Mo J W, Ogorevc B
Analytical Chemistry Laboratory, National Institute of Chemistry, Ljubljana, Slovenia.
Anal Chem. 2001 Mar 15;73(6):1196-202. doi: 10.1021/ac0010882.
Overoxidized poly-(1,2-phenylenediamine) (OPPD)-coated carbon fiber microelectrodes (CFMEs) exhibit, in combination with square-wave voltammetry (SWV) detection mode, the attractive ability to simultaneously measure low nM dopamine (DA) and mM ascorbate (AA) in a pH 7.4 medium. The PPD polymer film is electrodeposited onto a carbon fiber at a constant potential of 0.8 V versus Ag/AgCl using a solution containing sodium dodecylsulfate as the dopant. After overoxidation using cyclic voltammetry (CV) in the potential range from 0 to 2.2 V at a scan rate of 10 V/s, the resulting OPPD-CFME displays a high SWV current response to cationic DA at approximately 0.2 V and has a favorably low response to anionic AA at approximately 0.0 V vs Ag/AgCl. The preparation of the new OPPD-sensing film has been carefully studied and optimized. The OPPD properties and behavior were characterized using CV and SWV under various conditions and are discussed with respect to DA and AA detection. The linear calibration range for DA in the presence of 0.3 mM AA is 50 nM to 10 microM, with a correlation coefficient of 0.998 and a detection limit of 10 nM using 45-s accumulation. The detection limit for DA in the absence of AA was estimated to be 2 nM (S/N = 3). The linear range for AA in the presence of 100 nM DA is 0.2-2 mM, with a correlation coefficient of 0.999 and a detection limit of 80 microM. The reproducibilities of SWV measurements at OPPD-CFCMEs are 1.6% and 2.5% for 100 nM DA and 0.3 mM AA, respectively. Potential interfering agents, such as 3,4-dihydroxyphenylacetic acid, uric acid, oxalate, human serum proteins, and glucose, at their physiologically relevant or higher concentrations did not have any effect. These favorable features offer great promise for in vitro and in vivo application of the proposed OPPD-coated microprobe.
过氧化聚(1,2 - 苯二胺)(OPPD)涂层碳纤维微电极(CFMEs)与方波伏安法(SWV)检测模式相结合,展现出在pH 7.4介质中同时测量低纳摩尔浓度多巴胺(DA)和毫摩尔浓度抗坏血酸(AA)的诱人能力。使用含有十二烷基硫酸钠作为掺杂剂的溶液,在相对于Ag/AgCl为0.8 V的恒定电位下,将PPD聚合物膜电沉积到碳纤维上。在0至2.2 V电位范围内以10 V/s的扫描速率使用循环伏安法(CV)进行过氧化后,所得的OPPD - CFME在相对于Ag/AgCl约0.2 V处对阳离子DA显示出高SWV电流响应,而在约0.0 V处对阴离子AA的响应则低得多。对新型OPPD传感膜的制备进行了仔细研究和优化。在各种条件下使用CV和SWV对OPPD的性质和行为进行了表征,并针对DA和AA检测进行了讨论。在存在0.3 mM AA的情况下,DA的线性校准范围为50 nM至10 microM,相关系数为0.998,使用45秒积累时检测限为10 nM。在不存在AA的情况下,DA的检测限估计为2 nM(S/N = 3)。在存在100 nM DA的情况下,AA的线性范围为0.2 - 2 mM,相关系数为0.999,检测限为80 microM。对于100 nM DA和0.3 mM AA,OPPD - CFCMEs处SWV测量的重现性分别为1.6%和2.5%。潜在的干扰剂,如3,4 - 二羟基苯乙酸、尿酸、草酸盐、人血清蛋白和葡萄糖,在其生理相关浓度或更高浓度下没有任何影响。这些有利特性为所提出的OPPD涂层微探针的体外和体内应用带来了巨大希望。