Box Karl, Bevan Christopher, Comer John, Hill Alan, Allen Ruth, Reynolds Derek
Sirius Analytical Instruments Ltd., Riverside, Forest Row Business Park, Forest Row, East Sussex, RH18 5DW, United Kingdom.
Anal Chem. 2003 Feb 15;75(4):883-92. doi: 10.1021/ac020329y.
A procedure is described for measuring pKa values in a short time, e.g., 4 min/assay. Samples, as 10 mM solutions, are prepared in DMSO in 96-well plates. A flowing pH gradient is produced by mixing two buffer solutions containing mixtures of weak acids and bases that do not absorb significantly in the UV above 250 nm. The sample solution is diluted with water and then injected directly into the flowing gradient, which then passes through a diode array spectrophotometer measuring in the UV wavelength range. The buffer has been formulated so that its acid-base titration curve is linear over a wide pH range, such that the pH of the gradient is a linear function of time. The solution pH in the measurement flow cell is therefore proportional to the time elapsed since the start of gradient generation. The sample's pKa values are calculated from the change in UV absorbance at multiple wavelengths as a function of pH. The pKa values of 71 drugs have been measured, and results compare well with values measured by pH-metric or traditional UV methods. Rules are suggested for the rapid inspection of data and the choice of method for the calculation of pKa from the data.
本文描述了一种可在短时间内(例如,每次测定4分钟)测量pKa值的方法。将样品配制成10 mM的二甲基亚砜(DMSO)溶液,置于96孔板中。通过混合两种缓冲溶液产生流动的pH梯度,这两种缓冲溶液含有在250 nm以上紫外光区无显著吸收的弱酸和弱碱混合物。样品溶液用水稀释后直接注入流动梯度中,然后通过在紫外波长范围内进行测量的二极管阵列分光光度计。所配制的缓冲液使其酸碱滴定曲线在较宽的pH范围内呈线性,从而使梯度的pH值是时间的线性函数。因此,测量流通池中的溶液pH值与自梯度产生开始所经过的时间成正比。根据多个波长下紫外吸光度随pH值的变化计算样品的pKa值。已测量了71种药物的pKa值,结果与通过pH滴定法或传统紫外法测得的值相比吻合良好。文中还给出了快速检查数据以及从数据计算pKa值时方法选择的建议。