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作 者:林雁[1] 阮顺强[1] 詹雪果[1] 潘林琳[1] 韦寿莲[1]
出 处:《广东化工》2004年第6期16-18,共3页Guangdong Chemical Industry
摘 要:在0.66mol/L KCl(pH=6.70)的底液中,哌拉西林钠在汞电极上有一灵敏的导数还原峰,其峰电位Ep=-1.23V(vs.SCE).峰电流与哌拉西林钠的浓度在8.0×10-6至7.0×10-8mol/L范围内呈良好线性关系(r=0.9992),检出限为4.5×10-8mol/L,该法应用于注射用哌拉西林钠中哌拉西林钠含量的测定,结果令人满意。实验表明,该体系为一具有吸附性的不可逆过程。In a supporting electrolyte containing 0.66 mol/L KCl(pH=6.70), a sensitive reduction peak of piperacillin sodium was found by single-sweep oscillopolarography. The peak potential of piperacillin sodium was -1.23v(vs.SCE). There was satisfactory linear relationship between peak current and the concentration of analytes in the concentration range of 8.0×10-6-7.0×10-8 mol/L(r=0.9992) for pipercillin sodium with the detection limits of 4.5×10-8 mol/L. The methods were applied to the determination of piperacillin sodiumin the sample of drugs with satisfactory results. This indicated an irreversilde process with adsorption.
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