Brouwer E, Verweij J, Hauns B, Loos W J, Nooter K, Mross K, Stoter G, Sparreboom A
Department of Medical Oncology, University Hospital Rotterdam, Rotterdam, 3008 AE, The Netherlands.
Anal Biochem. 1998 Aug 1;261(2):198-202. doi: 10.1006/abio.1998.2746.
Cremophor EL (CrEL) is a polyoxyethylated castor oil surfactant used in the intravenous formulation of the anticancer drug paclitaxel (Taxol). Quantitative determination of CrEL in patient samples can be achieved by complexation of the compound with the Coomassie brilliant blue G-250 dye in protein-free extracts [Sparreboom, A., Loos, W. J., Verweij, J., De Vos, A. I., Van der Burg, M. E. L., Stoter, G., and Nooter, K., Anal. Biochem. 255, 171-175 (1998)]. A disadvantage of this method of CrEL determination is that the assay plot of absorbance at 595 nm, the peak wavelength of the CrEL-dye complex, versus the concentration of the surfactant is not linear. The present study shows that the nonlinearity is associated with a decrease in the free dye concentration and a reduction in complex formation by increasing the CrEL concentration. By measurement of the ratio of absorbances at the maxima of the red (450 nm) and blue charge forms (595 nm) of Coomassie brilliant blue G-250, a full-scale linear relationship can be obtained over the entire range studied (0.500 to 10.0 microliter/mL). Validation data revealed that transformation of the detection procedure exhibits significantly improved specificity, accuracy(</= 6.33% relative error), and precision (< 10.0%) compared to our previous assay. The modified method was successfully applied to the measurement of CrEL in plasma of 11 cancer patients treated with a 1-h infusion of paclitaxel.
聚氧乙烯蓖麻油(CrEL)是一种聚氧乙烯化蓖麻油表面活性剂,用于抗癌药物紫杉醇(泰素)的静脉制剂中。通过在无蛋白提取物中使该化合物与考马斯亮蓝G - 250染料络合,可实现对患者样品中CrEL的定量测定[Sparreboom, A., Loos, W. J., Verweij, J., De Vos, A. I., Van der Burg, M. E. L., Stoter, G., and Nooter, K., Anal. Biochem. 255, 171 - 175 (1998)]。这种CrEL测定方法的一个缺点是,在595 nm(CrEL - 染料络合物的峰值波长)处吸光度与表面活性剂浓度的测定曲线不是线性的。本研究表明,这种非线性与游离染料浓度的降低以及随着CrEL浓度增加络合物形成的减少有关。通过测量考马斯亮蓝G - 250红色(450 nm)和蓝色电荷形式(595 nm)最大吸光度的比值,在整个研究范围内(0.500至10.0微升/毫升)可获得全量程线性关系。验证数据表明,与我们之前的测定方法相比,检测程序的转变显示出特异性、准确度(相对误差≤6.33%)和精密度(<10.0%)显著提高。改良后的方法成功应用于11例接受1小时紫杉醇输注治疗的癌症患者血浆中CrEL的测定。