Arfaj Nawal Al, Abdine Heba H, Sultan Maha A
Department of Chemistry, College of Science, Women Student-Medical Studies and Sciences Sections, King Saud University, P.O. Box 22452, Riyadh 11495, Saudi Arabia;
Int J Biomed Sci. 2007 Jun;3(2):131-6.
A simple and sensitive chemiluminometric method using flow injection (FI) is developed for the determination of carvedilol, based on the reaction of carvedilol with tris (2, 2'-bipyridyl) ruthenium (II), and KMnO4 in sulfuric acid medium. Under the optimum conditions; the chemiluminescence (CL) intensity is a linear function of carvedilol concentration over the range of 0.04-1.0 µg ml(-1) (9.8 × 10(-8) - 2.5 × 10(-6) mol L(-1)) with a detection limit (S/N=3) of 0.025 µgml(-1) (6.2 × 10(-8) mol L(-1)). The relative standard deviation of the proposed method calculated from 10 replicate injections of 0.4 µg ml(-1) carvedilol is 0.95%. The sample throughput is 90 samples h(-1). The method is applied successfully to the determination of carvedilol in tablets dosage form and spiked human plasma.
基于卡维地洛与三(2,2'-联吡啶)钌(II)以及高锰酸钾在硫酸介质中的反应,开发了一种使用流动注射(FI)的简单灵敏的化学发光法来测定卡维地洛。在最佳条件下,化学发光(CL)强度与卡维地洛浓度在0.04 - 1.0 µg ml⁻¹(9.8×10⁻⁸ - 2.5×10⁻⁶ mol L⁻¹)范围内呈线性关系,检测限(S/N = 3)为0.025 µg ml⁻¹(6.2×10⁻⁸ mol L⁻¹)。由0.4 µg ml⁻¹卡维地洛的10次重复进样计算得到的该方法的相对标准偏差为0.95%。样品通量为90个样品 h⁻¹。该方法已成功应用于片剂剂型和加标人血浆中卡维地洛的测定。