Department of Chemistry and ‡MOAC Doctoral Training Centre, University of Warwick , Coventry, CV4 7AL, United Kingdom.
Anal Chem. 2017 Mar 7;89(5):3021-3028. doi: 10.1021/acs.analchem.6b04629. Epub 2017 Feb 10.
A multifunctional dual-channel scanning probe nanopipet that enables simultaneous scanning ion conductance microscopy (SICM) and scanning electrochemical microscopy (SECM) measurements is demonstrated to have powerful new capabilities for spatially mapping the uptake of molecules of interest at living cells. One barrel of the probe is filled with electrolyte and the molecules of interest and is open to the bulk solution for both topographical feedback and local delivery to a target interface, while a solid carbon electrode in the other barrel measures the local concentration and flux of the delivered molecules. This setup allows differentiation in molecular uptake rate across several regions of single cells with individual measurements at nanoscale resolution. Further, operating in a "hopping mode", where the probe is translated toward the interface (cell) at each point allows self-referencing to be employed, in which the carbon electrode response is calibrated at each and every pixel in bulk for comparison to the measurement near the surface. This is particularly important for measurements in living systems where an electrode response may change over time. Finite element method (FEM) modeling places the technique on a quantitative footing to allow the response of the carbon electrode and local delivery rates to be quantified. The technique is extremely versatile, with the local delivery of molecules highly tunable via control of the SICM bias to promote or restrict migration from the pipet orifice. It is expected to have a myriad of applications from drug delivery to screening catalysts.
一种多功能双通道扫描探针纳米管,能够同时进行扫描离子电导显微镜(SICM)和扫描电化学显微镜(SECM)测量,被证明具有强大的新功能,可用于空间绘制活细胞中感兴趣分子的摄取情况。探针的一个桶中充满了电解质和感兴趣的分子,并与主体溶液相通,以进行形貌反馈和局部输送到目标界面,而另一个桶中的固体碳电极则测量输送分子的局部浓度和通量。这种设置允许在单个细胞的几个区域进行分子摄取率的区分,具有纳米级分辨率的单个测量。此外,在“跳跃模式”下操作,探针在每个点都向界面(细胞)移动,允许采用自参考,其中在每个像素处校准碳电极响应,以便与表面附近的测量进行比较。对于活系统中的测量,这一点尤其重要,因为电极响应可能随时间而变化。有限元方法(FEM)建模使该技术具有定量基础,能够定量碳电极的响应和局部输送速率。该技术非常通用,通过控制 SICM 偏压,可以高度调节局部输送分子,以促进或限制从探针尖端的迁移。预计它将有从药物输送到筛选催化剂的众多应用。