1102-1106
    [75]李景虹,程广金,策绍俊.自组装技术在电分析化学中的应用[J].分析化学,1996,24(9):1093-1099
    [76]罗红霞,施祖进,李南强,等.羧基化单层碳纳米管修饰电极的电化学表征及其电催化作用[J].高等学校化学学报,2000,21(9):1372-1374
    [77]孙元喜.导电聚合物膜修饰电极及其分析应用[J].武陵周刊,1997,18(3):40-46
    [78]Barcndrecht E.Chemically and physically modified electrodes:some new development[J].Appl Electrochem,1990,20(5):175-180
    [79]董绍俊,车广礼,谢远武.化学修饰电极[M].科学出版社,2003年.
    [80]Singh H,Srivastava M.Fullerenes-Synthesis,Separation,Characterization,Reaction Chemistry,and Appllications-a Review[J].Energ.Source,1995,17(6):615-640
    [81]肖素芳.碳纳米管修饰电极对生物分子的电分离分析[D].青岛大学硕士学位论文,2004
    [82]Iijima S,Ichihashi T.Single-shell carbon nanotubes of 1-nm diameter[J].Nature,1993,363:603-605
    [83]Ebbesen T W,Ajayan P M.Large scale synthesis of carbon nanotubes[J].Nature,1992,358:220-222
    [84]Thess A,LeeR,Nikolaev P.Crystalline ropes of metallic carbon nanotubes[J]. Science,1996,273:483-87
    [85]Cheng H M,Li F,Sun X.Bulk morphology and diameter distribution of single-walled carbon nanotubes synthesized by catalytic decomposition of hydrocarbons[J].Chem.Phys.Lett.,1998,289:602-610
    [86]Kong J,Cassel A M,Dai H J.Chemical vapor deposition of methane for single-walled carbonnanotubes[J].Chem.Phys.Lett.,1998,292:567-574
    [87]Ebbesen T W,Lezec H J,Hiura H,et al.Electrical conductivity of individual carbon nanotubes[J].Nature,1996,382:54-56
    [88]Saito R,Fujita M,Dresselhaus G,et al.Electronic structure and growth mechanism of carbon tubules[J].Materials Science and Engieering,1993,19(2):185-191
    [89]徐国则,张立德.纳米复合材料[M].北京:化学工业出版社,2002,26-29
    [90]杨占红,李新海,李晶,等.碳纳米管纯化技术研究[J].中南工业大学学报,1999,13(4):389-391
    [91]李新海,杨占红,陈至国.炭纳米管的提纯一重铬酸钾氧化法[J].新型碳材料,1999,14(3):32-36
    [92]杨翔,陈代璋,方勤方,等.纳米碳管分离提纯技术[J].地学前缘,2000,7(2):527-534
    [93]Zhu W,Bower C,Zhou O,et al.Large current density from carbon nanotube field emitters[J].Appl.Phys.Lett.,1999,75(6):873-875
    [94]Ajayan P M,Iijima S.Capillarity-induced filling of carbon nanotubes[J].Nature,1993,361:333-334.
    [95]Rinzler A G,Hafner J H,Nikolaev P,et al.Unraveling nanotubes-field-emission from an atomic wire[J].Science,1995.269:1550-1553
    [96]Hafner J H,Cheung C L,Lieber C M.Growth of nanotubes for probe microscopy tips[J].Nature,1999,398:761-762
    [97]Liu C,Fan Y Y,Liu M,et al.Hydrogen storage in single-walled carbon nanotubes at room temperature[J].Science,1999,286:1127-1129
    [98]Chen J,Hamm M A,Hu H,et al.Solution properties of single-walled carbon nanotubes[J].Science,1998,282(5386):95-98
    [99]Luo H-X,Shi Z-J,Li N-Q,et al.Investigation of the Electrochemical and Electrocatalytic Behavior of Single-Wall Carbon Nanotube Film on a Glassy Carbon Electrode[J].Anal.Chem.2001,73:915-920.
    [100]Wang J,Li M,Shi Z,et al.Investigation of the electrocatalytic behavior of single-wall carbon nanotube films on an Au electrode[J].Microchem.J.,2002,73,325-333.
    [101]Wang J-X,Li M-X,Shi Z-J,et al.Electrocatalytic oxidation of 3,4-dihydroxyphenylacetic acid at a glassy carbon electrode modified with single-wall carbon nanotubes[J].Electrochim.Acta,2001,47:651-657.
    [102]肖素芳,王宗花,罗国安,等.L-半胱氨酸在环糊精复合碳纳米管电极上的伏安测定[J].高等化学学报,2004,25(10):1833-1835.
    [103]Wang G-Y,Liu X-J,Yu B,et al.Electrocatalytic response of norepinephrine at a β-cyclodextrin incorporated carbon nanotube modified electrode[J].J.Eleciroanal.Chem.,2004,567:227-231.
    [104]Wu K B,Hu S S,Fei J J,et al.Mercury-free simultaneous determination of cadmium and lead at a glassy carbon electrode modified with multi-wall carbon nanotubes[J].Anal.Chim.Acta.,2003,489:215-221.
    [105]Islam M F,Roias E,Bergey D M,et al.High Weight Fraction Surfactant Solubilization of Single-Wall Carbon Nanotubes in Water[J].Nano.Lett.,2003,3:269-273.
    [106].曾艳.破纳米管修饰玻破电极的研究和应用[D].华中师范大学硕士学位论文,2006
    [107]吕少仿,朱丽华.土霉素在碳纳米管修饰电极上的电化学行为研究及其测定[J].分析科学学报,2003,9(2):139-141
    [108]孙延一,吴康兵,胡胜水.阿霉素在多壁碳纳米管膜电极上的电化学行为及其分析研究[J].分析科学学报,2004,20(1):26-28
    [109]吕少仿.多壁碳纳米管化学修饰电极测定替硝唑的研究[J].分析化学,2004,32(3):412
    [110]赵长庆,钱彬彬,蔡跃娟,等.利用电化学及光谱方法研究环丙沙星与DNA 的相互作用[J].安徽师范大学学报,2007,30(4):477-480
    [111]王玉春,李将渊,刘赵荣.多壁碳纳米管修饰电极对抗坏血酸的电催化作用[J].内江师范学院学报,2005,20(2):57-60
    [112]王歌云,王宗花,肖素芳,等.碳纳米管修饰电极对多巴胺和肾上腺素的电分 离及同时测定[J].分析化学研究报告,2003,31(11):1281-1285
    [113]李玉平,曹宏斌,张懿.血红蛋白在碳纳米管修饰碳糊电极上的直接电化学行为[J].物理化学学报,2005,21(2):187-191
    [1]唐爱国,周霞.高效液相色谱法测定甲硝唑的唾液浓度.中国医院药学杂志,1990,10(12):539
    [2]何光耀,谭定定,钟春宁.高效液相色谱法测定胃液中甲硝唑浓度[D].色谱,1997,15(3):228
    [3]阎旭光,梁晓波.高效液相色谱法测定中西药复方乳剂中甲硝唑的含量[J].药物分析杂志,1994,14(6):23
    [4]N.Tavakoli,J.Varshosaz,F.Dorkoosh,M.R.Zargarzadeh.Development and validation of a simple HPLC method for simultaneous in vitro determination of amoxicillin and metronidazole at single wavelength.Journal of Pharmaceutical and Biomedical Analysis,2007,43:325
    [5]项新华,沈建忠.HPLC法检测硝基咪哗类药物残留及其有效化学测量的研究[J].卫生研究,2007,36(3):379
    [6]王慧琛,张永强,刘光赫.LPLC法同时测定复方甲硝唑软膏中甲硝唑和氯霉素的含量[J].天津药学,2006,18(3):14
    [7]丁涛,徐锦忠,沈崇钰,蒋原,陈惠.高效液相色谱-串联质谱联用测定蜂王浆中的三种硝基咪哗类残留[J].色谱,2006,24(4):331
    [8]陈丽佳,吴伟明.离子对高效液相色谱法同时测定人血浆中阿莫西林和甲硝唑浓度[J].儿科医学杂志,2006,12(4):4
    [9]殷居易,谢东华,李佐卿.HPLC-APCI(+)MS/MS分析动物源性食品中的硝基咪唑类药物残留量[J].分析测试学报,2007,26(3):385-388
    [10]于志庚,于颖佳,吴雅文,王鲁妹.HPLC测定痤螨灵搽剂中三组分的含量[J].药物分析杂志,2005,25(8):958
    [11]郝正华.HPLC法测定甲硝唑结肠定位肠溶胶囊含量[J].临床医药实践杂志,2006,5(6):427
    [12]刘晓哲,王丽娜.HPLC法测定甲硝唑漱口液中甲硝唑的含量[J].齐鲁要事,2007,6(3);153
    [13]中华人民共和国药典:二部[M],北京:化学工业出版社,2000
    [14]李宇,王术皓,杜凌云,刘洪海.反相流动注射化学发光法测定甲硝唑[J].分析科学学报,2006,22(2):237
    [15]吕经兰,路永.UV法测定甲硝唑硼酸胶囊中甲硝唑的含量[J].江苏药学与临床研究,2006,14(1):65
    [16]国平.分光光度法测定片剂和注射液中的甲硝唑[J].中国卫生检验杂志,2007,17(7):1220
    [17]正行,程光忻,应允明.示波极谱滴定法测定甲硝唑含量[J].药物分析杂志,1990,10(1):33
    [18]元华,高红艳.单扫示波极谱法测甲硝唑[J].伊犁师范学院学报,2005,9(3):55
    [19]俞英,龙朝阳.甲硝唑片及其伏安行为的示波极谱法测定[J].中国医药工业杂志,2004,35(11):672
    [20]玉忠,李蜀萍,阚显文,李茂国,方宾.头孢噻肟钠降解产物在银微电极上示差脉冲阴极溶出伏安法的测定[J].分析化学研究简报,2000,11(28):1371
    [21]淮凌,孙鲲,李贯良,凌翠霞.酮洛芬的电化学行为及测定[J].化学世界,2005,11:658
    [22]根珊.药物分类与药物学,北京:解放军出版社,1998:828
    [23]Tarmure,R.Sa ndulescu,C.Ionescu.Voltammetric determination of lactate dehydrogenase using a carbon paste electrode.Journal of Pharmaceutical and Biomedical Analysis,2000,22:355
    [24]B.E1-Hefnawy,I.S.E1-Hallag,E.M.Ghoneim,M.M.Ghoneim.Electrochemical behavior and determination of amiloride drug in bulk form and pharmaceutical formulation at mercury electrodes. Journal of Pharmaceutical and Biomedical Analysis,2004,34:899
    
    [25] Abbaspour, R. Mirzajani. Electrochemical monitoring of piroxicam in different pharmaceutical forms with multi-walled carbon nanotubes paste electrode. Journal of Pharmaceutical and Biomedical Analysis,2007,44:41
    [1]Richle R,Scholer H J,Angehrn P,et al(1978).Fundamentals of the chemotherapy of trichomoniasis and amebiasis with ornidazole[J].A rzneim ittelforschung.28(4):612-625.
    [2]Tabak F,Ozaras R,Erzin Y,et al(2003).Omidazole-induced liver damage:report of three cases and review of the literature[J].Liver Int.23(5):351-354.
    [3]戴景发,陈新峰,郭文献.奥硝唑的临床应用[J].海峡药学,2005,17(6):143
    [4]马传学,孙伟.硝基咪唑类药物的不良反应[J].江苏药学与临床研究,2005,13(1):41
    [5]Wu Q A(2007).Determination of Omidazole Suppository by RP-HPLC[J].Chin.MAP.24(8):710-711
    [6]Y Z,W W,C Y,et al(2005).Determination of Compound Ornidazole Emulsion by HPLC.China Pharmaceuticals.14(7):40-40
    [7]林朝晖.HPLC法测定奥硝唑葡萄糖注射液含量及有关物质[J].海峡药学,2003,15(4):45
    [8]田怀平,王美纳.HPLC法测定家兔奥硝唑的血药浓度[J].药学服务与研究,2004,4(3):278
    [9]马传学,孙伟,黄成琼,徐春燕.高效液相色谱法测定奥硝唑栓的含量[J].江苏药学与临床研究,2003,11(4):14
    [10]杨万兴,向明凤.人体血浆中奥硝唑的HPLC测定[J].第三军医大学学报,2004,26(12):1120
    [11]杨征,吴畏,陈雅,舒凌玲.复方奥硝唑乳剂的含量测定[J].药物鉴定,2005,14(7):4
    [12]陈蒂芳,易爱纯,张顺芝.UV法测定奥硝唑分散片的含量[J].中国药事,2004,18(1):44
    [13]钱小蔷.紫外分光光度法测定奥硝唑氯化钠注射液中奥硝唑含量[J].中国药师.2004,7(10):777
    [14]戴助.紫外分光光度法测定奥硝唑乳膏的含量[J].安徽医药,2004,8(1):56
    [15]Li Q B,Qiao M Y(2005).Determination of Ornidazole Sodium Chloride Injection by Differential Spectrophotometry.Strait Pharmaceutical Journal.17(6):77-78
    [16] Liu B, Wang J Z,Chen X (2006). Determination of Ornidazole tablets by fluorescence spectrophotometry. China W C J P S. 21(6): 604—605
    [17] Sun D, Wang H, Wu K B (2006). Electrochemical determination of 10-hydroxycamptothecin using a multi-wall carbon nanotube- modified electrode. Microchim Acta 152: 255
    [18] Peng Y, Lu C, Hu B L(2007). Development of an acetylspiramycin sensor based on a single-walled carbon nanotubes film electrode. Microchim Acta 158:79
    [19] Profumo A, Fagnoni M, Merli D, et al(2006). Multiwalled Carbon Nanotube Chemically Modified Gold Electrode for Inorganic As Speciation and Bi(Ⅲ) Determination. Anal. Chem. 78:4194-4199
    [20] Wan H J, Zou Q L, Yan R, et al(2007). Electrochemistry and voltammetric determination of tannic acid on a single-wall carbon nanotube-coated glassy carbon electrode. Microchim Acta 159: 109-115
    [21] Zhang H J(2004). Fabrication of a single-walled carbon nanotube-modified glassy carbon electrode and its application in the electrochemical determination of epirubicin. Journal of Nanoparticle Research 6:665-669
    [22] Wu F H, Zhao G C, Wei X W, et al (2004). Electrocatalysis of Tryptophan at Multi-Walled Carbon Nanotube Modified Electrode. Microchim. Acta 144:243-247
    [23] Gong K P, Zhang M N, Yan Y M, et al (2004). Sol-Gel-Derived Ceramic-Carbon Nanotube Nanocomposite Electrodes: Tunable Electrode Dimension and Potential Electrochemical Applications. Anal. Chem. 76: 6500-6505
    [24] SunY P, Fu K F, Lin Y, Huang W J (2002). Functionalized CarbonNanotubes: Properties and Applications. Acc. Chem. Res. 35: 1096-1104
    [25] Ooyang M, Huang J L, Lieber C (2002). Fundamental Electronic Properties and Applications of Single-Walled Carbon Nanotubes. Acc. Chem. Res. 35: 1018-1025
    [26] Byon H R, Choi H C(2006). Network Single-Walled Carbon Nanotube-Field Effect Transistors (SWNT-FETs) with Increased Schottky Contact Area for Highly Sensitive Biosensor Applications. J. AM. CHEM. SOC. 128: 2188-2189
    [27] Yang C H (2004),. Electrochemical Determination of 4-Nitrophenol Using a Single-Wall Carbon Nanotube Film-Coated Glassy Carbon Electrode. Microchim. Acta 148: 87-92
    [28] Wei S H, Zhao F Q, Zeng B Z (2005). Electrochemical Behavior and Determination of Uric Acid at Single-Walled Carbon Nanotube Modified Gold Electrodes.Microchim Acta 150:219-224
    [29] Wei S H, Zhao F Q, Xu Z Y, Zeng B Z (2006). Voltammetric Determination of Folic Acid with a Multi-Walled Carbon Nanotube-Modified Gold Electrode. Microchim Acta 152: 285-290
    [30] Wu K B, Fei J J, Hu S S (2003) Simultaneous determination of dopamine and serotonin on the glassy carbon electrode coated with carbon nanotubes film. Anal Biochem. 318: 100
    [31] Valentini F, Orlanducci S, Terranova M L, Amine A, Palleschi G (2004) Carbon nanotubes as electrode materials for the assembling of new electrochemical biosensors. Sens Actuators B 100: 117
    [32] Britto P J, Santhanam K S V, Ajayan P M (1996) Carbon nanotube electrode for oxidation of dopamine. Bioelectrochem Bioenerg 41: 121
    [1]黄波,邹国林,杨天鸣.阿霉素与牛血清白蛋白结合作用的研究[JJ.化学学报.2004,60(10):1867
    [2]陶清,韩莉,徐金光,吕鉴泉.诺氟沙星与牛血清白蛋白相互作用的拉曼光谱研究[J].河南科学,2007,25(3):391
    [3]邱瑾,邵爽,游金宗.荧光法研究奥沙利铂与牛血清白蛋白的相互作用[J].分析测试学报.2007,26(7):51
    [4]邬春华,吕元琦,袁倬斌.大黄酸与牛血清白蛋白相互作用的电化学研究[J].分析测试学报,2004,24(3):73
    [5]胡秋娈,赵风林,李克安.以偶氮胂K光度法测定蛋白质[J].分析测试学报,2000,19(1):45-47.
    [6]]王海人,肖忠柏,宋功武,等.荧光素与牛血清蛋白作用的光谱研究与分析应用[J].分析测试学报,2001,20(4):45-46.
    [7]吴婧,文凌飞,朱兴旺,等.用铍试剂测定人血清白蛋白的分光光度法[J].分析测试学报,1999,20(11):1697-1702.
    [8]WANG Y T,ZHAO F L,LI KA.Microdetermination of proteins by enhanced Rayleigh light scattering spectroscopy with morin[J].Fresenius J Anal Chem,1999,364(6):560-564.
    [9]ZHANG H M,ZHU ZW,Li N Q.Electrochemical studies of the interaction of tetraphenylporphyrin tetrasulfonate(TPPS) with albumin[J].Fresenius J Anal Chem,1999,363(4):408-412.
    [10]SUN W,J IAO K.Linear sweep Voltammetric determination of protein based on its interaction with alizarin red S[J].Talanta,2002,56(6):1073-1080.
    [11]BAO X Y,ZHU Z W,LI N Q,et al.Electrochemical studies of the interaction with hemoglobin and determination of hemoglobin[J].Talanta,2001,54(4):591-596.
    [12]LI Y Q,GUO Y J,LI X F,et al.Electrochemical studies of the interaction of Basic Brown G with DNA and determination of DNA.Talanta,2007,71:123-128.
    [13]李晓燕.用荧光和共振光散射光谱研究甲硝唑与牛血清白蛋白的相互作用[J].物理化学学报,2007,23(2):262-267

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