Yarman Aysu, Scheller Frieder W
Fraunhofer Institute for Biomedical Engineering IBMT, Am Mühlenberg 13, 14476 Potsdam, Germany.
Sensors (Basel). 2014 Apr 25;14(5):7647-54. doi: 10.3390/s140507647.
We present an electrochemical MIP sensor for tamoxifen (TAM)-a nonsteroidal anti-estrogen-which is based on the electropolymerisation of an O-phenylenediamine‒resorcinol mixture directly on the electrode surface in the presence of the template molecule. Up to now only "bulk" MIPs for TAM have been described in literature, which are applied for separation in chromatography columns. Electro-polymerisation of the monomers in the presence of TAM generated a film which completely suppressed the reduction of ferricyanide. Removal of the template gave a markedly increased ferricyanide signal, which was again suppressed after rebinding as expected for filling of the cavities by target binding. The decrease of the ferricyanide peak of the MIP electrode depended linearly on the TAM concentration between 1 and 100 nM. The TAM-imprinted electrode showed a 2.3 times higher recognition of the template molecule itself as compared to its metabolite 4-hydroxytamoxifen and no cross-reactivity with the anticancer drug doxorubucin was found. Measurements at +1.1 V caused a fouling of the electrode surface, whilst pretreatment of TAM with peroxide in presence of HRP generated an oxidation product which was reducible at 0 mV, thus circumventing the polymer formation and electrochemical interferences.
我们展示了一种用于他莫昔芬(TAM)——一种非甾体抗雌激素药物——的电化学分子印迹聚合物(MIP)传感器,该传感器基于在模板分子存在下,邻苯二胺-间苯二酚混合物直接在电极表面进行电聚合。到目前为止,文献中仅描述了用于TAM的“本体”MIP,它们用于色谱柱中的分离。在TAM存在下,单体的电聚合产生了一层完全抑制铁氰化物还原的薄膜。去除模板后,铁氰化物信号显著增加,再次结合目标物后信号如预期那样因空穴被目标物填充而再次受到抑制。MIP电极铁氰化物峰的降低与1至100 nM之间的TAM浓度呈线性关系。与代谢物4-羟基他莫昔芬相比,TAM印迹电极对模板分子本身的识别能力高2.3倍,并且未发现与抗癌药物阿霉素有交叉反应。在 +1.1 V下进行测量会导致电极表面污染,而在辣根过氧化物酶(HRP)存在下用过氧化物预处理TAM会产生一种可在0 mV下还原的氧化产物,从而避免聚合物形成和电化学干扰。