Signal enhancement and low oxidation potentials for miniaturized ECL biosensors via N-butyldiethanolamine
文献信息
Stefanie Kirschbaum-Harriman, Michael Mayer, Axel Duerkop, Thomas Hirsch
We present studies on ruthenium-based electrochemiluminescence (ECL) focusing on conditions supporting signal enhancement and low oxidation potentials. Low oxidation potentials (LOPs) are especially attractive for miniaturized ECL biosensors, as microfabricated electrodes tend to detach from their support when used with high currents and operated at high potentials. Furthermore, high potentials or current densities can lead to damage of typical biosensor surface coatings and biological probes. The possibility of generating LOP ECL signals at a potential below 900 mV was therefore studied for Ru(bpy)32+ with two typical coreactants, i.e. 2-(dibutylamino)ethanol (DBAE) and tripropylamine (TPA), as well as with the tertiary amine N-butyldiethanolamine (NBEA). Furthermore, the effect of buffer components and pH values on ECL signal generation was investigated. We could show a significant LOP ECL signal for NBEA. We found that Tris buffer, with its ability to form complexes with transition metal ions, has a positive influence on this ECL signal in terms of signal strength and LOP capabilities. Specifically, at basic pH values significant increases in ECL signals were observed at 900 mV and at 1.2 V. In fact, the ECL signal at 1.2 V was three times higher than the signal observed in phosphate buffer at a pH of 7, and it was thirty times higher than the ECL signal for TPA under these conditions. The LOP signal for NBEA in Tris buffer at pH 8.5 was similar to the signal obtained for TPA in phosphate buffer at pH 8.5 but three times higher than for TPA at pH 7.0. Interestingly, the coreactant DBAE was neither significantly influenced by the buffer system or pH nor did it present a valuable LOP ECL signal. Finally, it was found that high peak currents in cyclic voltammograms are not the indicators for high ECL signals, which should be obvious because the ECL mechanism requires more complex electron transfers. Overall, the standard TPA ECL at 1.2 V in phosphate buffer at pH 7.0 can successfully be replaced by NBEA ECL at 900 mV in Tris at pH 8.5 providing significantly higher signals accompanied by more gentle electrochemical conditions.
相关文献
Applying reversible chemistry of CO2 to supramolecular polymers
Heng Xu, Erin M. Hampe, Dmitry M. Rudkevich
DOI: 10.1039/B309580K
Molecular recognition. Self-assembly of molecular trigonal prisms and their host–guest adducts
James D. Crowley, Andrew J. Goshe, Brice Bosnich
DOI: 10.1039/B307385H
Competitive electron transfers from a tyrosyl side-chain and peptide bond in the photodegradation of N-tosyl α-aminomethylamides: an insight into photosynthesis and photodamage in the biological oxidation of water?
Roger R. Hill, Sharon A. Moore, David R. Roberts
DOI: 10.1039/B308525B
Porphyrin ring contraction: a one-pot reaction leading to divalent corroles
Christophe Jeandon, Romain Ruppert, Henry J. Callot
DOI: 10.1039/B400812J
Noncovalent attachment of oxidenanoparticles onto carbon nanotubes using water-in-oil microemulsions
Jing Sun, Lian Gao, Mikio Iwasa
DOI: 10.1039/B400817K
Room temperature borylation of arenes and heteroarenes using stoichiometric amounts of pinacolborane catalyzed by iridium complexes in an inert solvent
Tatsuo Ishiyama, Yusuke Nobuta, John F. Hartwig, Norio Miyaura
DOI: 10.1039/B311103B
Electrochemical lithography: fabrication of nanoscale Si tips by porous anodization of Al/Si wafer
L. Pu, Y. Shi, J. M. Zhu, X. M. Bao, R. Zhang, Y. D. Zheng
DOI: 10.1039/B315810A
Nanoprobe implantation into mammalian cells by cationic transfection
Yan Zhao, Bryce Sadtler, Min Lin, Gregory H. Hockerman, Alexander Wei
DOI: 10.1039/B317061F
Supramolecular assembly of a quaterthiophene surfactant
Lu Jiang, Robert C. Hughes, Darryl Y. Sasaki
DOI: 10.1039/B316657K
Mesoporous iron phosphate as an active, selective and recyclable catalyst for the synthesis of nopol by Prins condensation
Unnikrishnan R. Pillai, Endalkachew Sahle-Demessie
DOI: 10.1039/B313747C
您可能还喜欢
(5-氨基吡唑-3-基)乙酸(CAS号:174891-10-2)的物理化学性质是什么?
(5-氨基吡唑-3-基)乙酸是一种无色至白色固体,分子量为174.15 g/mol。它在水中具有较好的溶解性,在有机溶剂中的溶解度较低。该化合物具有较好的反应活...
3-氟-4,5-二氯苯胺(CAS号:35754-38-2)适用哪些法规指南?
3-氟-4,5-二氯苯胺受到多项法规指南的约束,包括但不限于GHS(全球化学品统一分类和标签制度)的危险分类标准、欧盟的REACH法规(注册、评估、授权和限制)...
什么是(R)-(+)-2,2',6,6'-四甲氧基-4,4'-联(二(3,5-二甲苯基基)膦基)-3,3'-二联吡啶(CAS号:442905-33-1)?
这是一种有机化合物,化学名为(R)-(+)-2,2',6,6'-四甲氧基-4,4'-联(二(3,5-二甲苯基基)膦基)-3,3'-二联吡啶,CAS号为44290...
1-氨基-2-氰基萘(CAS号:3100-67-2)应用于哪些行业?
1-氨基-2-氰基萘在医药、聚合物、传感器和半导体等行业中有应用。在医药领域,它可用作中间体合成某些药物。在聚合物行业,它可以用于制备具有特定性能的聚合物。此外...
如何处理含有1-溴-4-(异丙氧基甲基)苯(CAS号:98446-84-5)的废料?
处理含1-溴-4-(异丙氧基甲基)苯的废料时,首先应确保废液收集在防渗漏的容器中,避免泄露。然后,可以考虑采用化学降解法或物理吸附法进行处理。在特定条件下,可通...
6-Chloro-8-(trifluoromethyl)chroman-4-one(CAS号:1344889-75-3)的主要用途是什么?
6-氯-8-三氟甲基-2,3-二氢-4H-色喃-4-酮主要用于有机合成中的中间体,也可作为研究试剂使用。
7-乙氧基-2-萘酚(CAS号:57944-44-2)通常如何合成?
7-乙氧基-2-萘酚通常通过N-乙氧基化反应合成,首先将2-萘酚与乙醇钠在乙醇中反应生成7-乙氧基-2-萘酚钠盐,再通过酸化进一步得到7-乙氧基-2-萘酚。该合...
4-(1,1-二氧硫代吗啉)丁醇(CAS号:59801-41-1)适用哪些法规指南?
该化合物需遵循一系列的法规指南,包括但不限于GHS全球统一分类和标签制度,其分类可能包括易燃液体和可能危害水生环境。在欧洲,还需遵循REACH法规,确保物质和混...
4-甲氧基苄基叠氮甲酸酯(CAS号:25474-85-5)的物理化学性质是什么?
4-甲氧基苄基叠氮甲酸酯是一种无色液体,具有一定的挥发性。其分子量为198.16,熔点为-69°C,沸点为105°C。该化合物在水中溶解度较低,在有机溶剂如乙醇...
如何处理含有4-氯-2-氟嘧啶(CAS号:51422-00-5)的废料?
含有4-氯-2-氟嘧啶的废料应按照危险废物处理。首先,应收集并分类这些废料,避免与其他废物混合。然后,可以采用焚烧处理或者交由专业机构进行处置。在处理过程中,需...
来源期刊
Analyst

Analyst publishes analytical and bioanalytical research that reports premier fundamental discoveries and inventions, and the applications of those discoveries, unconfined by traditional discipline barriers.














