药学学报
藥學學報
약학학보
ACTA PHARMACEUTICA SINICA
2001年
2期
127-130
,共4页
钱永贵%鲁毅强%胡劲波%毛燕宁%李启隆
錢永貴%魯毅彊%鬍勁波%毛燕寧%李啟隆
전영귀%로의강%호경파%모연저%리계륭
氧氟沙星%电化学行为%Pt离子注入%修饰电极
氧氟沙星%電化學行為%Pt離子註入%脩飾電極
양불사성%전화학행위%Pt리자주입%수식전겁
目的 研究氧氟沙星在Pt/GC离子注入修饰电极上的电化学行为。方法 氧氟沙星在0.40 mol*L-1 KCl溶液中,用Pt/GC离子注入修饰电极进行伏安测定。结果 得到一良好的还原峰,峰电位Ep=-1.35 V(vs SCE)。峰电流与氧氟沙星的浓度在1.0×10-6-3.0×10-5 mol*L-1呈线性关系,相关系数γ=0.9992;检出限为5.0×10-7 mol*L-1。该法用于药片的测定,获得满意结果。用线性扫描和循环伏安法等电化学手段研究体系的电化学行为和电极反应机理。用俄歇电子能谱(AES)、光电子能谱(XPS)和扫描电子显微镜(SEM)等表面分析技术检测了注入电极表面的元素的组成、价态和深度分布,对离子注入电极的催化性质进行了探讨。结论 实验表明,体系属于两电子还原的不可逆过程。
目的 研究氧氟沙星在Pt/GC離子註入脩飾電極上的電化學行為。方法 氧氟沙星在0.40 mol*L-1 KCl溶液中,用Pt/GC離子註入脩飾電極進行伏安測定。結果 得到一良好的還原峰,峰電位Ep=-1.35 V(vs SCE)。峰電流與氧氟沙星的濃度在1.0×10-6-3.0×10-5 mol*L-1呈線性關繫,相關繫數γ=0.9992;檢齣限為5.0×10-7 mol*L-1。該法用于藥片的測定,穫得滿意結果。用線性掃描和循環伏安法等電化學手段研究體繫的電化學行為和電極反應機理。用俄歇電子能譜(AES)、光電子能譜(XPS)和掃描電子顯微鏡(SEM)等錶麵分析技術檢測瞭註入電極錶麵的元素的組成、價態和深度分佈,對離子註入電極的催化性質進行瞭探討。結論 實驗錶明,體繫屬于兩電子還原的不可逆過程。
목적 연구양불사성재Pt/GC리자주입수식전겁상적전화학행위。방법 양불사성재0.40 mol*L-1 KCl용액중,용Pt/GC리자주입수식전겁진행복안측정。결과 득도일량호적환원봉,봉전위Ep=-1.35 V(vs SCE)。봉전류여양불사성적농도재1.0×10-6-3.0×10-5 mol*L-1정선성관계,상관계수γ=0.9992;검출한위5.0×10-7 mol*L-1。해법용우약편적측정,획득만의결과。용선성소묘화순배복안법등전화학수단연구체계적전화학행위화전겁반응궤리。용아헐전자능보(AES)、광전자능보(XPS)화소묘전자현미경(SEM)등표면분석기술검측료주입전겁표면적원소적조성、개태화심도분포,대리자주입전겁적최화성질진행료탐토。결론 실험표명,체계속우량전자환원적불가역과정。
AIM To study the electrochemical behavior of ofloxacin at Pt/GC ion implantation modified electrode. METHODS With Pt/GC ion implantation modified electrode as working electrode, the behavior of ofloxacin was studied by voltammetry in 0.40 mol*L-1 KCl solution. RESULTS A sensitive reductive peak of ofloxacin was obtained by linear sweep voltammetry. The peak potential was -1.35 V (vs SCE). The peak current was proportional to the concentration of ofloxacin over the range of 1.0×10-6-3.0×10-5 mol*L-1 with the detection limit of 5.0×10-7 mol*L-1. The behavior of reduction wave was studied and applied to determination of ofloxacin in tablets. CONCLUSION The reduction process was irreversible. The element composition, atomicity form and depth of distribution at the surface of Pt/GC electrode were determined by Auger electron spectroscopy (AES), X-ray photoelectron spectroscopy (XPS) and scannig electron microscope (SEM). The catalysis behavior and reaction mechanism at Pt/GC modified electrode was also studied.