Kuroda Yukihiro, Yukinaga Hideo, Kitano Masahiro, Noguchi Taeko, Nemati Mahboob, Shibukawa Akimasa, Nakagawa Terumichi, Matsuzaki Katsumi
Graduate School of Pharmaceutical Sciences, Kyoto University, Kyoto 606 8501, Japan.
J Pharm Biomed Anal. 2005 Mar 9;37(3):423-8. doi: 10.1016/j.jpba.2004.11.025. Epub 2004 Dec 22.
On-line capillary isoelectric focusing-mass spectrometry (cIEF-MS) was applied to determine concentrations of peptides and proteins using angiotensin II and human tetrasialo-transferrin as the model samples. The concentration of the carrier ampholyte was optimized for both resolution and ion intensity. cIEF-MS employing 1% Pharmalyte 3-10 and a sheath liquid containing water/methanol/acetic acid (50/49/1) resolved angiotensin I and II (5 microM each, DeltapI=0.2) at an Rs value of 2.29. The determined concentration of angiotensin II (0.1-5 microM) well correlated (R=0.999) with that obtained by the conventional RP-HPLC method. The limit of detection was 0.22 microM, which was about 10 times lower than that by UV detection (2 microM). The repeatability and accuracy were <15 and <11%, respectively. cIEF-MS was also applied to determine human tetrasialo-transferrin concentration. The good linearity (R2=0.998) was also observed between the transferrin concentration (0.5-1.2 g/L) and peak area ratio (IS; beta-lactoglobulin B) with acceptable accuracy (<1.9%) and repeatability ( approximately 10% at 1g/L).
采用在线毛细管等电聚焦-质谱联用技术(cIEF-MS),以血管紧张素II和人四唾液酸转铁蛋白为模型样品,测定肽和蛋白质的浓度。对载体两性电解质的浓度进行了优化,以兼顾分离度和离子强度。采用1%的Pharmalyte 3-10和含有水/甲醇/乙酸(50/49/1)的鞘液的cIEF-MS,在Rs值为2.29时分离了血管紧张素I和II(各5 microM,ΔpI = 0.2)。所测定的血管紧张素II浓度(0.1 - 5 microM)与通过传统反相高效液相色谱法(RP-HPLC)测得的浓度具有良好的相关性(R = 0.999)。检测限为0.22 microM,约为紫外检测法(2 microM)的十分之一。重复性和准确度分别<15%和<11%。cIEF-MS还用于测定人四唾液酸转铁蛋白的浓度。在转铁蛋白浓度(0.5 - 1.2 g/L)与峰面积比(内标;β-乳球蛋白B)之间也观察到了良好的线性关系(R2 = 0.998),准确度(<1.9%)和重复性(1g/L时约为10%)均可接受。