Department of Chemistry, University of Warwick, Coventry CV4 7AL, United Kingdom.
Langmuir. 2010 Mar 16;26(6):4004-12. doi: 10.1021/la903438p.
Evanescent wave cavity ring-down spectroscopy (EW-CRDS) has been used to study in situ the kinetics of the adsorption of 5,10,15,20-tetrakis(4-N-methylpyridiniumyl)porphyrin (TMPyP) from pH 7.4 phosphate buffer solution (PBS) to the silica-water interface and the interaction of calf thymus DNA (CT-DNA) with the resulting TMPyP-functionalized surface. TMPyP was delivered to the silica surface using an impinging jet technique to allow relatively fast surface kinetics to be accessed. Adsorption was first-order in TMPyP, and the initial adsorption rate constant at the bare surface was found to be k = (4.1 +/- 0.6) x 10(-2) cm s(-1). A deceleration in the adsorption kinetics was observed at longer times that could be described semiquantitatively using an Elovich-type kinetic expression. The limiting value of the absorbance corresponded approximately to monolayer coverage (6.2 x 10(13) molecules cm(-2)). Exposure of the TMPyP-modified silica surface to CT-DNA, achieved by flowing CT-DNA solution over the functionalized surface, resulted in efficient desorption of the TMPyP. The desorption process was driven by the interaction of TMPyP with CT-DNA, which UV-vis spectroscopy indicated involved intercalative binding. The desorption kinetics were also simulated using complementary finite element modeling of convection-diffusion coupled to a surface process.
消逝波腔衰荡光谱(EW-CRDS)已被用于原位研究 5,10,15,20-四(4-N-甲基吡啶基)卟啉(TMPyP)从 pH 7.4 磷酸盐缓冲溶液(PBS)到二氧化硅-水界面的吸附动力学以及小牛胸腺 DNA(CT-DNA)与所得 TMPyP 功能化表面的相互作用。TMPyP 被传递到二氧化硅表面,使用撞击射流技术来允许相对较快的表面动力学得到访问。吸附在 TMPyP 中是一级的,并且在裸表面上的初始吸附速率常数被发现为 k =(4.1 +/- 0.6)x 10(-2) cm s(-1)。在较长时间内观察到吸附动力学的减速,可以使用 Elovich 型动力学表达式进行半定量描述。吸光度的极限值大约对应于单层覆盖(6.2 x 10(13)分子 cm(-2))。通过将 CT-DNA 溶液流过功能化表面,将 TMPyP 修饰的二氧化硅表面暴露于 CT-DNA,导致 TMPyP 的有效解吸。解吸过程由 TMPyP 与 CT-DNA 的相互作用驱动,这表明涉及插入结合的紫外可见光谱。解吸动力学也使用对流-扩散与表面过程耦合的补充有限元建模进行了模拟。