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出 处:《分析测试学报》2007年第3期352-355,共4页Journal of Instrumental Analysis
基 金:河南省自然科学基金(0511020300);河南省科技攻关项目资助(20055001)
摘 要:建立灵敏快速测定氯唑沙宗的新方法。在0.24mol·L^-1 KH2P04-Na2HPO4(pH6.81±0.1)支持电解质中,氯唑沙宗于0.80V(vs.SCE)电位处产生一还原波。加入过二硫酸钾后,该还原波峰电流增加约10倍,峰电位基本不变,产生一极谱催化波。其二阶导数峰电流Ip"与氯唑沙宗的浓度在2.0×10^-7~8.0×10^-5mo1·L^-1范围内呈良好线性关系(r=0.9981,n=8),检出限为1.0×10^-7mol·L^-1。该方法可用于药剂中氯唑沙宗含量的测定。A novel method for the determination of chlorzoxazone is established. The reduction wave of chlorzoxazone appears at 0.80 V (vs. SCE) in 0. 24 mol · L^- 1 KH2PO4 - Na2 HPO4 ( pH 6. 81 ± 0. 1 ) supporting electrolyte. In the presence of 0. 01 mol · L^-1 K2S2O8, the reduction wave is catalyzed to produce a parallel catalytic wave. The peak current of the catalytic wave is 10 times higher than that of the corresponding reduction wave. Based on the catalytic wave, a novel method for the determination of chlorzoxazone is proposed. The peak current of the catalytic wave is rectilinear to chlorzoxazone concentration in the range of 2. 0 × 10^-7 -8.0 × 10 ^-5 mol · L^-1. The detection limit is 1.0 ×10^-7 mol · L^-1 The proposed method can be applied to the direct determination of chlorzoxazone in pharmaceuticals and urine without preliminary separation.
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