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阿霉素吸附在石墨和汞电极表面的氧化还原动力学

Redox kinetics of adriamycin adsorbed on the surface of graphite and mercury electrodes.

作者信息

Komorsky-Lovrić Sebojka

机构信息

Center for Marine and Environmental Research Ruder Bosković Institute, P.O. Box 180 10002, Zagreb, Croatia.

出版信息

Bioelectrochemistry. 2006 Sep;69(1):82-7. doi: 10.1016/j.bioelechem.2005.10.006. Epub 2006 Jan 27.

DOI:10.1016/j.bioelechem.2005.10.006
PMID:16443398
Abstract

Kinetics of the surface redox reactions of adriamycin (doxorubicin hydrochloride) adsorbed on paraffin-impregnated graphite electrode (PIGE) and on mercury electrode is measured by square-wave voltammetry. In 0.9 mol/L KNO3 buffered to pH 4.65, the standard electrode reaction rate constants of the first quinone/hydroquinone redox couple (see Scheme 2) on PIGE and mercury are k(s1)=49+/-12 s(-1) and k(s1)=147+/-36 s(-1), respectively. Under the same conditions, the standard rate constant of the second redox couple on the PIGE is smaller than 4 s(-1) and the electron transfer coefficient of the reduction is alpha2=0.35.

摘要

采用方波伏安法测定了吸附在石蜡浸渍石墨电极(PIGE)和汞电极上的阿霉素(盐酸多柔比星)表面氧化还原反应的动力学。在pH值为4.65的0.9 mol/L硝酸钾缓冲溶液中,PIGE和汞电极上第一个醌/对苯二酚氧化还原对(见方案2)的标准电极反应速率常数分别为k(s1)=49±12 s⁻¹和k(s1)=147±36 s⁻¹。在相同条件下,PIGE上第二个氧化还原对的标准速率常数小于4 s⁻¹,还原反应的电子转移系数α2 = 0.35。

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